Fellow chronic pain sufferers?
misssmaria
Posts: 27 Member
Looking for buddies who are experiencing similar obstacles.
Open diary.
Open diary.
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Replies
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Hello, hope you find someone to share your journey with. While I don't suffer chronic pain, my mother has polymyalgea and my sister has lupus so I do have some understanding of the difficulties that you are probably facing. Happy to be a friend although not quite what you're looking for. xx1
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Hello. I have chronic pain due to having Ehlers-Danlos syndrome (and a few other things). I just joined this group and I'm looking for friends who understand too xx2
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I have joint hypermobility syndrome, fibromyalgia and a tear on my right hip. Happy to add friends from all backgrounds
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Hi I have cerabal palsey left side I have lots of meds everyday including morphine patches HRT patches and lexitrine for uat xx feel free to add me x0
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I can sort of relate, I have Auoimmune hepatitis, cfs, and the side effects of the meds mean i have pain almost daily although a different pain each day, so its a bit pot luck where it will be, amongst other stuff. I have found that going the gym has helped a lot with the CFS.0
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I definitely have chronic pain issues. I am 36, have arthritis throughout my body, made worse by my hypermobility. I've just started swimming again but even that hurts!0
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Hi, I have fibromyalgia, Raynaud's phenomenon, arthritis, Mortons neuroma, plantar fasciitis and hyper mobility. I'm currently trying to increase my movement, doing little walks and stretches to try and increase strength after being bed bound/ wheelchair bound for a very long time
It's nice to chat to people who understand being in pain. I also post in chronic pain and weight loss group0 -
Me. I have ME/CFS.0
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Hi I have nerve damage in my lower back and server migraine semi controlled by anti eplipic meds , just had a brain scan to see if they can do anything else.I've been here since 2010 had the nerve damage since 2005 but didn't Know until I had a relapse in 2014. So feel free to add me or inbox me0
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Chronic pain and fatigue from neuroma following abdominal surgery in 2001. Feel free to add me.0
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I don't have this thankfully but popping in as my mum and sister have fibro among other things (mum has loads!) but both are regulars at the gym. They just have to take a break now & again.
Hopefully I can share tips between lol0 -
Hi i have myotonic dystrophy it's a inherited muscle wasting condition0
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Hi I have Fibro , under active thyroid high blood pressure osteo arthritis and plantar fasciitis so I know your stuggles x some days are worse than others and I'm trying to push myself to walk a little longer and a little further every day . add me as a friend of you want to chat or friendly encouragement0
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I have lumbar degenerative disc disease, impinging on the L5 nerve which is the one running down the outside of my legs to my ankles. Also have hypermobility, most badly in my ankles1
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@susannah521 I also have EDS with DDD. My L5/S1 herniated into my spinal canal in January 2013. I also just found out that I have another 2 discs bulging in my lumbar region as well! Yippee!
I try to do hydrotherapy every weekend. Its been keeping me going for an age!0 -
Hi have ME/CFS - for 10 years now
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How are we all doing today? This changing weather is killing me!
If any of you fancy it, Manchester university are doing a study on how weather effects our pain. Look for 'Cloudy with a chance of pain'. It'll ask you some questions and then send you to an app called uMotif.
Enjoy!0 -
Struggling to keep track at the moment. My mums off her feet due to an abscess in her foot and my dads just found out he has cancer. Plus my body is struggling to cope.
Any advice for getting back on track is most welcome!0
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