I got Omicron in January '22 despite being double vaxx'd, and I felt totally fine until 3-4 mo. later when I started to get recurrent dizzy spells, major fatigue, and bouts of anxiety, which are all very unusual for me. Checkup / bloodwork showed nothing. I am 41 y.o. who exercise regularly, does not smoke, rarely drinks, etc.
So far I can still function and maintain a job, but it makes me wonder what's going on inside of me that 11 months later it's still causing these issues regularly. Our 4 y.o. son got it as well and although he was asymptomatic I am still very concerned about what the long-term effects on him may be.
I am not a doctor and this is not medical advice, but I read a paper saying that hyperbaric oxygen therapy helped some people, so I've been using Wim Hoff breathing as a poor man's version. It does seems to help with the fatigue but not the vertigo. Best of luck.
Wim Hoff Breathing: https://www.youtube.com/watch?v=tybOi4hjZFQ
Honestly, I feel very lucky to be as functional as I am. I do worry about how medical and political systems are responding to COVID and long COVID, but largely I think good care is going to come from the bottom up and not top down. I'm comfortable(ish) with a reality that I might just suddenly drop dead tomorrow, but this experience has given me a new appreciation for the health I have that I could not have fathomed before. Because I can alleviate symptoms with diet and directed exercise and it does appear to have a cumulative effect on their reduction, I think recovery is possible without intense intervention. I don't even mind being more spacey and a bit dumber. It suits me a bit and has changed the pace of my life in a way that once I embraced has been good.
My biggest worry is that if I suddenly die and how devastating that would be for people that depend on me, but I think without an infection of a new virus or several viruses I might live a shorter, but alright life. My chance of suddenly dying because I got light headed in an elevator now being slightly higher than my chance of being crushed by a vending machine.
Thank so so much for this. Very useful information.
One of my inner ear canal output signals dropped by about 75%. There is a diagnostic test they can do; more basic tests showed nothing but this more sensitive one showed it clear as day. No-one can tall me WHY the nerves are outputting a weaker signal and I couldn't tell you if it's related but it's something that doesn't get checked much.
If you had the information available, I'd be very interested to know the names of the diagnostic tests you took. Analysis of how I'm hearing is something I'm uniquely able to analyze over time and compare to medically conducted tests. While I think I know how the second test might have worked, I don't know what I'd call such a test to look for it.
I think analysis of hearing on newly infected to post care of people with COVID and Long COVID could provide useful hints that most other methods might not be able to detect.
It identified not just the issue but the actual specific structure that was giving me issues.
This has no impact on hearing, so wouldn't be caught by those tests.
I have no idea if it was anxiety or Covid, but the dizziness was disorienting, at the worst I couldn’t walk , it felt like I was on a boat. During this time I had anxiety attacks almost non stop-triggered by the vertigo. As soon as I started to notice the vertigo I would begin to spiral because it was so unprecedented and disorienting. It just cleared up on its own after 8 weeks.
Part of the vertigo was dizzy spells every time I stood up.
I had ~ptsd from it for a full year, every time I stood up I would brace for the vertigo ,
Hope you find some relief soon
[0]http://sanfordhealth.staywellhealthlibrary.com/Search/134,51...
Same thing can happen with EBV, where it is responsible for some flare up of symptoms post-infection, and chicken pox becoming symptomatic years after infection as shingles.
I wouldn't be surprised if long COVID symptoms are caused by latent COVID infections.
[1] https://www.sciencedaily.com/releases/2017/07/170717091954.h...
https://www.nationalgeographic.com/science/article/persistin...
Here is but one such paper - https://link.springer.com/article/10.1007/s11695-022-06338-9
> Gastric specimens from 26 (32.5%) patients and 4 (100%) cholecystectomy [gallbladder removal] specimens showed positive cytoplasmic staining for the anti-SARS-CoV-2 nucleocapsid protein in surface mucosal epithelial cells.
> The median time between initial COVID-19 infection and surgery was 274 and 380 days in the positive and negative staining groups, respectively (p = 0.371). It's not clear whether these had any long lasting symptoms since infection.
> The inclusion criteria were a history of COVID-19 with one or more gastrointestinal symptoms [during the acute phase] and a negative PCR test result at the time of bariatric surgery.
There are literally dozens of these.
The problem is that most people don't get tissues resected from inside their body when their alive and most such tissues are not tested for the virus.
With regards to the general question of persistent corona viruses, just look at FIP in cats for another such example.
The only confirmed cases of SARS-CoV-2 infections in humans lasting beyond a few weeks have been in immunocompromised patients. Their immune systems were able to somewhat suppress the virus, but not clear the infection. (There is a hypothesis that such patients were the sources for some of the variants because the extended infections gave the virus more time to evolve but that can't be conclusively proven.)
Thinking about this now though gives me some ideas that could even be testable that could help. Thank you for sharing this.
