Mitsubishi Tanabe Pharma America
@MTPA_US
MTPA is dedicated to making a real difference in the lives of people living with serious and debilitating diseases. Community guidelines: https://bit.ly/4e9gM93
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
ALS patients may wait 10–15 months for a definitive diagnosis, facing painful diagnostic tests and inaccurate diagnoses. The @alsassociation’s thinkALS™ tool may help doctors identify ALS earlier with clear clinical indicators. Learn more: bit.ly/4kkWMEh
We were honored to attend the @MDAorg'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

Discover the real impact of #ALS on our YouTube channel with stories from patients, caregivers & advocates sharing authentic experiences. bit.ly/4dJmeAM
Theresa found purpose and strength in being a care partner for her husband living with #ALS. A role that is deeply rewarding yet filled with challenges. Discover her powerful journey as a #CALS: bit.ly/4eltjYE
This week, we proudly celebrate three years of our #ALS treatment option! We're honored to support the ALS community and remain committed to providing care for people with #ALS. Learn more about our dedication to the ALS community: bit.ly/3G7dxnz
We’re joining the conversation at @EANeurology #EAN2025 and #ATMRD2025 to share our newest findings on #ParkinsonsDisease. Honored to help advance scientific understanding in this crucial research area. Learn more at bit.ly/4kMKbK5
At MTPA, we're dedicated to advancing cutting-edge research in ALS and PD that help create new possibilities. See how we're transforming science into progress: bit.ly/3Ri4hP7

The #ALS community has many inspiring stories filled with resilience and hope. These shared experiences can help offer strength to people who are impacted by similar challenges. Explore ALS stories here: bit.ly/4j6GzkT

Check out our podcast interview with @ReachMD! Gustavo Suarez, MD, Vice President of Medical Affairs, MTPA discusses advancing care for #ALS. Listen to the full episode here: bit.ly/4j5UvMW

This Men's Health Month, we remember that ALS still affects men 20% more frequently than women. A gap that continues to be studied by researchers. #ALSAwareness #MensHealthMonth
The #ALS diagnosis process is complex, often leading to delays in care. MTPA is committed to supporting patients earlier in their journey. In @medpagetoday, Stephen Apple, MD & Joseph Scalia discuss how industry and HCPs can help address these challenges. medpagetoday.com/ad-insights/in…
Don’t miss out! One week left to register for our FREE webinar on understanding ALS treatment access. Hear from an access expert and two ALS community members as they share personal experiences navigating insurance and financial assistance. Register now: bit.ly/3YRd5jq

We had a blast at the Yankees game on 6/3! Our team from Jersey City, NJ, came together to honor Lou Gehrig's legacy. A great opportunity for team building and honoring Lou's positive impact on the ALS community. #TeamMTPA

We had a great time at the Shady Strong BBQ Competition & Music Festival, and are proud to have sponsored this event in support of people impacted by ALS and their families! Thank you to Brian Bennati for supporting the community.
Lou Gehrig. The Iron Horse: 2,130 consecutive games. 493 homeruns. Then ALS at just 36. Yet he stood at Yankee Stadium and called himself "the luckiest man on earth." 80 years later, we’re still fighting for the cause. #LouGehrigDay #ALSAwareness
The #ALS community is filled with resilient people whose shared experiences can help inspire others going through similar challenges. Explore their stories here: bit.ly/4j8Qnul

Genetic ALS testing can contribute crucial data that researchers may use to identify patterns and develop treatments that may help fighting ALS. Connect with the @LesTurnerALS for more educational resources they have available. #ALSAwarenessMonth
We recently joined fellow research industry experts at the @PRDAssociation 30th World Congress on Parkinson’s Disease and Related Disorders in NYC. Read more about the importance of the Congress from Rebecca Vayalumkal’s recap below. #TeamMTPA #IAPRD2025
An ALS diagnosis has ripple effects beyond the patient, touching loved ones and friends. This #ALSAwarenessMonth, Theresa shares her story of caring for her husband with ALS in hopes to connect with the entire ALS community.