Feeling dizzy? More former COVID patients are being diagnosed with POTS. Here's what you need to kno

[@KelseyJacobson-zn3mw]

They ALWAYS blame it on anxiety!!!! This medical gas lighting is ridiculous!!!!!

[@no_country_for_real_men]

Yes medical degreed people are cowards wilfully dismissing patient concerns, signs and symptoms. Getting paid to do LITERALLY nothing

[@KelseyJacobson-zn3mw]

@no_country_for_real_men Why do you think many engineering students drop out and switch to medicine? They are dumb!

[@Zayday1993]

Watch a video on KZbin called covid survivors explain dysautonomia and listen to what they say regarding this comment

[@aminah761]

Yessssss

[@RockTheBoat404]

Doctors will even tell people who have cancer that their symptoms are "just stress" or anxiety and then they discover they have a tumor

[@gathercreatelivewithleslie8340]

We need doctors to actually listen to their patients. People have lost faith in doctors and the media.

[@VivaLasVegasX]

Eastern medicine is the only way to go. Western medicine are a bunch drug dealers and butchers

[@leos3003]

Yes and what is the next natural step when people loose any use for something???

[@MA-yl1er]

Because they are corrupt.

[@gme5802]

Doctors that listen to a patient. Yeah, right. Ain’t gonna happen. Doctors are only in it for the money not patient care.

[@lonebikeroftheapocalypse9527]

I've been misdiagnosed enough times to doubt every quack in a smock.

[@karenk9119]

I believe each and every one of my patients. Doctors that ignore or disbelieve their patients' complaints are trying to hide their incompetence and lack of clinical insight.

[@AldousHuxley7]

Insight yes. What else could be a factor here?

[@no_country_for_real_men]

one thing they are not hiding is how lazy they are. Getting paid to do LITERALLY nothing

[@RD9_Designs]

They ignore, or they gaslight! I've been gaslighted so many times through the span of several years when no doctor could figure out what it was making me hurt so bad! And because they had no clue, they told me it was all in my head! God finally hooked me up with the smartest man I ever knew... He had 8 doctorates and was board certified in 5 of them! That means he was 8 times the doctor as any onee of those who told me it was all in my head! He had planned to go back for a mathematical doctorate when I was going to him, but he was 67 years old, stooped over with back pain and had a lot of trouble walking, and a fire broke out at his house. His lungs were badly damaged. He was recovering for the better part of 2 years. He lost his clinic and all his employees but his head nurse, who, oddly enough, came to work in my office as a nurse recruiter. I went right back to that doctor when he began seeing patients again in one of the rooms of a skin care clinic that was run by a younger doctor whom he mentored (for greater work than skin care). My doctor only lasted about 6 months before he died of complications of smoke inhalation. But not before giving me, and my daughter our final diagnoses... he knew when he first met me that I had fibromyalgia and chronic fatigue syndrome, and through the years I had him, he ruled out all the diseases that I could have had but one, so, by process of elimination, his diagnosis was psoriatic arthritis. I immediately went to a rheumatologist, but she couldn't find any inflammation markers in my blood... but 5 years later, there it was! My daughter had hypothyroidism, but the pills weren't helping her, and she felt like crap, too! She was seeing the best children's endocrinologist, but he had no further answers, and was planning on doing a thyroidectomy on her. Thank God I took her to my dr, who diagnosed her almost immediately with Hashimos disease, another autoimmune disease, and if her endocrinologist had cut out her thyroid, the disease would have attacked other things in her body! With Hashimotos, she needs more than just her TSH (Thyroid Stimulating Hormone) checked, she needs something else checked too... She has always taken care of it herself, being an adult when Hashimtos was diagnosed. Today, she tells drs what tests to run, and what the results mean, and how to treat her. The really sad thing is that most doctors think that my doctor was a crazy, trying to help people with supplements, when he was the nicest, smartest man who was head and shoulders above all of them! But he's not the only super smart and nice dr God has gotten me to.... There have been 4! 2 have died, and I'm worried about my wonderful internist GP, but my pain specialist, who I think has his PhD in palliative care, is the only one I've ever met that never treated alll of his patients like junkies just because some were, he just got rid of them and continued to be a nice, compassionate man who wants to believe the best of us, but still has us pee in cups, just in case! I have never broken my contract with him and never will!

[@AtTheBarn]

Computers have really created this in doctors. Insurance companies pay for the design of the medical software used today. If doctors and health systems want access to insurance money they use the programs. If the doctors and health systems want protection from litigation they use the software. The patient left the practice two decades ago and Obama Care implemented this take over by giving insurance companies total power over the cash flow of the medical industry. Notice how the doctors trying to operate outside the insurance system disappeared after Obama Care? The Insurance lawfare lawyers shutdown or "scared straight any Doctor fighting back. Remember the Doctor's speaking out during Covid and what happened to them!!!

[@no_country_for_real_men]

@@AtTheBarn I think there's some truth to that because Obama use to be a lawyer for the insurance industry and he is the one that signed the Tort reform bill which essentially blocks patients from suing doctors for malpractice and people with medical degrees have been murdering people and getting away with it ever since and the insurance companies love it

[@becaSidekick]

Is it from getting covid or from the covid shot? There's a difference.

[@juliadenson8548]

I'm suffering from pots trying to say it's been coursed through long COVID I haven't had COVID but Iv had two shots .they won't admit it's the jabs

[@debbyrabold6069]

​@@juliadenson8548 o dear, I'm so sorry. There is a protocol to detox the shots out of you. I think it's called FLCCC Alliance.

[@ikvangalen6101]

No there isn’t!!!!

[@becaSidekick]

@@ikvangalen6101 Yes, there is.

[@dand33911]

​@ikvangalen6101 The fact you get to vote is terrifying

[@MOstix13]

Someone needs to be held accountable for everything COVID related. We were lied to for years.

[@Seaside_Gal]

Grow up

[@MOstix13]

@ Your comment makes no sense.

[@VictoriaRosario1]

trump

[@seeleygirl6178]

Do you mean from vax?

[@mingmen9908]

Was amazing

[@lizzardwizard2000]

Stop getting COVID boosters.

[@Dallasl_andscaping_.]

Never had one. Now I’m laughing at all the programming since escaping the matrix.

[@mynof1248]

I had to get the first clot shot due to Biden’s mandate and I am stuck with golden handcuffs at my job if I want to retire early. Fortunately I haven’t had any issues from it. Its time for me to find a new Dr. though because all my primary care doc does is advocate for the boosters.

[@librarynan4610]

Wonder how many of these patients had the vaccine.

[@Music2Desire]

BOOM. The sound of that OTHER shoe dropping.

