mes paskiepijom, 8 para prasidejo...limfmazgiai padidejo, ant tonziliu pulinukai, uzburkusios gleivines, kosulys... gydytojos spejimu cia viskas del to, kad maze buvo neseniai prasirgus pries pora menesiu...imunitetas dar silpnas...
special, manau kad jus liga ir skiepai nieko bendro neturi. pora menesiu po ligos, vaikui, neturinciam imuniniu problemu pilnai uztenka atsistatyti.
o mes tikriausiai sita skiepa atidesim neribotam laikui. labai jau sunku nuspresti, juk norisi kaip geriau vaikui...
O mes va snd pasiskiepijom MMR, kadangi ne LT gyvenam tai cia nuo siu ligu skiepija 12-15 menesiu, gudytoja sake, kad be tempos pakilimo, po mazdaug 4sav gali limfmazgiai padideti, mazdaug po 6sav isberti 
Tikiuosi viskas bus gerai. Ir JUms linkiu nesirgti ir lengvai pernesti skiepus
Tikiuosi viskas bus gerai. Ir JUms linkiu nesirgti ir lengvai pernesti skiepus
siaip nuo MMR reakcijos pasireiskia ne iskart, o 10 -14 dienu begyje, del 6 sav tai pirma karta girdziu , ir berti neturetu, jeigu isberia tai reiskais jus susirgot vakcinoasocijuotais tymais, reiktu kreiptis i gydytoja
cia apie tymu epidimijas Zydu gyvenvietese . reikejo vienam neskiepytam vaikui uznesti sia liga ir per 5 men susirgo 107 vaikai, 91.5 proc. neskiepyti
http://www.ncbi.nlm....l=pubmed_docsum
Jerusalem District Health Office, Ministry of Health, Israel.
In 2003 and 2004 two measles outbreaks occurred in Jewish ultra-orthodox communities in Jerusalem. The index case of the first outbreak (March 2003) was a 2-year-old unvaccinated child from Switzerland. Within 5 months, 107 cases (mean age 8.3+/-7.5 years) emerged in three crowded neighbourhoods. The first cases of the second outbreak (June 2004) were in three girls aged 4-5 years in one kindergarten in another community. By November 2004, 117 cases (mean age 7.3+/-6.5 years) occurred. The virus genotypes were D8 and D4 respectively. Altogether, 96 households accounted for the two outbreaks, with two or more patients per family in 79% of cases. Most cases (91.5%) were unvaccinated. Immunization coverage was lower in outbreak than in non-outbreak neighbourhoods (88.3% vs. 90.3%, P=0.001). Controlling the outbreaks necessitated a culture-sensitive approach, and targeted efforts increased MMR vaccine coverage (first dose) to 95.2%. Despite high national immunization coverage (94-95%), special attention to specific sub-populations is essential.
http://www.ncbi.nlm....l=pubmed_docsum
Jerusalem District Health Office, Ministry of Health, Israel.
In 2003 and 2004 two measles outbreaks occurred in Jewish ultra-orthodox communities in Jerusalem. The index case of the first outbreak (March 2003) was a 2-year-old unvaccinated child from Switzerland. Within 5 months, 107 cases (mean age 8.3+/-7.5 years) emerged in three crowded neighbourhoods. The first cases of the second outbreak (June 2004) were in three girls aged 4-5 years in one kindergarten in another community. By November 2004, 117 cases (mean age 7.3+/-6.5 years) occurred. The virus genotypes were D8 and D4 respectively. Altogether, 96 households accounted for the two outbreaks, with two or more patients per family in 79% of cases. Most cases (91.5%) were unvaccinated. Immunization coverage was lower in outbreak than in non-outbreak neighbourhoods (88.3% vs. 90.3%, P=0.001). Controlling the outbreaks necessitated a culture-sensitive approach, and targeted efforts increased MMR vaccine coverage (first dose) to 95.2%. Despite high national immunization coverage (94-95%), special attention to specific sub-populations is essential.
Labai sunku pasverti visus už ir prieš. Gyvenu Airijoje, čia irgi vaikai skiepijami 12-15 mėn. Aš gaunu tokį internetinį laikraštuką iš Patrick Holford, gerai žinomo Aglijoje ir šiaip visiems anglakalbiams, kurie rūpinasi savo sveikata. Kas labai nori, tegu parašo man, išversiu šį straipsnį. Patrick Holford nevienintelis taip manantis, kituose šaltiniuose irgi teko kažką panašaus skaityti.
