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Old 06-22-2007, 07:27 AM #1
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BobbyB BobbyB is offline
In Remembrance
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
BobbyB BobbyB is offline
In Remembrance
BobbyB's Avatar
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
Smile Help Fight ALS With S.5 Stem Cell Research Enhancement Act

Help Fight ALS With S.5 Stem Cell Research Enhancement Act

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The petition
Started: June 21, 2007

"Help Me Make A Difference"

Please help fight ALS "Lou Gehrig's Disease by signing the S.5 Stem Cell Research Enhancement Act Petition. When we get this act passed it will help find a cure faster for ALS and many other terminal diseases for which there is no cure.

Please Read About ALS and how it could affect you, someome in your family or a friend or someone you know!

This mystery of a disease that affects as many as 30,000 annually. With more than 5,600 people diagnosed each year - an average of 15 new cases each day - our mission is urgent. The search for answers knows no bounds.

ALS has no Prejudice - It occurs worldwide, with No Age, Ethnic or Economic boundaries.

ALS is a degenerative disease; it deteriorates the motor neurons in the brain and spinal cords. Motor neurons are the little messengers sent out by the nervous system to tell the muscles to move. ALS attacks these motor neurons, causing the victim to lose control of his muscles. Every year in America 1-2 people per 100,000 develop ALS; that figures out to about 5,000 new victims per year. Once a person has been diagnosed with ALS, they usually are given a life expectancy of 3-6 years. The disease can strike anyone at any age, but it most often it strikes in the middle-aged and elderly, more commonly in men. Although women do get it.

It's a rare disease, the truth be told; the rareness can be both fascinating and frustrating to victims and their doctors. For instance, victim'cognitive and imaginative brain function is left intact. Though the victim eventually cannot talk or move, they can still think, remember, hear, compute and daydream - and they are very aware of how trapped in their own bodies. Eventually resulting in death. Therefore depression is a common side effect of ALS. Please help my Brother Timothy and all other ALS Patients and those that will be diagnosed in the future. When Diagnosed with ALS a persons Life will never be like it was before, unless we find a cure.

Please sign my petition to help Fight ALS.

I sincerely thank you on behalf of all ALS Patients.

L.Walley-ALS Advocate

Sign the petition
http://www.ipetitions.com/petition/h...htalspetition/
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ALS/MND Registry

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