you know, just being there to listen as you do anytime is one of the best ways to help out. Even the little notes, cards you send to a caregiver mean so much, even if he does not say anything back.
all for now
Joyful50
Joyful50 - what is the best way for a family member, not the caregiver, to support both the caregiver and the person with Mito? This is wonderful for you to share your story and perhaps reach out to others who may be feeling all alone in dealing with this disease. Thank you.