GETTING TO THE GUTS OF TRUTH ABOUT AUTISM, ALLERGY AND MMR
WAS DR.ANDREW WAKEFIELD RIGHT ABOUT THE LINK BETWEEN AUTISM, THE GUT, ALLERGY AND THE MMR VACCINE?
Next month Dr Andrew Wakefield, who found a link between autism, the MMR vaccine, and abnormal gut reactions, is facing a hearing with the General Medical Council, and may be struck off for, in effect, challenging the status quo. If you think this is wrong, as I do, please click here to sign this petition.
If you are not sure, then please read on to find out what we know about autism, the gut, vaccinations and what food has to do with it. The strongest direct evidence of foods linked to autism involves wheat and dairy, and the specific proteins they contain - namely gluten and casein. These are difficult to digest and, especially if introduced too early in life, may result in an allergy. Fragments of these proteins, called peptides, can mimic chemicals in the brain called endorphins, so they're often referred to as 'exorphins'. These exporphin peptides have damaging opioid-like effects in the brain, leading to the many symptoms we describe as autism. Researchers at the Autism Research Unit at Sunderland University have found increased levels of these peptides in the blood and urine of children with autism [1].
What's Going on in the Gut
To understand how these common foods can be so harmful to sensitive individuals, we need to look at how they get into the body via the gut. Opioid peptides are derived from the incomplete digestion of proteins, particularly food containing gluten and casein. One such peptide, IAG, derived from gluten in wheat, is detected in 80 per cent of autistic patients [2], while another, gliadorphin-7, has been found in very large amounts in 54 per cent of autistic children, but only in very small amounts in just 32 per cent of non-autistic children [3]. So the first problem is the poor digestion of proteins. Zinc and vitamin B6 can help autistic children, and here it is worth noting that these two nutrients are essential for proper stomach acid production and therefore protein digestion. But even then, these partially digested protein fragments shouldn't enter the bloodstream. So how do they? Vitamin A deficiency is certainly one culprit, but there may be more.
A large proportion of parents with autistic children report that their child received repeated or prolonged courses of antibiotic drugs for ear or other respiratory infections during the first year of life, prior to the diagnosis of autism. Broad spectrum antibiotics kill good as well as bad bacteria in the gut, weakening the intestinal membranes. This can lead to what is known as leaky gut syndrome, in which large molecules that shouldn't be absorbed through the gut membrane do get through [4]. Dr Andrew Wakefield, in a now controversial study, published in the Lancet in February 1998, of 60 autistic children with gastrointestinal symptoms, found much greater incidences of intestinal lesions than in non-autistic children with similar digestive problems. Over 90 per cent of autistic children showed clinical evidence of chronic inflammation of the small and large intestine as a result of infection, at levels greater than six times that found in non-autistic children with inflammatory bowel disease [5].
Despite a concerted effort to discredit Wakefield's research, recent studies are confirming the link between autism, digestive problems, immune system abnormalities and the MMR vaccine. Wakefield's own research has shown that, in a group of 15 autistic children versus healthy children, there is clear evidence of immune dysfunction [6]. Three studies have shown measles antibodies in the central nervous system, with the potential to damage both brain and gut. [7;8;9]
So restoring a healthy gut in autistic children is very important. Supplementing digestive enzymes and probiotics is known to produce positive clinical results in autistic children, as these nutrients help heal the digestive tract and restore normal absorption [10]. Improving the healthy balance of bacteria in the digestive tract, which can be helped by taking probiotic supplements, may also help by digesting exorphins in the gut before they can be inappropriately absorbed [11]. The amino acid L-glutamine is especially important in restoring the integrity of the digestive tract. Drinking 5g dissolved in water just before bedtime can help heal the gut.
Cutting Out Wheat and Dairy
Clearly though, removing suspect foods from the diet is key, and there are many anecdotal reports of dramatic improvements from parents who remove casein and gluten from their autistic children's diet [12]. It can take some time for the harmful peptides to be removed from the blood and brain, so results can be slow to emerge. Dr Robert Cade, professor of medicine and physiology at the University of Florida, has observed that as the levels of peptides in the blood decrease, the symptoms of autism decrease. 'If they can be reduced to normal range,' he says, 'most patients either improve dramatically or become completely normal.' But you need to rigidly adhere to a gluten/casein-free diet to accomplish this [13].
