I love traveling. I mean, I LOVE traveling. Ever since I was 15 and ordered my first Guinness beer from a bar in Ireland (and … Read More ›
Category: Conditions and Diseases
*** Update: For dysautonomiacs who are filing for disability, my friend Stacy (see comments) has kindly offered the diagnostic code for dysautonomia: 337.9 (confirm this … Read More ›
For the past few days I have been pretty dehydrated. From what I understand, dysautonomia and ME/CFS can cause problems with water retention, and we … Read More ›
Note: I started writing this post before the bombing in Boston on Monday, but debated whether to continue with the post in light of the … Read More ›
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 ›
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 ›
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 ›
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 ›