@@user-ky2xo2ls4m I guess that's to be expected somewhat as they both have similar symptoms. I'm just struggling that my doctor seems to think standing up is causing me mass amounts of anxiety
@@user-ky2xo2ls4m absolutely at least now I know when I've overexerted or my HR has been too high for a bit I need to sit down or something. It's very annoying considering this only all started for me 18 months ago
@@user-ky2xo2ls4m I'm only 27 so I don't think I'm quite ready for the scrap heap yet. I'd just like the heart beating part to be a little slower 😂. Thank you and I hope you continue managing your SVT
There is so much more to this syndrome. I take offense at “patient complains” how about, “patient presents with.” There is such a lack of understanding on doctors’ part; we really need people to listen to us, perhaps strive to find underlying causes, and a tad of compassion and understanding go a long way. After all I’ve gone through over the last 15+ years, I’ve lost a lot of faith in doctors 😢
Literally came here to say that. Got instantly triggered by the word complain, goddam. What’s wrong with presents, or states said symptoms!! We’re not complaining we’re suffering.
It is interesting to note the interpretation of 'complain'. In this context, Dr Gupta is merely using the commonly used medical sense meaning 'suffering from' and is intending no detraction otherwise. @savannahstudley303
@@graniabenge2814 I hope you can understand that the use of the word ‘complain’ to a chronically ill person can be extremely damaging to their mental health. Especially when you consider most chronically ill women get medically gaslit often by male doctors. Yes it may be an interpretation, but when has the word complain ever meant anything good?? A coworker goes to their manager to express their ‘concerns’ about you, when the manager comes to you they say your coworker has been complaining about you… it hurts emotionally but the intention was originally from a place of concern. do you see the difference? Where they both mean the same thing but can actually have a negative impact when used in the wrong situation.
I got in touch with the BHF and they told me there has been an increase in POTS cases following Covid. That, my vaccination or a jet ski crash is what seems to have kicked mine off they all happened within a 2 months of eachother so its hard to pinpoint. Its very hard to get help with too, feels like pointless struggle
@@francescachristy8761 it's just getting to that point that is hard. A lot of doctors don't know about pots so just label you as anxious so you can never actually get a diagnosis or treatment.
Doctor you’re the best I learned a lot from you I live here in the US and I’m 75 years old and I watch your videos I have learned more than any cardio doctor or any other doctor besides my own doctor and when I watch of you keep the good work up I appreciate I learned a lot from you at 75 thank you so much
No , what he is implying is it is only a symptom which is medical term. There may be different underlying causes. He has so many videos explaining POTS and it's treatment.
What he is saying is that POTS isn't a syndrome on its own, but rather an effect of something wrong in the sympathetic-parasympathetic systems. It's not a heart condition.
I had a tilt table test done. They kept me laying down for 30 minutes (strapped in of course), then they finally tilted the table. The tilt was so slow that nothing happened. I'm talking almost 2 minutes to tilt the table from 180° to 90°. They told me to eat salt and so yoga. Fast forward 3 years, I now have a Cardiac alert service dog for my POTS.
Now I’m really confused. I’ve been dealing with this passing out thing basically since I got pregnant for my daughter. My doctor actually told me to look up what POTS was, I had no idea what it was before hand. I just knew that passing out every time in the shower makes life very hard. They gave me a heart EKG thing that I press every time I feel like lightheaded or I’m going to pass out. I don’t even have an official diagnosis yet but this whole process feels pretty official to me? I actually didn’t think it was that serious, but my doctor said that it is not normal to pass out when you stand up. I also have a lot of other weird health problems. That’s why I did not believe it was that serious because I thought it was related to something else. Is there a good video explaining what this disorder actually is and how to live with it properly?
Thank you so much for this comment!!! I have pots too, and I was really confused because I looked up the symptoms and I literally had all of them! Then he says it isn't real? It makes me really confused and kinda angry too 😂
POTS is real in the sense that patients are definitely being affected by something. But right now it isn't really known what the underlying cause is. I've heard people recommend a symptoms management perspective, like working a job that doesn't involve lots of standing to reduce the risk of falling over.
