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Biologic Drug Approved for Rheumatoid Arthritis

By Brenda Goodman

05/14/09 The U.S. Food and Drug Administration has given its nod to certolizumab pegol (Cimzia), a drug previously approved to treat Crohn’s disease, to also treat moderate to severe rheumatoid arthritis.

Certolizumab pegol belongs to a class of biologic drugs that block an inflammatory protein called tumor necrosis factor alpha, or TNF-alpha. Other drugs in this category include etanercept (Enbrel), infliximab (Remicade), adalimumab (Humira) and golimumab (Simponi), which was approved last month.

Cimzia’s molecule is slightly different from the other drugs in its class, however, because it is pegylated, or coated, a process that, in theory, should help it slip by the body’s immune system more easily and may make it less likely to cause an infusion reaction.

Pegylation may also help the drug work more quickly. According to UCB, the Belgian company that makes certolizumab pegol, when used in conjunction with methotrexate, patients in clinical trials for Cimzia reported a reduction in symptoms as early as the first week.

Certolizumab pegol is administered with at-home injections, which can be given every two or four weeks.

UCB also worked with industrial designers OXO Products, the same company behind the Good Grips line of kitchen tools, to redesign the syringe that patients use to administer the drug. Noting that the design of the classic syringe, which is very difficult for some arthritis patients to use, had not changed substantially in a century, UCB worked with OXO to add features like an extra large loop at the top which make it more patient-friendly. The new device has earned the Arthritis Foundation’s Ease-of-Use Commendation.

UCB, in a press release, said the drug would be made available to rheumatoid arthritis patients within a week.

