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.
• 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.