ME/CFS (Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome) Awareness Week 4

Welcome! Did you know that May 12th was MECFS International Awareness Day? With that in mind, during the month of May, I’m joining in on Instagram with other chronically ill people on the below pictured spoonie challenges, posting once daily as able, to spread awareness on a variety of MECFS topics. In order to try …

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What is your funniest holiday memory?

Well hi, thanks for popping by today! As you may or may not know this month’s Tuesday blog posts are dedicated to asking one light-hearted question. I have to confess, thinking up these questions was much easier in theory. 😊 Trying to be all inclusive has been the biggest challenge, but yep, always a but …

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A Few Things that have Helped me Live my Best Life, Alongside Chronic Illness

One to the blessings of social media, when living with a chronic illness, is the ability to learn what tools other people are using to live their best life with their disability. In the spirit of ‘sharing what’s worked for me but might not work for you as we are all different’, I’m going to …

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5-Part Series: The Truth about my Life with Multiple Chronic Illnesses, Part Five

Welcome back to the final chapter in this series, the last week in July was the week I got sick five years ago, just a few days before my son’s 18th birthday. If you’re just joining in and have some time or the desire to wander through my journey here are parts One, Two, Three, …

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5-Part Series: The Truth about my Life with Multiple Chronic Illnesses, Part Four

If you’re just joining this series, I’ll catch you up quickly. Five years ago, this month, I came down with Myalgic Encephalomyelitis (Chronic Fatigue Syndrome), a.k.a. MECFS. It’s been a rough road to put it lightly. If you feel like catching up here are Parts One, Two, and Three. Next Tuesday will be part Five …

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