The Autism Research Unit at Sunderland University recommend a gradual withdrawal of foods, waiting three weeks after the removal of casein (dairy) before removing gluten (wheat, oats, barley, rye) from the diet. Keep a food diary and note behaviours and symptoms alongside. This can help to identify other problematic foods, which commonly include citrus fruits, chocolate, artificial food colourings, salicylates, eggs, tomatoes, avocados, aubergine, red peppers, soya and corn [14]. Because you need to ensure that these foods are replaced rather than just removed, as well as being fully aware of all those foods that contain gluten and/or casein, this is best done under the guidance of a nutritional therapist.
The MMR Vaccine Debate
The official line is that there's no good evidence of a danger of the MMR vaccine causing autism in children. There's some truth to this, in that Dr Andrew Wakefield's research at the Royal Free Hospital [15], while important, was the first hint of a problem and it may be too early to jump to conclusions. Of course, the last thing the medical profession want is a whole lot of children not being vaccinated, since that increases the risk of epidemics. Here's what Wakefield actually said: 'Although MMR cannot by any means be described as a cause of autism, a child genetically predisposed to asthma, eczema , food allergy or intolerance, perhaps with possible disruption of the gut flora or with a fungal overgrowth, deficient in vitamins, minerals and essential fatty acids, may be at risk from MMR. For them MMR could be described as the straw that broke the camel's back, tipping the balance of normal childhood development into a retrogressive state. [16]' However, despite many attempts to discredit Wakefield, a recent review of all the available evidence on autism and vaccination concludes 'there has not been a single credible study that can robustly refute the claims of the parents that their children's acquired autism has been caused by MMR or related measles-containing vaccines, or thimerosal-containing vaccines.' [17] A recent study found that in 55 out of 824 children with autism, the parents reported clear signs of regression associated with the MMR vaccine. If correct, this means that 6.7 per cent of autistic children, or 1 in 15, are attributed to the MMR vaccine, according to parents. [18]
For most children, the MMR vaccine is unlikely to be a problem, but having said this, no one really knows the full consequences of giving a child three immune attacks - mumps, measles and rubella - all at the same time. Getting all three illnesses at once simply doesn't occur in nature, so there's a logical argument for single vaccines if a parent so chooses, especially for children with weakened immune systems. Perhaps for these children, with nutrient deficiencies, lacking essential fatty acids, susceptible to food allergies, infections and/or gut problems, these triple vaccines are the last straw.
So just what is the evidence against MMR? First, studies have shown a high incidence of autism in children whose mothers had received live virus vaccines (particularly the MMR or rubella vaccine) immediately prior to conception during pregnancy, or immediately following birth [19]. Secondly, there are two classifications of autism: the first where autistic traits are noted from birth and the second where symptoms are noted at 18 months plus. Autism onset at 18 months was uncommon until the mid-1980s, when the MMR vaccine came into wide use. After that the incidence shot up [20]. Thirdly, there is now evidence that measles antibodies can lie in the central nervous system, potentially damaging brain and gut. In fact, many autistic children are found to have measles antibodies in the gut. It's a bit like having a chronic infection. It seems that this triple vaccine makes measles persist. The antidote for measles is vitamin A. This is one of the most important infection fighters for this virus.
The late Dr Bernard Rimland said that the problem may not be the vaccine itself, but a preservative used in multi-dose vials of many childhood vaccines till very recently. Thimerosal, a preservative containing high levels of mercury, was used in many vaccines up until 2001. Before this, each vaccine injection exposed the child to levels of toxic mercury in excess of the US federal government's own safety guidelines, and a child receiving all their jabs could have received a total of 187.5mcg of mercury - enough to give them heavy metal poisoning [21]. Mercury is known to inhibit the enzyme that digests gluten and casein, possibly increasing a child's susceptibility to wheat and milk allergy.
Although it is too early to conclude, it is entirely possible that late-onset autism may be triggered by multiple vaccinations, allergies, toxic overload or nutritional deficiencies and especially combinations of any of these that send a child's gut and brain into distress.
If you've like to sign a petition to stop the General Medical Council striking off Dr Andrew Wakefield please click here.
Wishing you the best of health
Send to a Friend
If you have friends or relatives who you think would be interested in this e-letter, please forward it to them for their information.
