Guest guest Posted November 19, 2004 Report Share Posted November 19, 2004 > My question is if he gets an antibiotic, should I ask for a > prescription for Nystatin. Yes. I have GSE which I havent used with him > yet. I tasted it today. YUCK- I have warts all over my hands and > have been to Dr. 5 times to have them burned off and they are still > here even after a bunch of home treatments. I read where GSE helped > cure someone's warts so i figured Id try it first. I have not read that GSE worked on a viral issue, altho you can certainly try it. I recently started olive leaf extract myself [when I had the flu last month] and I have noticed that two small warts are gone. >> I can still give > him the Culturelle also right? Yes. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 19, 2004 Report Share Posted November 19, 2004 Thanks Dana: I just got back from Doctor. He has double ear infections. She gave me Diflucan, she felt it was easier. I have been thinking about all this yeast and viral issues. My son very rarely had infections or antibiotics when he was young. He has had quite alot in the past 2 years with ear issues. Either infections from colds or swimmers ear. Now it seems funny to me that his OCD has gotten way out of control in the past two years. I thought of this when you brought up that alot of parents have felt that OCD is connected to Viral issues. So this should be very interesting indeed to see how he progresses with the OCD. When he is better from ears I will have to try the OLE to see what happens. I was feeling a bit down as I have not really seen positives with the enzymes, but his BM are much more consistent, still watery and sponge like with the exception of the one day they were beautiful LOL. I did get a chance today to talk with his aide at school and she noticed that his OCD is better (not at home) his anxiety a bit higher, but other than that no real problems (also circle walking more she included this in anxiety). THanks for your help Eileen >From: " danasview " <danasview@...> >Reply- > >Subject: Re: Ear infection >Date: Fri, 19 Nov 2004 15:21:41 -0000 > > > > > My question is if he gets an antibiotic, should I ask for a > > prescription for Nystatin. > > >Yes. > > > I have GSE which I havent used with him > > yet. I tasted it today. YUCK- I have warts all over my hands and > > have been to Dr. 5 times to have them burned off and they are still > > here even after a bunch of home treatments. I read where GSE helped > > cure someone's warts so i figured Id try it first. > > >I have not read that GSE worked on a viral issue, altho you can >certainly try it. > >I recently started olive leaf extract myself [when I had the flu last >month] and I have noticed that two small warts are gone. > > > >> I can still give > > him the Culturelle also right? > > >Yes. > >Dana > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2004 Report Share Posted November 21, 2004 > Thanks Dana: I just got back from Doctor. He has double ear infections. > She gave me Diflucan, she felt it was easier. Diflucan is an anti-fungal, so far as I know. So she determined that these infections were fungus/yeast based? My kids will get yeast in their ears also. Is the Diflucan working? It can be hard on the liver, so watch for that. >>I have been thinking about > all this yeast and viral issues. My son very rarely had infections or > antibiotics when he was young. He has had quite alot in the past 2 years > with ear issues. Either infections from colds or swimmers ear. Chlorine can really aggravate yeast issues http://www.danasview.net/chlorine.htm For my son, milk will cause excessive ear wax, even with enzymes, even after being fully chelated. So you might want to reduce or remove milk. I don't give my son glasses of milk, etc, but I do allow butter, cheese, and cream sauce and other things. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2004 Report Share Posted November 21, 2004 Hi Dana: No the doctor didnt tell me if she determined if the ear infections were yeast based. I just asked her for a script for Nystatin and she gave DiFlucan (1) tablet. I have not given it to him yet. I have been giving him the Culturelle. I was going to give the DiFlucan today. He does not drink milk. Has refused it since he is about a year old or so. The only milk based product he likes is ice cream. Wont eat cheese or any other dairy products either. The chlorine is something I never knew, but I am learning alot that I never knew before. I suppose he is CF except for the occasional ice cream, which is not often. Dinner last night was Hamburger (no bun) has always eaten it this way, french fries (baked in oven) but they are store bought, string beans. Thanks Eileen >From: " danasview " <danasview@...> >Reply- > >Subject: Re: Ear infection >Date: Sun, 21 Nov 2004 15:39:24 -0000 > > > > > Thanks Dana: I just got back from Doctor. He has double ear >infections. > > She gave me Diflucan, she felt it was easier. > > >Diflucan is an anti-fungal, so far as I know. So she determined that >these infections were fungus/yeast based? My kids will get yeast in >their ears also. Is the Diflucan working? It can be hard on the >liver, so watch for that. > > > >>I have been thinking about > > all this yeast and viral issues. My son very rarely had infections or > > antibiotics when he was young. He has had quite alot in the past 2 >years > > with ear issues. Either infections from colds or swimmers ear. > > >Chlorine can really aggravate yeast issues > >http://www.danasview.net/chlorine.htm > >For my son, milk will cause excessive ear wax, even with enzymes, even >after being fully chelated. So you might want to reduce or remove >milk. I don't give my son glasses of milk, etc, but I do allow >butter, cheese, and cream sauce and other things. > >Dana > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2004 Report Share Posted November 21, 2004 Yes, you can give Culturelle and GSE in the same day. I wouldn't necessarily give them at the same time of day, especially in the beginning as die-off is difficult enough with one product, much less two at once. We give Culturelle at night, as the die-off issues are easier to manage when they sleep through the initial effects of it. GSE die-off can produce some real rage issues, weepiness, etc. I'd do it when you know you have a couple of days when you're not on a real tight time schedule. Most days I'm a drill instructor, with routine, but when I know I'll be treating for something, I make the time to explain " why " 50 toys can't go with us in the car, and why this is not a tragedy worthy of crocodile tears. Things like this pop up all day and night during die-off, but I know his body is hurting, the equivalent of a massive headache, body ache, tummy ache, etc. So I take my time with him. Sorry if this e-mail is too long, but boy is it worth all the trouble when you can get things cleared up. Ex. My Mom has a terrible infection that required two antibiotics and an inhaler for asthma like symptoms. My son caught it from her. After 4 days of Olive Leaf extract, with no alleviation of symptoms, and 2 days of Oil of Oregano, with fever gone, cough minimized, draining already occurring, definitely worth the weepiness we experienced for about 50 minutes prior to dinner last night. Good luck to everyone. Ask your doctor about Calcium Butyrate if your child tests positive for Clostridia, really made a difference here. Ear infection > > > Hi-Me again-My son is going to doctor tomorrow as I believe he has > an ear infection. He stayed home today with a soar throat. When I > got home from work he complained that his ear hurt and he was warm. > My question is if he gets an antibiotic, should I ask for a > prescription for Nystatin. I have GSE which I havent used with him > yet. I tasted it today. YUCK- I have warts all over my hands and > have been to Dr. 5 times to have them burned off and they are still > here even after a bunch of home treatments. I read where GSE helped > cure someone's warts so i figured Id try it first. I can still give > him the Culturelle also right? Thanks Eileen > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2004 Report Share Posted November 21, 2004 ear infections, allergy, autism & gluten Date: 19 Jul 1995 Jack Challem, Editor of The Nutrition Reporter newsletter, wrote: >I'm sure you'll hear a lot of opinions. But I'll point to you to a >specific journal citation that confirmed what people have been saying for >years. The fundamental cause of ear infections is allergy, which causes fluid >retention in the ear, which creates a great breeding ground for bacteria. The >most common allergens for small children are milk and wheat. >Nsouli TM, " Role of food allergy in serious otitis media, " ls of Allergy, >September 1994;73:215-219. This is quite interesting because the IgA antibodies formed in the gut are transported to all mucous membranes in the body and may react with appropriate antigens. Because intact antigens are taken up into the blood postprandially (1) and we have also demonstrated increased levels of IgA antibodies to gluten, gliadin and casein in some autistic patients (2,3); I can easily see a possible connection, where all mucosal membranes are irritated by the circulating antigen reacting with deposited IgA antibodies. References: 1: Husby S et al (1985) Scand J Immunol 22:83-92. 