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I am one of those people who has had remissions. I’ve had JRA (dx age 10) for 30 yrs. Each remission has been from 1-3 yrs. At the end of the remission my flare is usually so severe that it takes years and many many drugs to get it under control again. I’ve had 5 remissions in 30 yrs. 10 yrs ago I had a remission for 2.5 yrs after starting Enbrel. An emergency surgery at that point set off another flare. That was my last remission. I was hopeful that the Simponi I started 8 months ago would trigger another remission, but it is simply taking my disease activity down quite a bit, without a full remission. I can see a pattern, that the older I get, the longer between remissions. I wonder if I’ll ever have another.
My remissions were characterized no pain or joint symptoms and no need for medication. The last one, 10 yrs ago, I stayed in remission as long as I kept on the Enbrel. On it, I was completely asymptomatic.
On the other hand, remission sure is nice when you finally get lucky – it’s definitely worth trying for. Took five years, and cycling though hydroxychloroquine, MTX, Embrel, Humira, Remicade, Cimzia, and Orencia, most of which did nothing for me, before I hit the jackpot with Actemra.
Six months of feeling normal now, no swollen joints, no fatigue. A little pain from the wrist joints that now have no cartilage – being in remission doesn’t make the cartilage grow back – but nothing like before starting the Actemra.
I do wonder how many folks miss out on the possibility of remission because they, or their rheum, or most likely of all their insurance company, give up before cycling through all of the available medications.
Too bad there isn’t something better than trial-and-error to find out what meds will work for any particular RA patient.
When I was on Enbrel for 6 or 7 years, I considered it a near-remission – which is funny because I still needed 5 mg of Prednisone daily, and still had flares requiring short-term higher Pred. But it felt like a remission to me because I was able to do almost everything I wanted to do, which was wonderful. Unfortunately, I had to go off it because of a problem with my white blood cell count and I haven’t yet found anything else that works.
Jeff, I’m glad to hear your report on Actemra, because I have recently been discouraged about trying yet another med and that is the next one on my list.
I really think some day we will be able to have blood and/or gene tests that will identify which med is most likely to work for each individual – but I’m not sure how soon that will happen…
While “remission” is something that we all aim for, I am satisfied with my current “stable” status.
It isn’t perfect, but it is nearly a polar opposite of where I was a year ago.
I’LL TAKE IT!
I was in ‘remission’ for a couple of months, but still taking Enbrel and sulfasalazine. I’m now back to low disease activity and have started methotrexate again (I was on mtx holiday for 5 months). It’s kind of a bummer, but I feel lucky to have good response to the Enbrel…I hope this activity isn’t a sign of the Enbrel failing as it’s the second biologic I’ve been on. I have a rheum doc appointment coming up, and I’m interested in asking her if- based on her experience, my history, and the current meds available today- what my chances are (in percentage) of sustaining joint damage that will affect my abilities and range of motion in the next 5 & 10 years. I know that nobody can accurately answer this but I’m hoping that she’ll give me an ‘off the record’ opinion so I can add it to my own.
I do know things can change, but I think it’s time that our rheumies start giving us a prognosis opinion, even if they make it clear that they’re guessing. We are entering an age where many rheumatologists have had patients on biologics for several years- they should start to be getting an idea of what the future MAY hold for us, and if we request it, share what they think.
I’m a relative newbie to the world of RA, diagnosed on Jan 31, 2012. That said, while I long for remission, I’ve been pretty impressed with the symptom reduction in the last 2 months. I’m still in a flare that varies from a very low burn to an occasional forest fire, but the forest fires are less frequent and not quite as hot. While it would be nice if this got put out, right now I’m thrilled with better (was sick as a little yellow dog for over a year).
Medications: MTX, Prednisone, Mobic, Tramadol ER, Lidoderm Pain patch, Folic Acid.
My doctor has nothing to offer but more drugs and surgery. I don’t like either option.
My doctor has always aimed for remission, and I am glad that she does, because it’s hard for me to hope for. I’m on relafin, orencia, sulfasalazine, methotrexate, tremadol, vitamin D, vitamin B complex, iron, and folic acid. I still hurt, I still suffer from fatigue. I may not believe in a remission for me, but I guess what I do believe in, what I strive for, what I hunt for, is a healthier me. Right now, out of a week, I have about four, mostly fatigue free, mostly pain free days. I consider that a huge success. Is it possible I will have a remission some day? I’m not ruling it out. I might win the lottery some day too. But until that day either comes or doesn’t, I guess what I’m saying is that doesn’t rule out trying to be healthier and trying to do the best possible for my health.
Warriors are like that, I hear.
~Jennifer
thanks for your awesome comments, Jennifer. I think most people I’ve met w/RA have that warrior spirit. We encourage each other in it too – in case it wanes at times from the weariness of battle.
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