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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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That is horrible!

July 22 2008 at 7:54 AM
Amy, Quinn's Mom  (Login anmns)


Response to OT - anyone with advice, help, etc.....
 

I know it is a longshot but have you tried to contact Micheal Moore (he made Sicko). This is one of his causes and he is from your area, maybe he could help. Maybe the local news? All she needs is a hospital to feel sorry for her and offer to do it for free.

Yikes, what is this world coming to when you have a totally treatable cancer but no money to treat it!?

Amy

Amy....Mom to Quinn 4/20/04 (DS) and Cooper 6/16/06
Photo Sharing and Video Hosting at Photobucket
Photo Sharing and Video Hosting at Photobucket

Read his daily Blog @ http://qmb.blogspot.com/


 
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