2: Reichelt Kl et al (1990) J Applied Nutr. 42:1-11 3: Reichelt KL et al (1994) Develop Brain Dysfunct. 7:71-85 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2004 Report Share Posted November 21, 2004 Immunodeficiency, gastrointestinal Candidasis, wheat and diary sensitivity, abnormal urine arabinose, and autism: A Case Study by Shaw, Ph. D., Great Plains Laboratory Baptist, MD Ph.D., Speer Allergy Clinic & Geenens, D.O. Abstract A child with autism was found to have complete IgA deficiency (serum IgA <6 mg/dL; normal 33-235mg/dL), Candidiasis of the gastrointestinal tract based on evaluation of stool testing, elevated urine arabinose, and elevated serum antibodies to wheat and dairy products. The pretreatment urinary arabinose concentration (341 mmol/mol creatinine in this child was nearly six times the mean value (60.4 mmol/mol creatinine, n=20) of normal children and over ten times the median value (31.0 mmol/mol creatinine) of normal controls. After antifungal therapy for 4 months, the urine was retested. At the time the urine arabinose was measured at 51 mmol/mol creatinine, a value only 15% of the baseline sample. Restriction of wheat and dairy products from the diet and antifungal therapy led to a significant decrease in autistic behaviors and increased rate of learning. The Childhood Autism Rating Scale (CARS), an observational measure of various aspects of autism, for the child has decreased from a rating of 43 (severely autistic) prior to introduction of these therapies to a value of 29 (non- autistic) after therapy. Introduction Studies done by the late Warren Ph.D. at Utah State University and others indicate that most children with autism have a substantial immune abnormality of some type (1-20). Kontstantareas and Homatidis (21) at the University of Guelph in Ontario, Canada found a high correlation between the prevalence of ear infections and the incidence of autism. they found that the earlier the child had an ear infection, the more likely that child had a more severe form of autism. They also found that increased incidence of ear infections was associated with a more severe rather than a mild form of autism. Candida infection has been reported as consequence of frequent antibiotic usage in both humans and animals (22-30) and an abnormal increase in the sugar arabinose probably form Candida has been reported in urine sample of two siblings with autism (31). However, Candida infection may also be common in children with immunodeficiencies who do not have an unusually high number of infections treated with antibiotics. The patter of gastrointestinal Candida overgrowth, immunodeficiency, metabolic disorder and autism is well-illustrated in the medical history of the child evaluated by us. Previous medical evaluation The child evaluated is a five year old Caucasian male with a normal birth at term and normal apgar scores. Newborn metabolic screens for phenylketonuria, hypothyroidism, galactosemia, and sickle-cell disease were within normal limits. Both parents are college graduates; both parents are considered socially well-adjusted. The maternal grandmother suffered from multiple sclerosis and is now deceased. The maternal grandfather died secondary to viral cardiomyopathy; as a child he did not speak until three years of age but then talked and developed normally. The paternal grandparents are in good health. The child was evaluated by a pediatric opthalmologist at six months of age for intermittent crusting and tearing of the left eye which was non-responsive to antibiotic drops. The patient had surgery for the blocked tear-duct and a possible undescended testicle at 16 months. Exploratory surgery did not located the missing testicle; the patient was put on porphylactic antibiotics after surgery. Up to the age of three years, the patient had had only one or two ear infections treated by antibiotics, a couple of colds, and an upper respiratory infection. Immunizations were all on schedule. A routine physical examination at 15 months of age assessed development as normal although concerns about lack of speech were expressed by parents. The MMR vaccine was administered at this checkup. Assessment by the pediatrician at 18 months was a " healthy 1.5 year old " who " does not need to return until 2 years of age. " Deficiency of expressive language was noted in the medical record but the parents were not advised to seek additional consultation. At a pediatric evaluation at 2 years of age, lack of expressive language (only 5 words) was again noted by not follow-up was recommended. At a pediatric evaluation at 2.5 years of age, no expressive language was noted and the child was referred to a hearing and speech clinic for evaluation. Diet was noted to consist of bread, pancakes, milk peanut butter, and chicken. He was noted to always have loose stools. The subsequent hearing evaluation revealed normal hearing but recommended a developmental assessment of the child. Three months later at the age of 27 months, the child was diagnosed with autism by a developmental pediatrician at a university autism clinic using DSM-IV diagnostic criteria; developmental age was assessed as a t the 19-20 month level. At this exam, otitis media was diagnosed and treated with Amoxicillin. A MRI scan of the head revealed some atrophy of the frontotemporal lobe. EEG and fragile X chromosome studies were normal. The child was seen by a second university autism clinic in another state which confirmed the original diagnosis. The parents of the child were referred to support groups, to speech therapists, and to special schools for education and behavioral modification but were not referred for any evaluation of the child's immune or gastrointestinal function. When the child was 4.75 years of age, the parents decided to embark on additional biochemical assessment of their child including allergy assessment, routine chemistry and hematology, evaluation of stool microorganisms, evaluation of immune function, and urine organic acid testing. Comprehensive food allergy testing for 96 foods were performed using IgG specific enzyme linked immunoassay. The following allergens were positive for IgG-specific enzyme linked immunoassay: barley, gluten, heat, bran, cow's milk, cheeses (cheddar, cottage, and Swiss), beef, grapefruit, orange, peanut, soybean, and sugar. The IgA endomysial antibody test which is considered to be specific for celiac disease was negative in this child. Normal serum values were found for all of the following: glucose, urea nitrogen, creatinine, total protein, albumin, total bilirubin, alkaline phosphates, AST, ALT, LDH, calcium, phosphorus, blood lead, sodium, potassium, chloride, bicarbonate, uric acid, triglycerides, cholesterol, anion gap, thyroxine, antinuclear antibodies, thryotropin (highly sensitive), iron, copper, magnesium, corisol, zinc and ferritin. White cel count was slightly low (4900/mm3); normal: 5500-15,500/mm3. Hemoglobin and hematocrit were normal. The white cell differential was normal except for a slight elevation of atypical lymphocytes. The absolute number and percentage of CD3, Cd4, and CD8 cells, evaluated by flow cytometry were all within normal limits. Analysis of serum immunoglbulins revealed normal values for serum IgG, IgM, IgE and IgG subclasses but undetectable values for serum IgA (Table 1). Stool analysis revealed a 4+ overgrowth of Candida parapsilosis; normal is 0 and the highest possible overgrowth is 4+. Antifungal sensitivity of the organism indicated sensitivity to fluconzole, itraconazole, nystatin, ketoconazole, and garlic. Bacteria in the stool sample usually considred beneficial were Lactobacillus (2+) and Bifidobacteria (4+). Stool analysis also revealed 3+ levels of gamma streptococci and 4+ hemolytic E. coli. An evaluation of a urine sample by gas