

With exchanging on dingus@lemmy.world’s post, already covered that enough, I remember I read somewhere maybe here that people living with Tourette’s syndrome are saying the challenge should not identified to them, but to the world that is not adjusted yet to their living with Tourette’s syndrome. I am of two-minds really of this, dislike labels & having to use them (there is a famous & what 30-years old Alternative Music/Hard Rock song all about this) as having labels applied to me in at least a negative way (as who has not), because of the challenges. Plus I strongly agree that the worlds we all exist in are still moving way, way & way too slow to treat/respect/not use to manipulate people living with challenges/differences. With that being said I not believing it is just the outside of the person, with the challenges (reason I did not use people is because not all are not the problem as well; believing is disrespectful of full group they are, for lack of better words), that created the problem, it is also the challenge they live with. Not to say I want everyone the same mind functioning & quality, sure many readers with Tourette’s syndrome who reply with that argument against, but until someone has figured-out how to live in the world with a challenge (& yes, the world has changed enough) it is also causing the person with a challenge problems. I do not know, maybe I would change my mind on this in the future; after all, the next door neighbor’s roosters (50-ft. or more away from both free bedrooms’ & 30-ft. or more away from living-room’s hurricane widows) calls are limiting me under 6-Hrs. of uninterrupted sleep, every single night they are not wet or scared to make their calls to other neighbors’ roosters.

I already posted that very point myself, in a previous reply here. That is not my point at all, I am talking about the Tourette’s Syndrome challenge, not the challenge coming from experiences with the Tourette’s Syndrome challenge.
AGAIN, my whole point to this thread was about Tourette’s Syndrome, which is NOT a Mental Health issue, thus referring to there is insulting to people challenged with living with it & thus probably (because since not doing it, not 100%) a huge waste of time going to that feed. I am going to go to a organization for people with Tourette’s Syndrome & get the answer there. A better source, any ways, less Internet message boards-social media effects on information given.
I hope so, but does not address the question I have for people living with Tourette’s Syndrome or even Docs. that are experts in the field.
If you are saying there might be some small amount of people living with Tourette’s Syndrome or even Docs. that are experts in the field, the first been less likely & last being pretty rare (from my experiences here). Then I might as well skip coming for the answer here, go to more excusive website for the answer.