Live data from Hacker News

Burden of post-Covid-19 syndrome and implications for healthcare planning

journals.plos.org

181–190 of 280 posts

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#181

Earlier quoted context omitted.

In my early 30s: Pretty sure I had COVID-19 in early March 2020. I had shortness of breath for a couple of days and I was feverish for about 8 weeks. Afterwards, I have severe fatigue. I also experienced bouts, off an on for like a week or two at a time, where I could not physically get warm, and I was freezing to death, no matter what I did. I also have severe dysautonomia (autonomic nervous system dysfunction) whic…

Which Garmin watch model do you have ?

Here's a list of supported watches:

https://support.garmin.com/en-US/?faq=VOFJAsiXut9K19k1qEn5W5

By coincidence I was looking to buy a Garmin smart watch!

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#182
Been in lockdown for 18 months before I actually caught covid, to be perfectly honest most of the symptoms described for "long covid" I experienced from being locked down, after actually having covid I haven't noticed much of a difference (once my smell and taste returned, thankfully that was soon).

Low energy, out of breath, etc. You have to keep in mind most of us are doing a fraction of walking around that you would do from a commute and it can make a huge difference over time. I was already getting out of breath running up and down one flight of stairs to answer the door after 6 months staying at home, embarrassingly I was one day interviewing a potential hire over video chat, quickly had to collect a package and could barely talk after running back upstairs, completely out of breath. I can see how a sedentary life kills people.

This is before we get into what depression, doom scrolling,Journalist created hysteria fear and dread, realizing there isn't much to life once a few factors are removed, loneliness, video call fatigue and isolation, lack of distance between work space and life space can do to your body and mind.

Doubt we'll ever get a truly objective assessment for the past year and a half for at least 10-15 years, if ever.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#183

Earlier quoted context omitted.

I am having daily heart palpitations and they are almost unbearable now. Sometimes I wake up and feel fine almost all day but not a day has gone by in the past two months where I don't have some kind of chest discomfort around my sternum/xiphoid process. I have had a whole bunch of scans and everything is normal. I will be having an endoscopy next week to hopefully get to the bottom of it. I am 'hoping' it is somethi…

This sounds like dysautonomia. I have dysautonomia, which I had long before (probably) getting COVID-19. I have a rare form of dysautonomia. But, dysautonomia does happen, relatively frequently, as post-viral cases. The good news is that post-viral dysautonomia has high potential for improving and even (realistically) going away. Rest will be the best treatment. Check my profile if you want to email me or want help.

I acquired dysautonomia from toxic exposure.

Turned out to be an underlying autoimmune disorder (Sjogrens) and a clotting disorder “factor 5 Leiden”

The exposure triggered both from mild barely noticeable problems to I was completely disabled.

Took years to figure out it out.

When I got covid it was basically the same event again. Took months for body to calm down again.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#184

Earlier quoted context omitted.

> Expressing skepticism surrounding the efficiency of social distancing, masks, "non essential business" and all these lockdowns is not a "far right" talking point. You're absolutely right. This kind of misinformation isn't limited to the far right. > To this day we cannot say for certain that lockdowns did anything at all, LOL, what? This is a truly astonishingly statement. Literally every place that instituted lock…

I am absolutely making this claim in good faith. Where is your studies showing these restrictions worked well enough to justify their immense costs to society? They don’t exist. To date I’ve yet to see a single cost benefit analysis done for any of this. It simply wasn’t allowed to be done… you’d get shouted down by the mob. It worries me greatly how little critical thinking has been applied to the last 17+ months. I…

> Where is your studies showing these restrictions worked well enough to justify their immense costs to society?

And predictably the goalposts shift.

First it was that we "cannot say for certain that lockdowns did anything at all".

Now it's that the results don't "justify their immense costs to society".

> and even then we didn’t know it would work going in,

Again: Lockdowns are a basic application of germ theory.

The only way they could not work is if infection didn't pass from human to human but was transmitted via miasma or aether.

You could absolutely make valid arguments for or against specific lockdown policy choices (i.e. capacity limits, sizes of gatherings, types of businesses affected, etc).

But lockdowns in general? There's piles of evidence that shows they're extremely effective. Heck, in my own city, we saw a massive spike brewing prior to Christmas, and once a lockdown was instituted, the numbers immediately began to fall. That pattern is repeated anywhere you care to look.

I honestly refuse to spend any time citing data for you, as I do not believe for a second that you're arguing in good faith. If you really wanted to find facts, you could easily dig them up. That you haven't done so tells me everything about your willingness to question your own beliefs.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#185

Earlier quoted context omitted.

> [edit] here come the downvotes, for those that do, note that downvotes, at least on HN, are not meant to express disagreement, they are meant for content that is objectionable for other reasons. This is factually wrong. Search for posts by dang frequently explaining traditions and norms in this forum, including the downvote very much being a standard way to express disagreement (although it is better to voice your…

I didn't know that, frankly I remember reading, many years ago, people saying that downvotes are not meant to express disagreement. Maybe that changed, I personally don't agree with this and only consider downvoting if someone is not being civil, is not interested in discussion, or really voicing something obviously false. I was careful with my comment, I'm not selling anything, I was just interested in maybe nudging…

It's often said, but as pointed out not the case, and ~never has been for as long as there was anything resembling policy - pg commented on it in early days.

Fwiw, I'm not really a fan of it (and don't do it) either. But it's a lot harder to upvote not-objectionable things (so many!) and not upvote things purely because you agree (tempting!) - so I suppose it makes sense. I've thought before about making a 'proof of concept' type commenting system where its designed around not/objectionable; the default as you scroll past things would be to up-vote them (automatically), only down-voting on intervention when 'this does not contribute to the discussion'. Meh, might be interesting, but I'm not interested enough that I've gotten around to it :).