chromatography-mass spectrometry as described previously (31) taken at the same time indicated significant increases of the sugar arabinose as the major abnormality; there were no abnormalities associated with any recognized inborn error of metabolism. Therapy Because of elevated Candida in the stool sample, indicating a gastrointestinal yeast overgrowth, the child was placed on 100,000 Units nystatin four times a day plus alternating weeks of Nizoral or Diflucan (2mg/kg) and was also placed on a gluten and casein free diet approximately two months after beginning antifungal therapy. Both dietary and antifungal therapy are continuing five months later. The pretreatment urinary arabinose concentration (341 mmol/mol creatinine in this child was nearly six times the mean value (31.0 mmol/mol creatinine) of normal controls. After antifungal therapy for four months, the urine was retested. At that time the urine arabinose was measured at 51 mmol/mol creatinine, a value only 15% of the baseline sample. With two additional months of antifungal treatment, the urine arabinose value decreased to 26 mmol/mol creatinine. A follow-up stool test indicated the absence of Candida in the sample. Results of therapeutic interventions. The mother of the child reports a significant increase in eye contact, a significant decrease in self-stimulatory behavior, and increased use of spontaneous language shortly after beginning antifungal therapy. After beginning the casein and gluten free diet, the mother reports the child was able to follow three step verbal directions versus only one step directions previously. The mother also reported increased learning speed in the schooling program, increased verbal labeling, and increased spontaneous verbal initiations. The score for the child on the Childhood Autism Rating Scale (CARS), an observational measure of various aspects of autism has decreased from a rating of 43 (severely autistic) prior to introduction of these therapies to a value of 29 (non-autistic) after therapy. Cutoff for autism is 30 or above. The child is now considered by the assessment team at the sate university autism clinic to be a high-functioning individual with autism. The child can now parallel play with other children in class, demonstrates an interest in peers, shares toys, and is engaging in some imaginative play. Discussion Selective IgA deficiency. The most striking laboratory abnormality of this child is the absence of detectable IgA. IgA is the antibody that is involved with protection of the lining of the nasal passages and intestinal lining from microorganisms. Secretory IgA or sIgA is a special form of the IgA antibody that is secreted to protect the mucosa, which is the lining of the intestinal tract. Secretory IgA on a stool sample from this child was also noted as deficient. Secretory IgA is apparently secreted by the gall bladder and then trickles down the bile ducts into the small intestine. Some children with autism such as this one have very low or even completely absent levels of IgA (1,20); in such cases there is probably also a deficiency of a secretory IgA since IgA is derived from IgA. This extremely common immunodeficiency occurs in 1 in 600 - 1000 persons of European ancestry (32). The causes of IgA deficiency are not completely known. There are some cases in which the deficiency runs in families while in other cases it does not. It has been reported in association with abnormalities of chromosome 18, but most individuals with IgA deficiency have no detectable chromosomal abnormalities (32). IgA deficiency may also be cased by drugs or viral infection (rubella, cytomegalovirus, toxoplasmosis) and may be also be associated with intrauterine infections. Patients with IgA deficiency are usually deficient in both subtypes of IgA, IgA1 and IgA2. In Gupta's study (2), 20% of the children with autism had a deficiency of IgA and 8% lacked it completely. Warren and his colleagues (1) also found that 20% of individuals with autism had low serum IgA compared with none of the normal controls. Thus, complete IgA deficiency in autism is somewhere between 48 to 80 times higher in the autism population compared to a normal Caucasian population. IgA replacement therapy cannot be used currently because the short half-life of IgA would make it an extremely expensive therapy. However, bovine colostrum, which is commercially available is high in IgA and might be considered as a possible therapy for IgA- deficient patients. IgG therapy can be used with patients with low IgA values. If the IgA values are so low that they cannot even be detected, however, giving IgG therapy is too risky. It is possible that the immunodeficient person's body would produce antibodies against IgA present in gamma globulin, causing potentially fatal anaphylactic shock. The clinical consequences of IgA deficiency range from severe systemic infection to a perfectly healthy state. Many IgA-deficient persons are never aware of their antibody deficiency while others may have recurrent infections, allergic diseases, and autoimmune diseases (32). This child with autism had significant Candidiasis of the gastrointestinal tract despite the fact that the child had only two courses of antibiotics during his lifetime. Thus, intestinal Candidiasis following antibiotic therapy appears to be a much greater risk in a child with immunodeficiency. The decrease in symptoms of autism after antifungal therapy and gluten and casein restriction have been noted in many children with autism (33). (The authors are aware of three children with autism diagnosed at university autism centers who are now considered symptom-free after antifungal treatment and gluten and casein restriction). The child being presented was never considered a " sickly " child by the parents. It is possible that the difficult to treat eye crusting may have been related to the IgA deficiency since IgA is secreted in tears, saliva, and gastric juice; the deficient IgA in the tears may have led to a grater number of eye infections. The occurrence of multiple sclerosis in the maternal grandmother might be of significance but she was never evaluated for IgA deficiency. The remarkable spectrum of clinical manifestations of this immunodeficiency may be related to variations in the ability to replace IgA antibodies in the mucous secretions with IgM antibodies. IgG2 and IgG4 subclass deficiencies are common in IgA deficiency but were not present in this individual. IgA deficiency and celiac disease The incidence of selective IgA deficiency is 10 times higher in patients with celiac disease compared to the general population (34). The diagnosis of celiac disease cannot be excluded in an IgA deficient child because the endomysial antibody test uses an IgA antibody specificity and may yield false negative results in such cases (35) so the possibility that the child may have celiac disease cannot be excluded. The parents elected to place the child on a wheat and dairy-free diet based on the ELISA-allergy test results so a diagnosis of celiac disease by intestinal biopsy would not be valid for this child. Positive IgG antibodies to gluten were found in 100% of IgA-deficient persons with biopsy proven celiac disease but who were negative by the endomysial antibody test (35). Most children with autism are sensitive to both gluten, the major protein in wheat and barley, and to casein, the major protein in cow's milk (36-40). Elevation of IgG antibodies to wheat, barley and several dairy products is common in autism even though most children with autism do not have celiac disease (36-40). Candidiasis and abnormal arabinose: possible implications in brain structure and function The exact biochemical role of elevated arabinose is unknown but a closely related blood sugar alcohol, arabitol, has been used as biochemical indicator of invasive Candidiasis (41-43) We have never found elevated arabitol in thousands of urine samples tested, including many sample with elevated arabinose and high yeast counts in the stool. Elevated arabinose in the urine of two brothers with autism was first reported by Shaw et al. in 1995 (31) and has since then has been reported to prevalent in urine samples from people with autism (33); values as high as 4000 mmol/mol creatinine have been found in children with autism (unpublished data). We have found arabitol but not arabinose in the culture media of multiple isolates of Candida albicans isolated form stool samples of autistic children (unpublished data). Presumably elevated arabitol in the urine may only occur in systemic rather than