Tuesday, January 31, 2012

List of Supplements Related to T21

Now you have all the different posts on supplements, all in one place! I put them in order of which ones are most commonly used to treat Down syndrome as well as a couple of categories. You can find another list with lots of info at riverbendds.org. Just click the "Supplements & Drugs" folder on the right.


31 Year Old Study Supports Vitamin Therapy

Signs of Nutritional Deficiency

Which Multivitamin for the Down syndrome population?

How Much Vitamin D3?

Folic Acid Cut Alzheimer’s Risk in Half

Why B12 & Folinic Acid for Down syndrome?

Fermented Cod Liver Oil

Coconut Oil Info and Recipes

Probiotic/Yogurt Strains: Benefits and Uses

Gingko: The Hows and Whys for Down Syndrome

Longvida Curcumin

Pregnant & Nursing Moms Need Choline to Help Baby

Fats & Oils

Why supplement and monitor zinc?

Changing Minds Foundation Protocol

Jett's Complete Supplement List

Vitamin C Plays Important Role in Brain Function

Glutathione

Glyconutrients

The Importance of Magnesium

L-tyrosine: Building Block for Neurochemicals

Coenzyme Q10

Piracetam (not a supplement, an over the counter drug)

EGCG Green Tea Extract For Memory

Why Rhodiola Rosea?

Ashwagandha: Good for Brain

Roobios Tea Protects Brain Against CNS Damage

Goji Berries

Astragalus Promotes Growth Hormone Release

Noggin and BDNF Promotes Neurogenesis

How to Prevent DS in Your Next Child in 60% of Moms

Natural Ways to Help with ADD & Hyperactivity

Acetyl -L Carnitine (ALC)

Phosphatidylserine

Ginseng: Benefits to the Brain

Wild Blueberry Extract

Cinnamon can prevent and cure Alzheimer's

Why Evening Primrose Oil?

Why Milk Thistle?

Feed Memory by Kan Herb

Vinpocetine

DMAE (Dimethylaminoethanol)

Bacopa Monera Extract (BME)

Stimulating Growth

Why L-Carnosine for the T21 Population?

NeuroProtek

Royal Jelly for Neurogenesis

Monday, January 30, 2012

31 Year Old Study Supports Vitamin Therapy for Children w/DS

This article was recently brought to my attention:  Can nutritional supplements help mentally retarded children? An exploratory study. by Harrell RF, Capp RH, Davis DR, Peerless J, and Ravitz LR. Proceedings of the National Academy of Sciences USA, 1981. 78: 574–8. 
Abstract:
To explore the hypothesis that mental retardations are in part genetotrophic diseases (diseases in which the genetic pattern of the afflicted individual requires an augmented supply of one or more nutrients such that when these nutrients are adequately supplied the disease is ameliorated), we carried out a partially double-blind experiment with 16 retarded children (initial IQs, approximately 17-70) of school age who wee given nutritional supplements or placebos during a period of 8 months. The supplement contained 8 minerals in moderate amounts and 11 vitamins, mostly in relatively large amounts. During the first 4- month period (double-blind) the 5 children who received supplements increased their average IQ by 5.0-9.6, depending on the investigator, whereas the 11 subjects given placebos showed negligible change. The difference between these two groups is statistically significant (P less than 0.05). During the second period, the subjects who had been given placebos in the first study received supplements; they showed an average IQ increase of at least 10.2, a highly significant gain (P less than 0.001). Three of the five subjects who were given supplements for both periods showed additional IQ gains during the second 4 months. Three of four children with Down syndrome gained between 10 and 25 units in IQ and also showed physical changes toward normal. Other evidence suggests that the supplement improved visual acuity in two children and increased growth rates. These results support the hypothesis that mental retardations are in part genetotrophic in origin.
Since this study is 31 years old (!!) I was wondering why it's not more widely referenced. Then, I came upon this excellent article by Andrew W. Saul at doctoryourself.com:

The Pioneering Work of Ruth Flinn Harrell: Champion of Children
by Andrew W. Saul

(from the Journal of Orthomolecular Medicine, 2004. Vol 19, No 1, p. 21-26.)
The person who says it cannot be done should not interrupt the person doing it. (Chinese proverb.)


Early in 1981, the medical and educational establishments were shaken to their socks. Ruth F. Harrell and colleagues, in Proceedings of the National Academy of Sciences (1), showed that high doses of vitamins improved intelligence and educational performance in learning disabled children, including those with Down syndrome. Though to many observers this seemingly came straight out of left field, Dr. Harrell, who had been investigating vitamin effects on learning for forty years, was not inventing the idea of megavitamin therapy in one paper. But she had at last succeeded in focusing much-needed public attention on the role of nutrition in learning disabilities, a problem that ink-well-era US RDA's and pharmaceuticals by the lunchbox-full have failed to solve.
The start of the second World War was breaking news when Ruth Flinn Harrell conducted her first investigations into what she called "superfeeding." Her 1942 Columbia University PhD thesis, "Effect of Added Thiamine on Learning" (2), was published by the university in 1943 and would be followed by "Further Effects of Added Thiamine on Learning and Other Processes" in 1947 (3). Her research was not about enriched or fortified foods; "added" meant "provided by supplement tablets." World War II had just ended when Dr. Harrell stated in a 1946 Journal of Nutrition article (4) that "a liberal thiamine intake improved a number of mental and physical skills of orphanage children." By 1956, Dr. Harrell had investigated "The Effect of Mothers' Diets on the Intelligence of Offspring" (5), finding that "supplementation of the pregnant and lactating mothers' diet by vitamins increased the intelligence quotients of their offspring at three and four years of age."
THIAMINE (Vitamin B-1)
Most everyone has heard of beri-beri, and few are all that passionate about it anymore. But beri-beri, which literally means "I can't, I can't," may all too well describe the learning disabled child. Such children, recognized as truly disabled by the Americans with Disabilities Act, are not unwilling but rather unable to perform well in school. To see the physical incapacitation thiamine deficiency causes in impoverished countries is all too easy. To see the mental incapacitation in American classrooms is not difficult, either. Yet both may be caused by thiamine deficiency, and both helped by thiamine supplementation. Harrell zeroed in on this topic sixty years ago, demonstrating that supplemental thiamine improves learning. One reporter wrote, "An experiment was conducted by Dr. Ruth Flinn Harrell which involved 104 children from nine to nineteen years of age. Half of the children were given a vitamin B1 (thiamine) pill each day, and the other half received a placebo. The test lasted 6 weeks. It was found by a series of tests that the group that was given the vitamin gained one-fourth more in learning ability than did the other group." (6)
Carbohydrates, including sugar, increase the body's need for thiamine. Children eat a lot of sugar. An unmet increase is effectively the same as a deficiency. This may be part of the mechanism of ADHD and other children's learning and behavior disorders, as many so-called "food faddists" or "health nuts" have proclaimed for decades. Vitamin deficiency can become vitamin dependency. Chronic subclinical beri-beri may result in thiamine dependency in the same way that chronic subclinical pellegra results in niacin dependency.

B-COMPLEX
The B-vitamins as a group are absolutely vital to nerve function, and it would be difficult to imagine the juvenile owner of malnourished nerves performing well in school. Specifically, it is well established that thiamine deficiency causes not only loss of nerve function and ultimately paralysis, but also according to The Nutrition Desk Reference (7), "memory loss, reduced attention span, irritability, confusion and depression." (p 43) Riboflavin (B-2) deficiency causes "nerve tissue damage that may manifest itself as depression and hysteria." (p 45) Niacin (B-3) deficiency causes "loss of memory and emotional instability." (p 46) Pyridoxine (B-6) deficiency results in "impaired production of neurotransmitters (and) mental confusion." (p 48) Folic acid deficiency causes irritability, apathy, forgetfulness and hostility. (p 49). Cobalamin (B-12) deficiency causes "degeneration of the spinal cord, fatigue, disorientation, ataxia, moodiness, and confusion." (p 51)
Though these symptoms generally appear after prolonged deficiency, they are very serious and, if untreated, the ultimate result in each case would be death. Practically speaking, a shortage of any one of the B-vitamins can be seen to lead to neurological damage sufficient to contribute to learning and behavioral troubles.
Harrell recognized that thiamine and the rest of the vitamins work better as a team. She used two clinically effective but oft-criticized therapeutic nutrition techniques: simultaneous supplementation with many nutrients (the "shotgun" approach), and megadoses. Working on the reasonable assumption that learning disabled children, because of functional deficiencies, might need higher than normal levels of nutrients, she progressed from her initial emphasis on thiamine to later providing a wide variety of supplemental nutrients.

DEFICIENCY DEBATE
The only escape from the inevitability of concluding that vitamin deficiency is a serious factor in learning is the political one: declare a victory. Dodging the issue is as easy as proclaiming that, thanks to food fortification (coupled with a generous portion of wishful thinking), no child has such deficiencies. Though the processed food industry and its apologists continue to assert exactly this, statistics fail to bear this out.
An analysis of National Health and Nutrition Examination Survey (NHANES III) data from 1988 to 1994 by Gladys Block, PhD, indicates that over 85 percent of American elementary school-age children fail to eat the recommended five or more daily servings of fruits and vegetables. "NHANES III, a federally sponsored survey shows that on any given day, 45 percent of children eat no fruit, and 20 percent eat less than one serving of vegetables. The average 6 to 11 year-old eats only 3.5 servings of fruits and vegetables each day, achieving only half the recommended 7 servings per day for this age group." (8) Additionally, Dr. Block reports, 20% of children's caloric intake comes from junk snacks, such as soda pop, cookies, and candy.
Though it is a stretch to say that all learning and behavioral disabilities are due to inadequate vitamin intake, it is certain that some are. Behavioral deficiency tends to show up before nutritional deficiency is recognized. Arthur Winter, MD, writes that "In thiamine (vitamin B1) deficiency, symptoms such as lack of well being, anxiety, hysteria, depression, and loss of appetite preceded any clinical evidence of beriberi. Other studies using the Minnesota Multiphasic Personal Index (MMPI) have also demonstrated that adverse behavioral changes precede physical findings in thiamine deficiency." (9)

DOSAGE DEBATE
Dr. Harrell anticipated that her use of megadoses would result in "controversy and brickbats." (10) She was right. A number of well-publicized studies (11-15) conducted to "replicate" Dr. Harrell's work seemingly could not do so. Would-be "replications" fail the moment they start when they refuse to use adequate dosages. Surely it is the most basic condition for any replication that one must exactly copy the original experiment, or it is not a replication at all. When DNA replicates, it forms an exact and indistinguishable copy of the original. Even the smallest of changes can result in dysfunction, mutation, and death. Yet Harrell's "replicators" failed to adhere to her protocol, and consequently but not surprisingly, failed to get her results. (16)
Probably one of the closer replications was done by Smith et al (17) and even that study totally omitted dessicated thyroid, a component of the Harrell protocol that her coauthor Donald R. Davis, PhD, says was "emphasized to Smith (as) Harrell's subjects received thyroid continuously." (18)
F. Jack Warner, MD, a supporter the Harrell approach (19) writes: "Even today many medical professionals scoff at the validity of Dr. Ruth Harrell's study with nutritional supplements and the important addition of thyroid medication. Dr. Harrell pleaded with her replicators to use exactly the same chemical values of supplements and medications. To date, this still has not been accomplished." (20) In spite of obvious bias, negative "replication" studies using incomplete or low doses are the ones that have been accepted, and Harrell's work shelved. This is saying that the results of inaccurate replication are more valuable than the original successful research. Imagine cloning a sheep, getting a hedgehog, and then claiming that it was the sheep's fault. Incredible. But that is what politicized medical apologetics are capable of.
The Harrell study was successful because her team gave learning-disabled kids much larger doses of vitamins than other researchers are inclined to use: over 100 times the adult (not child's) RDA for riboflavin; 37 times the RDA for niacin (given as niacinamide); 40 times the RDA for vitamin E; and 150 times the RDA for thiamine. Supplemental minerals were also given, as was natural dessicated thyroid. Harrell's team achieved results that were statistically significant, some with confidence levels so high that there was less than on chance in a thousand that the results were due to chance (P < 0.001) Simply stated, Ruth Harrell found IQ to be proportional to nutrient dosage. This may simultaneously be the most elementary and also the most controversial mathematical equation in medicine.
There is a tone to the controversy that does more than merely suggest that Harrell's research was careless or incompetent. This is unlikely in the extreme; Dr. Harrell, formerly the chairman of the psychology department at Old Dominion University, had been studying children before many of her critics were even born. What is more likely is that Harrell's critics embrace the assumption that medicine must ultimately prove to be the better approach, and if there are any megadoses to be given, they shall be megadoses of pharmaceutical products. Vitamin therapy is unattractive to pharmaceutical companies. There is no money in products that cannot be patented. Children learn at an early age that mud pies don't sell. No investment is made, no research is done where no money is to be recovered. Drug companies do not expect to find, nor do they want to find, a cure that does not involve a drug. A tragic example is modern medicine's approach to Down syndrome.

