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Airing Pain 140: Out now!
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
PainConcernHelpline
Pain Concern
in
Pain Concern
11 months ago
PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
dmart7
in
PMRGCAuk
7 months ago
constipation from panadeine, or vertebra nerves, or both?
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
MayGodBlessYou
in
Bone Health and Osteoporosis UK
11 months ago
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Pelvic Pain Worse at Night
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
PBGV24
in
Endometriosis UK
11 months ago
Painkillers
I have been on Gabapentin and Tramadol for 5 years to help with pain. I have now been told GP will no longer prescribe as they are shown to have no effect on chronic pain and are addictive. Anyone else had the same?
I have been on Gabapentin and Tramadol for 5 years to help with pain. I have now been told GP will no longer prescribe as they are shown to have no effect on chronic pain and are addictive. Anyone else had the same?
Chardonnaylady
in
Fibromyalgia Action UK
11 months ago
Clinical trial - Recorded hypnosis or relaxation reduced cancer pain and anxiety. Hypnosis also improved fatigue and sleep.
Hypnosis and relaxation interventions for chronic pain management in cancer survivors: a randomized controlled trial Linda H. Eaton, Min Kyeong Jang, Mark P. Jensen, Kenneth C. Pike, Margaret M. Heitkemper & Ardith Z. Doorenbos Supportive Care in Cancer volume 31, Article number: 50 (2023) Cite this
Hypnosis and relaxation interventions for chronic pain management in cancer survivors: a randomized controlled trial Linda H. Eaton, Min Kyeong Jang, Mark P. Jensen, Kenneth C. Pike, Margaret M. Heitkemper & Ardith Z. Doorenbos Supportive Care in Cancer volume 31, Article number: 50 (2023) Cite this
Graham49
in
Fight Prostate Cancer
11 months ago
back spasm, can anything be done?
what do you do to get comfy or relieve pain? e.g take magnesium? something topical? thanks question 2, what pain medication have you used? i guess it'll be up to the prescribing doctor, but people here often have extra knowledge and tips
what do you do to get comfy or relieve pain? e.g take magnesium? something topical? thanks question 2, what pain medication have you used? i guess it'll be up to the prescribing doctor, but people here often have extra knowledge and tips
MayGodBlessYou
in
Bone Health and Osteoporosis UK
11 months ago
Does this sound like endo?
I have had chronic pelvic/ lower back pain for the past 12 years, it flares up to the point where I can't do anything, but lay in bed and then after a few days to weeks it calms down to just the "usual pain/ache" and the cycle continues. I have been to see so many doctors and trips to A&E over the years
I have had chronic pelvic/ lower back pain for the past 12 years, it flares up to the point where I can't do anything, but lay in bed and then after a few days to weeks it calms down to just the "usual pain/ache" and the cycle continues. I have been to see so many doctors and trips to A&E over the years
Shellbell2023
in
Endometriosis UK
11 months ago
Seeking advice on burning feet symptom and an endocronoligist recommendation in London
Hi everyone. Over the last two years I’ve learnt so much from this site and I’m very grateful. I’m looking for some advice relating to my hypothyroid symptoms. I was diagnosed nearly three years ago and am taking 50mg of Teva. My symptoms arrived suddenly, and I still have bouts of anxiety and depression
Hi everyone. Over the last two years I’ve learnt so much from this site and I’m very grateful. I’m looking for some advice relating to my hypothyroid symptoms. I was diagnosed nearly three years ago and am taking 50mg of Teva. My symptoms arrived suddenly, and I still have bouts of anxiety and depression
FW23
in
Thyroid UK
11 months ago
Negative SVT Ablation experience
Good Morning All, So I had my SVT Ablation on Thursday at St Thomas’. Not a great experience. Procedure took 3 and half hours. I was awake the whole time and conscious of everything! Four puncture wounds on groin. Two either side. I could feel the catheters going up into my veins and tweaking around
Good Morning All, So I had my SVT Ablation on Thursday at St Thomas’. Not a great experience. Procedure took 3 and half hours. I was awake the whole time and conscious of everything! Four puncture wounds on groin. Two either side. I could feel the catheters going up into my veins and tweaking around
Carolx
in
AF Association
11 months ago
Biopsy prior lap
Hello ladies! I am about to have a partial hysterectomy in december, i am already terrified, gutted, i am s...ing on myself with fear. My consultant told me I need to have a biopsy from my womb prior to surgery so he can know there is nothing dodgy there except a lot of fibroids he has already seen
Hello ladies! I am about to have a partial hysterectomy in december, i am already terrified, gutted, i am s...ing on myself with fear. My consultant told me I need to have a biopsy from my womb prior to surgery so he can know there is nothing dodgy there except a lot of fibroids he has already seen
Pisi
in
Endometriosis UK
11 months ago
Viral meningitis
My 17 year old daughter was diagnosed with viral meningitis last weekend and this was confirmed on Monday. Initially she was given antiviral and antibiotics because they was unsure if it was bacterial meningitis. She had been unwell for 5 or 6 weeks. Permanent headache that painkillers didn't touch
