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.

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  • Posted

    Hi everyone,

    Apologies - this is the first chance I've had to respond. Thank you all so much for taking the time to reply - I wasn't expecting it and it's very much appreciated.

    It really does help to hear that other people's symptoms have gradually eased and all the hints and tips are most welcome.

    We were hoping to extend our family before long. I certainly don't feel well enough right now but I'm hopeful it could still be an option down the line. Right now I need to focus on me and my health and the lovely little girl I'm so blessed to already have! If anything this has all been a huge wake up call to me how important it is to look after myself.

  • Edited

    Hi there,

    Just reaching out on here on the off chance anyone will read it!

    I'm coming up to 6 months of symptoms which had been attributed as post viral and having a wobble about something more sinister going on. With Covid-19 I'm not really in a position to seek further medical advice/tests. I just wanted to check if people found the buzzing legs, pins and needles, back and leg pains stuck around more so than fatigue? Obviously in the current situation I'm not going out and I have been furloughed at work so I feel that my energy levels are somewhat improved but some other symptoms are the same if not worse.

    I had a scare regarding changes in my nipple and breast pain and have been seen at the breast clinic and assured all is fine. I've always had pins and needles/buzzing feelings in feet and occasionally right hand but this has now progressed to a pain/burning sensation in my right shoulder around into my armpit and ribs and down one arm. This is the same side as breast pain. To a certain degree I think anxiety around my breast hasn't helped but I fear there could be other issues going on that may be being missed. Thoughts creeping in again about cancer or MS.

    I've been eating as healthy as possible and taking my supplements but I must admit lockdown has meant I've fallen off the wagon on occasion with gluten, occasional unhealthy foods creeping in and the odd glass of wine.

    I also wonder if any females have found their symptoms worsen at ovulation/menstruation? I find on particularly bad days which tend to be around these times I am more thirsty than normal and have an odd almost menthol taste in my mouth.

    It's all so random and I just feel worried with a lack of diagnosis. It's started to get me down that I struggle to do as much as I would like with my little one and I feel a lack of intimacy with my husband is affecting us both.

    I had a brief spell where I actually felt a little improved and did have a nasty virus a number of weeks ago which I guess will have set me back.

    If anyone read this far - thank you! I know I'm much luckier than many and should be remaining positive.

    • Edited

      Hi there.

      Oh my goodness. I feel your pain.

      This was me, over 2 years ago now. Started with pins and needles in both legs, numb arms and horrific shooting pains in my head. I couldnt function properly. Spent so much time at the doctors and they just used to look at me as if I was wasting their time.

      Had bloods done, all OK, apart from borderline underactive thyroid.

      Then, after six months of the above, I started getting twitching, i could see movement in my foot and then my leg just twitched all the time. This sent me over the edge as I googled it and it came up with MND!

      The twitching lasted 6 months also. I started to try and forget about it and try and get my head together for the sake of my family. Day by day, week by week, month by month, I got better.

      I still have a really achy body now, but I think the stress of all of the above has done this to it. I put myself through so much worry and in the end, it was post viral and I do think a bit of chronic fatigue syndrome as I was absolutely shattered all the time.

      My advice is please just take your mind off it, enjoy the sunshine and give yourself chance to relax. It might take a while, but you will get better.

      You do feel hopeless. I wish I could rewind and deal with all mind so differently.

      Take care of yourself and dont overthink. The nerve issues will go away, maybe get a magnesium rub or something.

    • Edited

      three years later and im pretty much back to normal. so grateful.

    • Posted

      Hi Jo,

      Thanks so much for the reply - I really genuinely appreciate it.

      The nerve issues are certainly unnerving (pardon the pun)! I'm so glad to hear things settled down for you.

      I'd got myself into a better headspace for a while and have had a wobble but you're definitely right keeping my anxiety in check is really important. I use a magnesium spray and taking some other supplements as well.

      Thanks again for taking the time to reply, hearing stories like this really helps xx

    • Posted

      hey lilium, is it okay if i dm you. I an going through something similar

  • Posted

    Hi Elle

    If you have MS they would have been able to tell from your MRI scan and bloods. My friend has Fibromyalgia she went through all the same tests as you but she kept pushing the Doctors as her symptoms persisted. I was diagnosed with MS, 5 years ago and some of my symptoms were the same as hers. The sex drive was the same for both of us but we are both going through the change of life too, so a double hit. You never said how old you

    are?

    Take Care

    Amanda

  • Posted

    Hi Amanda,

    Thanks for your reply - I'm not the OP (Elle). I posted on this thread a couple of months ago when I googled some of my symptoms. Apologies if I haven't posted in the correct way.

