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Symptoms > Pain > All About Pain > Living With Chronic Pain
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Living With Chronic Pain

For people with arthritis pain, life is full of challenges. Fight back by getting active, staying positive and taking your meds.

By Susan Bernstein

For millions of Americans who have some form of arthritis or a related disease, pain is chronic, or long-lasting. Technically, pain is considered chronic when it lasts three to six months or longer, but arthritis pain can last a lifetime. It may be consistent, or it can come and go. Repetitive motion, such as typing at a keyboard for hours or walking through the mall during holiday shopping season can cause pain.

Chronic pain can make it hard to perform daily activities like cleaning the house, dressing or looking after your kids. However, there are ways to effectively managing chronic arthritis pain, from taking appropriate medication, to staying active, to maintaining a positive outlook. Meet three people who refuse to let arthritis pain run their lives.

Mona Gardner: Managing Pain With Medication

Three years ago, Mona Gardner was active and healthy, working full time teaching research classes at a local university. One day, she woke up with terrible pain in her hands, feet and skin.

“I couldn’t even open the doors of my car,” says Gardner, 74, of Littleton, Colo. Her primary-care physician dismissed her symptoms at first as the typical aches and pains that one might expect at her age, but Gardner was unconvinced. “I said, no. I have friends who pop two Aleve pills in the morning and then they’re good to go. That was not working for me.”

Pressing for a more accurate diagnosis, Gardner went through a series of blood and imaging tests and learned she had rheumatoid arthritis, a condition in which the body’s immune system goes awry and begins to attack its own tissues, triggering painful inflammation in the joints. Gardner was stunned to learn she had this disease, which typically emerges in younger people.

“I never want to feel pain like that again!” says Gardner, recalling her early flares of joint inflammation before going on disease-modifying drugs for her RA. “My skin hurt. My joints all ached. I could have probably been overtaken by depression at the time. I couldn’t do anything. If it wasn’t for my husband, I don’t know what I would have done. My hands hurt so badly, I couldn’t buckle a belt. He had to do that too. I don’t want to feel like that ever again.”

Instead of giving in to her pain, Gardner sought treatment from a rheumatologist. She began taking the disease-modifying antirheumatic drugs methotrexate and hydroxychloroquine (Plaquenil) to control the physical processes that cause her inflammation. She also pushed herself to stay physically active by taking Arthritis Foundation Exercise Program and dance classes and continuing her work at the Regis University.

Gardner also made an effort to maintain a positive attitude about living with arthritis. “I thought, ‘I am not going to just sit here. If I have to deal with this pain when I am doing my exercise classes, that’s what I’ll do!’ The lucky thing for me is that I am not expected to move around a lot at my age. But I want to!” she says. 

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Diana G
27 Apr 2012, 12:27
I'm living with OA and the pain has become so bad lately. It seems every other month a new joint becomes disfigured and hurts too.
Is it possible to have OA AND RA?
I am schedule to have surgery on my foot in August 2012 to help the joint that is causing the worst of my foot pain. But at some point they can't keep doing surgery they'll have to stop and let it be.
I can't take NSAIDS so I'm on Vicodin just 2 pills a day which are not enough. I'll see the Rheumatologist next week about the newest joint to become painful and disfigured.
I workout both on a treadmill and in the pool. But I do it in pain every day. I've worked out at least an hour a day 5-7 days a week. Joined weight watchers to shed the pounds too.
I just feel defeated some days living with chronic pain. I keep active and go out with friends to enjoy my life to the fullest.
Thanks for being here to let me vent!
Jennifer
06 Apr 2012, 08:31
I run a facebook page called "Making Autoimmune Connections". I suffer with chronic pain from Fibro,RA and Sjogrens. My page is a positive and up lifting place of understanding, information and refuge. Please join us! * air hugs and much love*
Rhonda D.
21 Feb 2012, 01:37
I hear my own suffering echoed in the letters above and it helps to know that I don't suffer alone. I am sooooo tired of being told that my problems all stem from my weight! I am college educated and am well aware that weight is a factor in a lot of disease processes. But, it is hardly helpful when a specialist in sleep disorders declares that my health issues would clear up if I lost weight. The type two diabetes and sleep apnea maybe. OA would improve I am sure. However, thyroid issues and gluten intolerance, damage from Lyme's arthritis and past injuries! I don't think so. The surgeries for carpal tunnel, torn rotator cuff and heel spurs on both arms and feet was NOT related to FAT or diabetes, but undiagnosed thyroid disease and the nerve damage preceded the diabetes! I am sorry I am ranting, but please understand I am 50 years old and spent twenty plus years seeking help and a truly receptive physician. I am sick and have been for years but was told and continue to be told that my weight is the root of my issues and I must only lose weight to receive this miraculous relief. I have had numerous issues and have never been able to successfully lose weight. I am so tire of trying to live sometimes. I had to quit with my pain meds cause they were making me have rebound headaches. So I am a fish on dry land at night. OA in neck and hips, lower spine feet and hands, nerve pain in feet and shoulders, gallbladder issues, and pain from hysterectomy and IBS, and possible kidney stones in pelvic area. I don't work now and don't know if I will again. Thankfully hubs has income. I won't attend family get togethers often, or friends parties or church. I don't know from today to tomorrow what I will be able to do. I mention I hurt and I get "oh, I am sorry," let me tell how much my bruised shin hurts! It helps to vent, but so many are unwilling to really listen. I am sorry for ranting so long. I just know that each and every one of you know what constant pain and limitations can cause. Keep on sloggin through the mire, and I will too. Someday we will get to the other side one way or the other, wading, slogging or drowning.
Claudette
15 Feb 2012, 10:15
Today is a number 9 day in pain! I have Osteoarthritis in both knees, and both of my elbows and right ankle. It seems to be spreading and I hate every minute of it! I try my best not to complain, because complaining gets me no where and it doesn't make the pain any better. I have had more than several shots in both of my knees, because of my age (53) my insurance will not cover the type of strong pain medication that I need. I take over the counter pain medication which at this point I might as well be eating candy!

