Guest guest Posted February 22, 2006 Report Share Posted February 22, 2006 rebecca, your response to " richard " was very well put. after over 5 yrs of bio med treatments, i have finally come to the conclusion that my son's main problems are heavy metals and virals. so, i am currently focusing on the viruses and metals (valtrex, transf factor #8 and chelation). my son has had many underlying issues since the beginning of diag (stemming, hyperness galore, gut issues, ocd, sensory...) so far, NOTHING has been able to alleviate these. he sometimes literally bounces off the walls! he is almost 9 yrs old now. my son's develop ped wants to put him on risperdahl. but, i feel because of the metals, this is the real reason why nothing has seemed to work.. i always keep an open mind and research. i make the final decision on what i give my son. i feel a lot more comfortable this way. also, since my son is apraxic, he cant tell me how he feels or how something is affecting him. i HAVE to read thoroughly what i give my son. vicki Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2006 Report Share Posted February 22, 2006 Hi : I wold be happy to answer your questions off list as I worry about exhausting the patience of the people on this list. This is a list about , and I feel that everyone has been more than gracious in allowing me lengthy responses about other protocols, thanks guys!! Please feel free, to contact me off list and I will happily answer any questions in detail. /was:Re: neuroimmune research , Thanks for the very detailed and helpful response. You indicated how well your dauter is doing! I don't know if you saw Dr. G or any other docs. You said you you would not see 90% of the DAN docs. I know you would not presume to prescribe for anyone else's child, however, I know that I would like to know more about the process you went through in getteing your daughter well. What type of doctor did you consult with? What types of interventions proved successful for her? > > > > > > just fyi - there is a new group for discussion > of > > > > > neuroimmune > > > > > > issues called 'neuroendocrineimmune'. It is an > informal > > list > > > > for > > > > > > people interested in the discussion of all " aspects of > > > > > > NeuroEndocrineImmune issues and CNDS (Chronic > > > > > > NeuroendocrineimmuDysfunction Syndrome) -- whether > > specific to > > > > ASD > > > > > or > > > > > > not... " (from the homepage.) My understanding is that > the > > focus > > > > > will > > > > > > be on current research. > > > > > > > > > > > > fwiw, > > > > > > timary > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Responsibility for the content of this message lies > > strictly > > > with > > > > > > the original author(s), and is not necessarily > endorsed by > > or > > > the > > > > > > opinion of the Research Institute and/or the > > Parent > > > > > Coalition. > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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