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Pain relief
Hi can anyone say what type of painkillers they use to help with polymyalgia. Thanks
Hi can anyone say what type of painkillers they use to help with polymyalgia. Thanks
Uglow
in
PMRGCAuk
3 years ago
Low Level Laser Therapy for Fibromyalgia
Hi, I posted in the RA group asking about LLLT for
pain
management
to see if anyone had tried it. I have struggled to see reviews online that felt that genuine. A lot of great videos made by the company that do a home device.... for a lot of money.
Hi, I posted in the RA group asking about LLLT for
pain
management
to see if anyone had tried it. I have struggled to see reviews online that felt that genuine. A lot of great videos made by the company that do a home device.... for a lot of money.
charlie9
in
Fibromyalgia Action UK
3 years ago
Is this normal?
Hey everyone. My doctor has said after speaking with a gynaecologist that I have endo - I haven’t had a scan and finding it impossible to get one. I’ve been in agony for two weeks now, started during my period and still here afterwards - at first the pain was in the middle and now it’s moved to the right
Hey everyone. My doctor has said after speaking with a gynaecologist that I have endo - I haven’t had a scan and finding it impossible to get one. I’ve been in agony for two weeks now, started during my period and still here afterwards - at first the pain was in the middle and now it’s moved to the right
abbiecx_
in
Endometriosis UK
3 years ago
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Pain management consultant
Hello , I was told yesterday I have fibromyalgia , I also have severe Ankyolosing Spondylitis. My GP who is excellent said there is not really any treatment for it. I am on Adalimumab for the AS which doesn't really help. I ache all over have muscles that are too sore to touch and have severe fatigue
Hello , I was told yesterday I have fibromyalgia , I also have severe Ankyolosing Spondylitis. My GP who is excellent said there is not really any treatment for it. I am on Adalimumab for the AS which doesn't really help. I ache all over have muscles that are too sore to touch and have severe fatigue
Stephanie6637
in
Fibromyalgia Action UK
3 years ago
Flare or not
I reduced prednisone on 2/11 now 11:11 and my hips don’t lie lol I’m not sure if I’m having a flare or just in pain. But painkillers not shifting. I hate the idea of going up on pred again but will follow your advice. 14to 13 mg It’s really restricted my walking. Thank you folks
I reduced prednisone on 2/11 now 11:11 and my hips don’t lie lol I’m not sure if I’m having a flare or just in pain. But painkillers not shifting. I hate the idea of going up on pred again but will follow your advice. 14to 13 mg It’s really restricted my walking. Thank you folks
Uglow
in
PMRGCAuk
3 years ago
Zoladex for severe endometriosis
My endometriosis is very severe and my consultant has advised 6 months of Zoladex to try to assist with the
pain
management
whilst I am on the waiting list for extraction surgery. The list is obviously long with covid waiting times etc so this is a last resort to keep me going whilst I wait.
My endometriosis is very severe and my consultant has advised 6 months of Zoladex to try to assist with the
pain
management
whilst I am on the waiting list for extraction surgery. The list is obviously long with covid waiting times etc so this is a last resort to keep me going whilst I wait.
Spangalow07
in
Endometriosis UK
3 years ago
Pain advice
Hey guys Any advice on pain killers to take or any sort of therapy to relief pain n stiffness in top of back neck and shoulders
Hey guys Any advice on pain killers to take or any sort of therapy to relief pain n stiffness in top of back neck and shoulders
Chocolate-lady
in
Fibromyalgia Action UK
3 years ago
Temperature during Endo flare
Hi all, I am hoping that someone is awake and more knowledgeable than me about this. Today my flare up has well and truly arrived, I have had a worse build up in respect of migraines disturbing vision, nausea and muscular pain from my neck all down my back and now tonight the pain is really awful, I
Hi all, I am hoping that someone is awake and more knowledgeable than me about this. Today my flare up has well and truly arrived, I have had a worse build up in respect of migraines disturbing vision, nausea and muscular pain from my neck all down my back and now tonight the pain is really awful, I
HolsBamboozledwomb
in
Endometriosis UK
3 years ago
Insane lower back, buttock
Hi. From 3 nights ago, I was perfectly fine, I did some cleaning up about 4 hours before bed and layed on my back watching something on my phone, had to go toilet and realized severe lower pack pain that seems to be affecting both sides but mostly left side. I don't have any other symptoms or problems
Hi. From 3 nights ago, I was perfectly fine, I did some cleaning up about 4 hours before bed and layed on my back watching something on my phone, had to go toilet and realized severe lower pack pain that seems to be affecting both sides but mostly left side. I don't have any other symptoms or problems
Marot
in
Pain Concern
3 years ago
Bit of a setback after last chemo
Last chemo was on Friday October 29th. Usual after effects - i.e. OK Friday and Saturday up to the evening; not too bad Sunday until the afternoon. As usual started to feel yukky and went to bed. Had a bit of cornflakes Monday morning and then nothing and off to bed again. Taking anti sickness pills
Last chemo was on Friday October 29th. Usual after effects - i.e. OK Friday and Saturday up to the evening; not too bad Sunday until the afternoon. As usual started to feel yukky and went to bed. Had a bit of cornflakes Monday morning and then nothing and off to bed again. Taking anti sickness pills
magstherunner
in
The Roy Castle Lung Cancer Foundation
3 years ago
Should I be worried?
