About a week ago, I stopped taking all my dysautonomia/ME/CFS medication. I don’t exactly know why. One night before bed it was time to pop … Read More ›
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Last Saturday, March 16th, was the American Academy of Neurology Annual Conference and Brain Fair. This year it was located here in southern California, so … Read More ›
My fellow POTS blogger over at lethargicsmiles provides a great description of POTS, what it is, and what it would feel like if you had it. … Read More ›
A few weeks ago my fellow blogger, Kathryn, posted about participating in the annual Beauty of a Woman (BoaW) BlogFest. I thought it sounded interesting, … Read More ›
Last week I had an appointment with my POTS doctor. Many dysautonomiacs see a neurologist for help managing their condition, as dysautonomia is a dysfunction … Read More ›
To my gentlemen readers (do I even have any?…), I promise I won’t be offended if you want to skip this post. When I was … Read More ›
I won first place! I NEVER win anything! Those of you who are my Facebook friends will recognize the photo – It’s my favorite “I’m … Read More ›
After my last two posts, you are no doubt now very familiar with my exercise plight. In this post I will finally share my formulated … Read More ›
You may remember that my last post, Spaceman’s Disease, was the first of a two part series on the biology, difficulty (and necessity, perhaps) of … Read More ›
This is Part 1 of what will probably be a two part post about deconditioning and exercise. Hope you’re in the mood for a science … Read More ›