gastrointestinal Candidiasis since arabitol in portal blood is converted to arabinose in the liver. Arabinose in the urine decreased markedly after antifungal therapy, concomitantly with an elimination of stool Candida. Arabinose, a sugar aldehyde or aldose reacts with the epsilon amino group of lysine in a wide variety of proteins and may form cross-links with arginine residues in an adjoining protein (44), thereby cross-linking the proteins and altering both bilogical structures and functions of a wide variety of proteins including proteins involved in the interconnection of neurons. Decreased clinical symptoms of autism after antifungal treatment would be due to decreased arabinose and pentosidine formation, resulting in fewer random neural connections (neural noise) and increased numbers of neural connections that are oriented to the child's environment. This adduct of arabinose, lysine, and arginine is called pentosidine (Figure 1). The epsilon amino group of lysine is a critical functional group of many enzymes to which pyridoxal (vitamin B-6), biotin and lipoic acid are covalently bonded during coenzymatic reactions (45); the blockage of these active lysine sites by pentosidine formation may cause functional vitamin deficiencies even when nutritional intake is adequate. In addition, this epsilon amino group of lysine may also be important in the active catalytic site of many enzymes. Protein modification caused by pentosidine formation is associated with cross link formation, decreased protein solubility, and increased protease resistance. The characteristic patholigical structures called nerofibrillary tangles associated with Alzheimer disease contain modifications typical of pentosidine formation. Specifically, antibodies against pentosidine react strongly to neurofibrillary tangles and senile plaques in brain tissue from patients with Alzheimer disease (46). In contrast, little or no reaction is observed in apparently healthy neurons of the same brain. thus, it appears that the neurofibrillary tangles of Alzheimer's disease may be caused by the pentosidines. The modification of protein structure and function caused by arabinose could account for the biochemical and insolubility properties of the lesions of Alzheimer disease through formation of protein cross links. Similar damage to the brains of autistic children might also be due to the the pentosidine cross-links. Since pyridoxal (vitamin B-6) reacts with the same critical epsilon amino group of lysine, it is possible that the beneficial effects of vitamin B-6 in autism reported in multiple studies (48) may be mediated by prevention of further pentosidine formation. Analysis of brain tissue of people with autism for increased brain pentosidines could be invaluable in the confirmation of this hypothesis. Women with vulvovagnitis due to Candida were found to have elevated arabinose in the urine (49); restriction of dietary sugar brought about a dramatic reduction in the incidence and severity of the vulvovaginitis. Thus, one of the mechanisms of action of antifungal drug therapy for autism might be to reduce the concentration of an abnormal carbohydrate produced by the yeast that can not be tolerated by the child with defective pentose metabolism or an inability to remove harmful pentosidines. Arabinose tolerance tests should be able to rapidly determine if such biochemical defects are present in children with autism. A model for autism The success of Gupota (2) in treating the autistic symptoms of children with autism with gamma globulin therapy indicates an immune abnormality in autism. Based on these findings and our findings of abnormal arabinose and other organic acids in other children with autism (31,33), we propose the following model for autism. According to this model, immune deficiencies which may be genetic or acquired lead to an increased frequency of infections which in the United States are almost always treated with broad spectrum oral antibiotic usage and greater proliferation of yeasts and antibiotic- resistant bacteria, setting up a vicious cycle. These organisms produce high amounts of abnormal carbohydrates such as arabinose and Krebs cycle analogs such as citramalic and tartaric acids (31). there is no inherent reason that dramatic biochemical changes in multiple biochemical systems caused by microorganisms would not be expected to alter brain structure and function. In PKU, correction of the metabolic defect by restriction of phenylalanine during infancy allows for normal development; retardation occurs if dietary intervention occurs too late. If abnormally elevated metabolites cause autism, then it is reasonable to think that elevations of these compounds would have maximum negative impact during periods of critical brain growth and development. As in PKU, metabolic intervention in autism night only be possible in the early stages of the disorder before the brain has matured. The differences in severity of disease and individual differences in symptoms might be due to different combinations of metabolites become abnormally elevated, and the susceptibility of the individual developing nervous system to the different microbial metabolites. some children with autism have a history of frequent infections: two different parents of children with autism indicated to the authors that their children had over 50 consecutive infections (predominantly otitis media) treated with antibiotics. However, some children with autism such as the child presented here id not have excessive use of oral antibiotics and was not considered to be a " sickly child " by the parents or attending physicians. In this child the underlying immune deficiency and two uses of antibiotics apparently led to a persistent yeast overgrowth of the intestinal tract. Generic immunodeficiencies proposed as the major genetic factors in autism. Ritvo et al. (54) found a concordance rate for autism of 23.5% in dizygotic twins and 95.7% in monozygotic twins, indicating a strong genetic basis for autism. However, the results of the Stanford autism genetics study of 90 families affected by autism (55) indicate " that there are no genes with a major effect for autism. This is, our analyses show that autism is almost surely not a simply single major gene disorder, such as Huntington disease. Rather, the analyses from these 90 families indicate that there are likely to be a relatively large number of different genes related to susceptibility for autism, each with a minor effect. " We suspect that many of these " relatively large number of genes " are those that regulate the immune system. We have been impressed with the large number of studies that have indicated a wide number of abnormalities of the immune system in autism (1-20) including IgG deficiency, IgA deficiency, IgG subclass deficiency, myeloperoxiase deficiency (a genetic defect in an enzyme of the leukocytes that produces hypochorite ion to kill yeast), reduced natural killer cell activity, markedly elevated serum levels of cytokines interleukin-12 and interferon-gamma, increased anti-myelin and serotonin receptor antibodies, increased DR+ T cells, and a deficiency in complement C4b. In addition, some immune abnormalities in autism have been linked to adverse reactions to vaccinations (56). The two brothers with autism in which abnormal arabinose and abnormal organic acids were first reported (431) both had abnormally low concentrations of serum IgG. Autism has also been diagnosed in other children with defined inborn errors of metabolism such as biotinidase deficiency and isovaleric acidemia (Lombard, Personal Communication) in which yeast infections are common. Efforts to locate a single autism gene would fail since any generic factor that severely impairs the immune system may eventually lead to the proliferation of antibiotic-resistant yeasts and bacteria which then alter behavior of children at critical periods of development through the excretion of abnormal microbial metabolic products. Thus, autism appears to be a complex metabolic disorder involving immune deficiencies, autoimmune abnormalities, abnormal food sensitivities, and gastrointestinal microbial overgrowths that may result in altered human metabolism and protein function. Figure 1. Reaction of arabinose from yeast with amino groups of lysine to form a Schiff base adduct. The rearranged Schiff base then reacts with a guanido group on an arginine residue of a second protein, resulting in tow different proteins crosslinked through a pentosidine moiety. Figure 2. Immunodeficiency model for autism. In this