Couldn’t fit it all in the title, but he receives steroids and immunotherapies including an antibody treatment.

It also confirms that he got the virus that triggers his CFS from Hope Hicks about half way though.

  • Mrtryfe [none/use name]
    ·
    4 years ago

    What's the deal with Hope Hicks? Is she just there for Donald's viewing pleasure?

  • lvysaur [he/him]
    ·
    4 years ago

    Do you have CFS OP? I've been dealing with the aftereffects since march. fuck the medical system

    • lol [he/him]
      hexagon
      ·
      edit-2
      4 years ago

      I don’t have CFS, but I do have a bunch of autoimmune issues that took years to properly diagnose. I can definitely emphasise when you say fuck the medical system. I didn’t get onto some decent immunotherapies (plasma exchange) until about 5 years after I first had symptoms, and by then I had a lot of progression and irreversible damage.

      My main advice would be to consider your doctors as disposable (switch to someone else if your current one isn’t working out, assuming that you’re able to do this), keep level headed as possible during appointments, and make sure you explain how your symptoms are affecting your day-to-day life (i.e it’s not just a minor inconvenience for you, it actually hampers you from doing X, Y, Z).

      Finally (and I know this is verging on class-reductionism) remember that most doctors don’t really care about you and are mostly concerned about their side consulting gigs or practice fees, so if you think they’re kind of doing the bare-minimum to just get you out the door, then push them to do more in the most diplomatic way as you can.

      • lvysaur [he/him]
        ·
        edit-2
        4 years ago

        Thanks for the advice. Were your autoimmune issues preceded by some sort of viral or bacterial event?

        Many people with CFS and ME develop it after a virus. Including COVID long haul obviously. I'm trying to put the pieces together between CFS, ME and COVIDLH