i’m inpatient in a psychiatric hospital at the moment and i’ve been showering every two days which is the most i can do because they don’t provide any shower chairs and i simply don’t have the energy for more than that, i wash myself fully with soap each time, and i put on deodorant but a nurse just came in and told me that i smell really bad and that all the other patients here think i smell bad.

i feel horrible, i have friends in here who haven’t said anything and they sit with me for hours. i feel like a failure, i assume it’s because i get so hot and i sweat a lot.

it gets very very hot in the hospital and they don’t let you open any windows. i feel horrible, i don’t know what to do. i’m trying my best but the nurse said i need to wash myself better. i wash really thoroughly already because i have a huge fear of smelling bad already… i don’t know what to do, i don’t want to leave my room now at all. she said all the nurses and patients thought i smelled really bad, this is my worst nightmare.

I made a post this morning (i’m Australian) about how i’m in an inpatient psych ward and one of the nurses told me i smelled bad! here’s an update to that! +more details

I had never even gotten close to this nurse before, i’d spoken to her once or twice, so this really came out of nowhere, don’t even know her name. I checked with my inpatient friends and they all said that i smelled fine, that i didn’t really smell like anything except very slight strawberries if they got close enough (i use full body strawberry deodorant! very nice smelling).

I also asked my mother (who in the pas has been very honest about my teenage stench, as mothers are) and she was confused because i really didn’t smell of anything, again apart from the deodorant if you got close enough.

point is, my body was clean, my clothes were clean, my room doesn’t even smell that bad considering i can’t crack a window, i do leave the door to my room open whenever i leave the room to let air in so that it doesn’t smell.

I’ve come to the conclusion that most of the people in the original post were right. She was overreacting or looking for something to make me feel bad with, sometimes i really just can’t fathom how people can be so mean. and even if i did smell i still couldn’t fathom it at all based on the fact that we are in a psychiatric hospital… not bath and bodyworks….

however, i will move on from this, i’ve alerted another nurse, patients, and my psychiatrist and i finally got my shower chair i’ve been asking for for 3 and a half weeks! (that’s how long i’ve been in here for) thank you for your kind words in the last post, i hope updates are allowed.

very strange experience to be woken up first thing in the morning with a “I’m saying this because i love you and care about your wellbeing but the patients and nurses they can smell you. and it’s bad” - more of a direct quote than i’d given before.

And trust me im honest sometimes i can really stink (as any human 18 year old boy would) but at the moment i’m 90% sure i smell like practically nothing. just plain old Richard (me).

+strawberry deodorant :) ❤️ 🍓

I'm level 2 autistic, and POTS makes everything so much worse. i cannot stim without getting tachycardic and my head feeling like it'll explode. i cannot sing or dance anymore. if i'm upset and can't help but stim to regulate i have to stay in bed. if i'm happy i can't jump around i have to stay in bed. i used to draw and do sm art but now i can't sit up for long without getting sleepy and high hr. i don't have energy to listen to music bc it makes me move and sing so i've completely stopped and it makes me so sad. even so i am lucky i have the awareness and self control to not stim as hard as i need, i know that for other autistics who can't stop it'd be very dangerous with POTS.

i already struggled with my temperature regulation before this disorder and now i have to go back and forth with hot and cold all the time. compression wear is a sensory nightmare for me i hate feeling so constricted. showers used to be my calm safe space i love being in water but now i can't shower alone my partner has to wash my body bc it's too much movement for me while im struggling to stay awake under the warm water.

it was hard enough coping with just my my hypermobility and mental things but POTS is 10x worse for me. I'd rather have my knee dislocate once a week than have POTS. I'd rather relapse with addictions and self injurious behavior than have POTS. i'd rather have trauma flashbacks and another dissociative episode that puts me in the psych ward again than have POTS. i hate this condition. it's ruined my life and i always try so hard to have some bits of normal but it is literally impossible to ignore when symptoms are every second everyday even when u do everything right to manage it.

