Post Viral Fatigue Syndrome Diagnosis | Covid-19 Impact

Post Viral Fatigue Syndrome Diagnosis | Covid-19 Impact

Post-Viral Fatigue Syndrome is starting to gain more recognition THANK GOD! There is a huge amount of people that suffer with this illness everyday and doctors keep turning a blind eye. Maybe Covid-19 will MAKE these professional pay more attention. Getting PVFS diagnosis is a very long process and at times, difficult. In this video I tell you the steps and things that need to happen in order to get the appropriate diagnosis. I have many videos on my condition, so make sure to check out my PVFS playlist to learn more about more Post-Viral Fatigue and tips on how to manage this illness. Love you all and stay healthy !-- Morgan

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MOST HELPFUL HOSPITAL I'VE BEEN TO: MAYO CLINIC IN JACKSONVILLE FLORIDA

[GeorgiaLinders]

I just wanted to post a quick update, Morgan. I'm going back to watch this video because i was just diagnosed with Post-viral Syndrome and Chronic Fatigue Syndrome. thanks again for posting these types of videos.

[Mrsbaileys]

I have Fatigue Syndrom since 2018 as a side effect of my cancer journey. My doctors have said this can take months or years until it goes less or completely away or stays forever.

[susandegennaro]

I have a history of chronic reactivating mononucleosis. One time I got mononucleosis so severe it was in my blood for 1 whole year. I was sent me to an infectious disease Dr bc my neck was so swollen that I had balls in the back of my neck so they did biopsies of my neck. I got double lung covid pneumonia for 3.5 month that left me with lung scarring and multiple benign nodules. Then I got the shingles for 3.5 months and found out a lot of post covid patients are getting shingles. Then I felt beyond exhausted like covid reactivated my mononucleosis and research suggested that covid can also reactivate mononucleosis too. I am beyond exhausted all the time & it has been 1.5 years since my double lung covid pneumonia, I should of fully recovered by now, and I don’t feel the same and I have exercise intolerance, out of breath, winded, and I sleep a lot more and wake up exhausted like I never went to sleep too. I am finding it hard to fully function like this. I tried to exercise to get healthy and loose weight. I was profusely sweating when I went roller skating after 1 hour and I used to skate for 3 hrs with no prior issues. I fell down and even had a severe fall where I broke my T12 spine and I prior to this could figure skate and spin 6 times. I go to Dr and no one seems to know how to treat long haul covid and I am so beyond frustrated. What dr did you go to at Mayo Clinic.

[lauramcneill]

Thanks for your video. I had what I think was coronavirus for about 12 weeks (undiagnosed because I had it so early, before anyone knew what was happening). I have since 'recovered' 4 months ago now, but I'm still experiencing post viral symptoms, so I'm worried it won't ever go away. I'm really interested in what you said about how your neurologist helped you. I happen to have epilepsy, which like many people is accompanied by migraines. The migraines have got worse and far more frequent since I got ill. The seizures have been under control for years, but I wonder whether I should get back in touch with my neurologist to see if there's anything they can do to help. Do you mind if I ask - how did your neurologist help your situation?

[BullsEye]

Thanks for sharing. I have been tired for 6 months, better than the first 3 months when I couldn't move at all, and thought I should go to the hospital, but didn't. I have gone to all sorts of Doctors, and they're saying there is nothing wrong with me. At times I feel my breathing struggles more than others, I get headaches, am tired, have brain fog, and still can't smell. I am lost, not sure what to do. I often take time outs, just unplug, feel better. Been trying to eat better and do stretches. When I wear a mask, I get dizzy and almost pass out. Not sure if it is safe to work out? Or whether I should see a neurologist? I went to a pulmonologist, and he said my oxygen levels are good. When I asked if I should get a cat scan of the lungs or heart, he didn't recommend it due to radiation.

[donna]

Going through this for the second time - last year with Glandular Fever and now with Covid.

[dawnroberts]

i had a virus six weeks ago started with vertigo all day everyday then that went and then i started getting weird symptoms cold sensations in my arms legs face head weakness shakes in hands and legs but now my hands hurt feel like i have lost some strength in arms legs i got two mri both normal bloods normal so i wonder if it can last this long

[taraedney]

I'm in week 13 now and seriously had enough my life is completely different and I can't do anything I could before Dr keeps saying I'm anxious

[onetothree]

24 months in mental fatigue after horrible ebv infection. any tipps?

[dawnroberts]

you must have good doctor to send you to all these doctor i still am suffering with things they said its anxiety but all these syptoms started after a virus

[SA]

I dont know if this is what I have been left with after being ill, but sometimes the lethargy/exhaustion is so bad that I feel like if I dont lie down Im going to litterally unable to stay Ill lie down and sleep for 4 - 6 hours (after having slept 12 hours already).

[kincaid]

Multiple professionals lol yeah good luck with that living in the UK

[tessgirl]

I’ve got it & im not getting better !