As far as I know I did not contract COVID, however I was part of the early response team for isolation after travel for the US Military so was exposed on several occasions early on and could have been asymptomatic.
My first vaccine was a non-event; the second fostered a reaction so bad I almost went to the hospital. 103F fever, rigor (shivering so bad you lock up), etc. for about 8 hours, then the fever broke and I recovered fine.
I had an anxiety induced possible cardiac event about a year after that (March 22), but I went to the ER and there was no EKG evidence and no troponin. Was monitored for 12 hours to be sure.
I have had a weird vertigo issue crop up; I actually managed to have exactly what causes it diagnosed! One of the inner ear canals has dropped it's output signal about 75%; no evidence to why the nerves were damaged. I am slowly adjusting. I have no idea if it's related.
Thank you for sharing more (probably this was your first post and I missed it) about your story and diagnosis. Seriously. Very helpful.
Happy to help!
In general, regular exercise helps strengthen the heart and reduce risks of CVD. If you're generally only exercising when you feel chest pressure and you do have CVD, your heart muscles aren't as strong and strenuous exercise can lead to problems. Going for a walk everyday would be better than exerting yourself irregularly, as the regular exercise will lower your risk of having problems when you do exercise.
[0]https://twitter.com/drclairetaylor/status/158936959572682342...
Ugh. I'm just gonna do some deep breathing in cold baths, maybe DIY a hyperbaric chamber, get better at pullups, buy a rowing machine, and cut out sugar. Likely by the time that's effective the damage done will be compounded, but at least I won't be left in a holding pattern of how fucked US medicine is.
One day she heard a very loud bang that she described as sounding like it was coming from inside her head. Shortly after she started getting dizzy spells, specially when getting up in the morning and when lying down to sleep at night. Every once in a while her left arm would go numb and she would lose strength in it.
She went to many doctors and it was the same story, they thought it was vertigo. Thankfully she found a better one who requested a brain CT scan which showed that she actually had had a mild ischemic stroke on the right side of her brain.
Hope you are feeling better now, take care!
I can feel my vascular system radiating from the center of my chest up the sides of my neck and out through my shoulders. It's got a bit of a slow ache and upper body stiffness when it's flaring up. When it's bad, sometimes I wake up with numbness that radiates from my chest out to my finger tips on the top sides of my arms.
I have no problems taking deep breaths. The injury does not seem to be growing.
After the cardiac issue I had in 2020, my bloodwork showed signs that there was a possible event. My EKG was fine. This was days after. I have a constant dull to really shitty headache in the top front inside my head that has been persistent from the thing that seemed like a mini-stroke. I have never really had headaches without a serious hangover for all of my life. I couldn't see my regular GP, still haven't been able to, but the doc I did see basically told me she thought it was vertigo and I needed to clean my ears. She checked my reflexes and some other things and said she could not recommend any further action without more events.
I'm 6' broad shouldered, and 210lbs. A bit chubby. I don't exercise a ton, but do some exercise, especially when the dinner plate flairs up. I don't smoke.
I've had a chest x-ray and it shows what looks like scarring in vascular structures radiating from my lungs. The forms kind of look on x-ray like the "ground glass nodules" that some people are experiencing. It's VERY hard to get a doctor that wants to do anything with me about this stuff. The fact that cardio makes things better and not worse is counter intuitive from traditional issues that look the same like Angina Pectoris. I've said since I recovered the first time (I've had it at least once more post vaccination but nothing was quite as near death as the first) that I felt cognitively and physically like I was 10 years older. I turn 40 next year. New research has been coming out showing that some people suffering from long COVID show aging of their CV systems of about 10 years.
It is going to take a long time to figure out what Long Covid is really doing to people. Some people that never showed symptoms get these things. Children are showing it too. The diagnostic criteria is really difficult and there is almost no treatment aside from some success with similar treatments used for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome[0]. I have found that most doctors don't want to touch it with a 200ft poll. The Red Cross says I should join an online support group[1]. A lot of the research is being done by scraping subreddits for people reporting symptoms because they vary so wildly and seem to have little correlation with the perceived severity of infection.
I suspect we may find a high correlation with exposure to heavy airborn contamination. Like living in a very polluted city, exposure to lots of dust or chemicals, or living in a building with black mold for extended periods. The minor feeling or easy to ignore/temporary damage done by those experiences creating cellular damage that makes cells in CV systems pop like popcorn when COVID does it's very unique number on vascular structures. The word Blood Foam was used once in a very early study on people who died from COVID. The images I remember from that study demonstrated that it is a pretty accurate term for what happens in the worst cases. I'm sure there are people with genetic properties that could just make them more susceptible as well.
[0] https://www.frontiersin.org/articles/10.3389/fmed.2020.60682...
[1]https://www.heart.org/en/news/2022/03/31/after-covid-19-expe...