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Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis Treatment > Rheumatoid Arthritis: Remission is Possible
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Rheumatoid Arthritis: Remission is Possible

Achieving arthritis remission may not actually be as daunting as the death-defying tasks that brought super-spy Ethan Hunt out of retirement in Mission Impossible III. In fact, it may be well within the grasp of nearly half of the 2.1 million Americans with RA. The earlier one begins rheumatoid arthritis treatment, the better one’s odds are.

“If you have fewer than 15 minutes of morning stiffness and no tender or swollen joints for at least three months, that’s definitely remission,” says Salahuddin Kazi, the chief of rheumatology at the Dallas VA Medical Center in Texas. “From a functional perspective, you can do all that you want to do. You have no limitations and no pain.”

Sound too good to be true? It’s not, says Désirée van der Heijde, MD, a professor of rheumatology at the University Hospital Maastricht in the Netherlands. She says that with today’s newer rheumatoid arthritis treatments, as well as with more aggressive use of older treatments such as methotrexate, nearly half of people with RA can – and should – achieve remission.

In the Trial of Etanercept and Methotrexate with Radiographic Patient Outcomes (TEMPO), a two-year study of 682 people with RA from 92 treatment centers in Europe and Australia, more than three quarters of people treated with the biologic drug etanercept (Enbrel) plus the disease-modifying antirheumatic drug (DMARD) methotrexate experienced no progression of joint damage at three years. More than 40 percent achieved clinical arthritis remission.

“Treating early before damage occurs gives you a higher probability of remission,” says Dr. van der Heijde, adding, “TEMPO showed a high percentage of patients in remission, even in those with relatively longstanding disease.” Exactly how close you can get to arthritis remission depends on how aggressively you are treated early on, agrees Dr. Kazi. 

“If you get treated within two years of the onset of RA symptoms, you have more than a 50 percent chance of achieving remission.” Chances are even better if you have mild disease activity and test negative for blood markers such as rheumatoid factor, he says. “If you get treated within five years of onset, TEMPO shows you still have a good chance of achieving remission.”

“At least 60 percent of RA patients should have low or moderate disease activity with today’s treatments, including the subset of biologics called TNF inhibitors – adalimumab (Humira), Enbrel, infliximab (Remicade) – and the newer biologic agents, such as abatacept (Orencia) or rituximab (Rituxan),” he says.

Don’t take no for an answer, Dr. Kazi says. “Develop a partnership with your doctor where you can say, ‘I still have some disease activity; can I have a higher dose of medication or try something different?’”

Jeff
02 Sep 2010, 17:42
As the parent of a 10-year old who has had JA since the age of 3, I am both encouraged and concerned by this report. Of course, we all want remission and even a cure - and the advances have been great. But remission is tricky, just in terms of its definition alone. It also concerns me knowing how difficult it is to raise money for RA research and programs. I don't know how many times people have asked me if my daughter will "outgrow it". This disease suffers from lack of understanding and exposure as it is. It's hard enough to overcome the "every gets it eventually" stigma, without tossing in "you've got a 50% chance of remission" when we don't even fully understand what is meant by remission. Still, this is good news and my own daughter is evidence that early treatment with what we know today can make a huge difference.
Les
22 Aug 2010, 20:12
Jessica,

I was recently diagnosed as well & my doc didnt give me any options other than methotrexate or being crippled. I only have pain in my fingers & wrists and I felt it was only a flare up. I have been doing so much research & cannot find anyone with a similar situation so I have changed my diet & balanced my hormones in order to get my immune system strong & healthy in hopes that I will beat this thing. Reading your post just gave me the most hope Ive had in weeks! Thank you!
Maria Elena
13 Aug 2010, 22:27
Marie,
I have noticed that when I have fasted the pain goes away. There has got to be a diet connection to this, so I have started to explore what foods need to be eliminated in order to feel better.
Kayla
28 Jul 2010, 22:37
RON- I got turned down for long term care and when I spoke to the underwriter it had more to do with the use of prednisone than for having rheumatoid arthritis. It in there experience indicates that the disease is not well controlled and I am able to try again for insurance as well as a better life insurance premium within two years. I recommend trying another treatment since the long term side effects of prednisone can be worse than RA itself....good luck!
Jessica
15 Jul 2010, 14:13
I was diagnosed with RA just after my 17th birthday. I was experiencing extreme flare ups in all of my joints. It took only 4 months for my Dr to diagnose me, my RA factor was positive. I was crushed to be so young and to be diagnosed with such a crippling disease. I started getting depressed and sleeping all the time. I was constantly in pain and tired no matter what I did. My DR put me on prednisone and plaquinil with cortosone shots in my fingers for the swelling. It was terrible. Then my insurance changed and I had to start seeing another doc who decided that I should be on methotrexate. I didn't want to take it because of the side effects, but the doctor told me that if I didn't I would end up disfigured and unable to move. I was horrified so I started taking the meds. I also decided that I wasn't going to trust the doc anymore and that I was going to look into other methods of control.

