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Back pain and spasms
I was diagnosed with PMR in 2020. I have been on prednisolone since then trying to type it off but only actually managed to get off of the drug for about three weeks before having to restart. I’ve only really had pain in my lower body and legs, only occasionally in my arms. Recently I have had acute
I was diagnosed with PMR in 2020. I have been on prednisolone since then trying to type it off but only actually managed to get off of the drug for about three weeks before having to restart. I’ve only really had pain in my lower body and legs, only occasionally in my arms. Recently I have had acute
Ladybay0
in
PMRGCAuk
4 months ago
Adenomyosis diagnosis journey
Hi Everyone, This is a long one but I hope it helps someone out there who may be on the same journey! From my first period when I was 11 I had long heavy painful periods, It would wipe me out, I was told that it was normal and that periods were painful and that as a young lady I needed to get on with
Hi Everyone, This is a long one but I hope it helps someone out there who may be on the same journey! From my first period when I was 11 I had long heavy painful periods, It would wipe me out, I was told that it was normal and that periods were painful and that as a young lady I needed to get on with
HolsBamboozledwomb
in
Endometriosis UK
4 months ago
Pregabalin doseage
Hi, so i have now been on 150mg/day and i'm still experiencing very acute pain in my legs (quads mostly and calves) I have to get up and take ibruprofen plus co-codamol. As I am a PT and train a lot, it can be hard to separate what might be RLS vs training soreness. I first went on Ropinirole after
Hi, so i have now been on 150mg/day and i'm still experiencing very acute pain in my legs (quads mostly and calves) I have to get up and take ibruprofen plus co-codamol. As I am a PT and train a lot, it can be hard to separate what might be RLS vs training soreness. I first went on Ropinirole after
bluffpt
in
Restless Legs Syndrome
5 months ago
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Solutions needed to manage nerve pains ( Post herpetic neuralgia ) after shingles .
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
Oldscores1
in
CLL Support
5 months ago
Help please!
Goodmorning, I was first diagnosed with PMR back in 2014, usual treatment with pred, taper etc. Then diagnosed in 2021 with Fibromyalgia aand on 2mg maintenance dose of pred & 60mg Duloxetine plus Co codamol as needed. Then last month caught Covid for first time. Have had all vaccines. It really hit
Goodmorning, I was first diagnosed with PMR back in 2014, usual treatment with pred, taper etc. Then diagnosed in 2021 with Fibromyalgia aand on 2mg maintenance dose of pred & 60mg Duloxetine plus Co codamol as needed. Then last month caught Covid for first time. Have had all vaccines. It really hit
September17
in
PMRGCAuk
5 months ago
Yesterday Thursday 29th & 1000 Steps
So my dear wife wanted to go shopping for bits and bobs and was going to get a taxi both ways so I said I'd join her. Dunelm. Nice cafe's and cake's etc for when I get bored I too it really easy and wore my new Skechers with no socks. I used one crutch (please don't chastise me) I didn't go flitting
So my dear wife wanted to go shopping for bits and bobs and was going to get a taxi both ways so I said I'd join her. Dunelm. Nice cafe's and cake's etc for when I get bored I too it really easy and wore my new Skechers with no socks. I used one crutch (please don't chastise me) I didn't go flitting
Hidden
in
PMRGCAuk
5 months ago
LDN journey.
