Fibromyalgia Awareness Day is May 12. My Several Worlds has won a Best Fibromyalgia Blog award again. Today post is a tribute to my favorite fibro advocates in the world.
May Momentum and World MECFS Day – My story with MECFS and some information from experts who have found that COVID19 and MECFS intersect as viral illnesses.
Written in honor of World Mental Health Awareness Day and World Arthritis Day 2019 – Learning to love your chronically ill body is possible. Here are some things to remember.
September is Pain Awareness Month. 9/19/19 is Pain Action Day. I’m sharing my chronic pain story to help others understand what it is like to live with in pain. You are not alone.
MSW Interviews: Introducing professional artist Jennifer Walker, author of Unexpected Advocate. Jennifer has RA, Fibromyalgia, and SPD; among others.
Figuring, Completing, Boring, Cuddling, Chatting – August 2018 Linkup Party for People with Chronic Illnesses
A Chronic Voice hosts a link-up party each month for those of us who are chronically ill. Sheryl’s writing prompts for August are: Figuring, Completing, Boring, Cuddling, and Chatting.
Alternative Treatments to Chronic Illness: Do They Work? Here are the alternative treatments I’ve tried that did not work to alleviate my disease symptoms.
Letting Go with Chronic Illness – Learn to accept what you need and don’t need with chronic illness. Growth comes from making room for new things.
Chronic illness is hard to understand. There are many things to consider when you’re chronically ill. These are things I never thought of until I got sick.
This is my flare survival kit, which includes medications, supplements, and things I need to make myself comfortable when flares hit suddenly.