I started reading on changing diet and exercise. I started practicing yoga 2x weekly and pilates 2x weekly. Then I decided to work on my diet. I started reading all these articles about all the crap that is in our meats and dairy and the thought occurred to me that maybe my immune system was attacking my body because of the things I was eating. I first cut out soda and beef. I started to feel better and decided to continue by cutting out chicken and pork. I stopped having pain and swelling. I stopped taking the meds and stopped seeing the doc that recommened them. I have since been in remission and continued to cut out white flour and sugar. I use soy, but I might start cutting back because I have heard that it is better to use it in moderation. I am seeing a new doctor, but he told me that I am doing so well that he doesn't believe that I need any meds and to keep doing whatever it is that I'm doing. I am so blessed to be in remission. I am only 26 and I feel like I have my life back. I cannot tell you how wonderful it is. For all of the people who suffer, I understandwhat you're going through and I just want to encourage you to look into other methods of control for your pain. Exercises that strenghten and stretch with low impact are great, changing your diet can have an amazing influence, and above all please trust yourself and what you feel is right for you. I'm not saying stop all your meds right now, I'm just saying that you should consider all your options and see what works for you. I am still actively looking for ways to keep my RA in remission and I learn new things about nutrition and staying healthy all the time. Keep your eyes open and have faith and hope. There will one day be a cure for this disease and we will know the cause of it.
Ron
06 Jul 2010, 14:23
I was diagnosed with RA by my Rheumy in Fall 2009.Severe joint pain in my hands. The blood test indicated negative for RA. never-the less Insurance company turned me down for Long Term Care because of being treated with MTR ( 4 tablets of 2.5mg once a week...I am also taking 4mg of Pred 2 times per day. I am otherwise in excellent health (both of my parents lived well into their 80's). Currently I seem to be fairly well controlled from the pain.I am concerned about long term affects of the medicines.

Has anybody been turned down for LTC Insurance in a similar circumstance?

A note to others...my Doc could have responded to Insurance company query by stating that I had "arthritis"-that had a blood test result of "negative" for RA. Had he handled it that way I probably would have been approved (so please make sure you discuss in advance with your Docs when you are applying for insurances so that factual information that helps your case is provided instead of factual info that hurts your case.

I'd appreciate comments on any of the above.

God Bless everyone1
TLB
05 Jul 2010, 23:37
I've just been diagnosed with RA. I was given shot of cortizone to help the inflamation and pain temporarily. I have been given some info sheets with limited information about the different medication options which I'm supposed to choose from. I am trying to research the best options but am at a loss without a medical degree......
Does anyone have a "DMARDS & Biologic Agents Cocktail" that they have found effective. My goal of course is complete remission.
Karen
20 Jun 2010, 22:01
No need to be in pain. As soon as you are diagnosed find a rhuematologist. Only see a specialist! If you are in pain after being prescribed assorted pills make sure you take/try the biologics (newest class of drugs). I am on humira, plaquenil and prednisone and according to this website I am in remission. Sounds good to me. I have minimal if any pain. Life is good : )
Marie
13 Jun 2010, 21:05
I was diagnosed in Oct. 2009. Had a hard time accepting the RA. I thought it had something to do with the birth control shot I just started in Sept. of 2009. Everyone laughed at me. The rhuma doc started me on plaquinel, sulfasalazine, and prednisone. I refused the methotrexate and still do. The doc is upset with me because of that. She just doesn't understand why I don't want to take that "chemo drug". When I got rediculous swelling of ankles and lower legs my Prednisone was increased to 60mgs a day for a week. I started Humira 5 wks ago (1 shot every 2 wks), which I am scared of the side effects since I don't have a spleen, which leaves me even more prone to infections. It was amazing for the first 2 wks but has started to lose it's effects already.
In Feb 2010 i had emergency surgery for obstructed bowel & was taken off ALL meds & no food/drink for 4 weeks. I didn't have any flare ups or symptoms. It was amazing. The RA didn't return until April, and it hit me like a semi truck!!
I now wait...but can't help but think that fasting helps in some way.
perry fleming
11 Jun 2010, 01:42
not sure if all commenters are sufferers. my wife is. she speaks of constant pain and agony. she has progressed from tna inhibtors to (soon to be) infusion theropy. hopeful thoughts and prayers are not recipes for cures. contributions for ra research are.

