#cveds

I've recently started looking into EDS again, refresh my memory of the disorder and its types, and as I'm going through the types I'm certain I have a few of the rarer types. I'm likely 1 in a few million. So yeah I'd say I'm bound to be the worst they've seen, some too scared to actually help me bc they fear making things worse and I get it, but it leads to medical gaslighting and conjures my cptsd from medical maltreatment. I've had great doctors too, but even they have said they can only do so much.

Really makes me feel like a shepherd sometimes, I can recognize small symptom patterns and lead those with less severe cases to getting a proper diagnosis and can recommend treatment from experience, I can provide an understanding ear to listen to struggles, trials and tribulations, of having EDS.