Skip to navigation Skip to content

Share

Master Page Does Not Exist

    Services

    Master Page Does Not Exist
    1. Care Givers

      We recognize that MS impacts the person who has been diagnosed with the disease, and that it also affects people who are closest to that person.

    2. Join a Group or Discussion

      Looking to connect with other caregivers, family members, or people affected by MS? Self-help groups bring people together who share common life experiences for support, education and mutual aid.

    Resources

    Master Page Does Not Exist
    1. A Guide for Support Partners (.pdf)

      Practical issues faced by caregivers. Includes resource list. By Tanya Radford.

    2. Intimacy and Sexuality (.pdf)

      MS can affect sexuality, both directly and indirectly, but problems can be resolved or minimized. By Rosalind Kalb, PhD.

    3. Hiring Help at Home (.pdf)

      Checklists and worksheets for people who need help at home. Forms for a needs assessment, job description, and employment contract.

    4. Plaintalk — A Booklet about MS for Families (.pdf)

      Discusses some of the more difficult physical and emotional problems many families face. By Sarah Minden, MD, and Debra Frankel, MS, OTR.

    5. Someone You Know Has MS: A Book for Families (.pdf)

      For children, 5-12. A story about Michael and his family explains MS and explores children’s fears and concerns. Adapted by Martha King from original material by Cyrisse Jaffee, Debra Frankel, Barbara LaRoche, and Patricia Dick.

    6. MS & Pregnancy: Kara's Story Part 1 (video)

      This video features part one of a discussion about pregnancy and multiple sclerosis.

    7. MS & Pregnancy: Kara's Story Part 2 (video)

      This video features part two of a discussion about pregnancy and multiple sclerosis.

    8. Kids Get MS Too: A Handbook for Parents Whose Child or Teen has MS (.pdf)

      This handbook is a guide for parents with a child or teen with MS.

    9. Keep S'myelin: A newsletter about MS for children

      Keep S’myelin is a colorful, engaging, informative, and reassuring newsletter to help children and their parents talk and learn about MS together. Each issue is filled with stories, interviews, games, and activities that highlight a specific topic related to MS, as well as a special section just for parents.

    10. Family Matters

      MS happens to families, not just to individuals. You probably have many questions about MS – what will happen to my family member with MS, how can we plan, how do we manage the unpredictability of the disease? The National MS Society is here to help you navigate the challenges of living MS with a personalized response to your unique needs.

    11. Communication Tools for Maintaining Good Relationships (Teleconference Recording)

      Recorded February 6, 2014. During this teleconference, Catherine Freemire, LCSW, shared Tools for Creating Positive Emotion within Relationships, Tools for Making Requests vs. Making Complaints and Tools for Making Repairs in Relationships When Conflict Arises

    12. A History of MS (book)

      This work aims to answer some of the fundamental questions of the history of MS.

    13. Everyday Matters

      Everyone has their own idea of their best life. For people living with multiple sclerosis, the idea of that “best life” can change due to the challenges of having a chronic, unpredictable and lifelong disease. The National MS Society’s Everyday Matters, supported by Genzyme, a Sanofi company, was an interactive national project that uncovered stories of real people facing the everyday challenges that MS can bring on the path to one’s best life.

    14. Live Fully, Live Well

      Managing your health and wellness is an integral part of "living well" with MS. Live Fully, Live Well is a comprehensive wellness program from the National MS Society and Can Do MS, designed for people living with MS and their support partners. Live Fully, Live Well covers topics affecting the whole family living with MS in order to strengthen relationships, increase understanding and promote improved health and quality of life.

    15. From a Loved One's Perspective: Depression (video)

      Partners and family members of people with MS may experience normal grieving and other emotional changes, including depression.

Share

Master Page Does Not Exist
© 2024 The National Multiple Sclerosis Society is a tax exempt 501(c)3 nonprofit organization. Its Identification Number (EIN) is 13-5661935.