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