This petition was submitted during the 2015 to 2017 Parliament
Closed petition Ehler Danlos Syndrome NEEDS doctors knowledge! FUND IT!
Closed on
Ehlers Danlos Syndrome has different types, the common link between them is Pain. Most people affected by this illness aren't diagnosed until later on in their lives.It is mostly an invisible illness and can ruin your life completely. THERE IS NO CURE! Most doctors don't know what it is.#makeachange
I suffer from ehler danlos syndrome and life is hard at the best of times, when something goes wrong you would think a doctor to know at least a bit of background about it. NOT EDS! This is horrifying as so many people go undiagnosed and refused the help they need to manage it! Not all of us with EDS can make it to America for treatment so we need something set up to help people in the 🇬🇧. Every time a doctor says "i don't know what that is" it saddens me. Please help to change this😔
132 signatures
Petition progress
View all updates for this petition, with the most recent first.
-
Petition closed
-
Petition published
This petition can now be signed.
If this petition gets 10,000 signatures, government will respond to it.
If this petition gets 100,000 signatures, it will be considered for debate in Parliament.
This petition will stay open until 3 May 2017.