A lot of people mentioning faking hEDS here.
I was told by a GP that I would not be happy until my daughters were ill.
My daughters (both adults) would ask me to attend their GP appointments out of frustration as they thought they weren't being taken seriously.
They were diagnosed at University College Hospital in London a couple of years ago. They were 23 yrs and 25 yrs of age. One has hEDS and the other Classical EDS.
Since their diagnosis, I was diagnosed at the grand old age of 53 yrs - hEDS.
We were all previously diagnosed (incorrectly - from the consultant's mouth) - fibromyalgia.
We all have some form of autonomic dysfunction as a result of the Ehlers type condition.
My 'fantastic' GPs have always hoodwinked me into believing that my aches, pains, dislocations, dizziness, slow wound healing were due to hypothyroidism.
Good job I found a brilliant endocrinologist who pointed us in the right direction and we finally got a correct diagnosis because my 'fantastic' GP had ME questioning my own sanity. He was implying that I had projected my own health difficulties onto my daughters when in fact they had inherited my undiagnosed condition.
My daughters both have much worse problems with their conditions than I ever suffered.
Lots of medical people on here relating tales of how common mental health issues are with regards to people faking illness when there's many more suffering as a result of misdiagnosis by people who are well paid to do their jobs competently.