I have a dianosis of stills desease and orthoarthritis. I take methotrexate for the stills which my consultant says is well managed but the pain from the orthoarthritis causes me problems. What pain killers do other people take please.
Methotrexate : I have a dianosis of stills desease and... - NRAS
Methotrexate


as much as possible I try to use gentle approaches for osteo. So using splints, ice and heat packs, diclofenac gel and things like that. And paracetamol sometimes with anti-inflammatories..
I have been prescribed stronger stuff ut have never used it as holding off as long as possible.
I don’t know where your OA pain is but just in case like mine it's is in your foot (metatarsal) when you walk, I've found that new insoles have given me a dramatic reduction in pain.
In case you're interested they're Diaped Duosoft Insoles. Apparently they're NHS prescribed, but I think for diabetics.
X
Oh sorry, poor you, that must be very draining ☹️
making contact as a fellow member with Stills!
Hello there, how are you at the.moment? I was diagnosed with stills in july 2024 I was hospiised for 10 days, I was very ill until they knew was it was and medicated me . It's been quite a journey. I'm 64 in couple of weeks! Best wishes
Heather
I was diagnosed aged 17 in 1979 after months of being bedridden. After a week in hospital they diagnosed and prescribed and a few years later I weaned off meds. I’m 63 now with joint pain etc and it’s hit worse in the last 25 years …since menopause.
Hi there, It sounds like it's been difficult for you. I hope you have found a way to manage it.
They are starting me on a biodrugs on 22 April and I'm hoping my stills will be managed better because I'm on a lot of medication at the moment to keep me pain free and moblie. Methotrexate, hydroxychloroquine,steriods, folic acid alendronic acid. I don't like taking them but have no choice. I also have orthoarthritis in my upper,lower spine and knee. Without the medication the pain and other symptoms are unbelievable.
Best wishes
I know things will have changed dramatically since my diagnosis in 1979 but the RA drug I was given was Indocid slow release capsules and they worked for me without side effects as far as I can recall. Other drugs apart from steroids were distalgesics for pain, and DF118, large doses of enteric coated aspirin for example, I don’t expect this is of help to you today but just sharing. I also had splints for my wrists and braces on my knees and special shoes provided by the hospital. As I said, 1979 was a different time. One word of caution; since my late 20s I’ve used codeine based meds for pain relief and have recently been diagnosed with diverticulitis ( not uncommon in ones 60s) but GP did say codeine is a contributory cause. In the last few years I’ve discovered that Stills can damage organs which I was unaware of before. Even down to the workings of the ear, I now have treatments for tinnitus and vertigo for example. Other AI things have joined in such as Lichen Sclerosus, Intistitial Cystitis, dry eyes and Deputyrens Contracture (spellings sorry). I also have strange mole/rash/ growths all I er my torso which I’m certain RA based. I only took steroids for about 5 years and no stomach protectors were issued in those days nor anything for bone health. A dexa scan in my early 30s warned I was osteoporotic so I was able to take action then. I think that’s all I can offer you except that acidic food, and tannins in wine and tea definitely make it worse. I hope you have better days and meds that do the job 😀