Email a copy of 'I Failed the Rheumatoid Arthritis Control Quiz' to a friend
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E-Mail 'I Failed the Rheumatoid Arthritis Control Quiz' To A Friend
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LOL. Yeah, I don't need an online quiz to tell me my RA is so far out of control it is worse than a naughty teenager. Which is what I often compare my out of control RA to.
Grill is ready for me to make burgers on. I reign supreme griller in the hooooouse!
Good one. 😀
Kelly, do you know which drug company is sponsoring that online quiz?
It was WebMd's site.
In part, WebMd is funded by Abbott.
They make Humira.
However, WebMd claims to have editorial control over all of their own content.
Things like this make me so mad – I'm glad you can take a positive view and laugh at it, I think it could really upset some people.
We all know that there is a possibility of our symptoms getting worse, but sometimes you just don't want reminding (especially by something like this with zero bedside manner!)
Grrr
🙂
This kind of crap is just insulting. We have a progressive disease that causes joint destruction and functional disability, were not stupid. My favorite thing about it was "The condition is taking a toll on you, emotionally and physically" ROTFL This would really be hilarious if it weren't meant to be serious
Glad we can laugh about it!
I am so thankful to have ya'll to laugh about it with!
It's just one more: OMG, Can you believe this one?
I especially loved Purple's "bedside manner" one and Tharr's "that causes…disability… not stupid"!!
That is very funny, “control over RA” that is an oxymoron! I agree, if I had control over RA it wouldn’t exist!! I think RA’s first job is to take a toll on you, emotionally, physically, spiritually and so on. And lastly… If I did not have fear that it would get worse than someone better lock me in the loony bin for denial!
i got cocky over the last month and thought my RA was under control: glad it slapped me down before i assumed remission was possible! 😉
Sorry, Amy. “Remission” is possible for some – I hear about it like the pot of gold at the end of the rainbow. But dmards are still required to slow damage. More like fool’s gold? :rainbow:
Took the same quiz. Got the same results. thought the same thing as you: “Oh really? *said sarcastically* I know it’s not under control-that’s why I’m taking these outrageously expensive drugs, getting stuck with needles once a week, and then having extensive safaris for veins, once a month. Chemo, steroids, etc, I’m a walking pharmacy. I’m not taking all that because I have nothing better to do. …….thanks, I feel better after my little rant!
Hi Julie, Drugs ok – I’ll accept that. But, I can’t DO anything. That is not “getting your life back.”
I took that one too. Way to funny.
Yea, I wonder if the writers or the docs realize we think that?
At my last appointment at least they said they “believed” my pain was real.
I guess that’s a good step. I hate to say it, but I wonder whether women have more problems w/ that issue than men.
Sadly yes.
Housemaids’ knees.. hysteria (as in relating to the womb) yep. In fact googling hysterical and rheumatoid brings up your site in the top two hits!
I just found a few papers that have made me very mad. And then a few alternative medicine sites that pretty much accept the hysteria/neurotic woman as a disease in itself.
I really needed this laugh this morning. I believe WebMD went to the same medical school as my PCP. See, the last 2 times I have had blood work done his office has called to inform me ” You still have very active RA”. I laughed so hard she asked if I needed a psych consult as this “is serious and laughing is inappropriate response”
I took the quiz as well, and surprise; my RA is not in good control. I found the fact that it took longer to read the “very helpful and enlightening” response paragraph than it did to take the 5 question quiz. Oh the lengths we will go, even when we know the results won’t be helpful to find peace within thus disease.
Jenn
I so wish that you could see our pediatric rheumy’s. They are so completely amazing. Dr. Elder can *see* the pain. Even though Emily always tells her that she’s feeling good, she knows better. Last week Dr. E decided to add Orencia to Emily’s Remicade & Rituxan. Since she’s already on IViG she’s not worried about dropping her immune system off of the charts. I was a little shocked- I had thought that Rituxan was a biologic. Guess not. The point is, they want to see her running, jumping and playing again one day. It makes me so sad that not every doctor feels that way. I think that the majority of rheumies just don’t have a clue. 🙁 It isn’t right or fair.
Will continue to pray for Emily.
And what you said about the disparities in treatment was a shock at first & after years of seeing it, struck me as such a great injustice that I’m committing myself to improving care for all people w/rheumatoid disease (RA / JA) until it is accomplished.
