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June 2020 by Lisa Ditullio
A free wheelchair isn’t enough! Support therapies that work. Use the money from the ice bucket challenge which was six years ago !! 80 million ?!
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April 2020 by Sheri Strahl
A mission-centered organization that is truly and deeply committed to the ALS community.
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January 2020 by Gee Monny Wire Wire
A big thanks to Dr Jude Robert for reserving my ALS disease with his effective herbal formula. I was diagnosed of ALS disease 9 months ago of all the horrible experience, I was bitterly in pains. My symptoms progressed so fast that I couldn't eat proper, walk, work, breath well, it was my worse part of life then. On this fateful day, I came across a post just like this concerning a patient who used Dr Jude herbal medicine herbal formula to reserve her ALS disease for over 2 y
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November 2019 by Irene Mikitarian
Unfortunately, on Weds (the same day real ALS Advocates went to the White House to fight for access to Phase 3 therapies) ALSA National sent an Email directive to all its local chapters to make sure they did NOT post the news that NurOwn's Phase 2 results have now been peer reviewed and published in the most prestigious journal, "Neurology". It's powerful Golden West chapter did have time to make sure it put up this lovely poster though, at its Gala sponsored by (wait for it)
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October 2019 by Letty Padilla Vorgitch
Great organization to donate too, they are helpful with resources for ALS families.
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August 2019 by Michael Buttress
I have been honored to be part of the Golden West Chapter for two years now. They are a dedicated team and "together we can make a difference"!
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October 2018 by Sheryl Kern-Jones
Absolutely amazing and caring support from knowledgeable people.
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January 2018 by Carolyn A. Plaks
Our friends with ALS cannot wait any longer. Some are misdiagnosed and suffer privately. Barry died last year and was not even properly diagnosed. At the end he had just days.
