Saturday, 9 October 2010

Mini flare

Hmm so I'm 3 months into starting plaquenil. From what I've been told, if it works for me it's supposed to start kicking in about now, with the maximum effect being reached at 6 months.

I've got my 3 month check up at the hospital in 2 weeks and I know they'll ask me if I think it's helping. Trouble is, I have no idea.

As I've said before, I've had a pretty good 6 months with only minor complaints. This past week I've had the worst 'mini flare' I've had since april and it affected my foot and right hand but I thought it was going to get a lot worse and last weeks like it did last winter, instead it fizzled out after about 2-3 days. So I wonder whether that was the plaquenil helping?? Or maybe it was just a mini one anyway. I have no idea.. how do you know if a med is working or if it's just the natural ebb and flow of the disease??

7 comments:

  1. Hard to say when exactly you know that a med is working. For me, it's always been sortof retrospective - you realize that you've only had a 2 or 3 day flare, and that you don't feel quite so bad, you're not so stiff in the morning. Then you might think back a bit and you can associate it to the change of medication, diet, lifestyle, all of the above. For me, I walked down the stairs this morning after getting out of bed and the right knee didn't have the usual pain associated with coming down stairs. So I think "perhaps the dieting IS helping the knee pain" or maybe the injectible methotrexate really does make a difference. Whatever it is, I am thankful.

    Baby steps.

    Good luck.

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  2. I don't really have advice for you. When I have gone on medications I have been pretty severe and can tell whether they work or not with little difficulty. I guess you could say that you are doing fine so either the RA isn't acting up much or the plaquenil is working.

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  3. CFTC, yeah I think that's one of the difficulties, we're always trying to look for a pattern. I'm trying to figure out if I feel better after plaqunil, or after cutting out lots of meat, or after exercising more. I really don't know. I think the RA just does what it wants and it might all be a coincidence. But maybe not. I have no idea. :/

    Cathy, your post makes me feel grateful. I should just be thankful and not worry why this and why that. Thank you.

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  4. This is a good question. I have switched meds twice in the last year. I hurt everyday but for me, the real tell tale signs show up after physically exerting myself. I can tell if a med is working or not by how I feel after a rough 12 hour shift at work, or the day after a 140+ mile ride.
    Just as an outside observation, I would tend to think that the Plaquenil is doing pretty good from you being able to complete your 51 mile bicycle ride. No way I could do that.

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  5. I tend to go by if I'm having more good days than bad days (good being a relative term). It seems like it's such a slow, on-going process, that, like CFTC Admin says, is generally seen in retrospect.

    Ditto with what Tharr said, that's awesome on your bike ride!

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  6. It can be difficult sometimes to tell if meds are working. You may have a good couple of weeks then get hit with a debilitating flare. I've gone through 3 biologics with some relief then they seemed to quit working. The last one I was on, I had a bad reaction after an infusion.

    I am now starting all over again. I am on Arava and prednisone for now. I am hoping to start Actemra soon.

    The plaquenil may be helping you, so I would continue to use it. Sometimes you slowly get back to living life that you don't realize how bad things were before...

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  7. Thanks guys, I think it's just another case of 'wait and see'. I think my rheumy will just tell me to wait it out until 6 months and then decide if I want to add mtx or something to it. We'll see. But yes, I am lucky to be able to do my bike riding and I am concentrating on today, trying not to worry about tomorrow. :)

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