Started: June 21, 2007
We Can Put a Man on the Moon, but we can't find a CURE for ALS
Please help "CURE" ALS "Lou Gehrig's Disease
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 "CURE" ALS
I have selected Country on sign petition, because I want to help every one with ALS every where.
I sincerely thank you on behalf of all ALS Patients.
Please Pass on to everyone you know, so we can make a difference.
L.Walley-ALS Advocate
Please read Tim's Story Under My Links on the right side of this page.
***Your E-Mail Address will not be given or used for any other purpose than this petition.***
***You Can Click On Signatures To View Comments***
The medical establishment keeps ignoring this crisis while thousands of families lose everything. I am tired of the hollow excuses from the labs and the bureaucrats who claim this is just too rare to solve. We are not going away until they actually start funding a real solution.
Reached 100 supporters
June 25, 2007
6 Comments
M
Mike Tran
19 years ago
Featured
We need more funding for research asap. it is 2014 and we still have no real answers for families going through this.
L
Lisa Doyle
19 years ago
Featured
Truly heartbreaking to think about. Praying for everyone who has to live with this day in and day out.
D
David Kim
19 years ago
Featured
Been watching my neighbor fight this for two years. absolute nightmare.
J
Jessica Griffin
19 years ago
Featured
My heart goes out to anyone dealing with this. it is way past time for scientists to find a cure.
T
Tom Schwartz
19 years ago
Featured
TOO MANY PEOPLE DYING AND NOBODY SEEMS TO CARE UNTIL IT HITS HOME. LETS GET THIS DONE.
S
Sarah Schmidt
19 years ago
Featured
Lost my uncle to this horrible thing last year. it is just cruel watching someone you love fade away like that.
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Share it with friends to help reach
750 signatures.
Sign Petition
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Your signature will be added via
.
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Started: June 21, 2007
We Can Put a Man on the Moon, but we can't find a CURE for ALS
Please help "CURE" ALS "Lou Gehrig's Disease
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 "CURE" ALS
I have selected Country on sign petition, because I want to help every one with ALS every where.
I sincerely thank you on behalf of all ALS Patients.
Please Pass on to everyone you know, so we can make a difference.
L.Walley-ALS Advocate
Please read Tim's Story Under My Links on the right side of this page.
***Your E-Mail Address will not be given or used for any other purpose than this petition.***
***You Can Click On Signatures To View Comments***
The medical establishment keeps ignoring this crisis while thousands of families lose everything. I am tired of the hollow excuses from the labs and the bureaucrats who claim this is just too rare to solve. We are not going away until they actually start funding a real solution.
Reached 100 supporters
June 25, 2007
6 Comments
M
Mike Tran
19 years ago
Featured
We need more funding for research asap. it is 2014 and we still have no real answers for families going through this.
L
Lisa Doyle
19 years ago
Featured
Truly heartbreaking to think about. Praying for everyone who has to live with this day in and day out.
D
David Kim
19 years ago
Featured
Been watching my neighbor fight this for two years. absolute nightmare.
J
Jessica Griffin
19 years ago
Featured
My heart goes out to anyone dealing with this. it is way past time for scientists to find a cure.
T
Tom Schwartz
19 years ago
Featured
TOO MANY PEOPLE DYING AND NOBODY SEEMS TO CARE UNTIL IT HITS HOME. LETS GET THIS DONE.
S
Sarah Schmidt
19 years ago
Featured
Lost my uncle to this horrible thing last year. it is just cruel watching someone you love fade away like that.
Help this petition grow
Share it with friends to help reach
750 signatures.
Sign Petition
We never post to your account. Social sign-in is used only to verify your signature.
or sign with Email
Add a comment?
Your signature will be added via . Tell others why you're signing — it's optional.
Signing with Google or Facebook verifies your signature instantly — no email needed.
We need more funding for research asap. it is 2014 and we still have no real answers for families going through this.