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Juvenile idiopathic arthritis
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Poncet’s disease
Hello anyone out there like me whose rheumatologist thinks I’ve had Poncet’s disease? I’m now being treated for TB and hoping this may care my inflammatory/ reactive arthritis.
Hello anyone out there like me whose rheumatologist thinks I’ve had Poncet’s disease? I’m now being treated for TB and hoping this may care my inflammatory/ reactive arthritis.
MsPJ
in
NRAS
4 years ago
tenderness
I had my stepmom rub my back this evening and when she hit the area where I feel the arthritis in the upper part of mt back it hurt worse when she hit that area to massage it. It hurt bad enough for me to yell out ouch. What should I do about this or is there anything that can be done? Need suggestions
I had my stepmom rub my back this evening and when she hit the area where I feel the arthritis in the upper part of mt back it hurt worse when she hit that area to massage it. It hurt bad enough for me to yell out ouch. What should I do about this or is there anything that can be done? Need suggestions
JDQuinn75
in
Arthritis Action
4 years ago
Rheumatoid arthritis hot flushes
Does anyone else ever experience this ? It usually happens when I wake up my pjamas are drenched in sweat like I've been really hot overnight Is it connected with rA? Thanks x
Does anyone else ever experience this ? It usually happens when I wake up my pjamas are drenched in sweat like I've been really hot overnight Is it connected with rA? Thanks x
cpr02
in
NRAS
4 years ago
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Hello I am a 50 year old female and have pain in knee due to arthritis and burning nerve pain
Arthritis pain, my pain meds include pregablin 50mg twice a day and 20mg of amitriptyline at night I also take co codomol for the pain, the pregablin is for nerve pain due to a failed carpal tunnel surgery. I just can’t take it anymore, tired of trying to control the pain, I just feel so lost, any advice
Arthritis pain, my pain meds include pregablin 50mg twice a day and 20mg of amitriptyline at night I also take co codomol for the pain, the pregablin is for nerve pain due to a failed carpal tunnel surgery. I just can’t take it anymore, tired of trying to control the pain, I just feel so lost, any advice
days70
in
Pain Concern
4 years ago
Anyone else have this?
Looks like dried blood in the cuticle. My index finger on the other hand has it too. I have Inflammatory arthritis and Raynaud's, is it connected?
Looks like dried blood in the cuticle. My index finger on the other hand has it too. I have Inflammatory arthritis and Raynaud's, is it connected?
Brychni
in
Scleroderma & Raynaud's UK (SRUK)
4 years ago
Facebook 7pm nras online webinar. Vaccines and rheumatoid arthritis
Should be a good watch. Maybe they will answer the topics worrying us about rituximab, etc. Etc
Should be a good watch. Maybe they will answer the topics worrying us about rituximab, etc. Etc
allanah
in
NRAS
4 years ago
Hypothyrodism & autoimmune disease
Hi everyone. I'm new on here, so please bear with me. Following the removal of my left thyroid (it had been engulfed by a tumour - benign thankfully) in October, I have never felt more unwell in my life! I had a thyroid blood test on 5th Nov, which hospital said was 'in range, but at the very bottom'
Hi everyone. I'm new on here, so please bear with me. Following the removal of my left thyroid (it had been engulfed by a tumour - benign thankfully) in October, I have never felt more unwell in my life! I had a thyroid blood test on 5th Nov, which hospital said was 'in range, but at the very bottom'
Struddie
in
Thyroid UK
4 years ago
At last
Hi everyone finally got my sulfasalazine can't wait to get started never in a million years did I ever think rheumatoid arthritis was so painful so here's to better day's 👍
Hi everyone finally got my sulfasalazine can't wait to get started never in a million years did I ever think rheumatoid arthritis was so painful so here's to better day's 👍
Hidden
in
NRAS
4 years ago
Just had first phone consultation with rheumatologist
I have to have a face to face consultation with him but before this can happen he is sending me some blood tests to have done, which I assume I have done at my doctors. He said my ESR and CRP levels were raised when I had my first tests done and PMR diagnosis and my rheumatic levels were slightly raised
I have to have a face to face consultation with him but before this can happen he is sending me some blood tests to have done, which I assume I have done at my doctors. He said my ESR and CRP levels were raised when I had my first tests done and PMR diagnosis and my rheumatic levels were slightly raised
jaybee58
in
PMRGCAuk
4 years ago
New diagnosis of Fibromyalgia
Hi, just had appointment with consultant and very confused. I was diagnosed with psoriatic arthritis 5 years ago at a different hospital as well as having osteoarthritis. I have been having a bad flare up for months now. Given my symptoms now he thinks I might have fibromyalgia, and possibly not psoriatic
Hi, just had appointment with consultant and very confused. I was diagnosed with psoriatic arthritis 5 years ago at a different hospital as well as having osteoarthritis. I have been having a bad flare up for months now. Given my symptoms now he thinks I might have fibromyalgia, and possibly not psoriatic
FawltyTowerz
in
NRAS
4 years ago
Bloody Urine using Celebrex
