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Hello, I´m new in the group, my name is Edgar, I´m from Guatemala, central

America, my daughter Ivonne has MDS, 23% affected cells, she´s in good shape

and good health, but I´m a little concern that she can´t crawl yet, she´s 11

months old, and I would like to know about the experience of other people

with their children about this issue, she´s getting physical therapy 5 times

a week and early stimulation for his brain.

Thank you for your info

Regards

Edgar

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