Severe ME/CFS Caregiver: Kim Moy

Bateman Horne Center and Solve M.E. co-hosted this webinar for the benefit of patients and caregivers navigating life with severe ME/CFS. It focuses on navigating health systems, role changes, daily care, caregiver mental health, and maintaining healthy relationships. The panel of experienced caregivers share practical tips and resources.

This video shows Kim Moy's section of the webinar. She is one of three panelists.

Panelists include:
Kyle Kitzmiller, husband to a woman with Severe ME. (Physics Girl)
Amy Mooney, mother to a teen daughter with Severe ME.
Kim Moy, wife to a husband with Severe ME.
Galen Warden, mother to an adult son with Severe ME.

The content provided is for informational purposes only and does not constitute legal or medical advice. Viewers are encouraged to consult with qualified legal or medical professionals for specific advice tailored to their individual circumstances.

[lindybrockington]

Self care is SO important. I am the one with ME/CFS and my husband is my caregiver when I need it. I'm not severe. I always encourage him to meet his friends for happy hour, to keep riding his bike and going to see his family even when I'm not able to travel and well as anything else he wants to do.