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Our Fragile X World

Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. And www.fraxa.org. For Caroline social communication is very hard. She has sensory processing difficul...

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Our Fragile X World | fragilexworld.blogspot.com Reviews
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Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. And www.fraxa.org. For Caroline social communication is very hard. She has sensory processing difficul...
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Our Fragile X World | fragilexworld.blogspot.com Reviews

https://fragilexworld.blogspot.com

Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. And www.fraxa.org. For Caroline social communication is very hard. She has sensory processing difficul...

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fragilexworld.blogspot.com fragilexworld.blogspot.com
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Our Fragile X World: Help us help our kids

http://fragilexworld.blogspot.com/2010/08/help-us-help-our-kids.html

Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. Subscribe to: Post Comments (Atom). View my complete profile. Help us help our kids.

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Our Fragile X World: Caroline

http://fragilexworld.blogspot.com/2010/08/caroline.html

Our Fragile X World. Monday, August 16, 2010. This is my 1st post on this site. I'm married to Will and we have 2 children. Clark who is 4 and Caroline who is 7 yrs. old. Caroline is diagnosed with Fragile X. She has the full mutation of Fragile X. Fragile X is a genetic syndrome passed down on the X chromosome. Great websites to reference are: www.fragilex.org. And www.fraxa.org. She is receiving speech therapy, occupational therapy, and she is on a drug called minocycline. She started the minocycli...

3

Our Fragile X World: August 2010

http://fragilexworld.blogspot.com/2010_08_01_archive.html

Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. And www.fraxa.org. For Caroline social communication is very hard. She has sensory processing difficul...

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Our Fragile X World. Monday, August 16, 2010. Help us help our kids. Fragile X researchers are so close to developing drugs to help our kids. We live with this every day and pray that the researchers keep trying, that the FDA will approve, and that our kids will get the help they need. Please help too! They are a great organization and don’t forget your gift is tax deductible! Thank you - Thank you. And www.fraxa.org. For Caroline social communication is very hard. She has sensory processing difficul...

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