ADVERTISEMENT
Close
In This Issue, Subscribe, Free Issue, Contact Us
ADVERTISEMENT
 
Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis News & Research > New Rheumatoid Arthritis Drug
Print Email

New Rheumatoid Arthritis Drug

By Denise Mann

10/27/08 When taken with methotrexate, a new pill that blocks an inflammatory protein called syk kinase may be another weapon in the ongoing war against rheumatoid arthritis (RA), finds new research presented at the American College of....


Return to Article



Betty
09 May 2012, 12:52
I have a big problem with this web site, because it talks about Rheumatoid Diease as if it is some kind of causual diease. I have suffered with Rheumatoid Diease for 13 years.

I am down and in pain and have not found any relief! So many drugs and nothing works. I have lost my family members to this awful chronic diease!

I am alone in this diease and when these web sites talk as if everything is going to be o.k. it is not! Forgiven me for my negative posting but let's get real....
Paula
07 May 2012, 16:54
I have adult onset stills disease. I have started kineret three weeks ago and after48 hours all my symptoms have disappeared. However, I am experiencing severe brain fog that is unbearable. Apparently I am alone with the side effect. Kineret is an interleukin 1 blocker which seems to be the cure for me. This new drug is an interleukin 6 blocker. Would this have the same effect as far as helping me? If I don't take the kineret I have pain, but with it I am pain free but the brain fog is extremely difficult to live with. I would appreciate any response. I am always searching for help since it is difficult to find anyone who can help with adult onset still's disease.



claudia
14 Jul 2011, 04:01
I'm on methotrexate now about 1 year. I think it helps, my WBC's are ok. I noticed my hair is thinning. This really is not good. My hair. Is there anything else this disease is going to take? I try and not take Prednisone, bec it will make your bones brittle after long time use. Last thing I want to do is break a bone. Is there anything to lessen the hair thinning? I know it's to kill off or lessen WBC production, that attacks our joints causing pain, inflammation and disfigurement, but seriously anything to help with the hair ? I know it's vanity but I had good hair. and now I don't . thanks anyone
Rosalyn Mayeux
12 May 2011, 18:21
I have RA and was diagnosed in November, 2009, I started going progressivley downhill while on Methotrexate, from walking with a cane, to a walker to being bedridden for 6 months....started Remicade treatments in May of 2010 and it helped for 4 weeks out of the 8 week schedule, in August of 2010 my Doctor asked me if I would like to try a new medicine and enter clinical trail, I was all for it, all I can say is GOD BLESS HIM AND PHIZER the drug is known right now as CP-690-550 (Google it)and is a God Send, I went from the bed to asking my husband to take me dancing within 1 week, the good news is its pills and near ready to me put on the market, check it out and good luck to all of you, ask you RA Doctor about it. It has mild side effects such as, nausea, diahrrea, head ache, all of which I did not have, check it out at, cant buy it yet but hopefully soon.
Jeff C
24 Mar 2011, 17:41
I've had RA since 1990 and started on Methotrexate in 1991.(it was a new drug then and it was used more as a last resort med). I've also been on countless other drugs too. Most recently I've been on Orencia for the past several months and while it does help it doesn't last until the next infusion. On April 8th, 2011 I start a new infusible and have my fingers crossed it will work better and longer. I'm 51 now and chronic pain is starting to wear me down. With the exception of a couple of years living in Connecticut all of my RA doctors were very good.I moved to Central N.Y almost 10 years ago and shortly their after hooked up with
Arthritis Health Associates in Syracuse, NY. This is the best group of doctors, nurses and support staff anywhere. They are consumate professionals on every level.I wish I didn't have to deal with this depressing condition but it makes it a little more bearable when you know your getting the best treatment available from the best people.
suhanasoft
12 Mar 2011, 02:24
<a href="http://www.dilseindia.org/angioplastysideeffects.html">ANGIOPLASTY SIDE-EFFECTS</a>
Angioplasty has proved to be a boon for patients suffering from heart diseases in the last 2-3 decades. It is efficient, economical, time-saving and involves less fuss. But in spite of that, there are a few side-effects of angioplasty as well. Let’s have a look at what could be the possible risks involved in and how to overcome them.
Luz Pagan
06 Mar 2011, 13:45
I take Methotrexate 2.5mg every Wednesday and it helps me some. However, I have pain in my neck, shoulders, upper back, for 4 to 5 days, and is very painful. I also have pain in my chest. Four months ago I had a heart attack and had Angioplasty. I read that some people who have arthritis also have had a heart attack, and I one of them. Thanks God I have a good cardiologist reumatoligist and internist. They all wotk in coordination to provide me with the best medical care avaialble. God bless them.
Jennifer Cocuzza
03 Feb 2011, 01:03
Hello Joe Cocuzza, As your Mother and always being there for you I know how much pain you go through on a daily basis. Eighteen Surgeries huh, more like 8, I was there for all of them, Feet, Thunbs, Liver biopsy, both hips, 1 knee. You were not in a wheel chair from 3 to age 8, you walked. The only time you were in a wheel chair was when your feet were operated on in 94. Your wife is disabaling you by doing everything for you and all the work of getting you to stay mobile is now being reversed, but you enable her to do everything, not right at all. Your meds, you do not seem to take them the way you should. Now I do not know or understand why you exaterate the TRUTH, but you do and should stop it. You are my son and I love you very much but stop stretching the TRUTH to obtain sympathy. Life is too short and I am still waiting for you to remember the word's I had for you growing up which were never say you cannot unless you try and if you try and cannot do something than I would help you and this is something you should live by to live a somewhat normal life. Our bodies are like machines, if they do not move they will not work. I love you very much. Sorry about this on here but I did not like what I saw since I did not raise that you way. Love, Mom
Marj Scott
08 Jan 2011, 21:05
I have had r.a. For 30 years. I feel bad for so many of you. I have the best dr. He has kept me going great till a bit ago. After some surgery it became bad . I used solgnol for years and it ws great till I had a baby.now on enbrel ten years and thinking of changing. Keep looking till you can find a great dr. That is the most important thing. I am furious that they took darvocet off the market. It was the best drug for me. It has been around for 60 years and there are drugs newer that are much more dangerous. It should be up to patient. I think other drugs are worse.
Don
02 Jan 2011, 11:00
I have had RA for about six years. I tried all drugs and injections to no avail. That is when my Dr recommended Rituxan. The results have been great, as I have been able to stop taking prednisone and all pain meds. I only receive the injection once yearly and am now on my 4th year. Although I still required a knee replacement due to the years prior to the injections. I am know able to work and live pain free.
sunnynwarmer
28 Dec 2010, 12:45
I was somewhat diagnosed with RA in 2007. I am sero-negative so I am unsure of what I really have. Yes, I have a lot of pain in my fingers, toes, back, knees, shoulders and elbows. My hands are the only give-away with swelling in the joints and redness.
As far as meds, I take nothing. My sister had scleroderma; the extreme meds they had her take eventually caused her death. An innocuous-looking fever blister turned into a brain infection, she suffered bouts of shingles and other maladies due to the drugs suppressing her immune system.
I have chosen not to go this route, I need to stay healthy. I chose diet and exercise to help with the pain and depression.
Whatever I have has begun to affect my eyes ("floaters" in my field of vision and uveitis), but again, I am choosing not to medicate.