My husband has been on Eliquis 5 mg. for over 5 years. His arms have be discolored by the bruising. After a Rheumatologist put him on Celebrex for one month, he had bloody urine for 12 hours. I had him stop the Eliquis. Has anyone been switched to 2.5mg without any trouble? The Celebrex works well
My husband has been on Eliquis 5 mg. for over 5 years. His arms have be discolored by the bruising. After a Rheumatologist put him on Celebrex for one month, he had bloody urine for 12 hours. I had him stop the Eliquis. Has anyone been switched to 2.5mg without any trouble? The Celebrex works well
Butkie95
in
AF Association
4 years ago
Newly diagnosed & Struggling
Hi Just been diagnosed with Fibromyalgia and Osteoarthritis in most joints. I struggle with pain most days and I am worried what my future holds. Can anyone recommend any books etc. on Fibromyalgia? Help really appreciated. Thanks
Hi Just been diagnosed with Fibromyalgia and Osteoarthritis in most joints. I struggle with pain most days and I am worried what my future holds. Can anyone recommend any books etc. on Fibromyalgia? Help really appreciated. Thanks
samsara70
in
Fibromyalgia Action UK
4 years ago
New to forum but not to Fibro
Hi all I have lived with Fibro for more than 24 years. Also have Osteoarthritis, Chronic migraines and the usual whole host of other accompanying nasties! I have recently also been diagnosed with seropositive Rheumatoid Arthritis and this is why I'm posting to say to all ‘ do not be ignored!’ The
Hi all I have lived with Fibro for more than 24 years. Also have Osteoarthritis, Chronic migraines and the usual whole host of other accompanying nasties! I have recently also been diagnosed with seropositive Rheumatoid Arthritis and this is why I'm posting to say to all ‘ do not be ignored!’ The
Niao
in
Fibromyalgia Action UK
4 years ago
anyone?
Hi all I have Raynaud's and Inflammatory Arthritis. Today has been first proper white finger day as there was a frost but I expect it will be in full swing from now on and soon it will be all fingers and toes. I'm posting this here to see if anyone else gets these 'dents'? First there was one and since
Hi all I have Raynaud's and Inflammatory Arthritis. Today has been first proper white finger day as there was a frost but I expect it will be in full swing from now on and soon it will be all fingers and toes. I'm posting this here to see if anyone else gets these 'dents'? First there was one and since
Brychni
in
Scleroderma & Raynaud's UK (SRUK)
4 years ago
Newly diagnosed
Newly diagnosed, Hi to all! I'm a 56 year old woman, have been living with pain and fatigue for 24 years plus due to Fibromyalgia, Osteoarthritis, Chronic migraines and the usual host of other things that accompany this! Now, after spending the last 2 1/5 years in absolute agony, trying to get GPS/
Newly diagnosed, Hi to all! I'm a 56 year old woman, have been living with pain and fatigue for 24 years plus due to Fibromyalgia, Osteoarthritis, Chronic migraines and the usual host of other things that accompany this! Now, after spending the last 2 1/5 years in absolute agony, trying to get GPS/
Niao
in
NRAS
4 years ago
probable misdiagnose
hi ive just joined has anyone had a misdiagnose was told i have osteoarthritis but they couldnt tell me where ,, i tick most the boxes for fibromyalgia
hi ive just joined has anyone had a misdiagnose was told i have osteoarthritis but they couldnt tell me where ,, i tick most the boxes for fibromyalgia
dusty-pink
in
Fibromyalgia Action UK
4 years ago
Tocilizumab patients and the COVID Vaccine
My Rheumatologist has let me know that it is fine for me to have the COVID Vaccine and to continue having my Tocilizumab injections. I am also on 10 mgs of Prednisalone. I have Giant Cell Arteritis/Large Vessel Vasculitis.
My Rheumatologist has let me know that it is fine for me to have the COVID Vaccine and to continue having my Tocilizumab injections. I am also on 10 mgs of Prednisalone. I have Giant Cell Arteritis/Large Vessel Vasculitis.
SheffieldJane
in
PMRGCAuk
4 years ago
Does anyone suffer with hissing noise in head / ears . I have underactive thyroid and fibromyalgia/ possible Rheumatoid Arthritis?
Hissing head
Hissing head
Dottie19
in
Thyroid UK
4 years ago
Would love some advice
Hi. Firstly, I just want to say how grateful I am to have found this forum. It is invaluable and has answered some of my questions before I have even asked them - ie. blurry eyes etc. I would love some advice though if you can still put up with me. My consultant reduced my 40mg dose of prednisolone
Hi. Firstly, I just want to say how grateful I am to have found this forum. It is invaluable and has answered some of my questions before I have even asked them - ie. blurry eyes etc. I would love some advice though if you can still put up with me. My consultant reduced my 40mg dose of prednisolone
Sophiestree
in
PMRGCAuk
4 years ago
Oral thrush and RA meds
I take sulphasalazine and methotrexate for inflammatory arthritis. Condition is fairly well controlled but I have suffered with oral thrush and resulting very bad breath for over a month. I have been prescribed Nystatin and am on my second week of using this although the taste makes me gag. Any advice
I take sulphasalazine and methotrexate for inflammatory arthritis. Condition is fairly well controlled but I have suffered with oral thrush and resulting very bad breath for over a month. I have been prescribed Nystatin and am on my second week of using this although the taste makes me gag. Any advice
Horse_and_hound
in
NRAS
4 years ago
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