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compressed vertebrae, i asked dr about stronger pain medication and they said no -- i wonder why?
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
MayGodBlessYou
in
Bone Health and Osteoporosis UK
9 months ago
Feel like just giving up on any help from GP'S
Recently my Psychiatrist wrote to my GP as regards
Pain
Management
for me. I didn't expect much in response & I was right.
Recently my Psychiatrist wrote to my GP as regards
Pain
Management
for me. I didn't expect much in response & I was right.
maddie_1234
in
Pelvic Radiation Disease Association
11 months ago
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
9 months ago
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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
9 months ago
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
9 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
9 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
9 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
9 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
9 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
9 months ago
Pain Management after spine surgeries
I took a
pain
management
course through the VA which helped me manage the
pain
, but I still have, what I call, flares of break through pain. I also use heat, physical therapy, stretching, exercise and meditation as part of the management.
I took a
pain
management
course through the VA which helped me manage the
pain
, but I still have, what I call, flares of break through pain. I also use heat, physical therapy, stretching, exercise and meditation as part of the management.
mifel
in
Pain Concern
1 year ago
Private Consultation Findings - thoughts on next steps
Own GP has tried me on contraceptives & meds for
pain
management
, which nearly tipped me over the edge. After a scare with my mental health, I decided to come off everything and see a specialist privately.
Own GP has tried me on contraceptives & meds for
pain
management
, which nearly tipped me over the edge. After a scare with my mental health, I decided to come off everything and see a specialist privately.
usernames123
in
Endometriosis UK
10 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
9 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
9 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
9 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
9 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
9 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
9 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
9 months 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
9 months ago
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