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Sulfasalazine

Yes, I'd say that a visit to a consultant rheumatologist should definitely be on the cards if it hasn't happened already.
 
Yeesh... Hope it's improving!

Thought I had it bad having pipes shoved down my throat to see why I was suffering from such bad acid reflux... A horrible 2 weeks, sounds nowt compared to your issues
It's highly aggressive and affects most of my joints but primarily my spine, also my bowl, skin, nails and eyes are affected... but it's relatively well controlled, I manage to DJ once or twice a week with the help of a roadie and also manage to run another small business. I holiday abroad about four times a year so I'm not doing so bad. You just learn to live with/around it.
 
I'm in the RA club. Sulphasalzine was my first DMARD, added Hydroxychloroquine then Methotrexate. Gradually the triple therapy become less effective. Now on biologic therapy with Methotrexate and Hydroxychloroquine.

One thing about Sulphasalzine, not only does it make your urine yellow, it can stain your sweat and thus your light coloured clothes.
 
I'm in the RA club. Sulphasalzine was my first DMARD, added Hydroxychloroquine then Methotrexate. Gradually the triple therapy become less effective. Now on biologic therapy with Methotrexate and Hydroxychloroquine.

One thing about Sulphasalzine, not only does it make your urine yellow, it can stain your sweat and thus your light coloured clothes.

Yes, I think my meds are becoming less effective, I’m being woken with intense pain in my hips, legs, elbows and wrists and my eyes are sore a lot of the time. I’ve had a colitis flare too. I’ve got an appointment on the 8th of January to see about revising my medication. I’ve just had to de-ice my side windows on my car and it’s crucified me!
 
Yes, sulfasalazine is usually started by specialists medics in hospital. Complete blood counts should be performed before starting this treatment.


Thanks for the replies chaps.

Yes, the RA specialist put me on it, started the course yesterday and already have guts ache, eyes on stalks, dry mouth and a feeling of ' squirty bottom'.:(
 
Yes, I think my meds are becoming less effective, I’m being woken with intense pain in my hips, legs, elbows and wrists and my eyes are sore a lot of the time. I’ve had a colitis flare too. I’ve got an appointment on the 8th of January to see about revising my medication. I’ve just had to de-ice my side windows on my car and it’s crucified me!
We've discussed this before, but for what it's worth, the jab of Etanercept I give myself once a week seems to have stopped my RA in its tracks, with no obvious side effects. With me it was very much the Last Chance Saloon, having tried all the other types of AR-suppressing medication.
 
I know dozens of people who have reduced their oestoarthritus pains using a product called Lewtress super strength Rosehip. They offer a money back guarantee they are so confident it will work. My mum tried it and has told her friends and the word has spread. Zero side effects. Bit pricey, but the cheaper versions don't do anything.
 
I know dozens of people who have reduced their oestoarthritus pains using a product called Lewtress super strength Rosehip. They offer a money back guarantee they are so confident it will work. My mum tried it and has told her friends and the word has spread. Zero side effects. Bit pricey, but the cheaper versions don't do anything.

Rheumatoid Arthritis is a family of autoimmune diseases where the body attacks the joints and other parts of the body such as the heart, lungs and eyes. Supplements and complementary therapies do not have a good track record in helping with RA. RA can occur at any age, many children are affected by Juvenile Rheumatoid Arthritis.

I caution people with RA that much as they would like to try doing without the medications they risk irreversible damage to the joints and general health. RA is often associated with spells of extreme fatigue especially during flares. As RA varies so much it is often a matter of trial and error to find the correct medication to control the disease and tolerable side effects.

Osteoarthritis is very different and is caused by joints wearing out through over use and age, supplements can help in some cases and are often worth trying along with non load-bearing exercise.
 
Rheumatoid Arthritis is a family of autoimmune diseases where the body attacks the joints and other parts of the body such as the heart, lungs and eyes. Supplements and complementary therapies do not have a good track record in helping with RA. RA can occur at any age, many children are affected by Juvenile Rheumatoid Arthritis.

I caution people with RA that much as they would like to try doing without the medications they risk irreversible damage to the joints and general health. RA is often associated with spells of extreme fatigue especially during flares. As RA varies so much it is often a matter of trial and error to find the correct medication to control the disease and tolerable side effects.

Osteoarthritis is very different and is caused by joints wearing out through over use and age, supplements can help in some cases and are often worth trying along with non load-bearing exercise.
You’re spot on with this, it describes my experience perfectly. I suffer both extreme fatigue and insomnia at the same time thanks to my arthritis... I’m actually awake now because I’ve just got home from a gig... I will have a very slow Sunday and probably Monday too recouperating.
 
