Best Grants for Multiple Sclerosis Patients

The National Multiple Sclerosis Society offers a four-week clinical mentorship for psychology graduate students, focusing on the diagnosis and management of multiple sclerosis. This opportunity allows students to observe assessment strategies, learn about current research, and engage in comprehensive care. Open to U.S. citizens or permanent residents, the mentorship includes a $3,000 award. Students will gain invaluable experience addressing neurocognitive and psychosocial issues related to MS, promoting synergies in research and clinical practices.

The National Multiple Sclerosis Society offers the Sylvia Lawry Physician Fellowships to support MDs in acquiring essential clinical trial training. This fellowship aims to enhance expertise in conducting complex trials for MS therapies, fostering skills in protocol design, patient recruitment, and data analysis. Applicants must have relevant medical training and be engaged in ongoing MS clinical research. The program is vital for addressing the increasing demand for trained professionals in MS clinical trials, contributing to advancements in treatment.

Medical institutions and mentors training neurologists or physiatrists in multiple sclerosis care in the U.S. can apply for National Multiple Sclerosis Society support. Approximately US $225,000 funds mentor-institution programs that recruit and train postdoctoral fellows in comprehensive MS care, benefiting nonprofits and healthcare organizations serving MS patients through improved clinical expertise and multidisciplinary care.

Board eligible or certified neurologists and physiatrists in the U.S. can apply for the National Multiple Sclerosis Society’s one-year clinical care fellowship, which provides US $75,000 to the host institution for stipend and related costs. Fellows receive supervised MS patient care experience and multidisciplinary training to advance specialized MS clinical practice.

U.S. pediatric neurology physicians seeking advanced training in multiple sclerosis clinical care can receive one-year fellowship support for supervised patient care and multidisciplinary learning. The National Multiple Sclerosis Society funds board eligible or certified neurologists or physiatrists to develop expertise in pediatric MS and related demyelinating disorders, preparing them to lead MS clinical practices and support patient-focused services.

Postdoctoral researchers at U.S. academic, government, or nonprofit institutions conducting multiple sclerosis research can apply for the National Multiple Sclerosis Society’s Career Transition Fellowship. This five-year award supports advanced postdoctoral MS research training and early faculty-stage projects, and may benefit organizations and labs focused on improving outcomes for people living with MS.

Postdoctoral MS researchers at academic, government, or nonprofit institutions outside the U.S. can access funding through National Multiple Sclerosis Society Career Transition Fellowships. Awards up to US $650,000 support two years of advanced MS research training plus three years of early faculty research, which may benefit organizations focused on improving outcomes for people with multiple sclerosis.

Postdoctoral researchers in multiple sclerosis studies at U.S. institutions can apply for National Multiple Sclerosis Society fellowships supporting up to three years of research training. Funding is primarily for stipend support, backing laboratory, clinical, rehabilitation, and population-based MS research that aligns with the Society’s Pathways to Cures Roadmap and research priorities.

Early-career MDs and PhDs pursuing multiple sclerosis research training outside the U.S. can access postdoctoral salary support through the National Multiple Sclerosis Society. Grants from National Multiple Sclerosis Society help researchers worldwide conduct fundamental or applied MS studies, including patient care, rehabilitation, and population-based investigations that ultimately benefit people living with MS.

Neurologists and other MS-focused physicians seeking clinical training in Europe can receive up to €55,000 to learn advanced multiple sclerosis patient management and care. Grants from the European Committee for Treatment and Research in Multiple Sclerosis help cover stipends, travel to the host clinic, and congress participation at leading European MS centers.

Underinsured U.S. patients being treated for systemic sclerosis with interstitial lung disease can receive up to US $9,000 to offset prescription drug copays and Medicare Part B premiums. Grants from HealthWell Foundation help cover medications like Actemra, Cellcept, Ofev, Rituxan, and related biologics, and may benefit those also managing multiple sclerosis–related health access challenges.

Faculty-level medical researchers in Rhode Island can seek up to US $25,000 to strengthen resubmissions of highly rated but unfunded NIH proposals, including multiple sclerosis projects. Focused on medical research, the Rhode Island Community Foundation funds data gathering, travel, equipment time, and supplies to improve the competitiveness of planned NIH resubmissions.

Rhode Island medical research faculty whose work includes multiple sclerosis or related conditions can seek up to US $25,000 to redirect or expand their research focus. Rhode Island medical researchers can access funding through Rhode Island Community Foundation for data gathering, equipment time, supplies, support personnel, and other operating costs over a 12‑month period.

Students in the U.S. affected by multiple sclerosis, either personally or through a close family member, can receive help covering post-secondary education costs through the Multiple Sclerosis Scholarship. Battle Creek Community Foundation supports higher education expenses such as tuition, books, fees, equipment, and in some cases childcare or transportation for eligible MS-impacted students.

Individuals in the U.S. with a documented multiple sclerosis diagnosis can receive help covering reasonable paratransit fees and transportation to MS medical appointments. Grants from Multiple Sclerosis Foundation help multiple sclerosis patients access neurologist visits and infusion centers through partnerships with Lyft and Uber, supporting independence and continuity of care.

Individuals in the U.S. living with multiple sclerosis who are uninsured can receive help covering one specialist visit and a follow-up, including dental care costs. This Healthcare Assistance Grant from Multiple Sclerosis Foundation pays providers directly and may benefit patients needing prescription renewals or other essential MS-related medical care.

Individuals with multiple sclerosis in the U.S. and Puerto Rico can receive assistive technology support for daily living, communication, mobility, and home or vehicle modifications. Multiple Sclerosis Foundation may locate, partially fund, or fully fund devices that enhance independence, participation in education or work, and overall quality of life for MS patients and their families.