DOWN SYNDROME
If there is orthodox resistance to using vitamins to enhance student learning, there is positively a fortified roadblock to the suggestion that vitamins can help children with Down syndrome. Nutrition, critics say, can not undo trisomy 21. But nutritional therapy is not a science-fiction attempt to rearrange chromosomes. Nutritional intervention may help the body to biochemically compensate for a genetic handicap. Roger Williams, discoverer of the vitamin pantothenic acid, termed this the "genetotrophic concept." Genetotrophic diseases are "diseases in which the genetic pattern of the afflicted individual requires an augmented supply of one or more nutrients such that when these nutrients are adequately supplied the disease is ameliorated." (1) Ruth Harrell's decades of research showed that it is plausible. Conventional Down syndrome educational material holds that it is hogwash.
As of August 2003, the National Down Syndrome Society's "Position Statement on Vitamin Related Therapies" states that "Despite the large sums of money which concerned parents have spent for such treatments in the hope that the conditions of their child with Down syndrome would be bettered, there is no evidence that any such benefit has been produced." (21)
At the heart of the issue are the usual, and largely philosophical, front-line disagreements of definition and interpretation. First, what precisely constitutes a "deficiency" in a society that, as nutritional legend would have it, has eliminated vitamin deficiency? Adherents of conventional dietetics presuppose that anyone who claims that there are widespread vitamin deficiencies among children must proceed from a false assumption. Those who advocate vitamin therapy would answer that Down's creates a "functional deficiency" which must be met with appropriate supplementation. The very idea that doses sufficiently high to effectively do so should be 100 times the RDA is positively repellent to most investigators. When asked about whether she had received National Institutes of Health funding for her study, Dr. Harrell replied, "Heavens, no! Nobody knows anything about the area of dietary supplementation, but the National Institutes of Health knows for sure it's impossible." (10)
Some reviews of Down nutrition studies actually state that doses as low as 500 mg of vitamin C are unsafe, and that other Harrell-sized dosages are harmful as well. In one such article posted at the Down Syndrome Information Network, the authors conclude that "If it is necessary for additional vitamins to be given to someone with Down syndrome, all that is usually needed is a multivitamin tablet, not more than once a day, at a cost of about one penny per tablet. Meanwhile, the best nutritional advice anyone can honestly offer is to consume a varied and balanced diet - whether you have Down syndrome or not." (22)
Another popular argument is that, even allowing that children eat poorly, there is insufficient evidence that Downs is aggravated by poor nutrition, or helped by good nutrition. After all, Downs is a genetically-determined disease. But surely the genes do not operate in a nutrient vacuum. For example, vitamin E has recently been demonstrated to preferentially protect genetic material in Down patients' cells. "Vitamin E treatment decreased the basal and G2 chromosomal aberrations both in control and Down Syndrome (DS) lymphocytes. In DS cells, this protective effect, expressed as a decrease in the chromosomal damage, was greater (50%) than in controls (30%). These results suggest that the increment in basal and G2 aberrations yield in DS lymphocytes may be related to the increase in oxidative damage reported in these patients." The results would also suggest that antioxidant vitamin supplements would be an especially good idea for Down's individuals. (23)
Although the greater question may be, can optimum nutrition help compensate for a genetic defect, the essential question must be this: can nutrition help a given Downs child? Dianne Craft, a special education teacher, comments on Harrell's 1981 research:
"Dr. Harrell noted that one of the observations that they made during this study was that when there was a ten point rise in IQ, the family noticed it. When there was a fifteen point rise in IQ, the teachers noticed it. When there was a twenty point rise in IQ, the neighborhood noticed it.
"The story of one child is particularly poignant. This seven year old child was still wearing diapers, didn't recognize his parents, and had no speech. His motor skills were relatively unimpaired and he could walk and run fairly well. In forty days, after some of the supplements were increased, his mother telephoned. . . saying, "He's turned on, just like an electric light. He's asking the name of everything. He points and says, 'What zis?' Finally he pointed to his father and said, 'zis?' I said, 'That's your father and you call him daddy, and he looked at him and said 'daddy.' I'm your mother; can you call me mommy?" She went on to say, "I think he saw us for the first time." This little boy went on to do very well in his learning, and eventually tested with an IQ of ninety, which an average IQ." (24) I have seen a beautiful photo in Medical Tribune (9) of Dr. Harrell being hugged by one of the study group children. The kids noticed their own improvement.
Perhaps Harrell's dramatic IQ gains were merely due to the placebo effect. If so, I want every school district on earth to lay in a stock of sugar pills, for gains like this, in only eight months, are astounding. Perhaps success was due to Dr. Harrell's group's expectations or to her bedside manner. But, as Abram Hoffer has said, "I am nice to all my patients. Only the ones on vitamins improve." Harrell colleague Donald Davis writes, "No amount of matching or variable control with Harrell's subjects could change their large IQ gains which are the crucial and so far unexplained difference between the Harrell group and others." (25)
When Dr. Harrell died in 1991, she was far from being alone in reporting success with high-dose nutrition therapy. Dianne Craft writes, "For over forty years, Dr. Henry Turkel (26, 27) treated Down's children successfully using orthomolecular methods. He used a combination of vitamins, minerals, and thyroid hormone replacement. His patients improved mentally and they lost the typical Down's syndrome facial appearance. With over 600 children treated, he found an eighty to ninety percent improvement rate." (24)
To date, the orthodox Down authorities' position may be summed up as, there is no evidence that it helps, so do not try it. Dr. Harrell's view would be, there is reason to believe that nutrition might help, so let's see if it does. The first view prevents physician reports. The second generates them.
Theorization can only go so far. The proof is in the pudding, and Ruth Flinn Harrell's approach yielded smarter, happier children. Her results are sufficiently compelling justification for a therapeutic trial of orthomolecular supplementation for every learning-impaired child.

References:
1. Harrell RF, Capp RH, Davis DR, Peerless J, and Ravitz LR. Can nutritional supplements help mentally retarded children? An exploratory study. Proc Natl Acad Sci USA, 1981. 78: 574–8.
2. Harrell RF. Effect of added thiamine on learning. NY: Bureau of Publications, Teachers College, Columbia University, 1943. Issued in the series: Contributions to education, no. 877. Reprinted: New York, AMS Press, 1972. ISBN: 0404558771.
3. Harrell RF. Further effects of added thiamine on learning and other processes. NY: Bureau of Publications, Teachers College, Columbia University, 1947. Issued in the series: Contributions to education, no. 928. Reprinted: New York, AMS Press, 1972. ISBN: 040455928X.
4. Harrell RF. Mental response to added thiamine. J Nutrition, 1946. 31:283.
5. Harrell RF, Woodyard E and Gates AI. The effect of mothers' diets on the intelligence of offspring. Also known as: Relation of maternal prenatal diet to intelligence of the offspring. NY: Bureau of Publications, Teachers College, Columbia University, 1956.
6. Dr. Ruth Flinn Harrell: Effect of added thiamine on learning." The Health Seeker, p 18-19. http://www.geocities.com/HotSprings/2194/vitamin.html
7. Garrison RH and Somer E. The Nutrition Desk Reference. New Canaan, CT: Keats, 1990.
8. http://www.eurekalert.org/pub_releases/2002-05/pn-akp051602.php 16 May, 2002. Accessed August, 2003.
9. Winter A. Differential diagnosis of memory dysfunction: Finding the cause when your patient can't remember. http://www.afpafitness.com/articles/Memory.htm Accessed August, 2003.
10. Horwitz N. Vitamins, minerals boost IQ in retarded. Medical Tribune. Vol 22, No 3. Wednesday, 21 January, 1981. Pages 1 and 19.
11. Bennett FC, McClelland S, Kriegsmann EA, Andrus LB, Sells CJ. Vitamin and mineral supplementation in Down's syndrome. Pediatrics. 1983 Nov; 72(5):707-13.)
12. Bidder RT, Gray P, Newcombe RG, Evans BK, Hughes M. The effects of multivitamins and minerals on children with Down syndrome. Dev Med Child Neurol. 1989 Aug;31(4):532-7.)
13. Menolascino FJ, Donaldson JY, Gallagher TF, Golden CJ, Wilson JE, Huth JA, Ludvigsen CW, Gillette DW.) Vitamin supplements and purported learning enhancement in mentally retarded children. J Nutr Sci Vitaminol (Tokyo). 1989 Jun;35(3):181-92.
14. Smith GF, Spiker D, Peterson CP, Cicchetti D, Justine P. Failure of vitamin/mineral supplementation in Down syndrome. Lancet, 1983. 2:41.
15. Weathers C. Effects of nutritional supplementation on IQ and certain other variables associated with Down syndrome. Am J Ment Defic. 1983 Sep;88(2):214-7.
16. Pruess JB, Fewell RR, Bennett FC. Vitamin therapy and children with Down syndrome: a review of research. Except Child. 1989 Jan;55(4):336-41.
17. Smith GF, Spiker D, Peterson CP, Cicchetti D, Justine P. Use of megadoses of vitamins with minerals in Down syndrome. J Pediatr. 1984 Aug;105(2):228-34.
18. Davis DR and Capp RH. Vitamins and minerals in Down Syndrome. J Pediatr. 1985 March;106(3):531.
19. Thiel R.J. Facial effects of the Warner protocol for children with Down syndrome. Journal of Orthomolecular Medicine, 2002;17(2):111-116
20. Warner FJ. Metabolic supplement for correction of raging free radicals in Trisomy 21: A noncomparative open case study. http://www.warnerhouse.com/radicals.htm . Accessed August, 2003.
21. http://www.ndss.org/content.cfm?fuseaction=SearchLink&article=45 . Accessed August, 2003.
22. Sacks B and Buckley F. Multi-nutrient formulas and other substances as therapies for Down syndrome: An overview. Down Syndrome News and Update, 1998. 1(2), 70-83. http://www.down-syndrome.info/library/periodicals/dsnu/01/2/070/DSNU-01-2-070-EN-GB.htm
23. Pincheira J, Navarrete MH, de la Torre C, Tapia G, Santos MJ. Effect of vitamin E on chromosomal aberrations in lymphocytes from patients with Down syndrome. Clin Genet. 1999 Mar;55(3):192-7.

24. Craft D. Can nutritional supplements help mentally retarded children? 1998.
25. Davis DR. The Harrell study and seven follow-up studies: A brief review. J Orthomolecular Medicine, 1987. 2:2, 111-115.
26. Turkel H. Medical amelioration of Down's syndrome incorporating the orthomolecular approach. Journal of Orthomolecular Psychiatry, 1975. 4:102-115.
27. Turkel H. The medical treatment for Down's syndrome. Southfield, MI: Ubiotica. 1985.
More on Dr Turkel’s treatment: http://www.doctoryourself.com/turkel.html

Copyright 2004 and previous years Andrew W. Saul.
Andrew Saul is the author of the books FIRE YOUR DOCTOR! How to be Independently Healthy (reader reviews at http://www.doctoryourself.com/review.html ) and DOCTOR YOURSELF: Natural Healing that Works. (reviewed at http://www.doctoryourself.com/saulbooks.html )
For ordering information, Click Here .

