Hello everyone! Hoping everyone is staying safe and healthy! As many of you may know, I live with a chronic condition, Ehlers Danlos Syndrome, that caused my spine to become very unstable. Because of this instability we were left with no choice but to fuse my spine. I have no regrets on that front, but let me tell ya, there is a lot that they don’t tell you ahead of time. You have to become your own best advocate, and a lot of that is just knowing the right questions to ask.

Spinal Instability in EDS:    • Living with EDS: Spinal Instability  

My Diagnosis Story:    • Living with EDS: My Journey to Diagnosis  

My Jugular Stenting:    • Living with EDS: My Jugular Stent and...  

All About my Feeding Tube:    • Living with EDS: All about my feeding...  

What my Feeding Tube Looks Like/How it Works:    • What My Feeding Tube Looks Like and H...  

Chiari and Tethered Cord:    • Living with EDS: Chiari and Tethered ...  

POTS/ Dysautonomia:    • Living with EDS: POTS and Dysautonomi...  

My Embr Wave Heating/Cooling Bracelet: https://embrlabs.com/?utm_source=chri...
Where to find me:

My Instagram: @watercolor_me_impressed   / watercolor_me_impressed  

My Etsy Shop: https://www.etsy.com/shop/ChristinaPa...

My Teespring: https://teespring.com/stores/christin...

My Medical Facebook: https://www.facebook.com/LoveOnChrist...

My Personal Facebook:   / christina.doherty.315  

My Twitter: https://twitter.com/C_DohertyPaints?l...

My Email: [email protected]

My Silver Ring Splints:https://www.silverringsplint.com/