thanks,
perry
rocio
19 May 2010, 16:16
I was diagnosed with RA September of 2009. At the time my symptoms were very painful. I started taking Plaquenil and Prednisone. I stopped prednisone in February and just manage my pain with Plaquenil and Advil when needed. I practice yoga, spinning and walk everyday. I follow the blood type diet and my symptomps have improved 80%. I only have mild pain within the first our after I wake up. Good luck to ya'll.
Stephanie
18 Apr 2010, 02:06
I have an idea that fasting may help. For 3 years I fasted once a year and ate a diet consisting of 95% raw food. I totally excluded Meat, Chicken,Diary and Wheat.
During this time I did not take even one painkiller or supplement of any type. I just dont seem to have the emotional resources to do this again. I still do not eat meat or chicken, but am now on so much medication that I feel like I rattle. I am diagnosed with RA, Fibromyalgia, Chronic Myafascia Pain Syndrome and Astma.
Good luck to you all
Danny
05 Apr 2010, 15:22
I was diagnosed with RA back in 1999 when I was 38 years old. It was horrible. I was in extreme pain and could barely walk and could not button a button. I went on prednisone, but quickly tapered off of it and was on it for only 13 weeks. During that time, I fasted (2 days/week water only; 2 days/week juice fast). I was symptom free and my sed rate and RA factor plummeted. My doctor was amazed. I had been completely drug-free and symptom-free for almost 10 years. I compete in triathlons and I lift weights daily, etc. I am very athletic. But now it has come back. Has anybody else had success with fasting?
Bonnie
03 Apr 2010, 18:08
I was recently diagnosed with RA. I am 37, and I am about to begin tx with Metrotrexate. I'm scared of the side effects, but want remission. If I go into "remission", can I stop all meds or at least this Metrotrexate? Has anyone done that?
Diwakar
31 Mar 2010, 10:46
Very useful information. I have found other related information which helped me a lot here

http://www.vedantatree.com/2010/02/treatment-for-rheumatoid-arthritis.html

It may help others.