Hi all, So im new here but I have a few concerns that I was hoping to get some clarification on, so here goes……. Some time ago i was taken to hospital with a suspected PE (blood clot), I had some scans done and thankfully no blood clot was found. A few weeks later and I was looking over my medical records
Hi all, So im new here but I have a few concerns that I was hoping to get some clarification on, so here goes……. Some time ago i was taken to hospital with a suspected PE (blood clot), I had some scans done and thankfully no blood clot was found. A few weeks later and I was looking over my medical records
MRSB18
in
HFI Connect - Hepatitis
3 years ago
Endometriosis, adhesions and struggling to work.
Hi everyone, I’ve been off work sick for the last week with constant abdominal and lower back pain made worse when sitting. I suffer with my bowels and long periods and have spent the past two years trying different ways of resolving my issues. My job involves me spending hours on the phone so no alternative
Hi everyone, I’ve been off work sick for the last week with constant abdominal and lower back pain made worse when sitting. I suffer with my bowels and long periods and have spent the past two years trying different ways of resolving my issues. My job involves me spending hours on the phone so no alternative
Las20
in
Endometriosis UK
3 years ago
Endo specialist
5 weeks ago this phone call appointment was, and I’m yet to wait to hear back from with estimated dates of a pelvic MRI, a laparoscopy date and also the doctors cannot do anything about my
pain
management
until they sign off the all clear for my prostap injections.
5 weeks ago this phone call appointment was, and I’m yet to wait to hear back from with estimated dates of a pelvic MRI, a laparoscopy date and also the doctors cannot do anything about my
pain
management
until they sign off the all clear for my prostap injections.
louisepercy2000
in
Endometriosis UK
3 years ago
Castle Walt Disney designed the castle he built at Disney Land. This castle welcomes you to the outskirts of the diamond village of Toledo.
My name is Anna, I was officially diagnosed by BMB of a Myeloproliferative Neoplasm, Essential Thrombocytosis in December 2011. I have been aware of the condition due to the consistently high platelets counts since I got a DVT while travelling in 1999. I have also been informed over the years and
My name is Anna, I was officially diagnosed by BMB of a Myeloproliferative Neoplasm, Essential Thrombocytosis in December 2011. I have been aware of the condition due to the consistently high platelets counts since I got a DVT while travelling in 1999. I have also been informed over the years and
Gordito
in
MPN Voice
3 years ago
GP rant🥲
I had to se my GP following receiving a letter from my neurologist advising about the MSA & medication will be needed to be prescribed by them. It was 10 mins I won’t forget, he read the letter and then said ‘ I don’t know why they send you a copy, so misleading ‘probable’ might mean you don’t have
I had to se my GP following receiving a letter from my neurologist advising about the MSA & medication will be needed to be prescribed by them. It was 10 mins I won’t forget, he read the letter and then said ‘ I don’t know why they send you a copy, so misleading ‘probable’ might mean you don’t have
Bizzyissy
in
Multiple System Atrophy Trust
3 years ago
Mysterious chest pain
Hoping for someone experiencing similar issues. I have had excruciating upper left chest pain for over 5 weeks. My Gp has sent me to a and e twice because the symptoms match a heart attack. ECG bloods and chest X-ray all normal. Diagnosed first with Costochondritis and then Bornholm disease. No painkillers
Hoping for someone experiencing similar issues. I have had excruciating upper left chest pain for over 5 weeks. My Gp has sent me to a and e twice because the symptoms match a heart attack. ECG bloods and chest X-ray all normal. Diagnosed first with Costochondritis and then Bornholm disease. No painkillers
Ponkysue
in
Thyroid UK
3 years ago
LIDOCAINE 5% PAIN PATCHES
My sister-in-law has these patches for her back pain (she has a steel rod for a back), and one day at her house she gave me a few for my muscle spasms and nerve pain. They are miracle workers! I asked my doctor for a prescription. He said FDA only recognized them for permanent Shingle nerve pain. My
My sister-in-law has these patches for her back pain (she has a steel rod for a back), and one day at her house she gave me a few for my muscle spasms and nerve pain. They are miracle workers! I asked my doctor for a prescription. He said FDA only recognized them for permanent Shingle nerve pain. My
agapepilgrim
in
My MSAA Community
3 years ago
New and struggling
I take co-codamol and ibuprofen 500 but it doesn't seem to touch the
pain
. Any advice welcome on
pain
management
and mental health. I try swimming but I ache the next day.
I take co-codamol and ibuprofen 500 but it doesn't seem to touch the
pain
. Any advice welcome on
pain
management
and mental health. I try swimming but I ache the next day.
koala84
in
Fibromyalgia Action UK
3 years ago
Feel like I'm getting no where
They are now telling me that I need a bowel scan and to be referred to
pain
management
as they are saying of not coping well. I'm currently on tramadol for the pain.
They are now telling me that I need a bowel scan and to be referred to
pain
management
as they are saying of not coping well. I'm currently on tramadol for the pain.
Kelseyjw
in
Endometriosis UK
3 years ago
Painkillers?
Hi. Feel a bit of a fraud as after reading on here, I am def not as bad as others..sorry...however I constantly have pain in my lower back, my legs and hips ache if i stand/sit for any length of time, I regularly have throbbing pain in my shins- even lying in bed in the middle of the night. I have a
Hi. Feel a bit of a fraud as after reading on here, I am def not as bad as others..sorry...however I constantly have pain in my lower back, my legs and hips ache if i stand/sit for any length of time, I regularly have throbbing pain in my shins- even lying in bed in the middle of the night. I have a
Kaytlou
in
Fibromyalgia Action UK
3 years ago
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