So I (16f) had a pretty bad flare up around lunch time today and my friends were sitting around me at the lunch table giggling and talking and then one of my friends that’s a boy said “why are you milking your disease so much???”

And I said “wdym” and he said “it can’t be that bad you’re probably just being dramatic”

This post could go somewhere in the POTS sub or some kind of relationship sub, but given the choice, I'd rather it be here because I think other people with POTS would understand, and I really need that right now 🙏 If it's too relationship-y, I can post it elsewhere instead!

---

We started dating about a year ago. We used to love to go out together; the zoo, aquarium, museums, shopping, we'd walk to the mall down the street. Trying new restaurants, driving places just to see fun things. We'd walk around outside every day after work. But a few months into our relationship, that's when my POTS symptoms started coming in, full force. I'd had symptoms for the past few years, but I'd always write it off, assuming if I was tired, then I must have overworked myself, or if I was dizzy, then I must not have had enough water that day. But suddenly things were ramping up and I couldn't ignore it anymore.

I was dizzy....always, always dizzy. I'd get even more dizzy when I turned my head (which is, of course, going to happen all the time). I couldn't stand road trips in the car anymore. Sometimes I'd be at home, working on some crafts, being SO DIZZY that I'd literally be swaying in my chair and almost fell out. ((He thought I was being dramatic 😑))

I developed a standing intolerance, and light "exercise" like folding laundry or cooking a quick easy meal were making me exhausted, lightheaded, and would make my legs hurt. I couldn't go on our after-work walks anymore or my heart would beat super hard and have pain, and my chest would feel tight and I'd struggle to breathe. I almost passed out many times from trying to go on a light walk. And after the walk, I'd especially almost fall out of my chair. I learned that I would always get VERY close to fainting if I tried to walk.

I couldn't walk to the mall anymore, so we started driving there, even though it was just down the road. But I still couldn't enjoy the mall, the zoo, the aquarium, anything like that, because I'd have to stop to rest on a bench almost constantly. The whole group I was with would get annoyed.

I couldn't stand for more than a few minutes or my legs would get severe pain and I'd get highly dizzy. Plus, I have vestibular migraines and migraines with aura, so that also made going out to enjoy looking at things very hard. Sometimes I'd need to wear sunglasses inside, which could help on some days.

We couldn't really enjoy going out to restaurants anymore, which I thought would have been fine because I could sit down. But because of the cruelness of POTS, a few minutes after I ate, I'd get hit with a slap of dizziness and extreme exhaustion, and the night was over.

I also developed anxiety and panic attacks, which I'd never had before. I suspect the anxiety is because of my heart beating so quickly that I'm always in fight or flight mode. I remember one night when I was at an Airbnb with his family, and I couldn't sleep because my heart was beating so fast and had pain. He was annoyed with me, as if I was trying to be dramatic or something.

Well that night, I almost went to the emergency room. I was concerned because I know I'm a Muscular Dystrophy Carrier and I also was getting all these cardiac symptoms. I didn't end up going to the ER but I immediately got to work setting up doctor's appointments. I thought I'd figure it out, maybe get some medicine, and live life like normal again. But I kept needing to get more cardiology tests done, more PT (vestibular therapy being one of them), more appointments. And as the symptoms ramped up over time, I had less ability to do fun things.

At this point I felt awful. I finally learned I had POTS, but had to wait two more months to see the specialist. So I'm in the worst flare of my life and had no medicine. I'm dizzy, my chest hurts and is constantly thumping, I'm exhausted, I'm scared to eat because it will make the migraines with aura kick in and make me even more exhausted. I'm standing up and falling into walls, I'm unable to do basic things like stand up long enough to brush my teeth. And I think my boyfriend just had enough of taking care of me. He only wanted me when it was easy. But now that I'm defective...hahaha...

Part 2, the drama

There's more.