Diwakar
terry motley
19 Jan 2010, 15:44
Good news!! I have had RA now for 3 1/2 years. It took 2 years to get a proper diagnosis. My Rheumatiod factor in 03/08 was 177 at discovery. Today, it is 33!! Even my sed rate is normal and the pain is mercifully gone. Methotrexate did not work for me. It made me very,very ill. I did not like the horrible side effects of all the other RA drugs so I instead went to a Doctor of Traditional Chinese Medicine. He mixes an herbal formual specifically for my needs and I drink it twice a day. Dr Ma says that auto immune diseases can be controlled by non-toxic herbs just as well as by the toxic western drugs. He is my hero because he has given me my life back. It took a year and a half of drinking his herbs for all of the pain to go away, but the pain did subside gradually over this time. There is a way to control your RA without using toxic drugs with terrible side effects. If anyone reading this would like to ask more questions, you can email me at motley92@hotmail.com. Just put RA in the subject line so I don't think it is junk. My blood results are proof that chinese medicine works!
Melissa Jordan
13 Jan 2010, 22:01
I am a 38 year old female and I was diagnosed with RA about 3 months ago, right before my b/d. The prednazone I was on, then tapered off of completely, really helped me alot. I then started on the sulfasalazine for a month and my doctor called me and told me to stop immediately because my liver levels were up. That was 3 weeks ago and I am not taking anything right because she told me to stop all meds even my vitamin d. I have had injections in my shoulders and was pain free for about 2 mths. They are hurting again but not as bad as before. Before I would be up all night long in tears. I got an injection in my left thumb a few weeks ago and so far no pain or swelling. I am scared to try a new medication in fear of the damage I will do to my body. I have a good mind to tell my dr that I am going to try natural ways of getting better for a while just to see what happens. I really want to be in remission from this disease. I am praying daily to be healed or for a cure. Does anyone know of a good exercise program that will help with pain. I was told exercise may help. I enjoyed reading all the posts on here because it really did give me hope!
cj
13 Jan 2010, 21:36
I was diagnosed with JRA at the age of 3. Physical therapy, nsaids, sleeping with braces on my leg and wrist, cortisone shots, gold shots, hospital stays.... had it all as a child.
I have had no symptoms since I was about 15. When I turned 18 my rheumatologist said at that point with no symptoms, I was in remission and only needed to see a rheumatologist again if it ever started to bother me again. Just turned 40 and still haven't been back to a rheumatologist - so remission does happen!
CJ
02 Dec 2009, 20:29
I think that there maybe help out there if you want to try biologics like Humera Embrel Remicade??? not sure of the spelling but if you contact the companys directly they may help... that is what i have heard...Is there anyone who has tried herbal remedies and diet remedies together... I have had RA for over 3 years have been on hydroxycloriquin or (plaquinal) and pain management are the only things I could count on... had sever reactions to almost all meds for RA (have not tried Biologics) the pain is still sever and feel like you just do not want to move ever... am so afraid to try any of the biologics the reactions to sulphasalizine methotrexate pednisone very sever lost my eyesight my face became swollen breathing problems looking for something that will not make things worse than it already is as I am sure all of you are Hoping for the best for you all hope info helps thanks for listening cj
julie
19 Nov 2009, 12:06
I was diagnosed in 95 and went through 5 years of experimentation, trying this drug and that drug, nothing worked, then went on mtx orally plus prednisone and plaq. this helped but changing to mtx injectable and then adding enbrel really helped. but then 4 years later my skin developed crusty sores that were diagnosed as pre-cancerous. then the meds stopped working. I quit the shots for 3 months and the sores subsided but I was in bad pain. I started the shots again for 6 months and the pain lessened but the sores came back. in sept this year I stopped the shots again. no bad effects this time, so far no shots for 2 months and sores are going away again.some pain but I take 5 mg pred when I need it, every few days or so. maybe I am in remission? I hope so! if the docs only knew what this disease really is and really how to make it go away!
Kevin
16 Nov 2009, 20:10
This is in response to Karla, who on 30 Sep 2009, 15:08, wrote of not being able to afford medication.

I do not suffer from RA, but am very close to someone who does, so I know how awful the suffering can be. We also do not have very good insurance, but I've learned that the makers of Enbrel can offer assistance to those who cannot afford it (and if you are not independently wealthy and/or do not possess excellent insurance, you cannot afford Enbrel - that is for sure).

We have not yet contacted Amgen/Wyeth (the makers of Enbrel) but we are about to. The assistance information is here:

http://www.amgen.com/citizenship/encourage_about_amgen_wyeth.html

If the proprietors of this site would please forward this message to Karla, that would be greatly appreciated.

Thank you.
jojo
03 Nov 2009, 10:53
I've had RA for a year. Prednisone seemed to work to relieve symptoms. Methotrex. was awful-made me feel ill for several days a week. Not worth it to me. Very afraid to start injectables- fear of side-effects. Can people reach remission with alternative treatments?
Mei
12 Oct 2009, 12:34
I had RA since 95 and had all the up and down, tried a lot of med, now I am on Enbrel,Plaquinil, olchicine and Prednisone 2.5mg (trying to cut it out). I have been felling nearly normal almost 6 mon.

It took a long time for me to accept the reality of having RA and having an incurable disease. I did wrong choices on finding the treatment. Now, luckily I have a good RA doctor and I try to work with him. Eating healthy is important. Exercise is a must. Since I got RA, I practice Tai Chi daily and follow a wonderful teacher all those years. It helps me tremendously.