Well, after making enquiries here, reading what I could and talking to my GP I had my Dicksons Chemist appointment this morning at a cost of £50. They rang half an hour late and as the conversation went on they said - Oh, if we had known you were on Co-codamol (Zapane) we would not talked to you about
Well, after making enquiries here, reading what I could and talking to my GP I had my Dicksons Chemist appointment this morning at a cost of £50. They rang half an hour late and as the conversation went on they said - Oh, if we had known you were on Co-codamol (Zapane) we would not talked to you about
Onceabiker
in
Fibromyalgia Action UK
5 months ago
I think Tramadol has caused my RLS
Hi everyone, I'm new here and I'd love some advice, please. I have MS - I was diagnosed in the late 90s. I'm lucky that it hasn't affected me badly (yet), but I do suffer from pretty severe nerve pain. I managed it with Co-Codamol 30/500 for years. I'd been prescribed 8 per day but rarely took more
Hi everyone, I'm new here and I'd love some advice, please. I have MS - I was diagnosed in the late 90s. I'm lucky that it hasn't affected me badly (yet), but I do suffer from pretty severe nerve pain. I managed it with Co-Codamol 30/500 for years. I'd been prescribed 8 per day but rarely took more
Princegwyn
in
Restless Legs Syndrome
5 months ago
Co codamol
I take Co codamol for back and ankle pain but am finding it doesn't work as well..I've been on them for 3 years..any thoughts?
I take Co codamol for back and ankle pain but am finding it doesn't work as well..I've been on them for 3 years..any thoughts?
Glasgow1967
in
Atrial Fibrillation Support
5 months ago
lidocaine infusion didn’t work - I feel so down, what should I do?
I have severe chronic pain, and I’ve tried lots of medicines (nortriptyline, amitryptyline, co-codamol, codeine, tramadol, tapentadol), I’m currently on gabapentin 400mg x 3 times a day. But still in SO much pain. So I went to a private doc who suggested lidocaine infusions. I had my first infusion
I have severe chronic pain, and I’ve tried lots of medicines (nortriptyline, amitryptyline, co-codamol, codeine, tramadol, tapentadol), I’m currently on gabapentin 400mg x 3 times a day. But still in SO much pain. So I went to a private doc who suggested lidocaine infusions. I had my first infusion
roselavenders
in
Pain Concern
5 months ago
Clear liver on ultrasound but GGT and other markers rising.
Late 50s female, and TBH, I've always enjoyed wine. The whole dining experience thing and decompressing from a stressful job, wine has, in the past, helped. However, In the autumn of last year, I developed a pain in my right side. I went to the DR. Bloods revealed a GGT of 148. The GP told me to cut
Late 50s female, and TBH, I've always enjoyed wine. The whole dining experience thing and decompressing from a stressful job, wine has, in the past, helped. However, In the autumn of last year, I developed a pain in my right side. I went to the DR. Bloods revealed a GGT of 148. The GP told me to cut
Caringgirl1
in
British Liver Trust
5 months ago
Update on safe pain relief
Received phone call from Liver Doctor yesterday tea time. I was told that it was safe for me to take up to 3g Paracetemol daily which is up to 6 x 500mg tablets daily. 8mg of Codeine daily can be taken if necessary along with a laxative as it can cause constipation. Tramadol and other Opiates should
Received phone call from Liver Doctor yesterday tea time. I was told that it was safe for me to take up to 3g Paracetemol daily which is up to 6 x 500mg tablets daily. 8mg of Codeine daily can be taken if necessary along with a laxative as it can cause constipation. Tramadol and other Opiates should
Cat1218
in
British Liver Trust
5 months ago
Hip Pain
Hi, I am 21 years old and have been suffering with Endometriosis for 10 years now (although I was diagnosed in 2021). I have been on Prostap injections and Tibolone HRT since July 2021 as previous to this I was wheelchair bound on 3 occasions due to the severity of the pain and nothing else worked. Prostap
Hi, I am 21 years old and have been suffering with Endometriosis for 10 years now (although I was diagnosed in 2021). I have been on Prostap injections and Tibolone HRT since July 2021 as previous to this I was wheelchair bound on 3 occasions due to the severity of the pain and nothing else worked. Prostap
Football3018
in
Endometriosis UK
5 months ago
Pain relief medication
Hi there, I had a stent fitted in LAD in 2021. Have a mild to moderate aortic leaky valve. I also have two slipped discs in lower back. For the most part, I have no pain or restricted movement. Every now and again, I’m in excruciating pain with my back for a few days, then all goes back to normal
Hi there, I had a stent fitted in LAD in 2021. Have a mild to moderate aortic leaky valve. I also have two slipped discs in lower back. For the most part, I have no pain or restricted movement. Every now and again, I’m in excruciating pain with my back for a few days, then all goes back to normal
simplysal
in
British Heart Foundation
5 months ago
diagnosed recently and struggling
hi everyone I came across this group and joined in hopes I can find some solace with others who may be going through the same thing, if not similar. I broke my leg in 5 places a few years ago and I’ve never had a day pain free. The pain became widespread and has become worse as time has gone on. I
hi everyone I came across this group and joined in hopes I can find some solace with others who may be going through the same thing, if not similar. I broke my leg in 5 places a few years ago and I’ve never had a day pain free. The pain became widespread and has become worse as time has gone on. I
Huskymomma
in
Fibromyalgia Action UK
5 months ago
is everyone else not getting diagnosed or much treatment?
