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.

Monday, January 14, 2013

Hopefully a resolution

           On February we are finally going to have my son's Mediation Hearing with his school district. My advocate has put together a reasonable summary and demands and I'm hoping that the district will give us what we ask for, its scheduled from 9:30-4:30 so I am assuming that it's like a bankruptcy court where you show up and wait to be called...but then again does it really take 7 hours?
           Also his Tri-Annual IEP is coming up on January 30 and his IEP (Individualize Educational Program) is going to be revised to his needs, his old IEP goals seem to not make sense so I revised it to his specific needs and realistic goals. I looked up on how to write IEP's on the internet and found some very good advice and strategies. I believe every parent should really look at their child's IEP and determine the reality of   the goals and what is expected from their children.
          So till then we will await our outcome in February and hope for the best. Wish us luck.

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