thealsassociation's Channel

The ALS Association

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Uploads (53)

Charlie Guenard's Speech at the Boston Walk to Defeat ALS

412 views - 1 month ago

Action ALS

5,795 views - 1 month ago

Gandolfi's Goombas Walk Team.wmv

135 views - 1 month ago

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4-ALS Awareness (5)

NY Yankees 4 ALS Lou Gehrig Tribute July 4, 2009

srpmusicv... - 7,057 views

Lou Gehrig's Retirement Speech July 4 2009

moofus1 - 8,806 views

Lou Gehrig's 4ALS Awareness at AT&T Stadium

StarsAGlow - 1,289 views

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thealsassociation

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Name:

tina

Channel Views:

14,898

Total Upload Views:

117,967

Joined:

Mar 28, 2008

Latest Activity:

2 weeks ago

Subscribers:

161

Website:

http://www.alsa.org

This is the official YouTube channel of The ALS Association National Office. The mission of The ALS Association is 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.

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United States

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	reaganeyes (2 months ago) I feel your pain and frustration having lost my mother Sept. 14, 2010 to ALS. It is crazy to me that no one knows what it is. I have a word of advice: at one point they were looking into lithium as a treatment- stay away from that. It changed her. Feel free to contact me- i may not be an expert but i'm a realist who's seen it all the way through. I will tell you like it is.
	lbrownxx08 (2 months ago) my dad was diagnosed w/ als in 2010 i wish there was more medications out there something to SLOW it down,or cure this asap!! !!!!!!its been so long they have a cure for alot of cancers but none for this?!?!! i baffles my brain!?
	kidneybitch (3 months ago) My heart goes out to all who are suffering from this nasty monster. I lost my brother Shannon 9 years ago from ALS. We walk and raise money in hopes of a cure. I know first hand that the families of people with ALS suffer along with those who have it. Let's keep raising that money and find a CURE.
	LucasFFXI (3 months ago) My mother has the ALS disease for about a year. And now today her ALS keeps getting worse, and sadly, she's on her hospital bed with not much time left to live. She is my mother and I love her so much. I hope someday in the future, a cure for ALS will be discovered.
	thealsassociation (4 months ago) Do you have a creative side and know someone living with #ALS? Share your story with the 2012 Neuro Film Festival http://ow.ly/6vbus.
	captainfury2007 (1 year ago) Hey thealsassociation, My name is Steve - I am just trying to get the word out about my channel. If you get a second, stop by and check it out. If not, thats okay too.
	CatherineMcNally63 (1 year ago) My husband was diagnosed about one year ago with Als and frontal lobe dementia to go along with it. I have never know anyone with this desease.I am devastated along with the rest of my family. Symtoms are in his arms( no power) and is now effecting his speech along with severe change in personality. We did a walk on his behalf in June and raised 1500 for the foundation. I hope and pray they find a cure soon. Cathy
	annmarieslavin (2 years ago) Thank you for your informative channel. My brother was just diagnosed with ALS and I'm trying to learn as much as I can. I guess that's my way of coping with it.
	sessamo (3 years ago) Angela, Noooooo! I was so worried when they shot a bullet at her, I think a large population of the world would die should Angela ever come to harm.
	ofiverde (3 years ago) Congratulations for the campaing. We are an student scientific asociation from University of Murcia (Spain). And we want to encourage you in this fight against Amyotrophic lateral sclerosis. Good luck! Greetings!

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