Yes there is. Look up Summer Dashe. She excellently explains what it is because she has it and it ruined her job as a news anchor. She notes all the symptoms. A really great video. Hope it helps. 🌞🦋🌷
When i was a kid i fell on the ice near my tailboe area, and as an adult i still get pain there and have has pots since i was a teenager. Could it be from my fall?@@Shigami-lb6oc
When I get up I feel like I’m gonna fall over but I think that just iron deficiency (also last night I was laying down for hours and decided to get up and go to bed and I felt dizzy and lightheaded)
Hi Dr. Just a quick question. The criteria regarding POTS and the rasing/elevated Heart Rate upon standing is quite unclear. So my question is: should the heart rate be manitained @ >30 beats per minute uppn standing and for how long should it be maintained? (E.g if your HR increases to > 30 beats per minite but in the next minute it drops to below 30 beats and steadily decreases to a normal range within 3 minutes. Does this still fullfill the criteria or do you need to maintain the >30 beats for the time you are standing?) thank you for this channel you are creating such massive awareness. Respect to ypu sir!
@@renu653 It’s just if it increases by 30bpm (40 for adolescents) or to over 120bpm at any time within the first 10 minutes, it doesn’t say that it needs to be sustained in the criteria.
But it’s only happened like 4 times from completely diffrent stuff over a few months (don’t have it diagnosed but heard a part of it is linked to audhd so wanted to look into it bc i related to the other video)
Can you receive a diagnosis though? I’m so tired of being judged and people thinking I’m perfectly healthy because I look that way. And anxiety being blamed.
I get very tired an fatigued when I eat ,so I just eat in the evening before bed, an I have been dealing with a foggy headache for the last 3 years, I can't get in a car when my head is foggy, it's made my life really bad for the last 3 years, I have been trying to figure out what it is but I only have a few symptoms of POTS, Dysautonomia is one I found out about just today, I hate this I wish it would just go away, God bless
I have this, i always faint after long period of time or sweat, and feel weak when standing for something, once I did, tai chi and almost passed out and though I just had low stamina. Had semi seizures and complete blacks out all the time. I though it was normal.
Find the video on my channel called “causes of Dysautonomia.” Pots/dysautonomia is caused by damage to the neurons mine was caused by a TBI I got as a child. I was working as a medic in 2020 and got Covid and it made my pots/dysautonomia put me on my death bed for 3-4 years… I am now very well after I figured out neurogenesis. Still have dysautonomia/pots but very well managed
@@ExtraordinaryJam your not going to see it if you don’t subscribe. (I’m not some random wannabe UA-camr I’m legit person that was on my death bead with dysautonomia for years! If you feel that I could give you any useful information I will 100% make a video explaining everything)
My daughter is 14 and suffering with these symptoms for years now she’s her blood pressure is low but when standing her heart rate goes up fast Then it can drop fast too Nerdiing help as it’s taking her childhood away
Have you figured it out if you have Pots or not? It's been 9 months since you posted this reply. Look for the poor man tilt table test on youtube. It will give you an idea of how to test it on your own if you have it or not.
I’ve my TTT at kings college with Nick Gall on 30/5/23 finally the Northern Ireland Drs have sent me to get help after years of medical gaslighting. The medics over here really need to be trained on all types of dysautonomia ❤
This happens to me but I thought was from something else I wash I knew . I don't have a single doctor n I haven't gone or told them to much I get scared but I need some help
@@michele0324 others include pure autonomic failure and multiple system atrophy. Those disorders can cause supine hypertension as well as orthostatic hypotension. Studies have linked supine hypertension to the same cardiovascular issues as essential hypertension. They compared multiple system atrophy patients with supine hypertension to those without. Those with supine hypertension had increased left ventricular hypertrophy along with changes in white matter and renal function, and most importantly, shorter survival. I lost my dad after a diagnosis of MSA. It also affects peripheral circulation in a way that the extremities are cold. My dad had the "cold hand sign" and at the time I wondered about diabetes, as both his brother and their dad had type 2 diabetes.
Try a low histamine diet and increase water intake, also a daily vitamin. Of course to much water intake can also be dangerous and I'm not a doctor, but this works for me.
High stress level creates a histamine response, when you combine that with foods high in histamine, you can get pots symptoms. I've been taking a daily vitamin and implemented a low histamine diet. My symptoms are nearly unnoticeable now. I miss hot sauce and cheese but I love feeling good better.
