Julie, CRPS Onset at 13

My onset began when I was 13 years old, but I wasn’t officially diagnosed until I was 15. Over time, my condition progressed into systemic CRPS, affecting multiple areas of my body.

Alongside CRPS, I live with several other complex health conditions, including Ehlers-Danlos syndrome (hypermobile type), POTS, hypothyroidism, hyperparathyroidism, cervical instability, scoliosis, and more. I currently have a DRG implant.

I wrote a book and built a website to share resources and information. Everything is free, with the hope that it can support others navigating chronic pain.

Julie’s Resources:

Julie has generously shared her website and book, which are available for free:
https://68646c0152c04.site123.me/

Previous
Previous

Terri, Living with Chronic Migraines & CRPS Advocate

Next
Next

Pain News Network