Subscribe to 100%health Newsletter
If you would like to receive Patrick Holford's 100%health bi-monthly newsletter and get regular in-depth features on a range of health and nutrition issues - as well as discounts on books, seminars and other health products - click here to find out more.
References
[1] Whiteley, P, Sunderland University Autism Unit, talk given at the Autism Unravelled Conference, London, May 2001
[2] Whiteley, P et al, 'A gluten-free diet as an intervention for autism and associated disorders: preliminary findings', Autism: International Journal of research and Practice, Vol 3, 1999, pp45-65
[3] J Robert Cade, University of Florida Department of Medicine and Physiology, at www.panix.com/paleodiet/autism/cadelet.txt
[4] Letter to the Editor, 'Anti-fungal drugs more helpful than Ritalin in autistic children', Townsend Letter for Doctors and Patients, April 2001, p99
[5] A J Wakefield et al, 'Ileal-lymphoid hyperplasia, non-specific colitis and pervasive developmental disorder in children with autism', Lancet, Vol 351, 1998, pp637-41
[6] P. Ashwood and A Wakefield, 'Immune activation of peripheral blood and mucosal CD3 lymphocyte Cytokine profiles in children with autism and gastrointestinal symptoms', J Neuroimmunol, Vol 173(1-2), 2006, pp. 126-34
[7] V. K. Singh et al., 'Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism', J Biomed Sci, Vol 9, 2002, pp. 359-364
[8] J. J. Bradstreet et al, 'Detection of measles virus genomic RNA in cerebrospinal fluid of children with regressive autism: A report of three cases', JAPS, Vol 9 (2), pp. 38-45)
[9] H.S. Singer, 'Antibrain antibodies in children with autism and their unaffected siblings', J Neuroimmunol, Vol 178(1-2), 2006, pp. 149-55
[10] M A Brudnack, 'Application of genomeceuticals to the molecular and immunological aspects of autism', Med Hypoth, Vol 57(2), 2001, pp186-91
[11] P Varmanen et al, 'S54X-prolyl dipeptidyl aminopeptidase gene (pepX) is part of the glnRA operon in Lactobaccilus rhamnosus', J Bacteriol, vol 182(1), 2000, pp146-54
[12] P. Whiteley et al, 'A gluten-free diet as an intervention for autism and associated disorders: preliminary findings', Autism: International Journal of research and Practice, Vol 3, 1999, pp45-65
[13] J Robert Cade, University of Florida Department of Medicine and Physiology, at www.panix.com/paleodiet/autism/cadelet.txt
[14] M. Ash and E. Gilmore, 'Modifying autism through functional nutrition', paper given at Allergy Research Group conference, January 2001
[15] A. J. Wakefield et al, 'Ileal-lymphoid hyperplasia, non-specific colitis and pervasive developmental disorder in children with autism', Lancet, Vol 351, 1998, pp637-41
[16] Andrew Wakefield, speaking at the Allergy Research Foundation conference, November 1999
[17] D. Thrower, 'Autism and MMR - Summary of Published Research', available from www.foodforthebrain.org under ' reports'
[18] P. Shattock, presentation, Food for The Brain Conference, 1 October 2006
[19] F. E. Yazbak, 'Autism - is there a vaccine connection?' See www.autisme.net/Yaxbak1.htm
[20] B Rimland, J Nut Env Med, vol 10, 2000 pp267-9
[21] B. Rimland J Nut Env Med, vol 10, 2000 pp267-9; See also Ashcraft and Gerel (law firm), 'Autism caused by childhood vaccinations containing Thimerosal or mercury', which considers the litigation of individual claims, on www.ashcraftandgerel.com/thimerosal.html
GETTING TO THE GUTS OF TRUTH ABOUT AUTISM, ALLERGY AND MMR
WAS DR.ANDREW WAKEFIELD RIGHT ABOUT THE LINK BETWEEN AUTISM, THE GUT, ALLERGY AND THE MMR VACCINE?
Next month Dr Andrew Wakefield, who found a link between autism, the MMR vaccine, and abnormal gut reactions, is facing a hearing with the General Medical Council, and may be struck off for, in effect, challenging the status quo. If you think this is wrong, as I do, please click here to sign this petition.