I was prescribed Enbrel last fall and it worked wonder right away. My worry is how long the Enbrel will last. My doctor said that sometime the body will reject the med after certain years, and the med won't work. Then you have to try another kind. I used to ask often...why me?! When I read other people's suffering stories, I could totally feel it - I went through hell (if you didn't go through this that you could not understand the pain) and I am glad for now, I feel OK. All I could say is don't give up, rest well (good night rest is essential) and eat well and try to find happy thought while in misery.
valentine
08 Oct 2009, 08:37
i was diagnosed with RA at 16 years old. that was 13 years ago.
i have been thru it all and taken all there is to take.obvious;y by now i have irreversible joint damage and take prednisone, leflumonide,painkillers .
i just wonder is tehre any hope for a remision for a case such as mine?
i am now 29 yeras old and hoping to have a baby soon.
i need to keep informed and know if it is possible for me
LOIS
05 Oct 2009, 16:32
HI ALL. I AM IN REMISSION FROM RA. HAD IT FOR OVER 13 YRS. DID MY HOMEWORK AND READ THE BOOK "RHEUMATOID ARTHRITIS THE INFECTION CONNECTION" BY KATHERINE POEHLMAN PHD. GOT ON THE ANTIBIOTIC PROTOCOL AS DEFINED ON THE SITE WWW.ROADBACK.ORG.I AM NOW IN LESS THAN A YEARS TIME IN NO MORE PAIN AND MISERY! IN REMISSION AND FEELING GREAT! EDUCATE YOURSELVES FOLKS! YOU NEED TO TAKE CONTROL OF YOUR HEALTH AND DO IT NOW!
Karla
30 Sep 2009, 15:08
Hello, My name is Karla and I have had RA for 5 years. First I had no insurance so I did not go to the Dr. Now I have bad joint damage in my feet (Toes) and wrists. I live with pain and am now on Disability. Well, my Rhumy wants me to go on Orencia and medicare does not allow that infusion so I am on a limited income and cannot afford the medication as I understand it costs approx. 22,000 a year.... IS THERE ANY HELP WITH MEDICATIONS. I CAN ONLY AFFORD MEDICARE INSURANCE AND HAVE NO OTHER INSURANCE... HELP ME I CAN'T STAND THE PAIN
Wes
12 Sep 2009, 11:14
Well, I'm a 31 year old male and have been on Humira for almost a year...I was diagnosed with RA about a year in a half ago. I decided to stop Humira and its been a month since my last injection and I feel pretty good. I have been swimming 30 laps (25 meters is one lap) at the GYM pool twice to three times a week. My muscles get sore but I don't have joint pain yet so I am stoked. I take probiotics, fish oil, and pure encapsulations - Nutrient 950. Wish me luck that I can stay off Humira and go into remission. I need to make sure I have a little better diet too.
Michelle
12 Aug 2009, 07:33
I was diagnosed with RA in 2007. I was first put on Plaquenil. But this wasn't enough. So I was put on Sulfdasine(this is not the right spelling). This 2 meds did the trick. I then started a vitamin reg. I am up to taking 6 Omega complex a day. I see that alot of people are not eating wheat products, I eat wheat products everyday and I haven't had a problem. I just saw my Dr. and I haven't have any major flares, so I am slowly weaning off the sulf. I guess we will see. I am hoping to get off all the meds. But in reality I know that the ra can come back. But I will hope for that I may be the exception.
Paul Ely
09 Aug 2009, 08:35
I first had RA when I was 42 (18 years ago). Doctors then (in UK) told me that diet had nothing to do with it. Eventually I was put on Methotrexate and the RA went into remission after about a year. (I also cut out wheat for 5 years which helped immensely). I then had 5 years pain and medication free - even enjoyed wheat products again. However a year ago the RA symptoms all came back again. I am now struggling to get it into remission again. I just found a website that said methotrexate should be continued at a maintenance level - I wish I had known this 5 years ago. Just so others might be warned - RA ALWAYS COMES BACK!
Mary
05 Aug 2009, 11:00
Has anyone looked into the information/studies done through The Arthritis Trust - The Rheumatoid disease foundation at arthritistrust.org The results really make you wonder what the right direction is. The meds we all have been put on can be very damaging and have bad side effects to your system. I would love for someone elses opinion who has actually researched the protocal they have used..even someone like me just trying to help themselves out of frustration. I have read all the case studies and leaning toward it being worth it to get the outcome if it worked...I just dont want to fall in to the hands of a quake...this study could have some truth to it after reading others I really question it.
kate
26 Jul 2009, 08:04
I was diagnosed in march09 my father had RA my RA factor and CCP are very high and I was feeling horrible. I cut out wheat, dairy, red meat and soy through a comprehensive elimination diet. I feel so much better. I've just started 10 mg mtx since I was afraid of joint damage. Diet has helped 80% but I want it to be 100%. People have asked me how can I be on such a restrictive diet. I feel much more incontrol knowing that I can have a positive inpact on my disease. My hope is that I can go off the Mtx within a year.
Pim Collier
14 Jul 2009, 16:08
I was diagnosed w/ RA in April 2008 and I was heading down hill fast. Last August (2008), I went to a medical doctor who practices natural medicine, Dr. Asa Andrew, in Nashville (I am so blessed to be living in Nashville and working down the street from his clinic). You can visit his website at www.drasa.com - he also has a syndicated radio talk show. I recommend reading his book "Empowering Your Health" and getting the "Foundational Food Guide" which list the approved & unapproved foods for the anti-inflammatory diet (this is good all and not just RA). I went through his program at his clinic and changed my life. In this program, I went through a series of detox, 70-panel blood test to determine deficiencies in my body (which dictates the supplements I needed to bring my body back to balance), and changed the foods I eat - stay away from: gluten, white & processed flour, wheat, processed & fake sugar, dairy & soy as well as processed foods and foods w/ additives. I believe Dr. Asa is opening clinics in other cities and does long distance consultations.

