Post viral symptoms / syndrome
Posted , 87 users are following.
Hello eveyone,
I have been diagnosed with "post viral symptons". I have not got a clue what it is.Has anyone heard of this. For over two months I have been suffering from the following:
Heavy head feeling,
unbalanced.
constant pressure in the head
flu like symptons but no fever.
Pins and needles in left and right leg. Sometimes hot and cold flushes in the leg.
Prickly feeling in the arms
Muscle fatigue or cramping in the hands. I feel like my hands are so stiff sometimes.
Fatigue all the time ( despite having a good sleep).
Apparently I had a viral infection and then one by one these symptons appeared. it is dragging me down. I have MRI, blood test which came back okay except for slight raised "infection".
Does anyone else have these symptons? It is dragging me down. Is there a solution. The Dr says there is no treatment but it will disspear or subside on its own... when? when? when? Some days I can handle it other days I want to just curl up.
No offence but this syndrome just sounds so wishy washy. Could I be misdiagnosed?
Sad Elle.
4 likes, 464 replies
kat2016 Elle1234
Posted
Just wanted to know how everyone is doing 2-3 years down the line, as I too have been diagnosed with post viral syndrome with the pins and needles, muscle twitching, heaviness and dizziness or other bizarre symptoms. I hope most of you have recovered or improved!
lilum kat2016
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kat2016 lilum
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Hi LIlium,
Thank you so much for your reply and I m so glad you're doing better! I hope you're on your way to al full recovery. I will read your previous posts. All the best to you and everyone else x
Mic13 lilum
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deirdre01438 Mic13
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lilum Mic13
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Re peri menopause, I’m not saying it’s not possible, but there are guys with the same symptoms. And it’s something diagnosed starting at 30 until about 60, doctors love to say it’s peri/menopause. That means, we have no answers and don’t know what to do for you.
Re antihistamines and benzos. That’s the only thing that works for me so far but I read a pretty reliable study that links long term use of anticholinergics (Zyrtec, Benadryl etc) or benzos (klonopin, Ativan etc) to increased risk of dementia and Alzheimer. If you need to take it, and I do, take it, but be mindful of that risk and try to cut back as soon as you can.
https://www.health.harvard.edu/mind-and-mood/two-types-of-drugs-you-may-want-to-avoid-for-the-sake-of-your-brain
chris12276 Elle1234
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shani68304 Elle1234
Posted
It feels a bit weird to reply to your post 3 years later! But, when I read it just now, it was like reading exactly what I had been experiencing for the last few weeks...
I got exactly the same diagnosis yesterday and my symptoms where nearly word for word the same.
How are you doing these days? Have you managed to recover and function normally again.
I was so discouraged when all of my blood tests came back as normal, except for slightly lowered platelets but my muscle were so weak I could not even walk properly. My brain also felt like it was fuzzy and too big for my skull, and I watched my muscles twitch uncontrollably after I even used them just a little bit.
Bed rest and patience seems to be the only effective treatment! ( along with a lot of vitamins and fluids of course!)
For what it is worth, please let me hear back from anyone else with viral induced chronic fatigue syndrome?!
Guest shani68304
Posted
Sorry to hear you have been diagnosed, that’s really s**t news.
I’ve been suffering a while now and only starting to work out what to do to aid some recovery. Everyone’s symptoms seem to be different but one major tip I can tell you and this is as absolute must to follow. Do not catch ilnesses from other people. If your partner has a cold stay away or if your friend has a cough. My recovery has been stunted dramatically by the cold winter weather and extra ilnesses on top.
I’m going to be honest with you, this is s**t. Get your family around you close and hold tight because it’s a bumpy ride. I’m still on the ride with no sign of the light yet. You will have hard times when you want things to go back to the way they were and they will but you just don’t know when.
Doctors lack any knowledge regarding this illness so just eat well and cut out toxins like alcohol etc.
This is my first post since my intial post but seeing your post reminded me of myself when I first realised I had this mysterious illness so I had to respond.
Best,
Ed.
Guest shani68304
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lyndell22882 Elle1234
Posted
The only abnormalities in my blood test are vitamin B12 dificiancy and white blood cells are below normal and my blood test before this one, detected some sort of infection that I wasn’t aware of. The only massive thing medically that has been wrong with me is I’ve had a haematoma which A hematoma is an abnormal collection of blood outside of a blood vessel. It occurs because the wall of a blood vessel wall, artery, vein, or capillary, has been damaged and blood has leaked into tissues where it does not belong. I used to be a hell of a lot more unbalanced and dizzy when that was in my body and I believe that would of triggered all these other things but who’s to know.
I hope everyone is doing well now
Guest lyndell22882
Posted
The B12 deficiency can be key.
Take high potency b12 tablets and see if that makes you feel any better.
I knew someone myself who thought they had CFS but instead only had this deficiency and only had to have injections of b12 once a month and she was right as rain!
I really hope this works for you!
zlatka1990 Elle1234
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Hello again! I've been dealing with this for 10 months now and I see some positive changes in the last 2 months after natural treatment, including teas, spirulina, mushrooms, inhalations and circulation meds. I also avoid stress, try to sleep at least 7 hours...the result is increased energy level so I'm dealing much better with my persistent symptoms: pressure in head, blurred vision and vertigo. They are still here but they seem to be weaker. Goodluck to all
Guest Elle1234
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So I am new to this discussion but thought I would drop in.
I am a tennis pro and about 6 months ago I was giving a tennis lesson in the heat and started to get dizzy and really weak in legs. At first thought it may be de-hydration but it felt like a little more. Anyhow it turns out that I am still dealing with this and the term post viral has been thrown out there.l by some of my Drs. I don’t really buy that diagnosis to be honest.
I have seen numerous Drs including GP’s Neurologists and infectious disease.
Have had all the scans including Brain and Spine and so much blood work and everything has come back normal!!
Things have improved but it is so up and down. Some days I feel ok and other days not great.
My symptoms are weakness in upper legs, Tittinus and Little brain fog
I don’t have any fatigue in fact I feel like I still have quite a bit of energy just weak.
I am going crazy cause I can’t get a diagnosis! And I am tennis pro so it’s hard to work.
I have been super stressed about it so that I am sure is not helping!
Anyhow if you have any thoughts or advice would love to hear!
Thanks
Tim
mesut322 Elle1234
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