I am too you to file for disability and I am too young to retire. So I am in that in-between stage right now of enduring all of this pain.

I guess today is just one of those days I wish I could stay in bed and never leave the house days, but I have to work.

I am so afraid that one day I am going to wake up and I just won't be able to get out of bed, but until that time, I guess I just have to deal with it and keep moving.

Thanks for letting me vent!
Angela
14 Feb 2012, 14:46
Thanks so much for your comments. I too suffer from osteoarthritis, deteriorating disc disease, u have 5 herniated disks in my back and neck. I am 48 and have already had carpel tunnel surgery in both hands, a total knee replacement, arthritis surgery on rt shoulder and shits in back, knees, and shoulders. I also have fibrous. My husband feels that if I exercise everyday I would be fine but that's Just wishful thinking. I do try to get to the gym twice weekly but usually pay for it the rest of the week. I suffer constant Pain but try to still work outside home part time and i also take care Of a friend's 8 week old grandbaby. I Also suffer from depression. What can a visit to a RA Dr do for me.
karen
14 Feb 2012, 08:31
I just came upon these comments and I couldn't stop crying cuz I just relized that I'm not crazy. I found out about my arthritis in 2006. I went from two sets of injections that only lasted about 3 months and 1 pain pill a day to 3 or 4 a day at this time. Just so you all know, IT SCARCES ME VERY MUCH to be taken this much. I hate it. I have to set my alarm 30 to 45 minutes before I have to get ready for work so my body will let me get up. I need to work for 7 more years to be able to retire and I don't know how I will make it. I am active at work and on my feet at least 6 to 8 hours a day. I don't have time to exercise like I should cuz of working 5 to 6 days a week. I am scared because I am 56 single with a home I can hardly manage to keep up anymore. I see my friends and family look at me when they relize how much pain meds I take and I know they really don't know the pain I'm in. Last sunday, my only day off, I tried to not take any meds except for the morning one and made it only taken a half one in the middle of the day. Yeah, but I didn't get much work done around the house. I do know if I had to live with this pain without meds, I wouldn't want to live anymore cuz THIS IS NOT LIFE. I am glad I found these comments cuz I see someone out there knows my PAIN AND MAYBE i WILLNOT BE DEPRESSED TODAY!! THANKS FOR LISTENING!!
Donna B.
12 Feb 2012, 10:14
As a person living with chronic pain, my first rule is to carefully consider ANY suggestion or advice in terms of my current abilities and knowledge. I take time to understand the source of the suggestion or advice. If it lacks common sense, I dismiss it. If it comes as an anecdote (personal story) which hasn't been reproduced in scientifically-sound studies, I tuck it away until more information surfaces. If it's given by a medical professional or other reputable source, I figure out how I can gently try it out as part of my arsenal of pain management.
I've replaced "exercise" with "movement" to widen my selection of ways to keep my joints and muscles as flexible and strong as I'm able to do.
No matter how an article is written, I always take it "under advisement" until I can figure out how it might realistically work for me. So there's no need for frustration on my part, just gentle consideration of whether anything else will become part of my routine for management of that day's pain level.
Trish
05 Feb 2012, 17:00
I have DISH, fibromyalgia/chronic fatigue sydrome complex, osteoarthritis, degenerative joint disease throughout my spinal column and 11 bulging and/or herniated discs. In addition to the inflammatory problems of fibro, arthritis and DISH, the fibro has also caused the gastrointestinal diseases scientists are saying it may be responsible for and wonder if it may be the reason I have chronic kidney stone disease.