Tuesday, January 24, 2012

Goji Berries

I first learned about goji berries from Kristen Morrison's book, Naturally Better Kids. She believes that they have been beneficial to her son with T21, Gryffin. They are expensive, but are delicious and most importantly, full of quite an impressive list of health benefits. Fortunately, Jett loves them. He enjoys the frozen, organic type from Whole Foods (when on sale); the dried fruit reconstituted in water; and the juice, first thing every morning mixed with the seven other supplements that he needs to take on an empty stomach (l-tyrosine, l-tryptophan, probiotics, l-orthinine, l-carnosine, bacopa and Nutri-Meds). I've included two articles on the super berries as well as lower priced, organic products I've found.

For products, please see the DS Day to Day amazon store.

Organic is important, see http://www.suntenglobal.com/news/show.php?ID=138&page for details.
 
Ningxia Wolfberry is the most nutritious goji berry. 

I purchased the 8 oz dried, raw, organic berries from Whole Foods since it was on sale. The 8 oz. bag has lasted us a long time. I just take a handful and soak it in filtered water in a small baby food jar overnight. Jett didn't like to bite into juicy foods, so I just crush it a little first so it doesn't burst in his mouth. But, now he loves to eat them and asks for them.

If you go to vitacost.com, be sure to get $10 off your first  order.
 
Overview 

Goji Berries (sometimes called Wolfberries, scientific name: Lycium barbarum) are a deep-red, dried fruit about the same size as a raisin. The Goji berry tastes somewhat like a cross between a cranberry and a cherry.
Out of the 8,000 food-herbs in the systems of Traditional Chinese Medicine and the thousands of years of history that back it, Goji Berries are considered the number one food-herb, with the highest ranking. Super powerhouse in antioxidants. Highest food in antioxidants measured on the Orac Scale. Complete protein source with all 8 essential amino acids. Loaded with 21 trace minerals plus vitamins B1, B2, B6, and E. Regarded as a longevity, strength building and potency food of the highest order. Only fruit known to stimulate growth hormone naturally.

What nutrients are found in Goji Berries?

Although new to the cuisine of Western culture, the Chinese have known of the special powers of Goji Berries for thousands of years.
Goji Berries are:
  • a complete protein source. They contain 18 different amino acids (on par with bee pollen) and contain all 8 essential amino acids (such as isoleucine and tryptophan).
  • contain up to 21 trace minerals (the main ones being zinc, iron, copper, calcium, germanium, selenium, and phosphorus).
  • contain vitamins B1, B2, B6, and vitamin E.
  • Mature fruits contain about 11 mg of blood-building iron per 100 grams, beta-sisterol (an anti-inflammatory agent), linoleic acid (an essential fatty acid), anti-aging sesquiterpenoids (cyperone, solavetivone), antioxidant tetraterpenoids (zeaxanthin, physalin), and liver-healing betaine (0.1%).
  • contain polysaccharides which fortify the immune system. About 36% of the sugars found in Goji Berries are polysaccharides. A polysaccharide found in this fruit has been found to be an anti-aging secretagogue.
  • As we age, we produce less and less Human Growth Hormone (HGH). The decreasing levels of HGH have been linked to symptoms of aging. Goji Berries are the only food known to help stimulate the human body to produce more HGH naturally. This factor alone makes the Goji Berry perhaps the world’s greatest anti-aging superfood.
  • some of the highest antioxidant containing foods in the world. Goji Berries typically contain 2-4 times the amount of antioxidants found in blueberries.
  • Goji Berries have been traditionally regarded as a longevity, strength-building, and potency food of the highest order. In several study groups with elderly people several ounces of Goji Berries were given once a day for 3 weeks. Many beneficial results were experienced and 67% of the patients’ T cell transformation functions tripled and the activity of the patients’ white cell interleukin-2 doubled. In addition, the results showed that all the patients experienced an uplifted spirit and more optimism. Appetite improved in 95% of the patients, and 95% of the patients slept better.
  • Goji Berries contain complex phyto-nutrients and bio flavinoids:

    Betaine, which is used by the liver to produce choline, a compound that calms nervousness, enhances memory, promotes muscle growth, and protects against fatty liver disease.

    Physalin, which is active against all major types of leukemia. It has also been used as a treatment for hepatitis B.

    Solavetivone, a powerful anti-fungal and anti-bacterial compound.

    Beta-Sitoserol, an anti-inflammatory agent. It has been used to treat sexual impotence and prostate enlargement. It also has a cholesterol lowering effect.

    Cyperone, a sesquiterpene that benefits the heart and helps maintain normal blood pressure. It has also been used in the treatment of cervical cancer.  From: http://www.health-report.co.uk/goji_berry.html
The famed Li Qing Yuen, who popularized ginseng in Chinese culture and who apparently lived to the ripe age of 252 years (1678-1930), consumed Goji Berries daily. The life of Li Qing Yuen is the most well-documented case of extreme longevity known.

How To Eat Goji Berries?

A reasonable daily intake of Goji Berries is 15-45 grams (a handful).
Goji berries may be used as snacks or mixed with recipes or smoothies like other dried fruits.
Cacao and Goji Berries go particularly well when eaten together. Because of their combined antioxidant content, Cacao and Goji Berries make for excellent airtravel snacks.
Organic Goji Berries can be mixed with Sunfood’s Cacao Nibs and/or Sunfood’s Cashews and/or many other dried fruits, nuts, and seeds to make a Goji trail mix.
You can blend dried Goji Berries into smoothies, juices, and elixirs.
Goji Berries can be soaked and rehydrated in water. The Goji soak water makes for a wonderfully hydrating beverage. This soak water can also be used for the base “stock” of a soup.
Goji Berries are an excellent tea additive. Whatever tea you are making, throw 10-15 Goji Berries into the mix and notice how they take the harsh bitter edges off of medicinal herbs and how they accentuate and synergize all the tea ingredients. Try simply drinking Goji Berry Tea all by itself.

Expert Insights: The Himalayan Health Secret of Goji Berries

Excerpts:

Lycium Barbarum, commonly known as Goji, grows wild at high elevations throughout much of central Asia and its berries have been used as an herbal remedy by Tibetan and Chinese healers for thousands of years. The plants grow like bushes with vines that reach over 15 feet. The berries are never touched by hand as they will oxidize and turn black if touched while fresh. They are shaken onto mats, then dried in the shade.

It is the richest source of carotenoids, including beta carotene (more beta carotene than carrots), of all known foods or plants on earth!

Goji is a powerful antioxidant and is traditionally believed to fortify the body against disease and to provide the energy to overcome difficult obstacles in healing. Beta-carotene can be transformed into vitamin A under the influence of human liver enzymes. Being rich in trace minerals, Goji Juice contains significant amounts of zinc, calcium, germanium, selenium and phosphorus, plus small quantities of many others.

In Mongolia it is commonly used by first trimester mothers to prevent morning sickness. It is a gentle and soothing fruit that is loaded with available vitality.

The Goji berry has absolutely no toxicity. However like most fruits, it should not be used if you are suffering from Spleen deficiency with dampness (This is a Traditional Chinese Medicine term. Basically, hold off if you are congested, have phlegm when you cough or have diarrhea-Andi) and diarrhea.

What is Goji juice good for?

It is reported to improve eyesight, lower cholesterol, strengthen the immune system, burn fat, build muscles, inhibit tumor growth, promote healthy sleep patterns, relieve the symptoms of menopause, shrink enlarged prostates, alleviate arthritic pain, reverse aging, balance blood sugar, awaken sleeping libidos, and lift sagging spirits. Such wide reaching claims make it sound like the proverbial snake oil. Are these claims for real?

Fortunately, a lot of people are trying to find out. In the past few years there has been a fair amount of independent research into the health benefits of goji (visit pubmed.org and search for "lycium barbarum", goji's scientific name). There is also a growing body of anecdotal evidence and testimonials from consumers and health professionals.

Goji Juice is now undergoing intense scrutiny as a cancer drug in Tibet, Mongolia, China, Japan and Switzerland. It has been found that the fruit, as well as an extract from its leaves, can kill many kinds of cancer cells in vitro. In vivo studies and human studies are proving to be highly promising. Goji Juice contains approximately 124 ppm of organic Germanium. Germanium has been demonstrated to have anti-cancer activity. Japanese studies indicate that organic Germanium is effective in treating liver cancer, lung cancer, uterine cancer, cervical cancer, and testicular cancer when combined with other drugs. It has been found to induce the production in human beings of g-interferon. Interferon can depress and even kill cancer cells. Germanium possesses the power to take over the hydrogen ion from cancer cells. Losing hydrogen ions can cause depression and even death to cancer cells. Besides Germanium, this berry has other components that act against cancer. These other components appear to be able to depress or block the synthesis of the cancer cells' DNA, which interferes with the cells' ability to divide and thus lowers the reproductive capacity of the cancer cells.
  • Some scientists believe that Goji fruit may be a very good supplement to prevent liver cancer because it exerts liver protection and anticancer effects at the same time.
  • Japanese researchers reported Goji fruits could inhibit the growth of cancer cells.
  • The Goji berry has also been tested as an anti-obesity drug. Patients were given 30 grams each morning and each afternoon, made into a tea. Results were excellent with most patients losing significant weight.
  • Goji Juice is a wonderful and delicious tonic which have traditionally been used as a blood tonic, used to nurture the heart, to relieve heart palpitation, insomnia, forgetfulness and anxiety associated with blood and chi deficiency, especially when combined with chi tonics.
Sacred Goji Waters

During the Tang Dynasty (around 800 AD), a well had been dug beside a wall near a famous Buddhist temple that was covered with Himalayan goji vines. Over the years, countless Goji Berries had fallen into the well. Those who prayed there had the ruddy complexion of good health, and even at the age of eighty they had no white hair and had lost no teeth, simply because they drank the water from the well. The original Goji Juice! From this legend, a Poem was crafted.

Goji Berry Health Discoveries
  • Imagine -- a tiny berry that contains more beta carotene than CARROTS.
  • Picture this -- a berry that contains more Vitamin C than oranges!
  • Even more amazing -- a berry that contains germanium... unheard of in any fruit!
  • And totally incredible ... the wonderful side effect ... it makes you smile.
  • There are over 34 KNOWN HEALTH BENEFITS provided by this tiny berry which have already been proven in independent scientific studies.

Goji has been found to be the most nutritionally dense nutritional source on the planet! Scientists were amazed to discover that these unique Goji berries Extremely High in Antioxidants contain:
  • 18 kinds of amino acids (six times higher than bee pollen),
  • 21 Trace Minerals including Germanium (124 ppm), Zinc, copper and iron (Mature fruits contain about 11 mg. of iron per 100 grams) .
  • The 13% Protein is higher than Whole Wheat and displays an insulin like action that is affective in fat decomposition.
  • 500 times the amount of vitamin C by weight than oranges
  • More Beta-Carotene than Carrots
  • More Iron than spinach,
  • High natural content of Vitamin E
  • B-Complex Vitamins
  • 4 Unique Polysaccharides
  • beta-sitosterol (an anti-inflammatory agent), linoleic acid (a fatty acid), sesquiterpenoids (cyperone, solavetivone), tetraterpenoids (zeaxanthin, physalin), and betaine (0.1%).
Truly an incredible food nicknamed the "Happy Berry for Mood"

20 Reasons to Go For Goji Supplement:
1) A powerful antioxidant that can help prevent premature aging.
2) Immune System builder. Makes you look and feel younger.
3) Can help maintain healthy blood pressure, and strengthen your heart.
4) Can help improve your memory functions.
5) Can help maintain normal blood sugar level and can help reduce cholesterol.
6) Can help enhance sexual functions and treat sexual dysfunctions.
7) Can help promote weight loss.
8) Can help Relieve headaches and dizziness.
9) Can help Relieve insomnia and improve the quality of sleep.
10) Can help improve your appetite and digestion.
11) Can help maintain eye health and can improve your vision.
12) Traditionally used as a treatment for Cancer.
13) Can help reduce the risk of Cancer and can help inhibit tumor growth.
14) Can help support healthy liver and kidney functions.
15) Can help menopausal symptoms.
16) Can help prevent morning sickness during pregnancy.
17) Can help improve fertility.
18) Can help strengthen your bones and muscles.
19) Can help alleviate stress and anxiety, and can promote cheerfulness
20) Can help activate anti-inflammatory enzymes.