Meagan
07 Jun 2009, 12:16
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Anyone seeking alternative treatments (instead of drugs), may be interested in The Road Back Foundation website. Dr. Thomas McPherson Brown's antibiotic research and treatment, and Thomas Scammell's book about it, are explained there. Also clinical stidies, trials, etc.
Very interesting how money/funding for research for an RA cure got turned over into funding for more drugs, as drug companies became more powerful.
Some books I found very informative, in addition to Thomas Scammell's: 'Selling Sickness: How the World's Biggest Pharmaceutical Companies Are Turning Us All Into Patients' by Roy Moynihan, 'The Truth About the Drug Companies: How They Decive Us and What To Do About It'by Marcia Angell, 'On the Take:How Medicine's Complicity with Big Business Can Endanger Your Health' by Jerome P. Kass, 'The Hundred Year Lie: How To Protect Yourself From The Chemicals That Are Destroying Your Health' by Randall Fitzgerald,
'Inside the FDA: The Business and Politics Behind the Drugs We Take and the Foods We Eat' by Fran Hawthorne,'Overdosed America:The Broken Promise of American Medicine' by John Abramson.
I am being been treated with minocyclene for RA and feel more confident and less worred about side effects than with any of the RA drugs. So far the numbers have proven it is effective. At least for me. Who knows what the future holds for me, but for now, I am doing well with it.
Beth
04 Jun 2009, 18:58
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I thank God every day that a new medication for RA comes out. I was diagnosed 7 yrs ago--took methotrexate and prednisone for 3 of those years, enbrel for 2 and then humira for 2yrs until each one quit working. I am starting Simponi next week. I would be happy with 2 more years of relatively bearable symptoms. I am an RN who had to quit working in the hospital due to symptamatology and am now fortunate to have a job in the nursing field that is not as physically taxing as my previous job. I agree with whomever made the post regarding God giving researchers the wisdom to come up with improvements in the treatment of these horrible diseases.
suze
04 Jun 2009, 12:08
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Was diagnosed two years ago. SO much better now than at the beginning. Plaquenil. I asked my doc about side effects of this and other drugs. I wanted deatiled description of anything he has seen in his practice as far as side effects. He told me. None from plaquenil. But some of the others...frightening. I lost my Mother to pancreatic cancer, my father to liver cancer, my grandmother to colon cancer.he agreed with my family background, if possible stay off the stronger drugs. Had pouches on knees for a few weeks, swelling behind knees, started working out and they went away! Thought they would be permanent. They never came back. he said my legs were not RA and could not figure out what that all was was very happy that exercise (bike, teadmill, etc) got rid of whatever was going on. My internist thought it was a side effect of the plaquenil. He hates these RA drugs, grumbles about them,as he has seen their side effects also in his practice but understands their importance.He checks my liver as does my rheumi due to the plaquenil. I have my eyes checked twice a year to make sure they have not been effected. So far so good. I have been taking many natural supplements, and anti inflammatories, as he said the most important thing is to keep the inflammation down and it does not have to only be through drugs.And my numbers have gone down. My doctor is very happy about all that I ahve been doing. We tried anti biotic treatments also for awhile (after i asked him for them, after reading a wonderful book about this. I asked to be taken off for awhile kind of worried about my stomach but he said anytime i want to go back on them let him know. He was very happy with the results of that treatment.
Thought I'd list some of the things i feel have helped me.I also eat all the suggested foods. And avoid the bad ones. My nephew has it,and he refuses to stop drinking and smoking and eating bad food and he is really struggling with it and had to go on embrel. I would rather eat healthy, and I never drank or smoked anyway, than go on stronger drugs. He is too heavy also for a young guy and the doctor has told him to lose weight which isnot happening and he also does not exercise or walk much at all where he lives. It hit his legs, but he wont make any effort to walk even to at least try to push through and help his legs, get stronger, even being pain free from the embrel.With me it is the hands, wrists etc.)I try to gentley nudge him into at least trying to live healthier and see if it helps his RA. I