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new here any advice?
hi I have Fibromyalgia and find Naproxen seems to help. Does anyone have any other suggestions? I have had Butec patches and Duloxetine but they didn't help. I'm currently havingacupuncture. Has it helped anyone? Thanks in advance for any advice. Janet
hi I have Fibromyalgia and find Naproxen seems to help. Does anyone have any other suggestions? I have had Butec patches and Duloxetine but they didn't help. I'm currently havingacupuncture. Has it helped anyone? Thanks in advance for any advice. Janet
Jhiggy
in
My Fibro Community
2 years ago
Liver test & starting methotrexate.
hi everyone. I'm a bit confused, I had my chest x Ray and blood test ready to start methotrexate, but the nurse called and said my liver result was a bit high and also my immflamation markers were up although my CRP being raised doesn't surprise me in the slightest seeing as I'm still in my initial
hi everyone. I'm a bit confused, I had my chest x Ray and blood test ready to start methotrexate, but the nurse called and said my liver result was a bit high and also my immflamation markers were up although my CRP being raised doesn't surprise me in the slightest seeing as I'm still in my initial
Nelliekel
in
NRAS
2 years ago
Has anyone else experienced a flare then a paralysis the of hand and wrist
Hi there strange one to ask but I just wondered if anyone else has had a flare and when it's calmed down you find you can't move your wrist, hand or fingers at all and the pain is excruciating. I've tried hot water bottles and ice bandages, I've taken naproxen and tramadol and paracetamol. I've
Hi there strange one to ask but I just wondered if anyone else has had a flare and when it's calmed down you find you can't move your wrist, hand or fingers at all and the pain is excruciating. I've tried hot water bottles and ice bandages, I've taken naproxen and tramadol and paracetamol. I've
Sueh121268
in
NRAS
2 years ago
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your wonderful insights to my results would be very much appreciated. hoping to see GP on Monday.
Nov 21 T4 16.2 [10-22] TSH 4.8 mu/L [0.3-4.2] Dec 21 T4 17.2 [10-22] TSH 4.3 mu/L [0.3-4.2] Started trial of 25mcg Levo (Teva brand) April 22 TSH 5.2mu/L [0.3-4.2] Dose 50mcg Levo (Teva) May 22 TSH 3.3 [0.3-4.2] Dose 62.5mcg (50mcg MP and half Wockhardt 25mcg) TSH 3.77mu/L [0.27-4.2] July M
Nov 21 T4 16.2 [10-22] TSH 4.8 mu/L [0.3-4.2] Dec 21 T4 17.2 [10-22] TSH 4.3 mu/L [0.3-4.2] Started trial of 25mcg Levo (Teva brand) April 22 TSH 5.2mu/L [0.3-4.2] Dose 50mcg Levo (Teva) May 22 TSH 3.3 [0.3-4.2] Dose 62.5mcg (50mcg MP and half Wockhardt 25mcg) TSH 3.77mu/L [0.27-4.2] July M
Auders
in
Thyroid UK
2 years ago
Hope in sight
Back on July 21st I had an NHS consultation where I expected to be given MTX and be on my way to recovery but the consultant wanted to give me an MRI scan on my hips before prescribing targeted treatment. Fair enough as I am keen to get the correct diagnosis. I have semi private health insurance that
Back on July 21st I had an NHS consultation where I expected to be given MTX and be on my way to recovery but the consultant wanted to give me an MRI scan on my hips before prescribing targeted treatment. Fair enough as I am keen to get the correct diagnosis. I have semi private health insurance that
Gottarelax
in
NRAS
2 years ago
R/A and fibromyalgia
hi all I’ve not posted for a while but for the last month or so I’ve been sweating excessively on my head and neck an have a tingling sensation in my feet to my knees and in my hands I am also very thirsty All the time I also feel very weak and tired I’m currently on leflunomide 20mg naproxen 500mg
hi all I’ve not posted for a while but for the last month or so I’ve been sweating excessively on my head and neck an have a tingling sensation in my feet to my knees and in my hands I am also very thirsty All the time I also feel very weak and tired I’m currently on leflunomide 20mg naproxen 500mg
Fortune7
in
NRAS
2 years ago
frustrating
is there any one here that has had 2 heart attacks and is on the usual cocktail of heart medication? My frustration is that I have chronic back pain and am now no longer prescribed Naproxen or any other anti iflammatory medication. i refuse to believe that there is nothing else out there that I can
is there any one here that has had 2 heart attacks and is on the usual cocktail of heart medication? My frustration is that I have chronic back pain and am now no longer prescribed Naproxen or any other anti iflammatory medication. i refuse to believe that there is nothing else out there that I can
momander
in
British Heart Foundation
2 years ago
post surgery pain worse!
