This is the third year I have posted this guide for people with chronic illnesses and their loved ones. I wanted to share it again … Read More ›
Tag: POTS
I’d like to think I’m somewhat of an expert at doctor’s appointments. I rarely went to the doctor as a kid, so when I became … Read More ›
This post isn’t about catching a few extra zzzzzzz’s in the morning before it’s time to wake up. In fact, the only alarms I use … Read More ›
Gentlemen, this is another one of those posts you may want to skip. Although, like my other “female issue” posts, I promise to include some … Read More ›
Everyone loves babies, right? They’re cute and cuddly and they have that oddly appealing baby smell (not to be confused with the completely revolting dirty … Read More ›
Today I’m very excited to bring you a guest post from Caroline at The Little Things Blog. You may remember that Caroline allowed me to … Read More ›
October is Dysautonomia Awareness Month! To commemorate the occasion, Dysautonomia International is co-hosting a free webinar in conjunction with the Ehlers-Danlos National Foundation. The webinar … Read More ›
I’m a self proclaimed nerd. If you’ve been reading this blog long enough this may not come as a surprise, although I may have fooled … Read More ›
I’ve had an interesting week. It’s been a week of firsts. If you’ve been following this blog you know I’m in the process of weening … Read More ›
Every year I try to write a post for Invisible Illness Week and – guess what week it is??! To learn more about Invisible Illness … Read More ›