According to Dr. Asa and many medical doctors, the root of most inflammation starts in your gastrointestinal tract (most people don't know there is an issue). I strongly urge you to read his books and start changing what you put into your body – it would also help to do a liver & colon cleanse. Nothing changes over night, but if you stick with it, it does make a tremendous difference on how you feel.

I do not take any medication for my RA any more as of April 2009 and have no RA symptoms. I went to see my RA doctor in June 2009 & he pronounced me "in remission" & told me to come back only if I need to. My primary care doctor thinks very highly of Dr. Asa and was thrilled to hear that I am doing so well. I told him that this is the best I've ever felt...probably since my early 20's (I am 39).

I wish you all the best. If you have any questions, please feel free to e-mail me at pim_collier@yahoo.com.
donita
02 Jul 2009, 17:32
i have ra in my lungs rare i know but it happens i have tried many drugs to try to stop the ra from growing and taking over my lung density i am on oxygen 24/7 because my lungs aren't pumping enough to my other organs i have recently started rutuxin therapy and it has helped my pain and stiffness but it is so expensive (all the medicine i take for ra is) my question is if ra goes into remission does that also mean ra will stop growing in my lungs? my next question is there ways to get help with prescription cost? if there is can i get the information please? thank you donita
sonjia montgomery
28 May 2009, 23:23
I was diagnosed with RA April 08`.I have struggled with this disease for a year.I was considering disability because I felt to awful to work.I started on Methotrexate and Prednisone,then went to Hydrocloriquine and Sulfasalidine(these may be mispelled)because of elavated liver enzymes.I have gone off and on steroids for a year.I went to a different RA doctor I had no swollen joints,when I went to his office.He took me off all RA medicines,and gave me samples of Celebrex,Cymbalta 2 x 60mg per day,5mg. of Prednisone.Also I said I have Fibromyalgia which goes hand in hand with RA.Insurance Co. do not cover Celebrex,it is very $$$$$$$.So I am not taking it either.I beleive I am in a remission.This is the first time in over a year I have been able to function.Isure hope this lasts!!! Sonjia
Milan Darda
26 May 2009, 11:46
Hi!!
I am new member in the RA Family. Just few months back i was diagnosed with RA and my first Allopathic Doc started with steroids (preduisolone 10 mg). But my friends suggested me to consult a Rheumy, she started Etoxib 90 mg. Now i m feeling better, but my left shoulder keeps on paining often.
I am 30 and after understanding the (side)effects i am really worried. I tried Ayurved but in Vain, What should i do?? My wrist joints swells too often.
pam
19 May 2009, 13:53
When i was 23 and told I had RH i was not to worried I took the meds had the surgeries 60 and counting had my flare ups and very scary side effects from many meds. Stopped taking meds walked 5 miles a day I was winning this thing! I am now 46 am so ill and then find out my heart has been damaged from this horrible monster. I never new about organ damage I know now so all of you read and learn all you can so you are not like me with one chronic illness that has generated another. The thing is with most people with heart problems a change to there lie style will help turn around damage or even stop it. Not with RH it is just as bad in destroying organs as joints and there is no turning it off. So take care and keep informed.
costantino Micallef
06 May 2009, 08:49
Male 71 In previous email forgot to ask.