hi there, i have always struggled with period pain since school around 2015, which has got progressively worse over time. After years of misdiagnosis and GPS turning me away, I was diagnosed with severstage 4 endo in April 2022 via laparoscopy. They removed all scar adhesions,drained two cysts (
hi there, i have always struggled with period pain since school around 2015, which has got progressively worse over time. After years of misdiagnosis and GPS turning me away, I was diagnosed with severstage 4 endo in April 2022 via laparoscopy. They removed all scar adhesions,drained two cysts (
Mia843
in
Endometriosis UK
2 years ago
NSAIDs - anyone ? part 2.
I wrote , about a month ago , about groin pain from pelvic fractures ; prescribed naproxen , which proved a life saver for groin pain and RA pain in general ; rheumatologist instruction to taper off naproxen. I had a rheumatology meeting end July and went armed with all the information gained from
I wrote , about a month ago , about groin pain from pelvic fractures ; prescribed naproxen , which proved a life saver for groin pain and RA pain in general ; rheumatologist instruction to taper off naproxen. I had a rheumatology meeting end July and went armed with all the information gained from
Briefencounter
in
NRAS
2 years ago
how quick does increase in MTX take effect
Hi, I was diagnosed early March and was on steriods to bridge gap until MTX started working. I was initially on 15mgs. Whilst on oral steroids I became pain free but as I started tapering down I had aches/pains in feet /hands/shoulder and hips. Whilst not too bad and seem to plateau recently I have
Hi, I was diagnosed early March and was on steriods to bridge gap until MTX started working. I was initially on 15mgs. Whilst on oral steroids I became pain free but as I started tapering down I had aches/pains in feet /hands/shoulder and hips. Whilst not too bad and seem to plateau recently I have
Newbie73
in
NRAS
2 years ago
The Dreaded Pramipexole
Has anyone experienced augmentation symptoms following even a very low dose of Pramipexole 0.088mg? I am 73 and still quite active. I started with RLS about two years ago. Intermittent at first, but then worsened such that I was experiencing continuous disturbed nights. Classic symptom of a shaking
Has anyone experienced augmentation symptoms following even a very low dose of Pramipexole 0.088mg? I am 73 and still quite active. I started with RLS about two years ago. Intermittent at first, but then worsened such that I was experiencing continuous disturbed nights. Classic symptom of a shaking
Hobscave
in
Restless Legs Syndrome
2 years ago
Advice wanted please
Hello, I'm hypothyroid on 125 does of thyroxine, I just had my blood test done and the results are Serum free T4 level (XaERr) 14.5 pmol/L [11 - 22] Serum TSH level (XaELV) 1.39 miu/L [0.27 - 4.2] I am only asking as the GP says everything is fine and no further action is needed but I feel terrible
Hello, I'm hypothyroid on 125 does of thyroxine, I just had my blood test done and the results are Serum free T4 level (XaERr) 14.5 pmol/L [11 - 22] Serum TSH level (XaELV) 1.39 miu/L [0.27 - 4.2] I am only asking as the GP says everything is fine and no further action is needed but I feel terrible
tom210
in
Thyroid UK
2 years ago
NSAID alternatives
Hi, the last few days bones in both my wrists started aching badly without any reason. I didn`t think too much into it but the next day both my big toes really ached as well and I was in pain all night. My old Doctor said I had Arthritis in my left toe quite a few years ago and my Podiadrist said
Hi, the last few days bones in both my wrists started aching badly without any reason. I didn`t think too much into it but the next day both my big toes really ached as well and I was in pain all night. My old Doctor said I had Arthritis in my left toe quite a few years ago and my Podiadrist said
gentryman
in
Arthritis Action
2 years ago
An update on my journey
My journey is short so far and I'm still in the early diagnosis/treatment phase. It's being a drawn out process as I need to have further scans before decisions are being made. I was given the option to take steroids while I wait for the scans with the warning that the scans may be impacted by the steroids
