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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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We're not using any school services

March 14 2006 at 3:22 PM
  (Login karendg)


Response to Using the school district...
 

I have never had respite or anything either. I am not doing any private therapy at the moment (haven't had any since EI). I would have to take Connor to the school and I just don't think there is any there they can do that I can't do here.
HSLDA also recommends that you don't use school services but I do not agree with a lot of their advice so I don't let that factor into my decision much.




Wife of Rob and Mom to Becca (13),Erin (11), Rachel (10),Kaitlyn(8), Ryan(6), Connor (4) and Emma (3) and Jenna (5 months)

cjsmile_1_1_1


 
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