[@mbarn6633]

I wonder how many of these patients didn’t have the vaccine

[@NeighborhoodDada]

Probably most of them. "Long COVID" and all that bs

[@librarynan4610]

@@Music2Desire I had two vaccines and then my blood pressure went up so high the doctor wanted to put me on medicine, which I refused. It took 18 months for it to come back to normal. No more covid vaccines for me.

[@mbarn6633]

@@librarynan4610 I was vaccinated 3 times. Absolutely no side effects.

[@susettesantiago5509]

Yes…….yes…….i get this all the time……I also get chronic fatigue and there are days my joints feel like I was thrown down the stairs……..but feeling dizzy almost like your fainting……..god bless our health care workers who are really advocating for their patients and seeing the truth and helping us we are suffering and struggling

[@sandeewichkoski1574]

Dr. Dave Marquis, functional medicine, treats vax injured from the covid jab. He has a channel with contact information and does telehealth visits: DrDavesHeadSpace is the name of the channel.

[@jadedphoenixprojects]

This. It's the basically just being dismissive. I even explained my feeling so about being dismissed offhand before telling her my concerns, where she proceeds to dismiss it.

[@Americanmamaistired]

@@susettesantiago5509 since my teens! Once I hit my 40s and the last administration took away disability people's livelihoods we just been waiting on God or death. Nothing else anyone can do

[@dallaswieler3822]

Same. It's crazy. I never felt like this before getting vaccinated for covid. Now ever day since I've been dealing with these symptoms. I haven't seen a Dr about it because what's the use. It won't get me anywhere.

[@WillowRatLady]

It is called aging.

[@JustTheTruth-Please]

Yeah, got to LOVE the US healthcare system where you are required to convince the drs to give you the medical tests to prove you aren't a liar wanting disability, medication, an excuse for work or aren't having mental difficulties. I went to numerous drs with a list of over 32 symptoms and was told I needed to just exercise more. Found one dr that only took cash, no insurance and found out I had a thyroid issue, developed gluten and egg allergies, had an inflamed chronic gall bladder and another health condition that required surgery to save my kidney and colon. Medication, lifestyle and two surgeries that MULTIPLE drs over 2 years missed. When you have to convince a dr to run tests because the dr is going to get paid regardless of how well you do...dunno, sounds like systemic issue in the US. I was lucky to be able to afford a "boutique" dr and my health is great now but not everyone can do that.

[@solangelalebron1348]

@@JustTheTruth-Please I'm not as sick as most people and I can't go to various doctors for treatment anyhow. If the local doctor can't do anything for me and they will send me to a ton of specialists all over, then it means I won't get treated because I really can't go to so many places with a limping leg.

[@JustTheTruth-Please]

@@solangelalebron1348 Yeah, this country is about able bodied people working for businesses to make money for the C suite. I am so sorry you have to experience that. Hugs to you, friend.

[@breathoflifeacres939]

I agree and POTS does disable people. It's so unpredictable.

[@spoonypoon7998]

Well I've heard people from Canada complaining because they have cancer and they can't get screening and they have to go on waiting list for 2 to 3 years to get things done

[@JustTheTruth-Please]

@@spoonypoon7998 "Heard from people", well, that sure does cancel out my using statistics and historical data, doesn't it? And how many kids in Canada did you hear about dying because their insulin cost was obscenely high so they ration it? And how many people in ANY other developed world go bankrupt as we do in the US? Check your facts, not your gossip. The US allows politicians to be purchased by big companies so they allow insurance companies, hospitals, pharma companies to all bleed us dry because both the big companies and the politicians (who get the BEST healthcare plans and an onsite dr/pharmacy at their workplace, both funded by taxpayers!) get rich from it. Don't come for me with Canada and UK gossip.

[@georgelabottum7448]

Thank you for this. Within a week after getting my 2nd Covid shot I started falling backwards several times a day. I put 2 and 2 together and refused any more shots. It took 6 months but I no longer suffer from vertigo.

[@FuckYourFeelings914]

Your the dumbfucks who got the shot tho

[@weaksause6878]

Unjabbed. I had dizzy spells for a few weeks after both times I got covid.

[@georgelabottum7448]

@weaksause6878 We'll never really know whether it was COVID or the jab that's causing vertigo.

[@cheesehead4670]

I’ll take things that didn’t happen for $500, Alex.

[@lauriepuglia4431]

Go get another booster ​@@cheesehead4670

[@deanhenson3600]

Never trust these Evil people with your health

[@chris2906]

And how many of them got the jab? Wake up.

[@DaNinja60]

Exactly

[@GoodCitizen1300]

I didn't get the shot. Same dizziness tho.

[@swervedriver5260]

​@@GoodCitizen1300 I didn't get the shot, feeling great!

[@bella5875]

I was diagnosed with POTS in 2020 and Orthostatic Hypotension as well a while after. Likely not COVID-related but rather triggered by pregnancy and Ehlers-Danlos Syndrome. It’s been an adjustment. You don’t really stop grieving but it gets better. Salt, water, compression stockings, and meds don’t always help as much as they’re said to. If you suspect POTS, log your blood pressure and heart rate in a notebook for a couple weeks before you go in and give it to them. Avoid a huge list of symptoms and mountains of papers right off the bat. With the way doctors think it can overwhelm them easily and make you look anxious. Ask questions and, sad to say but… sometimes getting a doc to think something is their idea is the only way to get them on board. Drop clues without jumping to conclusions or outright saying it. Also, nurse practitioners are usually better at listening and collaborating

[@Joyinme-sg9tu]

This is so true because I was diagnosed with anxiety lol I should’ve written down my bp like you said. And yes, my nurse listened to me way more that the Dr did.

[@nightmaresturningoftendejavue]

Same thing happened to whole generation after flu. Some, got some miracle medicine from japan - like my granny (it took months to get it, but…) and now she is 102, while rest of her family (grandad, mom of gra y…they all perished on different things caused by hearth failure - enlenagrment, hearth attack, holes….).

[@xerilaun]

@@nightmaresturningoftendejavuewhat is the medicine?

[@bushveldkid7640]

It is also a side effect from multiple injection injuries.

[@rhphotocdn]

🤣🤣 there goes the Main Stream Media blaming COVID again… Try blaming the 💉 , that’s the cause… Not the flu!

[@GoodCitizen1300]

Never vaxed.. i have the same dizziness.

[@davidgsebastian5490]

I had all those symptoms and went to a Naturopath. I was on multiple meds for gout, arthritis. IBS, ulcerative colitis, leaky gut syndrome, etc.... The naturopath diagnosed I was intolerant to eating potato's. I am now med/pill free. My MD doctor of thirty years told me naturopaths are quacks even though I explained to him "BUT I AN FEELING BETTER."

