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Save Our Boy Foundation - Our Story

SaveOurBoy. Fighting to End Duchenne Muscular Dystrophy

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Save Our Boy Foundation - Our Story | saveourboy.com Reviews
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SaveOurBoy. Fighting to End Duchenne Muscular Dystrophy
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Save Our Boy Foundation - Our Story | saveourboy.com Reviews

https://saveourboy.com

SaveOurBoy. Fighting to End Duchenne Muscular Dystrophy

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1

Save Our Boy Foundation - EKDOR Golf

http://www.saveourboy.com/EKDOR-Golf.html

January 17, 2014. To learn  more about the. Meet Grant.Our Inspiration.

2

Save Our Boy Foundation - Houston Marathon

http://www.saveourboy.com/Houston-Marathon.html

Running for the boys who cant. Running to END Duchenne. In 2013, Grants Gang partnered with the largest Duchenne-specific organization, Parent Project Muscular Dystrophy (PPMD) for the Houston Marathon. With the help of all the runners and donors, we were able to raise thousands of dollars for Duchenne research. To be part of the team. For the 2014 Houston race on January 19, please  click here. 160;Wed love to run with you next year! Meet Grant.Our Inspiration. 160;to see his story.

3

My Blog

http://www.saveourboy.com/blog.html

4

Save Our Boy Foundation - Donate

http://www.saveourboy.com/Donate.html

Help Save Our Boy Now. Our life goal is to find a cure for Duchenne Muscular Dystrophy so that Grant and other boys around the world can enjoy a normal life and continue running, playing, dancing, living, and breathing for many years to come. We need everyones support. We thank you for taking the time to read our story and thank you for helping Save Our Boy Grant and ALL boys with Duchenne Muscular Dystrophy. Click Here to Make a Donation to Help in the. Fight to END Duchenne.

5

Save Our Boy Foundation - Grant's Video and News

http://www.saveourboy.com/Grant-s-Video-and-News.html

The Christmas Tree Luminary in Market Square. The Woodlands Paper, November 2012. Read about Grants Gang in the Houston Marathon. Houston Chronicle, January 2011. Read Grants Story as seen in the. Houston Chronicle, September 2010 . Read Grants Story as seen in the. Houston Chronicle, September 2009.

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What is Duchenne Muscular Dystrophy? Friday, October 2, 2009. It's been almost 6 months since we found out. It's been almost 6 months since we found out our 3 year-old son Grant has Duchenne Muscular Dystrophy (DMD). It is hard to believe it has been that long.it feels as if it has only been a few weeks. With time working against us these days.I wish it would just slow down! What have I learned in these 6 months? In these 6 months, I also had my genetics testing completed and found out I am NOT a carrier.

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To provide funds for advanced treatments. And a potential cure for Duchenne Muscular Dystrophy (DMD),. The most common fatal genetic disease diagnosed in childhood (afflicting 1 in 3,500 boys worldwide). Meet Grant.Our Inspiration. 160;kept surfacing. We took Grant back to several doctors and demanded testing. The results confirmed our greatest fears. . Grant was diagnosed with Duchenne Muscular Dystrophy (DMD) just before his 3rd birthday. What happened to Grant CAN happen to ANYONE. 1/3 of Duchenne MD&...

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To provide funds for advanced treatments. And a potential cure for Duchenne Muscular Dystrophy (DMD),. The most common fatal genetic disease diagnosed in childhood (afflicting 1 in 3,500 boys worldwide). Meet Grant.Our Inspiration. 160;kept surfacing. We took Grant back to several doctors and demanded testing. The results confirmed our greatest fears. . Grant was diagnosed with Duchenne Muscular Dystrophy (DMD) just before his 3rd birthday. What happened to Grant CAN happen to ANYONE. 1/3 of Duchenne MD&...

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