World M.E Day
Hello Friends,
Today is World M.E Day and to help people understand what M.E or Myalgic Encephalomyelitis actually is, I thought I’d publish an article giving you an overview of the disease. I felt this was especially important since there’s been so much in the media about Long Covid ~ which is remarkably similar to M.E and some with people with Long Covid are now being diagnosed with M.E…
Goodbye 2021 ~ Changes are Coming
Hello friends,
2021 is finally coming to a close; it both feels like its been a long year and yet flown by…this year for me personally, has been very up and down and it’s ending more on a down than an up.
This has lead me to think a lot about the content of this space and my social media…
My Bed and M.E
This month is National Bed Month and like many chronically ill people, especially those with Moderate/Severe M.E, my bed is very important to me. So I thought I’d tell you bit about why that is and what I feel are some of the important factors in ensure you bed is a cosy a haven as possible.
Since becoming seriously ill, my bed isn’t just the place I sleep anymore as I spend at least 3 days out of 7 each week in it resting. So my bed, and by extension my bedroom, has become a lounge, a dining room, an office/study, a library and at times even a kitchen!
University and Chronic Illness ~ Guest Post by Pippa Stacey
Above all else, I want to have an impact. I want to help other people get their foot in the door. I want to make sure that other chronically ill individuals also have a fair shot at chasing their dreams. It’s about time the world realises just how much we have to offer.