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HopeForSona - Cure FOP Disease

Sona is a sweet 7-year-old girl with the crippling genetic disease FOP. Please help us find a cure!

http://www.hopeforsona.org/

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HopeForSona - Cure FOP Disease | hopeforsona.org Reviews
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Sona is a sweet 7-year-old girl with the crippling genetic disease FOP. Please help us find a cure!
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1 hopeforsona
2 help cure fop
3 fibrodysplasia ossificans progressiva
4 sona's story
5 more about fop
6 fop research
7 donate now
8 optional email code
9 amount
10 your info
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HopeForSona - Cure FOP Disease | hopeforsona.org Reviews

https://hopeforsona.org

Sona is a sweet 7-year-old girl with the crippling genetic disease FOP. Please help us find a cure!

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hopeforsona.org hopeforsona.org
1

Sona's Story - hopeforsona

http://www.hopeforsona.org/sona-story

Sona is a bright, funny, happy little girl who loves to read, draw and paint, and run quite messy experiments with anything gooey and colorful. Sona has copious, highly specific opinions on Pop Music. She really enjoys playdates with her friends, keeping her little brother Taj in line, and helping-out her guinea pig Pickles. Every day and every dollar counts. Please help us fund crucial research on FOP! Do you like this page?

2

About FOP - Hope For Sona

http://www.hopeforsona.org/about-fop

Fibrodysplasia Ossifcans Progressiva ( FOP. Is an extremely rare genetic disease in which muscle and connective tissues are replaced by bone. This new bone builds up over time, locking-up good bones and joints in a second skeleton , why FOP is sometimes called. Healthy minds trapped in a prison of bone. FOP is caused by a genetic point mutation: a single DNA letter is wrong on one chromosome. Occurs in 1 out of 2 million people, one of the rarest diseases known to medicine. Presents in childhood and typi...

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HopeForSona - Cure FOP Disease

Help Me Find a Cure For FOP! I’m Sona. I’m seven years old and I have FOP. One of the rarest and most debilitating genetic diseases. FOP turns muscles and ligaments to bone, locking them in place. Eventually, I won’t be able to run or walk, move my arms or talk and eat normally. There is no cure for FOP. Yet there is hope for me and my friends! Exciting research is close to finding treatments for this terrible disease. Please help us fund this critical work! How You Can Help. Holy See (Vatican City State).

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