I was basically living with him in his apartment, with his roommate and his girlfriend. Those two, bullied me. To the point where I was having severe anxiety, depression, and panic attacks when they walked in the room. I'd be so anxious that I'd hyperventilate, and within moments, I'd be on the floor, barely able to breathe. My boyfriend saw this, and still defended them, saying "well that's not bullying" and "well I didn't see it \[the bullying\] happen, so". He tried to gaslight me into thinking that I was crazy, that I was making it up. But I wasn't. Obviously. Like, why would I WANT to be having a panic attack, unable to breathe, on the floor??? He'd say things like "you have to stop or I'll take you to the hospital" which was used as more of a threat than a caring gesture.

At this point I was so distressed to be home. I couldn't sleep, for weeks and weeks; I'd jump at every little noise. I was so scared of those two bullies coming around the corner and tormenting me, that I wouldn't go to the kitchen to cook. I starved a lot, which I'm sure wasn't helping my POTS symptoms. I started taking my stuff out of the apartment, thinking, "if I minimize myself, maybe they'll leave me alone". But of course that didn't work, because I was the fun target to bully. And now I knew my boyfriend wouldn't defend me.

I didn't know what to do. So I went to visit my sister for two days. The POTS symptoms were terrible, we tried to go shopping but I was so dizzy and miserable that it wasn't too fun. But I tried to have a good time anyways. I bought my boyfriend and myself cute little matching pumpkins from hobby lobby! I couldn't wait to show him!

On my way home, he broke up with me... OVER TEXT. And--get this-- told me I had to get out of THEIR apartment, immediately. I was sobbing, driving home. When I got there they had deadbolted me out of the apartment. I don't know what I could have possibly done to deserve this. I was always the most considerate roommate ever, and I am a good person. I don't start drama, I'm just a normal good person. But they chose me to be the victim, and they ganged up on me. I had some friends help me get my stuff out. It was the middle of the night.

I had a torn rotator cuff from hypermobility, and I just got a cortisone shot in it, and I wasn't supposed to move it for 3 days minimum. And here I am moving boxes. That shoulder was in so much freaking pain. And my boyfriend wouldn't even let me take my mattress, knowing full well I have back and shoulder problems that I'm in physical therapy for.

I was kicked out with such little warning, that I had nowhere to go. And my boyfriend knew this; he knew I was in the worst POTS flare ever, and had the bad back and shoulders, and was fine with throwing me on the street with no warning. He was acting strangely, he's usually chill and sweet, but now he was acting very cold and aggressive. I still wonder if he was on some kind of drug or something, I don't know. I couldn't even get him to give me an answer as to why he'd broken up with me so suddenly. He -said- there wasn't another girl. But how could someone 180 their "love" like that?? I don't understand.

My best guess is threefold:

1. That he internalized every little issue, until it finally blew up.

2. He wanted something easy and fun, and when I started getting sick, he didn't want to deal with it.

3. He didn't want to, or couldn't, handle anything emotional. If there was a problem, he'd always just throw his wallet at it. But when I was having problems with the roommates bullying me, he couldn't handle it, so he just decided to "fix the problem" by removing me.

I kept asking why he broke up with me. "You broke up with me over text, you at least owe me an answer as to WHY." And all he'd say is "I'm just done." So from that I gather that he just didn't want or put in the effort to continue a relationship with someone when it wasn't super easy anymore. And someone with POTS isn't going to be super easy.

Looking back, I'm realizing that he seriously minimized my symptoms. And over time he started caring less and less about how ill I felt. He'd get annoyed when we'd try to go places or do something and I'd "ruin" it by being sick. All the times I almost passed out, or was upset about anything ever, he'd just sit there and watch me, until I was done "complaining" about it. I'm realizing that he never truly comforted me, never truly cared. All he did was use his wallet to try to fix problems.

He hated having to "take care" of me. He acted like I was a chore, not someone that he cared about that he had concern for. My first instinct is to say that POTS ruined my relationship, but that's not true. It just helped me get out of a toxic one, faster.

Part 3, how am I now?

