Holy Heatwave, Batman! We have been having an unprecedented heatwave here in southern California. Certainly this time of year, temperatures are expected to rise – … Read More ›
Tag: myalgic encephalomyelitis
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 ›
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 ›
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 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 ›
*** 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 ›
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 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 ›