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.
I'm not sure it would work for classical EDS sufferers as it might cause more damage than benefit, but maybe for hypermobile sufferers...
My main issue is balance and the feeling like the lower half of my legs are wooden. 
University
Has anyone been to a residential pain management course? If so what was your experience.
EDS or HMS
Vitamin Deficiency/ Pernicious Anaemia : How Common Are They With EDS and What's The Best Treatment for Us ? Please Tell Me Your Experience 
