Guest guest Posted April 15, 2006 Report Share Posted April 15, 2006 Thanks for the advice Stan, I am on the fence with HBOT, everything new scares me though. I do plan on waiting now, mostly because we are seeing gains and don't want to *interrupt* the progress. Dylan is doing so well that it just amazes me daily. I need to reintroduce the nasal MB12, do you recall his aggressive reaction to nasal w/folinic Stan? Our phone conversation back in Jan.? It was then that you talked to me about valtrex and I am so glad you took the time to explain it to me and told me to consider trying it. Anyway, I found an old tube of Autistique cream in the back of the fridge (contains, mb12, TTFD and ALA) so I put a little on him this week and he has been making spontaneous vocalizations again, as he was when on nasal, so I know I need to order the nasal again, w/o folinic. By the way Stan, you are a popular man, I run into your name as a reference at other boards!! Parents love you!! Colleen Mom of Dylan, 8 autism > > > > > > > > Just looking to see if anyone is doing HBOT. When did you > > start? > > > > After valtrex? I have the opportunity to start at a new center > > in my > > > > area and am looking to see if 55 days in to valtrex, if it would > > be > > > > safe. > > > > > > > > Appreciate any input/experiences with HBOT. > > > > > > > > Thanks Colleen > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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