Severe ME Awareness Day is August 8.
I’m posting for awareness today for my fellow ME patients who are classified as ‘severe’ and ‘very severe’ MECFS patients. Many of them are completely bed bound and haven’t been able to walk, eat, talk, or get out of bed in years.
Walking for Ankylosing Spondylitis is challenging for me with fibromyalgia and MECFS to deal with as well. But May is here. Time for change!
Why Do Blood Draws Make Me Sick? Are you an FM/MECFS patient that experiences a flare-up of symptoms or a PEM crash from blood draws? If yes, I’d love to hear from you!
You’ll never think of the cost of chronic illness and maintaining an income until it happens to you. Here’s a breakdown of what Spoonies think about.
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.
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.
The holiday season for chronic illness warriors is stressful and hard. Here are some tips on surviving the holidays with chronic illness without flaring.
Chronic Illness Prompts: Meeting, Advocating, Tweaking, Working, Curating – What chronic illness bloggers write about when given writing prompts to write about their chronic lives.
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.