scoffed over all the suggetions of exercising, but seriously it is saving my life now. it also empowers me feeling like wow, if i can do all of this for all this time and feel great doing it and after doing it,, then i dont get AS depressed when i have a trouble with buttons or things around the house. for goodness sakes, i can do the treadmill for over an hour now and still keep going, so what is the big deal about buttons, bottles, opening cans?? i can deal with all of that with a much better attitude instead of getting depresseed or frustrated over it. so i cant relly use my thumbs and so those joints really kill me when i try to turn a key or get dressed. It just is not that big of a deal and I can cope with that since i am able to do other major exercises for long periods of time. I count my blessings of what i CAN do. and my rheumi tells me i am NOT am candiate for this spreading to other ogans or the heart since those cases seem to be patients who DONT exercise, or change their diets or take better care of their bodies. I dont know if this is true, but i have to accept it as true rather than think negatively and spend my life anxious and worrying about if those things can or will happen to me.
accuppuncture gave my thumb joints and y neck relief. cortizone did nothing for me. Pro Lo therapy shots were the best, But insurance does not cover that yet. Really really the best relief I got was with them.
here are soem of the things I have foudn that have helped me tremendously:
fish oils, flax oil
curcumin
tumeric
boswellia
bromelin
msm, hyaluronic acid
new chapter zyflmend softgels
xtendlife arthrit-eze
extra selenium
extra vitimin e,c,b-comples
potent mulitis
alamax cr (biotin,alpha lipoic acid,regenerates c,e, coQ10)
some other things. i do not take evey day. i play it by ear.
And please do not scoff at the food. Cherries and fruits really do help me. And lots of vegetables too. And I love them. If I am feeling fatigued etc. I know it is time to eat alot more greens again, and get out and do soem exercise.. But that is just me.
TONI
03 Jun 2009, 20:42
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I HAVE HAD RA ABOUT 4 YEARS THAT I KNOW OF.IM ON METRO,PREDISON IV TAKEN ALL KINDS OF INJECTIONS BUT ALWAYS STOPED BECAUSE OF INFECTIONS BECAUSE I SMOKE.TODAY I WENT TO MY R/A DR HE SAID IM JOINTS ARE ALL SWOLLEN ,IM VERY VERY TIRED HURTS ALL OVER MY BODY . I HAVE TAKING THIS R/A LIGHTLY BUT READING ALL OF YOU COMMINTS THIS IS REAL I CANT BELIVE I HAVE THIS IT SUCKS.BUY THE WAY NANCY C. YOUR STORY REALY INSPIRED ME THANK YOU. TO ALL OF YOU THANKS FOR ALL YOUR EXPERANCE IN SHARING THEM WE CAN ALL HELP EACHOTHER. GOODNIGHT GOD BLESS TONI
Nancy
03 Jun 2009, 16:20
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All drugs have side effects, Mr Rawlins. The FDA and manufactures put the information out there and the users have a responsibility to ask for it. check out the mayo clinic web site under drugs and supplements. It is the most complete listing of side effects I have seen and it is in plain English the majority of people can understand. Natural and alternative medicine is fine to a point, but when you are beyond mild RA you need more help than juices can give you. I eat healthy. I have my fruits and veges daily, soy products, fish, chicken, walk when my pain and inflamation allow, and try to maintain a healthy attitude. But it is not enough-I need the medication that God had given man the knowledge to manufacture and provide for us. Don't dismiss them out of hand. It is my responsibility to research what my doctor recommends and make my own decision based on my feelings, needs, and what I am willing to accept as my quality of life. Don't criticize me, Mr. Rawlins, for accepting the risk of side effects for the chance of less pain and inflamation, to be able to play with my 2 year old grandson, 1 and half year old great grandson, and unborn great grandson. I want to quilt and sew again and hike with my husband and ride in our car to our home in Florida for the winter. I want to hold my husband's hand with no fear of him hurting me. I want to get rid of the depression I fight daily because I can't lift a skillet or pan to cook his meal or cook a family dinner. I want to have a conversation that does not include "is this a good day today?" I want my wrist to quit hurting as I type this on my computer. I know the risks. and yes-the FDA and the drug company made them very clear. And I can't wait for my first injection of Enbrel!
Ginger
03 Jun 2009, 15:58
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As a person recently diagnosed with RA and overnight onset of major symptoms, I have been surprised how many people I have met who were also told by an M.D. that my pain and inability to move is "in my head".

