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MS is unpredictable, but the care for those living w/ this illness should not be. Protect Medicaid and consistent, comprehensive coverage most in need.

MS Activists know multiple sclerosis affects everyone - including 70,000 veterans and military service members. Ask Congress to restore the MS Research Program through the CDMRP: nmss.quorum.us/campaign/11940…

MS Activists register here for the "Save the MS Research Program" Webinar! Learn more about CDMRP funded research. nmss.quorum.us/event/23043/

Reminder! Calling all MS Activists to register here for the "Save the MS Research Program" Webinar! Learn more about CDMRP funded research: nmss.quorum.us/event/23043/

Have you registered for the Save the MS Research Program Webinar? We're calling all MS Activists to join us on April 29 and restore funding for the MSRP/CDMRP! nmss.quorum.us/event/23043/

To all of our MS Activists: THANK YOU! 🧡

Join us TOMORROW for the “Save the MS Research Program” at 2 pm ET! Click here to RSVP and learn more about the importance of the MSRP and how you can help: nmss.quorum.us/event/23043/

Eighty years ago, an ad in the New York Times sparked a movement. Sylvia Lawry, driven by her brother’s struggle with MS, refused to accept “no cure.” Today, we honor her legacy—one that has fueled hope for generations. Read Sylvia's story: ntlms.org/80Years

MS Activists were at the California State Capitol this week to advocate for improved healthcare for those living with MS. Let’s give them a 🧡to show our support! Our priorities: -Reforming the rules for Pharmacy Benefit Managers (PBM) -Care Denial Transparency

MS Activists: Take action today and contact your member of Congress and tell them to Protect Medicaid: nmss.quorum.us/campaign/12185…

MS Activists came together in Harrisburg earlier this week to meet with legislators, urging them to support SB 268. This legislation would ban copay accumulator programs and make #AllCopaysCount.

Medicaid is our country’s primary payer for long-term services and supports, including home- and community-based services that allow people with MS to remain independent and in their homes. MS Activists: Take Action, contact your member of Congress today! nmss.quorum.us/campaign/12185…

MS doesn’t wait, so getting treatment shouldn’t wait either. MS Activists met in Hartford last week to: ✔️Reform pharmacy benefit manager practices ✔️Create protections in utilization management to ensure that people with MS can get needed medications without harmful delays.

MS Activists were at the North Carolina General Assembly on Wednesday urging lawmakers to support prior authorization reform to address harmful delays in care!

🧡MS Activists at Massachusetts MS State Action Day met with lawmakers this week about legislation that would ensure all third-party financial assistance counts toward patients' deductibles & out-of-pocket maximum amounts. Let's make #AllCopaysCount!

MS Activists gathered in Ohio last week to support HB 257, The Ohio Medical Debt Fairness Act. They were joined by volunteers and staff from the Leukemia & Lymphoma Society to address the long term financial burdens that can come with accessing quality health care and treatments.

MS Activist Amy V shares “Your Views: Wisconsin must continue MS research” learn more about why the CDMRP MS Research Program is important to her gazettextra.com/opinion/letter… via GazetteXtra

📣Calling all MS Activists: contact your U.S. Senators today to help protect Medicaid and Affordable Care Act coverage! Take action: nmss.quorum.us/campaign/12565…

.Senator Thom Tillis thank you for spreading the word regarding the implications of the cap on the Medicaid Provider Tax Rate in the Big Beautiful Bill (H.R. 1) - 📢 MS Activists tell your U.S. Senators no more cuts: nmss.quorum.us/campaign/12776…

📝We need to hear from you! Email us at [email protected]