I think pots is secondary to mast cell activation. I think all pots is just mast cell activation. Maybe lyme disease, toxic mold exposure. If i follow a low histamine diet combined with pots recommended water and salt. I feel great.
@@adamjackson7585There is no one- size-fits-all amount and the guidelines you'll find online are just that; guidelines. Salt can worsen symptoms in those with Hyperadrenergic POTS.
Hello sir I am from India, the symptoms you are telling i am suffering from last 24 months and dr in india diagone with anxiety is there any cure for POTS please reply I am very help less
“Sometimes as doctors, when we can’t explain what’s going on we just give it a name ….” to shut the patient up. Hummm, we don’t investigate, we don’t attempt to figure it out, look into, etc. We don’t actually try to understand what the patient is suffering from that results in their symptoms. It could be something in the patient’s head, how are we supposed to find any cause if it is in their head? Ugh, why bother it’s easier to just slap a convoluted medical name on it and send the person on their way. Heck, I can be a doctor myself AND apparently no university degree, training, rotation, etc. required anymore! 😎
Should we say that you don't know what your saying either. Don't u do the same when a patient comes in your office with a concern. You go in your office and read a book on what might be going on!! How dare u!!! Your nor GOD !!! NOW GO READ THAT!!
RESPECTED DOCTORS "POTS"MEANS DOCTORS ARE PESHENTS HEALTH KEEPING POTS STOP THEY'RE SICKS DOING HUMANS IN TOPS ALWAYS DOCTORS ARE DURING PESHENTS HEALTH KEEPING SPOT A VALUABLE POST IS POTS For RESPECTED DOCTORS 💓 OKAY thanks LOVE EVERY THINKS UNDER THE ⛅ SUN K A HABEEB RAHAMAN ROWTHER PALAKKAD BHARAT 👍 JAI HIND JAI BHARAT
No when patients stand they get said symptoms, there's muscle instability, tremors, hot sweats, chest pains, passing out & an increased heart rate yes are symptoms but that's not all too it. The sickness that's been no reason till then, the excessive bleeding it can cause. Juat because some patients only have said symptoms a lot of us have a lot more than that.
@annie.hi. pots is an inherited issue, and goes hand in hand with other issues, along with having pots, I also have celiac diesease, ehlers-danlos-syndrome, and Mast-cell -ctivation-syndrome. Some of these issues like ehlers-danlos-syndrome goes back hundreds of years.
Dude please....😂 Enough with the fear mongering. There were WAY more complications including death with Covid. No matter what your UA-cam ex-doctor says.
Ya, that is not how it works. What he is describing is similar to nauseousness, big word describing a symptom people feel. If you ever felt nauseated in your life? Then you are a hypochondriac? Ridiculous … POTS is a symptom of a bigger problem. I had pots as a teen because I was on a doctors order, for an extremely reduced salt diet. Was I making up pots or purposely causing myself to faint? And almost faint on a tilt test? NO! I was born with a narrow Aorta and a Hole in my heart. Many people who have pots have physical heart problems and/or EDS, or Post Covid symptoms. Do your research please. Just because you can not see it with your eyes does not mean it is not real. In fact that attitude is dangerous. I had people in my life push me past my physical limit, more than once, outside of the medical world because they did not believe a young person, of good weight, who looked well-ish, could surely not have serious heart issues. That theory is beyond dangerous and factually incorrect. And beyond critically dangerous.
Lastly and my final statement. After brexit in 2022 there was a shortage of 11,000 physicians in the nhs. And here in America we have a massive shortage as well. The idea that a physician would feel the need to make happy and “feed a faker” to acquire money for appointments, financially for a living is absolutely insane. And factually invalid. But cool … you do you 😎
When drs can’t explain what’s going on they tend to diagnose you with anxiety and send you on your way.
That's been my experience for the last 18 months unfortunately, I've been looking into private which is something I don't want to do particularly
Exactly 😂
@@user-ky2xo2ls4m I guess that's to be expected somewhat as they both have similar symptoms. I'm just struggling that my doctor seems to think standing up is causing me mass amounts of anxiety
@@user-ky2xo2ls4m absolutely at least now I know when I've overexerted or my HR has been too high for a bit I need to sit down or something. It's very annoying considering this only all started for me 18 months ago
@@user-ky2xo2ls4m I'm only 27 so I don't think I'm quite ready for the scrap heap yet. I'd just like the heart beating part to be a little slower 😂. Thank you and I hope you continue managing your SVT
There is so much more to this syndrome. I take offense at “patient complains” how about, “patient presents with.” There is such a lack of understanding on doctors’ part; we really need people to listen to us, perhaps strive to find underlying causes, and a tad of compassion and understanding go a long way. After all I’ve gone through over the last 15+ years, I’ve lost a lot of faith in doctors 😢
Yup
Literally came here to say that. Got instantly triggered by the word complain, goddam. What’s wrong with presents, or states said symptoms!! We’re not complaining we’re suffering.