I take my meds, I regularly visit my docs, I exercise when I can, I write in a journal, I try to keep busy to keep my mind off the pain and the fear and the fatigue. What is happening is seeing less and less of my family and friends, doing less and less of what I love to do and a decrease in quality of life.

I try to remain positive, but I am depressed and I am angry. I lost my job because of the pain, depression and fatigue and often times feel worthless. Sometimes I don't want to live.

Linda M
05 Feb 2012, 13:30
To "just new" and others who don't have health coverage: Does your town or county have free medical clinics? Call United Way to find local help, or ask at a hospital, large church or county health department. Doctors can sometimes give free samples of medications, and drug companies have programs to help people who can't afford their prescriptions. It's hard to find out about all these things when you're in pain, but you may find what you need. There may be a support group near you as well, to provide people to talk to who feel what you feel. Ask at a hospital or senior center. (A group of senior citizens has experienced nearly every ailment in the book!) Best of luck.
Cynthia
30 Jan 2012, 15:56
I am 48 yrs. old and I have suffered with RA, osteoarthritis, fibromyalgia, raynauds disease, and a muscle disease for 11 yrs. I have went to many different drs. over the course of those years. What I have learned is that if you have arthritis you must see a rheumatologist. He is a specialist who knows how to treat arthritis. He has greatly helped me. I also see a pain specialist who prescribes Hydrocodone, Gabapentin, Diclofenac for pain and Celexa for Fibromyalgia. My rheumatologist prescribes Methotrexate for lupus. I have pain in the morning when I wake up, but for the most part I can function pretty well now. You do what you have to do to survive. I don't like taking these meds everyday but I want to enjoy life somewhat. As far as exercise, I know none of us feels like exercising but if you don't try to move your body a little you will get worse. I do a very easy arthritis swim class and ride a stationary bike for 10 minutes at a time. Space exercise out. A 10 min. walk, a 10 min. ride on a bike, a few stretches, or in a warm pool swim a little. We are not working on getting in fantastic shape, just moving a little and stretching our joints. I know for a fact that when I get out of my chair in the morning nd get working on something, I feel much better than if I sit there thinking about my pain. Anything at all. Dust a table, clean up yesterdays dishes that you never got done. I know how you all feel. Do you want to let these diseases get the better of you. I don't!! And try to eat well . That is my biggest problem. I need to eat better and lose some weight. I know that would also help. Less weight on your joints. I feel a little stiff right now but I am going to ride my stationary bike now. I hope you all will maybe feel like trying a little exercise. I have tried it both ways. And I choose living my life not letting illness take it away.bestsde
teri
30 Jan 2012, 14:29
I have Rheumatoid arthritis and had found a wonderful rheumatologist dr. that got me to the right meds. I take Plaquinal and metholtrexate and the combo really helps me to walk. If i don't have it i'm am down for the count. thank goodness we have this medication to help us! if your not on it find a Dr will will put you on it! it was a life changer for me with little side affects! So glad i can join life again!
Nancy Thompson
30 Jan 2012, 13:48
I have been struggling with chronic pain for 3 years now. I have degenerative disk disease,osteoarthritis and a ruptured disk in my spine. I also have arthritis in both knees. I take narcotics and aleve every day,otherwise I would not be able to function. I have had injections several times,but didn't help. I am not a candidate for spinal fusion so I just have to tough it out. I force myself to keep moving every day,but sometimes the pain is unbearable. My faith in god is all that keeps me going and the promise that one day I will be free of this curse.
just new
27 Jan 2012, 09:42
I am new at this I have arurits and fibro and lups I have no meds right now and lost meicade and am trying to cope I have no friends who can help i also have a husband and two small kids at home i try to coppe the best I casn but not very good at it there are day i like to give up any way just talking
Becky
25 Jan 2012, 15:16
"Living with chronic pain," Uhm, how 'bout 'Let's Not!'. There needs to be dramatic improvement with pain relievers for chronic pain, especially if doctors are not going to write prescriptions for narcotics. There is only so much pain a person can put up with when they do not even want to get out of their chair to do anything because of the pain. I am pretty tired of hearing people recommend exercise when a person is in pain and exhausted from being in pain.
Arthritis flare ups are really a pain in the a$$ when I lose a day or two due to not being able to use a limb and it takes me twice as long to do the things that I absolutely have to do. Enough already, time to switch drugs for RA.
Irish
22 Jan 2012, 17:18
