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When Jett was first diagnosed with T21, my family and I were drowning in a sea of information. I did not like a lot of what I was reading. Much of it was depressing and negative with a focus on accepting the fate of your child with DS instead of assisting in finding answers, treatment and solutions. Please benefit from our experience and enjoy this...
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Content provided in this website is given as information only and should not be taken as a professional medical diagnosis or opinion. Be sure to check with your physician.