@@savannahstudley303after this comment I'm kind of glad your suffering. Moan moan moan. Go home karen
It is interesting to note the interpretation of 'complain'. In this context, Dr Gupta is merely using the commonly used medical sense meaning 'suffering from' and is intending no detraction otherwise. @savannahstudley303
@@graniabenge2814 I hope you can understand that the use of the word ‘complain’ to a chronically ill person can be extremely damaging to their mental health. Especially when you consider most chronically ill women get medically gaslit often by male doctors. Yes it may be an interpretation, but when has the word complain ever meant anything good?? A coworker goes to their manager to express their ‘concerns’ about you, when the manager comes to you they say your coworker has been complaining about you… it hurts emotionally but the intention was originally from a place of concern. do you see the difference? Where they both mean the same thing but can actually have a negative impact when used in the wrong situation.
I got in touch with the BHF and they told me there has been an increase in POTS cases following Covid. That, my vaccination or a jet ski crash is what seems to have kicked mine off they all happened within a 2 months of eachother so its hard to pinpoint. Its very hard to get help with too, feels like pointless struggle
There are treatments. Diagnosis is normally done with a tilt table test
@@francescachristy8761 it's just getting to that point that is hard. A lot of doctors don't know about pots so just label you as anxious so you can never actually get a diagnosis or treatment.
My sister was diagnosed with POTS after having covid.
@@mylittlefamilyabroad finally got my diagnosis yesterday, have to meet with my doctor to discuss different treatment paths
Try a low histamine diet. It worked for me.
I get it turning over in bed, in the mornings
That's different though, you're lying down... Are you anemic?
That not pots. You prob are having vertigo..it's from crystaks in ear or you may be anemic.
@@Esther216or cervical spine instability..
I get it laying down too
Doctor you’re the best I learned a lot from you I live here in the US and I’m 75 years old and I watch your videos I have learned more than any cardio doctor or any other doctor besides my own doctor and when I watch of you keep the good work up I appreciate I learned a lot from you at 75 thank you so much
he is awesome !
This is why we love this guy.
Very true what you said Dr patients actually don’t understand the terms and get scared listening to such jargon’s
❤ TY FOR SPEAKING STRAIGHT.
So basically it’s “all in our heads”.. just a label. Not a diagnosis. Great… 😔
Even though he just said that when they measure the heart rate it is indeed higher? That made no sense.
No , what he is implying is it is only a symptom which is medical term. There may be different underlying causes. He has so many videos explaining POTS and it's treatment.
What he is saying is that POTS isn't a syndrome on its own, but rather an effect of something wrong in the sympathetic-parasympathetic systems. It's not a heart condition.
What can we do then?
Thank you for expounding on the term...❤
Thank you for the explanation! I saw a POTS short and was curious as to what it was from seeing a short on yt! :)
Dr. Gupta, can you explain what tests can be use OR helpful in diagnosing POTS?
I had a tilt table test done. They kept me laying down for 30 minutes (strapped in of course), then they finally tilted the table. The tilt was so slow that nothing happened. I'm talking almost 2 minutes to tilt the table from 180° to 90°. They told me to eat salt and so yoga. Fast forward 3 years, I now have a Cardiac alert service dog for my POTS.
Now I’m really confused. I’ve been dealing with this passing out thing basically since I got pregnant for my daughter. My doctor actually told me to look up what POTS was, I had no idea what it was before hand. I just knew that passing out every time in the shower makes life very hard.
They gave me a heart EKG thing that I press every time I feel like lightheaded or I’m going to pass out. I don’t even have an official diagnosis yet but this whole process feels pretty official to me?
I actually didn’t think it was that serious, but my doctor said that it is not normal to pass out when you stand up. I also have a lot of other weird health problems. That’s why I did not believe it was that serious because I thought it was related to something else.
