Smarterthnavg
Greenlighter
- Joined
- Jul 16, 2012
- Messages
- 1
I am a female who is dx with Ehlers Danlos Syndrome Type Hypermobility. Ive been in pain management for yrs and yrs and lookin for suggestions help info or other sufferers with EDS. Im obviously on some decent meds but need sporaditic tune ups. EDS is a genetic cond. in which my body produces faulty collagen and/or insufficient collagen/tenascin. I will never get better but dont mean i dont deserve to feel better. so anyone with suggestions to go wit a medicinal regiman would be f-in great!!!!!

