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NSAIDs
Hi everyone, hope you are having a good day. After my angioplasty I was put on Clopidogrel and I have read that you cannot take NSAIDs with them as it increases bleeding risks. I suffer with condrochronitis(inflammation of the chest wall) and I am having a flare up. This flare up has been going on for
Hi everyone, hope you are having a good day. After my angioplasty I was put on Clopidogrel and I have read that you cannot take NSAIDs with them as it increases bleeding risks. I suffer with condrochronitis(inflammation of the chest wall) and I am having a flare up. This flare up has been going on for
MB1969
in
British Heart Foundation
2 years ago
NSAIDS anyone ?
When I was diagnosed with RA in 1989 , along with other medication , I was given diclofenac as a NSAID . This was later changed to Meloxicam by my rheumatologist . Which I took daily until this year . Fast forward to May 2021 and I tripped on a step in the house and fell heavily onto my left hip
When I was diagnosed with RA in 1989 , along with other medication , I was given diclofenac as a NSAID . This was later changed to Meloxicam by my rheumatologist . Which I took daily until this year . Fast forward to May 2021 and I tripped on a step in the house and fell heavily onto my left hip
Briefencounter
in
NRAS
2 years ago
Getting diagnosed
I’ve recently been diagnosed with fibromyalgia by gp. Got to see a specialist in a couple of weeks. They won’t give me any stronger pain killers than naproxen. But I can’t cope I’m in agony as soon as I wake up till I go to sleep, I have a 16 month old who I can barely pick up or even sit and play on
I’ve recently been diagnosed with fibromyalgia by gp. Got to see a specialist in a couple of weeks. They won’t give me any stronger pain killers than naproxen. But I can’t cope I’m in agony as soon as I wake up till I go to sleep, I have a 16 month old who I can barely pick up or even sit and play on
Yellowbing24
in
Fibromyalgia Action UK
2 years ago
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Hi, I started experiencing lower back pain last year and over the course of a few month the pain spread to my lower abdomen. I was referred to a gynaecologist in April but as yet , I’ve still not herd anything . My doctor suggested that I have the implant taken out as it was nearly time for it to come
Hi, I started experiencing lower back pain last year and over the course of a few month the pain spread to my lower abdomen. I was referred to a gynaecologist in April but as yet , I’ve still not herd anything . My doctor suggested that I have the implant taken out as it was nearly time for it to come
Gretna02
in
Endometriosis UK
2 years ago
An unfortunate series of events
Hi I’m in a bit of a dilemma. Recently several things happened to me in quick succession. 1. My RA specialist ( locum ) advised me to reduce my MTX doseage. 2. I had a heart attack and my anti- inflammatory stopped ( naproxen ) I am now experiencing what I think is a flare ( shoulders / neck / back pain
Hi I’m in a bit of a dilemma. Recently several things happened to me in quick succession. 1. My RA specialist ( locum ) advised me to reduce my MTX doseage. 2. I had a heart attack and my anti- inflammatory stopped ( naproxen ) I am now experiencing what I think is a flare ( shoulders / neck / back pain
Chris_O
in
NRAS
2 years ago
Update : getting the right treatment
Update about the crystal maze that is my gp practice! So tried Naproxen for a week to be a compliant patient and not surprisingly it was awful. Shoulders as bad as ever but nausea and headache to boot 🙁 So stopped them and made yet another appt with the afor mentioned Extended scope practitioner .
Update about the crystal maze that is my gp practice! So tried Naproxen for a week to be a compliant patient and not surprisingly it was awful. Shoulders as bad as ever but nausea and headache to boot 🙁 So stopped them and made yet another appt with the afor mentioned Extended scope practitioner .
Romilly2
in
PMRGCAuk
2 years ago
Which anti inflammatory for RA?
Ibuprofen and Naproxen do not help. I've heard there is an alternative that can be prescribed, but can't remember the name of it. Anyone know?
Ibuprofen and Naproxen do not help. I've heard there is an alternative that can be prescribed, but can't remember the name of it. Anyone know?
tazman3
in
NRAS
2 years ago
Went from Psoriatic arthritis to fibromyalgia to osteoarthritis
Hello everyone. It’s been awhile since I’ve used this account. I was previously diagnosed with endometriosis. After two surgeries I’m mostly symptom free. Then found out I also have hemochromatosis. Psoriasis runs in the family as well as arthritis but no one I know of has gone to a specialist.
Hello everyone. It’s been awhile since I’ve used this account. I was previously diagnosed with endometriosis. After two surgeries I’m mostly symptom free. Then found out I also have hemochromatosis. Psoriasis runs in the family as well as arthritis but no one I know of has gone to a specialist.
Sunshine23
in
Arthritis Action
2 years ago
Diagnostic laparoscopy on Friday
The date is getting closer but the pain is much much worse. I finally was told that I had a cyst on my left ovary a month after having my ultrasound scans, and also after being given the date for my laparoscopy. I recently had to go back to taking desogestrel as I had ran out of the new one and with
The date is getting closer but the pain is much much worse. I finally was told that I had a cyst on my left ovary a month after having my ultrasound scans, and also after being given the date for my laparoscopy. I recently had to go back to taking desogestrel as I had ran out of the new one and with
Hidden
in
Endometriosis UK
2 years ago
Struggling to get the right treatment !