Is there a good video explaining what this disorder actually is and how to live with it properly?
Thank you so much for this comment!!! I have pots too, and I was really confused because I looked up the symptoms and I literally had all of them! Then he says it isn't real? It makes me really confused and kinda angry too 😂
POTS is real in the sense that patients are definitely being affected by something. But right now it isn't really known what the underlying cause is.
I've heard people recommend a symptoms management perspective, like working a job that doesn't involve lots of standing to reduce the risk of falling over.
Yes there is. Look up Summer Dashe. She excellently explains what it is because she has it and it ruined her job as a news anchor. She notes all the symptoms. A really great video. Hope it helps. 🌞🦋🌷
It could be cervical spine instability...
Ur vagus nerve or jugular is been pinch by the c-1/c-2 vertebrates... prolotherapy can help...
When i was a kid i fell on the ice near my tailboe area, and as an adult i still get pain there and have has pots since i was a teenager. Could it be from my fall?@@Shigami-lb6oc
Thank you, I found what you said to be informative.
When I get up I feel like I’m gonna fall over but I think that just iron deficiency (also last night I was laying down for hours and decided to get up and go to bed and I felt dizzy and lightheaded)
Not all people collapse though and it can be when you stand up suddenly that you experience symptoms like an increase in heart rate of 30bpm or more
Postural (pertaining to posture)
Ortho (upright) static (standing)
Tachy (fast) cardia (heart)
Literally fast heart rate related to upright posture
Thank you Sir for your explanation. What causes those symptoms doctor ?
SNS activation due to autonomic nervous system dysfunction (Dysautonomia).
Hi Dr. Just a quick question. The criteria regarding POTS and the rasing/elevated Heart Rate upon standing is quite unclear. So my question is: should the heart rate be manitained @ >30 beats per minute uppn standing and for how long should it be maintained? (E.g if your HR increases to > 30 beats per minite but in the next minute it drops to below 30 beats and steadily decreases to a normal range within 3 minutes. Does this still fullfill the criteria or do you need to maintain the >30 beats for the time you are standing?) thank you for this channel you are creating such massive awareness. Respect to ypu sir!
The criteria says that you should have sustained heart rate increase by 30 points or 120 per minute at the end of 10 minutes.
@@renu653 It’s just if it increases by 30bpm (40 for adolescents) or to over 120bpm at any time within the first 10 minutes, it doesn’t say that it needs to be sustained in the criteria.
Somehow people are not discussing the usual drop in blood pressure with POTS. And the elevation in heart rate is not necessarily a tachycardia.
Medicine is so fascinating
I have POTS. Can I get rid of it? I have had it for almost 12 years. It is probably caused by EDS.
Check " cervical instability " and pots
Really? Interesting, I'll look that up.
But it’s only happened like 4 times from completely diffrent stuff over a few months (don’t have it diagnosed but heard a part of it is linked to audhd so wanted to look into it bc i related to the other video)
Can you receive a diagnosis though? I’m so tired of being judged and people thinking I’m perfectly healthy because I look that way. And anxiety being blamed.
Yea
Yeah, you can. I was diagnosed with it thru a tilt table test.
I had this for a while but I also got blind for some seconds and I could only see blacl I thought it was nothing and I stopped having it
I get very tired an fatigued when I eat ,so I just eat in the evening before bed, an I have been dealing with a foggy headache for the last 3 years, I can't get in a car when my head is foggy, it's made my life really bad for the last 3 years, I have been trying to figure out what it is but I only have a few symptoms of POTS, Dysautonomia is one I found out about just today, I hate this I wish it would just go away, God bless
I have this, i always faint after long period of time or sweat, and feel weak when standing for something, once I did, tai chi and almost passed out and though I just had low stamina. Had semi seizures and complete blacks out all the time. I though it was normal.
Omg i had this condition 😮. I thought it was due to lack of physical exercices or anemia.
Had? What was it? Can you explain? Thank you
Find the video on my channel called “causes of Dysautonomia.”
Pots/dysautonomia is caused by damage to the neurons mine was caused by a TBI I got as a child. I was working as a medic in 2020 and got Covid and it made my pots/dysautonomia put me on my death bed for 3-4 years… I am now very well after I figured out neurogenesis. Still have dysautonomia/pots but very well managed
What did you do to get better?
