Guest guest Posted July 5, 2005 Report Share Posted July 5, 2005 Hi everyone, My doctor just confirmed on Friday that I have RA. I first went to him 3 weeks ago after about 2 months of severe pain, swelling and stiffness. He put me on Celebrex and 10mg of prednisone and I had relief the next day. (I had forgotten how it felt to be pain free). Anyway, on Friday he told me that he wanted to start me on Methotrexate and either Remecade or Enbrel. I went back to work and did a bit of research and was horrified to see the side effects associated with all of these. It seems to me that he's jumping way ahead considering that the MRI showed no joint damage. From what I've been reading, I appear to be in the first stage. So, my questions to everyone are - what other options are available? What about alternative remedies? Does anyone have advice on following a particular diet? Thanks in advance! Amy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 16, 2007 Report Share Posted March 16, 2007 Hi Kris, I'm Steph in VA. I'm 29 & was dx'd with RA in 1999 when I was 22. My advice is: 1. See a rheumatologist. Having a GP is necessary but you can't expect your GP to know everything about RA too. 2. You'll have to make a choices about meds -- it is a personal decision that all of us must make. You must weigh the risks vs. benefits. For me, early, aggressive treatment has kept me working full time and have a fairly functional life (research confirms this too). 3. Listen to your body. Eat when you're hungry, rest when you're tired (easier said than done with 3 kiddies!) Take care, Steph in VA Morning all, I was just sort of diagnosed last week with RA from my GP. I am seeing a Rheumy April 3rd to confrim. My bloodwork was pretty good but for a few things. Sed rate was normal but Rfactor was off the charts. Also urine came back with wbc and moderate rating for squamous and bacteria. So of course I am worried. I had an uncle die of RA 22 years ago. He had one of the bad cases, totally crippled and never went into remission. Only joints so far are my hands and feet, can't wear my heels anymore lol, and am always tired it seems. My GP put me on Feldene and the lowest dosage of celexa to try to control my worrying and stressing out. So of course my mind is in overdrive thinking of all these terrible things. I am a single mom, 44 years old, 3 kids one of whom has Down syndrome. So can anybody give me some advice on all this? Thanks so much. Kris ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ " Never underestimate the power of a small, dedicated group of people to change the world -- indeed, it's the only thing that ever has. " (Margaret Mead) AmeriCorps Alums -- We're Still Getting Things Done --------------------------------- Now that's room service! Choose from over 150,000 hotels in 45,000 destinations on Travel to find your fit. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 16, 2007 Report Share Posted March 16, 2007 Kris, Welcome to the group. Your children sound like they are teenagers or close to it. As the daughter if a someone who had RA, let me tell you they will survive. Both my brothers and I did, well even I wanted to take out my younger brother... Okay and unfortunately they will still act like teenagers, so don't take what they do, and act like personally. They will with time get used to " The New You " , and work around it. My mom and I argued, fought, and had a great time together. I still miss her greatly. Find things you can do with each of your children that is special to them. When my mother got to the point where she could no longer walk much, we took drives, we also did china painting together. She went fishing with my older brother, and painted for us, I knew her hands must have hurt horribly. She gave each of us alone time with her. We didn't talk about being sick much, even when we took her to the doctor. That was just part of the package of getting to have her around. The point I am trying to make, is not to worry about your children, this is going to be their 'normal'. If you do not make a fuss, they will learn to work with it. Children, even teenagers are remarkably resilient. Fortunately, we have RA at a point in time where there have been some incredible advances in treatment. Don't be afraid of the side effects, compared to the side effects of RA, they are nothing. Okay, the commercials on TV paint much to rosy a picture. Yes, your Rheumatoid Factor is high, luckily for you, that means you are not going to have to work at getting a diagnosis. The SED rate measures the amount of inflammation in your body, normal is under 20. Mine regularly measures around 80, and I know it when it gets higher than that. Check if your Doctor did a blood test for CRP, C-reactive Protein, that also measures inflammation. You mentioned that your feet were swelling because of the anti-inflammatory(NSAID), ask your doctor for a diuretic (water pill). That will help with your feet, who knows maybe you will at least be able to put on your high heels. lol People on the list already mentioned DMARDS like methatrexate (MTX), and the biologic DMARDS. You may be put on a combination of the two as soon as you see a Rheumatologist. It really is a double whammy, that can stop the progression of RA in it's tracks. There are a lot of reasons to optimistic today. Our lifes will not be like your uncle's or my mother's. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 16, 2007 Report Share Posted March 16, 2007 Well I feel much better after reading the responses I received. I am going to a RA doctor April 3rd, can hardly wait and I did have my CRP tested also. That was normal 5.6 so just the high RF number and the wbc, squamous and bacteria were slightly off. I call the dr again tomorrow after being off the Feldene and low and behold the water retension is gone in my feet and fingers. So we shall see what she does next. Today wasn't too bad of a day really. Thanks again so much. I am learning tons reading all of the posts. Kris Quote Link to comment Share on other sites More sharing options...
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