[@quebecpatriot1874]

I was on 13 pills/day high blood pressure on top of it and injecting me with poison 5 years ago; removed 1 crucial thing from my life: stress. Retired, moved in the sticks and enjoy the wild. 0 pills today.

[@ruidadgmailcanada8508]

Thanks for sharing David. I’m with you 100%. Look into how the Rockefellers (John D) destroyed natural medicine that had worked for 1000’s of years, replacing it with his allopathic western medicine of today - dependent on pharmaceuticals to treat symptoms and not the underlying condition. 😮 That’s why the doctor couldn’t figure your issues out…not trained to. Yes $ gets you power and control. It’s interesting history but will make you hate globalists…as they should be. 😊 He also screwed the educational system in the US. 🤦 The more you know!

[@Zoomville]

Every doctor was a naturopath until Rockefeller started funding medical Schools in the 1920’s and beyond to use drugs.

[@Brumasterj]

Thats awesome! Have several friends who swear by them! Glad your off the pharmaceutical’s

[@vallang4832]

My integrative doctor also diagnosed me with sensitivities to foods. I feel so much better knowing what I can and cannot eat. I do believe GMO had a huge handle on in this.

[@FlushaArt]

Safe. And effective.

[@xstorm_8_shadowx]

Crimes against humanity

[@blusnuby2]

@@xstorm_8_shadowx Nuremberg Code 2.0

[@breathoflifeacres939]

Fauci should be in prison for treason and crimes against humanity

[@neilkurzman4907]

No one ever said the virus was safe or effective.

[@notbarbie582]

Even for pregnant women!!

[@semperparatus3685]

Take a notebook with your questions and symptoms. Don't let them cut you off or dismiss you. Check off each question and symptoms. The "good" doctors will see you're serious and will take you serious if you do. I'm a 100% Disabled Veteran because until my wife sarted bringing a notebook with symptoms with date and times did they realize I had 24 hours to get surgery before permanent nerve damage but that was 6 month too late.

[@GeorgeH-j1x]

You also need another interested party

[@GoodCitizen1300]

Holy crap! Ive been dealing with this for almost 4 years now. Im gonna ask my pcp if he thinks it could be POTS. Thank you for the video!

[@meatpopsicle1567]

I love how they never mention that a majority of the people affected by all the long termed symptoms related to COVID are pretty much those who got the jab, got boosted, got jabbed, got boosted, ad nauseam.

[@garytorresani8846]

Bs. Having a jab has nothing to do with long covid. Take a class in cellular biology to understand how virus work. People fell into the misinformation generated by Trump and Fox and his reluctance to do anything about it and 600,000 Americans died who didn’t need to. I was one of the ones on the firing lines trying to help people survive this and anti vaxxers were among the worst patients in their denial. if you’re going to make claims like this, show me the data.

[@shawnaellcey6970]

Pots can be caused by various things, viral injury, which causes automatic nervous system disorder. But not to be confused with pots caused by a traumatic brain injury. Is was first called soldier’s heart, then later efforts syndrome. Pots can be severe, they are not mentioning this, as gastrointestinal issues such as gastroparisis can occur with development of SIBO. You cannot exercise or condition yourself out of POTS. It’s more than dizziness, often your blood vessels are damaged and are not constricting to aid out your heart upon standing. Make sure you know what type of pots you have. She was correct no pots patient will ever pass a tilt table test. (Correctly done with isoproterenol)

[@breathoflifeacres939]

That is the best description I've ever read. People sometimes don't understand that you cannot exercise it away. It can cause disability. I've heard of people committing suicide because it's so frustrating and disruptive to people's lives. I've had it for years and I also have the digestive conditions you mentioned. It's tough to deal with.

[@pg3541]

Autonomic nervous system. Meaning the the part of the nervous system that makes decisions for the body unconsciously. Many parts of the body are affected. When it goes sideways it is very difficult to navigate. This is POTS. I have this now for over 50 years. See a good doctor that understands this condition. Salt, water, protein, mild exercise on floor to begin and with progress move to more if capable without crashing, sleep, know your limitations, take supplements to keep you immune system strong, and medicines to ameliorate symptoms. Most important people will not understand what you are going through, so protect yourself. It’s your body and your experience is real not anxiety. Good luck to everyone who lives with this! ❤

[@too-girly]

But patients with other forms of Dysautomia may pass the tilt table. It's too easy to think all Dysautomia is POTS.

[@too-girly]

​@@breathoflifeacres939Between the GI symptoms and the erratic heart rate and BP, it's very disturbing.

[@nektariosandmagdalena4985]

​@@Kris-ib8sn I was two points from the 30bpm sustained increase, but I was on a beta blocker that I cant get off of because i have prolonged qt. I was dismissed completely many many symptoms of dysautononomia including very labile extreme blood pressure flucuations. I was hung up on when I was begging the neurologist to please listen to me. She gaslit me said it's anxiety. Tech also noted all my symptoms during TTT (hot flash, tremors, dizziness, ect) and saw and noted moderate blood pooling in my feet. I was told this was all normalby neuro. My blood pressure was also very labile during the TTT.

[@sonjebianca2483]

POTS has been around for years. I’ve had it since childhood and I’m 60 years old. Tall, thin teenagers are particularly susceptible.

[@zensoundsarah9209]

yes! POTS has been around however, it sounds like there's an increase in that diagnosis related to heart conditions with the uptick in covid and I can totally see why that is. Kind of scary to think the damage covid has the potential to do to damage the heart.

[@Nuggetsoffudge]

You might want to look at grabbing some Benfotiamine to assist with a thiamine deficiency. I'm guessing you might have had one since childhood. It seems to potentially run in families who don't pass along dietary habits that are high in thiamine and could also be passing along a reward seeking mood disorder like ADHD and or Autism. If you love sweets or intermittent fast or drink caffeine or have had chronic stress, you might want to check out what a thiamine deficiency is and what the indicators are that deplete it.

[@sonjebianca2483]

@@Nuggetsoffudge I actually take that, even though that has been ruled out for me. I can’t tolerate meat or high amounts of dairy, so I’m careful to supplement all the B vitamins and such. But thanks for the tip.

[@couch-m5j]

Almost 70 years old. Had POTS my entire life. I am a short, petite woman I was never a tall thin teenager. stop with that.

[@sonjebianca2483]

@ I said they were “particularly susceptible,” not that they were the only ones to develop POTS.