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#186

Earlier quoted context omitted.

This sounds like dysautonomia. I have dysautonomia, which I had long before (probably) getting COVID-19. I have a rare form of dysautonomia. But, dysautonomia does happen, relatively frequently, as post-viral cases. The good news is that post-viral dysautonomia has high potential for improving and even (realistically) going away. Rest will be the best treatment. Check my profile if you want to email me or want help.

I acquired dysautonomia from toxic exposure. Turned out to be an underlying autoimmune disorder (Sjogrens) and a clotting disorder “factor 5 Leiden” The exposure triggered both from mild barely noticeable problems to I was completely disabled. Took years to figure out it out. When I got covid it was basically the same event again. Took months for body to calm down again.

Yep, I am in the exact same position as you. I lost at least a year of my life due to this post-viral syndrome. I am back to where I was prior to getting COVID-19, though. When I was really sick in March 2020, I thought "wow, I haven't been this sick in a long time". It really was like going back to square one. It was super scary, too, given the health problems that I have.

I have autoimmune autonomic ganglionopathy (autoimmune dysautonomia), which is believed to have caused my type 1 diabetes (autoimmune and insulin-dependent). It is also believed to have caused other endocrine problems and other neurological problems (I have another immune-mediated neurological disease affecting my peripheral nervous system). Anyways, autoimmune autonomic ganglionopathy is very rare, and I have the antibodies (about half of people do not), so I am tremendously lucky.

Anyways, I would be interested in chatting with you. If you want to do so, my email is in my profile information. I am very resourceful and I have tips.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#187
A theory that I ascribe to is that Long Covid is viral induced CFS/ME. As someone with hEDS I've battled CFS/ME for most of my life. I don't want to celebrate too soon but in the last few weeks do I feel like I have now won the battle. I just started using a combination of very powerful but targeted drugs. I feel 110% and no longer get Post Exertion Malease (PEM) which is a major indicator of CFS/ME.

I take Low Dose Naltrexone, Testosterone Cypionate, BPC-157, TB-500, Mod GRF, Ipamorelin, Thyroxine (T4), and Triiodothyronine (T3). I take a ton of vitamins but the effective ones seem to be the megadoses of B1 and B3. I also take NMN for NAD+ deficiency but I'm not sure if that is doing anything. I eat a low carb diet and take cold showers and work out every other day.

Low Dose Naltrexone is great for brain fog and I've been taking it for 5 years.

The Test, hGH peptides, and T3/T4 is probably responsible for the bulk of my improvement. I've only been taking them for a few weeks and it's night and day difference.

I'm not saying this is for everyone but it definitely worked for me so it may help others looking for ideas.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#188

Not “long Covid” but my sense of smelling/tasting is still not the same after 6+ months. I had mild symptoms, but my sense of smelling and tasting were totally gone for a few weeks. After a few weeks it turned almost back to 80% only intense smells (like gasoline, garlic and diapers :shrug:) were filtered out. Since ~3 months these things stink intensely with an indescribable way… (I guess the diapers always did ;))…

I feel for you, I completely lost smell and taste and it was extremely scary, you don't know how bad it is until it happens and you can't tell if your teeth are clean, your clothes are clean, your milk has gone off, it's crazy to put fragrance on and put your wrist to your nose and there's nothing. Eating suddenly becomes a miserable chore, I normally cook a lot but just ended up eating ramen and fruit and only when my stomach called for it.

Thankfully mine returned mostly after 2 weeks, some things maybe smell slightly different but I think if I was one of the people to have it for 6 months or not at all I'd be pretty deep in depression by the end of it.

I saw some comments online saying long term sufferers returned after taking Vitamin-D and Zinc. I was already taking D but ordered zinc and started taking it as soon as it happened. Could be quackery, normally wouldn't post something like that on HN but only doing it in case that was the reason mine came back so quickly because I know how much it impacts your quality of life.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#189
post #58

Earlier quoted context omitted.

Ah yes, the heart thing. Forgot to mention that because it hasn't happened for a couple of months now but I would wake up at night every now and then with my heart going like I just ran a marathon. But that fortunately completely went away. As for lung capacity: I used to play saxophone pretty fanatically and I think that is one of the reasons I got through this with a relatively low amount of damage.

Sounds terrible. Did you (and u/mygoodaccount) have loss of smell among the symptoms? I recall reading somewhere that it correlates with protracted recovery.

My sister had this. Even today (5 months after infection) she says some things taste and smell funny. She can't eat mint ice cream anymore because she says it tastes like cigarettes.

Re: Burden of post-Covid-19 syndrome and implications for healthcare planning

#190
How do you disambiguate "long Covid" from the very real fact that people are incredibly suggestible.

My father-in-law was convinced he had long Covid. He talked about it all the time.

He was never diagnosed, but he had a cold near the beginning of the pandemic and he decided it was Covid.

He claimed he could run up and down the steps at the park before getting Covid. Now, he claimed, he was always breathless. I exercise him and he'd be convinced exercise will do nothing because of his long Covid.

Of course when he got tested he had no antibodies.

But it's not just that. During the height of the pandemic, did you notice yourself, or notice in others, that people were always thinking Covid was coming on? Every little pain or weird breath and people became very worried.

The brain is incredible at turning normal sensations into symptoms. We don't realize all the sensory input we're constantly discarding until we start becoming hyperaware.

The incentives for the media to hype long Covid and for researchers to find long Covid is incredibly intense. Every shred of evidence will by hyped to the moon. Every other person you meet with a panic disorder or heart condition will have a story attributed to Covid. Ordinary people will have absolutely zero way to contextualize the true risk.

Post reply on HN