It has been challenging to fully explain to co-workers, friends, family and others how much pain I am in, and how it varies from day to day.

I'm pretty confident my RA was brought on by stress. My heart goes out to ALL arthritis sufferers. I read information about RA everyday and can never learn enough.
jennifer
03 Jun 2009, 12:08
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i feel the same way as sandee and im am going to be 27 in july, and all i know is that this sucks and everyday is a day of not knowing how you are going to feel or if you even want todo anything .. i tired and worked as long as i could and then when day i was just at the breaking point and i have made alot of friends on some fibromyalgia sites and ra sites..and know one else can know what we are going through unless they have it. and i am tired of hearing people that have addictive personalities tell me i should get off my meds when they have no idea how that would effect my everyday life.. and dont have md behind there name... i dont know about this new meds. i know i am on a lot and then know methoxtrate and all this hair is falling out (thank god i have alot ) and my rhuem told on last apt that there is a new med coming out cause i have tired everything and nothing seems to help and we just keep adding on the diagnosis .. long list of them.. i pray everyday and so does my mom that never thought she would see her daughter like this. i used to be a cheerleader and dancer and run track and play baseball.. all things i cant do anymore.. and for all the people that say its in our heads, you come live a day in our shoes and You would never be able to do it!!!!!!!!!!!!!!!!!!!!!!!!!!!!!...
shimels
03 Jun 2009, 08:39
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It is realy a great news
Sandee
03 Jun 2009, 02:36
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Time takes it't toll especially with RA. I am diagnosed with RA and Fibromyalgia. Embrel is my cocktail..not great but better than before without it. Somedays pain seems almost tolerable,yet never a day without pain.
Until my diagnosis 10 years ago, most of my family, co-workers, friends and even my Primary Care Doctor would actually tell me I should be feeling good...after all, up until the diagnosis', I really did not show very much joint damage.
But there was another monster lurking in my life...Fibromyalgia..and it is a ghost. I almost started to believe I was crazy...and sudddenly finding ways to avoid my world, because I no longer fit in it. Fibromyalgia creeps into everyday of my life. It eliminates the essecence of the joy of making decisions about everyday choices...time with friends, community and family. The pain so real, so dibilitating.Together, my days can be long. Yet, I am still here and grateful for any news in the horizons that show indications these diseases will some day be out of our lives.
For someone who has just be given the news of RA, Fibromyalgia, or any of the other autoimmune diseases it is a long road to hoe until we find what works for us. I pray for cures, because all life, whether young or old should be of quality. To people who are in the labs looking for answers, I say good work. Don't give up! I certainly am not.
Nancy E Compton
02 Jun 2009, 21:55
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By the way - AGAIN! Wish I could let this go, but I don't seem to be able to. Mr Rawlins, I managed to get through to the end of your post and saw your info about Johns Hopkins and how they are working to build up the immune system in combating cancer. I'm assuming your making a connection between this and RA because ???? what? - methotrexate? or the side effects of the biologics? I'm not sure, but obviously you're unaware that the whole problem with RA is a revved up immune system that is attacking the body, specifically the joints; under the worst conditions it will turn on organs of the body. We don't want an IMPROVED immune system, ours is way too good already.
Mr Rawlins, I'm curious, what possessed you to read this article? Do you know someone that has this disease? There must be some reason that you were interested enough to read this information. I'd like to encourage you to go back and get some basics first. Get the "How, and Why." of RA so you'll have a fundamental understanding of it's workings. Then go on from there and read some of the info about a few of the other auto-immune disorders like Lupus, Crohn's, ankylosing spondylitis, and the numerous types of RA there is. I think you'll find that you never offer natural or holistic help to anyone ever again.
Nancy E Compton
02 Jun 2009, 21:12
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I would like to add that of all of us that have this confounding disease, the ones I feel the most distress over, are the children. I didn't develop this condition until my late 40's, but it is just plain so unfair for them to have this almost from the beginning of their lives. A great deal of my time is spent "managing" my disease and the associated pain and fatigue. It is never far from my mind, and I forget how much it has become woven into the planning of each day. At least since they are young, there is the hope they will see and experience a cure.
I am so sorry for the folks who's disease has not responded to any treatments. My heart breaks for you. I will say my prayers for you and send out as much positive energy as I can muster.
Oh, and thanks Sven for your thoughts, that felt really good to hear that.