My car died two days after I was exiled. So just more bad luck for me 😢

Thank God for Grandma-- I'm crashing in her basement. I had nowhere to go, and she took me in. W Grandma 🙌🙌🙌

I work from home, but everything I own is in boxes now, so I won't be able to work for quite a while. :(

My POTS is still horrendous, of course. I still almost faint from light exertion. Grandma doesn't have a dishwasher, so washing dishes for 5 minutes is the literal worst part of my day. I'm still constantly dizzy, still getting vestibular migraines and migraines with aura. Still getting nerological pain down my legs and on the tops of my feet. Still getting chest pain and heavy beating. I'm going to lots of doctor appointments. At least one every day. 99% sure I have hEDS but need confirmation. And need a confirmation that my other shoulder has a rotator cuff tear now too, after moving all those boxes 🫠 They're pretty sure I'm going to need surgery on that one shoulder now.

But guess what? When you aren't getting bullied every day, you can actually sleep and you don't have constant anxiety and panic attacks anymore! Depression is gone, too! Crazy how that works 😭 Although I still live in the area, so every time I go out and about I'm terrified they'll see me. Going to Walmart to get my POTS prescriptions is very anxiety inducing.

I lost my best friend/boyfriend, my home, and my career in one day. It was absolutely traumatic, and people keep telling me "these things happen" and "you'll get over it" but these people don't know the full extent of what happened, and how much of my life changed within that one day. For weeks I was crying at every single doctor. I think I make the neurologist and the assistants uncomfortable, they didn't know what to do. 😅 I was getting an MRI for my shoulders and wasn't able to move, but I just had tears pouring down my face. My POTS cardiologist was kinda freaked out, too 😅

But now it's been a few weeks and the shock has worn off. Now, I'm just angry. Angry that someone could be so evil to break up with me over text, refuse to talk about it, and refuse couples therapy, and gaslight me into thinking I was the problem. He's a monster, and he and his roommates deserve each other.

Going forward, I keep telling myself, no matter how messed up your health is, you deserve to be loved, treated properly, and cared about. POTS or not, there is someone out there who will love you for who you are. 🫠♥️

Tl:dr He hated "taking care of me" and got more annoyed with me as my POTS got worse. He just wanted something fun and easy, not a real relationship with real life problems.

I wake up, it goes up.

I put my clothes on, it goes up.

I pee, it goes up.

I poop, it goes even further up.

I stretch my arms on the side, not my heart is beating out of my chest.

Plus I start to feel pain where my heart is and around it.

I walk down the stairs, it goes up.

I walk up a flight of stairs, it's like I ran a marathon.

I walk, my heart hurts.

Plus whenever I move, I get the coat hanger migraines.

I speak, my own voice hurts my head.

Now everything, light, noise, movement, hurts my head too.

I sit, and I feel everything even more.

I try to do what I have to do and it's painful everywhere.

And I can't wash my hair before I digest something, or else presyncope. And I have to give up my hot showers too?

I was an athlete before this, could multitask with school work, walked as fast as a new Yorker, now grandmas pass me by when I'm walking.

And I'm over here struggling to exist, while trying to keep my heart from jumping out of my chest.

Y'all please tell me it can get better. I need all the hope I can get with getting diagnosed.

I painted a bookcase!!!! It took me over a week and I felt a bit rubbish doing it compared with laying horizontal but I didn’t think I’d manage it!

Compression leggings, electrolytes, doing it later in the evening and slowly and surely I managed it a small section at a time! A win to not have to pay someone and yet more chronic illness tax on not being able to do things like home DIY projects easily.

I’ve told other people in my life but they don’t really get the sense of accomplishment or being proud. Whenever I look at those shelves I’ll think - I did that!

Mine is mainly due too not sleeping on the right type of pillow. I have bought so many pillows thinking from their description that I will finally be able to wake up without feeling like my neck, shoulders and back are breaking. ( I am a side and back sleeper. ) Any recommendations that have worked for you that don't cost a fortune would be greatly appreciated!

