Welsh Government is Starting to Pay for EDS Treatment
It has been difficult in many countries, including the US, to get insurance and government agencies to pay for Ehlers-Danlos Syndrome treatment. Many doctors do not understand this disorder and most do not know how to treat this condition. This is a story of a successful result of a public appeal for a teenager with this rare condition which causes her limbs to dislocate She is now starting specialist treatment.
Click picture for full article
We welcome comments and Likes regarding this story
Loading ...
