Rheumatoid Arthritis

I was diagnosed with RA 20 years ago. With me it was only in my hand, so its not quite comparable to what you're going through. The worst part was the fatigue. Some days I could barely move I was so tired.

They treated it with cortisone shots and drugs like methotrexate and NSAIDs. I took that for a couple years until I started developing psyrosis of the liver. When they took me off the drugs the swelling never came back.

I tried really hard to exercise through everything. If I was too tired to run I'd try to walk. That's when I started swimming. Just a couple laps at first and then gradually adding a lap until I was up to a mile. I still swim a mile 2 to 3 times a week. I felt that if I stopped moving I'd never get up again so I just kept on going.

The RA has been in remission for 18 years now. If I stop doing aerobic exercise for a while I feel the fatigue start coming back. I credit aerobic exercise for the success.

Don't give up. Just do what you can and do it every day. Now I run, swim, ride my bike and do strength training. Keeping the weight off, your muscles toned and your aerobic capacity high will do wonders.

Good luck.

I agree with Mike, keep moving.

Two years ago I didn't exercise and ate more than I should have. At one point I was so stiff that if I dropped something on the floor I would leave it there or find a stick to pick it up because bending down was very difficult. Now I'm careful about my dietary choices and I exercise on a regular basis. I have far less pain than I did two years ago and I feel better overall. I can bend down and pick up after myself now I plan on keeping up with the exercise as long as I'm able. I think if I stopped moving the stiffness would start creeping back in.

I was diagnosed with RA about 18 months ago (Rheumatoid Factor positive), although I think I've had it for a least 8 years undiagnosed. I just assumed I was following my mothers footsteps with osteoarthritis. I was in so much pain. I had it in my feet (I walked like an 90 yr in the mornings) I also had it in my ankles, collar bone, hands, wrists and elbows. I was so sore I couldn't even lift the weight of my blankets, I could hardly dress myself and just lying in bed, the 'burning' in my wrists nearly had me in tears.

My CRP was 17 which should be 0-6 and my ESR 47 which should be 1-20. (These are inflammation marker in our blood) I didn't want to be on the toxic drugs for long so I spent weeks turning the internet upside. I used my body as a guinea pig and illimunated certain foods, then reintroduce them to see if I would react.

This is what I discovered... I can't eat sugar, processed foods, meat or dairy and I also cut back on coffee to keep my ph levels balanced. I am off all medication. I do however take an iron tablet once a day and probiotics from time to time. My CRP is now 5 and my ESR 19. I still have minimal pain in my right wrist as my MRI scan show bone erosion.

My life has done a complete turn around just by simply swapping sugar for honey, meat for fish and cows milk for soy milk (Soy milk in Australia is GM free) and eating more fruit and vegetables. I also try to incorporate turmeric, ginger and garlic into many meals.

If you want to learn more I wrote a short ebook which you can get here... http://naturalraremedy.com you can also follow me at https://www.facebook.com/NaturalRARemedy

I sincerely hope this info helps many

it there a group of RA sufferers ?if not would anyone like to start one ?

I have Rheumatoid as well as Psoriatic arthritis.

The most important thing is to listen to your body. Don't push it to do something that is very painful. Its quite a balancing act, but every person I know eventually figures it out to some extent. Maybe others can chime in, but I know for me getting my weight lowered helped immensely on lowering the pain levels on my joints. Especially the knees, hips, and ankles. So if you have weight to lose I would concentrate on the diet aspect just to start out. Keeping active as you can without pushing the limits.

Depending on what exercises you are interested in or capable of, I can probably give you some tips to lower the impact yet give your body a workout that is just as intense.

I am med free do to the cancer risks so I go about it 99% med free with popping a prednisone for a day or two about every 10 months when I know I am going to abuse my body as I am extremely active now. that I found a balance that works for me.

I have the same main issues as you. Walking was very difficult for many years and i needed a cane. My rheumatologist was very leery of my exercise plan at first. Now he says he definitely rethinking some of his initial thoughts. My theory is our joints are getting eatin' up so they need more support. In my mind more muscle is more support to hold the joints where they are suppose to be. Hence less pain.

Feel free to stop by my profile page and see my accomplishments while dealing with RA. PM me anytime with questions.

Hi..new to myfitnesspal..I too, was recently diagnosed with RA. On one hand a relief...on the other, not so much! The meds are helping..I'm finally WANTING to work-out. Do you have any suggestions on how to keep it up? I feel good on some days and then it seems maybe I over-do it when I workout and then feel crappy for the next two days...

Im 34 and was diagnosed with RA 5 years ago just after I had my first son. For me I suffered with small joints first (ankles, wrists and knuckles) but as the years went on I suffer more now with the larger joints - hips, shoulders, knees mostly.
I have a little bit of an addictive personality - when I decide to do someting I give 100% so I was getting really frustrated if I started something like 30DS and had to stop due to a flair up. I was a great runner and had to buy a bike to lessen the impact on joints.
I am on the highest dose of methotrexate and taking daily pain killers. BUT this year I decided to take charge, I am lucky that on good days I am completely normal. I can run etc no bother. I do TRX and kettlebells classes. On bad days I can do nothing.
Again I find the tiredness is the worst, and I am in bed at 9pm every night. Im sick of hearing people say its natural to be tired with two kids aged 5 and 1 but its not normal!

I started taking two tablespoons of apple cider vinegar every morning - idea being my body is too acidic as it is which contrbutes to the inflamation so this will bring the acidity of my body closer to neutral.
I also have bursitis which causes me chronic pain during a flair up so thats another motivation factor to keep taking the apple cider vinegar coz its disgusting!!

Ideally I would LOVE to be off medication in 12 months time.

I hope you're coping ok and remember you can only do what your body allows you to do... dont force excerise if you are in pain.

I was diagnosed with RA six months ago. Among other things, I was put on prednisone, which helped the pain but stimulated my appetite dramatically -- even such that I would wake up in the middle of the night extremely hungry. It was a disaster for my eating plan, which in turn put me on a negative spiral. I gained quite a bit of weight.

I'm trying to do a reset now. I still struggle with significant fatigue along with some arthritic discomfort, but my doc says that will all improve when we finally get my RA under control. I know I need to find a balance that includes exercise, and I like the idea of swimming. Anyway, I really appreciate the information in this chain. If any of you are still logged in, I hope you will continue to post your comments.

My wife has spondyloarthrisis. It is another form in the family of autoimmune arthritis.
Her favorite aerobic machine is a seated elliptical made by Octane Fitness. No joint impact at all. No soreness after in the joints. And full body workout.
Swimming is another very good no impact workout.
My wife does various weight machines *kitten* well. The more she moves the better she feels.
She also battles 3 other autoimmune conditions that effect her endurance. But she still pushes herslef as much as she can.