Unique

After David being diagnosed with a rare chromosome "genetic" disorder I was referred to a web site called rarechromo.org and I found there facebook page for parents who have children with a rare chromosome disorder. There is approximately 3 families that are registered in the United States and most of the families are registered in the UK. My son was tested by his Metabolic and Genetic doctor for Fragile X Syndrome and even though he had the defect of the "X" chromosome he did not have Fragile X. It's not until 3 years later that he got tested for the deletion of his genetic chromosome and therefore diagnosing him properly. I recommend that ALL parents have their children tested by a genetic doctor, you just never know what you'll find out.

Saturday, July 2, 2011

Guardianship for your disabled child

I read on my quarterly magazine from The National Fragile X Foundation a report about guardianship for our children who are disabled and turn 18. It stated " At age 18, children become legal adults, which means the parents are no longer their legal guardians, even if the children have disabilities". That kind of gave me a rude awakening, I had no idea that my husband and I would still have to file for guardianship for our son. Take the steps early on so that your child remains part of your family and not the courts, they will always need you to protect them and love them.

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