About Patient Advocate Foundation

Patient Advocate Foundation is the nation’s most comprehensive nonprofit dedicated to helping patients navigate, access, and afford the care they need—while improving the healthcare system for all.

Who we are and our impact

Patient Advocate Foundation provides financial assistance to help patients afford treatment and cost of living needs, personalized case management to navigate complex healthcare and social needs challenges, and a wide array of resources to empower people to take charge of their health. Since our founding in 1996—and joining forces with the PAN Foundation in 2026—we have helped 3.8 million patients navigate and access care, granted over $7 billion in financial assistance, served 350,000 people through personalized case management and elevated the patient’s voice to drive improvements in the healthcare system.

Multiple sclerosis (MS)

Help with healthcare costs for Multiple sclerosis (MS)

This TotalAssist fund helps you pay for out-of-pocket healthcare costs, including medication copays, coinsurance, and deductibles, health insurance premiums, and other expenses.

About the disease

Multiple sclerosis (MS) is a potentially disabling disease of the central nervous system in which the insulating covers of the nerve cells in the brain and spinal cord are damaged. MS is a chronic disease that affects the nervous system.

About Patient Advocate Foundation

Patient Advocate Foundation is the nation’s most comprehensive nonprofit dedicated to helping patients navigate, access, and afford the care they need—while improving the healthcare system for all.

Who we are and our impact

Patient Advocate Foundation provides financial assistance to help patients afford treatment and cost of living needs, personalized case management to navigate complex healthcare and social needs challenges, and a wide array of resources to empower people to take charge of their health. Since our founding in 1996—and joining forces with the PAN Foundation in 2026—we have helped 3.8 million patients navigate and access care, granted over $7 billion in financial assistance, served 350,000 people through personalized case management and elevated the patient’s voice to drive improvements in the healthcare system.

Multiple sclerosis (MS) health equity

Help with healthcare costs for multiple sclerosis (health equity)

This TotalAssist fund helps you pay for out-of-pocket healthcare costs, including medication copays, coinsurance, and deductibles, health insurance premiums, and other expenses.

Health Equity Funds offer help to eligible patients living in areas identified as having increased social and financial needs, as well as higher rates of chronic conditions. Eligibility is determined in part by home address zip code. 

About the disease

Multiple sclerosis (MS) is a potentially disabling disease of the central nervous system in which the insulating covers of the nerve cells in the brain and spinal cord are damaged. MS is a chronic disease that affects the nervous system.

The National Multiple Sclerosis Society offers a Medical Student Mentorship Program that provides a four-week clinical experience for medical students who have completed at least one year of school. This program aims to raise awareness about the challenges faced by individuals with MS and generate interest in careers focused on MS care. Students gain hands-on experience under the guidance of MS specialists, enhancing their understanding of the disease and its management.

The National MS Society offers Harry Weaver Scholar Awards to support emerging researchers in multiple sclerosis. This prestigious award honors Dr. Harry Weaver's legacy and aims to facilitate independent research careers. Eligible candidates must have a doctoral degree and relevant postdoctoral training. The funding is designed to provide salary and grant support for five years, allowing awardees to establish competence in their research area. Applications should align with the Society's Pathways to Cures Roadmap.

The National MS Society's Clinician Scientist Development Awards aim to cultivate promising young investigators in multiple sclerosis research. This program supports postdoctoral fellows with three years of comprehensive training in academic medicine focused on MS. Applicants must hold a clinical degree and be licensed in the U.S. The Society prioritizes research that aligns with its Pathways to Cures Roadmap, which emphasizes stopping disease progression, restoring function, and preventing MS.

Biogen Corporate Sponsorships provide funding to support congresses, events, and initiatives in exchange for tangible benefits such as marketing opportunities and recognition. Applications are reviewed on a rolling basis, and requests must be submitted 50 days in advance. Biogen considers various disease areas for sponsorship, including Alzheimer’s and Multiple Sclerosis. Approval depends on funding availability, alignment with interests, and event details, ensuring transparency for all potential sponsors.

The Christopher & Dana Reeve Foundation's Expanded Impact Grants Program aims to support previously awarded Quality of Life grantees in expanding successful initiatives for individuals living with paralysis. Offering up to $100,000 for each of the four grants, this program seeks to enhance evidence-based practices that improve the quality of life for both patients and their caregivers. Eligible organizations must demonstrate previous success and be capable of scaling their impactful projects within 24 months.

The Hanger Foundation's Empowerment Grants aim to positively impact individuals with physical challenges by supporting 501(c)(3) organizations in the U.S. The foundation focuses on rehabilitation services, athletic programs, and social activities that empower those with limb loss or differences. Grants are available for one year and prioritize projects that engage communities and enhance the quality of life for those in need. Organizations are encouraged to apply for funding that directly supports these goals.

The Quality of Life Grants Program, managed by the Christopher & Dana Reeve Foundation, provides funding of up to $25,000 for projects that support individuals living with paralysis. This program emphasizes community engagement and health promotion in all U.S. states and territories. It focuses on funding initiatives that directly impact those affected by various conditions, such as spinal cord injuries and multiple sclerosis, fostering inclusion and well-being.

The National MS Society offers annual Research Grants for investigator-initiated proposals addressing key research questions from the Pathways to MS Cures Roadmap. These grants support diverse studies, including clinical and nonclinical research aimed at stopping MS disease activity, restoring function, and preventing new cases. Eligible applicants must hold an M.D. or Ph.D. and demonstrate relevance to the Society's research priorities. This funding opportunity promotes collaboration and focuses on underserved MS populations.