You may remember that I previously wrote about a recently released documentary, Unrest, which portrays how myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome … Read More ›
Tag: ME
In this post, I’m actually going to talk about an illness I don’t have: myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Prior to my postural orthostatic tachycardia … Read More ›
This is the third year I have posted this guide for people with chronic illnesses and their loved ones. I wanted to share it again … Read More ›
The immune system is my favorite system (with my least favorite obviously being the nervous system. Stupid autonomic dysfunction). I like the immune system because … Read More ›
This is the second third time I have written this post. WordPress decided it wanted to be a jerk and deleted previous drafts, so I … Read More ›
I have talked about the difficulties of exercising in a previous post, and as it’s a constant battle, will probably post many more. I have … Read More ›
Don’t get your hopes up – this post is not about sick people…you know, getting “on top” of sick people. Sorry if you were kind … Read More ›
I posted this guide for people with chronic illnesses and their loved ones last year. I wanted to share it again this year, as I … Read More ›
After being diagnosed with POTS, the first medication I was prescribed was a selective serotonin reuptake inhibitor (SSRI). SSRIs are antidepressants but are often prescribed … Read More ›
As I’ve mentioned previously, I’ve been experiencing more pain than usual in my back and neck. At least part of it is caused by the … Read More ›