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Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis News & Research > Doctors Should Watch for Depression in Rheumatoid Arthritis Patients
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Doctors Should Watch for Depression in Rheumatoid Arthritis Patients

Patients with rheumatoid arthritis are twice as likely to experience depression but are unlikely to talk to a doctor about it, according to researchers at the University of North Carolina at Chapel Hill. In the study, published in Arthritis Care & Research, researchers found that almost 11 percent of RA patients had moderately severe to severe symptoms of depression, demonstrating a worrisome link between rheumatoid arthritis and depression. 

The study also found that only one in five of the patients with arthritis and depression discussed it with their rheumatologists. Those who did were always the ones to bring up the topic – not the physician. When it was brought up, it was often not discussed at any length.

Why not? Because when patients visit their specialists, their arthritis is understandably the main focus, says Betsy Sleath, PhD, the study’s lead author. But in discussing a patient’s arthritis, depression is a topic rheumatologists should consider broaching.

"Chronic diseases can greatly affect a patient's psychosocial well-being, and depression can also affect a patient's adherence to treatment regimens," Sleath says. "Since many arthritis patients see their rheumatologist more often then their primary-care physician, we recommend that rheumatologists take steps to screen patients for signs of depression."

Hannah
10 Feb 2010, 11:43
Hello everyone. WOW. Reading all of these comments is so bittersweet. First of all, I am 18 years old and its my senior year in high school. But two years ago I was diagnosed with RA (which actually now I have psoriatic arthritis) but I am on enbrel (which was veryyy hard to get btw.) and methotrexate and the physical pain is slowly going away. However, my arthritis has also caused idiopathic condylar resoprtion which I have suffered from all my life. I have seen numerous doctors and specialists and I am getting jaw surgery in the summer right before I start college. I'm so sick of being sick. But I am glad to know I'm not alone. I dont know of any support groups and I think all anyone needs is to talk with people who understands. Thank you for listening and remember to laugh and smile!
Carrie
24 Jan 2010, 20:17
I am 31 years old and was diagnosed with RA about 6 months ago, but in all reality have been batteling RA for a couple of years due to denial. I am a Paramedic and would blame my pain on lifting heavy patients or just pulling muscles...etc. I have never up until now had the feelings that I have with RA. I have days that all I want to do is cry, then I have days that I am mad at the world, then there are the mornings where I literally have to crawl out of bed. I often feel that I am in worse shape than most of my patients. I guess my question is: Are these feelings normal and will they pass? OR..is this something I am going to have to learn to deal with?
JOHNNA
14 Jan 2010, 14:25
I FEEL FOR ALL OF YOU SO MUCH. I HAVE HAD RA FOR OVER 2 YEARS NOW AND SOMETIMES LIFE IS SO HARD TO LIVE EVERYDAY. IT HAS BEEN A NEVERENDING BATTLE EVEN WITH ALL THE MEDICINES, PAIN PILLS, AND INFUSIONS.I PRAY FOR ALL OF YOU. IT IS GOOD TO SEE SOME PEOPLE UNDERSTAND HOW HORRIBLE THIS DISEASE IS FOR US.
Egondu
14 Jan 2010, 12:21
Hi everyone! I was diagnosed with RA 3 years ago, but I've been living with the disease for at least 4 years, probably longer. In February of 2006, I started experiencing severe pain in my shoulders - as if I pulled or strained something. I thought it was from working out. As the months went by, the pain worsened, and began affecting most of my joints, symmetrically. Eight months later, I had lost about 20 pounds, which was a lot for my already slim frame, I could barely walk up or down stairs, and I was still terrified to go to the doctor! Looking back, I wish I had gone to the doctor early, because I really think I could have slowed or prevented some of the progression of the disease/joint damage. I feel much better today than I did before I received my diagnosis, but I still have really bad flares sometimes, and I know the RA has had a direct affect on my mood/mental health. I'm currently taking methotrexate w/folic acid & naproxen, but I will start on simponi soon, as the methotrexate alone hasn't been working as well as expected. I can empathize w/so many of your feelings and experiences - believe me, you're not alone. Help people to understand your RA & everything that comes along w/it. Don't feel guilty when you don't feel well, whether it be physically or emotionally. And know that you should be able to receive the best treatment that's out there right now. I think the most important thing that we can do is educate ourselves and do everything we can, through diet & fitness, along w/medication, to live as optimally as is possible w/RA.
marty wilder
25 Dec 2009, 16:30
It's Christmas day and my husband, who has RA (and diabetes, among other things) is in bed. He's been there a couple hours which is actually a pretty good day for him. I'm on this site in absolute frustration and despair as to how I can help him. He not only has extreme fatigue but severe pain much of the time. I keep trying to search the internet as to what might be causing his problems but it always comes back to ... R.A. I just read an article on RA and depression. No shit, Sherlock. How depressed would anyone be to have this horrendous disease and almost nobody who understands?
Can anyone help me understand if what he has is typical or R.A. or not? We've asked his doctor(s) and even been to Cleveland Clinic. I guess I just can't accept the simple truth that this is all just R.A.
