National Multiple Sclerosis Society
Caring for someone with a chronic illness like MS can be deeply satisfying. Spouses and partners, family, and friends can be drawn more closely together by their shared concerns and collaborative efforts. But caregiving can also be physically and emotionally exhausting, particularly for the primary caregiver. While this is most often a partner or spouse, the primary caregiver may also be an adult child, parent, or friend. Whoever you are, remember that paying attention to your own health and well-being is essential to being able to care for someone else.
Resources for Cargivers:
Well Spouse Association
CaringBridge is a free one-stop shop that connects and updates communities of supporters on a person's ongoing health status, treatment, surgeries, progress in therapies and recovery. A personalized CaringBridge website helps keep loved ones informed during difficult times. In return, family and friends give support through guestbook messages.
A Guide for Caregivers
Someone You Know Has MS: A Book for Families