COVID-19 (Coronavirus) discussion

I wonder what the chemical triggers for that were? As someone who's heart can occasionally decide to jump to 130+ for no reason I know its an uncomfortable feeling.
The thinking is that the vagus nerve can be attacked during covid and that controls all the automatic processeses.

The theory is there is viral persistence that is delaying repair.
 
The thinking is that the vagus nerve can be attacked during covid and that controls all the automatic processeses.

The theory is there is viral persistence that is delaying repair.

I was wondering more which food or ingredient triggered the tachycardia? I sometimes suffer from supraventricular tachycardia and it can last from a few seconds to 20+ minutes, that is rare though. I have had spicy food trigger it in the past. I can often stop it by taking a deep breath, holding it and bearing down like you are having a poop, it can stop it instantly. Fortunately I don't get shortness of breath or feel feint. That must make it feel so much worse.
 
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I was wondering more which food or ingredient triggered the tachycardia? I sometimes suffer from supraventricular tachycardia and it can last from a few seconds to 20+ minutes, that is rare though. I have had spicy food trigger it in the past. I can often stop it by taking a deep breath, holding it and bearing down like you are having a poop, it can stop it instantly. Fortunately I don't get shortness of breath or feel feint. That must make it feel so much worse.
I think in this case it is probably the dark chocolate cocoa I was eating.

I also seem to get problems when I take vitamin d drops with olive oil. I'm going to get a different type of vitamin d soon just to make sure it's not the vitamin d itself.
 
The thinking is that the vagus nerve can be attacked during covid and that controls all the automatic processeses.

The theory is there is viral persistence that is delaying repair.
You probably have POTS. I developed that as part of my long covid. I couldn't take anything with caffeine in it, including chocolate otherwise it would make me feel considerably worse. In POTS, your body pumps out excess noradrenaline ( and sometimes adrenaline ) which is what precipitates the fast heart rate and other related symptoms which can include nausea, migraines, anxiety and panic. Any substance that exerts a stimulatory effect will exacerbate the situation eg. caffeine.
 
A note to myself, don't have a curry and then later eat dark chocolate. My heart rate went up to 152 :eek:

I'll be glad when this is over.

Wow that must have been strange considering you didn't do any exercise / movements. I mean when I'm doing a MMA session I know it can get high but having that without any physical activity my be quite disconcerting. Do you know how to do some meditative breathing? Might help bring it back in control quicker.

4 months on and the tinnitus I got from covid still hasn't completely gone away. Might end up trying prednisolone and see what happens.

I've had tinnitus for 16+ years so I feel your pain - but then again I also suffer from hearing loss (head injury - also caused the tinnitus). I did some CBT-style sessions to learn to cope with it, but I also often put some background noise on to mitigate it which is really helpful (especially if you wear hearing aids).
 
Wow that must have been strange considering you didn't do any exercise / movements. I mean when I'm doing a MMA session I know it can get high but having that without any physical activity my be quite disconcerting. Do you know how to do some meditative breathing? Might help bring it back in control.
It was very odd as I was wearing an oximeter that reads oxygen and heart rate, so I was sitting still watching it going up. I could feel the adrenaline before it set off.

I'm going to look in to breathing exercises.

I think I have some kind of pots because I've noticed if I drink water and take some magnesium it tends to keep under control.

I had asked the doctor for a beta blocker but they don't want to give me any because I already have breathing issues and they are hoping it goes away eventually.
 
It was very odd as I was wearing an oximeter that reads oxygen and heart rate, so I was sitting still watching it going up. I could feel the adrenaline before it set off.

I'm going to look in to breathing exercises.

I think I have some kind of pots because I've noticed if I drink water and take some magnesium it tends to keep under control.

I had asked the doctor for a beta blocker but they don't want to give me any because I already have breathing issues and they are hoping it goes away eventually.
Good luck with whatever solution you find to it :)
 
It was very odd as I was wearing an oximeter that reads oxygen and heart rate, so I was sitting still watching it going up. I could feel the adrenaline before it set off.

I'm going to look in to breathing exercises.

I think I have some kind of pots because I've noticed if I drink water and take some magnesium it tends to keep under control.

I had asked the doctor for a beta blocker but they don't want to give me any because I already have breathing issues and they are hoping it goes away eventually.
You'd probably still be safe with cardio-selective beta blockers eg. bisoprolol. Failing that ask for a referral to a Cardiologist. They could prescribe ivabradine as an alternative which won't affect breathing/asthma. Does seem likely you have some form of dysautonomia - POTS falls into that category, as does IST ( isolated supraventricular tachycardia ) and both are common in the aftermath of covid.
 
Wow that must have been strange considering you didn't do any exercise / movements. I mean when I'm doing a MMA session I know it can get high but having that without any physical activity my be quite disconcerting. Do you know how to do some meditative breathing? Might help bring it back in control quicker.



I've had tinnitus for 16+ years so I feel your pain - but then again I also suffer from hearing loss (head injury - also caused the tinnitus). I did some CBT-style sessions to learn to cope with it, but I also often put some background noise on to mitigate it which is really helpful (especially if you wear hearing aids).