If you are not sure, then please read on to find out what we know about autism, the gut, vaccinations and what food has to do with it. The strongest direct evidence of foods linked to autism involves wheat and dairy, and the specific proteins they contain - namely gluten and casein. These are difficult to digest and, especially if introduced too early in life, may result in an allergy. Fragments of these proteins, called peptides, can mimic chemicals in the brain called endorphins, so they're often referred to as 'exorphins'. These exporphin peptides have damaging opioid-like effects in the brain, leading to the many symptoms we describe as autism. Researchers at the Autism Research Unit at Sunderland University have found increased levels of these peptides in the blood and urine of children with autism [1].
What's Going on in the Gut
To understand how these common foods can be so harmful to sensitive individuals, we need to look at how they get into the body via the gut. Opioid peptides are derived from the incomplete digestion of proteins, particularly food containing gluten and casein. One such peptide, IAG, derived from gluten in wheat, is detected in 80 per cent of autistic patients [2], while another, gliadorphin-7, has been found in very large amounts in 54 per cent of autistic children, but only in very small amounts in just 32 per cent of non-autistic children [3]. So the first problem is the poor digestion of proteins. Zinc and vitamin B6 can help autistic children, and here it is worth noting that these two nutrients are essential for proper stomach acid production and therefore protein digestion. But even then, these partially digested protein fragments shouldn't enter the bloodstream. So how do they? Vitamin A deficiency is certainly one culprit, but there may be more.
A large proportion of parents with autistic children report that their child received repeated or prolonged courses of antibiotic drugs for ear or other respiratory infections during the first year of life, prior to the diagnosis of autism. Broad spectrum antibiotics kill good as well as bad bacteria in the gut, weakening the intestinal membranes. This can lead to what is known as leaky gut syndrome, in which large molecules that shouldn't be absorbed through the gut membrane do get through [4]. Dr Andrew Wakefield, in a now controversial study, published in the Lancet in February 1998, of 60 autistic children with gastrointestinal symptoms, found much greater incidences of intestinal lesions than in non-autistic children with similar digestive problems. Over 90 per cent of autistic children showed clinical evidence of chronic inflammation of the small and large intestine as a result of infection, at levels greater than six times that found in non-autistic children with inflammatory bowel disease [5].
Despite a concerted effort to discredit Wakefield's research, recent studies are confirming the link between autism, digestive problems, immune system abnormalities and the MMR vaccine. Wakefield's own research has shown that, in a group of 15 autistic children versus healthy children, there is clear evidence of immune dysfunction [6]. Three studies have shown measles antibodies in the central nervous system, with the potential to damage both brain and gut. [7;8;9]
So restoring a healthy gut in autistic children is very important. Supplementing digestive enzymes and probiotics is known to produce positive clinical results in autistic children, as these nutrients help heal the digestive tract and restore normal absorption [10]. Improving the healthy balance of bacteria in the digestive tract, which can be helped by taking probiotic supplements, may also help by digesting exorphins in the gut before they can be inappropriately absorbed [11]. The amino acid L-glutamine is especially important in restoring the integrity of the digestive tract. Drinking 5g dissolved in water just before bedtime can help heal the gut.
Cutting Out Wheat and Dairy
Clearly though, removing suspect foods from the diet is key, and there are many anecdotal reports of dramatic improvements from parents who remove casein and gluten from their autistic children's diet [12]. It can take some time for the harmful peptides to be removed from the blood and brain, so results can be slow to emerge. Dr Robert Cade, professor of medicine and physiology at the University of Florida, has observed that as the levels of peptides in the blood decrease, the symptoms of autism decrease. 'If they can be reduced to normal range,' he says, 'most patients either improve dramatically or become completely normal.' But you need to rigidly adhere to a gluten/casein-free diet to accomplish this [13].
The Autism Research Unit at Sunderland University recommend a gradual withdrawal of foods, waiting three weeks after the removal of casein (dairy) before removing gluten (wheat, oats, barley, rye) from the diet. Keep a food diary and note behaviours and symptoms alongside. This can help to identify other problematic foods, which commonly include citrus fruits, chocolate, artificial food colourings, salicylates, eggs, tomatoes, avocados, aubergine, red peppers, soya and corn [14]. Because you need to ensure that these foods are replaced rather than just removed, as well as being fully aware of all those foods that contain gluten and/or casein, this is best done under the guidance of a nutritional therapist.
