so here is the latest development in my EDS journey: I am in several Ehlers Danlos groups on Facebook. And they gave me a few names of geneticists who are listed as pediatrics but also do see adult patients with EDS. So I called the one that was named multiple times to confirm that they still do this and they do and also take Medicaid. So I will give their name to my GP on wed. when I go for a medical checkup so they can refer me. #Amen #GodBless might finally be getting answers .
Just the tellings of life through the eyes of a 29 year old, Cajun Louisiana Native with Scoliosis, Kyphosis, EDS(Ehlers Danlos Syndrome), and other medical issues, just trying to get by. :)
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