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.
BELIEVE US: Invisible Illness Awareness Week 2019 – How to show compassion when someone says they are disabled or have an invisible illness.
Let’s talk about pain for chronic pain awareness month. This is my chronic pain story. I hope it helps others understand what it is like to live with in pain. You are not alone.
Chronic Illness Prompts: Meeting, Advocating, Tweaking, Working, Curating – What chronic illness bloggers write about when given writing prompts to write about their chronic lives.
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.
Chronic Fatigue Syndrome: I Am One of the Millions Missing – When I have a Grey Day, aka a Missing Day, my ME/CFS hits overdrive and I go missing. Where do I go?
This is my flare survival kit, which includes medications, supplements, and things I need to make myself comfortable when flares hit suddenly.
A friend recently asked me, “What is a flare?” Flares are a sudden increase in symptoms from my normal day-to-day levels of energy, fatigue and pain.
One of the biggest challenges with chronic illness is learning how to live with limitations. These limitations range from small to severe disruptions that leave people housebound.
My struggle with the severe and debilitating symptoms of Fibromyalgia in Taiwan as a Canadian expat.