I've had tinnitus caused by my TMJ since 2016 - it was triggered when I clenched my jaw far too hard one time. I have no idea exactly what that did to cause it, but there was always the hope that one day it could get sorted. I still haven't gotten used to the constant flashbang in my head. The covid infection adding another new tone is just a nail in the coffin as far as I'm concerned.

I had no obvious signs of any kind of ear infection while I had covid, but I did lose my ability to pop my ears (which I have regained). I'm hoping it is just latent inflammation of the Eustachian tubes and a course of steroids will fix it right up.
 
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You'd probably still be safe with cardio-selective beta blockers eg. bisoprolol. Failing that ask for a referral to a Cardiologist. They could prescribe ivabradine as an alternative which won't affect breathing/asthma. Does seem likely you have some form of dysautonomia - POTS falls into that category, as does IST ( isolated supraventricular tachycardia ) and both are common in the aftermath of covid.
I'm due to have a phone appointment tomorrow, though the whole process is very slow. I'm still waiting for a radiologist to read a high contrast ct scan I had done about 5 months ago.

When I was in hospital for checks they didn't do much apart from an x-ray (that hasn't been looked at) and some blood tests. Then they mentioned about the gp giving me a heart monitor belt. But I haven't heard anything so far. They have an appointment for an echocardiogram waiting for a date. These tests are in preparation for hopefully a cardiologist referral, which I think the gp as to make as hospital doctors can't refer to each other.

The whole process seems like a very long drawn out process.
 
My echocardiogram took about 5 months, I’m still waiting for the cardiology dept to get in touch after being referred last November (or maybe February as I’m sure my GP forgot). My issues are Atrial Fibrillation which used to be 20 second episodes occasionally over 10 years, till last October with 2 hours over 200bpm. A few long ones since resulting in long waits in A&E, one of which felt like a fish flopping about in my chest which woke me up, thought it was in its last gasps.

Hope you don’t have to wait as long.
 
I had no obvious signs of any kind of ear infection while I had covid, but I did lose my ability to pop my ears (which I have regained). I'm hoping it is just latent inflammation of the Eustachian tubes and a course of steroids will fix it right up.
Could be mucous I had the same with the last bad chest infection I had, once the antibiotics cleared that up the tubes cleared after a few days (like a dam bursting, had this revolting taste at the back of my mouth)
 
I'm due to have a phone appointment tomorrow, though the whole process is very slow. I'm still waiting for a radiologist to read a high contrast ct scan I had done about 5 months ago.

When I was in hospital for checks they didn't do much apart from an x-ray (that hasn't been looked at) and some blood tests. Then they mentioned about the gp giving me a heart monitor belt. But I haven't heard anything so far. They have an appointment for an echocardiogram waiting for a date. These tests are in preparation for hopefully a cardiologist referral, which I think the gp as to make as hospital doctors can't refer to each other.

The whole process seems like a very long drawn out process.
Hospital specialties can make referrals to each other, unless they are being lazy. But waiting lists for things like echocardiograms can be very lengthy ( almost a year in my neck of the woods ). For diagnosing POTS, you can do a quick test yourself if you have a device that can measure your heart rate eg. fitbit, Apple watch etc. Lay down for several minutes and measure your resting heart rate, then stand for 10 mins. If your heart rate increases by 30bpm or more there is a strong chance you have POTS. Anyway, sounds like you're on the path to being investigated, which is the main thing. Hopefully you get to the bottom of it soon.
 
Could be mucous I had the same with the last bad chest infection I had, once the antibiotics cleared that up the tubes cleared after a few days (like a dam bursting, had this revolting taste at the back of my mouth)

One of my colleagues recently had it for the 3rd time, 3 weeks on from returning to work still have a lot of mucous and sound like they are 2 days into a cold still which is a bit disturbing. Surprised no one else got it as they came into work symptomatic and only had 3 days off before returning again.
 
Now on the nasal steroids for a month. GP who previously did ENT says it sounds like classic ETD, so wants to see how I get on with the roids for now.

If no improvement, stronger roids.
 
Really nasty run of colds going around here at the moment, doesn't seem to be COVID, think it is the same one as people getting the same horrendous runny nose/bunged up sinuses as above one of my colleagues still sounds bunged up weeks on, just started going around at my brother's work and he has got it at the moment :( so dunno if I'll escape it. So far not picked it up, at least symptomatically, from people at work or other acquaintances.
 
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Really nasty run of colds going around here at the moment, doesn't seem to be COVID, think it is the same one as people getting the same horrendous runny nose/bunged up sinuses as above one of my colleagues still sounds bunged up weeks on, just started going around at my brother's work and he has got it at the moment :( so dunno if I'll escape it. So far not picked it up, at least symptomatically, from people at work or other acquaintances.
I think my brother and I had that about 6-8 weeks ago, nasty cold type thing, seems to go away for a few days then comes back, largely clears off again but lingers for weeks.

It did a good job of knocking me flat enough that I did several covid tests to make sure it wasn't that.
 
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