@SkinnytuX@leo_leo_X When someone - such as yourself - behaves in a way which is expressly and aggressively transphobic, I respond with the assertion "trans rights are human rights" because it is a statement of fact.
Sometimes, this leads to productive discourse.
Sometimes, I am called a bot.
@sunsopeningband Well said. I noticed some #pwLC are admonishing you for this gently expressed observation and the ironic nature of their pushback is not lost on me.
ME/CFS and Long COVID share similar symptoms and biological abnormalities: road map to the literature https://t.co/2W2aaaLGCG
@endthetti Left a reply under this less than an hr ago, only to find it gone when I returned to attach an addendum of sorts. Nothing inflammatory or inappropriate was said but if someone happened to see and flag it for removal, please feel encouraged to reach out to me with your feedback.
@griminthenorth@areyoflight Oh. I now see there are conflicting guidelines.
This one encourages saying "disabled people" instead of "the disabled."
That said, even when posts must adhere to a character count, I think "people with disabilities" is top-tier terminology.
https://t.co/mp99K8Rj8D
@areyoflight "Advocates of person-first language believe that a person with disabilities is an individual first and shouldn’t be identified by their disability. Examples include “people with disabilities” instead of “disabled people." https://t.co/EAGrAShFfF
@endthetti It was my experience ('98-'00) that most everyone had AM and PM cleaning duties but "kitchen duty" could mean cooking/serving/washing/or... hrs spent within a walk-in freezer, wearing no gloves and slides because closed-toed or nonslip shoes = run plans.
Also: basket weaving.
@DiaryofaSickGrl Brain inflammation & a "type III hypersensitivity" which was triggering my immune system to attack my CNS on a near daily basis.
Being a foster adopt w/ no family history, my adoptive family quickly accepted the explanation that "anxiety can manifest physically."
@adamrocketblack @Finn000000000 @PlzSolveCFS I've been living with these afflictions for twenty-one years. I think you might be misunderstanding my point and I apologize for conveying it poorly.
@Finn000000000 @PlzSolveCFS Have you given up on the possibility that your condition could someday be treated and improved? Perhaps not cured entirely but what if you could someday experience brief periods of wellness? Would choosing to be active in those times make your illness less real?
@PunkyBrewstuh@dryostradamus@PlzSolveCFS I understand the point you are attempting to make but only a small percentage of people with epilepsy are photosensitive.
@dryostradamus@PlzSolveCFS Speaking only for myself, the inflammation (and many other symptoms) that I experience is not 24/7 for all 365 days each year. This does not change my diagnosis.
@YEP4Rights While I do recall a lighter hue of blue, these shades of green and pink appear identical to what was being issued at Cross Creek Manor in 1998/1999/2000 (presumably until closure). Supply chain contracts for #WWASP remain undisclosed, yet it seems someone's business is thriving.