This week, an article was published on CNN discussing hypermobile EDS with the headline “This mysterious disease affects millions – why isn’t the medical profession paying more attention?” I was so glad to see this “rare” disease for once get the recognition and eye it deserves. It gives me hope that one-day medical professionals will recognize this condition sooner, genetic testing will be available, and treatment modalities will be developed.
I’ve hyperlinked the article for your reading here.