    I haven't had an MRI. I did have a full blood count last year - I'm not sure which blood test might be MS related? Fibromyalgia has crossed my mind.

    I'm 33 so nowhere near menopause (I hope!)

    Thanks again

  • Posted

    Hi Elle,

    Im sorry to hear you have been suffering these symptoms.

    post viral fatigue / post viral syndrome is a term given by doctors following a bad virus or flu where you never fully recover, feeling very wiped, heavy, headachy etc.

    did you suffer a virus?

    i did when i first got sick in late 2016. then tingling and pins and needles crept in and ended up all through my body. its very scary in the beginning but try to not let the fear take over because it makes evrything much worse.

    It helps to see the virus or whatever preceded your symptoms as the straw that broke the camels back. Most people with these illnesses have had a lot of stress, overwork, trauma or physical burnout prior to becoming ill.

    i went through the cycle of specialists and doctors, naturopaths, for over a year and allnit did was create trauma and panic. i was diagnosed with lyme by aternative practitioners and all their treatments only made me sicker.

    i came to the realisation that i needed to focus on health rather than illness and become my own doctor. I then started healing.

    I got so sick i ended up bed/housebound for most of 2017. Fatigue was not my most debilitating symptom in the beginning, it was horrific nerve pain in my hands and feet. i think the fatigue was difficult to see though as i was in high adrenaline mode as my body was shutting down.

    FYI here are my symptoms:

    pins and needles

    crawling skin

    burning skin sensations (particularly at hormonal times)

    nerve pain

    numbness in lower legs and groin

    blurry vision during cycle

    pressure headaches

    sinus headaches

    blocked ears

    swollen glands in throat

    overloaded lymph detox pathways

    freezing feet and hands

    dizziness

    migratory athralgia in knuckles and toes

    forearm and shin aches

    ibs - weight loss

    gut issues

    phantom smells - headaches upon smelling perfumes etc.

    nervous system overload - huge anxiety

    insomnia

    the list goes on!!

    i have healed so much through diet, gentle exercise,

    change of lifestyle, removing toxic relationships, self work, finding my tribe, rest!!

    I'm getting there and working part time now but patience and trust is the most important. I know i will recover fully.

    It is important for you to have tests to rule out MS etc. but remember, the western medicine system has a completely different view of illness and health. your symptoms are messages from your body to take action. not something to be covered or suppressed with drugs. Trust your body's wisdom!!

    all the best!!

    Monika

  • Posted

    Hi Monika,

    Thanks so much for your reply. Yes, it all started after a run of colds and being generally run down followed by a virus with upset stomach. Looking back I was struggling to cope juggling work and family life and I had a stressful year on the whole.

    I can relate to a scary number of your symptoms - its the nerve related stuff that worries/scares me. I definitely need to keep my anxiety in check. It's great to hear you're getting better. I can't imagine my nerve issues ever going away completely but I know it's only been 6 months.

    I'm going to push for further investigations when I can as I feel like I need to rule some things out to be sure. I'd hoped to have another baby in the not too distant future so that's all on hold for now but I know I'm incredibly blessed to have my little girl already!

    Thanks again xx

  • Posted

    Hi Vikki,

    i can also very much relate to most of the symptoms you are describing.

    my episode started 3 years ago, and it took me over a year to see improvements. i am mostly ok now, still have what i call short relapses for a few days if i m particularly stressed or have a viral illness of some sort.

    i still get tired quite easily, but life is pretty normal. like everyone else on here, i tried many different things, but in the end, it was just down to good self care, good diet, sleep and time. Be kind to yourself, and try not to take your symptoms too seriously, when you are very anxious and focus on them, it only seems to make them worse!

    take care xx

  • Posted

    Hi Kat,

    Thanks so much for your reply, I know you were one of the people who replied to me last time. It's comforting to find people who can relate - I find it hard to talk to people in real life as they just don't get it or think it's all in my head I suspect!

    So glad to hear you're recovered for the most part xx

  • Posted

    Hi Elle

    I had a nasty viral infection 9 weeks ago (negative covid test) and normal blood tests. It felt similar to glandular fever which i had 20 years ago.

    Ever since, if i overdo it , a walk or housework, i come down with awful fatigue , heavy head feeling and slighty dizzy. It can take a week or so to return to say 70% better. Its so dibilitating.

    It means its hard to make plans.

    I was fairly fit before this happened and cant believe i am now unable to so any proper exercise.

    How are you doing now?

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