An entire book could probably be written about simple things that are made much more difficult by dysautonomia and ME/CFS. Some I have mentioned before … Read More ›
Category: Uncategorized
I just realized that Musings of a Dysautonomiac celebrated its one year anniversary! June 21st, 2012 I posted my very first post. I started this … Read More ›
Gentlemen, this is another one of those posts you may want to skip. Although, if you choose to continue, I have included some special treats … Read More ›
I have been bad about posting lately, but certainly not for lack of topics. There are a number of things I plan to write about, … Read More ›
Update: After publishing this post, my fellow POTS blogger at With a Side of Salt alerted me to her post about airplane travel with POTS. … Read More ›
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 ›
I’m about a week late celebrating International ME/CFS Awareness Day, but this is a great post nonetheless so I wanted to share! Linds
*** 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 ›