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Takayasu arteritis
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J1707 Leflunomide
When i started taking this drug some 4 years ago sulfasalasine had stopped working & Mx actually made my arthritis much worse. I've found it to be a very good drug for me although the initial side effects did take a bit to get used to. These were mainly digestive (diarrhoea l change of taste which put
When i started taking this drug some 4 years ago sulfasalasine had stopped working & Mx actually made my arthritis much worse. I've found it to be a very good drug for me although the initial side effects did take a bit to get used to. These were mainly digestive (diarrhoea l change of taste which put
Gardenlassy
in
NRAS
4 years ago
Shopping to help NRAS
I've just received this notification. Whatever your feelings about shopping at Amazon, if you do need to, then make it count! [i]This is your quarterly AmazonSmile donation notification. Your chosen charity, The National Rheumatoid Arthritis Society, recently received a quarterly donation of £416.06
I've just received this notification. Whatever your feelings about shopping at Amazon, if you do need to, then make it count! [i]This is your quarterly AmazonSmile donation notification. Your chosen charity, The National Rheumatoid Arthritis Society, recently received a quarterly donation of £416.06
oldtimer
in
NRAS
4 years ago
Tapering
I was down to 3mg which l had been for a month, tried to come down to 2 mg and had a flare, was not sure if this was pmr fibro or arthritis. I have bad arthritis in my left shoulder, l asked dr. for naproxen she agreed to see if it helped with arthritis but it didn’t, tramadol did not help either, so
I was down to 3mg which l had been for a month, tried to come down to 2 mg and had a flare, was not sure if this was pmr fibro or arthritis. I have bad arthritis in my left shoulder, l asked dr. for naproxen she agreed to see if it helped with arthritis but it didn’t, tramadol did not help either, so
Fifelassieo
in
PMRGCAuk
4 years ago
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Bakers cyst - rupture and treatment
Has anyone had a bakers cyst that has ruptured and how long is recovery time. For some time have had pain and tightness in calf after walking for short period.(have already been told Ihave arthritis in that knee and awaiting knee op) However earlier this week back of calf really tight after walk ( I
Has anyone had a bakers cyst that has ruptured and how long is recovery time. For some time have had pain and tightness in calf after walking for short period.(have already been told Ihave arthritis in that knee and awaiting knee op) However earlier this week back of calf really tight after walk ( I
Red1973
in
Arthritis Action
4 years ago
Vitamin d and k2
Hi can anyone tell me if vitamin d3 and k2 can help as I’m on hrt patches and I need to come off soon and am worried about arthritis as it runs in the family and I’m 48 years old. Now I’m soon to start warfirin and need to protect my bones..
Hi can anyone tell me if vitamin d3 and k2 can help as I’m on hrt patches and I need to come off soon and am worried about arthritis as it runs in the family and I’m 48 years old. Now I’m soon to start warfirin and need to protect my bones..
Aihpos
in
Hughes Syndrome APS Forum
4 years ago
Pelvic mesh
Has anyone had arthritis since this type of gynae op? I am still questioning the terrible knee and ankle problems I suffered and recovery has taken 4 years. Scans showed only very early arthritis in my knees. The pain was debilitating and I was crawling around on the floor at worst. I feel I was
Has anyone had arthritis since this type of gynae op? I am still questioning the terrible knee and ankle problems I suffered and recovery has taken 4 years. Scans showed only very early arthritis in my knees. The pain was debilitating and I was crawling around on the floor at worst. I feel I was
Emmeline3
in
Arthritis Action
4 years ago
TV vaginal Sling
Has anyone had this surgery and had problems with arthritis in knees and feet. Its taken me 4 years to recover from a severe flare up when I was badly immobilised. My sister has had severe problems with pelvic mesh surgery. I am wondering if that was the route
Has anyone had this surgery and had problems with arthritis in knees and feet. Its taken me 4 years to recover from a severe flare up when I was badly immobilised. My sister has had severe problems with pelvic mesh surgery. I am wondering if that was the route
Emmeline3
in
Arthritis Action
4 years ago
RA on my local news
Just watched my local news and they showed the NRAS video. They also showed a local woman who suffers with RA . They called it a hidden disability. She has been abused in the past for using her blue badge and described how the rheumatoid part of the disease effects her and the how the arthritis part
Just watched my local news and they showed the NRAS video. They also showed a local woman who suffers with RA . They called it a hidden disability. She has been abused in the past for using her blue badge and described how the rheumatoid part of the disease effects her and the how the arthritis part
Hidden
in
NRAS
4 years ago
RA factor all of sudden normal and now intense Psoriatic Flare?
Hello everyone, it's been awhile since I have posted as I mostly recovered in October 2019. I was diagnosed with RA in 2018 with a good probability of Psoriatic Arthritis. The story is long and my hands hurt a bit too much to detail today, but I was treated for RA in 2019 for about 10 months on methotrexate
Hello everyone, it's been awhile since I have posted as I mostly recovered in October 2019. I was diagnosed with RA in 2018 with a good probability of Psoriatic Arthritis. The story is long and my hands hurt a bit too much to detail today, but I was treated for RA in 2019 for about 10 months on methotrexate
RAlife2018
in
NRAS
4 years ago
Warfarin
Hi everyone is there anyone on this site taking warfarin and meds for arthritis 👍
Hi everyone is there anyone on this site taking warfarin and meds for arthritis 👍
Beth72
in
NRAS
4 years ago
Advice please!