Any input would be helpful.
Marty'
Steve
14 Dec 2009, 11:19
I am glad to see that I am not losing it, or at least not losing it alone. I feel so stupid when I find myself unable to watch a simple movie or even commercial without braking down in tears. I am a grown man for heaven's sake. I am sneaking around hiding it from everyone because I don't want people to think I am some kind of pansy. Is it the medicine, or is it the disease? I want it to stop. Tired of being sad and tired of the tears.
shona russell
13 Dec 2009, 16:28
hi to all the people out there who, suffer from .R. A can relate to person who said to depressed to comment,,,,
i have nearly crawl in the mornings, i stiffen up and get up, walking like i have something up my backside, untill i warm up,, ands then same things over and over, do not much support from spouse either,,, but i guess when they no in pain, and it does not effect them, its ok. im starting to sound bitter, but it sure sucks, right,,,,, shona
Michelle
11 Nov 2009, 13:46
Do I feel all your pain - both physically and emotionally. It is the worst pain and does suck the life out of you sometimes. Reading all of these posts I feel so sad for all of you - including myself! Right now I have a huge flare up in both of my shoulders, on t3's all night. It gets hard working and dealing with clients and trying to put on that happy face when all you want to do sometimes is crawl in a hole. But everyone hang in there. Try different foods, omega 3 fish oil is good for you I try lacota and I am on 2 different kinds of meds. Try and stay positive, trust me I know it's hard. I would love to start a support group as there is not one where I live - even an online one - maybe meeting once every 2 weeks just to compare notes, maybe different things people are trying, etc, etc. If anyone is interested my email is mknudsen@telus.net. Thanks for listening.
Leasha
27 Oct 2009, 10:28
Don't give up on life Lynn, life hasn't given up on you at all. It may be really tough for you and not having the support of your husband sounds awful. But please don't give up. People on this site understand how you feel and maybe its better for now if you vent to us. At least we will not judge you or think you are a faker as we all know what it is like, good days and bad. But please don't give up on yourself. Its not your fault or your bodies fault you ended up with this horrid disease.
ravenscry
19 Oct 2009, 23:56
Be sure that your doctor is checking your Vitamin D levels. I experienced a tremendous relief of pain as my D level came up from 12 ng/ml to 39 ng/ml with Vitamin D supplementation and more sunlight. My mood is also much brighter. Which came first? I think it was the mood. After a year of higher D levels my joints are all fine instead of swollen and achy. I have been able to go off the methotrexate and reduce the Enbrel as well. I also do 20 min. of functional exercise every morning before I get out of bed, which I think helps as well. I have been able to increase my activity from about 1,200 steps a day to 8,000-12,000 a day. Envision yourself healthy.
Lynn
19 Oct 2009, 12:03
I was just at the Rheumatologists office last week. I was in tears venting about my frustration with this disease. I feel so alone. My husband has disconnected from me completely and makes me sleep on the couch. The kids stil expect mom to do everything and I just seem to explode then cry and no one cares. No one cares I'm sick of being sick. I'm sick of being a walking pharmacy and pin cushion for tests. The girls I work with don't understand and treat me as if I'm just a complainer. How can I not give up on life when it's given up on me?
Leasha
13 Oct 2009, 08:26
I totally understand what you are all saying and sometimes im so thankful for getting this disease when i was a young child. Ive had RA since i was 4 yrs old and im now 25 and Ive always said to my parents how bad it would be to have had a " Normal" life and then to have been struck down with the disease- I guess because i have grown with it, Ive become more accepting. Doesn't mean i don't have my down time either and i can understand how frustrating and lonely it can be at times when no one else understands the pain and what you are going through. This disease most certainly does suck a lot and well i guess all we can hope for is a cure someday- But try not to get too down on yourself, as hard as that sounds. At the end of the day, YOU are not just the disease. That's something that took me a lot time to learn.
Shelley
11 Oct 2009, 12:33
I can't believe the hopeless I feel because of the pain. No one understands what it feels like not to be able to do the little things in life. If I do the little things then the pain is so extreme that I go into a depression. It's hard to explain even to my spouse who is a very loving and sensitive man. I can't even find a doctor to treat my arthritis in my town. My grandkids are always asking "do you feel better grandma so we can spend some time with you?" I finally got time with four of them and now I'm exhausted. Along with the RA I suffer from neck and back problems. I wish there was a blue sky in sight bringing a better day.
just a mom
06 Oct 2009, 14:06
Ever since the RA started the doctors told me to 'hang in there, the cure will be here soon'. Sometimes the pain is so bad I have no hope. The other times the side effects of the medicines are so bad, I have no hope. My quality of life is that of an old vegetable. Now that I look back, I've been waiting 11 years. My youngest daughter is only 12 and I just haven't been able to run and jump with her like her older sister. This disease really sucks, not to mention all the infections we get. I hope the flu shots actually work this year.
k
19 Sep 2009, 23:43
I'm too depressed to comment.

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