I have suffered from RA and Osteoarthritis since 1980. I am never in remission from pain. I started on Rituxin over 3 years ago. It does help for about 3 months and then the cycle of pain and stiffness as well as the swelling starts all over again. I also take methotrexate. Which causes a small amount of side effects which keeps me with an upper respiratory infection/cold every few months. I can't sleep but a couple of hours a night. Walking is difficult always and with my hands all swollen and trigger fingers, holding a walking cane can be quite painful. As one person mentioned about depression, not having access to help from others like family or friends. All have dispersed and or stayed away because they feel I am a hinder for them. Or they look at me as if I am going to break or cry out in pain. I never complain and when I do mention how I am feeling my young adult kids and others don't seem to care like they have heard this song and dance before. But let one of them get a paper cut and they act like they are going to die. I have shut myself off from anything but my house the drs and the grocery store a few times a month. Stress with finances and copays when I have a drs appointment stops me a lot of times from seeing my Rheumatologist. I get the impression when the billing office calls me two days ahead of my appointments to ask if I am going to keep the appointment or/and will I have something to pay on my bill. Because it is so high, that the billing office does not give a care about this RA chose me not I had a choice. Sorry for the rambling but I feel like the comments here relate to me totally. I hurt when I move and move and move. I exercise and only to hurt something fierce afterwards. I walk for 30 minutes in front of my house around the circle and struggle after the 3rd lap getting to sit down. But prayer keeps me grounded and sane or depression and not being able to fully enjoy my life would take over. Wishing better days for everyone. Irish.
Sandy Thielke
18 Jan 2012, 21:57
Someone mentioned water therapy, what a blessing for me! I have a excellent therapist who works with me and really switches up the exercises. The pool I go to has a underwater threadmill, I just love beening able to walk without pain! The hot tub is so good for the aches and pains!
Rose Miller
18 Jan 2012, 20:25
I've had RA for about 5 years and have gone through at least that many meds looking for the "right one " finally, finally after 3 infusion and one self-injection treatment my Dr. "hit"upon Actemera...I've been on it for almost 2 years and it has helped more than any other infusion med. Pain not completely gone as I also have Fibro. Will begin Reclast this Feb.
Life is not easy, when I go out my husban has to push me around in a wheelchair ... he's 71 and I'm 225. Good thing he's healthy and has always been physically active.
I have an RA Dr. that really listens and takes time to hear my concerns.He does seem to care and understand my condition.
Lindy
18 Jan 2012, 18:33
I have been in pain with RA everyday for 25 years. I work full time and I'm a pretty happy person. The only piece of advice I have ever gotten that has seen me through--and there have been hundreds of pieces of advice--is to write. Keep a journal and write it out. If all you can write is "I don't know what to write", write that. Soon ideas will form. Studies actually show that people who keep a journal have reduced pain and a brighter outlook. But, studies can prove anything. I have about 32 journals--my study says--try it.
gayle
18 Jan 2012, 16:03
For the person in ATLANTA/ RIVERDALE AREA, check at Piedmont Fayette Hospital, specifically Dr. Rod Duralde. I've been under his care since 1982. Now getting the selective nerve root block injections that help plus starting body massage in the next few weeks. Due to several colon surgerys I am very limited on medications ,there's a cream Voltarian that you can use on your painful places ,its prescription and I've found it to work very well.
Frances Stotts
18 Jan 2012, 11:39
My comment is in response to Faith Neff...she wrote nearly everything I was thinking!! While this article may have intended to encourage those of us living with chronic dibilitating pain...it did not. Also, Lisa Berlowitz made some very good points! I received more from the comments than I did the article itself!
Please Arthritis Today...take a few moments & check out the "American Pain Foundation" there are thousands/millions of suffering Americans living with chronic dibilitating pain everyday, with so many having to fight just to get a Dr. to hear/believe them...let alone their own family &/or friends!! So sad...
NEHYRI CONTRERAS
18 Jan 2012, 01:08
I HAVE PAIN EVERY DAY AND NIGHT ON MY BACK
AND NECK I TAKE ADVIL IN THE NIGHT
Jenn Burns
18 Jan 2012, 01:01
I had a back injury in 2004 and surgery in 2006, one that failed me and yet made me worse than before. Over 3 years ago I was one of the many that suffered from the swine flu, that seemed to take weeks to recover from, after i started to feel better the body pain i had lightened but never went away. I went to my doctors and was told I now have fibromyalgia. I thought oh how nice (NOT), so here i am today with severe constant pain from that, along with my regular back pain, and to add to the list, my knees now have arthritis that is getting worse by the day and I find myself unable to walk somedays and have to rely on my walker just to get around my house. The doctor told me almost a year ago i would be in a wheel chair within 6 months to a year and it seems the more i fight it , the closer i can feel myself slipping to that point. I try not to think about it, hoping i can prove him wrong. There are days that my fiance looks at me and knowing he is baffled on what to do to help ease my pain, and i have to tell him I hurt so bad, it is hurting my body when he looks at me, not to mention my eyelashes hurt I have such severe pain some days. My back is in a multiple "S" shape but from side to side rather than front to back, leaving my tailbone on a slant to the left. When i drive for more than a short trip to the store, i can't get out of my vehicle without help or wait it out til i can move, also sometimes to get in, once leaving me in the pouring rain 1/2 in 1/2 out of my vehicle and noone that walked by would help nor would the store mgr that i called , would send out help so i could get in and get home. I often am sick with colds from these type of situations which just adds to my already medical problems. There are days I want to stay in bed but I force myself to get up , which only leads me back to bed a few hours later on bad days. It's not fun, however i make the best of it and keep plugging away day to day. It's best to keep moving most of the time, but not to over due it, it will land you in bed. Do i follow these rules of mine, umm not usually but am getting better because i know it does work. Take care of yourself
