PMG left School Board Services

[Guest guest]

Hi everyone! !

My daughter was diagnosed with Left PMG when she was 6 months old. She has had

OT and PT since then. Until recently, our new insurance is now refusing service

and I must go through their appeals process. (She is now 4 years old)

She has done great with early intervention and I would like her to continue to

recieve services so she does not regress. Her biggest issues are neglecting her

right " helping hand " and some mild weakness in her right leg.

I had her evaluated at age 3 by the school board and they said she is

" functional " and does not qualify for the educational approach to therapy.

I will once again take her this year for an evaluation, since now we have no one

providing services. I would like to know if anyone has faced this sitution and

how have you presented the case to the school board to help your child receive

services.

Thanks for your help!