There is no doubt that 2023 saw significant breakthroughs in advocacy, care and research. Here's a look at the top ten blogs of the year that covered it all.
Mike will never forget receiving a phone call telling him that his best friend, Matt, had been diagnosed with ALS. The first event Mike attended for The ALS Association was a golf event in Janesville with Matt. That one event has now become years of walks and third-party events supporting The ALS Association Wisconsin Chapter.
We’ve developed several materials as communication and educational tools to help inform medical providers, as well as provide pertinent insurance and family information. Access them now.
The Suzanne Rogers Weber Memorial Fund honors Suzanne and her family’s gratitude for the Chapter’s assistance throughout her illness and her faith in a future world without ALS by supporting the Chapter’s Care Programs and ALS Research.
John Hedstrom, Executive Director of The ALS Association Massachusetts Chapter, greets the Massachusetts ALS community with a Happy New Year and robust plans for the Chapter at the start of 2021.
There can be no doubt this time of year means “back to school” to so many families around the country. As students return back to campus, this year, we wanted to take the opportunity to introduce you to some of this year’s recipients of the 2023 Jane Calmes Scholarship Fund.
Since our founding in 1985, we have put collaboration at the forefront of everything we do. The gift of the ALS Ice Bucket Challenge in August 2014 gave us the unique opportunity to up our game in establishing innovative research partnerships around the world.