Anyone else with CFS suffer from achy legs?

Posted , 10 users are following.

Hi everyone,

I've been suffering with CFS symptoms for around ten years, but was only diagnosed in the past twelve months. For a while now, I've been experiencing a dull ache in my leg muscles, as well as in my hips. It used to only happen at night when I'd been lying on one side for too long, but now it's constant. Has anyone else experienced anything like this?

Thanks so much!

0 likes, 28 replies

28 Replies

Next
  • Posted

    Hi Jamie,

    I used to have sever pins and needles as well as a dull ache in my left hand and arm. I found taking magnesium and vitamin D completely cured this (was advised by a CFS specialists to take this)

    Hope this helps.

    Haylee

  • Posted

    Hi Jamie

    Like Haylee I suffer with pins and needles and aches, I also take Magnesium and vitamin D but as yet still suffering with it. Its just another one of the lovely symptoms.

    A hot bath helps when I'm really struggling 

    • Posted

      When I first started taking the magnesium and vit D it didn't really work but once I doubled the dos the symptoms disappeared. Even find some days I have more energy. I definitely notice it when I forget to take them! All the symptoms come crashing in...

      Best of luck x

  • Posted

    Hi Jamie,  I've had CFS/ME since 2003, following a back injury which resulted in tears to two of the discs in my lumbar/sacral spine.  As well as having some  loss of sensation to the skin around my trunk I do also get hip pain/sacroiliac pain/sometimes sciatica.  I saw a physio some years ago, on and off for a few years. She gave me some stretches to do, for my hip pain do which do ease the pain to a degree.  The cold, damp weather make the pain worse. Hope the pain improves, Claire.
    • Posted

      Thanks so much for your reply, Claire. So sorry to hear you've been in all that pain. Mine is more an annoying dull ache than anything, but I have noticed it gets worse when I'm cold.

      Take care xx

    • Posted

      Hi Claire,

      I felt I had to reply because I too had a back injury, I too have loss of sensation around my trunk and cfs/me as a result. I am no longer ticklish. Are you the same? Mine was from a car accident.

      B

  • Posted

    Hi yes Jamie was diagnosed with CFS 18 years ago now, its only been the last two that my legs are really bad and hips too. The smallest task seems to go straight to my legs, strange thing is its actaully  worst  after ive been laying down for a while like at night, wake up to go to the loo, when i get back into bed they throb like blazes.

    Was put on vitamine D but when i requested a repeat prescription was told this would be the last lot! Dont know why?

    Of course the achy legs and hips can be just the hips are playing up leading to a hip op in the future, My mum started of just like me and ended up with having both hips replaced but she hasnt gor CFS though but arthritis. Signs of hip problems are when lying on your side at night too.  Hard to say as when you have CFS they tend to blame that for everything.

    Sue

     

    • Posted

      I'm exactly the same, Sue. My legs ache worst when I'm in bed. Being 33, I'm guessing it's a CFS symptom rather than something else, but it's impossible to tell.

      Thanks so much for sharing. xx

    • Posted

      I think if its arthritis you get other parts hurting and swelling like knees and knuckles where as this doesnt happen with CFS, do you find it affects your vision as well?  x
    • Posted

      Hi Jamie,

      My legs were aching more recently and one leg has been locking up when walking? I had It xrayed and no issue there but when I mentioned maybe just cfs to doctor, he said it could be other things and referred me to physio. Check it out with your gp. I'm also taking vit d but with calcium. The locking up seems to have gone away last couple of days. With the aching it sometimes feels like there going to fall off. I also get restless legs with It sometimes. Hope that helps.

      B

    • Posted

      Well, I'm visually impaired anyway, so it's hard to tell. I do find my brain gets sort of hazy though and it's really hard to concentrate. XX
    • Posted

      Thanks, Beverley. I'll certainly mention it to my doctor next time I go. XX
    • Posted

      The different symptoms with this condition are mind boggling. I often get one red hot cheek and ear! I put it down to my system thinking it has to fight something in my sinuses but just on the one side : )

      B

  • Posted

    Sometimes my legs are very heavy, painful, thick feeling, like walking in mud. I just stop walking! It frightens me, and I never know when it's coming. I lie on my back, and sometimes my buttocks ache. It's something new. I suppose I should get up more.....but when movement means pain, it feels best to just stop.
    • Posted

      Wow, how horrible. Perhaps see your GP about it as well. XX

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.