@@ExtraordinaryJam it’s a lot to explain. I’ll make video and post it subscribe
@@SethWebb-fr8tx I'll be waiting for it then, thanks for replying!
@@ExtraordinaryJam your not going to see it if you don’t subscribe. (I’m not some random wannabe UA-camr I’m legit person that was on my death bead with dysautonomia for years! If you feel that I could give you any useful information I will 100% make a video explaining everything)
My daughter is 14 and suffering with these symptoms for years now she’s her blood pressure is low but when standing her heart rate goes up fast
Then it can drop fast too
Nerdiing help as it’s taking her childhood away
Dysautonomia International is a phenomenal resource for information.
This happens to me too
I wouldn't cause 2mins prolonged personally. I couldn't stand for a prolonged period.
Lord help us
Wait so thats probably why I feel like ima pass out if I stand too long or get up too fast? 😬
Have you figured it out if you have Pots or not? It's been 9 months since you posted this reply. Look for the poor man tilt table test on youtube. It will give you an idea of how to test it on your own if you have it or not.
Tremulousness? Is that a weak shaky feeling?
Yes.
I’ve my TTT at kings college with Nick Gall on 30/5/23 finally the Northern Ireland Drs have sent me to get help after years of medical gaslighting. The medics over here really need to be trained on all types of dysautonomia ❤
@@PoTSdysautonomia Glad to hear that!
@@Catlily5 I’m so glad to be getting tests finally then hopefully some treatment options! Thank you for your reply x
@@PoTSdysautonomia It took me 10 years to get diagnosed with POTS. It can be very frustrating. I wish you the best!
This happens to me but I thought was from something else I wash I knew . I don't have a single doctor n I haven't gone or told them to much I get scared but I need some help
.My husband has heart condition he has vomitied in these two days he says he is fine, do l have to worry?
oh uh, my name is pots... uh oh.
So what is actually going on
a drama
SNS activation due to autonomic nervous system dysfunction (Dysautonomia).
I think it's in the dysautonomia family, not sure.
POTS what is the most common form of Dysautonomia (autonomic nervous system dysfunction).
@@michele0324
others include pure autonomic failure and multiple system atrophy. Those disorders can cause supine hypertension as well as orthostatic hypotension. Studies have linked supine hypertension to the same cardiovascular issues as essential hypertension. They compared multiple system atrophy patients with supine hypertension to those without. Those with supine hypertension had increased left ventricular hypertrophy along with changes in white matter and renal function, and most importantly, shorter survival. I lost my dad after a diagnosis of MSA. It also affects peripheral circulation in a way that the extremities are cold. My dad had the "cold hand sign" and at the time I wondered about diabetes, as both his brother and their dad had type 2 diabetes.
Why is my heart beating hard and irregular when i lay down? It is since having COVID
Dysautonomia.
Follow a low histamine diet with salt and water.
Please ask your people that make all the videos about “pots” why they don’t allow comments….
what can we do
Try a low histamine diet and increase water intake, also a daily vitamin. Of course to much water intake can also be dangerous and I'm not a doctor, but this works for me.
For engineers it means plain old telephone service 😀
Yep, old box of adapters, plugs, testers in my garage has POTS written on it. About to get pitched out.
I think it may be connected to trauma/stress
High stress level creates a histamine response, when you combine that with foods high in histamine, you can get pots symptoms. I've been taking a daily vitamin and implemented a low histamine diet. My symptoms are nearly unnoticeable now. I miss hot sauce and cheese but I love feeling good better.
Can u pls tell what foods u need to avoid pls u said hot sauce and cheese and what vitamins do I need to take@@brandyanon8789
I think pots is secondary to mast cell activation. I think all pots is just mast cell activation. Maybe lyme disease, toxic mold exposure. If i follow a low histamine diet combined with pots recommended water and salt. I feel great.
Also autoimmune conditions.
How much water and salt is recommended ?
@@adamjackson7585There is no one- size-fits-all amount and the guidelines you'll find online are just that; guidelines. Salt can worsen symptoms in those with Hyperadrenergic POTS.
POTS is heterogeneous. Meaning there are multiple etiologies (root causes).
