Also often since its rare people don't know...my mom has it and did not realize until my diagnosis. Both of my daughters have it as well.
Thanks for that bit of info, I was not aware of that...good to know.Something to look into further when we get to see the geneticist, I am sure they can answer this question.
I wanted to add that I was doing some research, and although very rare, eds, at least the vascular type has been known to spontaneously mutate and have no genetic relatives that had the disease. I read a study on a 15 year old boy who had this..
I may be wrong on this, but I think you can carry the mutated gene but not actually have EDS, so its very possible that nobody in your family has it or has symptoms and you can still have it.
Hi and welcome to the EDS group.
Yes, it is highly possible that u have more symptoms and issues then others in ur family....not all with it have the same issues.
I never realized how flexible I was until I was dx with EDS at age 48....my sister's always seemed to be very flexible, I never attempted to move like that as the thought of doing it hurt...lol....I know it is possible to have this condition and not know it or be aware...so, do get seen by a good rheumatoid Dr that knows EDS.