Susie
02 Jun 2009, 20:49
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As a person with very advanced RA, I look at all information that comes out and could possibly make things better. I have tried the diets, raw, vegan, natural etc. They have not helped. I also have Diabetes, so the fruit juices and fresh fruit played heck with the blood sugar. I have lupus and fibromyalgia to boot, so I do work closely with my Doctors. I have tried all the medications, and being allergic to all but the Enbrel has made it more difficult. The low dose chemo aka Arava, methotrexate were tried, and I was allergic to both of those. This, with the combo of medical conditions I have make life more difficult and painful, so if there is a better drug, then Hooray! Maybe it will work better. I can either take the meds and have the risk of side effects, or I can be in chronic pain, wheelchair bound and hopeless. Don't be quick to judge anyone for the choice they make. If it works for them, then God Bless.
DLM
02 Jun 2009, 19:47
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I HOPE AND PRAY EVERY DAY THAT ANY NEW MEDIATION CAN BE FOUND THAT RELIEVES AS PEOPLE AS POSSIBLE...I AND MY SON BOTH ARE PAIN CONTROLED WITH VERY HEAVY MEDICATIONS WHICH DON'T ALWAYS WORK BECAUSE WHEN YOU FEEL THE EFFECTS OF WEATHER IT IS SIMPLY A WARNING WHAT'S GONNA HAPPEN IT'S YOU BODY HELPING YOU AND TELLING EITHER U'RE DOING TO MUCH OR THE WEATHER IS CHANGING..I MUST TELL I HAVE BEEN ON BOTH SIDES I LOOK AT THIS AS AN ACCOMEDATION TO HELP ME TO HAVE AS MUCH NORMALTY WITHOUT PAIN..EACH PERSON BODY IS DIFFERENT AND NO TWO PEOPLE'S FEEL PAIN THE SAME..I HAVE HAD MANY ACCIDENTS NOT MY FAULT USUALLY SAFETY ISSUES...OR BAD TIMING..OR "RUSHING" WHICH ALL OF US HAVE HAD HAPPEN TO US AT SOMETIME DO TO OUR PAIN ISSUES...I AM HAPPEN WHEN I SEE PEOPLE WHO HAVE AND CAN ADAPT TO ANY FORM OF MEDICATION THAT HELPS...MY SON HAS VERY HIGH LEVEL AT 26 DOCTOR'S COULD NOT AGREE ON TREATMENTS NOT MANY DO..BUT I JUST AM GLAD THAT 1 FINALLY LISTENED AND HELPED HIM DEAL WITH SOME OF HIS ISSUES...TO HEAR SOMEONE CRY IS WORST PAIN YOU CAN DEAL WITH UNLESS YOU ARE A COLD COLD PERSON...WHICH I HAVE ENDEAVORED ALOT EMPATHY IS SURPOSED TO BE THE FIRST ON YOUR LIST...CARE AND COMFORT IS INDEED THE BIGGEST REWARD THAT A DOCTOR CAN DO FOR US ALL..MANY ARE SADLY OVERWORKED AND SHORTAGE IN THIS FIELD GETS WORSE EACH DAY I PRAY THAT WHAT EVER WORKS FOR ANYONE KEEP WORKNG...AND HOPEFULLY WE WILL GET SOMEMORE HELPS WITH THIS DEADLY DISEASE WHICH CAUSES SOME MANY DEATHS EACH YEAR...THE RATE FOR SUICIDE DUE TO THESE ISSUES HAS REACH A NEW LEVEL...THE APPROXIAMETLY AGE IS USUALLY 20 YRS OF AGE..DOCTORS HAVE TOLD THEM THAT THEY SHOULD LEARN TO LIVE WITH THE PAIN THEIR TO YOUNG TO HAVE SO MUCH PAIN..IT'S A TERRIBLE THING I MYSELF HAVE HEARD FROM SOME DOCTOR'S OWN MOUTHS..THAT IS WHY I FIGHT FOR THESES YOUNG ADULTS...PAIN IS DIFFERENT FOR ALL OF US...GOD BLESS YOU ALL AND I HOPE THAT SCIENCE CATCHES UP FASTER..I DON'T WANT TO HAVE TO GO TO ANY MORE FUNERALS....A SILENT ANGEL OF MERCY I USED TO WORK TAKING CARE OF PEOPLE WHO HAD SURCOMED TO PHYSICAL HOSPITALIZATION FOR THE REST OF THEIR LIVES...SO I DO KNOW WHAT YOU ALL FEEL...I HAVE BEEN RELIEVED AND STRIPPED OF MY DUTIES FOR CARING AND BEING ONE OF THE PEOPLE I SO LONG FOR AND MISS...I CAN NO LONGER WORK DOING WHAT WAS MY CALLING...FORMER NURSING ASSISTANT...
Beth
02 Jun 2009, 18:38
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My 12 yr old son has jra and aknylosing spondylitis and he has been on everything. Homeopathic treatment, remicade, orencia, enbrel, methotrexate, arava, rituximab , cortisone injections in his hips and spine. NOTHING HAS WORKED!He has gone from walking to no stairs in March of 08, then a cane to a walker and now since Sept 08 a wheelchair I have to assist in dressing, bathroom, ect.
Life stinks for this 12 yr old boy. I would give my life to have him walk . PAIN!!! all
day everyday.

