Battling Invisible Illness

One of the main reasons for a. starting this page, and b. changing my diet, was because, since 2014, I’ve been battling invisible illness. I was undiagnosed and made to feel like my symptoms were all in my head for a long time until I finally got some answers in early 2016 when I was diagnosed with Posturals Orthostatic Tachycardia Syndrome (POTS) and Ehlers-Danlos Syndrome- Hypermobile Type (EDS3) and started being investigated for a potential CSF (Brain Fluid) Leak. For a long time I feared telling people I was really sick, especially when I didn’t know what was wrong with me but this is my space to share how my illnesses affect me and spread a little awareness for my pretty rare and little known conditions.