[@ursulaglissmann6905]

postural orthostatic tachycardia syndrome

[@SusanClemens-pd4pt]

Thank you. Now I don't have to look it up. I didn't know what pots was.

[@heatherallen2236]

I was doubted and not believed for years by almost everyone, until I finally ended up at the Cleveland Clinic. I was diagnosed with Hyperadrenergic POTS in 2016 by my Neurologist Dr. Wilson. This disease is a nightmare that I would not wish on anybody. It is a sister disease to MS as well. Many POTS patients go on to develop MS and many MS Patients also have POTS. Thankfully people are finally starting to become aware.

[@AndreaCrisp]

I have MS. POTS was my first symptom over 20 years ago. I had a bunch of tests run, but no problems were found. Instead they offered an SSRI. 🤬 At least they ran a bunch of tests before offering that. Now they would just offer SSRIs or some kind of gas lighting. Back then (early 2000s) I ended up self-diagnosing POTS and treated myself by switching to only drinking water & the appropriate amount (gave up juice or soda) and use sea salt. Prior I did not use salt in cooking or eating at all. Additionally, over time I started using electrolytes in all of my water. No flavor just electrolytes. I haven't suffered from POTS for years. Still developed MS though. POTS seems to be related to a lot of auto immune disorders, not just MS. It is also very common in EDS patients as well. I suspect hEDS or hypermobility syndrome. Definite connective tissue problems. Totally sucks. I've been able to avoid COVID thus far. But I likely won't be able to forever.

[@heatherallen2236]

@AndreaCrisp Oh wow, I''m so sorry about everything you have gone through 🥺💖 I have hEDS as well, and I'm having more and more orthopedic problems from that, the combination of the two diseases is really awful. Thank you for taking the time to reply, I hope that you can continue to avoid covid and that you are able to find treatment and relief of symptoms for your MS ❤️ Stay strong my friend

[@GeorgeH-j1x]

Cleveland clinic never gave me the time of day. They help some

[@kelsokreations8285]

Thank you for bringing awareness to this! My 15 year old son recently was diagnosed and it’s been rough for him adjusting to this new normal. He has his ups and downs throughout the day.

[@lauriepuglia4431]

Did he get the covid vaccine?

[@cica8427]

How the hell you can recommend gatored to drink? Here is the list of ingredients"Water, Sugar, Dextrose, Citric Acid, Natural Flavor, Salt, Sodium Citrate, Monopotassium Phosphate, Gum Arabic, Sucrose Acetate, Isobutyrate, Glycerol Ester of Rosin, Yellow 6." Do you need electrolites,drink coconut water!

[@too-girly]

She needs the sodium to help keep her blood volume up. She knows what she needs and her doctor advised. Don't presume to know better.

[@Mick698]

Too-girly Ha ha Gatorade is healthy right? Maybe some coca cola and McDonald's for recovery 😂😂😂

[@studio107bgallery4]

I’m really surprised that doctors and sports professionals recommend using Gatorade. They must get kickbacks because it’s not good because of the additives and sugar. Coconut water is good and also apple cider vinegar with honey in water is better.

[@crosslink1493]

Gatorade's formula has changed quite a bit since it was first developed by a biochemist working with the U of Florida football team. It moved away from electrolyte replacement ingredients to sugar and flavoring. Some folks like me find it nauseating, its just too strong. A little salt and a little salt substitute (potassium) mixed in plain water and I'm good.

[@robertpesa4157]

​@@Mick698Iced Tea 😂

[@shawnaellcey6970]

I am seeing a lot of comments pertaining to gaslighting so please note this: Multiple sclerosis (MS) and postural orthostatic tachycardia syndrome (POTS) are both conditions that can cause orthostatic intolerance, fatigue, and anxiety, and are more common in women between the ages of 20 and 50. POTS is more prevalent in people with MS than in people with orthostatic intolerance but no neurological illness. POTS can develop years before an MS diagnosis, or as part of the autonomic dysfunction associated with MS.

[@czerniana]

It took me 17 years to get diagnosed with MS instead of anxiety. The medical gaslighting is ridiculous and it’s costing people their lives. I’m fully disabled now, because I didn’t get started on drugs early enough.

[@gardenjoy5223]

So sorry to read that. Indeed, the medical gaslighting is insane and it should be a crime!

[@fidelcatsro6948]

im sorry

[@melissaseago536]

The sad part is that it maybe caused by herpes viruses left untreated. Carnivore diet will help. Dr. Terry's protocol got her out of bed and back to living a good life. Don't give up.

[@gardenjoy5223]

@@melissaseago536 Stop pushing your faulty agenda. This is also a form of abuse and ridiculous.

[@BonnieTietjen]

Yes, out the carnivore diet...it has many health benefits for ailments that some Drs say there's no cure. Look up Dr. Shawn Baker & Dr. Ken Berry for more info ❤

[@Solscapes.]

The pots sucks hard. The vertigo was the worst.

[@mrsjamessmom9044]

I just started having symptoms. I slid down a wall to keep from falling, Scary.

[@solangelalebron1348]

​@@mrsjamessmom9044LMAO!!!!!😂 Those are the kind of things the potter's house will make you do. Like the guy running around the church this Sunday like a crazed lunatic and nobody stopped him. That's like an insane asylum.

[@AprilTeniente-eu1mj]

I had a bit of the vertigo after the iron infusion, but I am fine. I need three more months till I stop taking the Integra Plus, the iron medicine for the low iron. I hope my iron will go back to normal soon

[@staceywilliams1863]

@@solangelalebron1348Wtf is funny you ignorant mfer!

[@Chucker973]

I have had an issue like this, I’m a electrician/mechanic, every time I’m under a piece of equipment or automobile on my back and I roll or move around, I get very nauseous and dizzy to the point of throwing up, never had this problem before I had COVID!

[@bg370z9]

I had this same problem for a while. Not to the point of getting nauseous, but felt dizzy when I turned my head, looked up or down. Definitely didn’t trust myself on a ladder. 72 hr heart monitoring didn’t show anything abnormal. Fortunately it slowly went away.

[@Ben-Rogue]

Sounds more like positional vertigo, which can be helped by the Epley Manoeuvre. Its a very common inner ear disorder

[@katherinemitchell4226]

If using salt, please use a fully mineralized product like Celtic Salt or Baja Gold. Also, you may want to hear Barbara O 'Niells' suggestion on how to use/injest the salt in the mouth before drinking water throughout the day. Of course, only follow your healthcare providers directions.

