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Groin pain
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How to deal with side effects of feeling hot from pain meds and antidepressants for pain?
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
Hidden
in
Neuropathy Support
10 months ago
RSV and Flare
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
MegfromOz
in
PMRGCAuk
10 months ago
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
10 months ago
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Adenomyosis/Endometriosis Pain Management
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
ABFr23
in
Endometriosis UK
11 months ago
pain in knee
pain in knee and body the answer is green lipped mussel extract works for me better than new knee helps fm pain to
pain in knee and body the answer is green lipped mussel extract works for me better than new knee helps fm pain to
Eastwood1
in
Pain Concern
1 year 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
11 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
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
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
Intense groin pain
My surgery confirm OA and general wear and tear of hip and yes I understand about referred
pain
in the
groin
but I have no other
pain
in the hip area at all and I am completely mobile, so am still confused - on the positive side I have an appointment with my requested GP on13th April.
My surgery confirm OA and general wear and tear of hip and yes I understand about referred
pain
in the
groin
but I have no other
pain
in the hip area at all and I am completely mobile, so am still confused - on the positive side I have an appointment with my requested GP on13th April.
Oboes22
in
PMRGCAuk
2 years 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
High Folate with PA terrible GP
I still don't know what's going on with me from the
groin
pain
, but the ER ruled out appendicitis and diverticulitis or any infection with a ct scan. They don't know why I'm in this pain but they gave me a steroid shot in my hip.
I still don't know what's going on with me from the
groin
pain
, but the ER ruled out appendicitis and diverticulitis or any infection with a ct scan. They don't know why I'm in this pain but they gave me a steroid shot in my hip.
EllaNore
in
Pernicious Anaemia Society
7 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
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