The ALS Association is the only national not-for-profit health organization dedicated solely to lead the fight against ALS. The Association covers all the bases - research, patient and community services, public education, and advocacy - in providing help and hope to those facing the disease.
MISSION: To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.
VISION: In the quest to create a world without ALS, our vision is to care for and support all people living with Lou Gehrig’s Disease as we leave no stone unturned in our relentless search for a cure.
Order your ALS Awareness Postage Stamps here.
4 comments:
I agree with this so much, I won't even try to say anything funny.
I have so many things running through my head right now! The most important issue surrounding ALS, I think, is treatment!! There are nowhere near as many advanced treatments for this illness as there are for more common serious illnesses. It's unfortunate that a political agenda has stood in the way of this kind of progress. The second most important issue: support! It's such a tragic illness that tears down a human being bit by bit, attacking their senses and ability to communicate while leaving their sound mind in tact. I wouldn't wish it on my worst enemy, even though it took one of my most cherished :(
Wow...thanks for the info Ann. This sounds horrid.
I agree with Jen.No treatment equals No hope.
Love Chris
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