Legendary health benefits

Many of the legendary health-giving properties of lycium barbarum (goji's Latin name) are today being confirmed in modern scientific studies, and this has led to the possibility of even more far-reaching benefits.
Scientific research from major universities around the world has validated the remarkable health benefits of the goji berry claimed by the Himalayan Healers thousands of years ago. Over 50 studies have already been published in prestigious health journals, including:

British Journal of Nutrition
International Immunopharmacology
Journal of Chinese Herbal Medicine
Journal of Ethnopharmacology
China Pharmacology and Toxicology
Chinese Herb News Magazine
Research Communications Molecular Pathology and Pharmacology
Chinese Patent Herbs
Chinese Herbs
Chinese Oncology Magazine
Hygiene Research
Physiology Academic Journal
Chinese Stomatology


Recent Research
• Lycium fruit (Fructus lycii) has significant antioxidant activity.
• Lycium fruit contains substances that protect DNA.
• Lycium fruit contains polysaccharides that have been demonstrated to potentiate the immune system.
• Zeaxanthin, a carotenoid abundant in Lycium fruit, may produce functional improvement in vision.
• Lycium fruit has been given to improve sexual function. It was reported that by taking Lycium fruit orally and in the form of an alcohol extract, it could markedly increase androgen levels in the blood, making patients feel more energetic.
• Lycium fruit may help athletes produce more lean muscle mass and experience strength gains.
• Consumption of Lycium fruit increased SOD levels in the blood.
• Consumption of Lycium fruit reduces free radical (lipid peroxide) levels in the blood.
• Consumption of Lycium fruit may increase hemoglobin levels.
• Lycium fruit has immune potentiating activity.
• Lycium as a source of immune-enhancing polysaccharides.

Goji - Strengthening The Immune System
The immune system is what keeps your body well. If it is not functioning as well as it should, you get sick when your body cannot fight off an invading illness. When the immune system is overworking, it will turn on you and start killing off healthy cells.

Things that weaken the immune system are poor nutrition, lack of exercise, stress, and lack of sleep. These all increase the risk of getting sick. Anti-oxidants such as Vitamin C and Alpha Tocopherol (Vitamin E) are considered to be good for the immune system.

The immune strengthening effects of complex sugars called polysaccharides found in Goji are not so commonly known. Polysaccharides are complex sugars, consisting of multiple linked simple sugar (monosaccharide) molecules. They are a glue-like material formed by microorganisms in the process of mineralization, or breaking down organic matter.

If it's so powerful, why haven't we heard about the goji berry before now?

Great question! For starters, imagine how long it took to find the original strain of berry... next, the need to develop and apply the right technology to find the right berries... and then there is the harvesting itself, which can be a complicated process.

The truth is as far back as 1936, British explorer Colonel Reginald Schomberg (1880 - 1958) may have made the original important observation: "...there is such a direct relationship between the sun and fruit. Fruit, more obviously than other foods, ripens and colors in the sun. Sunlight is the carrier of the sun's quality. Through it that quality comes direct from the great orb of our being. It stores itself in sun-bathed food, as in a minor way electricity is stored in a battery. The eating of fruit releases the sun's quality in its most direct and least interfered-with form."
The unfortunate thing for Schomberg is that he never presented his theory in a scientific treatise, but merely described it in the notebooks of his Himalayan expeditions. Consequently, his scientific observations went undiscovered for many years until they were recently unearthed.

What is the Schomberg effect? Simply put, foods with a high Schomberg effect are said to be able to keep us healthier by facilitating the transfer of energy.

When scientists first found, then tested, a variant of Lycium barbarum known as goji, they were astounded. The Schomberg effect measured off the scale.

Don't be fooled by inferior berries, or dried goji berries... if you want to experience the FULL EFFECTS of this amazing fruit, you want to be certain it is a juice that matches the optimum potency spectral signature of the original bloodline. In fact, "a one-liter bottle of a good Himalayan-quality goji juice product  should provide the polysaccharide equivalent of more than two pounds of fresh goji berries!

STUDIES

Below, are links to 4 out of over 50 studies listed on the National Library of Medicine web site about "Lycium Barbarum" the Latin name given to the Himalayan Goji Berry from which is extracted Goji Juice. Please be informed, Click Here to search Pubmed.com for Lycium Barbarum,

Enhanced Immune Response
[A polysaccharide-protein complex from Lycium barbarum upregulates cytokine expression in human peripheral blood mononuclear cells.]
Gan L, Zhang SH, Liu Q, Xu HB.
Institute of Pharmacy, Huazhong University of Science and Technology, Wuhan 430074, People's Republic of China.

Anti-Fatigue Effects
[Isolation and purification of Lycium barbarum polysaccharides and its antifatigue effect]
Luo Q, Yan J, Zhang S.
Department of Hygiene, Hubei Medical University, Wuhan 430071, China.

Free-Radical Prevention
[Experimental research on the role of Lycium barbarum polysaccharide in anti-peroxidation]
Zhang X.  Beijing Military General Hospital.

Weight Loss
[Study on the composition of Lycium barbarum polysaccharides and its effects on the growth of weanling mice]
Zhang M, Wang J, Zhang S.
Food Science Department, Huazhong Agricultural University, Wuhan 430070, China.

Gong H, Shen P, Jin L, Xing C, Tang F.
Therapeutic effects of Lycium barbarum polysaccharide (LBP) on irradiation or chemotherapy-induced myelosuppressive mice.
Cancer Biother Radiopharm. 2005 Apr;20(2):155-62.
PMID: 15869449 [PubMed - in process]

Zhang M, Chen H, Huang J, Li Z, Zhu C, Zhang S.
Effect of lycium barbarum polysaccharide on human hepatoma QGY7703 cells: inhibition of proliferation and induction of apoptosis.
Life Sci. 2005 Mar 18;76(18):2115-24.
PMID: 15826878 [PubMed - indexed for MEDLINE]

Zhi F, Zheng W, Chen P, He M.
[Study on the extraction process of polysaccharide from Lycium barbarum]
Zhong Yao Cai. 2004 Dec;27(12):948-50. Chinese.
PMID: 15807251 [PubMed - in process]

Sytnik E, Komarnytsky I, Gleba Y, Kuchuk N.
Transfer of transformed chloroplasts from Nicotiana tabacum to the Lycium barbarum plants.
Cell Biol Int. 2005 Jan;29(1):71-5. Epub 2005 Jan 26.
PMID: 15763502 [PubMed - in process]

Wu SJ, Ng LT, Lin CC.
Antioxidant activities of some common ingredients of traditional chinese medicine, Angelica sinensis, Lycium barbarum and Poria cocos.
Phytother Res. 2004 Dec;18(12):1008-12.
PMID: 15742346 [PubMed - indexed for MEDLINE]

Hai-Yang G, Ping S, Li JI, Chang-Hong X, Fu T.
Therapeutic effects of Lycium barbarum polysaccharide (LBP) on mitomycin C (MMC)-induced myelosuppressive mice.
J Exp Ther Oncol. 2004 Oct;4(3):181-7.
PMID: 15724837 [PubMed - indexed for MEDLINE]

Cheng CY, Chung WY, Szeto YT, Benzie IF.
Fasting plasma zeaxanthin response to Fructus barbarum L. (wolfberry; Kei Tze) in a food-based human supplementation trial.
Br J Nutr. 2005 Jan;93(1):123-30.
PMID: 15705234 [PubMed - indexed for MEDLINE]


Since the early 1980s, the Goji (known botanically as Lycium barbarum) has been the subject of a number of clinical studies - including several published by the State Scientific and Technological Commission in China. These studies have documented its antioxidant and immune-stimulating effects. More recent studies in the 1990s have contributed additional scientific support.

Role of Lycium barbarum Polysaccharide as an Antioxidant Author: X Zhang Journal: Chung Kuo Chung Yao Tsa Chih 18 (Feb 1993) Location: Beijing Military Hospital, Beijing, China Conclusion: The effect of free radical damage on red blood cells can be prevented and reversed by incubation with either Lycium barbarum polysaccharide or superoxidide dismutase. Abstract: Researchers incubated cells (Xenopus Oocytes) in a solution containing a free-radical-producing system for 6 hours. The changes in the electrical profile of the cell membranes were measured using a microelectrode electrophysiological technique. The results showed that Lycium barbarum polysaccharide both prevented and reversed free radical damage to cells.

Protective Action of Lycium barbarum on H2O2-induced Lipid Peroxidation Author: B. Ren, Y. Ma, Y. Shen, B. Gao Journal: Chung Kuo Chung Yao Tsa Chih 20 (May 1995) Location: Faculty of Preventative Medicine, Ningxia Medical College, Yinchuan, China Conclusion: Lycium barbarum protects red blood cell membranes against lipid peroxidation. Abstract: Hydrogen peroxide (H2O2), a powerful promoter of oxidative damage, was used to promote lipid peroxidation of the red blood cell membranes of rats. Dried Lycium berries showed the greatest protective effect against H2O2 damage, followed by Lycium barbarum polysaccharide.

Effects of Lycium barbarum and on the Attachment and Growth of Gingival Cells to Root Surfaces Author: B. Liu Journal: Chung Kuo Chung Yao Tsa Chih 27 (May 1992) Location: College of Stomatology, Fourth Medical University, Xian, China Conclusion: Lycium barbarum improved the attachment and growth of human gingival cells to root surfaces. Abstract: A dose of 1.25 mg/ml Lycium barbarum was used to stimulate the in vitro attachment of human gingival fibrobasts to the surfaces of dental roots. In response to Lycium barbarum exposure, cells on diseased root surfaces increased in quantity, exhibited better growth and distribution. Drynaria displayed similar effects but was not as potent as the Lycium barbarum.

Effects of Lycium barbarum and Radiation in Treatment of Lung Cancer Author: Lu, C.X., B.Q. Cheng Journal: Chung Hsi I Chieh Ho Tsa Chih 11 (Oct 1991) Location: Cancer Institute, Ningxia Medical College, Yinchuan, China Conclusion: Lycium barbarum enhanced the effects of radiation therapy in the treatment of Lewis Lung cancer.

Reference
1. Qi Zongshao, Li Shufang, Wu Jiping, et al. Chemical Analysis on Lycium Barbarum Fruit and Leaves. Zhong Yao Tong Bao (Chinese Herb News). 1986, 11(3):41.
2. Wang Qiang, Chen Suiqing, Zhang Zhehua, et al. The Measurement of Lycium Barbarum Polysaccharide (LBP) in Lycium Barbarum Fruit. Zhong Cao Yao (Chinese Herbs). 1991, 22(2):67.
3. Zhong Guo Shipin Bao (China Food News). March 2, 1998.
4. Data in Rich Nature Nutraceutical Laboratories. 1998.
5. Geng Changshan, Wang Geying, Lin Yongdong, et al. Effects on Mouse Lymphocyte and T Cells from Lycium Barbarum Polysaccaride (LBP). Zhong Cao Yao (Chinese Herbs). 1988,19(7):25.
6. Huang Guifang, Luo Jieying. Immune Boosting Effects from Fu Fang Wu Zi Yang Zong Wan (a Chinese patent herb containing Lycium barbarium fruit). Zhong Cao Yao (Chinese Herbs). 1990, 12(6): 27.
7. Li Wei, Dai Shouzhi, Ma Fu, et al. Active Lymphocyte Effects Observed after Taking Lycium Barbarum Fruits. Zhong Cao Yao (Chinese Herbs). 1991, 22(6): 251.
8. Tao Maoxuan, Zhao Zhongliang. In Vitro Anti-Mutation Effect of Lycium Barbarum Polysaccaride (LBP). Zong Cao Yao (Chinese Herbs). 1992, 23(9):474.
9. Cao GW, Yang WG, Du P. Observation of the Effects of LAK/IL-2 Therapy Combined with Lycium Barbarum Polysaccharides in the Treatment of 75 Cancer Patients. Chunghua Chung Liu Tsa Chih. 1994, Nov.; 16(6): 428-431.
10. Lu CX, Cheng BQ. Radiosensitizing Effects of Lycium Barbarum Polysaccharide of Lewis Lung Cancer. Chung His I chieh Ho Tsa Chih. 1991, Oct.: 11(10): 611-612.
11. Kim HP, Kim SY, Lee EJ, Kim YC. Zeaxanthin Dipalmitate from Lycium Barbarum Has Hepatoprotective Activity. Res. Commun Mol Pathol Pharmacol. 1997, Sep.; (3): 301-314.
12. He Jie, Pan Li, Guo Fuxiang, et al. Hepatoprotective Effects from Lycium Barbarum Fruit in a Mouse Experiment. China Pharmacology and Toxicology. 1993, 7(4): 293.
13. Li yuhao, Deng Xiangchao, Wu Heqing, et al. The Effect on Lipid Metabolism of Injured Liver Cells in Rat. Zhong Guo Zhong Yao Za Zhi (Journal of Chinese Herbal Medicine). 1994, 19(5):300.
14. Ding Aurong, Li Shuli. Effects on Activities of Na+, K+-ATP Enzymes from Huang Jing and Five Other Herbs. Zhong Cheng Yao (Chinese Patent Herbs). 1990, (9): 28
15. Cheng et al. Fasting Plasma zeaxanthin Response to Fructus Barbarum L. (Wolfberry; Kei Tze) in a Food-based human Supplementation Trial. British Jounal of Nutrition (2005), 93, 123-130

Related Posts

Saturday, January 7, 2012

Support Durkin's Dragons

From time to time, parents express an interest in showing their appreciation for this blog... Well, here's the opportunity you've been waiting for!