[@14luirod]

Just putting this out there, some of the "healthier" varieties of salt have shown to have larger amounts of heavy metals like lead, cadmium, arsenic and mercury. Obviously more testing needs to be done and from different sources but I'd recommend staying away from the brands you just mentioned in the meantime

[@TAHSIYN]

Love Celtic salt it does not give me chest pains like Morton’s table salt at all. I also put a pinch under my tongue and drink a lot of Good water throughout the day! O’Neill is the TRUTH! No doubt about her❤❤❤❤

[@dtropolopicus3602]

Redmonds is a good 1.

[@maryrodgers7898]

That's what my Dr says. She drinks water with salt in it everyday.

[@MyTNMtnHome]

I shouldn’t be that hard for a woman to get help. Experienced the brush off before finally finding what was wrong…pancreatic cancer and a heart attack. Doctors need to believe patients when they say something is wrong.

[@James-f1h7h]

Yes.Because America is still SOOO against women right?😂Men deal with the same thing.Get over it

[@debhart1160]

@@James-f1h7h Yes, I think there is ample evidence that men in America still hang on to privilege over women.

[@James-f1h7h]

@ There really isn’t any evidence whatsoever.Youre just a liberal looking to be a victim.All the women I’m around are either WELL taken care of or have jobs that pay more than the men around them so you can never persuade me if that nonsense yall keep trying to spread

[@James-f1h7h]

@ Na really there isn’t any

[@Noneyourbusiness-d8ball]

Of course the vaccines for COVID has nothing to do with this medical issue.

[@danielwoolman8969]

They should compare the rates of it with those who got the jab and who didn’t get it. Would be interesting.

[@robert-wr6md]

Can't for the life of me think why this is happening. It would have nothing to do with safe and effective prior medical actions would it?

[@Gina-dn6xm]

You can develop POTS after numerous diseases. I developed POTS after being diagnosed with lyme disease after severe fatigue for two years.

[@sarahMuahahaha]

Same... they still continue to ignore lyme and call us crazy

[@gardenjoy5223]

Yep, also got POTS after chronic Lyme Disease!

[@mrsjamessmom9044]

My daughter had Ehlers Danlos Syndrome and chiari malformation, which are genetic conditions. She suffered with POTS as well. She passed away in 2016. I have started having symptoms of POTS as well. I have a connective tissue disease and a couple of autoimmune conditions. I hope the doctor is ruling out the connective tissue connection on these patients and well as post covid.

[@SharkyJ40]

Hello from a fellow zebra! Lots of love for you, your daughter’s legacy. ❤

[@couch-m5j]

MCAS

[@mrsjamessmom9044]

@@SharkyJ40 Oh thank you. I love finding other zebras! I hope you are getting the care you need and deserve. Much love back to you and your. I miss her every day but I try to educate people when possible with her story and now mine. Both diagnoses were scary and nobody really knew anything about either. I found people who knew more than doctors did at the time so I help newbies navigate and how to advocate for yourself or a loved one.

[@mrsjamessmom9044]

@@couch-m5j You know that is the one comorbidity of EDS that my girl didn't suffer with, my niece however has crazy mast cells with her type of EDS. It's crazy all that cones with an EDS diagnosis. (gentle hug)

[@SharkyJ40]

@@mrsjamessmom9044 Very nice to meet you, and thanks so much for the advocacy efforts, a beautiful way to honor your daughter. Were you just diagnosed as well? I got support for the immune deficiency with infusions finally at 36 but not a lot of help from cardiology or neurology with POTS, and they looked the other way with TIAs and myocarditis from vax injury. PCP is caring and fights for me. Endocrinology helps with adrenals but doesn't understand my HPA axis issues well enough. Pain mgmt is hard since they won't learn about the med processing issues we have, learning how to help myself more on YT than drs or PTs. And therapists and DO drs like to blame us! "Just heal yourself and your tissues will heal." I had a time with SSA getting SSDI, and my employer was terrible, still retaliating through their long term disability carrier any way they can. I started filing board complaints now when I am gaslit. Truly hanging in there best I can! 💜

[@krissnov9072]

I just got diagnosed with this a couple months ago. It's more annoying than anything. You have to be careful when getting up, wear compression socks, drink A LOT of water, increase salt intake.

[@drscott1]

@@krissnov9072 …and stop getting experimental immunotherapies if one does not have a legitimate condition that makes them susceptible to a bad outcome from the bio weapon.

[@gruntgamer4204]

I just took some cold medicine, and nausea medicine, when I got it last December. I was able to improve within a week as opposed to several weeks or months. I also didn't receive the vaccine or anything from Pfizer. I threw the Pfizer medicine in the trash soon as I seen it in my prescription bag.

[@dragondancer1814]

My older daughter caught Covid in 2021, and she developed symptoms of POTS afterwards. She wasn’t diagnosed until 2023, and that was after a prolonged battle to find doctors who would even _listen_ to her, much less do the testing that ultimately confirmed it! She’s now on medication that will (hopefully) control the symptoms, and she’s determined to live as normal a life as possible-she was very athletic before this all started, and she refuses to let having POTS slow her down!

[@da1stamericus]

Hmm what medication has she gotten for it. Were using socks and physical therapy.

[@LoriJMarshall]

Oh my goodness - this sounds like my daughter 😢

[@breathoflifeacres939]

Can I give some advice? I've had this for 20 years. Fighting against it and pushing herself will make things worse. It's more helpful to listen to her body and slow down when the symptoms hit. A lot of people cannot do that because of family or work obligations. Exercise helps but not the kind of Exercise that most people do. See a physical therapist, reduce stress, avoid caffeine, check all her meds to see if they have side effect of low BP, be sure not to get dehydrated especially when she has diarrhea, meditation, gentle yoga ( not the kind where you get up and down. But Seated on the floor or in chair. Acceptance is key to getting better.

Vaxxed?

[@dragondancer1814]

Vaxxed and boosted! Unfortunately, many of her coworkers at the restaurant where she was a server were not.

[@OfficialFoodForThough]

I was diagnosed with pots three weeks ago. My md team thinks it’s because of having a severe case of Covid. Best suggestion is lay down and put your feet above your head. It’s hard because I can have an episode at anytime. I had one at petco two days ago when I was looking at frontline for our cats. I wish other like me get the right diagnosis and treatment.

[@mrsjamessmom9044]

Compression socks work pretty well too.

[@solangelalebron1348]

My spirit doesn't even want to raise my leg not even a little bit. So I won't. I'll just wait for the pots to overcome me watching the potters house.

[@solangelalebron1348]

​@@mrsjamessmom9044Not even a little bit do I want to wear compression socks.

[@OfficialFoodForThough]

Compression socks don’t seem to help. I wear them everyday day. I’m open to all suggestions, please. The only way we can learn truly through helping each others. General online education only goes so far. My doctor just parrots normal stuff socks and salt.

