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Hello and Welcome. As someone who suffers from HMS (Hypermobility Syndrome) or EDS type III (Ehlers Danlos Syndrome)
I found that getting information was difficult and frustrating. I have put together infromation from various sources to give
friends, family and those who have been diagnosed some tools for a better understanding of what this HMS/EDS is and how it
works.
I hope that this site gives everyone a little insight into what a complicated thing this is and lend support to those
of us who "don't look sick" but suffer on a daily basis.
Thank you for caring!
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