model, immunodeficiencies lead to antibiotic use that stimulates yeast overgrowth (primarily Candida) of the gastrointestinal tract. Certain strains of Candida produce immunosuppressant compounds called gliotoxins that further weaken the immune system and may lead to additional infections. Arabitol produced by Candida in the gastrointestinal tract is converted to arabinose in the liver. Elevated arabinose then leads to pentosidine formation, leading to increased neurofibrillary tangles in the brain. Table 1. Serum immunoglobulins in child with autism Immunoglobulins class Child's value Reference Range IgG 833 mg/dL 593-1723 mg/dL IgA <6 mg/dL 33-235 mg/dL IgM 51 mg/dL 36-314 mg/dL IgE 10 IU/ml 2-35 IU/ml IgG-1 444 mg/dL 370-994 mg/dL IgG-2 180 mg/dL 88-455 mg/dL IgG-3 30 mg/dL 11-108 mg/dL IgG-4 33 mg/dL 1-97 mg/dL References Immunodeficiency, gastrointestinal Candidasis, wheat and diary sensitivity, abnormal urine arabinose, and autism: A Case Study by Shaw, Ph. D., Great Plains Laboratory Baptist, MD Ph.D., Speer Allergy Clinic & Geenens, D.O. Abstract A child with autism was found to have complete IgA deficiency (serum IgA <6 mg/dL; normal 33-235mg/dL), Candidiasis of the gastrointestinal tract based on evaluation of stool testing, elevated urine arabinose, and elevated serum antibodies to wheat and dairy products. The pretreatment urinary arabinose concentration (341 mmol/mol creatinine in this child was nearly six times the mean value (60.4 mmol/mol creatinine, n=20) of normal children and over ten times the median value (31.0 mmol/mol creatinine) of normal controls. After antifungal therapy for 4 months, the urine was retested. At the time the urine arabinose was measured at 51 mmol/mol creatinine, a value only 15% of the baseline sample. Restriction of wheat and dairy products from the diet and antifungal therapy led to a significant decrease in autistic behaviors and increased rate of learning. The Childhood Autism Rating Scale (CARS), an observational measure of various aspects of autism, for the child has decreased from a rating of 43 (severely autistic) prior to introduction of these therapies to a value of 29 (non- autistic) after therapy. Introduction Studies done by the late Warren Ph.D. at Utah State University and others indicate that most children with autism have a substantial immune abnormality of some type (1-20). Kontstantareas and Homatidis (21) at the University of Guelph in Ontario, Canada found a high correlation between the prevalence of ear infections and the incidence of autism. they found that the earlier the child had an ear infection, the more likely that child had a more severe form of autism. They also found that increased incidence of ear infections was associated with a more severe rather than a mild form of autism. Candida infection has been reported as consequence of frequent antibiotic usage in both humans and animals (22-30) and an abnormal increase in the sugar arabinose probably form Candida has been reported in urine sample of two siblings with autism (31). However, Candida infection may also be common in children with immunodeficiencies who do not have an unusually high number of infections treated with antibiotics. The patter of gastrointestinal Candida overgrowth, immunodeficiency, metabolic disorder and autism is well-illustrated in the medical history of the child evaluated by us. Previous medical evaluation The child evaluated is a five year old Caucasian male with a normal birth at term and normal apgar scores. Newborn metabolic screens for phenylketonuria, hypothyroidism, galactosemia, and sickle-cell disease were within normal limits. Both parents are college graduates; both parents are considered socially well-adjusted. The maternal grandmother suffered from multiple sclerosis and is now deceased. The maternal grandfather died secondary to viral cardiomyopathy; as a child he did not speak until three years of age but then talked and developed normally. The paternal grandparents are in good health. The child was evaluated by a pediatric opthalmologist at six months of age for intermittent crusting and tearing of the left eye which was non-responsive to antibiotic drops. The patient had surgery for the blocked tear-duct and a possible undescended testicle at 16 months. Exploratory surgery did not located the missing testicle; the patient was put on porphylactic antibiotics after surgery. Up to the age of three years, the patient had had only one or two ear infections treated by antibiotics, a couple of colds, and an upper respiratory infection. Immunizations were all on schedule. A routine physical examination at 15 months of age assessed development as normal although concerns about lack of speech were expressed by parents. The MMR vaccine was administered at this checkup. Assessment by the pediatrician at 18 months was a " healthy 1.5 year old " who " does not need to return until 2 years of age. " Deficiency of expressive language was noted in the medical record but the parents were not advised to seek additional consultation. At a pediatric evaluation at 2 years of age, lack of expressive language (only 5 words) was again noted by not follow-up was recommended. At a pediatric evaluation at 2.5 years of age, no expressive language was noted and the child was referred to a hearing and speech clinic for evaluation. Diet was noted to consist of bread, pancakes, milk peanut butter, and chicken. He was noted to always have loose stools. The subsequent hearing evaluation revealed normal hearing but recommended a developmental assessment of the child. Three months later at the age of 27 months, the child was diagnosed with autism by a developmental pediatrician at a university autism clinic using DSM-IV diagnostic criteria; developmental age was assessed as a t the 19-20 month level. At this exam, otitis media was diagnosed and treated with Amoxicillin. A MRI scan of the head revealed some atrophy of the frontotemporal lobe. EEG and fragile X chromosome studies were normal. The child was seen by a second university autism clinic in another state which confirmed the original diagnosis. The parents of the child were referred to support groups, to speech therapists, and to special schools for education and behavioral modification but were not referred for any evaluation of the child's immune or gastrointestinal function. When the child was 4.75 years of age, the parents decided to embark on additional biochemical assessment of their child including allergy assessment, routine chemistry and hematology, evaluation of stool microorganisms, evaluation of immune function, and urine organic acid testing. Comprehensive food allergy testing for 96 foods were performed using IgG specific enzyme linked immunoassay. The following allergens were positive for IgG-specific enzyme linked immunoassay: barley, gluten, heat, bran, cow's milk, cheeses (cheddar, cottage, and Swiss), beef, grapefruit, orange, peanut, soybean, and sugar. The IgA endomysial antibody test which is considered to be specific for celiac disease was negative in this child. Normal serum values were found for all of the following: glucose, urea nitrogen, creatinine, total protein, albumin, total bilirubin, alkaline phosphates, AST, ALT, LDH, calcium, phosphorus, blood lead, sodium, potassium, chloride, bicarbonate, uric acid, triglycerides, cholesterol, anion gap, thyroxine, antinuclear antibodies, thryotropin (highly sensitive), iron, copper, magnesium, corisol, zinc and ferritin. White cel count was slightly low (4900/mm3); normal: 5500-15,500/mm3. Hemoglobin and hematocrit were normal. The white cell differential was normal except for a slight elevation of atypical lymphocytes. The absolute number and percentage of CD3, Cd4, and CD8 cells, evaluated by flow cytometry were all within normal limits. Analysis of serum immunoglbulins revealed normal values for serum IgG, IgM, IgE and IgG subclasses but undetectable values for serum IgA (Table 1). Stool analysis revealed a 4+ overgrowth of Candida parapsilosis; normal is 0 and the highest possible overgrowth is 4+. Antifungal sensitivity of the organism indicated sensitivity to fluconzole, itraconazole, nystatin, ketoconazole, and garlic. Bacteria in the stool sample usually considred beneficial were Lactobacillus (2+) and Bifidobacteria (4+). Stool analysis also revealed 3+ levels of gamma streptococci and 4+ hemolytic E. coli. An evaluation of a urine sample by gas chromatography-mass spectrometry as described previously (31) taken at the same time indicated significant increases of the sugar arabinose as the major