The title of this post is a long overdue follow up to my post, a dysautonomiac walks into a gym. In the near future, I … Read More ›
I’m going to tell you a story about the woman in this photo. This was taken a little over six years ago. She … Read More ›
Standing Up to POTS (an organization for which I serve on the Board) is partnering with counselors and suicide prevention specialists to tackle the issue … Read More ›
I expect this post will be wildly unpopular, but I am going to say it anyway. Stop comparing every illness to cancer. The day I … Read More ›
Hi friends, I’d like to tell you that the title for this post is some deep metaphor for the wisdom I’m about to bestow, but … Read More ›
Hi friends! In my previous post about the POTS/MCAD/EDS conference I went to in December, I promised I would let you know as soon as … Read More ›
I was really hoping to get this out to you all before the end of 2016, but I’m 23 hours late. I hope you’ll all … Read More ›
One year ago today, my life changed. This handsome fella came into my life: Today is Fletcher’s one year adoption anniversary. I first came across … Read More ›
Every year I post this guide to the holidays for loved ones of the chronically ill. Friends, I’d love to hear your suggestions/challenges for the … Read More ›
Great post about autoimmune diseases (which may include POTS) from my blogging friend. Check it out: autoimmune disease is a major health issue Why aren’t more … Read More ›