I've had rheumatoid arthritis (RA) for 15 years. It was reasonably well controlled until a few years ago when I developed a chronic bladder condition with recurring urinary tract infections. One UTI bug managed to get into my bloodstream causing septic arthritis in my hip...ouch!! which required surgery. To cut a very long story short...eventually, and following a second bout of sepsis, it was decided that I had to stop taking all specialised immune suppressing medication for my RA because of frequent recurring UTIs and the high risk of sepsis. This was over a year ago and I have not had a single UTI since, would have had at least two, probably three during that time when I was taking immune suppressing medication. Because I've had so many UTIs my bug, an E. coli type, is now resistant to all of the common antibiotics that GPs can prescribe meaning that should I get a UTI, then I will have to be admitted to hospital to be treated with strong intravenous antibiotics.
People need to take heed of that TV advert warning about over use of antibiotics for minor ailments can lead to big problems when you really need them for more serious infections.

The only specialised RA med I can take is hydroxychloroquine, which although not as effective as methotrexate and etanercept, that I used to take, is helping me. Just hope it doesn't stop working which can happen. I also take strong pain killers.

If that wasn't bad enough, two years ago I was diagnosed with RA related lung disease, which I don't want to go into here. Enough to say that the disease has been stable since it was diagnosed 2 years ago. I see my chest consultant again in May and if there's still no change then he will discharge me...keeping all digits metaphorically crossed for that one.

Regarding the OPs post... I tried sulphalazine and developed a rash and was told to stop taking it immediately. So do be aware of even seemingly minor issues as they can be signs of a serious underlying problem.

Apologies for the long post, just thought I'd elaborate a bit on the sort of damage this shitty disease can do.

Linnfomaniac, if you remember I did speak with you when you were being diagnosed and in a bad state. Sorry to hear that things are not too good, but glad that the medication is at least helping some.

Rheumatoid Arthritis is a family of autoimmune diseases where the body attacks the joints and other parts of the body such as the heart, lungs and eyes. Supplements and complementary therapies do not have a good track record in helping with RA. RA can occur at any age, many children are affected by Juvenile Rheumatoid Arthritis.

I caution people with RA that much as they would like to try doing without the medications they risk irreversible damage to the joints and general health. RA is often associated with spells of extreme fatigue especially during flares. As RA varies so much it is often a matter of trial and error to find the correct medication to control the disease and tolerable side effects.

Osteoarthritis is very different and is caused by joints wearing out through over use and age, supplements can help in some cases and are often worth trying along with non load-bearing exercise.
 
Rheumatoid Arthritis is a family of autoimmune diseases where the body attacks the joints and other parts of the body such as the heart, lungs and eyes. Supplements and complementary therapies do not have a good track record in helping with RA. RA can occur at any age, many children are affected by Juvenile Rheumatoid Arthritis.

I caution people with RA that much as they would like to try doing without the medications they risk irreversible damage to the joints and general health. RA is often associated with spells of extreme fatigue especially during flares. As RA varies so much it is often a matter of trial and error to find the correct medication to control the disease and tolerable side effects.

Osteoarthritis is very different and is caused by joints wearing out through over use and age, supplements can help in some cases and are often worth trying along with non load-bearing exercise.

Yep, that pretty much sums things up.
 
Thanks for your post moffer, you've reminded me of hydroxychloroquine, couldn't remember the name. I was on this for a short time, but I found it adversely affected my eyesight; most unpleasant! Fortunately, after leaving off the stuff for a few days, my eyesight returned to normal.

I do worry about folk recommending "alternative" treatments for RA (and other diseases). There is no cure for RA, only the chance of slowing its progress, and by spending time trying scientifically unproven medication the irreparable damage to your joints will continue. Beware!
 
I am surprised that there are so many RA suffers on this forum. By it's nature the forum will have a male majority and RA is more common in women.
 
It can adversely affect eyesight in some people as you found out. Were you advised to have your eyes tested before starting hydroxy, then at least once a year after? Glad your eyesight returned to normal. I think it's causing a bit of acid reflux, but I daren't stop taking it.

Entanercept worked wonders for me - I was like a new man a couple of days after starting it...well almost! As no doubt you know, it's a very strong immune suppressor. Apparently it was this very med that helped make thing easy for the UTI bug get into my bloodstream and cause the septic arthritis in my hip. The docs told me not to take again...other meds later followed suit. :(
 
I've had rheumatoid arthritis (RA) for 15 years. It was reasonably well controlled until a few years ago when I developed a chronic bladder condition with recurring urinary tract infections. One UTI bug managed to get into my bloodstream causing septic arthritis in my hip...ouch!! which required surgery. To cut a very long story short...eventually, and following a second bout of sepsis, it was decided that I had to stop taking all specialised immune suppressing medication for my RA because of frequent recurring UTIs and the high risk of sepsis. This was over a year ago and I have not had a single UTI since, would have had at least two, probably three during that time when I was taking immune suppressing medication. Because I've had so many UTIs my bug, an E. coli type, is now resistant to all of the common antibiotics that GPs can prescribe meaning that should I get a UTI, then I will have to be admitted to hospital to be treated with strong intravenous antibiotics.
People need to take heed of that TV advert warning about over use of antibiotics for minor ailments can lead to big problems when you really need them for more serious infections.

