Email a copy of 'Swollen Knees Are Smoother: The Glad Game in Rheumatoid Disease' to a friend
Loading ...
E-Mail 'Swollen Knees Are Smoother: The Glad Game in Rheumatoid Disease' To A Friend
Loading ... Loading ...20 thoughts on “Swollen Knees Are Smoother: The Glad Game in Rheumatoid Disease”
Comments are closed.
I finally got a handicap placard. Some folks think it’s cool to park close to the door in a “special” spot. I did. Getting the placard was really hard for me. I resisted a long time. Till I hit a day when I had to park far away. Going into the store was fine. After awhile in the store and standing in line, the walk to the car was painful. I still don’t park in a blue spot if I can get close. There are others who may need it more. I think my town only has one Disabled parking spot on Main St. Pretty sad. But I never noticed before I got a placard.
Doug,
I go tomorrow (BMV is closed on Mondays) to get mine. I, too, have put it off for as long as possible but it is getting harder and harder to walk halfway across a parking lot and then shop (I pretty much only shop for groceries anymore). I have mixed feelings about getting a tag but the time has come. And my friends who understand the struggles I have wonder why I didn’t do it before. I’ve had RA/RD for 15-20 years although only “officially” diagnosed 5 yrs ago. I, too, will only use my placard when I have to but we should be glad that when we need it, we will have it! Take care of yourself!
I was diagnosed with RA about 2 years ago. I really suffered for the first year. In August 2012 I started taking Actemra infusions. I am now about 95% pain free about as close to remission as I think I will ever get. Actemra was the 3rd biologic I tried and the only one that worked.
My point is don’t give up, try every available type of medication. RA is very complex and a medication that works for one person may not work for another.
I am not recommemding Actemra for everyone but, it works for me and Enbrel and Simponi did not. Also, i no longer take MTX and have weaned myself off of Prednisone.
I agree Tom. I’m glad you found something that’s helping you.
The problem with RA is that you are not only dealing with one joint’s inflammation and pain, but all too often you are dealing with MANY joints at the same time. So perhaps your knees were less swollen than doc’s wife’s ankles, but you have multiple other areas in your body wearing you down also, making you more exhausted, lessening your tolerance for pain in the knees because you are trying to ignore pain in so many other areas as well. Tell doc it’s sad his wife’s ankles are so bad, but you are not there to discuss his wife’s ailments. You are searching for some relief from yours. Ask him to be the same attentive compassionate doctor to you that he would expect of the doctor who treats his wife. P.S. I too have smooth knees! Lol (Diagnosed with RA in 2008)
I thought my knees had just gotten fat, like the rest of me, since I’ve had RA! I take 7.5 mg of prednisone daily (can’t seem to function below that, tho my rheumy would like me to.) prednisone makes you want to gnaw your own arm off, so hungry always! That and the lack of mobility have packed the pounds on the last 16 years. I have a pool so ido pool exercises several times a week. Can’t do laps now cause I have a torn rotator cuff. I’m doing pt for that now and for my balance issues. (I fall easily and can’t get up by myself.) ugh!! I will proably end up getting a shoulder replacement (the 4tendons are irreparable), to go along w/my bionic knee and titanium rod in my back! I take 15 mg of mtx weekly and orencia infusion monthly. Both of those used to do the trick but ever since I was taken off relafen, due to bad kidney numbers, I’ve been getting flares in hands and feet. It’s always sumthin, right?
Kelly, thank you for finding that silver lining and making us laugh! A little humor really helps a lot.
I’ve got a strange situation going on right now that has me shaking my head – the middle finger of my left hand is getting noticeably more stiff than the other fingers. Is it possible that I’m going to end up with THAT FINGER in a permanently straight position? Oh no ….
Martha… You sure you are not developing Trigger finger? Does it lock up in a fist position? Mine does this quite a bit, usually when I’m sleeping. I wear a finger brace most nights or I would have to soak it in warm soapy water to loosen up enough to forcefully straighten it out. Once I get it straighten then it functions normal (normal as an RA warrior can be. My mother had trigger finger also and was given a cream to use and did some PT. I know a few people at work decided to have surgery for theirs. All they do is go into the palm of your hand and slice a tendon.