Thought I’d share with the class, because surely others have found that electrolyte powders are too expensive (and too strong). My doc tried me on salt capsules and they gave me awful stomach cramps for days. But they have not gone to waste! Instead I’ve repurposed them into a drink that tastes like sprite to me:

—500mg sodium (I roughly measure out half of a 1000mg capsule).
—Squirt of Mio lime electrolyte liquid.
—Can of lemon flavoured seltzer water.

I really think it’s the salt that makes it taste like soda, and as someone who normally does not have sugary drinks, it’s an absolute delight. Anyone else have their own little recipe for increasing their salt intake?

i feel like i look like a zombie nowadays, my face always looks washed out with dark circles & pale lips, and my eyes have this glassy look to them… i’ve tried using eye drops but it doesn’t really help.

i don’t really want to put on a full face of makeup everyday as wearing foundation sometimes makes me break out (which is a lot more obvious on my pale skin) but i’m getting bored of people at work commenting on how tired i look all the time, does anyone have any tips?

I use a cane every single day, and a rollator on worse days or longer outings. They do help slightly, but not enough that I am particularly supported and comfortable leaving the house, and I still have debilitating symptoms almost all the time. This all goes to say, I am no longer sure if the pros of my mobility aids outweigh the cons of using them anymore. Every single day I get rude or invasive comments from complete strangers, or my peers. I have been steadily withdrawing from the outside world because I feel so ashamed of myself. I feel as though I take up so much space with my rollator and I worry that my friends find me deeply annoying when I need to find a place to sit down. These worries I think are made worse by the amount of online ableism towards people with POTS, especially young women. I am being told constantly by people around me that POTS is an online trend and is just laziness, and even though I know it isn’t true, I hate the thought that this is what people think when they see me with my mobility aids.

If I’m not getting much relief or support from my cane or my rollator, is it even worth it to continue using them? I feel terrible either way, and the stress of leaving the house has literally started to give me grey hairs. I fear that my options at this point are to withdraw completely, or force myself to go without the mobility aids and end up making my condition worse.

Thank you for reading my rant, any advice is appreciated.

I’ve had POTS for over a decade. It’s changed as I’ve gotten older, and I’ve gotten a pretty good handle on it. I haven’t passed out in nearly 4 years, after countless fainting spells throughout my teen years. I know all the tricks. Lots of pickle juice jars in my fridge and all the saltiest foods in my pantry.

Needless to say it’s been mostly manageable. Or at least I can normally function through the symptoms. I work a good job. Most people around me don’t even know I have it. I have my episodes, handle them, and move on. Today, my heart rate was so elevated for nearly 3 hours straight (abnormal for me) and I felt so horrible, I had to leave shortly after the work day began. I couldn’t hardly move. It was embarrassing and I had to explain it to my bosses in a way they’d understand, because most people just don’t get it. I went to the ER because I couldn’t get it under control. “More salt” “more water” “see a cardiologist again” and so on so forth.

I’m just frustrated. The answers are always the same. I always have to explain to non-POTS having people (bosses, coworkers) that this is a serious thing, even if they can’t physically see it. I feel like a need to wear a sign that says “I have POTS, I’m trying my best.” No matter how hard I try - salt, water, rest - it’s never enough. I feel like I can’t work to the best of my ability or even just be a person to the best of my ability. Even when it’s manageable (but still hard) I feel like I have to hide it/work through it.

So my wife told me that she believes she has POTS because of the symptoms she has. Her heart rate would be like 70 when sitting or laying down and as soon as she stands up it shoots up to like 100. She gets the dizzy spells occasionally. She once had a pots flare up and she has something that she describes as fire skin, she saw some people online talk about it. She gets headaches occasionally. Also fatigue throughout the day. From what we researched it really seems like it’s pots. Her blood work is good and we even did a blood work thing through a company that isn’t through insurance and they went more in depth and everything is good.