I am not sure what will happen over the next few years. The pain gets pretty bad at times, (especially if I am stressed and/or the weather is cold and damp), so before I go to bed, I take two Advil or Motrin and lay on a heating pad.
Doctor Zaius
10 Dec 2010, 15:20
Very interesting piece.

Rigel's drug and many others are discussed here...

http://earningsview.blogspot.com/2010/12/new-drugs-in-development-for-rheum atoid.html
Deborah
08 Dec 2010, 17:24
I was diagnosed with RA 2 years ago, and began taking methotrexate. It made me sick, and my hair fell out, but the doc. said that it was the best med.

Last year, I was in excurciating pain, on a walker, in a wheelchair, and ended up having to having a hip and knee replacement! At that time, the Doc. changed my meds. DUH??? yes, my fault, for not changing doc's! I am now doing the Ebrel injections (10 mo. now) along with taking Plaquinel. Together they are working GREAT!!!! The only pain I have is when it is cold and rainy.

Everyone is different. I pray you will find the right combination for your RA! God Bless you. Oh, my hair is still falling out, and I do get exhausted. :(
nitya narayan
03 Dec 2010, 01:40
I am suffering fm RA for the last 11 yrs.I was put on various DMRD drugs. But my main problem now is my hairfall. I lose a lot of hair daily. I just need to know how to stop this hair fall, without stopping the medicines for RA.
Rj
18 Nov 2010, 15:00
I was diagnosed 3 years ago with severe RA I was 27. I have been off all meds for 1.5 yrs due to no ins, but more importantly the Dr i have been to are just idiots. The first almost made me sterile, and the second refused to look at my wrist which has a bone chip certainly caused by my RA. I am in NJ and am able to travel if anyone know of a great DR please let me know.