Our local Down Syndrome Foundation of Florida is having their 2nd Annual Tour of Champions Valentine's Bowl-a-thon event this February 12th. The Foundation is all about "striking" Down barriers to inclusion and I'd LOVE for you to sponsor our bowling team, Durkin's Dragons!
 
Simply click this link to sponsor us:
http://bowlathon.net/event/DSF_Florida_2012/donate.  All donations are tax-deductible.  


Last year Durkin's Dragons raised over $1,000, and we'd love to do it again this year! Especially since each team that raises over $1000 is eligible to participate in the grand prize drawing for an iPad! Jett would greatly benefit from having an iPad (and maybe have some fun with it too!).

As a special incentive, anyone kind enough to donate $50 or more will receive a free caricature of their family (face only, color, drawn in the same style as my blog header). Just type in "We'd love a caricature!" in the comment section when you sponsor us. Then email us photos of your family members, along with hair and eye color, to kennydurkin@gmail.com.


The Foundation is run 100% by volunteers so all proceeds go directly to families for scholarships and programs!  Last year they raised $50,000 -- $34,000 went towards scholarships and $13,000 went towards programs.  It is their goal to raise more money this year so they can support the growing number of scholarship requests and implement some additional programs such as Lose The Training Wheels and iCan Work program. 

Jett has gotten many scholarships from DSFF for his speech therapy evaluations, swimming classes and therapeutic Gymboree classes.

Photo Highlights from 2011

 Volunteers, in light green shirts, were there to help the families when needed.
 
Jett was irresistible, as usual, and at one point we had FIVE volunteers "helping" with Jett.
Here's Kathy, Jett's sister, and the "Valentine's Day Bowling Ball of Destruction"
 
 Alex, Jett's brother, and "Goldie the Demolisher"
 And, Jett's Daddy with "Kermit the Annihilator".

Saturday, December 31, 2011

Join Me on Facebook!

I don't really know what this means, yet, but... I do have a page or a group or community or something on facebook... It's at:
http://www.facebook.com/pages/Down-syndrome-A-Day-to-Day-Guide/193837467378474


Monday, December 12, 2011

NeuroProtek for those with T21?

I am just amazed and elated by the progress Jett has made through taking the supplement, NeuroProtek, which he started about a year ago. While I am quite pleased about the improvements in cognition and speech--what I'm most thrilled about is the eye contact, the smiles--the first belly laugh EVER! The self-initiated hugs, the "air kisses" (doesn't initiate kisses--yet) and the... (sob) "I lub you soooooooo much!" Thank you, Dr. Theoharides, for creating NeuroProtek!

It's like "Jett" is standing before me for the first time, catching my eye, really acknowledging my existence instead of this being that I feed, diaper and clothe. Yes, okay, so it may be selfish of me to be more pleased by this new sociability than the improvements in cognition but, I'm only human and I need sustenance--through a little sweetness from my own child--to keep me going.

To all of you with a "cuddly" and friendly child with DS, eat those hugs and kisses up! Please, appreciate them--we don't all get them! Imagine if you didn't get any positive feedback. Imagine wondering: Would my child even care if I was suddenly replaced by an equally attentive mother? Does he even notice if I'm gone for the day? (He didn't even smile when I'd come home.)

And to those of you who don't get much eye contact or affection from your child... read on... NeuroProtek may be of particular interest to you...

What is NeuroProtek?

It's simply a concentrated amount of the flavonoids Luteolin, Quercetin and Rutin. Bioflavonoids are naturally found in various fruit and vegetable skins. NP harnessed those beauties to better reduce inflammation in the brain and in the gut, help clear up the effects of allergies, and, in some, help alter mood through regulating dopamine (Jackpot!) and even lessen the effects of some metal toxicity. Here is Algonot's information on NeuroProtek.

Prior to NP, Jett rarely smiled (didn't smile at me until 7 months old and I had to stimulate him vestibularly to "force" him to) and his laugh was a short "Key!" and that was it. If I hugged him, he would go so far as to "lay into" my hug, but no arms/legs around me, no pressure of reciprocation, certainly no initiation. Little positive reinforcement. I saw improvement on NP--after only 14 days-- I soon saw an increase in smiling, actual laughing -- his first belly laugh, initiated a hug (once) for the first time, initiated kisses (once) for the first time, more eye contact, even more verbal (didn't think that was possible), more organized play and thought... I saw no change in stomach issues that I can directly attribute to NP. I believe his constipation has been cleared up because of the Vitamin C, but it's true that it can take months for the full effects of NP to appear.

NeuroProtek and Mercury
    So how could such a huge change in sociability come from bioflavinoids? Could be one or the combination of two benefits of NP: increase in dopamine level and prevention of mercury toxicity.

    Jett's symptoms or "autistic traits" could be from mercury toxicity, which are almost identical to autistic symptoms (dare I say cause and effect?).

    In the study, Luteolin and thiosalicylate inhibit HgCl(2) and thimerosal-induced VEGF release from human mast cells., it states: "Luteolin...may be useful in preventing mercury-induced toxicity".

    I'd love to test his mercury level, but his pediatrician said that "unless he's been chewing on a thermometer and it broke, I'm not testing." So, I have to go by symptoms and the fact that he did get 5 vaccines in the first 5 months of age and I have 4 mercury fillings and breastfeed.

    Exclusive of the characteristics that we can contribute to Down syndrome, Jett has (had) many of the telltale symptoms of ASD that coincide with mercury toxicity including
  • Social deficits 
  • Lack of eye contact 
  • Sound sensitivity 
  • Self injurious behavior, e.g. jabbing himself in the head with his thumb & kicking himself repeatedly in the "diaper area." 

For more details, check out this comparison of symptoms between autism and mercury toxicity.

NeuroProtek Side Effects

The regular version of NP has a lot of phenols in it so symptoms of phenol sensitivity may appear. If your child has a low tolerance of phenols, which Jett has to some degree, you may want to look into the low phenol version. When I switched Jett's to the low phenol type, the 3-4 symptoms he showed disappeared. (They reappear whenever I increase his phenol intake in another way, like almonds.) Here is a great explanation of phenol sensitivities and an excerpt of the symptoms:

Symptoms of phenol intolerance include (not all of these need be present):

  • night waking for several hours, night sweats, difficulty sleeping 
  • dark circles under eyes, 
  • irritability, hyperactivity, aggression 
  • red cheeks/face/ears, 
  • lethargy, 
  • self-injurious behavior, head banging 
  • inappropriate laughter 
  • diarrhea, 
  • eczema, and other skin conditions. 

Mood Swings (negative) or Mood Changes (positive)

Some parents of children on the autism spectrum (not many w/ DS are on NP) have seen anger and/or mood swings when taking NP. This may be because, in addition to being an anti-inflammatory, quercetin is also a catechol o' methyltransferase (COMT) inhibitor (also, it turns out that it is a MAO inhibitor!). This means that by inhibiting this enzyme, dopamine turnover may also be altered. Therefore, the fluctuations in dopamine can cause mood swings. The degree to which mood swings can flare up depends on COMT status. Therefore, if your child is COMT+ (genetic 'overmethylator'; limited tolerance for additional methyl donors) his/her dopamine will be already relatively high. Hence, inhibiting his/her COMT enzyme will cause more dopamine to hang around longer and the result is one crabby child.

Conversely, if your child is COMT-(genetic 'undermethylator'; can tolerate additional methyl donors), he/she will generally have a lower dopamine status. This ties into histamine because frequently, some (Pfeiffer method) will define methylation status by histamine levels i.e., low whole blood histamine will denote overmethylator, while high whole blood histamine will denote undermethylator. While this biochemical marker can be useful, it is prone to fluctuation because of supplementation e.g., MB12, TMG, 5-MTHFolate and SAM-e can alter methylation status in an individual.


For products, please see the DS Day Today amazon Store.

They have two formulas, regular and the low phenol.


My notes on Jett's experience with NeuroProtek


Originally, I was keeping notes on Piracetam, but I also restarted NeuroProtek the day after I started Piracetam. I had Jett on NP much earlier, but it disturbed his sleep so I had stopped it. (Boy do I wish I had continued!) So, as I wrote these notes, I didn't realize until later that it was the NP that was making the difference. When I ran out of the P and continued w/NP, I saw no difference in him when I stopped the P! I may restart P at a later date when I can afford the choline. But, for now, Jett is doing very well on NP with the P.


Day one
Age: 20 months   
Piracetam Dosage: Jett weighs 19.8 lbs which is 8.98 kilos. So he'd get 673 mg of Piracetam per day. One capsule is 800 mg. So I will give him 1/2 a capsule (400) in the morning and 6 hours later, give him a third of a capsule (266) and see how it goes. But for day one, I'm giving him 1/3 of a capsule in the am and 1/3 in the afternoon.

Notes:
He's not on Prozac anymore and we ran out of Longvida Curcumin and EGCG (green tea extract) but, have a full bottle of Piracetam that I haven't tried so... I'll let you know what I see... I'm a little apprehensive because I rely on Prozac, LC and EGCG to support him cognitively. The last time he was off LC, I saw noticeable decreases in speech that were very uncomfortable to watch. (My mother even noticed and agreed to pay for the next bottle. Bad news/good news.)
I take 840 mg of choline a day and Jett still breastfeeds, so I am assuming that he is getting some choline 3 times a day. (I did look this up and a study supports the fact that breastfeeding woman who supplement with choline have higher choline content in their breast milk.)
Cognition pretest: I wrote 6 words on the magnadoodle, one at a time and showed him what they were in the room:  bean bag, chair, cow (a picture), shoe laces, stool and umbrella. (Bean bag, shoe laces and umbrella are brand new words. The others he has seen this week.) Sometimes he wanted to write them as well after I wrote them (I mean that he made me hold his hand and he wrote them with me). Then I immediately wrote each one again and asked him where they were. He got them all right. I called my husband and stepdaughter into the room and although he was distracted and "talking" to them, he got them all right again. He's taking a nap now, but I'll try again when he wakes up to see if he remembers.
He did remember when he woke up and remembered all but one (bean bag) the next night.
I'm excited to see the results because he's not on Prozac, LC or EGCG-- my "go to" list for cognitive support. Just ginkgo and vitamins (and Piracetam). Hopefully we can afford LC and EGCG again soon. He's not been hyper at all and he actually crawled around the house and played a lot on his own (w/out being irritable--being happily independent). I did read a lot of books to him and did some Little Reader and magnadoodle, as I mentioned. When I do a lot of that, he seems to feel happier and more independent. If I don't spend a lot of time with "lessons" he gets really irritable and whines for me to read to him.
Obviously, it's caused no sleep issues so far because he's taking a nap now.