I’ve had severe period pain for years, when I wasn’t taking painkiller in time I would be sick and feel faint. I have tried paracetamol and ibuprofen in the pad which did nothing. I took naproxen 500mg which used to completely block my pain but now only stops it being severe. More recently I’ve been
I’ve had severe period pain for years, when I wasn’t taking painkiller in time I would be sick and feel faint. I have tried paracetamol and ibuprofen in the pad which did nothing. I took naproxen 500mg which used to completely block my pain but now only stops it being severe. More recently I’ve been
pinkie25
in
Endometriosis UK
6 months ago
Sunbathing with Butec patches
I’m using Butec 10mg patches which do help slightly. The most benefit from changing from Co codamol is that I no longer feel bloated. I have recently read that you shouldn’t sun bathe whilst using the patches. I am due to go abroad in May and possibly in August. I find the warmth helps my pain somewhat
I’m using Butec 10mg patches which do help slightly. The most benefit from changing from Co codamol is that I no longer feel bloated. I have recently read that you shouldn’t sun bathe whilst using the patches. I am due to go abroad in May and possibly in August. I find the warmth helps my pain somewhat
Wilson16
in
Fibromyalgia Action UK
6 months ago
Low Dose Naltrexone (LDN)
Hi, this is my first starter post although I have replied to a few questions from others. After being run over by a car 40 years ago and suffering multiple skeletal fractures I have undergone 14 operations so far. Around 2019 I was further diagnosed with Fybromyagia. Multiple medicines later and serious
Hi, this is my first starter post although I have replied to a few questions from others. After being run over by a car 40 years ago and suffering multiple skeletal fractures I have undergone 14 operations so far. Around 2019 I was further diagnosed with Fybromyagia. Multiple medicines later and serious
Onceabiker
in
Fibromyalgia Action UK
6 months ago
Endometriosis
I've had period pain since I was 15 and each year the pain only gets worse. When I became 18, the pain became crippling. The pain will start mildly a week or two before I start my period. Then when I start my period the pain intensifies. I find it hard to walk, I feel like I have a fever then have an
I've had period pain since I was 15 and each year the pain only gets worse. When I became 18, the pain became crippling. The pain will start mildly a week or two before I start my period. Then when I start my period the pain intensifies. I find it hard to walk, I feel like I have a fever then have an
Tigerlily34
in
Women's Health
6 months ago
Endo diagnosis
I've had period pain since I was 15 and each year the pain only gets worse. When I became 18, the pain became crippling. The pain will start mildly a week or two before I start my period. Then when I start my period the pain intensifies. I find it hard to walk, I feel like I have a fever then have an
I've had period pain since I was 15 and each year the pain only gets worse. When I became 18, the pain became crippling. The pain will start mildly a week or two before I start my period. Then when I start my period the pain intensifies. I find it hard to walk, I feel like I have a fever then have an
Tigerlily34
in
Endometriosis UK
6 months ago
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