From websites to videos, to books to support groups; there are plenty of ALS-focused resources specifically for caregivers. But not all caregivers feel they need to attend an ALS caregiver support group; and sometimes these groups don’t provide enough help.
If you don’t attend an ALS caregiver support group, where do you find your support, respite and relief? Do you turn to a club, neighbors, a group of friends or other similar groups? What do you recommend for new caregivers?