Details
May is also Ehlers-Danlos Syndromes Awareness Month, which makes sharing this story feel even more meaningful to me. 💜
A year ago, I was fighting for answers while trying to hold onto pieces of myself that illness was slowly taking away.
Today, I’m incredibly honored to share my story with the Amyloidosis Foundation to help raise awareness for hereditary ATTR amyloidosis (hATTR-PN), Ehlers-Danlos Syndrome, and the reality of living with invisible illness.