Day two/20 months 
I noticed by day two on Piracetam that it doesn't support the eyes as well as: LC, Prozac & EGCG since his eyes are crossing very badly. (Shows that the communication between the brain and eyes are not doing well, but it's only been a day...) We've ordered LC (yeah!!!) and should expect it in 3-5 days. But, his language is coming along nicely. Usually, off LC, he either stops talking or really regresses language wise, but yesterday he said a bunch of words, actually repeated after me. (Unfortunately one was "shut up"...I did say PLEASE, first...) which of course he repeated like twenty times with enthusiasm. And then it was the first thing he said this morning. I said, "Good morning, Jett." and he smiled and said, "Shut up!" Hopefully people will think it's cute... like Ann Hathaway in Princess Diaries...
I did also added one capsule of Neuroprotek which he took before w/no side effects.
I showed Jett colors, but he didn't get them all right. I'll try again another day. Maybe the concept is more difficult than just learning words? 

Day three/20 months
I'm upping the dose of P to 1/2 in morning and 1/3 in the afternoon. Ooops... Jett was fed the last dose of Piracetam at 7pm! So, he didn't sleep very well at all. He didn't fall asleep until 2 am. Once he fell asleep, he was fine though. So, it looks like it takes about 7 hours to get out of his system... We won't make that mistake again!

Day four and five/21 months
He turned 21 months old on Nov. 25, 2011. These past two days he has been playing independently for very long periods of time! And instead of sitting and going "ehhhhhh" when he wants me to read a book, he takes the book, crawls over to me and hands it to me to read. He also has been more interested in his bath time and has been taking an hour long bath and not wanting to get out, for the first time. (He's always enjoyed bath time, he's just more engaged now and for a longer period of time.) So, it appears to me that he's more focused with a longer attention span on the Piracetam and NeuroProtek.

Day six/21 months
Saturday, Nov. 26, 2011 I had to work (I do, 2-4 times a month) and there was a "miscommunication" so Jett got 1/2 a capsule of Piracetam at 10am and then another 1/2 at 1pm. (I fixed the small bowls of supps, but my husband got the times wrong--I didn't write it down for him this time.) He seemed fine though and Kenny said that he didn't "give him any trouble" which means that Jett did a lot of independent play, was in a good mood, ate well and took almost a 2-hour nap. :D

Day seven/21 months
Sunday, Nov. 27, 2011 My mother came over and had Jett outside for his 30 minutes of sun. While outside, Jett stood up and walked behind a rolling toy car! She said that he took three steps! I took him outside an hour later and he took five steps! So I got my husband and stepson to see and take a video. I'm excited!! I would love for him to walk soon! (As part of the ND program, I haven't initiated much walking because crawling is so important for brain development. I don't know if my mother "put him up to this" or if he thought of trying to walk behind the toy on his own... I do wonder how long he's been able to do this. I don't really think I'm supposed to encourage him to walk like this...) He has taken a couple of steps forward on his own initiative (but supported) just in this week, so maybe it was his idea? The average age of a child w/DS who can walk 10 feet with a push toy is 22 months and 11 months for a typical child. Jett did walk about 5 feet today. I'm not sure how much Kenny recorded. I don't think it would hurt for me to try this again tomorrow.

Day eight/21 months 
I played Little Math for the first time and he LOVED it. He shouted with protest when it was over. They counted to five really fast and he shouted out "six"! So funny because no one taught him any of that! (There is a Readeez song that counts to 12 very fast so he probably learned it that way.) He did it twice more when my husband played it later on in the day, so it wasn't my imagination. 

Day 11/ Dec. 1/ 21 months
Jett's finally back on curcumin. Yeah! He said five recognizable words in front of the speech therapist today. I figure that's pretty good for an hour, right? (Horse was one.)  His walking is progressing as well. And he learned to read the names of some of his instruments: drum, tambourine, morocco and xylophone as well as "shake" and "beat". He was very excited to learn these and would play each one when I wrote the name. He also loves to dance, bounce and shake. He wouldn't vocalize for "sing" but he did sway his arms from side to side and looked toward the computer where I play pandora.com (music).
When I wrote "together" he laced his hands together. I only showed him that word once a couple of days ago. But it's one of his favorite words, so it makes sense that he learned it immediately. When I wrote "chair" he pointed to the chair closest to him then he also pointed to the chair that was on the other side of him. These chairs look very different so he does understand what a chair is and not just the chair I showed him first (showing transference). He remembered all the old words except bean bag--again! It's not a word we use a lot so maybe that's why. We worked on shapes yesterday and colors the day before, but he didn't seem to either get them or be too interested so I didn't check today to see if he magically got them. I know that he knows star, though because he's said it a couple of times and will point to one.
Some meaningful words he said today were: Jett, yes, eyes, "S", "Ah" (for A-apple), "kuh" for book (upon request), "zzz" for buzz, shapes... that's all I can think of off the top of my head. He jibber jabbers constantly so I forget to remember all the stuff he says. His favorite book today is Mr. Brown Can Moo, Can You? He was having fun tonight pretending to read it out loud. He made a lot of noises but they didn't exactly match the word. I'll have to teach him those words tomorrow--he'll love that!
Oh, we did Little Reader in Chinese and he freaked out. He hated it! He rolled off my lap onto the floor he was so disturbed by it. I think it's because it was all too foreign to him and he LOVES reading English so much that it was not a pleasant experience. I'll have to try again later--once he's got a good grasp of the English language. (Learning another language is really good for the brain.)
I gave him the Piracetam a little after 5 so he fell asleep about an hour late (midnight). I have to remember that he won't fall asleep until 7 hours after the last dose -- so no later than 4pm.

Day 14/Dec. 4/21 months
Discovered for sure that he knows and will verbally say ten letters of the alphabet. He says the sound, not the letter name. When I read the alphabet to him, I say "wuh" instead of "double-u", etc. He knows A, C, E, O, P, S, T, W, X and Z. (I found out the next day that he knew M as well.)
Yesterday, he spontaneously gave me a hug for the first time and my mother said he hugged her too. This afternoon, when he was supposed to be napping, he spontaneously gave me like 5 kisses on my nose. He never initiated kisses and hugs before. But he recently started to give me kisses from afar by making the smack sound.
Yesterday I also noticed that he put a lid on a container which I don't think he's done before.

Day 19/Dec. 11/21 months
Okay, so now Jett can put in a puzzle piece for the first time. (It was the Melissa & Doug farm sound puzzle of the sheep.) And he wanted to put the shapes into the shape sorter, but was having difficulty so he had me come over. I set it up so he could succeed better (less choice of shapes, at the right side where the correct shape hole is, etc.) and he was able to do it better and better! He put them in himself! (He's not great at it yet, but he understood the concept and was interested and tried and did it!)
Yesterday, he spontaneously said, "A B C" while playing in the bathtub and my husband parroted him and then Jett said, "D!" He's started singing (ba, ba, ba) and has been singing with the Readeez version of the alphabet song. (I mean that he tries to, he can't actually sing the alphabet song.) I can tell that his brain is more organized... He went around and gathered all the parts of his floatable xylophone where each musical bar is on its own colored puzzle piece. So, he's picking through his toys and brings me a pile of his xylophone and says "together" (his version of the word) so that I will put it together for him! (Then he immediately ripped them apart so I'd do it again.)
He did something similar last night, he sorted out the red puzzle pieces from only one puzzle and just brought those to me.
I was unhanging socks that were dry and I dropped each one on his head as if it were raining socks and then I rolled the matching ones together into "sock balls." So he gathered the sock balls and we played catch for a while and then he gathered them and carried them all through his crawl tube and went back and got the ones he dropped, etc. And played with them for a good while, very creatively!
All this type of play is NEW NEW NEW! I don't know if it's the Piracetam or the NAET or what, but I'm loving this burst of amazing cognitive progress!
And his mood... he is smiling much more and seems to be an all around happier kid! His eyes are doing great as well. Very little crossing. Yes, we are still doing the neurodevelopmental exercises for his eyes. I'll have to ask around and see what other moms have seen in their child on Piracetam.
He also has been reading--out loud--words that I haven't specifically taught him, from his books. Like in the Hide and Squeak book, he read: Pup and the Mr. Brown book, he read: Hoo, Buzz, Pop, Klopp, Boom, and Grum... In a pig book, he read splash and like three other words. And in other books, I see him react to the words before I say them. Like a Barney book says "pat your head" and he's already doing it before I read it out loud.

Day 25/Dec. 17/21 months


We have contact! Eye contact, that is! I didn't realize what little eye contact Jett had before, but today, he really held my gaze. Because of this, he parrots more--both verbally and "gesticulaterly." I'm rather animated with my hand movements when I talk and I see him copying me. Too funny. I always thought he was engaged, but the change has been amazing.
Also new--I had noticed that when I pointed, Jett looked at my finger or the end of my finger and not at the object to which I was pointing. This is significant because studies show that children who can follow where you point learn better. Jett just started looking at the object! I try this everyday so I can tell you that this is the first time he's done it!

Day 26/Dec. 18/21 months


I've readded TriEnza enzymes to help w/Jett's bowel movements. Because of the uncomfortable nature of getting his stomach in order, he was very clingy and irritable all day and night. He had 2 BMs in one day--1 BM a week is "normal" for him, so this will take some time for him to adjust.
As I learn more about Neuroprotek, I'm thinking that I need to attribute all the elimination of Jett's borderline Autistic tendencies on it rather than the Piracetam. I don't know how much of the P to attribute the speech and cognitive advances, but I am quite pleased so far!

May 11, 2012/24 months 

Repeats everything we say, even double words and multiple syllables. Also repeats words in songs, on TV and radio and people in other rooms. Yesterday he repeated perfectly: "I love you sooo much!" That's the most he's repeated at one time.
Collaborates: He sings parts of songs with me. All of itsy bitsy w/ hand motions but he only does the whole song once a day. He sings the last parts usually and holds the note and shows inflection. Like he sings the word "i-dol-lize" w/the "do-re-me" melody. He knows many, many songs.
Initiates: He talks to himself/toys a lot. He sings to himself. He sings with the piano. He initiates "itsy-bitsy" a lot. The word he uses most often is "up." He uses it for us to pick him up when hungry, have to potty, just to be held, etc. It does frustrate him some because we pick him up but don't know what he wants after that.
He now uses the phrase "smookey, smookey" as a term of endearment (which I use). He uses it with me all the time and used it when my friend, Nina was cuddling & breastfeeding her Hunter and used it when he was approaching Hunter on his own. (As if to say, "hey there, little baby").
Before, when he wanted something, he'd smack his knees/bounce his head and go "eh, eh!"
He still does this BUT I've been saying "What do you want, Jett?" and looking at him. He will say something instead of "eh, eh" but I usually can't figure out what it is. At night, he's highly frustrated and says something that sounds like "eat" or  "deeth" or "teeth" and repeats it emphatically over and over. We put him on the potty but that's not what he wants. He may be saying "drink" because when I give him water he drinks it like crazy and goes back to sleep. For the past 3 days, he has been actually asking for "drink" or "sip" or pointing to our drink instead of smacking himself and saying "eh, eh." When he's hungry, he still doesn't say "eat" or "hungry" or "bite." Instead, he will go to his high chair and stand up holding it and go "eh, eh!" and bounce his head. If we are eating, he will come up to us and say "bite." When he wants milk he just comes to me and makes it obvious w/out using words.
Just yesterday, we were on the couch and he was wearing a diaper and he said "Pee pee" to let me know that he had just peed in his diaper! On the potty, he will say "pee pee, poopy and potty" but doesn't usually initiate it.
Reads words aloud much more and more loudly. So in public, he points to a sign and reads it loud enough and clearly enough that strangers immediately notice that he is reading out loud. He does draw attention, which makes our shopping trips much longer (small price to pay!).

