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We are a group of friends who have come together because we share the common bond of caring for someone who has Trisomy 21. We are here to share therapy tips, medical issues, laughs, accomplishments and yes, even frustrations. We embrace what Trisomy 21 has brought into our lives. We feel that it has taught us to appreciate the true meaning of life. We count our children as blessings! We will fiercely protect them and fight for their lives to be valued just as all other peoples' are. We share our pictures, our stories and our hearts here not only to provide friendship and support for each other, but also in the hopes that others will open their minds and their hearts to our unique children and, in turn, make a better world for everyone.
 

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MRI Advice

June 26 2008 at 2:54 PM
Terri (Sam's Mom)  (Login tmorris3133)

 

Sam will soon be 14 mos old and he is still not sitting on his on. He is finally being referred for an MRI because the DDS worker is pushing it. (The pedi wanted to wait when I asked for it at 12 mos.) However, they are referring him for a brain MRI, not for the sacral dimple. Has anyone had this done? What should I expect? (I thought that when we see the neurologist, I will voice my concerns about the sacral dimple.) Any advice would be appreciated. Thanks in advance.

Terri



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DOB: May 07,2007


http://sam-samuelaidanm.blogspot.com/

 
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