The homeopathic stuff didn't help nor did the meds and now he has to stop taking everything. LIVER DAMAGE!!!. So people stop arguring and complaining about what works better, each person is different. Just be thankful you have something that helps. Not all of us can say that. PLEASE be thankful for each step you take and each painless moment. There are some who don't have that!


Carole Mitchell
02 Jun 2009, 17:44
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My husband has been on the Enbrel injections for a few years now and has had no side effects at all and is relatively pain free. Everyone is different. Thanks for all your comments.
Jamie Lee
02 Jun 2009, 15:58
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PS. Put it in a pill, a ptach, or cream man!!! I'm also a big neddle sissy.
Jamie Lee
02 Jun 2009, 15:54
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I must admit. Im a bit of a chicken. I suffer with cripping RA but will not try any new drugs untill they have been out for at least five years. Let someone else suffer devistating side effects, or death. I don't want to be one of those people who say I got great realif for years BUT NOW!!! EEEKKKK!!! No thanks. I wait a few years and then see what helps...
Nancy Martens
02 Jun 2009, 15:10
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Five years ago I was being treated with physical therapy for a ruptured Baker's cyst behind my knee and the therapist remarked upon my swollen finger joints and said "that looks like RA to me". Up to that time I had not been bothered by any other joint problems other than OA in my left thumb joint. That remark concerned me, so I went to my MD, who conducted some blood tests and xrays and then referred me to a rheumatologist for further testing. My rheumatologist did a lot more testing and in a few months diagnosed me with RA. By this time I was feeling real pain in my joints--and not only my fingers, but also wrists, elbows, ankles, feet and even my neck. I was having difficulty with everyday tasks, getting dressed, was developing those typical RA bumps on my wrist and elbows. Like the other Nancy who commented, I was getting very depressed, figured I would have to move out of my 2 story home and be in a wheelchair before long. When my doctor put me on Enbrel it was like a miracle--the pain and swollen joints gone in a few weeks and I felt like a human again. Yes, there certainly are risks with the biologic drugs, but I would rather enjoy life than be in pain and misery. Each person has to choose the medication route that they are comfortable with, but for me I am very happy to be enjoying life. Incidentally, I'll be 75 in September...and I'm still in my 2 story home that I clean myself and take care of my small yard and my 2 little dogs as well...
KRISTEN
02 Jun 2009, 14:43
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I tried embrel years back,for just over a year i gave myself these painful shots, ive got scars on my stomach and both legs, I hated that each new shot made most other injection sites puff right back up and hurt. I endured as I am desperate to be human again. Now I am on disability, and medicade pays for nothing that helps, oh the embrel did nt help, but it turned out that was becuase inow also have lupus, it did keep some of the disfiguring at bay, but thats it, and now again it starts... i am using a natural item for some of the pain, it eases my back but i also have a few other health concerns..I really just want to be like others,ride my bike again,live....i will pray for each name ive seen here.
Graciela
02 Jun 2009, 14:40
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I am in agreement with all who say until one has had to deal with RA they shouldn't try to push their advice on you. I am on Humira, I tried Enbrel and it worked for about 10 months and then my doctor switched me to Humira. It has worked about 30% more effective then Enbrel but I am not at 100% which I don't know is a realistic hope but I am very happy and embrace the effectiveness of this drug. I have been warned about the side effects but before these drugs I sat up night after night rocking myself back and forth with wreaking pain so I will take my chances with the side effects. I say whatever works for you then just do it and embrace each day of life.
Sven
02 Jun 2009, 14:23
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oops! Typo! I have NEVER considered taking alt meds.

Sven
02 Jun 2009, 14:21
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I am always so glad to read people like Nancy speaking out. I have considered
taking alternative or "natural" meds for the very reasons you state, Nancy. But, it is all the more profound when it comes from someone like you who was once on the alt med bandwagon.

There really is a thing called science and it really works way better at treating and curing diseases than non-science nonsense.

Pomegranate juice? Puhleeez!