I have one swollen knee, one swollen hand and this morning I could barely walk with my left foot. Everyday it is something. My Doctor has put me on geneeic for Arava plus Methotrexate. My question is why am so tired ? The swollen knee is also smooth and round as you described.
Alyce, I hear you when you say you are tired. Fatigue has been a problem for me for years. Have the doc check if you need iron or are anemic. Lord bless you.
My knees where the first to swell and my back is messed up neck and lower back. Now my ankles are going the same way. My doc added immuniran to embrel and plaquenil and have gotten 2 sinus infections back to back. My lower body has had more problems than upper body, have the crepitius in lower body awlful. Will not,give up.
I have also experienced the hair and makeup changes as my hands got more involved the past 7-8 years. It IS like a burden lifted when you realize that it’s just not going to happen anymore! I’m getting a bit of gray hair, and have decided not to start coloring it… I can’t stomach the salon costs, and would want to do it at home, but doing ANYTHING with my hair already takes it out of me, so why add one more thing? (plus my husband says my hair looks great the way it is, isn’t that sweet?)
I used to spend more time worrying about matching my outfits and now I’m more concerned with comfort. With less shoes that are comfortable, it’s easier to get ready in the morning! Less choices. So I see the same silver linings Kelly 🙂
I can relate, but with my puffy swollen cartoon balloon hands. Now, I’ve always had fat hands, but this is ridiculous. I have these round pinkish brown things with no bones or veins, with fat little sausages poking out one end and an arm poking out the other!
If they didn’t hurt so bad, I’d laugh at them.
Silver lining: on prednisone all my wrinkles disappear!
Suggestion: keep a photo collage of your entire body when it’s “normal.” Then you have concrete evidence of you “before” and “after.”
ugh, memories of pure hell. I used to get a swollen knee so bad I couldnt extend/bend it to walk, and I have a job that requires me to be on my feet all day. I told lots of excuses like a pulled muscle etc, just to avoid having to tell the real story. One particular time both knees got in on the action and I went to the Rheumy, he tapped one knee for fluid to “look” at it. Never did find out what the conclusion of the fluid they drew was, but it filled 2 vials and the aspiration hurt awful bad. I will never allow them to drain a knee again, no point in doing it… I’m so lucky that Enbrel has put me back to normal again, but the memories of what happens should it quit working haunt me daily. I hope you find some relief somehow someday Kelly.
Yes! I do have a positive comment on RA…my hands are swollen all of
the time (no joint deformity yet…) and so, look very young! The
skin is taught and there are no wrinkles. My 62 year old hands appear
30 years old! That is a positive thing, for now at least!!!
Just have to say it’s pleasant reading your article, I was diagnosed with Rheumatoid arthritis in 1981, my father said “Honey if you wake up and nothing hurts, it means you died”.. I didn’t know what he meant then, my knees had swollen and my parents were forced to bring me to a Dr. for school. The doc said “Hell she as Juvenile Rheumatoid Arthritis.” Mom said “ok” and that was it. No meds no special treatment and barely a word about the ailment ever. When my knees hurt I wrapped them and when my feet hurt I wore flat shoes, when my hands stopped working I forced my self to play the guitar all the while never going to a doctor myself. I lived with it med and doc free for 25 years. Then one day it looked like someone took hammers to my feet they were horrible black and blue and green, twisted and deformed. I rushed myself to the hospital and they were shocked that I could walk with what looked like broken feet. No breaks just arthritis. So I went to a specialist and of course by then the flare had faded, I had to beg get them to do the bloodwork, I am not afraid of Rheumatiod arthritis while it really annoys me some days. But every member of my family has AI of some sort so I was concerned it may be more than the initial diagnosis. Turns out I am a thick headed woman living with RA with little or no medication for as long as I can. But it is nice to be reminded that there are other people with all the same symptoms. I literally have every single one you described here. We are not alone.
I am so thankful for my warriors. I am unable to get off prednisone. 4mg every other day. In the beginning, I took 80mg every day. My body didn’t get big, but my head was huge. Lol. I laugh every day.
I guess that is why we are “warriors”. We learn to adjust our strategy to fight the war to live! Thanks for the “silver lining”. I can certainly use it today!
I was able to remember a benefit to rheumatoid arthritis. Having to make good food choices because my hands could not scoop the ice cream out of the carton! Thank you RA