Guest guest Posted January 15, 2006 Report Share Posted January 15, 2006 Hi, Thursday a.m. I'm taking my 26 month old son to a pediatric neurologist for our first visit. He's seen the EI SLP (well, actually 2 or 3 different ones) and a private SLP and they all believe he has apraxia. We are only getting one visit a week with EI and we just began the other SLP service through our insurance " network " , which is quite limited. The insurance is already being difficult about what they might cover and won't commit to anything. SOOO, what do I need to ask at the neurologist appointment? What should he ask me? What EI papers/assessments should I try to take there? If my goal is to get more/increased service for my son, who is making some progress, but very very slowly, what " should " happen at this appointment? I know many many of you have already been down this road ahead of me, so please let me know what to expect, etc. Thanks, Quote Link to comment Share on other sites More sharing options...
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