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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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LOL! I just read your question again

February 15 2006 at 8:52 PM		   (Login HollieV)


Response to Here is our current plan....but I am not sure it will help much
 

and nothing in the above post had anything to do with it. Sigh...sorry!!

Noah's EI is with our Dept of Special Needs and I think we can stay with her until he is 6yo. Beyond that, I don't know. We currently get respite money to pay for his one day/week at Mom's Morning Out and that will only continue until age 3yo. So I've wasted a lot of space and your time and have been no help at all.

Sorry.

Hollie, Homeschooling mom to Eli (7yo), Kyle(5yo) and Noah(20 months, T21)



 
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