abnormality; there were no abnormalities associated with any recognized inborn error of metabolism. Therapy Because of elevated Candida in the stool sample, indicating a gastrointestinal yeast overgrowth, the child was placed on 100,000 Units nystatin four times a day plus alternating weeks of Nizoral or Diflucan (2mg/kg) and was also placed on a gluten and casein free diet approximately two months after beginning antifungal therapy. Both dietary and antifungal therapy are continuing five months later. The pretreatment urinary arabinose concentration (341 mmol/mol creatinine in this child was nearly six times the mean value (31.0 mmol/mol creatinine) of normal controls. After antifungal therapy for four months, the urine was retested. At that time the urine arabinose was measured at 51 mmol/mol creatinine, a value only 15% of the baseline sample. With two additional months of antifungal treatment, the urine arabinose value decreased to 26 mmol/mol creatinine. A follow-up stool test indicated the absence of Candida in the sample. Results of therapeutic interventions. The mother of the child reports a significant increase in eye contact, a significant decrease in self-stimulatory behavior, and increased use of spontaneous language shortly after beginning antifungal therapy. After beginning the casein and gluten free diet, the mother reports the child was able to follow three step verbal directions versus only one step directions previously. The mother also reported increased learning speed in the schooling program, increased verbal labeling, and increased spontaneous verbal initiations. The score for the child on the Childhood Autism Rating Scale (CARS), an observational measure of various aspects of autism has decreased from a rating of 43 (severely autistic) prior to introduction of these therapies to a value of 29 (non-autistic) after therapy. Cutoff for autism is 30 or above. The child is now considered by the assessment team at the sate university autism clinic to be a high-functioning individual with autism. The child can now parallel play with other children in class, demonstrates an interest in peers, shares toys, and is engaging in some imaginative play. Discussion Selective IgA deficiency. The most striking laboratory abnormality of this child is the absence of detectable IgA. IgA is the antibody that is involved with protection of the lining of the nasal passages and intestinal lining from microorganisms. Secretory IgA or sIgA is a special form of the IgA antibody that is secreted to protect the mucosa, which is the lining of the intestinal tract. Secretory IgA on a stool sample from this child was also noted as deficient. Secretory IgA is apparently secreted by the gall bladder and then trickles down the bile ducts into the small intestine. Some children with autism such as this one have very low or even completely absent levels of IgA (1,20); in such cases there is probably also a deficiency of a secretory IgA since IgA is derived from IgA. This extremely common immunodeficiency occurs in 1 in 600 - 1000 persons of European ancestry (32). The causes of IgA deficiency are not completely known. There are some cases in which the deficiency runs in families while in other cases it does not. It has been reported in association with abnormalities of chromosome 18, but most individuals with IgA deficiency have no detectable chromosomal abnormalities (32). IgA deficiency may also be cased by drugs or viral infection (rubella, cytomegalovirus, toxoplasmosis) and may be also be associated with intrauterine infections. Patients with IgA deficiency are usually deficient in both subtypes of IgA, IgA1 and IgA2. In Gupta's study (2), 20% of the children with autism had a deficiency of IgA and 8% lacked it completely. Warren and his colleagues (1) also found that 20% of individuals with autism had low serum IgA compared with none of the normal controls. Thus, complete IgA deficiency in autism is somewhere between 48 to 80 times higher in the autism population compared to a normal Caucasian population. IgA replacement therapy cannot be used currently because the short half-life of IgA would make it an extremely expensive therapy. However, bovine colostrum, which is commercially available is high in IgA and might be considered as a possible therapy for IgA- deficient patients. IgG therapy can be used with patients with low IgA values. If the IgA values are so low that they cannot even be detected, however, giving IgG therapy is too risky. It is possible that the immunodeficient person's body would produce antibodies against IgA present in gamma globulin, causing potentially fatal anaphylactic shock. The clinical consequences of IgA deficiency range from severe systemic infection to a perfectly healthy state. Many IgA-deficient persons are never aware of their antibody deficiency while others may have recurrent infections, allergic diseases, and autoimmune diseases (32). This child with autism had significant Candidiasis of the gastrointestinal tract despite the fact that the child had only two courses of antibiotics during his lifetime. Thus, intestinal Candidiasis following antibiotic therapy appears to be a much greater risk in a child with immunodeficiency. The decrease in symptoms of autism after antifungal therapy and gluten and casein restriction have been noted in many children with autism (33). (The authors are aware of three children with autism diagnosed at university autism centers who are now considered symptom-free after antifungal treatment and gluten and casein restriction). The child being presented was never considered a " sickly " child by the parents. It is possible that the difficult to treat eye crusting may have been related to the IgA deficiency since IgA is secreted in tears, saliva, and gastric juice; the deficient IgA in the tears may have led to a grater number of eye infections. The occurrence of multiple sclerosis in the maternal grandmother might be of significance but she was never evaluated for IgA deficiency. The remarkable spectrum of clinical manifestations of this immunodeficiency may be related to variations in the ability to replace IgA antibodies in the mucous secretions with IgM antibodies. IgG2 and IgG4 subclass deficiencies are common in IgA deficiency but were not present in this individual. IgA deficiency and celiac disease The incidence of selective IgA deficiency is 10 times higher in patients with celiac disease compared to the general population (34). The diagnosis of celiac disease cannot be excluded in an IgA deficient child because the endomysial antibody test uses an IgA antibody specificity and may yield false negative results in such cases (35) so the possibility that the child may have celiac disease cannot be excluded. The parents elected to place the child on a wheat and dairy-free diet based on the ELISA-allergy test results so a diagnosis of celiac disease by intestinal biopsy would not be valid for this child. Positive IgG antibodies to gluten were found in 100% of IgA-deficient persons with biopsy proven celiac disease but who were negative by the endomysial antibody test (35). Most children with autism are sensitive to both gluten, the major protein in wheat and barley, and to casein, the major protein in cow's milk (36-40). Elevation of IgG antibodies to wheat, barley and several dairy products is common in autism even though most children with autism do not have celiac disease (36-40). Candidiasis and abnormal arabinose: possible implications in brain structure and function The exact biochemical role of elevated arabinose is unknown but a closely related blood sugar alcohol, arabitol, has been used as biochemical indicator of invasive Candidiasis (41-43) We have never found elevated arabitol in thousands of urine samples tested, including many sample with elevated arabinose and high yeast counts in the stool. Elevated arabinose in the urine of two brothers with autism was first reported by Shaw et al. in 1995 (31) and has since then has been reported to prevalent in urine samples from people with autism (33); values as high as 4000 mmol/mol creatinine have been found in children with autism (unpublished data). We have found arabitol but not arabinose in the culture media of multiple isolates of Candida albicans isolated form stool samples of autistic children (unpublished data). Presumably elevated arabitol in the urine may only occur in systemic rather than gastrointestinal Candidiasis since arabitol in portal blood is converted to arabinose in the liver. Arabinose in the urine decreased markedly after