The only specialised RA med I can take is hydroxychloroquine, which although not as effective as methotrexate and etanercept, that I used to take, is helping me. Just hope it doesn't stop working which can happen. I also take strong pain killers.

If that wasn't bad enough, two years ago I was diagnosed with RA related lung disease, which I don't want to go into here. Enough to say that the disease has been stable since it was diagnosed 2 years ago. I see my chest consultant again in May and if there's still no change then he will discharge me...keeping all digits metaphorically crossed for that one.

Regarding the OPs post... I tried sulphalazine and developed a rash and was told to stop taking it immediately. So do be aware of even seemingly minor issues as they can be signs of a serious underlying problem.

Apologies for the long post, just thought I'd elaborate a bit on the sort of damage this shitty disease can do.

Linnfomaniac, if you remember I did speak with you when you were being diagnosed and in a bad state. Sorry to hear that things are not too good, but glad that the medication is at least helping some.
It sounds like you’ve had a rough time too, and yes I’ve had to stop my meds a few times too thanks to pneumonia. I still just get on with it as much as I can though... I was working until 2.30am entertaining people and I’ve dug my car out (admittedly with some help) and have been ferrying family around and shopping for building materials to het my parents garden room finished in time for Christmas day... I don’t let it stop me.
 
It can adversely affect eyesight in some people as you found out. Were you advised to have your eyes tested before starting hydroxy, then at least once a year after? Glad your eyesight returned to normal. I think it's causing a bit of acid reflux, but I daren't stop taking it.

Entanercept worked wonders for me - I was like a new man a couple of days after starting it...well almost! As no doubt you know, it's a very strong immune suppressor. Apparently it was this very med that helped make thing easy for the UTI bug get into my bloodstream and cause the septic arthritis in my hip. The docs told me not to take again...other meds later followed suit. :(
Aye, had my eyes tested, and was supplied with a card to regularly test my eyesight against. I noticed a problem when I was driving - things in the distance started to swim about in a most disconcerting way. Luckily, my wife was in the car & took over driving.

Sorry to learn you had problems with etanercept. I've been on it for over a couple of years so far, and have yet to contract any infection. Fingers crossed...
 
It can adversely affect eyesight in some people as you found out. Were you advised to have your eyes tested before starting hydroxy, then at least once a year after? Glad your eyesight returned to normal. I think it's causing a bit of acid reflux, but I daren't stop taking it.

Entanercept worked wonders for me - I was like a new man a couple of days after starting it...well almost! As no doubt you know, it's a very strong immune suppressor. Apparently it was this very med that helped make thing easy for the UTI bug get into my bloodstream and cause the septic arthritis in my hip. The docs told me not to take again...other meds later followed suit. :(
There is a limit to how much I can safely suppress my immune system, being prone to severe chest infections that have hospitalised me on several occasions. I’d rather deal with arthritis pain and poor mobility than not being able to breathe.
 
There is a limit to how much I can safely suppress my immune system, being prone to severe chest infections that have hospitalised me on several occasions. I’d rather deal with arthritis pain and poor mobility than not being able to breathe.

Same here. I'd rather deal with debilitating arthritis pain than have an arm or leg amputated, or maybe something even worse! :eek: After I was discharged from hospital for the septic hip, it scared me that much having sepsis that I went cold turkey and stopped RA meds, including steroids and anti inflammatories, which I still can't take, and relied just on strong pain relief. It took about 4 weeks for the meds to leave my body and start feeling the effects of the RA returning. Another fortnight and I was crippled with pain and at times was unable to move from room to room without help. I just couldn't get over how bad the pain had become in most of my main joints. I was nigh on housebound for the next 4 months...how I lasted that long in such constant pain I'll never know. Eventually I had to give in and my rheumatologist started me on methotrexate, which I'd been on in the past. I had to have a chest x-ray to start methotrexate and that's when the abnormalities were found in my lungs so I had to stop taking that as well because it can cause lung problems of its own. Thankfully, and probably due to starting hydroxy, the pain has not returned to anywhere near as bad as when I went cold turkey. I'm still not in a good place and my mobility ain't too clever either, but like you I try to keep on truckin' as much as I can.

Hope things stay steady for you.
 


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