RA Causing a lot of pain! Any helpful hints?
I have had RA for several years have tried many medication‘s and I am in so much pain. I would love any kind of helpful hints that you can give me! thank you so very much for your help!!’
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@lindaadele When we say "I have RA", it's kind of like saying "My back hurts" - that is, there are many types of RA, that can cause pain in many different parts of the body.
I happen to be lucky enough to have both RA and osteoarthritis (OA), as well as fibromyalgia and an aggressive inflammatory response to many triggers, so treating pain takes a multi-pronged approach. My primary treatments are a healthy diet and as much activity (note I didn't say exercise) as possible. As to the specific ailments, for RA, we have settled (for now) on 15 mg leflunomide daily, which mostly controls pain and swelling in my hands and feet, I handle the breakthrough with topical Voltaren gel. We may be headed for a biologic in the next year. For OA, I use Tylenol to manage pain, add ibuprofen for bad days, and am exploring adding meloxicam with my rheumatologist. For fibro & reactions, I was using duloxetine, but weaned off and will be exploring options (too brain-fogging).
Through it all, I have stayed as active as possible - one of my fabulous rheumatologist's favorite lines is "motion is lotion." My Mom lived 40 years with RA & OA, and when people told her to take it easy, she would reply "If I sit down, I'll rust up and not be able to get up" - I try to keep both these adages in mind.
In 2020, after all of these diagnoses, plus a chronic lung condition, I was headed for being a permanent couch potato. I was referred to a pain rehab clinic through my health provider, where I learned to LIVE, not just exist, in spite of pain. The treatment included learning to acknowledge and see the pain differently, manage it with (non-opioid meds), physical therapy, meditation, behavior mod. Also to learn how to get decent sleep. I saw a pain management doc, a PT, and a psychologist. I also have a pulmonology team managing my lung condition, and a cardiologist for my heart.
Most of the time, being active - gardening, doing a lot around our 50 yo house (currently in a complete refresh/redec/cleanout), volunteering, walking, traveling, painting, fiber arts, hanging out with friends from 8 to 80+, and playing with my grandsons keeps my mind off how I hurt. If I sit down, I start cataloguing how many parts hurt (or don't work.)
When that's not enough, I resort to surgery if needed - I have had both hips replaced (OA), both thumbs repaired (OA & RA), my ACL/MCL replaced & rotator cuff repaired (trauma). This week, I will have my wrist replaced (OA & RA).
Yes, I have BAD days, or days when my body refuses to do ...anything. Then I take a day off, rest, read, take a hot bath, sit and enjoy my gardens.
Do you know your specific type of RA, and what parts of your body are affected. It would also be helpful to know if you have osteoarthritis (OA) or fibromyalgia in addition to RA.
What non-drug methods have you tried to manage pain and improve your quality of life?
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10 Reactions@sueinmn
Your treatment sounds worse than the disease.
I'm not active and there's a lot of truth in the "I'll rust up" adage.
Jake
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2 ReactionsI've had RA for over 25 years. Sue is right. Stay as active as is possible.
And diet is really important too. The more junk type food like chips, etc. you eat, worse you will feel. I find even eating too many supposedly healthy type cracker aren't great either. The less processed foods you eat the better you will feel.
Sugar is also a big culprit . I usually feel pretty bad by the time Christmas is over and I've over indulged.
And try to keep your weight as close to a healthy weight as possible. I know that is hard for a lot of us.
You didn't mention a rheumatologist or the types of medicines you are taking or have tried.
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4 Reactions@sueinmn
Sue, are you in Phoenix? I ask as my body has all the symptoms of RA. I have had a terrible time getting in to see a Rheumatologist. Do have a Mayo appt 7/22, with a resident. 2 month wait. I have Myasthenia Gravis, broke 5 metatarsals in 2022,23,24, which are healed but last winter my feet just went off the charts with pain! Swelling, a whole shoe size, burning, skin sensitivity. Due to the broken metatarsals, and a improper gait, then my hip went wonky, i learned i had 2 tears in labrum, Glute tears and Bursitis, which then caused awful pain all down the legs, most issues on the right, then of course i have a 72 year old back who is severely degenerated. At the end of now, after searching so many paths and have had RA tests negative, but i learned that seronegative is a potential possibility,. I did not mean to give an entire history, but with so many problems, pain, autoimmune MG,, which after 12 years only became significantly managed with a new biologic a year ago, i am so tired of chasing doctors, ones who sincerely are incompetent. I am left with a fracture in my right ankle which could be causing inflammation in one foot but certainly not 2. So I think I am left with a rheumatology issue. I have done all potential testing of any other things. SOOOO when i aw your post, sounds like you may have some experience in similar issues. The feet specifically. I so fear any surgery. Anyway, if you have a wonderful smart Rheumatologist, would you be willing to share? I appreciate any input. From you or any other patient onn here that sees this. Thank you!
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1 Reaction@theresaag My great rheumatologist is in Minnesota, and not looking to move.
I understand the frustration of trying to find good docs. We have been extremely fortunate to find each doc by referral from another we trust. Being near Mayo, a medical school and many teaching hospitals is an advantage.
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1 Reaction@sueinmn when you say swelling do you mean just the joints or the fingers and such??
I have had RA and then osteo and erosive for over 40 years untreated until 3 years ago. I'm allergic to aspirin and NSAIDS. I just put up with it.
The standard RA drugs didn't work.
I started low dose Naltrexone last year. The relief is amazing. I have no side effects and the everyday quality of life is much improved.
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3 Reactions@sueinmn Your uplifting mindset is powerful. I plan to hand your post in the frig!💕
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1 Reaction@tisme My joints and the soft tissue in my fingers/hands/wrists (and sometimes feet) swell and get red/warm/even hot to touch. Leflunomide is keeping it mostly controlled, but I am at my maximum dose. My Rheumatologist says when it ceases to work, we will look at biologics because I am not a candidate for methotrexate, sulfasalazine or hydroxychloroquine. I also use topical Voltaren gel at bedtime on bad days.
@jdnc2023 So glad to hear low-dose Naltrexone is working for you. We may try it if I ever have to stay home in the cold Minnesota winter. That is the WORST for me - but so far I escape to warmer climates from Halloween to late April.
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