We are proud parents of 5 children, three of whom have been diagnosed with Fragile X Syndrome and Autism. William, my husband of 16 years owns a brokerage firm but his passion is advocating for the special needs population on a local,statewide and national level. He has been able to help innumerable people throughout the entire United States though his advocacy. In a few words, I am also an advocate, soccer mom, fundraiser, supporter, volunteer, therapist, chauffer, and friend.
In my blog, I will talk about our family's life with Fragile X Syndrome and autism. However, we are not here to offer you scientific information about the genetics and biological side of Fragile X and autism. Rather, the more personal and emotional aspect of raising a family with typical and special needs children. Welcome on this journey with us.
To find the most accurate and up-to-date information on fragile X syndrome please visit:
The National Fragile X Foundation,
FRAXA Research Foundation
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