Is Long Covid The Same As Chronic Fatigue Syndrome?

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Being diagnosed with Covid-19 is a worrying experience for anyone. But for some people, the virus doesn't go away after a few weeks. Instead, they develop what's known as long covid, which can cause a range of symptoms that can last for months or even years.

According to a recent study, long covid can cause your nervous system to become hypersensitive. The study, which was conducted by researchers at the University of Glasgow, found that covid patients who developed chronic fatigue syndrome (cfs) were more likely to have heightened sensitivity to light, noise, and touch. This can also lead to symptoms such as brain fog, memory problems and difficulty concentrating. The findings suggest that long covid can have lasting effects on the nervous system, even after the initial infection has resolved.

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Tags: Cns fatigue, cns burnout, nervous system burnout, nervous system fatigue, cns exhaustion, chronic fatigue, cfs, chronic fatigue syndrome, bedridden, housebound, adrenal fatigue, chronic fatigue syndrome treatment, cfs symptoms, cfs recovery, cfs health, chronic pain, chronic pain syndrome, chronic pain explained, chronic pain meditation, post-viral fatigue syndrome, long covid, covid long hauler
#cfs #cfsrecovery #cfsme #bedridden #anxiety #somaticsymptoms #somatic #panicdisorder #panicattacks #chronicpain #chronicsymptoms #longcovid #postviralfatigue

DISCLAIMER: I am not a medical doctor or therapist. I am sharing my own experience and research. My video content is for information and educational purposes only. Please consult with your medical professional.

[cfsrecovery]

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[suepritchard]

I had Covid and it immediately became chronic fatigue and I was pretty much bedridden. The doctors said it was long Covid until it went on for a couple months. Then they started referring to it as chronic fatigue. After almost 8 months now I am slowly getting stronger thanks to the positive information from CFS Recovery! I’m now out of bed and able to get out of the house for short periods of time. Feeling stronger every day!

[ljon]

I got covid while recovering from CFS and i am back on track and getting so much better, sleep as well and also able to digest food that I couldn’t eat a month ago. This is all from putting the knowledge to work that Miguel is teaching. Listen openly and apply them thoroughly, it works trust me. 🙏

[kathygreen]

My doctor says long term Covid and I never tested positive. Went down with MECFS soon after I caught a respiratory virus. First symptom was my legs felt like they wouldn't hold me up. So weak. Then came burning arms, legs, and brain, always around 3-5am. Covered in first time unresponsive to treatment Psoriasis. Definitely have PEM. Has been a year. I am better than last year but far from normal. Definitely dysautonomia. Have panic and anxiety for no reason. Sometimes depression in the morning. Typically better at night. Low diastolic blood pressure too. Fluctuating between 48-53. Have Hashimotos and been on Synthroid for 40 years. Sigh....I really need one doctor looking at the whole body instead of an Endo, a dermatologist, a general practice dr. Dont like being treated compartmentally. My ANA test is sky high.

[lindascott]

Hi Miguel, another Great Video.. It's people like you who continue to hope this Hell will go away .. Thank you❤

[steffenrunge]

wow 100% living all of this since 19 months now. And since Tuesday finally next round of it. I so hope that there is an escape out of this nightmare. I used to be an happy, sportive, warm hearted guy with a good job and a big heaart. Now am sitting home alone, falling asleep constantly, feeling weak, crying a lot, but hey apart from my CRP all blood result are perfect. Nobody knows how frustrating this is when they have no clue and just send you home another monh to relax.🍀 best wishes from Germany, Steffen.

[tlsmith]

I had Covid last January 2023. But I thought I recovered. By Jan 2024 I’m in bed a lot. I have to plan when I go out and recovery time. But you said it right. My friends started asking me if I was on drugs or benzos because my speech got weird. I can only handle going out about once a week (it takes me now 1-3 days to recover)

I have all the typical symptoms of CFS now. Dr not sure if it’s Long Covid or typical CFS. But when people don’t know is Long Covid REACTIVATES dormant viruses… I’m now testing positive for EBV, MONO, and even things like chickenpox’s, androgen virus and a host of others.

When you said the doctor give you electrolytes that just happened to me and I wanted to throw it at her. I used to work out every morning and she told me to work out in the afternoon in the afternoon. I’m basically done in afternoons . She gave me a powdered drink with electrolytes and caffeine in it. I want to throw it back at her.

[c.taylor]

Miguel, thank you so much for this and how you covered this information! As someone living with long covid for over 2 years and now diagnosed ME/CFS by my rheumatologist i couldn’t agree more with you and your perspective! For me, i can see that is is absolutely my nervous system gone wild! Very, very grateful to have found your channel and to be part of your CFS Recovery Jumpstart program 🙌

[ezza]

Great video thanks 🙏 we will all recover. I like what you said about how covid can push us over the stress threshold, why is it some people get covid and recover so quick and then other get long covid, maybe those people were already stressed before the onset of covid

[beatepaschilke]

Thank you so much for this video and all the informations. The way you explain this make a lot of sense to me. You do a great job. Thank you.

[tlsmith]

I have long covid and I’m so exhausted I was in bed all day today. It’s exactly like CFS. The way you describe the exhaustion is exactly the same. I couldn’t even walk to the kitchen. I was just too tired to stand.

I thought I was getting better and I walked for exercise this week, but now I’m bedridden and I don’t know when it’s gonna stop. I learned my lesson. Last time I felt this bad was January. I just can’t handle the cardio of walking. I’m the girl that was at the gym every single day so this is really frustrating. I just don’t know what to do.

[cathycoppin]

How. Do you get. Help. Hyper sensitivity, nervous system.
?? Tljx
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[EllaSloman]

This is an absolutely brilliant video . I have had lc for 20 months and it’s definatelŷ nervous system damage . I’ve upped meditation and vagus nerve stimulation.

[deborahasher]

I had CV in March 2020 it's at that time I developed CFS. Before that time, I had energy galore.

[rosarioparedes]

Do you have videos here on yt that will help heal the nervous system? Do you have them in one place to access?

[SPIRITWILDCHILD]

I'm just recovering from COVID and suffer from CFS. For me COVID felt similar yet very different. I'm eating very healthy to see if I can recover from all of this.

[kaylaberry]

I have very high cytokines. Can chronic fatigue cause this? I am taking a binder, Nattokinase and ivermectin for long Covid. I didn’t have a severe case but I was dizzy and it didn’t go away.

[Jane-pgjv]

Luckely you are helping so many people!!! 🙏 Amen

[techsavytronicstechsavytro]

Hey man, do u help with OCD thought compulsions - it hurts my head and get very fatigued throughout the day. I tried a hypnotherapist but it didnt help. Just trying to think if it’s related to a hypersensitive nervous system issue

[DawnTiburzi]

I did suspect cfs because all my life i couldnt just stand around without moving and now i have exacerbations when standing up and the only thing that will stop it is prednisone. Thank you