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Unexplained Leg and Thigh Pain
Morning all, not sure that this anything to do with the forum and I wasn't going to mention it until my long chat with the doctor yesterday morning. Since Thursday I have been suffering from excruciating pain in my right leg, which appears to start in/around my knee and which then radiates up to my thigh
Morning all, not sure that this anything to do with the forum and I wasn't going to mention it until my long chat with the doctor yesterday morning. Since Thursday I have been suffering from excruciating pain in my right leg, which appears to start in/around my knee and which then radiates up to my thigh
Bcol
in
PMRGCAuk
2 years ago
Sciatica hell
Hi. I have been diagnosed (over phone!) either sciatica. It crept upon me over a few days, no obvious cause, I've now had it 2 weeks. Its so very painful - a gnawing deep ache across right buttock down back of leg into calf. Can't get comfortable anywhere and difficulty walking without holding on
Hi. I have been diagnosed (over phone!) either sciatica. It crept upon me over a few days, no obvious cause, I've now had it 2 weeks. Its so very painful - a gnawing deep ache across right buttock down back of leg into calf. Can't get comfortable anywhere and difficulty walking without holding on
Lunadoo
in
Pain Concern
2 years ago
Help with unexplained weight loss
Hello all, I am waiting upon the fitting of an ICD. In the meantime, as a type II diabetic, I have been having terrible problems with my guts. Lost 20lbs in just a month. Seems my medications had pushed me into Ketosis which probably is the cause. This came on top of painful cramps and griping in my
Hello all, I am waiting upon the fitting of an ICD. In the meantime, as a type II diabetic, I have been having terrible problems with my guts. Lost 20lbs in just a month. Seems my medications had pushed me into Ketosis which probably is the cause. This came on top of painful cramps and griping in my
Brunovsky
in
British Heart Foundation
2 years ago
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Cerrelle constant bleeding
I was given the progesterone only pill because I can’t take the combination pill as I have aurora migraines and it increases the risk of stroke. Well I have been bleeding constantly for two weeks. I’ve been on it for 5 weeks. I can handle the annoyance of a constant period but not the pain and discomfort
I was given the progesterone only pill because I can’t take the combination pill as I have aurora migraines and it increases the risk of stroke. Well I have been bleeding constantly for two weeks. I’ve been on it for 5 weeks. I can handle the annoyance of a constant period but not the pain and discomfort
ZebraZone
in
Endometriosis UK
2 years ago
Please help. Where do I go next?
I had my first gynaecology appointment this morning and have come away feeling like I haven’t been listened to and my symptoms are not real. I am considering my next steps and whether to go back to my GP. I had been waiting 1.5 years for this appointment and feel very upset that I may now not get any
I had my first gynaecology appointment this morning and have come away feeling like I haven’t been listened to and my symptoms are not real. I am considering my next steps and whether to go back to my GP. I had been waiting 1.5 years for this appointment and feel very upset that I may now not get any
sweetpea2288
in
Endometriosis UK
2 years ago
Painkillers
I have cirrhosis and my back has just given out on me (I have a dodgy disc) I know my pain relief options are limited but I need something as it is extrememly painful. What is the latest advice about what painkillers are best for the liver? Co-codamol is what I have here (and paracetamol) but I know
I have cirrhosis and my back has just given out on me (I have a dodgy disc) I know my pain relief options are limited but I need something as it is extrememly painful. What is the latest advice about what painkillers are best for the liver? Co-codamol is what I have here (and paracetamol) but I know
theoldboiler
in
British Liver Trust
2 years ago
Is it a flare?
Diagnosed last September and have been able to lead a fairly normal life since apart from stiffness and tiredness. Had got down to 11 mg tapering slowly until this morning when I got out of bed and felt as if someone was sticking red hot knives into my left hip. I can honestly say it’s the worst pain
Diagnosed last September and have been able to lead a fairly normal life since apart from stiffness and tiredness. Had got down to 11 mg tapering slowly until this morning when I got out of bed and felt as if someone was sticking red hot knives into my left hip. I can honestly say it’s the worst pain
Jayveedee
in
PMRGCAuk
2 years ago
Pip
Well just been signed off sick from work pain and exhaustion so bad, gp has upped my gabapentin and put me on co codamol I feel so sick on them, phoned citizens advice regarding pip does anyone else receive this can my husband claim carers allowance? Never been on benefits so we have no clue what to
Well just been signed off sick from work pain and exhaustion so bad, gp has upped my gabapentin and put me on co codamol I feel so sick on them, phoned citizens advice regarding pip does anyone else receive this can my husband claim carers allowance? Never been on benefits so we have no clue what to
Minniebuttons
in
Fibromyalgia Action UK
2 years ago
Feeling so fed up
Hey fellow spoonies. Just after some advice on how you'd approach this situation. I feel like I've pretty much been in a flare on and off since Christmas. I was given some pred tablets (v low dose) for some of Jan and Feb, which really helped. But since then it's gotten worse agqain. Then two weeks
Hey fellow spoonies. Just after some advice on how you'd approach this situation. I feel like I've pretty much been in a flare on and off since Christmas. I was given some pred tablets (v low dose) for some of Jan and Feb, which really helped. But since then it's gotten worse agqain. Then two weeks
SlothSandpit
in
NRAS
2 years ago
help
I had my laparoscopy a month ago and have a lot of pelvic pain even after one month taking two co codamol three times a day but still have stool leak and anal pain.are these normal symptoms after surgery 😢
I had my laparoscopy a month ago and have a lot of pelvic pain even after one month taking two co codamol three times a day but still have stool leak and anal pain.are these normal symptoms after surgery 😢
Mylovepari1
in
Endometriosis UK
2 years ago
Symptoms abate when the immune system has something else to deal with ?
