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A question for those with older kinds...

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We are going to Mayo Clinic on Friday to see Dr. Edyth Strand. Our son, Josh,

has had a dx for a little over a year (along with PDD-NOS) and we have done the

usual (private SLP/OT 3X/ week, EI through the sachool district, neuro workup,

genetic workup, fish oil, etc.) He is 3 1/2 and has been in therapy since he was

2. I have my list of questions for her, but was looking to pick your brains

about potential questions I *should* ask. I am most curious about topics that we

(my family) haven't experienced yet--but things you wish you would have asked

about when your child was younger. Maybe things about appropriate therapy

recommendations for the school aged years, or types of supplemental therapies

that would be of benefit.

Any ideas? Thanks in advance!

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