My 17 year old daughter was diagnosed with viral meningitis last weekend and this was confirmed on Monday. Initially she was given antiviral and antibiotics because they was unsure if it was bacterial meningitis. She had been unwell for 5 or 6 weeks. Permanent headache that painkillers didn't touch
Sylv1969
in
Meningitis Now
11 months ago
To family and friends who help us
HiThis post is a bit different from me. Those who have read any posts I've written know I have health conditions that like all of us we have to get on with no matter how much they suck. The side most people know about me where I live is that I'm a family carer. I have been a carer for different family
HiThis post is a bit different from me. Those who have read any posts I've written know I have health conditions that like all of us we have to get on with no matter how much they suck. The side most people know about me where I live is that I'm a family carer. I have been a carer for different family
19581979
in
British Liver Trust
11 months ago
coccyx pain
hello, I’m having issues with coccyx pain and am wondering whether it’s another exciting (😒) symptom of FA. I’m still ambulatory so not a wheelchair user but am having the problem when sitting on an upright chair- so I’m avoiding doing that as much as I can but it’s not always possible. I bought a
hello, I’m having issues with coccyx pain and am wondering whether it’s another exciting (😒) symptom of FA. I’m still ambulatory so not a wheelchair user but am having the problem when sitting on an upright chair- so I’m avoiding doing that as much as I can but it’s not always possible. I bought a
dansybelle
in
Ataxia UK
11 months ago
update on my health issues
Hi everyone, I can no longer work and had to give my job up due to my many disabilities that I have. I receive Personal Independence Payment and Employment and Support Allowance. Today I received a phone call to tell me that I can no longer get Employment and Support Allowance. I received nil points
Hi everyone, I can no longer work and had to give my job up due to my many disabilities that I have. I receive Personal Independence Payment and Employment and Support Allowance. Today I received a phone call to tell me that I can no longer get Employment and Support Allowance. I received nil points
Imagine1
in
Pain Concern
11 months ago
Surgery follow-up appointment
Hi all I had my surgery on the 30th of March, where they found four bits of endo. I did have stomach pains in my first month, but then I had an infection. From the second month after my surgery, I had stomach pains again, although it was at a lower intensity and frequency. Over the last couple of
Hi all I had my surgery on the 30th of March, where they found four bits of endo. I did have stomach pains in my first month, but then I had an infection. From the second month after my surgery, I had stomach pains again, although it was at a lower intensity and frequency. Over the last couple of
Bookobssessed
in
Endometriosis UK
11 months ago
Endo Diagnosis
Hi, I am unsure where to start off trying to get a diagnosis of endometriosis. I've been struggling for about 4 years now and have found out my gran and my mum both have endometriosis with them experiencing the same symptoms. All my symptoms line up with others that have endometriosis as well. My first
Hi, I am unsure where to start off trying to get a diagnosis of endometriosis. I've been struggling for about 4 years now and have found out my gran and my mum both have endometriosis with them experiencing the same symptoms. All my symptoms line up with others that have endometriosis as well. My first
LivePink
in
Endometriosis UK
11 months ago
newbie uc proctitis
Does anyone here have it, and what do u do for
rectal
pain
. I sit on ice packs, also have hemmoroids. ? Is it possible proctitis can trigger chronic utis?
Does anyone here have it, and what do u do for
rectal
pain
. I sit on ice packs, also have hemmoroids. ? Is it possible proctitis can trigger chronic utis?
Sdone
in
Crohn's and Colitis Support
1 year ago
sciatica and PD?
2 months ago after 2 10 hour train journeys I developed severe sciatic nerve pains down my right let and hip. these are making it very difficult/impossible to do my PD excercises. The GP only prescribes pain killers which don't really help. Web research seems to only suggest excercise stretching baby
2 months ago after 2 10 hour train journeys I developed severe sciatic nerve pains down my right let and hip. these are making it very difficult/impossible to do my PD excercises. The GP only prescribes pain killers which don't really help. Web research seems to only suggest excercise stretching baby
Nickcc
in
Cure Parkinson's
11 months ago
Oral thrush
Hello!:) I need some advice for this. I'm using Fostair, I really think it's from that inhaler. I have some white and red spots on my throat, nothing on my tongue yet. I have a few questions because this never happened before. Is oral thrush contagious? I'm afraid because I don't want to give it to
Hello!:) I need some advice for this. I'm using Fostair, I really think it's from that inhaler. I have some white and red spots on my throat, nothing on my tongue yet. I have a few questions because this never happened before. Is oral thrush contagious? I'm afraid because I don't want to give it to
VanillaCoffee
in
Asthma Community Forum
4 months ago
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