Debbie Geisler
My son was diagnosed at 4 years old with developmental dyspraxia. After 2 years of wasted therapy, what a relief to find a center who not only knew the problem, but could help with appropriate therapy. It, too, became a full time job to go to therapy 3 days a week - from 2-3 hours each session. He received not only speech, but occupational and physical therapy as well. He is now 11 years old and receives only occupational therapy twice a month. He is doing GREAT!!! There is help out there. We did not have insurance either for this therapy. It is considered a medical disability and thus makes the child elligible for medical benefits from the Department of Welfare, regardless of income. We never could have afforded therapy without it. We also investigated alternative methods of therapy that helped such as theraputic horse back riding (which he loved) taught by an occupational therapist and theraputic massage from a licensed physical therapist. A combination of early intervention and the appropriate center has made the difference in my son't life. I would be happy to talk to anyone with a child with this diagnosis. Even though he is doing great, we still have minor delays and struggles. It will always be an ongoing challange, but with education of this diagnosis not only for parents, but also for educators, our children are making leaps and bounds.