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  1. After I was diagnosed with EDS, I started doing research and found this doctor, Dr Brad Tinkle who is supposed to be the Dr Grubb of EDS. He's written a few books about it, this being his newest & most up to date: http://www.amazon.com/gp/product/098257715X?ie=UTF8&force-full-site=1 I bought it and think its a wonderful book. I found I've had so many more EDS symptoms & complications that I knew. He breaks down each body system and how it can be affected by EDS and hypermobilty. It's a great reference to have when something goes wrong to take to your dr. It has a lot of practical tips for coping, too.
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