March 24, 2012/24 months

Jett's been off P and only on NP for months and he's still doing great! I'm going to reintroduce P along with BodyBio PC soon and see if I observe a difference. (Update: I never have reintroduced it.) He's 24 months and has been putting together the Melissa and Doug stacking puzzle, the M & D wooden puzzles with the little red knobs, reading words out loud like "helicopter, enterprise, happiness" and has been repeating two-three words at a time instead of just one. He's also been playing appropriately with cars and has been showing me things (new behavior). He recently starting following my point to far away objects instead of just looking at the end of my finger. And now he points himself. Last week he pointed excitedly to a flock of birds flying overhead and said, "Birds! Birds!" He didn't point to anything except for things up close until about 3 weeks ago. (This is another autistic tendency that is going away.) And just today, he called out to a boy on a bicycle as he rode by. So, he's wanting to be more social. And the past two weeks he's been memorizing songs including "Itsy Bitsy Spider" and the ABC song. He hasn't gotten it perfect yet, but he's having fun with it. And he's been playing with stuffed animals and dolls--brand new behavior as well!

April 10, 2012/25 months

Jett read a whole book out loud, by himself for the first time on Saturday! It was 27 pages long-- The Eye Book by Dr. Seuss. It's late kindergarten level. (I need to record it but he says a lot of it very quietly... will try!)

He's also enjoying activities that involve more fine motor skills, is using his words to ask for things rather than just naming things and is following more commands. (He washed himself last night--rubbed each body part as I requested!) He can sing most of "Itsy Bitsy Spider" with the hand motions (not perfect) as well.



July 5, 2012/28 months old

Over the months, NP has moved into one of the "must have" slots on Jett's Supplement List. I continue to see social gains. He's still not initiating hugs or kisses but six weeks ago, I increased his dose of l-carnosine, which has helped to increase his expressive language. He now asks for "drink, sip, cup, milk or coconut(water)" when thirsty as well as "piece, bit, food, eat, pizza, soup, etc." when hungry. He wakes up and immediately asks for "Mary Poppins" or "Pooh" or "Readeez." Usually, about 25 times a day, it's "Mary Poppins." Check out my post on L-carnosine  for more details. He uses at least 50 words from his own head, not counting when we ask "What's this?" or when he's reading.

July 8, 2012/28 months old

Jett's been sick so hasn't taken his NP or most of his other supplements. I've been able to get only his thyroid, probiotics and l-carnosine in him consistently. (He had a little bit of magnesium and a little bit of zinc.) His amount of speech has dropped off considerably although he does find his words when he's thirsty, hungry or wanting to watch Mary Poppins.  

August 7, 2012/29 months

We hear two word sentences much more often now although most of what he says we can't understand. He talks a lot-- it's usually when he wants something that he looks at us and clearly states his needs. "Mommy milk", "Where's the pillow?", "Pizza food eat PLEASE!", "I see it!" and "I lub you so much!"

September 22/ 30 months

He reads really, really fast. Faster than he can talk. The speech therapist was shocked when she tried to get him to read a word out loud on the page. He wouldn't do it. Then he read the entire paragraph as fast as he possibly could out loud. (And I do mean as fast as you can read it out loud.) 
He's experimenting with language even more. "Just a little bit" and "I like it!" are his newest phrases. Today he said my shirt was "pretty" which he had just learned what that meant yesterday from a conversation my husband and I were having. And he pointed out that something was "shiny" on my shirt which he had just learned from watching Project Runway. So he is building his vocabulary on his own, without me having to sit and teach him what words mean.
He is also showing more interest in people other than just himself. Two days ago he sat on the couch between me and my husband. He touched my husband and me and said: "Mommy and Daddy. Mommy face." (and looked at me) "Daddy face." (and looked at my husband.) Then yesterday, in the same situation, he said, "Daddy's eyes. Mommy's eyes. Daddy's glasses." And took my husband's glasses off. "Mommy's glasses." And took mine off as well. Then he looked at us both and smiled. Then he tried to put our glasses back on us. (He probably hadn't really noticed our faces before this.)In the last couple of weeks he also started feeding me-- crackers and grapes. 

At 32 months, about a year on NP, he still isn't affectionate on the level of a typical child w/T21, but he does initiate gentle "head bumps" as he calls it. And will say, "Kisses!" so that everyone will kiss HIM. His idea of kissing is to lean toward you, forehead first. He has actually kissed me a couple of times with his mouth, and, although it wasn't his idea, he actively participated.

Update: 4.5 years old. He's been off NP for quite a while, over a year, at least. We just haven't been able to afford it. But I recently readded it. Wow! Love it! He had stopped playing with stuffed animals and just started up again. He also just started feeding my husband again. He has a baby brother now (who is 14 months old) and he spent the most time today that he ever has socializing with him. Granted, I said to Jett, "I wonder what Oliver's pajamas say today." And that's just too irresistible, so he had to go over and read his pajamas. And then I told Jett to ask Oliver what he wanted and he did, twice! Before, the only way I knew that Jett knew that Oliver existed was that Jett would carefully walk over him when he was on the floor. (And would mention Oliver's name in any word games we did.) Other new things I've seen so far:

He said goodbye to the principal at school and goodbye to every other adult on the way out--- normally he wouldn't even NOTICE anyone, let alone look at them, wave and say good bye!

And this morning he sang 5 songs--- full songs, from beginning to end, full melody. Of songs he hasn't heard in months.

And he's saying more specific things like: I have a hair in my mouth. Which is significant because he could feel it, figure out what it was, and was telling us to get it out. (He does speak very well, like 10 word sentences, etc.)

Also, we were at Whole Foods yesterday and there was this striking young black girl with an Afro and purple shirt and Jett said "Oh, she's cute!" Which was surprising, because, again, he normally doesn't notice people at all.





At 5 years old, we continue to see social progress on NP. I understand that he will gently rest his hand the back of another child in school that he likes. (That actually was the first sign of affection he gave to me when he started NP.) I know that he knows all the names of the kids in his class, but he still doesn't talk about any of them. At home, I feel that he's appropriately affectionate now. He even walked quickly toward me and smiled at me when I picked him up from school. We're almost done with the school year and this is the first time he did this. ALL the other kids run to their parents and hug them and smile. So we are getting there!

Research

Rutin and Quercitin are also known as Vitamin A and Carotenoids which act as an antioxidant, aids detoxification, aids the immune system, supports the microvilli in the digestive system, aids in the health of the thyroid gland.


Querecetin and T21
 
The potential use of diet for rational gene targeting in treating genetically-defined pathologies

Shazaan Hushmendy1, Lalithapriya Jayakumar1, Amy Hahn1, Devang Bhoiwala1, Dipti Bhoiwala1 and Dana Crawford11 Albany Medical College, Albany, NY





ABSTRACT

We have considered the novel possibility of treating pathologies whose genetic bases are defined with diet and nutrition. We reason that some healthy dietary nutrients can modulate the expression of disease-causing genes back toward the normal, attenuating the disease process while lowering treatment cost, toxicity, long-term risks, and improving compliance. Here, we chose clinical immunosuppression and Down Syndrome, genetically-defined pathologies caused by excessive IL-2 production and an extra chromosome 21, respectively. For immunosuppression, berry extract, curcumin, quercetin, sulforaphane, EGCG, Echinacea and others were tested on anti-CD3 activated primary human T-lymphocytes and mouse splenocytes in culture. Curcumin, sulforaphane, quercetin (in vitro and in vivo) and EGCG all significantly inhibited T-cell proliferation and IL-2 production, suggesting their potential in treating auto-immunity and transplant patients. The expression of two major Down syndrome candidate genes (RCAN1 and DYRK1A) was also evaluated following mouse dietary supplementation for 10 days. Quercetin and Echinacea both suppressed RCAN1 and DYRK1A protein levels. These results support our strategy of using healthy dietary supplements to treat genetically-defined pathologies; an approach that we believe is simple, healthy, and cost-effective. This research was supported by the Community Foundation.


Teratog Carcinog Mutagen. 2001;21(5):369-82.

Aneuploidy induced in lymphocytes of parents of trisomic 21 children.

Caria H, Chaveca T, Rueff J.

Source

Department of Genetics, Faculty of Medical Sciences, New University of Lisbon, Lisbon, Portugal.

Abstract

A possible predisposition to aneuploidy in trisomic 21 individuals, their parents, and a control group was evaluated. Peripheral blood lymphocytes from those three groups were used to study the induction of micronuclei (MN) by mitomycin C, cyclophosphamide, and quercetin. Induced MN were further analysed by C-banding and CREST antibody. Trisomic 21 individuals have spontaneous frequencies of MN significantly higher than their parents and the control group. Quercetin without metabolic activation induces MN in trisomic 21 and their parents at a significantly higher level than in control group. The group of the parents of trisomic 21 individuals exhibits higher frequencies of induced MN by mitomycin C and cyclophosphamide than controls. Mitomycin C significantly induced CREST-positive-MN in ten of the sixteen parents evaluated. The results obtained seem to suggest a unique behaviour for the parents of trisomic 21 patients consisting in an increased susceptibility to chromosome loss in the presence of clastogenic genotoxicants, suggesting a higher predisposition to aneuploidy.

Copyright 2001 Wiley-Liss, Inc.

PMID:

11746251

The following article discusses quercetin in some detail as it relates to dopamine.

http://www.ncbi.nlm.nih.gov/pubmed/12711835

Quercetin benefits

Excerpts:

Quercetin is a naturally occurring substance known as bioflavonoid that is found in high concentrations in the skin of apples, red onions, citrus fruits and red grapes. Quercetin benefits are numerous. It is a potent antioxidant that has anti-inflammatory properties and it is known to decrease allergy symptoms. It does this by blocking histamine action in the body...

...People who take 500 milligrams of quercetin three times a day find that their allergy symptoms are greatly relieved. Quercetin’s antihistamine action may also help some people relieve asthma symptoms as well. Other quercetin benefits include the anti-inflammatory properties of this substance that may help to reduce pain from disorders such as arthritis....

Some more quercetin benefits include the reduction of anxiety, depression and even fatigue. Collagen is needed for organ health and skin. Quercetin benefits the maintenance and health of collagen in the body and helps slow down the breakdown of collagen. This means that wrinkles and the aging and sagging of the skin can be slowed down as one grows older if they are getting enough quercetin in their daily diet. Internal organs stay stronger and healthier longer too.

One of the well known quercetin benefits is that of its ability to act as a natural blood pressure reducer. It has been shown through clinical studies that people who supplement daily with 730 milligrams of quercetin can significantly drop both their diastolic and systolic blood pressure. However, these were people who are in the initial stages of hypertension and are just beginning to have problems with their blood pressure. People who are established as being hypertensive and are having problems controlling their blood pressure with prescription medications may not be able to control their blood pressure by supplementing with Quercetin alone. You should always consult your doctor if you want to try another way to control your blood pressure.

Quercetin also benefits the entire cardiovascular system. People who have a high intake of Quercetin tend to have a lower risk for heart disease and stroke. Quercetin benefits the capillaries and connective tissues of the body which can help alleviate varicose veins, bruising and edema. Research into quercetin benefits also show that it can neutralize free radicals and prevent cell damage. It improves lung functioning so it is extremely beneficial to help in cases of bronchitis, asthma and emphysema.

...Some doctors caution that taking Quercetin as a daily supplement may interfere with medications they are taking because it can interfere with the liver’s ability to break them down. If you are taking prescription medications of any kind you should consult with your doctor before taking Quercetin supplements.

Luteolin and T21

Plant flavonoid found to reduce inflammatory response in the brain
May 19, 2008
Source: University of Illinois at Urbana-Champaign

...Inflammation plays a key role in many neurodegenerative diseases and also is implicated in the cognitive and behavioral impairments seen in aging.

The new study looked at luteolin (LOO-tee-OH-lin), a plant flavonoid known to impede the inflammatory response in several types of cells outside the central nervous system. The purpose of the study was to determine if luteolin could also reduce inflammation the brain, said animal sciences professor and principal investigator Rodney Johnson.

“One of the questions we were interested in is whether something like luteolin, or other bioactive food components, can be used to mitigate age-associated inflammation and therefore improve cognitive function and avoid some of the cognitive deficits that occur in aging,” Johnson said.

The researchers first studied the effect of luteolin on microglia. These brain cells are a key component of the immune defense. When infection occurs anywhere in the body, microglia respond by producing inflammatory cytokines, chemical messengers that act in the brain to orchestrate a whole-body response that helps fight the invading microorganism.