Am member of Life Extension Foundation and they say that they have advised countless 70 + men to adjust and balance their Testosterone to the upper 1/3 of the scale and estrogen to the lower 1/3 of the scale ie. youthful parameters and often inflammation disappears. Also that one should use natural testostorone cream not Penteston pill which can damage liver. Do you hold these views.
Regards C. micallef - NZ
Nel
25 Apr 2009, 17:07
I've had this coming on for about 4 years..they still don't know for sure which autoimmune disease it is...Was put on prednisone and Metrotrexate..started at 40mg pred, but am down to 2 or I should say was down to 2. Went to see my Rheumy Thursday and he said my sed rate was still up in the 40's so I'm going up to 3mgpred..darn...just once in a while I feel a bit better, but I don't think I've had many remissions, if any..They think I may have Polymyagia Rheomatica..
I take coumadin also, so I'm so bruised that's it's pathitic..my hands and lower legs..I have Afib, so have to be careful what I got to take for the RA..Tylenol..is it.....good luck everyone....Nel
Sally
22 Apr 2009, 18:39
I was diagnosed with RA at 27 years old. I am 55 years old now. Over the years I have been on many different prescription drugs. I started taking biologics (first Enbrel and currently Humira) at least 10 years. The biologics keep me in remission.

Remission IS possible and CAN last a long time (I'm talking years!) Remission is what you and your Rheumatologist are working toward, so don't ever give up. The journey sometimes can be difficult, but there are meds out there that can work for your...some times it takes a combinations of meds to achieve this. I just cannot "stress enough" the need to have a good relationship with your Rheumatologist because you have to work as a team to reach this goal. Remission is worth it! Good Luck!
Angela
19 Apr 2009, 19:43
RE: Patricia

I was diagnosed and started with MTX last year. I didn't have a fast response to the drug, but my RA is bordering severe category. If you are not experiencing some relief after 4 weeks, ask Doc to increase dose, I am currently at 8 2.5xs a week, plus recently added Enbrel due to a flare about a month ago.

Don't give up and insist your doctor look at other options. The meds can take a while to work, so give them a fair shot, but always ask "Why, and Why not?"!

Good Luck!
patricia gullage
16 Apr 2009, 09:21
I started to take methotrexate four weeks
ago and I am still in quite a bit of pain. I
am taking 2.5mg six pills every Saturday.
When do most people start to feel some kind of relieve or do I just need for the doctor
to increase my dose. I am very discouraged.
zalikha ibrahim
20 Mar 2009, 00:53
i started taking combination therapy (MTX + arava)in january 2009. within 1 week after taking the medication, i experienced no more morning stiffness also no tender joints. is that mean im in remission?

i was thinking to further my study, but afraid the pain will come back during the time. how long does the remission last? what can i do to maintain the period? what makes me confuse is, how am i going to arrange my future which enables me to continue my study without pain?
catalina morvant
15 Mar 2009, 13:54
i've been in remission for during my pregnancy in 2005 . symptoms came back 2 months after i had my baby.
started again with meprednizone and humira. had another remission that last 6 months. last night i had an episode like when i just was diagnosed with ra. unbearable pain in my right side. i immediately started w humira, medrol that i have still at home . also took a mobic.
i had slight symptoms along the week -before last night-but i refused to accept that it could be ra again.
how long does the remissions last? how could i extend that period? what can i do to not reach this level of pain?

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