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The Resources Are There. How Can We Connect More Families to Them?

The stress, emotion, and confusion that accompany a diagnosis for your child can be overwhelming. We are excited to share an article by Ricki Meyer, Exceptional Lives’ Director of Policy and Legal Operations, that discusses how our free resources can help parents and caregivers navigate the various disability systems and accompanying emotions upon receiving a diagnosis for their child.

From the article: “You’ve just received your child’s diagnosis: autism, intellectual disability, cerebral palsy, or visual impairment. Sifting through websites, you start thinking of many questions. How will you find occupational therapists for your child? How will you learn what occupational therapy is? Will your child ever live on his own? Will she have a job? What about your other children — how will you support them while caring for your child who is going to need extra resources? As you become immersed in trying to understand what this means for your child and family, you hear many new terms: Supplemental Security Income (SSI), Individualized Education Program (IEP), Medicaid, special education. You have started to explore government websites but there is too much text and the quantity of information is overwhelming.”

Click here to read the full article, and please share with family, friends, and coworkers who can benefit from our resources!

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