The MMR Vaccine Debate
The official line is that there's no good evidence of a danger of the MMR vaccine causing autism in children. There's some truth to this, in that Dr Andrew Wakefield's research at the Royal Free Hospital [15], while important, was the first hint of a problem and it may be too early to jump to conclusions. Of course, the last thing the medical profession want is a whole lot of children not being vaccinated, since that increases the risk of epidemics. Here's what Wakefield actually said: 'Although MMR cannot by any means be described as a cause of autism, a child genetically predisposed to asthma, eczema , food allergy or intolerance, perhaps with possible disruption of the gut flora or with a fungal overgrowth, deficient in vitamins, minerals and essential fatty acids, may be at risk from MMR. For them MMR could be described as the straw that broke the camel's back, tipping the balance of normal childhood development into a retrogressive state. [16]' However, despite many attempts to discredit Wakefield, a recent review of all the available evidence on autism and vaccination concludes 'there has not been a single credible study that can robustly refute the claims of the parents that their children's acquired autism has been caused by MMR or related measles-containing vaccines, or thimerosal-containing vaccines.' [17] A recent study found that in 55 out of 824 children with autism, the parents reported clear signs of regression associated with the MMR vaccine. If correct, this means that 6.7 per cent of autistic children, or 1 in 15, are attributed to the MMR vaccine, according to parents. [18]
For most children, the MMR vaccine is unlikely to be a problem, but having said this, no one really knows the full consequences of giving a child three immune attacks - mumps, measles and rubella - all at the same time. Getting all three illnesses at once simply doesn't occur in nature, so there's a logical argument for single vaccines if a parent so chooses, especially for children with weakened immune systems. Perhaps for these children, with nutrient deficiencies, lacking essential fatty acids, susceptible to food allergies, infections and/or gut problems, these triple vaccines are the last straw.
So just what is the evidence against MMR? First, studies have shown a high incidence of autism in children whose mothers had received live virus vaccines (particularly the MMR or rubella vaccine) immediately prior to conception during pregnancy, or immediately following birth [19]. Secondly, there are two classifications of autism: the first where autistic traits are noted from birth and the second where symptoms are noted at 18 months plus. Autism onset at 18 months was uncommon until the mid-1980s, when the MMR vaccine came into wide use. After that the incidence shot up [20]. Thirdly, there is now evidence that measles antibodies can lie in the central nervous system, potentially damaging brain and gut. In fact, many autistic children are found to have measles antibodies in the gut. It's a bit like having a chronic infection. It seems that this triple vaccine makes measles persist. The antidote for measles is vitamin A. This is one of the most important infection fighters for this virus.
The late Dr Bernard Rimland said that the problem may not be the vaccine itself, but a preservative used in multi-dose vials of many childhood vaccines till very recently. Thimerosal, a preservative containing high levels of mercury, was used in many vaccines up until 2001. Before this, each vaccine injection exposed the child to levels of toxic mercury in excess of the US federal government's own safety guidelines, and a child receiving all their jabs could have received a total of 187.5mcg of mercury - enough to give them heavy metal poisoning [21]. Mercury is known to inhibit the enzyme that digests gluten and casein, possibly increasing a child's susceptibility to wheat and milk allergy.
Although it is too early to conclude, it is entirely possible that late-onset autism may be triggered by multiple vaccinations, allergies, toxic overload or nutritional deficiencies and especially combinations of any of these that send a child's gut and brain into distress.
If you've like to sign a petition to stop the General Medical Council striking off Dr Andrew Wakefield please click here.
Wishing you the best of health
Send to a Friend
If you have friends or relatives who you think would be interested in this e-letter, please forward it to them for their information.
Subscribe to 100%health Newsletter
If you would like to receive Patrick Holford's 100%health bi-monthly newsletter and get regular in-depth features on a range of health and nutrition issues - as well as discounts on books, seminars and other health products - click here to find out more.
