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Spinal Muscular Atrophy Cure

Spinal Muscular Atrophy Cure

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Age Defying Surgical Center

BRETT BOLTON

PO B●●●●1664

fort ●●●●●rdale , Florida, 33339

United States

1.95●●●●5868
dr●●●●●●@live.com

View this contact

Age Defying Surgical Center

BRETT BOLTON

PO B●●●●1664

fort ●●●●●rdale , Florida, 33339

United States

1.95●●●●5868
dr●●●●●●@live.com

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1

Spinal Muscular Atrophy Cure

http://www.helpmiafightsma.com/mia.html

Mia was born on May 7, 2009. Everything about her birth was completely normal; she sat up around six months, learned to crawl at about ten months. However, Mia was never able to bare enough of her weight to fully stand. And not know what’s going on is awful! It is an experience that I never want any other mother to have to go through. Finally, Mia’s physical therapist asked me to test Mia for SMA. Although we had desperately wanted to know for a whole year what was happening to our baby, we quickly reali...

2

Spinal Muscular Atrophy Cure

http://www.helpmiafightsma.com/about.html

About Spinal Muscular Atrophy. Spinal muscular atrophy (SMA) is a rare genetic disorder that affects the voluntary muscles that are used for activities such as crawling, walking, head and neck control, and swallowing. It refers to a group of diseases that affect the motor neurons of the spinal cord and brain stem. The ability to feel is not affected and intellectual activity is normal. It is often observed that SMA patients are unusually bright and sociable. Or Werdnig-Hoffman Disease is generally diagno...

3

Spinal Muscular Atrophy Cure

http://www.helpmiafightsma.com/index.html

October 2nd, 2014. For the Gala of Hope. We invite you to join us in what is sure to be a night full of memories, good times, and most importantly, hope. Our dream is to live in a world were no mother will ever have to hear the words your baby has Spinal Muscular Atrophy. There is no treatment and no cure. Please join us in our fight to raise awareness and help fund research. Help Us Find a Cure for Our Daughter. Spinal Muscular Atrophy (SMA). The Israels with their daughter Mia.

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October 2nd, 2014. For the Gala of Hope. We invite you to join us in what is sure to be a night full of memories, good times, and most importantly, hope. Our dream is to live in a world were no mother will ever have to hear the words your baby has Spinal Muscular Atrophy. There is no treatment and no cure. Please join us in our fight to raise awareness and help fund research. Help Us Find a Cure for Our Daughter. Spinal Muscular Atrophy (SMA). The Israels with their daughter Mia.

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