Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 I still cannot get over the amount of information I am gathering from this one place. Thank you a million times over. I was feeling confident last night and composed a thoughtful letter to Liam's current school SLP politely inquiring her specific experience working with apraxia and requested an IEP meeting to increase his speech time from 60 minutes. I also started the ball rolling to request therapy through the summer. I feel with what I have learned here and from 'Latetalkers' my requests were based on knowledge and not just a mother's whim. I'll let you know. 1)However, I am still in search of the right doctor to work with. The ped neuro wasn't the help we had hoped for. I found the name of a developmental pediatrician and a name of a pediatric physiatrist but only from internet research...not from recommendation. Anyone have someone they know or have heard good things about? 2) Same thing as far as finding an SLP. I was wondering if there is an SLP association that would have records of who has taken the PROMPT training? 3) Is it worth taking Liam to a specialist, even if they are out of state? If so, who would you recommend. I read about Dr. Agin but don't know if this step is necessary. 4) Lastly, Liam's hypotonia (I think) continues to effect his ability to stand or walk unsupported. From what I read this is much more than a soft neuro sign. Does anyone else have a child who was still not walking unsupported at 3 y/o? On a sweet note, Liam got to spend time with his grandparents this weekend. They haven't seem him since we adopted him last May. They were having a hard time believing that a child who couldn't talk could truly understand everything we said he could. We they happily have eaten their humble pie and are in shock of how smart (and cute and sweet) their newest grandson is Thanks for the answers and support Paige Quote Link to comment Share on other sites More sharing options...
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