I am glad you are feeling better, Nancy.
Christina
02 Jun 2009, 14:11
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So many people are "ignorant" when it comes to RA~ they think it's just like OA, which all of us sufferes know is so not true. I get tired of others telling me to try this or that because it helps joints. RA does not just make your joints swell. I too was diagnosed with RA 13 years ago, it's been a very long journey to get to the Enbrel which I just started a month ago and I already have a big part of my life back. I am concerned with the side effects as well but that is the chance we are all taking to live as "normal" life as possible.
Nicole
02 Jun 2009, 12:14
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I can understand everyone's position, I however have to say that without the benefit of Remicade I would have almost no quality of life. I have had to experience life without it and I prefer to be walking than in a wheelchair for as long as it is possible. Despite trying every "home remidy" that is available Remicade is the only thing that has produced results for me. Each person is an individual and that is why I do not agree with people handing out their "hard and fast opinions" on any treatment plan, as there is no treatment plan that works for every person, just because it works for you does not mean that it will for others and likewise. As for the people who have died during clinical studies; one must "pull back the onion" prior to passing judgement on the trial and any outcomes of it; perhaps the best way to decide for yourself is to go to a medical library and actually read published studies, because until one does it is pure speculation.
barron Joel Glass
02 Jun 2009, 12:04
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Dear author of this article the new drug for pain does not minimize the detrimental effects of damage to not just the immune system, but also other auto response systems in place in the afflicted body.If the drug could be used in additional to several other medicines only in a much lower dose the afflicted body could readjust it self to be recptive and change how and where it will be more effective.Dosage is the key for any new agent to introduced into any living body as well as reactive chemical response or responses to such affliction. Pain will be evident for some time in any case because of the human brains response to any new medicine introduced as well as several other inlaying effects not recognized at this time.Thank you good luck in modifying and send me reply with questions to want answered. Barron Joel Glass bglassya@yahoo.com
Nancy E Compton
02 Jun 2009, 12:02
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Mr. Rawlins,
Your experience with RA is obviously limited. I have had the condition for approximately 15 yrs. The first 3 I spent treating myself with homeopathy, herbal, vitamin/mineral therapy and other anecdotal treatments that were reported to be effective in the control, management or cure of rheumatoid arthritis. All that happened was that I got progressively worse, the pain became unbearable, and I was depressed and exhausted constantly. As a matter of fact at one point, I was so tired from the unending pain that I began to think of suicide. It took a long time for me to get diagnosed. I have no idea why. I think the doctors were more willing to see me as a chronic complainer and drug seeker, but once I did get a diagnosis, I had to demand a referral to a specialist. I finally was able to receive treatment specific for RA, and my rheumatologist had been treating me for several months without improvement, when he decided to offer me treatment with one of the biologics. He informed me of the possible side effects and the possible benefits. Without hesitation I wanted to give it a try. Within 48 hrs of my first dose of Enbrel, I was symptom free.
I realize that is not the norm and it takes most people longer to experience the benefits of a biologic, but if you ever once experience RA at the level some of us have, you would understand why we are willing to accept the risk of some of the side affects.
Oh, and by the way, I have been on a biologic of one form or another now for about 10 yrs and haven't died yet. Life has been worth living, and I haven't thought of killing myself once.
I'm sorry if this sounds to confrontive of you Mr. Rawlins, but I was once just like you. I believed passionately in natural healing, but I have seen that industry become a racket and just as greedy as the drug companies. My experience is, they don't work over half the time. There are no regulatory agencies watching them or conducting studies to back up any of the claims that they make.
For me taking/using ANY of those so called cures or treatments was like taking a water pistol to a forest fire. I could never see or feel any improvement from any of the so called treatments.
jim
02 Jun 2009, 11:57
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The FDA is corrupt. Read any of the books out about them ( a huge awakening for me!!)and you will realize how easy it is for things to get by them, sometimes "politics" sometimes money or certain factions pushing them relentlessly to approve something. People have died in studies of some of the drugs they have passed. Yet they still will not back any or approve any of he supplements carried in health food stores. This news that the FDA has approved yet another RA drug means nothing. Do the research yourselves before you accept their approval, before you take anything the FDA approves.
annie
02 Jun 2009, 11:41
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Forgot to mention, Arthritis Today would not be in business without all the Drug Company Ads they carry.
Dawn
02 Jun 2009, 11:40
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I agree with you prof girl .I really wish people would learn more about a disease before giving advice.Mr. Rawlings must not know that people with RA and other Autoimmune diseases can still develop alot of damage and even develop other autoimmune diseases even if we get pain relief. Mr.Rawlings do a little more homework please.
Carol
02 Jun 2009, 11:34
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Right on Annie!.Sadly, Arthritis Today would not be able to stay in business without all the multitudes of Advertising from all the Drug Companies! We all need to be aware of whom the messenger is.
annie
02 Jun 2009, 11:27
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I for one am grateful for Fred's information or ANY natural healthier way to help me battle this disease. Any natural thing that keeps down the inflammation and slows down the deterioration of the joints. I am fed up with all the drug companies who have the funding to continue to come up with more harmful drugs while there is very little funding to find a cure. "One of the most under researched yet most disabling" diseases" is what my rheumotologist says. I have a great doctor, who is open to anything natural that I find in all my own research and take in addition to the plaquenil he has me on. He is not happy about having to prescribe these awful harmful drugs. With mine the liver and eyes need to be monitored but that is nothing compared to some of the others with way worse side effects. I consulted with another rheumotologist back in the beginning who was very aggressive as far as drugs and would have put me on a "Drug cocktail" as they cal them, also told me there is no cahnce of "remission" so dont even think about it. I left with no hope after that visit and was so happy he was not my doctor. Interesting thing is, he is in research at a major hospital here, research for more harmful drugs to slow it down.And was thrilled about all these drugs. That was about all he wanted to talk about. Big difference between him and my doctor. I am grateful that I have not had to go to anything stronger and he is very pleased with how I am doing and feels it has alot to do with taking things in my own hands (he knew I was determined from the get go to not have to go on anything stronger and he is now talking about the possibly of weening me off of the plaquenil at the end of the year to see how I myself to believe it will worsen, and not being o.k. with any stronger drugs. I exercise regulary, treadmill, eliptical,do weights and weight machines,, dance classes, bicycle, making every effort to get and stay stronger, warding off this from moving from my hands to places like my legs, my strongest part of me body and I will not accept that it will move to those places and he does not believe it will either with all I am doing .In the first (20 minutes on the treadmill my hands and fingers start feeling relief), anti inflammatory diet, holistic supplements, I never ate meat anyway, very low fat diet, lots of fruits (I think Fred is right about all the fruit-it really helps me-so happy cherries are back!) lots of vegetables,salmon, I never ate junk or deserts anyway, always watching my weight and diet. In a way if anything, this has made me take better care of myself and MOVE, not easy living in L.A. with all the driving, so I now make time every day for some kind of physical exercise. Some sun and light seems to help tremendously also and sleep and rest, and petting the cats makes me feel nice and calm and happy.. And I try to have a positive, happy outlook, and I also pray and friends pray for me. The drug companies are getting fat and rich off of people with these illnesses. I pray for a CURE, and have become an advocate for the new Arthris Prevention Bill helping get bigger name politicians to sponsor and sign onto it. So this news of yet another harmful drug, being pushed by the big drug comapnies is not great news to me. Greater news would be that RA people will never have to take this garbage another day in their lives. Greater news would be that MORE money would be used in research for a cure and not for harmful drugs. I am happier hitting the healthful stores for the tons of natural, harmless, safe, yet helpful supplements and including in my diet all the good things that help stave off this disease and moving moving moving. And drug companies be damned as far as I am concerned.
Barbara
02 Jun 2009, 11:05
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Thank you Fred for all the great info.
W. Wilson
02 Jun 2009, 10:49
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Sounds like old Fred might just have a few shares of stock in that company.
Prof Girl
02 Jun 2009, 10:30
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Does that Fred Rawlins who felt the need to post three times have RA? Does have have any other inflammitory disease?