Hi everyone, always wonderful supportive advice on these groups ! I’m struggling at the moment getting a confirmed diagnosis of PMR , and consequently being put on steroids. I have all the classic diagnostic criteria, acute onset back in Jan of pain and stiffness both shoulders, am 65 year old Caucasian
Hi everyone, always wonderful supportive advice on these groups ! I’m struggling at the moment getting a confirmed diagnosis of PMR , and consequently being put on steroids. I have all the classic diagnostic criteria, acute onset back in Jan of pain and stiffness both shoulders, am 65 year old Caucasian
Romilly2
in
PMRGCAuk
2 years ago
Moving and recent Drs visits
Well finally hit our time frame, listed our house, and moved. It’s been a stressful few weeks but it’s over and I’m thankful. Just before that we went to UCLA and saw quite a few Drs so heres how it went: Rheumy 1 : thinks Lupus is attacking my right knee. She said something about it being different
Well finally hit our time frame, listed our house, and moved. It’s been a stressful few weeks but it’s over and I’m thankful. Just before that we went to UCLA and saw quite a few Drs so heres how it went: Rheumy 1 : thinks Lupus is attacking my right knee. She said something about it being different
JennaShi
in
LUPUS UK
2 years ago
pain medication
Hi everyone, I wonder if there is anyone here suffering the same as I am?? I have 2 herniated discs and sciatica. I also have early signs of mild osteoarthritis of the spine. I had a HA last year and can no longer take naproxen. I am wondering what others take as pain relief? I take co codamol and gabapentin
Hi everyone, I wonder if there is anyone here suffering the same as I am?? I have 2 herniated discs and sciatica. I also have early signs of mild osteoarthritis of the spine. I had a HA last year and can no longer take naproxen. I am wondering what others take as pain relief? I take co codamol and gabapentin
momander
in
Pain Concern
2 years ago
Advice on Pramipexole Withdrawal?
I was as diagnosed with PD in 2012.. At that time I was put on Pramipexole and Rasagaline and several years later- Sinemet. When I transferred to a movement disorder specialist in 2016, I was on 1mg of Pramipexole- 5 times a day (No this is not a misprint) I did not know any different until I started
I was as diagnosed with PD in 2012.. At that time I was put on Pramipexole and Rasagaline and several years later- Sinemet. When I transferred to a movement disorder specialist in 2016, I was on 1mg of Pramipexole- 5 times a day (No this is not a misprint) I did not know any different until I started
Park4me
in
Restless Legs Syndrome
2 years ago
Struggling with a diagnosis
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Ryane96
in
Fibromyalgia Action UK
2 years ago
Struggling for a diagnosis
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease ,apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease ,apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Ryane96
in
NRAS
2 years ago
Struggling to get a diagnosis.
Hello, I have been suffering with what I believe are all symptoms of lupus, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme debilitating fatigue
Hello, I have been suffering with what I believe are all symptoms of lupus, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme debilitating fatigue
Ryane96
in
LUPUS UK
2 years ago
TCZ 7 months in, and tapering Pred,- update.
Hello friends ! Long post, hope it’s of use to someone…! Since early April I’d been intending to write an update on my progress at my 6-months-on -TCZ- point . There had been a request on the forum here for info at that time, and I’d reached zero Pred point, on my rheumatologists scarily fast taper
Hello friends ! Long post, hope it’s of use to someone…! Since early April I’d been intending to write an update on my progress at my 6-months-on -TCZ- point . There had been a request on the forum here for info at that time, and I’d reached zero Pred point, on my rheumatologists scarily fast taper
Jonimoroni
in
PMRGCAuk
2 years ago
Costochondritis getting worse
I was diagnosed with costochondritis about a year ago , it’s getting worse as the months go by . Last weekend we were away and as I wasn’t doing all the usual housework I had a lovely pain free weekend . Since getting home and back to all the usual chores my pain has returned worse than ever . My bra
I was diagnosed with costochondritis about a year ago , it’s getting worse as the months go by . Last weekend we were away and as I wasn’t doing all the usual housework I had a lovely pain free weekend . Since getting home and back to all the usual chores my pain has returned worse than ever . My bra
Westie2012
in
British Heart Foundation
2 years ago
RA and lungs
Hello, I'm anti CCP positive RH neg and awaiting formal diagnosis. I'm only taking Naproxen to ease symptoms until then. The onset of symptoms has been rapid and most joints affected now but worst in shoulders, hips and knees. Alongside onset of these symptoms has been a general tickle in my lungs. I'm
Hello, I'm anti CCP positive RH neg and awaiting formal diagnosis. I'm only taking Naproxen to ease symptoms until then. The onset of symptoms has been rapid and most joints affected now but worst in shoulders, hips and knees. Alongside onset of these symptoms has been a general tickle in my lungs. I'm
Gottarelax
in
NRAS
2 years ago
Costochondritis
I was diagnosed with costochondritis about a year ago , it’s getting worse as the months go by . Last weekend we were away and as I wasn’t doing all the usual housework I had a lovely pain free weekend . Since getting home and back to all the usual chores my pain has returned worse than ever . My bra
I was diagnosed with costochondritis about a year ago , it’s getting worse as the months go by . Last weekend we were away and as I wasn’t doing all the usual housework I had a lovely pain free weekend . Since getting home and back to all the usual chores my pain has returned worse than ever . My bra
Westie2012
in
Pain Concern
2 years ago
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