The ALS Association

Freedom of movement—walking, going up and down stairs, getting off the floor, completing daily tasks, exercising—are just a few of the activities that many of us take for granted. But for people living with ALS, these often become difficult to do. Physical and occupational therapy can help. Physical therapy (PT) is the use of exercises and treatments to improve mobility. For example, a physical therapist might prescribe stretching exercises to limit discomfort or use pool therapy to help you walk and improve joint function. Occupational therapy (OT) is similar but focuses on the physical skills needed to perform everyday tasks. An occupational therapist may help you find new ways to brush your teeth or recommend equipment to make your daily living activities easier. Learn more: https://lnkd.in/eTeKqdEi

We are already a couple of weeks into 2024! Let's take a quick look back at the top 10 posts from our blog last year. https://lnkd.in/eJvyKfeM

Stories have connected us for generations, often providing impact and making waves of change. Discover some of the most powerful stories from the #ALS community and share this post to help spread awareness of this disease today. https://lnkd.in/eTzRmH5d

Congratulations to our research committee chair, Dr. Michael Benatar, neurologist and #ALS researcher at the University of Miami Miller School of Medicine, 2023 recipient of the Sean M. Healey International Prize for Innovation in ALS. Recognized for his exceptional discoveries, his research has influenced the development of ALS treatments, notably the ATLAS trial with tofersen. Thank you Dr. Benatar, for all that you do to help the #ALS community. Learn more about Dr. Benatar and his work: https://lnkd.in/ezV243qe

Congress is back in session deciding on the future of #ALS research right NOW. Take action to urge your lawmakers to #FundALSResearch: https://lnkd.in/etuPBDE7

Are you facing challenges, seeking advice, or simply looking for a safe space to connect with others in the ALS community? Support groups are a great resource for people to give and take the wisdom and experience that comes from living with a devastating illness. Find support: https://lnkd.in/eRGx3-Rf

Depending on where you live, cold weather is likely something you have to deal with during the winter months. While lower temperatures can present special challenges for people living with #ALS, it doesn’t mean they can’t enjoy the season. https://bit.ly/Tips-Cold

The ALS community proudly cheered on San Diego State University men's basketball vs. University of Nevada-Las Vegas on Sunday where awareness of #ALS ran wild amongst the crowd. From PA announcements and signs throughout to inspiring chants from the fans, we proved we are all one team versus ALS. #AllvsALS

A lot happened last year, from the FDA approval of Qalsody to the development of My ALS Journey™ Read about 2023 highlights in our year-in-review: https://lnkd.in/evagahd4

Visit als.org/research to dive into the latest ALS research findings, learn about ongoing studies, and discover how your involvement can impact the search for a cure.