Thanks,
RJ
alma
11 Nov 2010, 20:22
i read all this and i feel the same way tired bones hurt... i wish that i didnt have to feel this way any more.......i hate this too many medication and i am 37 yrs old hispanic
sundaram
10 Nov 2010, 20:09
please suggest me a newely invented medcine for rhemutaid athrties
ed sanders
10 Sep 2010, 07:02
I've been dealing with RA for 14yrs. DON'T GIVE UP trying. REMICADE with Methotrexate and Prednisone control, not alleviate, the pain and depression. I also use an anti-depressant, pain relievers, anti-anxiety, and Neurontin. The result is I play basketball regularly, walk three miles every day, eat smart, keep the weight down and feel better at 62 than I have in the past 13 yrs. How long this mix will work is a crap shoot, but never be afraid to try and get better. Prayer, exercise, family support, diet all play an important role in working with your doctor. Give her (him) all the info you can and get control of your depression, it's more dangerous than the RA. Please give prayer a chance, with close friends and family, it can't hurt and I can attest to the comfort I have received thru the years.
Nancy Tobin
02 Sep 2010, 20:57
to whom it may concern,
i have been diognosed with ra about 8 months ago. My doctor gave me a script of PIROIXAM for it and recomended me to see a specialest in wanatche wa which is about 200 mile from where i live. I asked my doctor if he could find someone closer and he said that medicade in washington state wont do it. I need to see someone about it because the problems are getting worse and i cant see no one about it because the only doctor that i am allowed to see is too far away and i cant take that long of a trip because of the ra and other problems. I've been searching for help from any one who will listen to me. i am running out of options. please respond asap. I live in the mid valley of yakima county. thank you. Nancy tobin
virginia Bone
26 Aug 2010, 07:48
Have been struggling with RA for over 12 Yr.Was afraid to take all that was avaible . I am hoping they will come out with a pill that has very little side effects. Need help
Amanda
18 Aug 2010, 10:13
I am 30 years old and have been formally diagnosed with RA for 3 years now. I have tried everything from injections to infusions and pills. Nothing has helped and recently have had reactions to meds that RA doc has put me on. I am a medic on an ambulance and love my job but struggle everyday with pain and not being able to lift or walk. I need help of suggestions of medications as it seems I am running out of options fast. Started out on methotrexate along with folic acid and enbrel injections had reaction to metho so had to quit, then switched to Humera which I had to stop taking due to my bloodsugar spiking over 250, then went to Orencia with no relief,then cimzia and had allergic reaction with hives all over my body and swelling to tounge and face. Recently was given Luflonomide and can not take due to stomach upset with vomitting. I feel like the RA is winning and I am a fighter but like I said above am VERY QUICKLY running out of options, if anyone is out there that could give suggestion it would be greatly appreciated.
Shirley
17 Aug 2010, 18:05
I've had RA for 5 years and osteo-arthritis in the back for 2 years. Like most of you I have tried many different drugs. Humira seems to help me the most at the moment but I'm getting some side effects. The white blood cell count is extremely low. I gained a lot of weight due to being inactive. I'm depressed because I can't do the things I love, dancing. I would be grateful if it all ended today because I don't believe there will ever be a cure. There's too much money in it for the drug companies. Why would they want the find a cure.
estela
08 Jul 2010, 02:38
a year ago,I was diagnose with ra.I am taking methotraxate weekly,and at least 5 other pills daily as part of my ra treatment.

One cold night last year,my right knee was in such a extreme pain that I tried keeping it warm and comfortable, so I could go to sleep. The pain got worse,so I decided to reverse the warm nice treatment; I applied ice to the knee and the frozen knee hurt as if it was broken,but suddenly,I fell asleep and the following morning felt much better.

I believe that my pain has a mean level of tolerance, but to quickly ease my flare ups, I fight back utilizing Frozen packs.
good luck


kranthi
30 Jun 2010, 10:00
good for research
Margie
19 Jun 2010, 13:30
I am 61 years old diagnosed with R.A. when I was 21. So, had 40 years of a challenge. Good days and bad days. I have been through the traditional medical, alternative, experiemental etc. treatments. Probably spent two fortunes between the out of pocket and inusrance payments, to try and keep functioning and always praying for a cure.

Some treatments helped, some did nothing, some I actually got worse. I have been taking enbrel injections since 2001, that with pain meds and vitamins and supplements has kept me going me off and on through the years.