I have osteoarthritis in one hip and knee and feet for which I take codydramol at maximum dosage. I had a TIA in February and now have to take clopidogrel plus blood pressure meds. I came off statins because of severe muscle and joint pain. This has eased but my joints are all deteriorating including
I have osteoarthritis in one hip and knee and feet for which I take codydramol at maximum dosage. I had a TIA in February and now have to take clopidogrel plus blood pressure meds. I came off statins because of severe muscle and joint pain. This has eased but my joints are all deteriorating including
mkcd
in
Cure Arthritis Community
4 years ago
NRAS on BBC Radio 4 today at 10am
Tune in to BBC Radio 4 at 10am today to listen in to Woman’s Hour, where Clare Jacklin (NRAS CEO) and Yulanda Sabrina will be interviewed about rheumatoid arthritis and it's autoimmune roots.
Tune in to BBC Radio 4 at 10am today to listen in to Woman’s Hour, where Clare Jacklin (NRAS CEO) and Yulanda Sabrina will be interviewed about rheumatoid arthritis and it's autoimmune roots.
Hidden
Partner
in
NRAS
4 years ago
Marina coil. Removed and best my arthritis has been for years
My friend had a marina coil and within months was being diagnosed with fibromyalgia. I did a bit of Internet searching and as a result had mine removed about 3 or 4 years ago. I then stopped my medication and although I wouldnt say I'm cured I haven't had a flare up in my knees since. I have just recently
My friend had a marina coil and within months was being diagnosed with fibromyalgia. I did a bit of Internet searching and as a result had mine removed about 3 or 4 years ago. I then stopped my medication and although I wouldnt say I'm cured I haven't had a flare up in my knees since. I have just recently
Mishkasmum
in
Arthritis Action
4 years ago
hydroxychloroquine vs sulfasalazine
hydroxychloroquine vs sulfasalazine would anyone know which one is better for rheumatoid arthritis?
hydroxychloroquine vs sulfasalazine would anyone know which one is better for rheumatoid arthritis?
Frankiefocus
in
NRAS
4 years ago
MRI in PMR diagnosis
I am wondering if anyone has had an MRI that showed evidence of PMR? I have been experiencing symptoms of PMR since February (stiffness and pain/aching in my muscles in neck, shoulders and hips), and my rheumatologist has ordered X-rays of hip and shoulders as well as MRI of c-spine (my neck and shoulders
I am wondering if anyone has had an MRI that showed evidence of PMR? I have been experiencing symptoms of PMR since February (stiffness and pain/aching in my muscles in neck, shoulders and hips), and my rheumatologist has ordered X-rays of hip and shoulders as well as MRI of c-spine (my neck and shoulders
Anna135
in
PMRGCAuk
4 years ago
The wrong forum!
https://www.rheumatologyadvisor.com/home/topics/rheumatoid-arthritis/undifferentiated-arthritis-identifying-candidates-for-early-treatment-to-prevent-progression-to-ra/ The above article explains fully. Essentially I'm in the wrong forum; Undifferentiated Inflammatory Arthritis which, is my diagnosis
https://www.rheumatologyadvisor.com/home/topics/rheumatoid-arthritis/undifferentiated-arthritis-identifying-candidates-for-early-treatment-to-prevent-progression-to-ra/ The above article explains fully. Essentially I'm in the wrong forum; Undifferentiated Inflammatory Arthritis which, is my diagnosis
Brychni
in
NRAS
4 years ago
First Video Rheumy Appointment on Monday
I haven't seen the Rheumatologist since last year, so I am probably due for a consult. I have a 1.5 hour drive to attend the Rheumy clinic, so if the video appointment works, it will be a relief. How do they do a DAS though, taking my word for 'I don't have any joint tenderness or swelling' probably
I haven't seen the Rheumatologist since last year, so I am probably due for a consult. I have a 1.5 hour drive to attend the Rheumy clinic, so if the video appointment works, it will be a relief. How do they do a DAS though, taking my word for 'I don't have any joint tenderness or swelling' probably
Brushwork
in
NRAS
4 years ago
New Kid on the Block
Hi,everyone,just joined the group and reading the posts really feel for those suffering with fatigue, something fortunately I have never had with P.M.R..I do however get flare ups with SEVERE pain mainly in the neck and shoulders.Difficult sometimes to know whether its P.M.R. or a trapped nerve or pulled
Hi,everyone,just joined the group and reading the posts really feel for those suffering with fatigue, something fortunately I have never had with P.M.R..I do however get flare ups with SEVERE pain mainly in the neck and shoulders.Difficult sometimes to know whether its P.M.R. or a trapped nerve or pulled
BeeDee1940
in
PMRGCAuk
4 years ago
Kick up bum needed lol
I am in a hole nt eating then when I do it the wrong food I have arthritis which stops me walking and moving much need the kick up the bum to get back on plan
I am in a hole nt eating then when I do it the wrong food I have arthritis which stops me walking and moving much need the kick up the bum to get back on plan
Howshort
2020 August
in
Weight Loss Support
4 years ago
Nose bleeds.
Hi. I’m new here. I have been diagnosed with rheumatoid arthritis and have recently started on methotrexate. I am having lots of nose bleeds. I was wondering if this is common and wether it is caused by the treatment. Does it go away ?
Hi. I’m new here. I have been diagnosed with rheumatoid arthritis and have recently started on methotrexate. I am having lots of nose bleeds. I was wondering if this is common and wether it is caused by the treatment. Does it go away ?
Hidden
in
NRAS
4 years ago
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