References
[1] Whiteley, P, Sunderland University Autism Unit, talk given at the Autism Unravelled Conference, London, May 2001
[2] Whiteley, P et al, 'A gluten-free diet as an intervention for autism and associated disorders: preliminary findings', Autism: International Journal of research and Practice, Vol 3, 1999, pp45-65
[3] J Robert Cade, University of Florida Department of Medicine and Physiology, at www.panix.com/paleodiet/autism/cadelet.txt
[4] Letter to the Editor, 'Anti-fungal drugs more helpful than Ritalin in autistic children', Townsend Letter for Doctors and Patients, April 2001, p99
[5] A J Wakefield et al, 'Ileal-lymphoid hyperplasia, non-specific colitis and pervasive developmental disorder in children with autism', Lancet, Vol 351, 1998, pp637-41
[6] P. Ashwood and A Wakefield, 'Immune activation of peripheral blood and mucosal CD3 lymphocyte Cytokine profiles in children with autism and gastrointestinal symptoms', J Neuroimmunol, Vol 173(1-2), 2006, pp. 126-34
[7] V. K. Singh et al., 'Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism', J Biomed Sci, Vol 9, 2002, pp. 359-364
[8] J. J. Bradstreet et al, 'Detection of measles virus genomic RNA in cerebrospinal fluid of children with regressive autism: A report of three cases', JAPS, Vol 9 (2), pp. 38-45)
[9] H.S. Singer, 'Antibrain antibodies in children with autism and their unaffected siblings', J Neuroimmunol, Vol 178(1-2), 2006, pp. 149-55
[10] M A Brudnack, 'Application of genomeceuticals to the molecular and immunological aspects of autism', Med Hypoth, Vol 57(2), 2001, pp186-91
[11] P Varmanen et al, 'S54X-prolyl dipeptidyl aminopeptidase gene (pepX) is part of the glnRA operon in Lactobaccilus rhamnosus', J Bacteriol, vol 182(1), 2000, pp146-54
[12] P. Whiteley et al, 'A gluten-free diet as an intervention for autism and associated disorders: preliminary findings', Autism: International Journal of research and Practice, Vol 3, 1999, pp45-65
[13] J Robert Cade, University of Florida Department of Medicine and Physiology, at www.panix.com/paleodiet/autism/cadelet.txt
[14] M. Ash and E. Gilmore, 'Modifying autism through functional nutrition', paper given at Allergy Research Group conference, January 2001
[15] A. J. Wakefield et al, 'Ileal-lymphoid hyperplasia, non-specific colitis and pervasive developmental disorder in children with autism', Lancet, Vol 351, 1998, pp637-41
[16] Andrew Wakefield, speaking at the Allergy Research Foundation conference, November 1999
[17] D. Thrower, 'Autism and MMR - Summary of Published Research', available from www.foodforthebrain.org under ' reports'
[18] P. Shattock, presentation, Food for The Brain Conference, 1 October 2006
[19] F. E. Yazbak, 'Autism - is there a vaccine connection?' See www.autisme.net/Yaxbak1.htm
[20] B Rimland, J Nut Env Med, vol 10, 2000 pp267-9
[21] B. Rimland J Nut Env Med, vol 10, 2000 pp267-9; See also Ashcraft and Gerel (law firm), 'Autism caused by childhood vaccinations containing Thimerosal or mercury', which considers the litigation of individual claims, on www.ashcraftandgerel.com/thimerosal.html
Mums arteja sis skiepas,eisim jau kita savaite,skaitau ir baisu darosi 
Iki siol dar nepastebejau nieko blogo po praejusiu skiepu.
Iki siol dar nepastebejau nieko blogo po praejusiu skiepu.
QUOTE(mamiux @ 2007 08 02, 23:47)
Mums arteja sis skiepas,eisim jau kita savaite,skaitau ir baisu darosi Iki siol dar nepastebejau nieko blogo po praejusiu skiepu.
Iki siol dar nepastebejau nieko blogo po praejusiu skiepu.pries darydami skiepa paskaitykite CIA
Manau ši vakcina gali palaukt ir vėlesnio amžiaus. Aš už skiepijimą jei vaikas nepersirgs iki paauglystės. Manau skiepyti 6 ir 12 metų. Šiaip jei turėčiau mergaitę tai tikrai neskiepyčiau MMR o pasirinkčiau vienvalentę raudoniukės vakciną.
Donalita, tik pamacius refrences'e Wakefieldo pavarde... abejoju straipsnio objektyvumu...
gal pasikarotsiu bet manau tymu skiepas yra butinas. o radoniuke tik mergaitems ir parotitas berniukams nepersirgus
gal pasikarotsiu bet manau tymu skiepas yra butinas. o radoniuke tik mergaitems ir parotitas berniukams nepersirgus
Dėl tymų skiepo būtinumo abejoju ne vien aš bet ir daugelis mano sutiktų medikų.
