Doctors really need to stop saying things like “Sick people itch” my goodness. I had my tonsils out and so did my ex’s son because they were essentially collecting strep throat and every time I’d start getting better I’d get it again. He was asymptomatic lucky him, but was a carrier reinfecting people wherever he went. That and being told “it’s all in your head” or “you must be making yourself sick” when they don’t know what else to test for or how to resolve symptoms are probably on the top 10 playlists of inane things really smart people say but should not.

If you haven’t yet, you might want to look into mast cell disorders. There are several types, and itching is part of all of them as can be other symptoms, and some people with mast cell disorders have other comorbid immune issues/deficiencies or genetic mutations causing them symptoms some have had their whole lives and just accepted as their norm priori to diagnosis. I had daily i hives most of my life. Dermagraphia, muscles becoming highly fatigued immediately after or during exercise, frequent migraines, often nausea or vomiiting after eating, cyclical IBS, exercise induced asthma, passing out during certain sports activities like mid flip in the pool, pain in my joints, skin, and deep in my bones, dislocations, feeling weak or fatigued, knees going out when i got excited, enough injuries just from doing normal kid things like climbing trees or trying to hang upside down, they threatened to report my mom for child abuse and told her she had munchausens by proxy, had been told when I went away to college that i had an eating disorder because my mom had been told i wasn’t allergic to the things she’d been avoiding giving me, because they didn’t show up as “true” IGE allergies, so she didn’t bother telling me I was or what she had been avoiding giving me, so I later ate things in the cafeteria not knowing they were triggers, would have an allergic reaction i did not recognize as one and puke in the trash can on my mad dash for a restroom, was told my GI pain was gastric reflux, and other things which turned out to be all explained by Primary MCAS, EDS and POTS as well as the preexisting diagnosis of Hashimotos thyroid disorder, sleep apnea and diabetes type 2 or 3.

I don’t list these off for people to feel sorry for me or what not, i have a wonderful productive and connected life. I mentioned them in case others are having similar symptoms and being blown off by doctors or told to just suck iit up, or “get used to it” as I was any time I or a loving relative sought answers. I went for 43 years without diagnosis just dealing with the symptoms because of doctors who didn’t know what to treat for so mistreated my mother or me. I had life threatening anaphylaxis multiple times and finally I refused to take the confused doctors as gods anymore and pursued answers until I got them in 2014 because i was having allergic reactions every time I ate, was exposed to the smell of hand sanitizer or certain foods being cooked, had gone into anaphylaxis when someone lovingly put essential lavendar oils on my pillow trying to help me sleep, and was in the ICU after almost needing a blood transfusion because I was passing blood after a “Perfect storm” of triggers one day. Where they kept almost killing me with hand sanitizer and various antibiotics i didn’t need, because they were just trying to help me and did not know how or why. Thankfully someone on facebook recognize my symptoms and told me to look in to Mastocytosis. Nurses at the mastocytosis society helped the doctors stabilize me enough to send me to mayo where ht why did I tests and decided i had some kind of mast cell disorder and helped stabilze me further, allowing me to fly to see a doctor who literally had hundreds of mast cell patients instead of a handful. (Sadly he has partially retired and stopped treating adult patients and is only focusing on pediatric) but thankfully i have doctors now who work together to keep me at my best health and give me advice on the tough questions like since I’m anaphylactic to flu vaccines should i risk the covid I vaccines or wait...etc.

Hope others find their answers no matter how bizarre or rare they are.

@lorirenee1 Thanks for the gentle introduction to the oddness of neuropathy. What is a "curable app"? I always see you as quietly interjecting or carefully reminding. Bring it on.......I can handle it.

May you be free of suffering and the causes of suffering.
Chris