VL
18 Jan 2012, 00:59
Lisa and Faith-
Thanks for saying what needed to be said better than I could!
It is frustrating to be misunderstood by friends & family and to feel isolated by pain, fatigue & chronic illness. That an article like this came from the very group we hope will not only support & educate us, but conduct research on our behalf is disappointing.
I know the AF can do better.
NEHYRI CONTRERAS
18 Jan 2012, 00:20
I HAVE PAIN EVERY DAY AND NIGHT IN MY BACK AND NECK, ESPECIAL WHEM I CLEAM MY HOUSE, I TAKE ADVIL EVERY NIGHT AND HEATER PACK IN MY BACK.
tracy mazzagatti
17 Jan 2012, 22:27
I have been living with chronic pain for the past two years. I'm tormented by this disparaging way of life. It all started after trauma to my upper extremities. I've had 3 surgeries to fix the ulnar nerves in my arms. However the trauma to my extremities seems to have caused some severe degeneration. I spent my life being physically fit and always active. Now all I have is the memory of my yesterdays joy. Its a hard pill to swallow since I am only 50.
Faith Neff
17 Jan 2012, 19:17
I have to be honest hear, I am honestly sick and tired of these articles that boast about having a "positive attitude" and "staying active". Yes, being positive can certainly go a long way to helping stave off a bout of depression and can aid in persevering the many dead ends one will meet when they have an autoimmune or chronic pain disorder. And staying active is important, but to each their own and up to their personal limits. This thing about fighting through the pain in a dance or exercise class is ludicrous. Pain does not equal gain in this case. If you are in the throws of an RA flare up, you can literally cause long-term significant damage by trying to fight through the pain for an exercise routine. What needs to be promoted more in these articles is seeking physical therapy programs that are catered for those who live with chronic pain and physical disorders that can and do contribute to physical pain. There is an excellent program here in Charlotte run by the Presbyterian Rehabilitation (Outpatient) specifically for those who suffer from chronic pain. Also, there is not enough imphasis on warm water aerobics and water yoga classes which are available at almost any YMCA or YWCA. It is discouraging to see this attitude of almost ignoring the pain, or pushing through it, with this idea that if you just keep your chin up all will be well. But let me tell you, it was very hard for me to find doctors that were even willing to help me with my pain, and then find doctors who were progressive with it in the right ways. Pain medications are not evil. Yes, they can cause physical dependence, but that, in itself, is not addiciton. Most people, who do not have any history of addictive type behavior, will not become addicted to pain medications and will follow their prescription as directed. In fact, most of the time, I end up with a surplus at the end of the month as I truly only take them as needed (prn) as the doctor wrote. Please, Arthritis Today, stop perpetuation this insane overreaction to the use of pain medications and equating them with a sure likliness of getting addicted. Its bogus! Also, why not do several articles on several different people on how they had to maneuver the healthcare field to get the right treatment, be taken seriously, and the many various ways they sought relief from pain. Such as me, I now take epsom salt pepperment essential oil baths every day for 30 minutes to 1 hour for 2-3 hours of pain relief. I use ice packs for my pain (which help better than heat for chronic pain), I do a daily regimine of physical therapy exercises that are gentle but very helpful in keeping my muscles limber and my joints lubricated, I take cayenne pepper capsules, use the spice turmeric, drink rooboi tea and pepperment tea regularly, and eat copious amounts of ginger to help with inflammation, and I have developed relaxing meditation techniques that work for me. These are all very helpful in coping with the pain and do not require me to push through pain, which inevitably would hurt me.
Sandy Thielke
17 Jan 2012, 19:06
I work closely with a pain mgt dr, I can not take arthritis meds because of gastric by-pass. I survive with injections in back and knees. I also sleep in a recliner, far better best than a bed. My hands are really starting to bother me, can never ger anything open and the pain wakes me up at nite. Getting older and falling apart is no fun! I envy older people who do not have arthritis!
LaVerne Hensley
17 Jan 2012, 17:17
Dogs are my reason to be active they always make me feel much better. I wake during the night hurting then I take a Percocet which lets me go back to sleep. My pain is caused by osteoarthritis and pain eds help.
Kathy Grove
17 Jan 2012, 14:30
Dear Lisa,

