This July 4th, we honor veterans who face a 2x higher chance of developing #ALS. Scientists are working to solve for why. If you, or a veteran you know needs support with ALS resources, find local advocacy organizations here: bit.ly/4jwp9y8

Discover the real impact of #ALS on our YouTube channel with stories from patients, caregivers & advocates sharing authentic experiences. bit.ly/4dJmeAM

We were honored to attend the Muscular Dystrophy Association's 25th Annual Wings Over Wall Street Gala in NYC! We joined researchers, advocates & families, all united by one cause – a world free from ALS. 25 years strong and still going. #WOWS25 #ALSAdvocacy

ALS patients may wait 10–15 months for a definitive diagnosis, facing painful diagnostic tests and inaccurate diagnoses. The The ALS Association’s thinkALS™ tool may help doctors identify ALS earlier with clear clinical indicators. Learn more: bit.ly/4kkWMEh

Interested in sharing an #ALS experience to inspire others living with ALS and their caregivers? Every story can help connect people living with ALS to a larger community where they feel seen and supported. Learn more here: bit.ly/4kOITOm

We’re proud to share the first issue of The Parkinson’s Perspective, an MTPA educational newsletter shaped with input from Parkinson’s disease advocacy organizations. Explore patient stories, expert insights and more: bit.ly/4fe64A4

This National Wellness Month, we want to remind ALS caregivers that prioritizing your health is not selfish, it's essential to help support the people you love. The best care starts with self-care. Learn more: bit.ly/44y0wvr

We don't just show up—we bring it! We're a team of bold thinkers who are taking on complex medical challenges. Every day is an opportunity to discover a scientific breakthrough that can help make a meaningful difference. Learn more: bit.ly/3TiAVl9

This #SummerSunSafetyMonth, we’re reminded that for people with erythropoietic protoporphyria (EPP) and x-linked porphyria (XLP), sun safety isn't seasonal. These rare conditions cause severe pain within minutes of exposure. Year-round protection isn't a choice, it's a necessity.

We proudly joined ALS leaders from around the globe at the The ALS Association’s 2025 #ALSNexus Conference—driving progress toward making a meaningful difference in the ALS community. #TeamMTPA

Just in: New research in Muscle & Nerve showcases the latest data analysis for our #ALS treatment. Read more here: bit.ly/4oJhekQ

"To us, success is measured in patients helped." Dive into our candid Q&A with MTPA President, Yasutoshi Kawakami, on our vision, rare disease innovation, and unique approach to healthcare challenges. Read more: bit.ly/4knqkQV

ALS and Parkinson's disease (PD) are finally receiving more awareness. We're not just watching this momentum, we're here to contribute to it by supporting patients, caregivers, and advocacy organizations. Find ALS and PD community resources here: bit.ly/3J6ymAQ

We had the privilege of hosting #ALS patient advocate and author Andrea Lytle Peet for a Meet the Author event at #ALSNexus 2025. Thank you to Andrea, her care partner Annie, and all who attended this thoughtful discussion on what it means to live with ALS.

Clinical trials can transform scientific discovery into treatments that may enhance the lives of patients. These carefully designed studies help us understand how treatments work. Learn more here: bit.ly/4mpFfvk

The energy at the International Neuropalliative Care Society #INPCS25 in Phoenix was incredible! We connected with brilliant minds advancing neuropalliative care at the meeting. Grateful for everyone who shared insights that will help us better support ALS and Parkinson's communities.

What a powerful September we've had supporting the #ALS community across the country. At these walks, we meet families, hear stories and see determination up close, which fuels our team to discover research that may have an impact on people living with ALS. #TeamMTPA

A little goes a long way when it comes to physical therapy. This National Physical Therapy Month, we're taking a moment to acknowledge the role of PT in helping those with neurodegenerative diseases to stay active in daily life.

We are honored to attend the NEALS Consortium Annual Meeting in Clearwater, FL., where our team will present eight posters focused on treatment effectiveness, safety, and disease burden in #ALS. Read more about our presentations at #NEALS2025 here: bit.ly/42PK49O

We’re looking forward to sharing our latest #ParkinsonsDisease research at the MDS #MDSCongress and connecting with the PD community. Read more here: bit.ly/4mR8pTY See you in Honolulu!