Multiple Sclerosis

Resources

The following links to local and national resources provide additional information you may find helpful in managing your disease and living your best life with MS:


  • National MS Society - National nonprofit providing navigation, information, referral and support services for MS patients.

  • MS Connection - A social network designed for living with MS.

  • Multiple Sclerosis Association of America - National non-profit providing information and resources for individuals living with MS, their family and care partners. 

  • Brighter Tomorrow Grants and Health and Wellness Programs - Grant recipients receive funds for goods and services not covered by other programs. The grant is designed to improve quality of life.

  • The Consortium of MS Centers (CMSC) - Organization offering networking, research and other services to MS health care professionals.

  • HealthWell Foundation - Gives grants and other financial assistance for coinsurance, copayments, health care premiums and deductibles for certain medications and therapies.

  • Patient Access Network Foundation - Ensures underinsured patients living with chronic disease get financial help to focus on what matters most - their health. 

  • Friends of Man - Helps with a large variety of needs, such as mobility equipment, wheelchairs, van lifts, home modifications, medical equipment and procedures, prescriptions and more.

  • American Academy of Neurology - A professional society representing more than 32,000 neurologists and neuroscientists. The website contains information on various neurological conditions.

  • Multiple Sclerosis Navigators - The NMSS has a new program designed to connect patients and families with local resources to help with a wide range of issues. They are professionals trained to assist you with accessing local resources and services to help you with the many challenges that comes with living with MS.

  • North American Research Committee on Multiple Sclerosis (NARCOMS) - A global registry containing research, treatment and patient education.

  • National Organization for Rare Disorders - A patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them.