"For more than thirty-two years, she has put up with my multiple sclerosis and me. Through good and bad times, she has remained a constant beacon of joy and hope - I could not wish for more or for anyone better." Michael M.
At the Minnesota Chapter, we care, and are committed to speaking up for care partners and their needs.
Spouses and partners, family, and friends can be drawn more closely together by a chronic disease like MS. But providing care can also be physically and emotionally exhausting.
MS doesn’t change the fact that the relationship between a care partner and the person receiving care is always a two-way street. The Minnesota Chapter acknowledges the unique challenges care partners face, and we’re here to provide resources and support.
Click here to learn about different programs and services designed specifically for caregivers and their needs.