My journey is short so far and I'm still in the early diagnosis/treatment phase. It's being a drawn out process as I need to have further scans before decisions are being made. I was given the option to take steroids while I wait for the scans with the warning that the scans may be impacted by the steroids
Gottarelax
in
NRAS
2 years ago
dealing with pain and grief
hello, I’ve had a rough couple of years and I’ve noticed that the past year my flare ups have been getting longer and longer it is also making me feel very anxious. At the beginning of the year I left my job stopped leaving my house and was doing nothing other than struggling I didn’t even contact the
hello, I’ve had a rough couple of years and I’ve noticed that the past year my flare ups have been getting longer and longer it is also making me feel very anxious. At the beginning of the year I left my job stopped leaving my house and was doing nothing other than struggling I didn’t even contact the
Ksxo
in
Fibromyalgia Action UK
2 years ago
endo/adyno/pcos and depression
Hi everyone, this is my first post so not sure how to start. I know everyone on here will have suffered similarly to myself so I think I am just looking for better coping mechanisms and advise. I have suffered with endometriosis, adenymiosis, pcos, and ibs for nearly 20 years now, but more so in
Hi everyone, this is my first post so not sure how to start. I know everyone on here will have suffered similarly to myself so I think I am just looking for better coping mechanisms and advise. I have suffered with endometriosis, adenymiosis, pcos, and ibs for nearly 20 years now, but more so in
Rachelsalondo
in
Endometriosis UK
2 years ago
Best Treatment if you’re already on Opioids
Hi, I’ve just arrived. I have only recently begun suffering from RLS. I’m on a ton of very strong pain killers for Fibromyalgia, CRPS, a bowel disorder, Chronic Fatigue Syndrome, Acute Anxiety & Clinical Depression & more. So my pain meds already include: Diazepam, Oxycodon, Fentanyl Patches, Zapain
Hi, I’ve just arrived. I have only recently begun suffering from RLS. I’m on a ton of very strong pain killers for Fibromyalgia, CRPS, a bowel disorder, Chronic Fatigue Syndrome, Acute Anxiety & Clinical Depression & more. So my pain meds already include: Diazepam, Oxycodon, Fentanyl Patches, Zapain
Jellylegs21
in
Restless Legs Syndrome
2 years ago
Advice Please, feeling a bit lost.
hello everyone, I've recently been diagnosed by the GP with Rheumatoid arthritis. This was 2 weeks ago when I went with sore hands and my bloods came back with extremely elevated CRP. Since those 2 weeks I've now got 2 painful swollen knees, an ankle I can barely walk on & 2 hands and wrists that
hello everyone, I've recently been diagnosed by the GP with Rheumatoid arthritis. This was 2 weeks ago when I went with sore hands and my bloods came back with extremely elevated CRP. Since those 2 weeks I've now got 2 painful swollen knees, an ankle I can barely walk on & 2 hands and wrists that
Nelliekel
in
NRAS
2 years ago
Scalp nerve pain
Hello, I’m new to this group. I’m waiting to be seen by a Neurologist who specializes in headaches, but have been started on treatment for Trigeminal Neuralgia by my Primary doctor. He believes I have a form of Trigeminal Neuralgia, based on how my scalp pain began suddenly and how it has behaved. I
Hello, I’m new to this group. I’m waiting to be seen by a Neurologist who specializes in headaches, but have been started on treatment for Trigeminal Neuralgia by my Primary doctor. He believes I have a form of Trigeminal Neuralgia, based on how my scalp pain began suddenly and how it has behaved. I
Sissy62
in
Neuropathy Support
2 years ago
How long do b vitamins take to work
Hi guys I hope you can give me some hope. I’ve had bilateral paresthesias in my feet and lower legs for a good year now and 2 months ago I realised that b 12 deficiency is a strong possibility. ( I’ve had loads of other treatment previously from chiropractor, physio and doing lots of core strengthening
Hi guys I hope you can give me some hope. I’ve had bilateral paresthesias in my feet and lower legs for a good year now and 2 months ago I realised that b 12 deficiency is a strong possibility. ( I’ve had loads of other treatment previously from chiropractor, physio and doing lots of core strengthening
Cookiedough2022
in
Pernicious Anaemia Society
2 years ago
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