Long COVID: What is it?

Long COVID: What is it?

Long COVID: What is it?

Describe ME/CFS. 

Post-exercise malaise: what is it?

What's going on with my friend?

Will a treatment ever exist?

COVID-19 is a recently discovered illness. It just dates back a few years. COVID-19 cannot exist without COVID-19. Additionally, it occurs in those who contract COVID-19 and experience these post-COVID symptoms for weeks, months, or even longer. COVID-19 is that. 10% to 30% of those who contract COVID-19 may also develop long-term COVID-19. Numerous, such as weariness, coughing, problems thinking, or even plain pain, are associated with long-term COVID-19.

These are the most typical. Some people will experience one or two of these symptoms, while others will experience all of them. There is a lot to discuss in this case. Therefore, to figure out what's going on and see if there's anything we can do, many patients with long-term COVID-19 experience brain fog, exhaustion, dysautonomia, etc. But long-term COVID-19 is much, much more than that; it's not just that. Many people suffer from heart disease, renal disease, diabetes, and excessive cholesterol. These are therefore the main long-term health repercussions of the SARS-CoV-2 infection, which affect almost all organ systems in the body.

Additionally, it exhibits similarities to the ailment known as ME/CFS, or myalgic encephalomyelitis chronic fatigue syndrome. The good thing about medical terminology is that it can explain what is happening just by reading it. Muscle pain, often known as myalgic pain, is present. Brain or spinal tissue inflammation is referred to as encephalomyelitis. Chronic implies that it occurs repeatedly. It is persistent, consistent, and repetitive. The two are not the same. It resembles running a long race more. You're worn out. Your battery is dead. The syndrome is also Because diseases typically have a recognized unique clause, syndromes are not always recognized as diseases. The virus that causes it is COVID-19. We don't always know what causes syndromes. A 2019 NIH report on ME/CFS states.

In addition to focusing and short-term memory issues, there can also be orthostatic intolerance, which is the inability to sit upright for therapy due to physical limitations. Not that a cure is readily available currently, however. Naturally, COVID-19 is the source of long-term COVID-19. Since it has been around for so long, ME/CFS may result from numerous infections. We're not completely certain. But are they equivalent? It's difficult to draw any clear distinctions between long-term COVID-19 and ME/CFS because we still don't fully understand both conditions. Between ME/CFS, also known as chronic fatigue syndrome, and long-term venous insufficiency, there is a great deal of overlap in the symptomatology, or the symptoms, clinical presentations, and phenotype if you will.

Long ago, COVID-19 encountered a sickness that they were unable to ignore. Although it is also believed that infection can cause ME/CFS, there has never been a widespread pandemic that has affected millions at once. But it was more difficult to identify the virus that might have been to blame. Additionally, the fact that ME/CFS is accompanied by post-exertional malaise, or PEM, does not help. And others are experiencing it in this way. When this happens, even small tasks like checking your email or getting out of bed to boil water for pasta cause the body to require an absurdly high quantity of rest. This is not like depression when you lack drive, and it comes from within.

Physical exhaustion from this is likely to make resting ineffective. Even hours after going to bed, you could still feel worn out. 12 hours or 2 days after the physical or mental action that caused them, symptoms may start to show. Yes, mental exercise once again, reading texts and checking email. This may lead to an escalation of PEM. Imagine being rendered unconscious for days by simply reading about your disorder or listening to a doctor. Now that there are so many overlaps and a lengthy history of COVID-19 mimicking ME/CFS, it's difficult to deny that anything is wrong. We don't understand why some individuals contract COVID-19 and then experience severe exhaustion, post-exercise malaise, mental confusion, and muscle discomfort.

And some individuals, you know, manage to survive it unharmed. It could be a genetic predisposition, environmental variables, the severity of the first illness, how their body and immune system responded to the infection, or the fact that their body did not eliminate the virus. Depending on how much overlap there is with long-term COVID-19, there may be between 800,000 and 2.5 million ME/CFS sufferers in the United States now. It has been difficult to identify ME/CFS because of the anomalies that have been discovered in so many systems throughout the past 35 years of research, starting in the 1990s. Not simply because it has such a large impact, but also because doctors don't think anyone has it. Doctors believed.

All of it was in your head. And even now, although millions of people are affected, that mindset persists. These two situations, in my opinion, are positively genuine. I believe that ME/ECFS has received insufficient funding, research, and evaluation and that patients have not been truly treated seriously. For more than a century, we did nothing about the post-viral state. As a result, we underinvested in that, and when Long COVID appeared, we were taken off guard. We would be in a much better position right now than we are if we had paid heed to the ME/ECFs immunity. Research on long-term COVID-19 and ME/CFS has benefited from their similarities. Do individuals have ME/CFS or not? Was the main worry in the largest study I could find.

If we don't know what the underlying reason is, how can we be certain?

They were also very selective about who could participate in the trial. A “two-plus-week stay” was reported for potential patients at an NIH facility. Exercise tests, mitochondrial evaluations, metabolic chambers, immunological assessments, brain scans, muscle biopsies, and spinal fluid pulls were all performed on the subjects. Up here, this is comparable to House, MD. Although the study has not yet been published, it is currently undergoing peer review, and once it does, the ME/CFS and long-covid communities could benefit. Once there has been a “real study” of these phenomena, it is difficult to deny that they exist.

Additionally, the overlap does suggest that funding for both types of studies may be available, which is positive and suggests that we may eventually find a cure for both. There are no medications for long-term COVID-19 on the list of FDA-approved ones. Countless millions of people have long-term COVID-19. Not one or two, this. Depending on the figures you use, there are essentially 14 million, 20 million, or 26 million individuals in the United States alone who have long-term COVID-19 and millions more who are afflicted with it. COVID-19 is a fundamental problem, and we need to know how to handle it. It is comparable to plumbing. We were able to stop the leak.

It's catchable in a bucket. We can replace the items that have been damaged by water, but we can't stop the flood because we can't locate the leak. However, there are some hypotheses about the origins of long-term COVID-19 and ME/CFS. Pavloxid is being studied for its ability to get rid of lingering infections in the body. That might be one reason. In cases where micro clots are impairing blood and oxygen flow, studies are looking into blood thinners and anticoagulants. Of course, there is also the option of treating the disease's symptoms. Beta-blockers are a treatment option for someone whose heart beats rapidly. We offer a remedy for people who are experiencing muscle soreness.

However, many medical professionals are mono-specialists who focus on the nose, throat, feet, eyes, brains, and overachievers. The funding for research is often divided to account for those specialties. Normally, brain and lung specialists do not work together, but in this case, they must. ME/CFS and long-term COVID-19 are multi-system syndromes. Since Long COVID didn't exist before 2019, there was no single research organization to address it. But that's no longer the case. Numerous medical professionals, including experts in Alzheimer's, infection, neurology, and nephrology, are all concentrating on this.

However, it takes time. We just cannot afford to say things like, “Oh, yeah, I'll conduct a trial and report back to you in ten years.” To determine which pharmaceuticals on our list of possible ones work and which ones don't, we need to keep hunting for items that work. What about PEM, then, if we can just focus on symptoms? How do you handle fatigue? Pacing is the term used for that. It's a lifestyle change. In essence, you organize your day knowing how much energy you have to work with, similar to the stamina gauge in “Zelda: Breath of the Wild.” You must exercise self-control to avoid falling off a precipice.

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