#ehlers danlos doesnt effect me TOO bad. like im sweaty and oily and hairy and i dont have much cartilage in my nose.

[panuccispizza]

I'm like. yea whatever cool to know abt learning about autism comorbidities for myself. like it just makes sense. then I realize my dad has these symptoms too and I start crying

#ehlers danlos doesnt effect me TOO bad. like im sweaty and oily and hairy and i dont have much cartilage in my nose. #at worst its in my knee and the cold weather makes my knee hurt a LOT like it gets stiff #then i think about in 2020 when my dad couldnt wear a mask properly or at all bc he has like the most minimum amount of cartilage #like his ears are basically soft rubber. they just kept flying off his face like they really did not stay on at all #not to mention like the other things. i do not believe he masks but i do believe he copes with living thru drugs and alcohol #like he doesnt have stims or echolalia (i don't either really though) but he smokes a lot. and mood. bc dealing with the world is hard #ive always thought he didnt understand living in the modern day but looking at it differently i think its that he doesnt get social cues #that well. a little more similar to agoraphobia since he gets along with his choice of people #but not anyone or anything else outside of his choice in people #and my brother is severely the most neurotypical person in the family aside from his adhd but hes on meds so.