I understand your exasperation. For the past three years, I have suffered such pain that I can only stay on my feet for 2 - 5 min. The pain is excruciating and there is no way to ignore it and go on with life. I have seen six different doctors and all said the same thing. It's just osteoarthritis and nothing can be done about it.

I have tried meds., exercise, physical therapy, acupuncture, and massage. I have been relegated to sitting in a recliner for most of my days. I cannot take care of my family or my home, nor look forward to the traveling my husband and I had planned to do upon retirement.

I try to be positive about life, but it can be a real challenge.



Mike Felter
17 Jan 2012, 14:25
Forgot to put my e-mail if anyone can tell me how to get in touch with the Sanford people,, hazelton4316@yahoo.com I wish you could make those letters and # care at the end my eyes are not that good
Mike Felter
17 Jan 2012, 14:18
I don't know why you would prohibite, service and products that would help people,, I know your going to tell me some thing,,save it,, you have to have the pain to know, like I would love to know how to get in touch with the people at Sanford,, even my doctor things I'm lieing,, and said the pain meds are no good for me,, If he had my pain he would he would have a bag full of pain meds, you can use my e-mail maybe some one will tell me how to get in touch with the people at Sanford ,, thank you
latonya burke
17 Jan 2012, 14:02
i would like to find a program in the riverdale area i live in atlanta, ga
Marcia
17 Jan 2012, 13:46
The whole "pain thing" is really discouraging. All my doctor, including my arthritis specialist wants to do is prescribe pain meds such as lyrica, neurontin, or prescription NSAIDS (which can have adverse effects on the heart). I already have 4 risk factors for heart disease.
Caryn Amster
17 Jan 2012, 11:59
I recently joined Weight Watchers and after 6 months I find that not eating sugar - the refined kind - really helps keep my pain lower
Lisa Berlowitz
17 Jan 2012, 10:21
I am disappointed that this article didn't cite any of the studies that have shown exercising during an RA flare is detrimental and can cause further damage to swollen joints and increased pain. Further, there was no discussion of how beneficial it is to share with others who also suffer from this disease, forming supportive relationships that can help you during the most trying times. And I am in favor of a positive attitude, but most times when I am honest with others about my pain they don't believe me or seem to feel that I am either complaining or exaggerating. So another article about just exercise more, just lose weight and just smile through the pain, denying what you are really going through does NOT feel helpful. In a world where few understand the challenges, biases and realities of what our pain costs us, I expected more from the Arthritis Foundation.
Valerie Wilson
17 Jan 2012, 09:23
Stanford University developed a program called "Take Charge of Your Health" for people who live with chronic pain. The 6-week course is offered all over the country. Look for a class in your area. Class participants learn a wide variety of self-management techniques for living with chronic pain and disease. I took the class myself; then I took the training to become a class leader. It is a wonderful program that offers people a new lease on life.

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