This response is associated with many of the most obvious symptoms of illness: sleepiness, loss of appetite, fever and lethargy, and sometimes a temporary diminishment of learning and memory. Neuroinflammation can also lead some neurons to self-destruct, with potentially disastrous consequences if it goes too far.

Graduate research assistant Saebyeol Jang studied the inflammatory response in microglial cells. She spurred inflammation by exposing the cells to lipopolysaccharide (LPS), a component of the cell wall of many common bacteria.

Those cells that were also exposed to luteolin showed a significantly diminished inflammatory response. Jang showed that luteolin was shutting down production of a key cytokine in the inflammatory pathway, interleukin-6 (IL-6). The effects of luteolin exposure were dramatic, resulting in as much as a 90 percent drop in IL-6 production in the LPS-treated cells.

“This was just about as potent an inhibition as anything we had seen previously,” Johnson said.

But how was luteolin inhibiting production of IL-6"

Jang began by looking at a class of proteins involved in intracellular signaling, called transcription factors, which bind to specific “promoter” regions on DNA and increase their transcription into RNA and translation into proteins.

Using electromobility shift assays, which measure the binding of transcription factors to DNA promoters, Jang eventually determined that luteolin inhibited IL-6 production by preventing activator protein-1 (AP-1) from binding the IL-6 promoter.

AP-1 is in turn activated by JNK, an upstream protein kinase. Jang found that luteolin inhibited JNK phosphorylation in microglial cell culture. The failure of the JNK to activate the AP-1 transcription factor prevented it from binding to the promoter region on the IL-6 gene and transcription came to a halt....

The findings indicate a possible role for luteolin or other bioactive compounds in treating neuroinflammation, Johnson said.

“It might be possible to use flavonoids to inhibit JNK and mitigate inflammatory reactions in the brain,” he said. “Inflammatory cytokines such as interleukin-6 are very well known to inhibit certain types of learning and memory that are under the control of the hippocampus, and the hippocampus is also very vulnerable to the insults of aging,” he said. “If you had the potential to decrease the production of inflammatory cytokines in the brain you could potentially limit the cognitive deficits that result.”

 ---

Luteolin flavonoid health benefit by Ray Sahelian, M.D.

Luteolin is a flavonoid, and more precisely one of the citrus bioflavonoids. Just like most flavonoids, it has antioxidant, anti-inflammatory, and anti-tumor properties. It is found in high amounts in parsley, thyme, peppermint, basil herb, celery and artichoke.


How it works
Luteolin exerts a variety of pharmacological activities and anti-oxidant properties associated with its capacity to scavenge oxygen and nitrogen species. It also shows potent anti-inflammatory activities by inhibiting nuclear factor kappa B (NFkB) signaling in immune cells.

Luteolin and brain inflammation
University of Illinois researchers report lutelin, found in celery and green peppers, can disrupt a component of the inflammatory response in the brain. Rodney Johnson of the University of Illinois at Urbana-Champaign and graduate student Saebyeol Jang found that luteolin inhibits a key pathway in the inflammatory response of microglia -- brain cells key to the body's immune defense. Microglial cells exposed to luteolin show a significantly diminished inflammatory response and there was reduced production of interleukin-6 -- used in cellular communication -- in the inflammatory pathway.

Luteolin Research

Decreased pro-inflammatory cytokine production by LPS-stimulated PBMC upon in vitro incubation with the flavonoids apigenin, luteolin or chrysin, due to selective elimination of monocytes/macrophages.
Biochem Pharmacol. 2005.
Apigenin and its structural analogues chrysin and luteolin were used to evaluate their capacity to inhibit the production of pro-inflammatory cytokines by lipopolysaccharide (LPS)-stimulated human peripheral blood mononuclear cells (PBMC). Furthermore, flowcytometric analysis was performed to compare the effects of apigenin, chrysin, luteolin, quercetin and naringenin on the different cell types present in PBMC. LPS-stimulated PBMC were cultured in the presence of the flavonoids and TNFalpha, IL-1beta and IL-6 were measured in the supernatants. In parallel, metabolic activity of the PBMC was determined by measuring succinate dehydrogenase activity. Apigenin, chrysin and luteolin dose-dependently inhibited both pro-inflammatory cytokine production and metabolic activity of LPS-stimulated PBMC. With increasing concentration of apigenin, chrysin or luteolin the monocytes/macrophages disappeared as measured by flowcytometry. This also appeared to occur in the non-LPS-stimulated PBMC. At the same time there was an increase in dead cells. T- and B-lymphocytes were not affected. Quercetin and naringenin had virtually no effects on cytokines, metabolic activity or on the number of cells in the studied cell populations. In conclusion, monocytes were specifically eliminated in PBMC by apigenin, chrysin or luteolin treatment in vitro at low concentrations (around 8 microM), in which apigenin appeared to be the most potent.

The flavones luteolin and apigenin inhibit in vitro antigen-specific proliferation and interferon-gamma production by murine and human autoimmune T cells.
Biochem Pharmacol. 2004.
Plant-derived flavonoids are inhibitors of various intracellular processes, notably phosphorylation pathways, and potential inhibitors of cellular autoimmunity. In this study, the inhibiting effects of various flavonoids on antigen-specific proliferation and interferon-gamma (IFN-gamma) production by human and murine autoreactive T cells were evaluated in vitro. T-cell responses were evaluated for the human autoantigen alpha B-crystallin, a candidate autoantigen in multiple sclerosis, and for the murine encephalitogen proteolipid protein peptide PLP (139-151). The flavones apigenin and  luteolin were found to be strong inhibitors of both murine and human T-cell responses while fisitin, quercitin, morin and hesperitin, members of the subclasses of flavonoles and flavanones, were ineffective. Antigen-specific IFN-gamma production was reduced more effectively by flavones than T-cell proliferation, suggesting that the intracellular pathway for IFN-gamma production in T cells is particularly sensitive to flavone inhibition. These results indicate that flavones but not flavanoles or flavanones are effective inhibitors of the potentially pathogenic function of autoreactive T cells. The effects of flavones were the same for human and murine autoreactive T cells, stressing the usefulness of animal models of autoimmunity for further studies on the effects of flavonones on autoimmune diseases.

Determination of free radical scavenging activity of quercetin, rutin, luteolin and apigenin in H2O2-treated human ML cells K562.
Neoplasma. 2004.
We investigated protective effects of four flavonoids against H2O2- induced DNA damage in human myelogenous leukemia cells (K562) using the comet assay. The structural difference of studied flavonoids -- quercetin, rutin, luteolin and apigenin -- are characterized by the number of hydroxyl groups on the B ring. The presence of an o-dihydroxy structure on the B-ring confers a higher degree of stability to the flavonoid phenoxyl radicals by participating in electron delocalization and is, therefore, an important determinant for antioxidative potential. The results correlate with earlier published data obtained in murine leukemia cell line L1210. Hydrogen peroxide induced in human K562 cells a concentration-dependent increase of single cell DNA strand breaks. The strongest inhibition against H2O2-induced DNA damage (44%, 42%) was found in a range of luteolin and quercetin concentrations of 20-100 micromol/l. Protective effect of rutin was only marginal (8-10%). Apigenin had no protective effect on DNA single strand breaks induced by H2O2. Luteolin and quercetin are therefore effective in the protection of human single cell DNA from oxidative attack.

Flavonoids such as luteolin, fisetin and apigenin are inhibitors of interleukin-4 and interleukin-13 production by activated human basophils.
Int Arch Allergy Immunol. 2004.
We have previously shown that fisetin, a flavonol, inhibits IL-4 and IL-13 synthesis by allergen- or anti-IgE-antibody-stimulated basophils. This time, we investigated the inhibition of IL-4 and IL-13 production by basophils by other flavonoids. We additionally investigated whether flavonoids suppress leukotriene C4 synthesis by basophils and IL-4 synthesis by T cells in response to anti-CD3 antibody. Highly purified peripheral basophils were stimulated for 12 h with anti-IgE antibody alone or anti-IgE antibody plus IL-3 in the presence of various concentrations of 18 different kinds of flavones and flavonols. IL-4 and IL-13 concentrations in the supernatants were then measured. Leukotriene C4 synthesis was also measured after basophils were stimulated for 1 h in the presence of flavonoids. Regarding the inhibitory activity of flavonoids on IL-4 synthesis by T cells, peripheral blood mononuclear cells were cultured with flavonoids in anti-CD3-antibody-bound plates for 2 days. Luteolin, fisetin and apigenin were found to be the strongest inhibitors of both IL-4 and IL-13 production by basophils but did not affect leukotriene C4 synthesis. At higher concentrations, these flavonoids suppressed IL-4 production by T cells. Based on a hierarchy of inhibitory activity, the basic structure for IL-4 inhibition by basophils was determined. Due to the inhibitory activity of flavonoids on IL-4 and IL-13 synthesis, it can be expected that the intake of flavonoids, depending on the quantity and quality, may ameliorate allergic symptoms or prevent the onset of allergic diseases.

Characteristic rat tissue accumulation of nobiletin, a chemopreventive polymethoxyflavonoid, in comparison with luteolin.
Biofactors. 2002.
Nobiletin, a polymethoxyflavonoid, is an effective anti-inflammatory and chemopreventive phytochemical found in citrus fruits. We compared the absorption and metabolism characteristics of nobiletin with those of luteolin in male SD rats. Our results suggest that the metabolic properties of polymethoxyflavonoids are distinct from those of other general flavonoids, because of their wide distribution and accumulation in tissue.

---
Can celery boost the memory?

The researchers suggested that aged mice may have more brain inflammation and therefore worse memories, so should normally perform worse in the test. Here they wanted to test how luteolin might affect this. They used 26 adult mice and 26 aged mice. Half of each group was given a standard diet while the other half was also given a supplement of 20mg of luteolin a day for four weeks.

After the experiment, the researchers assessed how much luteolin had been absorbed into the mouse blood. They also looked at which genes had been switched on in the hippocampus, a region of the brain that is associated with spatial memory. They determined the activity of the genes by looking at how much RNA was produced by each gene.


What were the basic results?

When exposed to LPS alone, the inflammatory response in the BV-2 cells was characterised by a greater release of a peptide called interleukin -1 (IL-1 ) and an increased activity in the gene that produces IL-1 and three other genes involved in inflammation that were measured.

BV-2 cells that had been treated with 50 mol/L of luteolin released 70% less IL-1 when exposed to LPS. Luteolin also reduced the activity of the gene that produced IL-1 and partially prevented the activity of the three other genes from being increased.

When the liquid (in which the BV-2 cells had been grown and treated with LPS) was mixed with neurone-like cells, some of the neurone-like cells died. However, BV-2 cells that had also been treated with luteolin caused a reduced amount of death of the neurone-like cells.

The researchers found that aged mice performed poorer on the water maze task, swimming further before they found the target. However, aged mice that had been given luteolin performed as well as the younger adult mice on this task. There was no difference in the performance of younger adult mice that had the luteolin-supplemented diet or normal diet.

The aged mice had higher levels of IL-1 mRNA in their hippocampus than adult mice, indicating that the IL-1 gene is more active in aged mice. The IL-I gene was less active in the aged mice that had been fed luteolin.


How did the researchers interpret the results?

The researchers suggest that luteolin improves spatial working memory in aged mice by affecting the microglial-associated inflammation in the brain's hippocampus. They suggest that luteolin consumption may be beneficial in preventing or treating conditions that involve increased microglial cell activity and inflammation.

Conclusion

This small animal study demonstrated that luteolin can interfere with microglial-mediated inflammation and improve spatial memory in aged mice, suggesting that microglial inflammation may play a role in spatial memory loss in mice.

Rutin and T21  










Rutin is a bioflavonoid found in rose hips, black currants, the rind of green citrus fruits, in tea, in buckwheat seeds and in berries like mulberry. While it has many potential benefits, more scientific research is needed to confirm them. Always consult your doctor before trying a new supplement and be aware that no regulated manufacturing standards for herbal compounds are in place, making it important to use products from reputable manufacturers.
Read more: http://www.livestrong.com/article/347639-what-are-the-health-benefits-of-rutin/#ixzz203BLIQXi


http://www.vaccinationnews.com/scandals/feb_15_02/comparison_symptoms.htm


Related Posts