There has been a lot of interesting news about POTS recently. I want to share one study in particular with you that I think you … Read More ›
Tag: Dysautonomia
I don’t want to brag, but I’m pretty awesome at sleeping. Pretty much anytime, any place, for any length of time. If there was a … Read More ›
Today is my POTSiversary. What is a “POTSiversary” you might ask? It’s the totally clever way of saying it’s my illness anniversary! Three years ago … Read More ›
It occurred to me recently that I have a bad habit of writing a post about some issue that I’m currently having and then never … 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 ›
A good friend of mine wrote a blog series for the Spirit of War military blog about suicide in September for suicide awareness month. As … Read More ›