But really though. 🥴
I had to.
This is seriously the face we all make when we try to get help and answers for #longcovid, #mecfs, #dysautonomia, #potssyndrome, #mcas, #lymesdisease, #endometriosis, #multiplesclerosis, #fibromyalgia, #cysticfibrosis, #asthma, #ibs, #lupus, #sleepdisorders, pretty much any #womenshealth pains and issues, and the list goes on and on and on...almost as long as we’re waiting to have our #chronicpain and #invisibleillness recognized, understood and properly and accurately treated!
Like, “doc, the physical pain causes the anxiety and depression; wouldn’t it do the same for you if you literally had a seizure in your doctor’s office and they told you it’s because of anxiety and you just need to try yoga or rest more?!”
(And also masks (Covid!!), gloves and jackets all applicable because... #immunesystem probz makes your body a living popsicle 🥶.)