CFS recovery

Posted , 16 users are following.

Have any of you begun to recover or recovered significantly from CFS?

I want to get a feel for if recovery is age related (do younger folk recover more quickly?) Or if it's related to how badly you suffered from CFS in the first place.

I've that broadly, younger folk get better quicker.  I've also heard that if somebody has had sudden onset, maybe caused by a virus, then they are more likely to recover in about three years.

What do you know?

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  • Posted

    I'm 44, was diagnosed after a virus, came into it pretty fit and have noticed overall improvements in stamina and symptoms over the last 6 months (I'm about 16 months in). 

    I was bed bound at my worst last year and still have poor periods, but things are slowly getting better. I was able to quit work and dedicate my time to it though. I think this is one of the key things.

    • Posted

      I can operate around the house ok as long as I pace myself. I can't really go out alone but do go out walking and shopping with my wife on good days. It's still very limited though and sometimes when we get where we were going we have to come right back again. smile
    • Posted

      I know the feeling!  Apart from the fatigue / loss of stamina, do you get the post Exhertion malaise the next few days?  How quick has your recovery been?  Just trying to compare things!  24 months in I saw zero improvement myself, probably slight decline.
    • Posted

      PEM yes. Thats another improvement I've noticed. Before it could take weeks for the PEM to improve, now its mostly days.

      I would say its taken 6 months of pretty much doing nothing but waking each morning and dedicating myself to getting better that has gotten me to this point. Plus a good diet and supplements.

    • Posted

      After 24 months of gradual decline I just felt different one day.  That's 16 days ago.  During those 16 days I've increased from hardly ever walking, but maybe 3 miles on my e-bike, to 12 miles on e-bike and 2.5miles walking in 50minutes - with no PEM,

      I'm trying to judge if I'm totally OK again, but needing to get fit like normal.  I think I could do more, but my consultant advises caution.

      All I'm left with now is frequent headaches, which I rarely had before CFS, and a bit of a fuzzy head - which doesn't limit me at all.

      Feeling hopeful!

    • Posted

      Sounds hopeful and good luck. Be cautious though as your Dr advised. 

      My improvements have come suddenly as well, then there is a plateau for a bit, then another small one. 

  • Posted

    Hi I am 51.  I was diagnosed 7 years ago.  I was no exercise fan, but a pretty busy mum with a part-time job that kept me out and about.  Part-time however, never really is part-time.  In the beginning I was quite ill and was off work for a couple of months.  But being careful and listening to my body I went back to work and remained there until 2013.  I then had one major relapse ( I fully believe this was due to work pressure and lack of support) and unfortunately I too came out of the workforce.  My mobility was affected, I too became bedbound, housebound, and had to use a wheelchair at times.  My home had to be adapted in places.  Today, I still suffer with mobility issues and walk with a crutch and can not walk very far.  I rarely go out and if so have someone with me.  I am doing much better than I was back in 2013 but still have a very long way to go.  I cant stand a cook a meal,  I can't walk all the way around the supermarket, and yes I too find once we got there we have to go straight back.

    I think it really depends on the individual on how quick recovery comes if at all.  I have just read  "from ME to you with Love", by Louise Harding.  I would thoroughly recommend any M.E. Sufferer to read this.  It gives you an insight to how other people are suffering, on family and friends, employers, and professionals who do not understand the condition.

    I agree the key thing is to dedicate your time to it and listen, listen, to what your body is telling you.

    All the very best.

    Tx

    • Posted

      So sorry to hear that Tina.  Thanks for replying.  I think I have CFS but not ME.  I don't get sore throat or anything, just mainly the fatigue and PEM, until a couple of weeks ago.
  • Posted

    I've heard of older people recovering, though some still have to pace themselves. It seems to often be related to how much rest and help people can get.

    It can be harder for those who live alone as I do. I'm inbetween carers and trying to get another one (my previous one got cancer and had to quit).

    Some symptoms have improved but the worst ones i.e. brain fog, exhaustion etc haven't and I've suffered from ME for over 10 years. I haven't given up hope though because George, a member of this group, recovered after 10 years of it and puts it down to a nutritious diet and cutting a lot out.

    So as one of the previous posters said, I think it's posible for people of any age to recover.

    • Posted

      Thanks so much for your detailed reply Georgia.  I'm lucky to have a fantastic wife who looks after me.  Without her, I don't know what would have happened.
    • Posted

      What's your diet like? I've learnt a lot about what to eat and what not to eat but it's hard to put it into practice because I don't have any help at the moment. I try though. Tell me about your diet because I think that following George's advice to pay it a lot of attention is important, after all he recovered through his diet. razz
    • Posted

      I think I've a good diet. Lots of fresh fruit and veg, home made bread, drink mostly tap water, moderate amounts of meat, eggs, cheese. Cereal breakfasts.

      Very little processed foods.

  • Posted

    I was 32 when I got sick after a 6 week bout of mono.  For a few years I was close to my pre-sickness level.  I think the problem was that I kept pushing my body hard because I refused to believe I was sick.  Over time I kept getting sicker.  Now at 43 years old, I am mostly house bound.  I work from home and only go out a couple of times a week for little jaunts.  Even grocery shopping can be too much if I am not careful.  This disease kicked my butt over time.  I hope you have better luck.  Take care.biggrin
    • Posted

      Ouch!  We are quite different then.  I went from very fit to unable to walk 50metres overnight!  Because of a virus.  When that cleared, I was left fatigued.  After 24 months I still couldn't do more than walk half a mile slowly.  I have found an electric bike really good.  It's easier than walking and gets me around for several miles.
    • Posted

      I really think my problem is that I have a hard time slowing down.  I still work 8 hours a day; although, I work from home.  I wonder if I didn't work (although I'd lose my house, car, etc) if I would start to feel better.  Maybe the 8 hours of work a day is too much and is sapping my energy.  I wish I knew.  I feel so bad that sometimes I just can't go on and lie on my bed in tears of exhaustion and pain.  I just wish I had my old life back.  I didn't know back than how good I had it. 
    • Posted

      I tried working two hours a day and couldn't - I doubt any clued up medic would abide it.

      Weve found we can live on far less money than we used to.  Fortunately, we didn't have to lose our house.  We did consider downsizing, but it didn't come to that.

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