[@donnajean9805]

​@@solangelalebron1348 Maybe a message that frontline & like products actually poison our pets.

[@chrisking-jp5kj]

How many of those people took the jabb?

[@lindasutton4014]

More issues continue with Covid. Welcome to the new patients of this generation. Business is booming for Drs.

[@gabriellagrace4734]

Big time

[@wcwright44]

Better tha been diagnosed with polio or TB…such strange conspiracy theories about doctors.

[@VivP532]

@@wcwright44Unfortunately there will be an increase in polio, measles and other infectious diseases due to RFK influence on policy. Wait til these people lose their health insurance when Trump repeals the AFC, and he will this time around, and they can’t get insurance due to existing conditions.

[@lindasutton4014]

@@wcwright44 Read Book. Rockefeller Medicine Men:Medicine and Capitalism in America. By E. Richard Brown

[@pandemicoftheunvaccinated5367]

Are you denying people the right to make a living?

[@terrapinflyer273]

There are many medications which can deplete your blood sodium levels as well! Which can be much more prevalent in the elderly. I believe anti-depressants are a big one for sodium depletion. Most (if not all) anti-depressants are derived from anti-histamines also, which can sometimes cause delirium, or dementia-like symptoms. It's also difficult to stay hydrated when you're older. I've heard that adding a few granules of celtic or himalayan salt can drastically increase the body's ability to actually absorb water and keep you hydrated. Chronic dehydration can lead to kidney issues. However, too much salt intake can cause swelling of extremities, and all sorts of other potentially serious issues. It's all about balance!

[@josephburleton9758]

It would be interesting to know how many of these cases are in patients who were vaccinated for Covid.

[@dalegray3188]

I am 67 years old. Back in 1979 I got mononucleosis. Anyone that's ever had that know that that is a pain in the butt to have and it can take up to 6 months to get over it. And that virus never leaves your body it just goes dormant. So let's jump to 2021, I caught covid pneumonia in February and I spent the month in the hospital. But I was never able to get rid of the fatigue that you get with it. But last year I went and found the doctor and he had a CAT scan right on me and a blood test run on me. He did not find anything particular in the CAT scan, but he called me and asked me have you ever had mononucleosis? And I told him yeah back in 1979. And he said well it looks like covid has reactivated that virus. He says you're not contagious it's just that the switch got turned on again and nobody knows if that switch will ever go off or not. So I'm stuck with this fatigue 24 hours a day 7 days a week and I'm just about 4 years into it. He told me there's nothing you can take for it and there is no cure for it. Unless somebody comes up with a way to get rid of that virus that causes mono.

[@jonathanisrael9714]

I too have long covid for three years, and perhaps my having mono in 1979 has made things worse for me.

[@Matthew-f9s]

@@jonathanisrael9714…both of you guys should go get a pack of nicotine gum(or the patch) and try for a day and see if your symptoms improve..there’s now evidence that the “spike protein” aka synthetic snake venom is blocked from being taken up by nicotine at the receptor sights(which btw is non addictive). This is why smokers were not hit hard by cov id.

[@thermitegrenade]

That's horrible.

[@charlottesmom]

I had mono at 16 years old, took months to get better.

[@mitchdegrace2040]

Research Sr Ardis re nicotine

[@TheDerangedBlood]

funny how people can have "long COVID" but mention you haven't felt right since the vaccine and you get shut down by doctors. I'm so fed up with the medical industrial complex. My pain is NOT in my head. Doctors get paid regardless if they help people get well and that needs to stop.

[@andrearobinson3911]

We're just addicts in their mind.. 7 million out of 10 million pain patients have had our pain meds ripped away from us. The overdoses skyrocketed in 2016 because that when the mandatory cut off started, sending patients to the streets to get poisoned instead of treated like a patient by their doctors.

[@Mick698]

Try black seed oil,serrapeptese, nattokinase and NAC. Research it yourself

[@gregg5958]

I haven’t had the vaccine and still have issues. So to blame vaccines for things while ignoring the illness itself is just wrong. There can be many causes.

[@pamalojo]

I'm vaxxed to the hilt and never had a reaction.But that's just me. I know several people who had such bad reactions to the vaccine that they decided not to get any more. Doctors need to listen because not everyone reacts the same way. I hope you find the care you need.

[@sportgoofy1975]

​@gregg5958 I'm sure you have had the covid vaccine. In fact I would bet on it.

[@marilynchapon357]

I have POTS. I am a member of a support group. Many members had their onset after Vaxx or boosters. It's debilitating to many of us.

[@Adam-gm5tm]

Every person who I personally know who have had it ‘not pots’ but the preventive shot have been ill more than once! Those who haven’t had the treatment have not gotten ill. Sorry for the vague description, but that’s where we are today!

[@ryansmiley5495]

Good thing for the vaccine 😂 you probably had covid after anyway.

[@jgarland3581]

I would suggest reading Doctor A.r.d.i.s’s book…no periods in the name. Don’t want to trigger anything🙄

[@joan.nao1246]

​@@Adam-gm5tm same here; everyone I know has been ill a few times after "prevention", as well as developed other issues, vs those who haven't partaken of "prevention" and have never gotten ill or have been ill just once.

[@uptoolate2793]

The inoculation was an eye que test. Those who took it, even once, failed. As a pure blood who told my Dr to sod off, I have a hard time feeling sorry for people who were jerks to me for thinking critically and having the spine to say no.

[@EndPoliceBrutailty]

I think I have this. My sports watch keeps giving me abnormal heart rate alerts even though I'm an athlete. I'll get most of those alerts when I'm not working out. I've had to quit running again because of the symptoms. I'm worried about a heart attack. I also feel lightheaded and dizzy from time to time. I haven't been myself since catching COVID in Oct. 2019.

[@mrsjamessmom9044]

Get it checked out please.

[@SharkyJ40]

Yep get it checked out. Could be having TIAs. Former Ironman triathlete living on disability now.

[@chanchan5349]

Same. Caught covid spring 2020. Long covid until 2024; just started last 4-5 months feeling more normal. Rare POTS & PEM lately. I’m so thankful to finally feel more normal. Lost stamina but I can slowly build back.

[@dethray1000]

i was getting like a a-fib--ekgs and everything else checked out ok--i had 3 bouts of covid--no vaxx--finally one doc told me i might have a viral bug running rampant and it will go away eventually,viral infection in the heart--took 6 months--but it still hanging around but barely--the worst was the joint pain coming and going-joint pain 90 percent gone--a friend's daughter gave me a big part of it 18 months ago--and it will take probably another 6 months to go away--some people call it long covid but who knows? not even the doctors...

