Yes This! I Was Absolutely Talking About Abled People Playing With Our Mobility Aids. If It It Yours

Yes this! I was absolutely talking about abled people playing with our mobility aids. If it it yours do what ever you want with it and have fun with it! We might as well make our lives a little more enjoyable

MOBILITY AIDS ARE NOT FUCKING TOYS GODDAMN IT. THEY ARE NOT HERE FOR YOU TO PLAY WITH!!!

Non caps: mobility aids are not fucking toys goddamn it. They are not here for you to play with!!!!

Had a group of teens laugh at and make fun of me for walking with my cane today. Wtf y’all wtf.

Is decency not a thing? Is kindness non existent? I am just a person and sure I use a mobility aid but goddamnit that doesn’t mean you cam/should laugh or make fun of me or any other disabled person for how they walk or behave and what not

I HATE cobbled streets with a passion OML my cane and crutches both struggle with them and keep slipping into cracks especially since it rained today

🎶 Tell me why

My body hates me so much

Tell me why

I’m in so much pain all the time

Tell me why

Everyone always says

Get well soon 🎶

(To the tune of I want it that way by the Backstreet boys)

Mobility Aids should be free.

Y’all, what’s the benefit of getting a hEDS diagnosis? Every Doc I’ve seen has brought up that I probably have it but none will actually evaluate me for it (based on the criteria to my understanding I definitely fit it) and I keep getting told there’s no point in actually getting the diagnosis so they don’t want to do the evaluation. They’ve offered genetic testing which is nice but that shits expensive and I know technically necessary for the diagnosis but if they won’t even do the in office evaluation what’s the point of it (I mean unless I have one of the other types)

Can I claim it for myself? I understand if not since I’m not formally diagnosed but I’m just curious.