
Kary Pearson
Mar 15, 20231 min read
Is M.E. Contageous?
The short answer is that Myalgic Encephalomyelitis is not contageous. However, it is usually caused by viruses which are contageous....

The short answer is that Myalgic Encephalomyelitis is not contageous. However, it is usually caused by viruses which are contageous....

Fear is a very real and constant part of my M.E. experience. I fear that I'll never get any better than my current condition, even as I...

If I can ask one thing of you, it's to become an advocate. People with M.E. do their best to advocate for themselves, but it can be...

Brain fog from M.E. can be difficult to describe because it's so many different things. Still, I'll try to explain how I experience it....

I can't think of what to write today, so I'd like to ask if you have any questions for me about M.E. or my experience with it. Want to...

If you have a chronic illness or know someone with one, you've probably heard of the spoon theory. The term was coined by Christine...

M.E. affects the brain and muscles as well as the digestive, immune, and cardiac systems. It's a complex illness, so why was it...

M.E. gets categorised as mild, moderate, severe, and very severe. I'm mostly moderate, but closer to mild than severe. That's only...

It took me over a year to identify as disabled. I kept telling myself that I wasn't doing that badly, that just because I couldn't do a...

Self care is big business, from fancy smelly candles to retreats that cost thousands of dollars. The self care options seem endless for...

I once read that the only way to avoid becoming disabled is to die young, and that's still no guarantee. Most people, especially healthy...

It's not quite noon and I already overdid it. I woke up feeling like a human being. Daniel kindly brought me breakfast in bed. I checked...

I'd like to ask you a favour the next time you go out - count the number of steps you have to go up or down. Notice if ramps or elevators...

There is one question that fills me with dread because I'm usually unsure how to answer it, "What do you do all day?" That question comes...

People with M.E. talk a lot about crashes, which are exacerbations of symptoms. A crash is very similar to a flair-up, but it tends to be...

I usually consider myself an optimistic realistic, I accept the things I cannot change and look on the bright side. But optimism isn't...

Many people with chronic illnesses and disabilities use mobility aids such as walking sticks, crutches, rollators, or wheelchairs. A lot...

M.E. feels like an invisible illness in more ways than one. Firstly and obviously, there are no physical markers, no scars, no splints,...

For me, M.E. feels like having jet-lag, the flu, a concussion, and a migraine all at once. Some of my symptoms are severe tiredness after...

These are some of the things I use to conserve energy. On days when I can't manage a shower but can brush my hair, I depend on dry...