[@instro3304]

Same, I've run many marathons b4 covid, then i started having the same issues seen a cardiologist abnormal heart rythem besided that they found nothing. I take b complex magnesium, and turmeric helped. Also, ice or heat the back of my head helps a lot

[@hilpei3675]

YES - freaking dizziness is a drag.

[@rabbitrabbit1243]

When U faint with pots your heart actually stops so yeah it's a fkg drag ding dong

[@kathyh4804]

Ironically, everyone I know with recent ( last 3 years) heart “issues that were previously healthy have had the cvd shot and NOT covid! So it’s not “long covid” as much as the shot it seems

[@urbugnmetoday3183]

What is the percentage of these people that were experimented on?

[@Earth2Flo-v6f]

I have dizziness and heart racing, got 2 Moderna shots and this started about a year later.

[@jab16399]

Moderna-carditis?

[@clydedenby1436]

We CALLED it. I also said that the lawyers are going to get involved. Wait for the class-action lawsuit advertisements.

[@a.scotth.9955]

Is this a disorder thats popped up after being vaccination?

[@trildi]

Report clearly says she had Covid.

[@dublingirl1470]

It's been around long before COVID or the vaccinations

[@Sctronic209]

@@trildia lot of people had Covid and still took the arm ticket.

[@Sctronic209]

@ I don’t believe that for a minute. I see research to the contrary you need to dig deeper.

[@Yamamanosuke]

​@@Sctronic209 these people are tards

[@MrJfont]

Natokinase,bromelian, tumeric for 3months minimum.

[@Islamisthecultofsin]

Definitely couldn't be the "safe and effective".

[@KeepPrayingCA]

How many of them got the vaccine??

[@cloudie9druoid172]

More Covid patients or more ppl who took the vaccine???

[@erikarobinson3557]

I’ve had Covid twice. I see spots more than ever now and irregular heartbeats

[@iainnicholson4399]

From COVID or the COVID vaccine?

[@billbradley2480]

Many of my family members have had health issues since 2020. They stood in line to comply. I don’t comply with what Drs recommend and at 66 I haven’t had a cold or flu in many years. My heart rate and blood pressure is excellent. My trick to great health is detox every 3 months.

[@peace5647]

Who took shots plus boosters? I am curious if there is a correlation.

[@no2thenwo737]

My brother did and he now has the shingles every few months. My brother in law did and now has boils that won't heal.

[@peace5647]

@ I’m so sorry to hear that. Same with a 21 yo family member… Shingles.

[@roxyiconoclast]

I had pre-existing POTS, which got worse after I got Covid. Only mild leg exercise was called for due to other health issues, and as usual for POTS standing and slow walking exacerbates tachycardia symptoms. Medication didn’t work. Now I need a wheelchair to go to medical appointments. Anyway, POTS is an example of how even a short acute Covid infection can leave you with serious lifelong symptoms. The cardiology test referred to is a Tilt Table Test, which is very expensive and may not be available to everyone. An alternative is an in-office test that primary care providers can offer, called the NASA Lean Test, which has been validated in a small study for Long Covid as well as other patients. The Bateman Horne Center has information in their article “Why the 10-Minute NASA Lean Test?”

[@gardenjoy5223]

Why is a Tilt Table Test so expensive where you live? It's a simple and short procedure. Shouldn't even cost a few hundred bucks, including the personnel, incl. everything.

[@roxyiconoclast]

@ have you ever had one? A few hundred dollar IS expensive. In Seattle, it required two visits with a cardiologist, pre and post, plus a procedure with a technician and a room full of expensive equipment. I don’t recall the cost as I had it 20 years ago, but most definitely not cheap. A NASA Lean test costs only what you pay for one non-cardiologist doctor’s appointment and equipment required is a blood pressure gauge and finger pulse gauge.

[@gardenjoy5223]

@@roxyiconoclast Yeah, I had one. In Europe. Didn't pay a cent, for we are all insured by law here, but was done quick and easy. Compared to many other things they ask money for in the USA a few hundred dollars is crazy cheap there. That system is broken so badly.

[@roxyiconoclast]

@ yes, it is crazy over here! Long ago I stayed more than a week in hospital as a student in France and paid nothing. 😊 In the US, serious hospital stays frequently bankrupt people. Since I didn’t recall the charges for my TT, I googled and found this 2009 post on a dysautonomia chat board: “I can give you exactly what it cost me and i have BCBS [large health insurance company]. $2698.00 for test. $1888.60 hospital charge. $686.00 to read it. less ins[urance] my actual charges equal-$2105.54” Yikes.

[@jhdholiday7253]

I have it since kindergarten. I'm 58 now. Got my diagnosis in 1999. Have been on meds since. I am blessed to have Dr. Blair Grubb from University of Toledo Hospital in Toledo. He has written textbook on the subject. I encourage anyone suffering to seek him out or any healthcare professional. Pots is part of a larger disorder called dysautonomia.

[@too-girly]

Agreed. What meds do you take?

[@jhdholiday7253]

@too-girly propranolol and methylphenidate. I will eventually be getting a pacemaker. But the meds have worked well and I will do that as last resort. I have resting heart rate in 20's the methylphenidate increases it and the propranolol increases the strength of heart contractions, or push of blood out to body

[@evonne315]

Oh no I dont have POTs I am just an older woman being paranoid, I just need to take care of myself better. 🤨

[@tinadiesman5442]

Is this from the jab?

[@JessicaD.-vb9ho]

No my son and I ended up with permanent vertigo after having COVID.

[@lorietaylor4665]

Yes it is

[@PAPOOSELAKESURFER]

Spike proteins have multiple symptoms?

[@janeshipley6993]

pots can be caused by an injection, but it is mostly caused by a viral infection, such as covid. why are people so stuck on “is it the shot?”! it’s been known to be caused by viruses for ages.

[@builderboy1646]

Indeed!

[@myforever13]

how do you get your doctor to test for this? i have a lot of POTS symptoms and the doctors just keep checking my blood sugar and thyroid

[@cindyhurzeler3885]

You need a tilt-table test from a cardiologist.

[@nope123-w6d]

I’ve had this POTS since being sick with covid. POTS is terrible. I can’t even count the number of times I purposely dropped to the floor when feeling like I was going to pass out. Then the amount of time I spent laying on the floor waiting for my body to recover from being dizzy, racing heart, uncontrollable full body shakes….then I’d slowly crawl back to bed. In Dec it will be 5 years since I got covid, things have slowly gotten better. Though my “before covid normal” seems to be long lost.

[@CheshireCat-w5s]

One of my children and I both developed POTS after having Covid.