antifungal therapy, concomitantly with an elimination of stool Candida. Arabinose, a sugar aldehyde or aldose reacts with the epsilon amino group of lysine in a wide variety of proteins and may form cross-links with arginine residues in an adjoining protein (44), thereby cross-linking the proteins and altering both bilogical structures and functions of a wide variety of proteins including proteins involved in the interconnection of neurons. Decreased clinical symptoms of autism after antifungal treatment would be due to decreased arabinose and pentosidine formation, resulting in fewer random neural connections (neural noise) and increased numbers of neural connections that are oriented to the child's environment. This adduct of arabinose, lysine, and arginine is called pentosidine (Figure 1). The epsilon amino group of lysine is a critical functional group of many enzymes to which pyridoxal (vitamin B-6), biotin and lipoic acid are covalently bonded during coenzymatic reactions (45); the blockage of these active lysine sites by pentosidine formation may cause functional vitamin deficiencies even when nutritional intake is adequate. In addition, this epsilon amino group of lysine may also be important in the active catalytic site of many enzymes. Protein modification caused by pentosidine formation is associated with cross link formation, decreased protein solubility, and increased protease resistance. The characteristic patholigical structures called nerofibrillary tangles associated with Alzheimer disease contain modifications typical of pentosidine formation. Specifically, antibodies against pentosidine react strongly to neurofibrillary tangles and senile plaques in brain tissue from patients with Alzheimer disease (46). In contrast, little or no reaction is observed in apparently healthy neurons of the same brain. thus, it appears that the neurofibrillary tangles of Alzheimer's disease may be caused by the pentosidines. The modification of protein structure and function caused by arabinose could account for the biochemical and insolubility properties of the lesions of Alzheimer disease through formation of protein cross links. Similar damage to the brains of autistic children might also be due to the the pentosidine cross-links. Since pyridoxal (vitamin B-6) reacts with the same critical epsilon amino group of lysine, it is possible that the beneficial effects of vitamin B-6 in autism reported in multiple studies (48) may be mediated by prevention of further pentosidine formation. Analysis of brain tissue of people with autism for increased brain pentosidines could be invaluable in the confirmation of this hypothesis. Women with vulvovagnitis due to Candida were found to have elevated arabinose in the urine (49); restriction of dietary sugar brought about a dramatic reduction in the incidence and severity of the vulvovaginitis. Thus, one of the mechanisms of action of antifungal drug therapy for autism might be to reduce the concentration of an abnormal carbohydrate produced by the yeast that can not be tolerated by the child with defective pentose metabolism or an inability to remove harmful pentosidines. Arabinose tolerance tests should be able to rapidly determine if such biochemical defects are present in children with autism. A model for autism The success of Gupota (2) in treating the autistic symptoms of children with autism with gamma globulin therapy indicates an immune abnormality in autism. Based on these findings and our findings of abnormal arabinose and other organic acids in other children with autism (31,33), we propose the following model for autism. According to this model, immune deficiencies which may be genetic or acquired lead to an increased frequency of infections which in the United States are almost always treated with broad spectrum oral antibiotic usage and greater proliferation of yeasts and antibiotic- resistant bacteria, setting up a vicious cycle. These organisms produce high amounts of abnormal carbohydrates such as arabinose and Krebs cycle analogs such as citramalic and tartaric acids (31). there is no inherent reason that dramatic biochemical changes in multiple biochemical systems caused by microorganisms would not be expected to alter brain structure and function. In PKU, correction of the metabolic defect by restriction of phenylalanine during infancy allows for normal development; retardation occurs if dietary intervention occurs too late. If abnormally elevated metabolites cause autism, then it is reasonable to think that elevations of these compounds would have maximum negative impact during periods of critical brain growth and development. As in PKU, metabolic intervention in autism night only be possible in the early stages of the disorder before the brain has matured. The differences in severity of disease and individual differences in symptoms might be due to different combinations of metabolites become abnormally elevated, and the susceptibility of the individual developing nervous system to the different microbial metabolites. some children with autism have a history of frequent infections: two different parents of children with autism indicated to the authors that their children had over 50 consecutive infections (predominantly otitis media) treated with antibiotics. However, some children with autism such as the child presented here id not have excessive use of oral antibiotics and was not considered to be a " sickly child " by the parents or attending physicians. In this child the underlying immune deficiency and two uses of antibiotics apparently led to a persistent yeast overgrowth of the intestinal tract. Generic immunodeficiencies proposed as the major genetic factors in autism. Ritvo et al. (54) found a concordance rate for autism of 23.5% in dizygotic twins and 95.7% in monozygotic twins, indicating a strong genetic basis for autism. However, the results of the Stanford autism genetics study of 90 families affected by autism (55) indicate " that there are no genes with a major effect for autism. This is, our analyses show that autism is almost surely not a simply single major gene disorder, such as Huntington disease. Rather, the analyses from these 90 families indicate that there are likely to be a relatively large number of different genes related to susceptibility for autism, each with a minor effect. " We suspect that many of these " relatively large number of genes " are those that regulate the immune system. We have been impressed with the large number of studies that have indicated a wide number of abnormalities of the immune system in autism (1-20) including IgG deficiency, IgA deficiency, IgG subclass deficiency, myeloperoxiase deficiency (a genetic defect in an enzyme of the leukocytes that produces hypochorite ion to kill yeast), reduced natural killer cell activity, markedly elevated serum levels of cytokines interleukin-12 and interferon-gamma, increased anti-myelin and serotonin receptor antibodies, increased DR+ T cells, and a deficiency in complement C4b. In addition, some immune abnormalities in autism have been linked to adverse reactions to vaccinations (56). The two brothers with autism in which abnormal arabinose and abnormal organic acids were first reported (431) both had abnormally low concentrations of serum IgG. Autism has also been diagnosed in other children with defined inborn errors of metabolism such as biotinidase deficiency and isovaleric acidemia (Lombard, Personal Communication) in which yeast infections are common. Efforts to locate a single autism gene would fail since any generic factor that severely impairs the immune system may eventually lead to the proliferation of antibiotic-resistant yeasts and bacteria which then alter behavior of children at critical periods of development through the excretion of abnormal microbial metabolic products. Thus, autism appears to be a complex metabolic disorder involving immune deficiencies, autoimmune abnormalities, abnormal food sensitivities, and gastrointestinal microbial overgrowths that may result in altered human metabolism and protein function. Figure 1. Reaction of arabinose from yeast with amino groups of lysine to form a Schiff base adduct. The rearranged Schiff base then reacts with a guanido group on an arginine residue of a second protein, resulting in tow different proteins crosslinked through a pentosidine moiety. Figure 2. Immunodeficiency model for autism. In this model, immunodeficiencies lead to antibiotic use that stimulates yeast overgrowth (primarily Candida) of the gastrointestinal tract. Certain strains of Candida produce immunosuppressant compounds called gliotoxins that further weaken the immune system and may lead to additional infections. Arabitol produced by Candida in the gastrointestinal tract is converted to arabinose in the liver. Elevated arabinose then leads to pentosidine formation, leading to increased neurofibrillary tangles in the brain. Table 1. Serum immunoglobulins in child with autism Immunoglobulins class Child's value Reference Range IgG 833 mg/dL 593-1723 mg/dL IgA <6 mg/dL 33-235 mg/dL IgM 51 mg/dL 36-314 mg/dL IgE 10 IU/ml 2-35 IU/ml IgG-1 444 mg/dL 370-994 mg/dL IgG-2 180 mg/dL 88-455 mg/dL IgG-3 30 mg/dL 11-108 mg/dL IgG-4 33 mg/dL 1-97 mg/dL References http://www.parentsofallergicchildren.org/autism.htm Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 22, 2004 Report Share Posted November 22, 2004 > Dinner last night was Hamburger (no bun) has always eaten it this way, > french fries (baked in oven) but they are store bought, string beans. My son did not tolerate orange or green foods, even with enzymes. You might try removing foods with those colors, see if things might improve. