I AM ALS
@iamalsorg
I AM ALS is the largest community movement made up of the very people living with, impacted by, and highly motivated to end ALS.
The Tim Lowrey ALS Panel Series brings ALS education to any setting, and they tailor their presentation to their audiences. Check out this recording of a panel for PT & OT students, & request a panel for your classroom or workplace: bit.ly/45xdhst bit.ly/4lyfyIZ
⭐️ YOU can help secure the future of ALS research. Feel the joy of moving the needle toward unlocking resources for care, research, and treatments. It's easy! Contact your elected officials about what ALS research means to you: bit.ly/3F1TS8c

As we begin working to reauthorize ACT for ALS in 2026, we're reminiscing about all the amazing elected officials who voted for this critical piece of legislation. Help us thank them, and remind them how much this bill means to you: bit.ly/4mPg1aJ

You know him as an all-star volunteer, a writer, and an I AM ALS Board member. Now, "the Juan and Only" Juan Reyes is adding "published author" to his lengthy resume! Check out Juan's new book, The ALS Express: amzn.to/4nZoXef

I AM ALS is delighted to welcome Chuck Smith to our Board of Directors! Learn more about Chuck and his motivation to end ALS in our update: bit.ly/4l0GZtU

We've set a date for the 2025 Artistry of ALS Gallery Opening! Join us on September 10 at 7pm ET for an unforgettable evening, co-hosted by the one and only Dr. Rick Bedlack. We hope you'll join us! bit.ly/3GHzzgW

Thank you @RepDavidValadao for standing with us as part of the ALS Caucus! The ALS community is so grateful for your commitment to prioritize the urgency of ALS, funding for research, support for people living with ALS, and more.
We learned so much about brain and tissue donation at last week's webinar, and we hope you did, too! Thank you so much to our panelists. If you missed the live event, don't worry—you can watch the full recording on our YouTube channel! youtu.be/xlUHg2ktEzM
Sometimes the best support comes from someone who knows exactly what you're going through. Whether you're living with ALS, a caregiver, a loved one, or grieving, we have a support group for you! iamals.org/action/join-a-…
It's finally here! Join the Many Shades of ALS Team TONIGHT at 7pm ET for this critical discussion of ALS care in long-term settings. This webinar will have valuable information for everyone, so make sure you sign up! bit.ly/3HzteV2
"[In my time at the FDA] I'd like to see a cure for... neurodegenerative diseases like ALS." We couldn't agree more, @DrMakaryFDA. Glad to have you as part of the movement to #EndALS! bit.ly/4kRsqZq
![iamalsorg's tweet image. "[In my time at the FDA] I'd like to see a cure for... neurodegenerative diseases like ALS." We couldn't agree more, @DrMakaryFDA. Glad to have you as part of the movement to #EndALS! bit.ly/4kRsqZq](https://pbs.twimg.com/media/GwlMI0jWkAI9hVv.jpg)
There's still time to sign up for the next session of the ALS Comedy Crew! Starting August 7, this group will meet on Thursdays for six weeks to do comedic exercises and connect with one another over a healthy dose of laughter. Sign up today: bit.ly/4nDKaKq
Last week's Ask Me Anything ALS all about writing was a smash hit! Huge thank you to the Scribes of Strength team and all of our panelists. In case you missed it, you can watch the full recording of the session on our YouTube channel: youtu.be/zl3pRP2IXAM
Thank you for everything, Phil. Thank you Lori Andre (second from right) for sharing this photo.



Imagine giving back to those who give their all: caregivers. Well, you can! Your support of the Credit for Caring Act will help provide caregivers with the support they deserve. Ask your elected officials to support this bill: bit.ly/4mw7klu

Mike and Linda are partners in love and in life—and they advocate to end ALS together! These two are just the best. 🌟 Listen to Linda's powerful testimony to her Congressman from this year's ALS Community Summit: bit.ly/3UhQdGZ

Please join us on Thursday, 7/24, at 5:00 pm ET for a research access discussion and Q&A session with Catherine Small and Judi Carey, RN from the Healey & AMG Center for ALS. #ALSResearch Register: mgb-org.zoom.us/webinar/regist…
As we seek to reauthorize the ACT for ALS next year, we're collecting stories that highlight the immense value of this bill and the programs it supports. If you're involved in an Expanded Access Program funded by ACT for ALS, tell us your story! bit.ly/441wYHo
One of the most powerful ways to make meaning out of a difficult situation is to share your experiences to help others. The Peer Support Initiative can match you with someone who needs someone just like you to support them. Learn more about the PSI: bit.ly/40iIk7X

If you've ever wished you could help with I AM ALS' legislative efforts but just haven't had the time, we have good news. By signing up to become a constituent, you can help with specific legislation without lifting a finger! Learn more: bit.ly/4kuH7Cw