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autism and autoimmune disorders

16 replies

saintlydamemrsturnip · 05/09/2010 20:45

Parental Autoimmune Diseases Associated With Autism Spectrum Disorders in Offspring. New abstract posted. Haven't read the paper yet, no sign from abstract of any attempt to identify subgroups but thought it might interest some.

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ArthurPewty · 05/09/2010 21:34

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saintlydamemrsturnip · 05/09/2010 21:43

Yes. We're not (dh and I) but just about every member of our extended family is. A lot seem to be autoimmune conditions that have been associated (in the literature) with viral triggers as well. DS1 regressed after a virus - does make me ponder (along with a lot of other stuff).

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WetAugust · 05/09/2010 22:41

I am autoimmune (Lupus) [sad}

ArthurPewty · 05/09/2010 22:46

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bettyswoobies · 05/09/2010 22:47

rheumatoid arthritis for me

Ineed2 · 05/09/2010 22:49

My mum has RA my niece Wagners and my cousin celiacs, that is seriously scary !!
Loads of family with probable but un dx'ed ASD's

rosie39forever · 06/09/2010 08:39

2 people in dh family have lupus and he has psiaratic arthritis!!

Davros · 06/09/2010 09:00

I have Scleroderma and it developed just after DS was born. But no-one else in my family has any auto-immune disease but there are 3 with AS and 1 with ASD (so far) so I have always thought that genetics play a bigger part in my family.

I also have friends with kids with ASD who have Lupus, Diabetes, Shergens(?) disease and I have noticed it. But a high number of my friends have kids with ASD so I'm not sure how common it is in the "outside" population.

CFSKate · 24/09/2010 16:40

This might be of interest. Warning, it is quite long.

www.ageofautism.com/2010/09/my-wife-my-daughter-and-xmrv.html

saintlydamemrsturnip · 25/09/2010 22:47

Thank you for posting that. I'll follow up those paper references. I've been meaning to find out more about xmrv and our family is so full of autoimmune issues.

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colabottles · 26/09/2010 01:17

umm I fit under this heading and thanks for that article CFSKate....

I am allergic to eggs/milk/wheat..scored 99.2% on the gluten wee test in sunderland. I did the diet for 8 months and to be honest it picked me up as turned mid 30's and I just hit the deck for 18 months couldn't do anything...had constant brain fog, weak terrible skin couldnt sleep and constantly tired. I started to scratch on ds when pregnant and have not stopped since. My liver is terrible painful and I have liver disease (non alcohol) I had asthma and have eczhma and my mother has diabetis and we both have low B12.

My dad and sister have alopeacea my sister bald since she was 24yrs and she has hypothyroidism. My mum has anemia but her twin sister has opposite (to many red blood cells ...heama ????forgot name) we are a walking autimmune time bomb....and when ds had MMR the to many injections caused a metobolic crisis and mito problems attacking the brain (mbp auto antobodies extremely high in ds results...conected to measels/egg)

Dr at biomed confirmed I had CFS but I could not afford their input so have just left it. I have been a lot better since the diet even though not on it now (CFGF) milk is defo a problem for me (fog/liver/stomach). So glad I got ds on strick diet though.

Dr Goldberg in USA who does NIDS discovered that when he was looking at kids with autism they had same results as his wife who has CFS so he says their is a link also!

CFSKate · 25/10/2010 09:54

saintlydamemrsturnip - I've just seen a video, it's an American ME/CFS patient giving testimony about how CFS spread within his family, and how both his children are autistic - the interesting part is that the man is adopted, so he is not genetically related to his parents and siblings, and his biological family are not ill, which he feels lends support to infectious virus as the cause.

CFSKate · 25/10/2010 09:56

trying that again

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HelensMelons · 25/10/2010 10:58

Yep, also auto immune in both mine and dp's family, particularly, allegies, nefrotic (sp? syndrome.

auntevil · 25/10/2010 11:15

Fascinating articles saintly and CFS.
As you know saintly I'm interested in trying to find out why my 3 DSs all have various immune issues and can't believe that there is no genetic link.
As an aside i am adopted too - and have applied for my records so that i can see if there is anything medical in them that might shed light on how i can best take their health matters forward.

DBennett · 25/10/2010 13:23

Thoroughly recommend this for people looking for a primer into XMRV.

Very readable and from a guy who was at the heart of a similar virus discovery 20yrs ago.

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