I'm glad that even though I've not helped anyone here (yet, perhaps), my thread has started a number of people writing about their experiences with hyperparathyroidism.

A very strange thing happened to me last Nov. on 3 consecutive days, a Monday, Tuesday and Wednesday. I had to go to the ER on the Monday and the Wednesday due to this mysterious medical thing that hit me. On each of those 3 consecutive days I, out-of-the-blue, would *suddenly* be extremely nauseous which never led to vomiting. These bizarre "spells of incredible nausea" would only last under a minute or maybe as long as minute, then end. This happened about 4 or 5 times on each of those 3 days. Another very strange aspect about this: immediately after each "nausea spell" ended, I couldn't recall the simplest of things I otherwise always know. These are basic things in my life such as where I have something stored, etc., etc. On the Wednesday, when I drove home from the ER, I couldn't figure out how to get the powered garage door open to park under my apartment building. I sat there, at night, in the car for some seconds before I happened to look up to the car's right side sun visor where I saw an object. I grabbed it, pushed the button on it, and the garage door went up. Other things I suddenly forget in those 3 days of "spells of the worst possible nausea" took many hours to I think a few days to come back to me. Now when I was in the ER on that Monday and Wednesday I never thought to mention my hyperparathyroidism but even though this ER place has all my medical records, the young MDs I'm always made to see (since it's a teaching hospital which I dislike so much) no young MD could explain why I suddenly would become SO nauseous for such a short "spell" repeated a number of times each of those 3 consecutive days.

After leaving the ER on that Wednesday I thought the nausea might have been caused by a terrible abdominal surgical outcome I had 10 years ago. For bilateral hernia repairs (only the LEFT groin was painful- the RIGHT groin one was painless but found by an eminent radiologist I had to consult in a distant state-- he's famous for finding hernias that other MDs fail to diagnose and he did find both of mine when my local MDs just couldn't properly detect the very painful LEFT side one), I was blown up as if I was a balloon. This inflation of my ab directly caused my linea alba to be wrecked. Every one on Earth has a key linea alba which runs down the midline of the ab, running from the end of the sternum to the center of the pubic bone. When it reaches the belly button, it splits to go around it but hugs the belly button snugly. The linea alba keeps LEFT side ab muscles tied nicely to the RIGHT side ab muscles with both sides meeting on the key linea alba which I figure is Latin for 'white line' since in anatomical illustrations it's shown as a whitish, ligament or tendon-like band. When the linea alba's wrecked, the permanent medical problem is called diastasis recti which often occurs in women due to pregnancy. Years after this happened to me I read on the Internet that men who have abdominal surgery can wind up with ugly diastasis recti. Nothing can be done for this. I'm forced to wear an ab binder which is a rather wide band running around me-- I reduced the width of mine and my former MD said I'm at the limit for the reduction of the ab binder. Anyway, I thought that the ab binder had stretched out, something I couldn't detect. But I tightened it up after that Wednesday and never had that horrible nausea again. Therefore, I suppose that those 3 consecutive days of unbelievable nausea might have been due to a stretched out ab binder and not to my hyperparathyroidism. I'll have to tell this though to a parathyroid surgery to see what that MD thinks about those 3 days last November. [But in the ER those 2 days I also never mentioned the possibility of the ab binder become a bit too loose on me. You see this only occurred to me *AFTER* the last ER visit on that Wednesday.]

In Aug. 2021 I nearly died from what turned out to be a 99% blocked key LAD artery ("the widow maker") over the heart. Fortunately, I listened to the ER triage RN who told me to get to the ER which I did. Treponin and other parameters were studied in the ER and I was hospitalized at once. More testing soon done in the hospital and a single stent was put into my LAD and that's why I'm here today telling you about my hyperparathyroidism. I do wonder though if my LAD artery was so, SO close to becoming 100% clogged/blocked (causing death) due to unrecognized but existing hyperparathyroidism in me. My blood calcium scores have been awful for many, many years but no one was concerned about this 'til Dec. 2022 when an MD suspected I might have hyperparathyroidism and that Dec. 2022 suspicion led to proper testing. In US medicine, there's always way too much unacceptable neglect, indifference, blasé and non-chalant attitudes along with the incompetence and ignorance of one thing or another. Too many MDs see us as walking, talking meat. [I noticed in the online Norman Parathyroid Ctr form (to fill out for desiring to be a patient there) that there was a question on a stent having been put into one's body. This probably or must mean that hyperparathyroidism's connected to some heart troubles. Right?]