Kelly, my RA is under control too. I don’t know whose control, but someone does stuff to my joints while I sleep so they don’t function the next day. And I’m sure the pain is in my head, as well as my fingers, wrists, feet, ankles, elbows, knees, and man, my hips got so bad a while back I couldn’t walk for 3 days.
Been there, felt that…
Keep up the good work!
Thank you for the smile 🙂
If some of these people would get RA even for just a week they wouldn’t write such nonsense. I think having RA should be a requirement to be a rheumatologist. At this point have have stopped most drugs except for my pain meds due to side effects from all that I have tried which are a lot over the years. So hope is something I am hanging on to by a thread.
It’s propaganda like this that makes my parents (who are retired and watch way too much TV)tell me that I am being overly dramatic about the effects RA is having on me. My dad just yesterday told me that I shouldn’t be taking “all that medicine” because it’s “just arthritis”. I have explained to my parents until I’m blue in the face that RA is not “just arthritis” and can affect the organs in your body, too. But it falls on deaf ears. My mom even goes to my rheumatologist, who has prescribed methotrexate for her (she has an autoimmune disorder – they just haven’t figured out which one yet). She refused to use it because one of the side effects was thinning hair. She won’t take any oral medication that has corn starch as a filler (which is anything in pill form) because of a mild allergy to corn. She “diagnosed” me with allergies to milk, wheat, and citric acid as a child (my rheumy said I probably had RA as a child), and looks up all my medications and finds that (surprise!) most oral medications have at least one of these as a filler.
I am so fed up with these “tra-la-la, everything’s better with medication” television ads. They practically tell you they have a cure, and you can go on as if nothing is wrong. The drug companies (and sites like WebMD) are responsible for the public’s misunderstandings of a serious disease.
Hi Jaynie. I’m lying here today working on a presentation for next month and you hit the nail on the head so well. This is what a majority of people with RA face. Sadly. … but we’ll change that.
Do your parents use the internet? You could use the email button under any article to send it to them or send them a link so they can read thru other comments too and see how very many people are like you are.
Unfortunately, my parents DO research on the internet. However, there is so much misinformation that my mom seems to always find and believe the “wrong” source. For example, just yesterday, I found a YouTube channel that sent me into space, I was so angry! The video clips were from “patients” who claimed to have had rheumatoid arthritis and were “cured” miraculously by this quack’s recommended diet. I’m pretty sure this is the last “cure” my mom emailed me. I left a scorching message for the uploader, as had several others, I noticed.
My parents spent the better part of this weekend visiting relatives whom they informed that I was NOT on chemo as I had told them, that I was just “over-reacting”. (A cousin – who also has RA – called to report this to me.) When will all the misinformation and quackery end?????
I’m sorry. I hope your parents will also be willing to read some accurate information about RA eventually. Combatting bad information about RA is one of the reasons I founded this site over 3 yrs ago. You’re right there is a lot of garbage about RA out there – and on YouTube too.
Crazy!!!!! I was just taken off mtx after a little over a year because of horrible migraines. Now I am left to just deal with the pain for 6 weeks until we decide which drug I go to next. RAD is in total control and it scares the crap out of me. I do have pain meds to help me through. This is my first time having to change meds. I know so many of you have been doing this for years. You are all an inspiration to me, especially you Kelly!!!!
Amen!
I am going through the same as you here in the U.K – taken off mtx 7 weeks ago ( I had bad cough from mtx and possible lung scarring plus mtx not working for me) and still waiting for new meds whilst going through more tests. How long does it take to decide what to try next?? Painkillers are a small help.You have my sympathy.
Kelly, I just saw this and it made my day.. Test after test, doctor after doctor.. they couldn’t figure out what was going on with me! The 3rd doctor got mad at me because I told him “WebMD has already diagnosed me, why is it taking you guys so long?!” Luckily, 4th doctor listened and didn’t wait for lab results to refer me to an excellant Rheumatologist! 🙂
Thanks Norma. I’m sorry it took me a few hours to approve your comment – have been in transit to board meeting. So glad you found dr #4.
A few minutes ago I stumbled across this site. What a wonderful thing you are doing, connecting people who have this horrible thing called RA. I’m a little bit tearful at the moment because I feel I’ve found people who understand what it means to have RA and what we all go through day after day. I’ll be back because suddenly I feel “lifted up”. By the way, loved your post about WebMd. My Rheumatologist told me years ago to avoid that site. So glad you validated his opinion and in such a fun way.
Thanks