Guest guest Posted July 31, 2002 Report Share Posted July 31, 2002 Hello All, I need help understanding how to best help my son. has been seeing Dr. Goldberg for about 6 months now and over all we have been very happy. I do however need help with the following: 1. has done very well being on Valtrex, however he seems to be regressing in the last 2 months. Is it possible that the Valtrex can lose its effectiveness? 2. About 4 weeks ago Dr. G started on Paxil and he did not do well at all. We have just recently changed to Celexa and the first day I noticed that had a need to have his hands in his mouth all day. As the days have continued his need for oral stimulation has become less but he still has his hands in his mouth a lot. We have noticed some improvement in potty habits, but he is still not doing as well as when we first had him on the Valtrex solely. 3. has been on a GF/CF diet and we have now allowed him to have some Gluten (not a lot) per the " does and don'ts of the diet " . Should I keep him off of the Gluten completely? 4. My son is a VERY picky eater (like most of our kids). He will hardly ever eat meat. Can anyone suggest a good amino acid supplement that is ok with Dr. G. Sorry for all of the questions, any help is appreciated. Otila Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2004 Report Share Posted March 11, 2004 Hi everyone, Does anyone know the answer to these questions in North Carolina? or are they federal? Basically, i have received only quarterly reports from my son's special ed teacher, nothing daily or weekly and he has not made any of his goals. She did start a biweekly report that also goes for the typical kids and gives me no relevent information--just he behaved or did not etc--very vague. He is in a FOST classroom--part of the time with typical kids and part in a resourse class. The other 4 kids are goiing on to first grade and will be repeating kindergarden. (2 of the other kids have repeated kindergarden) This was a new program this year and did not get under way for a least 4 months. I feel like they have not given a chance. He is in a verbal behavior school/home program in the afternnoons and is doing good, not great. Any advice will be a big help. I asked for lawyers before in my area, but cannot find my info. Was Joy ston one of them? thanks, a stressed out mom in NC need some help > Hi Ms. , > > I need the answer to a couple of questions. > > What kind of communication between teacher (special ed teacher) and parent > do the schools have to do? Both you and Martha have said parents should > have daily/weekly communication about the childs goals/progress etc--does it > say so in writing anywhere? 2) The school just had my son reevaluated by a > pychologist with little/no experience evaluating autistic kids and the same > with the SLP. Based on the information from their evals, they think he > should go to a self contained classroom since he is not at the level of the > other 4 kids in the Fost program (only 2 diagnosed with Autism). The > director at the school had the temerity to tell me 'Janine, at least you'll > get the more communication there.' I told her that communication should not > determine placement, we should have that kind of communication here as well. > We have not had our IEP meeting yet, they shared! this information with me > at a meeting to discuss his psych eval. If we disagreed with this and the > IEP team insisted, is it a majority rules or if we do not sign the IEP, it > cannot happen? I have heard that we can request an independent evaluation > with people experienced in testing autistic kids, is it better to do this or > to go get some evals done privately. We have had some done lately for our > neurologist (research) i'm not sure if they were doing the same tests. > Thank you for your help Janine Govert > Quote Link to comment Share on other sites More sharing options...
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