I really liked the video. Thank you! The little girl is beautiful, particularly her movements and expressions. My son Christopher has an extra copy of Chromosome 21 too. Chrissie has quite severe dyspraxia. Have you ever checked out "Communicating Partners" at http://jamesdmacdonald.org/Articles/MacDonaldStart.html? We have found it a real help. He can't talk much, but he communicates very nicely, thank you!
I have stumbled upon your Blog and I am so grateful! I have such a heart for those with Down Syndrome. Your daughter is beautiful and I pray she never has to live a day knowing what a precious gift from God she is. God Bless...
Hi Quinn´s Crusade. Really I love the video. It´s incredible when the family are there ALWAYS.! I´m student & I´m only pass to check another blogs, but really.... She´s so BEAUTIFUL.! Thanks for make me SMILE :D My best wishes for the family.! She´s a gift from God, take care
This blog is about our journey raising three bright, gorgeous kids (Riley, Aidan, and Quinn). Miss Quinny happens to have an extra 21st chromosome (Down syndrome) along with Infantile Spasms (West syndrome) and Stereotypic Movement Disorder. This blog is for awareness and advocacy for families with children with special needs.
I am loving mom of three children, two boys and one girl. Riley is age twelve; Aidan is eight; and Quinn is five. I have been married to my husband, Neal, for 14 years.
Down Syndrome Awareness Month Blogging Challenge - I DID IT 2009
Deep Thought by Jack Handy
“If you define cowardice as running away at the first sign of danger, screaming and tripping and begging for mercy, then yes, Mr. Brave man, I guess I'm a coward.”
This is great! Those kids are adorable!
ReplyDeleteI really liked the video. Thank you! The little girl is beautiful, particularly her movements and expressions. My son Christopher has an extra copy of Chromosome 21 too. Chrissie has quite severe dyspraxia. Have you ever checked out "Communicating Partners" at http://jamesdmacdonald.org/Articles/MacDonaldStart.html? We have found it a real help. He can't talk much, but he communicates very nicely, thank you!
ReplyDeleteThis is so precious..special.. just like Quinny and the amazing young man who tells her she is so beautiful just the way she is!
ReplyDeleteI have stumbled upon your Blog and I am so grateful! I have such a heart for those with Down Syndrome. Your daughter is beautiful and I pray she never has to live a day knowing what a precious gift from God she is. God Bless...
ReplyDeleteHi Quinn´s Crusade. Really I love the video. It´s incredible when the family are there ALWAYS.!
ReplyDeleteI´m student & I´m only pass to check another blogs, but really.... She´s so BEAUTIFUL.!
Thanks for make me SMILE :D
My best wishes for the family.! She´s a gift from God, take care
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