Hello sir I am from India, the symptoms you are telling i am suffering from last 24 months and dr in india diagone with anxiety is there any cure for POTS please reply I am very help less
Hi contact Deepak padbanaman cardiologist in Bangalore.
This is so difficult to treat.
His voice is so smooth. He’d make a great narrator
“Sometimes as doctors, when we can’t explain what’s going on we just give it a name ….” to shut the patient up. Hummm, we don’t investigate, we don’t attempt to figure it out, look into, etc. We don’t actually try to understand what the patient is suffering from that results in their symptoms. It could be something in the patient’s head, how are we supposed to find any cause if it is in their head? Ugh, why bother it’s easier to just slap a convoluted medical name on it and send the person on their way. Heck, I can be a doctor myself AND apparently no university degree, training, rotation, etc. required anymore! 😎
Oh yea when i stand up, then im blind
What’s pots
my least favorite doctor word is idiopathic, even tho i get the need for it
Oh I thought fibromyalgia was the catch all! 😂
Should we say that you don't know what your saying either. Don't u do the same when a patient comes in your office with a concern. You go in your office and read a book on what might be going on!! How dare u!!! Your nor GOD !!! NOW GO READ THAT!!
Most doctors are dismissive, aloof and generally not interested.
RESPECTED DOCTORS "POTS"MEANS DOCTORS ARE PESHENTS HEALTH KEEPING POTS STOP THEY'RE SICKS DOING HUMANS IN TOPS ALWAYS DOCTORS ARE DURING PESHENTS HEALTH KEEPING SPOT
A VALUABLE POST IS POTS For
RESPECTED DOCTORS 💓
OKAY thanks
LOVE EVERY THINKS
UNDER THE ⛅ SUN
K A HABEEB RAHAMAN ROWTHER PALAKKAD BHARAT 👍
JAI HIND JAI BHARAT
No when patients stand they get said symptoms, there's muscle instability, tremors, hot sweats, chest pains, passing out & an increased heart rate yes are symptoms but that's not all too it. The sickness that's been no reason till then, the excessive bleeding it can cause. Juat because some patients only have said symptoms a lot of us have a lot more than that.
MEE
POTS is a vaccine injury.
I never got the vaccine or any vacccines, nor did my mom, but I have eds, pots and mcas, so....?
@@staym925 is that true
@@staym925yeah same. I’m pretty sure my teenager has POtS and was never vaccinated at all
@annie.hi. pots is an inherited issue, and goes hand in hand with other issues, along with having pots, I also have celiac diesease, ehlers-danlos-syndrome, and Mast-cell -ctivation-syndrome. Some of these issues like ehlers-danlos-syndrome goes back hundreds of years.
Dude please....😂 Enough with the fear mongering. There were WAY more complications including death with Covid. No matter what your UA-cam ex-doctor says.
Yeah. I can make up 💩 by myself and save myself a few $K.
Well hypochondriacs love having fancy sounding "conditions", and Doctors a way to stop malingerers wasting their time.
You can't really understand another person's experience until you've walked a mile in their shoes."
Ya, that is not how it works. What he is describing is similar to nauseousness, big word describing a symptom people feel. If you ever felt nauseated in your life? Then you are a hypochondriac? Ridiculous …
POTS is a symptom of a bigger problem. I had pots as a teen because I was on a doctors order, for an extremely reduced salt diet.
Was I making up pots or purposely causing myself to faint? And almost faint on a tilt test? NO!
I was born with a narrow Aorta and a Hole in my heart.
Many people who have pots have physical heart problems and/or EDS, or Post Covid symptoms.
Do your research please.
Just because you can not see it with your eyes does not mean it is not real.
In fact that attitude is dangerous.
I had people in my life push me past my physical limit, more than once, outside of the medical world because they did not believe a young person, of good weight, who looked well-ish, could surely not have serious heart issues. That theory is beyond dangerous and factually incorrect. And beyond critically dangerous.
Lastly and my final statement. After brexit in 2022 there was a shortage of 11,000 physicians in the nhs. And here in America we have a massive shortage as well. The idea that a physician would feel the need to make happy and “feed a faker” to acquire money for appointments, financially for a living is absolutely insane. And factually invalid.
But cool … you do you 😎
Do you have pots? If not please don’t comment. We know what we are going through. Definitely not a hypochondriac situation.
He literally said that when measuring the heart rate it does elevate upon standing. There is even a test for yhis