[@waynesmith6325]

Did you both get the Jab though? Just curious....my whole Family got Rona in the 2nd wave of it and we still didn't get the jab. I know multiple people who got the jab and they seemed to get covid more....we only all had it once. I'm not anti vax just anti NEW untested unproven vax.

[@CheshireCat-w5s]

@@waynesmith6325 Nope. We got Covid in 2020, before the vaccine was even available.

[@CheshireCat-w5s]

And I would agree that our friends that got the vac and boosters came down with Covid quite a few times. Our family has had it twice. Once in 2020 and one more time in 2023.

[@Yamamanosuke]

​@@CheshireCat-w5s so can you solve the 2+2 there?

[@davestark2015]

My Daughter has it after COVID don't know whether to blame it on the shot or COVID

[@Yamamanosuke]

Well seeing as C19 was seasonal flu with a new name and fake test should be easy to determine

[@davidbognacki8606]

How many were ALSO vaxxed?

[@wplants9793]

I had POTS after Lyme disease, luckily it went away within 18 months. I also have EDS and as a kid I had MCAS, which are related to POTS. It was terrible though, I had flares all day long, I could hardly move and going up and down the stairs was awful. My house became so messy because I couldn’t bend over to pick things up

[@Bettinasisrg]

Unless you're one of the millions in America without insurance, then you're screwed.

[@bgmullins]

Is it correlated more with COVID-19 infection, or is it correlated more with having taken the vaccine???

[@Bayoucityconstruction]

We will not know for a few years

[@plowboy8123]

This is all pointing directly at the jab !! Wake up!

[@GeorgeH-j1x]

I'm never vaxxed. Still have it.

[@TexSquirrel]

My daughter didn’t get it, but has POTS.

[@dianegreen6635]

Injection side affects ?

[@34BGIRL]

I suffer from this but was told it was vertigo. Sent me on my way & no medicine. Its horrible

[@brazil7028]

I want to know how many were treated with gene therapy

[@TT-cu7ze]

As part of the Ehlers Danlos community maybe we will finally get more attention.

[@gmac8586]

My mother had these symptoms but she also had chest pain and fatigue for weeks. Her doctor kept telling her she was having panic attacks. Her symptoms were never constant and her doctor would never catch her during her symptoms. I've had panic attacks and they were never painful. Finally, we took her again to emergency for the third time. She was in serious pain and the nurse could finally catch how dangerously high her heart rate was. They found out she had a lung embolism (blood clot in the lung)!! Her heart was trying to compensate for the lack of oxygen due to the blocked artery. She was kept in hospital for a week. Thank God she survived and is currently on blood thinners. Please don't ignore symptoms! She almost died and I'm glad we just kept on it, and insisted she returned to emergency. She now has a new doctor.

[@DaveBegotka]

Tell the truth....did these people have the "Warp Speed" it not.....i bet so

[@ChimmyChimChim95]

I feel seen! Diagnosed with Pots after developing symptoms literally the week after i tested positive in 2021. Have never had these issues in my life until i got covid.

[@Yamamanosuke]

Injections?

[@JescaML]

That’s why this wasn’t good to force people to take an inexperienced drug

[@mickeyandres2651]

We were given junk and now we’re suffering. People need to be held accountable.

[@Star-c6d7h]

I wasn't given junk because I didn't go get the vaccine. I'm not suffering anything.

[@Betty-qz5zd]

Yes, the ubiquitous "they" must be held accountable, for everything. Bad teeth, inflation, lack of affordable healthcare, lack of good paying jobs, lack of housing, poor education, racial injustice, homelessness, superficial values, everything we hate.

[@debhart1160]

What junk were you given, how are you suffering, and who's fault is it that you're suffering?

[@Yamamanosuke]

​@@Betty-qz5zd "they" are wee hat people. The Geaus and yes they are responsible for almost all that

[@poormanagement1722]

Told I had anxiety for past 4 years, constant congestion and tired. Stopped taking meds, and replaced with Shunghite water and Celtic salt. No more congestion, no more tired.

[@OhsoScary]

Are they vaxxed?

[@RandallWilliams-b7f]

Nothing to help us at all almost 4 years later

[@HypatiaMuse]

After I had COVID my blood pressure went crazy.

[@AliceHolbrooke-lc4ty]

Crimes Against Humanity.

[@mikefrederick4096]

Don't you just love the double speak... early in the video they say 1 in 500 people have it but later the doctor says he's seeing several patients with it....well if hes seeing several and hes just one doctor and there's millions of Doctors then the 1 in 500 is more lies

[@kellymcclendon6601]

You should have refused the jab.

[@Beaver108]

Is this a side-effect of the Jab or just Covid in general?

[@josephstory6461]

POTS or CLOTS?

[@mrsjamessmom9044]

or STOPS..

[@robertyoung2819]

Yep...

[@paulettebarrow9791]

Iv had PVC'S for along time but never had Tachycardia before I had Covid in Dec 2019 sine then Iv been in the hospital I think 4-5 times with it, I just have not been the same since Covid in many areas like memory for 1,dizziness, headachs, Tach, no energy, etc

[@elisaorozco9494]

Me, too..................

[@backcountyrpilot]

Have any cases of POTS been diagnosed in un-vaxxed adults or children?

[@KmusikOne]

Nope

[@benlawson4640]

My wife is unvaxxed and has terrible Pots after Covid. Days of being bed bound due to dizziness and fainting

[@KmusikOne]

@@benlawson4640 Bot

[@KmusikOne]

@@benlawson4640 Lies

[@KmusikOne]

@benlawson4640 Pics or it didn't happen

[@nonnalovepriceless]

I’m going threw this it’s awful

[@Kelly-yx9tn]

The jab! The gift that keeps on giving.

[@marilynngray-raine7581]

Not the vaccination! The disease itself !

[@beckysartor]

Definitely Maga there!

[@Kelly-yx9tn]

@beckysartor definitely not a goofy leftist liberal 🙄

[@beckysartor]

@Kelly-yx9tn I'm definitely not a rude, bully maga.

[@americanandpunjabilifevlog3951]

I have been feeling dizzy for so many years, one minute I’m fine and other I need to lay down, feel unconscious, I have neck pain for so many years. I had trouble explaining to my doctor. All my blood test reports come good.

[@doubletapgaming1189]

I wonder how many got the jab...

[@ericwethington]

Wonder how many of these people had the vaccine

[@Cat22275]

Kaiser Oregon refuses to diagnose me. I ended up with a rare Takotsubo heart attack in the emergency room because they didn’t take my dehydration seriously.

[@Yamamanosuke]

Google says thats caused by having a b**** fit