Was speaking to my Mum today about artificial limbs and she said "can't you have all your tendons replaced with these new spider silk ones?" You can imagine my face as I burst out laughing. However, I then googled it and she's right....here's the article, sounds as though this could be helpful with EDS people.
Another Rheumatologist Dissapointment
Diagnosed with Joint Hypermobility Syndrome but I’m not sure.
Has anyone been to a residential pain management course? If so what was your experience.
Should I go to the doctors with these symptoms 