Hi. I’ve broken my ankle and was expecting that with the PMR too, using crutches was going to be very painful with my shoulders and also shuffling upstairs on my bum using good leg and arms for leverage. In fact. I’ve not felt a twinge from PMR since doing it two weeks ago today. I’ve stayed on my
Hi. I’ve broken my ankle and was expecting that with the PMR too, using crutches was going to be very painful with my shoulders and also shuffling upstairs on my bum using good leg and arms for leverage. In fact. I’ve not felt a twinge from PMR since doing it two weeks ago today. I’ve stayed on my
Buttonshutton
in
PMRGCAuk
2 years ago
Knee pain can't take naproxen. Any suggestions please?
Hi. I'm new here. Can anyone recommend any alternatives to naproxen. I can't take them now as have afib and on apixaban. I have knee arthritis and only ever took them for walking / exercise and pain going down stairs. I realise many are suffering much more. But now after about 30 mins of walking the
Hi. I'm new here. Can anyone recommend any alternatives to naproxen. I can't take them now as have afib and on apixaban. I have knee arthritis and only ever took them for walking / exercise and pain going down stairs. I realise many are suffering much more. But now after about 30 mins of walking the
Sue2528
in
Osteoarthritis Action
2 years ago
Progress and any info on ranolaxine?
Had an appt with cardiologist next week (face to face) but this has been cancelled via email ,due to unforeseen circumstances and they cannot arrange a new appt so now on a waiting list. This was very important to me after contacting heart nurse three weeks ago and visit to A&E a week ago. It was also
Had an appt with cardiologist next week (face to face) but this has been cancelled via email ,due to unforeseen circumstances and they cannot arrange a new appt so now on a waiting list. This was very important to me after contacting heart nurse three weeks ago and visit to A&E a week ago. It was also
Hidden
in
British Heart Foundation
2 years ago
Acalabrutinib
Hi everyone, I'm new here. I started on Acalabrutinib in February 2022 after being in remission for 12 years. Unfortunately I started getting awful headaches, sickness, palpatations, confusion, itching, pain and blood pressure shot up. Eventually was taken off all the other drugs I was taking (Allopurinol
Hi everyone, I'm new here. I started on Acalabrutinib in February 2022 after being in remission for 12 years. Unfortunately I started getting awful headaches, sickness, palpatations, confusion, itching, pain and blood pressure shot up. Eventually was taken off all the other drugs I was taking (Allopurinol
BethIlia
in
CLL Support
2 years ago
Numbness problems
I have GPA and am currently on azathioprine, prednisone and
Co
trimoxazole
.
I have GPA and am currently on azathioprine, prednisone and
Co
trimoxazole
.
Vqueen
in
Vasculitis UK
3 years ago
Fed up with pain
I haven’t been officially diagnosed with IBS and have been fine for months and in the last month have had a flare up. (I can only put this down with doing an aspect of my old job with my old boss as a temporary fix in the business, loved the job didn’t like the boss). Left side pain which constantly
I haven’t been officially diagnosed with IBS and have been fine for months and in the last month have had a flare up. (I can only put this down with doing an aspect of my old job with my old boss as a temporary fix in the business, loved the job didn’t like the boss). Left side pain which constantly
Epiphanies
in
IBS Network
2 years ago
Are my expectations too high?
I was diagnosed 15 months ago. I was started on prednisolone then added methotrexate then sulfasalazine then abatacept. I am now taking all four plus co codamol and naproxen occasionally. I would have expected to be able to function but my hands are still very stiff and painful and am very fatigued.
I was diagnosed 15 months ago. I was started on prednisolone then added methotrexate then sulfasalazine then abatacept. I am now taking all four plus co codamol and naproxen occasionally. I would have expected to be able to function but my hands are still very stiff and painful and am very fatigued.
Oscardoggy
in
NRAS
2 years ago
Online doctor's service ordered to pay £13k for providing unregistered services
We often see members asking about pharmacies which offer some form of consultation before prescribing and supplying prescription-only or pharmacy medicines. This story is about one with a very questionable way of working:
[i]Online doctor's service ordered to pay £13k for providing unregistered
We often see members asking about pharmacies which offer some form of consultation before prescribing and supplying prescription-only or pharmacy medicines. This story is about one with a very questionable way of working:
[i]Online doctor's service ordered to pay £13k for providing unregistered
helvella
Thyroid UK
in
Thyroid UK
2 years ago
Alternative to naproxen
Alternative to naproxen Hi I’ve been taking naproxen for some years now for RA, but I also have CKD ( chronic kidney disease). After going for my six monthly checkup with the RA specialist, she has suggested I stop naproxen and switch to co-codamol, which I reluctant to do. Has any one been in the
Alternative to naproxen Hi I’ve been taking naproxen for some years now for RA, but I also have CKD ( chronic kidney disease). After going for my six monthly checkup with the RA specialist, she has suggested I stop naproxen and switch to co-codamol, which I reluctant to do. Has any one been in the
Chris_O
in
NRAS
2 years ago
8 days post ablation
What a week?! I had an RF ablation at the start of last week but felt, what I thought, was excessive pain in my chest (particularly when lying on my back) 2/3 days after but just stuck with it thinking it was a standard recovery symptom for RF as I’d only had cryo done before. However on Thursday night
What a week?! I had an RF ablation at the start of last week but felt, what I thought, was excessive pain in my chest (particularly when lying on my back) 2/3 days after but just stuck with it thinking it was a standard recovery symptom for RF as I’d only had cryo done before. However on Thursday night
Safc1983
in
AF Association
2 years ago
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