Advocacy Initiatives, A Move, and More for May 2021! Ah, where to start? Today’s post is a personal update post. I rarely take the opportunity to do these types of posts, but we’ve had a lot happening and there’s no better way to update than by telling it like it is! Read on to learn more about my May initiatives – my busiest month by far in 2021.
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!
Chronic pain quotes that pain patients can relate to – When life has you down and you’re not sure if you have words to describe your pain, you can trust that someone somewhere has helped. Chronic pain quotes like these let chronic pain patients know they’re not alone.
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.
Most chronically ill patients struggle to find purpose and meaning in life, and a great number of us do so with advocacy work. Some of us also seek volunteering opportunities, so today’s post is about finding the right kind of volunteer work when you are chronically ill.
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.
Life with COVID19 and Chronic Illness in Taiwan Update – Life in Taiwan during a global pandemic and having to visit a hospital in Taiwan each month.
BELIEVE US: Invisible Illness Awareness Week 2019 – How to show compassion when someone says they are disabled or have an invisible illness.