OUR CAREGIVERS ONLY GROUP
My personal experience: it was hard to consider my caregivers when I was extremely sick because it is like I had no room to consider how hard it was on them. I carried intense guilt but I was too focused on surviving. Over time, I found taking the time to tell them how very much I appreciate them, validating how hard it was for them too, and showing them how I cared for their health too.. helped create a better balance of love and support.
"Chronic illness often results in not one but two patients: the person ill and the person caring for them. Lyme Caregiving - Providing Care without Losing Yourself"
"10 Life Lessons I Learned as a Caretaker for Chronic Lyme"
https://medium.com/@DebOberly/10-life-lessons-i-learned-as-a-caretaker-for-chronic-lyme-3a7fde0d6aea
"Being in a caregiving role can be extremely challenging. Over the four years I’ve spent supporting my chronically ill partner I’ve made dozens of mistakes."
"You didn’t sign up for this. It’s a blessing that neither of us knew what fate had in store when we met. I’m not sure that I would have been brave enough to carry on and I know that I would not have wanted to bring you on this grisly journey with me."
Meeting for CAREGIVERS
PARENTS OF CHILDREN WITH LYME
COMPASSION OVER TOUGH LOVE
SUPPORT FROM LOVED ONES POST with video
Disclaimer: Rise Above Lyme makes no claims about any possible benefit of using any product mentioned within this site. Always consult with your doctor before adding anything. The information shared is based on personal experience, years of accumulated researched resources from Lyme Literate doctors and polls conducted within Lyme groups from actual patient experience using these solution ideas.
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