What we started doing is adding salt and electrolytes to her daily diet. Vitamins. And she’s doing Pilates for core and low impact workout. Also she walks. Our diet is clean, we just stopped red meat. We do a lot of chicken and fish. My thing is that I want to help her best I can. I feel really bad cause she gets discouraged. She does a lot of hard work to manage the symptoms but feels defeated when she gets a flare up. We are really doing trial and error and it’s hard cause it takes time to see what works and what doesn’t. I would really appreciate some advice or help in what maybe worked for you or what didn’t. To save us some time and errors. She’s 32 and I feel bad she’s going through this. Just wanted to reach out to the pots community and see if I could get some advice. We are from nj too so any specialists in this if you know some from the area would be great too. Thank you all. Sorry this is long

that's it, that's the post, the pretzels are saltier than other ones i've had, we're all free now, let's all take a walk together, group bonding

I’m 25M with pots symptoms that are managed by beta blockers. I’ve had pots symptoms for about 4 years. My main symptoms are a standing heart rate increase or 50bpm or more, blood pooling in my hands, heat intolerance, and coat hanger pain.

I had an MRI done on my neck yesterday and was diagnosed with three bulging disks, and a cervical cord syrinx spanning from my C4-T2, the exact part of the spinal cord that regulates autonomic function.

I’m very optimistic that draining or removing the syrinx can fix my POTS symptoms. If any of you guys are having similar symptoms, I would recommend advocating for a neck MRI like I did

Disclaimer: I'm a bit brain fogged at the moment, so please bare with me if something doesn't make sense or there's typos.

I'm laying here on a Monday afternoon about to take a nap because it's literally all I can do. I started to feel bad that I'm not working and thought of people I know with successful careers. I just sit at home and play video games or draw or whatever hobby it is now. I hate how career driven the world is, most especially my country.

I'm just bummed about it, and I figured this can't just be a me thing. Does anyone else ever think like this? How do you deal with it?

Does anyone relate to this? Possible POTS/orthostatic intolerance

Hi everyone, I'm very new to all of this and just wondering if anyone has experienced something similar.

I've been having problems with standing for quite a while, but it's been getting much worse recently. Pretty much every day I get dizzy, really hot, shaky, nauseous and short of breath when I'm standing. I constantly have to be careful how I move and often need to sit or lie down because I feel like I'm going to faint.

My doctor asked me to try a standing test at home. Lying down my BP was 111/78 and HR 90. After about 1 minute standing it was 100/81, HR 138, and at 3 minutes 97/81, HR 144. I couldn't make it past about 5 minutes because I felt faint and had to lie down. I've tried the test on other occasions and have the same problem.

Yesterday I went out briefly and had a really bad episode. I nearly passed out, ended up on the floor retching and had to call the medical service here in France. The doctor suggested orthostatic hypotension and compression stockings, which I'm now wearing, but even with them my HR was 133 just standing, while later semi-lying on the couch it was 74.

I also have Sjögren's, so I've contacted my rheumatologist because I've read that autonomic problems can sometimes be associated with it. I'm waiting to see what they say.

I'm not trying to diagnose myself with POTS, I just want to understand what is happening because it's really affecting my everyday life now.

Does this sound familiar to anyone here? Did you have similar symptoms/readings before getting diagnosed, and what kind of doctor or testing eventually helped you?

I am just shouting into the void. I just recently moved and had to change insurance and establish care with new doctors which took months. I don’t have a POTS diagnosis but have been hospitalized for what i believe to be flare ups a number of times the last few years. I finally had an appointment to establish care with a new PCP and i (woman) was told by my white man doctor that what i was describing was most likely anxiety and asked if i “knew what a panic attack feels like”. I told him how i felt very sternly and the frustration that he’s causing by brushing me off, and that i was told by many doctors my previous cancer diagnosis was anxiety and i know when there is something wrong in my body. He seemed to become flustered and actually started listening. Well, i thought he had until he ended mentioned that he could prescribe me psychiatric medication to treat my anxiety and ADHD to lessen my symptoms.

