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Is it normal for RA symptoms to be worse after infusion before they get better?View Thread
Is it normal for RA symptoms to be worse after infusion before they get better?View Thread
https://adobeformscentral.com/f=dLDH2jBw8nHc3%2Ar6B6kzeg
If you have 10 minutes to spare please complete
Feel free to ask any questions
Thank yoView Thread
This is a 60-minute in Phone/Web Interview.
Who: Rheumatoid Arthritis Patients
Topic: RA Sufferers
Date: Tuesday, May 21, 2013
Time: Times to be scheduled upon your convenience
Honorarium: $100
Where: Phone/Web Interview
Confidentiality is strictly maintained and only statistics are used. Your opinions, as a patient, are invaluable to our research.
If you are interested and would like to participate, please call Cathy at 212-217-2000 x2048 at your earliest convenience. Please reference job number 13-190 when you call.
We understand your time is valuable and as an appreciation of your help, you will receive an honorarium of $100 for your participation.View Thread
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Poll Results
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Non-Biologic75% (3)
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Biologic25% (1)
Just looking to see if anyone has had the experience of their biologic stop working.
I've been on Simponi for over two years and it's been fine, however, I'm starting to think it may not be working. I had a really hard time finding a med that worked. It was a rough experience. The last thing I want to do is switch. I can't take methotrexate or Enbrel.
Just looking for some information.
Thanks,
LCView Thread
Any suggestions, input on this would be greatly appreciated. I am feeling like I am making this up in my head now, that is the way he made me feel.
View Thread
I was diagnosed with RA three years ago and I have been taking monthly injections of Simponi for about 2 1/2 years and it has worked great. Haven't had a flare in 2 years.
Lately I have been waking up in the middle of the night with an extremely painful knee, ankle or foot (knee was the worst). All I kept thinking was this feels like a flare. When I wake up in the morning, I feel fine aside from the regular stiffness in feet, etc. My blood work also showed that my C-reactive protein has gone up a little to 1.3 (previously it's been at 0.
. So there is some inflammation.Has anyone else experienced something like this?
Thanks,
LCView Thread
Additionally, I've osteoarthritis in both hands. The finger joints & on ea knuckle of the pointer finger are always swollen & painful. I've noticed that on each finger's nailbed is slightly purple. Is this a cause for concern?
Best to all,
KimView Thread
http://www.forbes.com/sites/rickungar/2012/02/12/proof-of-the-failure-of-free-markets-in-medicine/View Thread
My symptoms have become worse and worse; fatigue, malaise, aching in my shoulders, ankles, calves, shines, wrists, neck and elbows. The worst is the fatigue and I'm thinking depression. Yesterday and today I woke up in pain whereas before it was aching and all I want to do is sleep. I've had to resort to putting a gate up in front of my daughter's door so I can have an extra few minutes to get myself going and I'm safe in the knowledge she's contained in her room. She asked that we read and I could not even hold the book my wrists hurt so badly. She wants to go outside and play and I'm sitting here trying to get the energy to shower let alone chance after a 3 year old. I feel like the worst mother ever. Does anyone have any good tips on raising kids with these symtoms?
I've read and understand these are all basically normal side effects of RA but my question is what do I do to manage until I can see my Rheumatologist and get the right medications etc. My husband although a great man and father just doesn't understand he has read that exercise is key and I'm not disputing that because when I do get up and moving I feel better but I crash so hard after. I tried to tell him I need to conserve my energy for things like housework and playing with the kids and doing my homework (I'm a full time online student). How do I get him to understand that as well? Or is he right do I just shake it off and push through the pain and fatigue?
View Thread
I feel terrible for my husband. He's had joint pain for two months now, which came on suddenly. I've been researching information for him online, he had some blood work done, and talked to a Rheumatologist, who said he didn't have RA or Lupus and did not give a definitive diagnosis, so he's frustrated to say the least. He're are his stats:
-42 years old, decent weight, fairly active (runner)
-No real health problems in the past, but has high cholesterol (family history of high cholesterol)
-Pain is primarily in his hands and joints, worse in the morning and at night (when he turns in bed and tries to pull the blankets, he's in pain)
-Some swelling of the fingers, but not consistent
-Pain appears to be symmetrical
-More recently, he has had pain in both knees (for 4 days out of the last 60 he's been feeling like this)
-Experiencing fatigue, but not sure it's because he is not getting a restful sleep b/c of pain
-Running sometimes helps, but not always. Lately, he's saying that it hurts to swing his arms fully while running.
-I've helped him by soaking towels in warm water and wrapping them, and buying him Capsasin cream, but it's a temporary fix. He still needs to work, and can't be home all day to treat himself.
Doctor put him on Meloxicam (15mg) about a month ago, and an anti-malarial about two weeks ago. I want him to feel better, but having no clear diagnosis is hard because once we know what it is, we can treat it and he can feel better. At the very least he could have more good days than bad.
Sorry for the long post. If anyone has any additional information that they could share to help us out, I would appreciate it. Thanks so much for your help.View Thread
What is the outlook / prognois for newly diagnoised individuals. I know there are a lot of variables so feel free to be vague. Everything I read online says EVERYONE gets erosions. Is this true?
In my case my rf is 21, my ESR and CPR have been consistently low/ normal but my ccp is above 250. I started medication within three months of the onset of symptoms. Does early intervention counteract the high ccp number?View Thread
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