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For Care Partners


Caring for someone with a chronic illness like multiple sclerosis can be deeply satisfying. Partners, family and friends can be drawn more closely together when they meet the challenges. Providing care can also be physically and emotionally exhausting, especially for the person who is the primary care partner. The Greater Carolinas Chapter is proud to provide support for families and care partners.

The National MS Society also provides a host of resources from brochures to books on advice for hiring home health aides and caregiver related research. Find out more here.

Programs and Services for the Care Partner

Additional Programs and Services

For all Programs and Services offered, click here.

Books available through the chapter’s Lending Library:

  • Living with Multiple Sclerosis: A Handbook for Families by Robert Shuman and Janice Schwartz
  • Creative Caregiving, Positive Caregiver Attitudes, Preventing Caregiver Burnout, Coping With Caregiver Worries, and The Magic of Humor in Caregiving by James R. Sherman, PhD
  • Always On Call: When Illness Turns Families Into Caregivers by the United Hospital Fund
  • Dirty Details: The Days and Nights of a Well Spouse by Marion Deutsche Cohen
  • Mainstay: For the Well Spouse of the Chronically Ill by Maggie Strong
  • Multiple Sclerosis: A Guide for Families by Rosalind Kalb, PhD
  • The Comfort of Home: An Illustrated Guide for Caregivers by Maria M. Meyer with Paula Derr, RN
  • Love, Honor, & Value: A Family Caregiver speaks out About the Choices & Challenges of Caregiving by Suzanne Geffen Mintz
  • Many more...

Care Partner Interviews

Meet Elsie and her care partner, Art.

Meet Blanche and her care partner, Larry.