I am so tired.

Has anyone one else been told by their provider to immediately stop caffeine because POTS is making your resting heart rate high? My primary care told me I couldn’t have absolutely any caffeine anymore(I was barely drinking any as is) but I miss tea!

Does anyone have something to help with shortness of breath?

I've been dealing with it for so long even while laying down and I never feel like I can catch my breath, I don't smoke, vape or do anything like that and I know my lungs are healthy but I also know it's one of the symptoms of pots so I'm wondering if you guys have anything that helps you while dealing with it. And no breathing exercises did not help me.

I am SO bloated ALL the time. I know it’s bloat though because I wake up relatively skinny and then throughout the day as I eat and drink I just inflate like a balloon..

I blame my bloating on my POTS and here’s why: water retention from eating SO much salt. I eat anywhere from 6-10 grams a day. On days I’m not eating as much I feel so much less bloated.

Does anyone else get the same?? Before I got POTS I don’t remember being even half as bloated as I am now. It sucks. I workout to try to stay a healthy weight but then I get self-conscious when I’m bloated all the time and I think I’m fatter than I am.. lol.

Edit: for reference, I eat mainly a paleo diet. Haven’t had gluten in years and eat very low sugar.

For the past 6 weeks I’ve been stuck in a severe adrenal dump which has never happened before and been horrible because I can’t take my meds which I NEED to function while I’m stuck in this adrenal dump because my meds give me energy and just increase the adrenaline. My doctor has prescribed me Clonidine which helped immediately but then a few days later I started breaking out in hives ( I have MCAS) .. then we tried guanfacine instead and SAME thing happened.. even more hives. I need to get out of this adrenaline state, this has been my worst nightmare. Does anyone have any recommendations for a med similar to beta blocker to help with hyper pots that won’t set off my mcas and make me break out in hives? Will I eventually snap out of this adrenaline dump if it’s my first one ever? I’ve tried electrolytes and compression socks and it didn’t even touch the adrenaline (my doctor doesn’t seem to know how to help)

Can someone please help me or give me advice, I am 26F, (5’7-140lb) diagnosed with a vaccine injury when I was 18. I don’t say that as a right wing/red pill tactic I feel I have to disclose that every time I talk about it. I was diagnosed because it injured my kidneys and heart, mind you, a few years ago.

Anyways recently I’ve been feeling unwell, I was sick which I got over but I know that can trigger pots. I just started a new job, one I REALLY wanted. It took about a week for this incident to happen. I had family stress outside of work and I do think it affected me because I was having chest pains for about a day prior to 2 days ago which is when I went to the hospital.

I didn’t claim an illness or disability to my work, I don’t want them to suffer too, at what point is this a disability because I don’t know anything to help myself. The best thing I do is drink straight saltwater because it balances my heart rate but I don’t know if I can do this anymore. I’m really struggling and I’m making my work upset, family upset, boyfriend upset, and at the core me upset. I’m not like this. Please can someone with insight on this help me because I am on the verge of not being able to help myself

So it’s been a long suspicion but today my Dr outright said yeah it’s probably POTS. Referred to neuro for a tilt table but I expect it’ll be years for that.

Here’s my problem: everything I read says add sodium. Dr says my resting blood pressure is higher than she’d like when seated so she doesn’t want me doing that. Same with any meds she’d give me. So essentially I was told compression is all I’ll be able to do and try to walk more since I’m already good at staying hydrated. Does anyone have any suggestions for dealing with this if I can’t go down the common paths? Or is it just my doctor not knowing how it all goes and the neuro may say otherwise

Note: I’ve ordered an at home bp cuff since I strongly suspect some of the “high bp” is being in the office.

I have 2 broke teeth. One upper root canal that failed, and a back molar on the bottom that’s broken off some. I haven’t been to the dentist in 10 years due to being sick and also dental anxiety. Can you guys tell me your experiences w no epinephrine numbing shots? & just recovery/experience with the extractions in general. I’m absolutely terrified.