As a special needs family that relies on medications to help improve ours kids quality of life, we have had mostly a positive experience. We have also had some negative experiences as well.
I know that placing your child on medications is never an easy decision and can be downright scary. I thought we could discuss our experience and maybe ask or answer some questions about medicating our children with #Autism. How have you weighed the risks vs the benefits?
This was posted via WordPress for Android, courtesy of Samsungs Galaxy S III. Please forgive any typos. I do know how to spell but auto-correct hate me.
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