It's so easy to condemn medicines that keep those of us who do have RA from become crippled. These medications don't just "take away the pain" they keep our immune systems from attacking our bodies.

I'm glad to see that there are new medicines still being created and produced.
Fred Rawlins
02 Jun 2009, 09:32
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Does the FDA maake the side effects clear to potential usrs? Mostg of the other drugs mentioned will cause a supression of the immune system and greatly increase your chances of serious infections and other ailments related to a weaken immune system. The recent finding that Pomegranate juice, and fruit, eats up the acid that cause the cartildge damage and inflammatilon from arthritis has been suppressed by the pharmaceutical companies. There are many natural cures for inflammation. There is a drink called Poga Moonga, that is a mixture of pomegranate, aloe vera, and moringa. These three ingredients have 11 anti-inflammatories and are all used seperately to treat arthritis. With a antural solution you go after the root cause of the problem and have no harmful side effects. The doctor's don't want you question their authority so go to www.pubmed.org and find out for yourself. You can put each ingredident, with the word arthritis, into their seach box and find one paragraph summeries of the published studies on that subject. This is all from the database of the Library of Medicine; third party and scientific. Print them and show them to your doctor and then try something natural for a few months. I can tell you I know several people, including myself, who have used it sucessfully. You can find out more at www.pogamoonga.com/fred and then decide for yourself. I did and I found out it works without harmful side effects; and in fact every side effect is a healthy one! Moringa is a whole food and with medicinal qualities, see pubmed article #17089328, used safely for thousands of years with not one alergic reation or negative side effect ever reported. Do the research and you will find it's just the opposite; moringa, and the other two ingredients, all build up the immune system and protect you from harm. This other class of drugs does the exact opposite; you may not have pain but your own immune system will let an invading infection or disease kill you because it is disabled by the use of these drugs. Do you think that you, or they, are smarter than God; who gave yo an immune system? The latestest cancer break through is to promote the immune system to fight the cancer not suppress it with chemo and radiation. Doctor's, starting at Johns Hopkins, are beginning to focus on building up the immune system instead of treatments that tear it down. Check it out for yourself you will be happy you paid attention to the details.

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