I had an appointment with my cardiologist yesterday to discuss the bradycardia I had been experiencing. However, it takes about 6 weeks to get an … Read More ›
I’ve been tai chi’ing like a grandma. Wait…..let me back up. As you may remember from a post earlier this year, my goal for 2013 … Read More ›
It’s no secret I don’t like being on medication. I’m still skeptical about the long term effects of putting chemicals in my body. And while … Read More ›
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 ›
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