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 My son is in DOC band for two months now. He started pulling his ears a week after he got started on his band. When i mentioned that during our 2nd week visit to Cranial Tech we were told that it should be an ordinary ear infection and it is not related to his banding. My son is still suffering from ear infection and cold and cough (and fever sometimes). Is there any relation between using band and ear infection ? Please let me know. Thank you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 My son is in DOC band for two months now. He started pulling his ears a week after he got started on his band. When i mentioned that during our 2nd week visit to Cranial Tech we were told that it should be an ordinary ear infection and it is not related to his banding. My son is still suffering from ear infection and cold and cough (and fever sometimes). Is there any relation between using band and ear infection ? Please let me know. Thank you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi!! I have read that kids with plagio may have a higher incidence of ear infections due to misshapen ear canals. I don't know how true this is. But, Sophie's ear infections were always on her 'bad' side. Interesting. Have you done antibiotics? Also use tylenol and sudafed under your doctor's recommended doses. This really seems to help with the discomfort. Our first son (non-plagio) did have lots of ear infections and we ended up getting him tubes in his ears. This was a great decision as he STILL gets infections and now they can drain and be treated at the source! I hope your son feels better. I know they can be miserable. Sorry for the sleepless nights!! - Boise, Idaho Sophie - 10 months - STAR helmet 3/15/06 > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi!! I have read that kids with plagio may have a higher incidence of ear infections due to misshapen ear canals. I don't know how true this is. But, Sophie's ear infections were always on her 'bad' side. Interesting. Have you done antibiotics? Also use tylenol and sudafed under your doctor's recommended doses. This really seems to help with the discomfort. Our first son (non-plagio) did have lots of ear infections and we ended up getting him tubes in his ears. This was a great decision as he STILL gets infections and now they can drain and be treated at the source! I hope your son feels better. I know they can be miserable. Sorry for the sleepless nights!! - Boise, Idaho Sophie - 10 months - STAR helmet 3/15/06 > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi there. My son had 2 starbands and a docband and he is 18 months old. He is yet to have an ear infection (knock on wood). He did grab at his ears all the time, I am not sure but I think he just likes playing with them. He and his twin sister (who does not have plagio) did go through a period when they were always sick with a cold or flu. I can't tell if that is from the band or from the travelling we did to get the band or being run down from the extra stress of going to the chiro 3 times a week. I have read alot about plagiocephaly causing ear infections though it has never been an issue for us. I hope your son feels better soon. It can be such a handful caring for a sick child especially when there doesn't seem to be any sign of it letting up. Good luck. Haylee Mom to Andre DOC band grad > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi there. My son had 2 starbands and a docband and he is 18 months old. He is yet to have an ear infection (knock on wood). He did grab at his ears all the time, I am not sure but I think he just likes playing with them. He and his twin sister (who does not have plagio) did go through a period when they were always sick with a cold or flu. I can't tell if that is from the band or from the travelling we did to get the band or being run down from the extra stress of going to the chiro 3 times a week. I have read alot about plagiocephaly causing ear infections though it has never been an issue for us. I hope your son feels better soon. It can be such a handful caring for a sick child especially when there doesn't seem to be any sign of it letting up. Good luck. Haylee Mom to Andre DOC band grad > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi, Welcome to the group. There is no relation to bands and ear infections. I have read that plagio babies w/ear asymmetry are more prone to ear infections though. Keep us posted on your little one's progress. > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi, Welcome to the group. There is no relation to bands and ear infections. I have read that plagio babies w/ear asymmetry are more prone to ear infections though. Keep us posted on your little one's progress. > > My son is in DOC band for two months now. He started pulling his ears > a week after he got started on his band. When i mentioned that during > our 2nd week visit to Cranial Tech we were told that it should be an > ordinary ear infection and it is not related to his banding. > > My son is still suffering from ear infection and cold and cough (and > fever sometimes). Is there any relation between using band and ear > infection ? Please let me know. > > Thank you. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2006 Report Share Posted May 16, 2006 Hi, I am hoping that you can help me with the following. My 18 month old nephew has just had an ear infection, his elder brother (7) is asd. Is there any cause for concern regarding his ear infection? if so, what steps/precautions should we take? Thanks. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2006 Report Share Posted May 16, 2006 The path you don't want to take with ear infections is antibiotics. They rarely help, but do a great job depressing the immune system and setting you up for problems down the road. I have used garlic/mullein oil drops (eclectic kids brand) with great success. They are a bit messy, but generally work overnight. They cannot be used if there is a perforation--that is, if you notice fluid leaking from the ear. If ear infections are a rare event, then the drops should do the trick. If they are common, you need to address the root cause (diet perhaps) and find ways to boost the immune system. I think there are a number of us whose children are ASD in part because of antibiotics from ear infections. Don't let a doctor scare you into using them as anything but a very last resort. Anita > > Hi, > > I am hoping that you can help me with the following. > My 18 month old nephew has just had an ear infection, his elder > brother (7) is asd. Is there any cause for concern regarding his ear > infection? if so, what steps/precautions should we take? > > Thanks. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2006 Report Share Posted May 17, 2006 > > Hi, > > I am hoping that you can help me with the following. > My 18 month old nephew has just had an ear infection, his elder > brother (7) is asd. Is there any cause for concern regarding his ear > infection? if so, what steps/precautions should we take? For many kids, removing milk will eliminate ear infections, so you can try that. For my son, I had to address improper fat digestion before his ear issues were gone. My son needed mito cocktail and amino acids, I wrote about it here http://www.danasview.net/mar05.htm Dana Quote Link to comment Share on other sites More sharing options...
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