I take cortisol for the low adrenal function, westthroid for hypothyroid and bio-identical hormones.

Today I am having morning stiffness and pain, swelling and heat in various joints. Even my new knee, got my first surgery with right knee replacement last June.

In April I somhow ended up with an infection/inflammation/pain in my stomach which landed me in the hosptial for 3 days on I.V. antibiotics. So,I am wondering now if this is what has stirred up this flare-up like I have not had in many years???

Maybe R.A. does have an infection component as many have said for years. Maybe some of the bacteria was killed off and this is a die off reaction.

Since when I was a young teenager I had infections in my gums and lost front 4 upper and lower teeth I have always wondered if that isn't where this all started.

God I wished I knew. But God bless all who suffer. I am humbled by reading all of these posts, many so young and so many sufferring. I praise God we have what we have and I pray for a cure for this very painful conditon. Keep the faith and never give up, I know it is a difficult path but hopefully someday we will know what it feels like to live without pain and restrictions. God Bless You All!
krishnan
11 Jun 2010, 06:26
For all those suffering from RA, theres hope round the corner. Pfizer is conducting a phase III trial for its new immunoupressant across 135 countries ( you too can sign up for the trial). So take heart
Renee White
03 Jun 2010, 18:21
I was diagnosed with RA 5 years ago. My rheumatologist set me up on a experimental drug, Tocilizumab, about 2 years ago. Prior to that I was on Methotrexate (2.5mg x 8 every Friday) and Folic Acid. I no longer take Naproxin for pain and the Methotrexate and Tocilizumab together have eliminated all pain. When first diagnosed, I could not get out of bed by myself, I had problems walking and thought I would wind up in a wheel chair for the rest of my life.

I've been told by my rheumatologist's nurse that this experimental drug has been approved by the FDA but I have not seen anything about this drug anywhere.

I am so thankful that the 24/hr a day pain has been aleviated. I hope this drug comes out soon (I take it once a month by infusion) so all of you who suffer pain from this debilitating disease get the relief that I now have.
vivica
02 Jun 2010, 06:37
i have ra and diagnosed 5 yrs ago i am51 and
take mehrextrate 2.5 mg x 8 every friday,folicacid 2 a day ibuprofen,nexium,vitamin b-12 my most pain is in hands,wrist,knees,feet, and neck some days are good worst time is first thing in the morniings and i also take 2 injections a week of enbrel pain every day
Jenn
19 May 2010, 20:58
Hi- I was diagnosed with JRA at 14- now 30. I used to take metho, humira, and many more. I found changing my diet helped me alot! Particulary Wheat- makes me flare up and others. I still have pain- but no meds for now. Hope this helps.
DONNA MEZZAPESA
10 May 2010, 14:48
Anyone needing help with paying for meds, should look up Caring Voices Coalition and Patient Advocate Foundation. They helped me in many ways and monies!
Beth
01 May 2010, 23:59
For all of you who are having trouble paying for your meds: please contact the makers of the drugs you are taking--practically all of them have programs for the uninsured, and others who can't pay full price--the meds are available at greatly reduced cost.
ELIZABETH
14 Apr 2010, 02:18
Hi, i was diagnosed to have RA last dec. I took plaquenil and decilone forte.I am able to do my normal works but i learned decilone has side effects (eyes and kidney). So am worried. Hope to have new meds for this illness.
b.a.brickley
03 Apr 2010, 20:43
I have had RA since having my daughter at
age 27. I work 40 hours a week and have had
to give up bowling, and a few things I like
to do, but I am fighting this disease. It is
a disease and I have to live with it, but I
try to stay positive. Stress, worry and
sad feelings all increase it and give it life. I am 62 years now. I take Enbrel weekly, which was a life saver. Some day I
pray it will disappear as quick as it started. It is a hideous disease, robbing a
person of their vitality, energy and bones.
Keep fighting. Some one will find a cure.
esther
31 Mar 2010, 00:38
Does any one Know Where I can Get the test drug at .Will my own doctor in AZ.GET IT FOR ME .I take simponi no difference yet taking my 3rd injection with methotrexate,celebrex predisone , would love to try the new medicne.I have had RA for 18 months can not get releif I am 36 do not know if you just always have pain and discomfort
Lynda
15 Mar 2010, 22:35
I was diganoised with Ra, 2 yrs ago. i am on metho. folic acid, plaqunil.. Lefeumoid, arthotec and ibrofuen. At first the drugs seem to be working,but a few mths down the road all the pain and swelling came back, I have not been able to work now for 2 yrs and not sure if i will ever get back to work.My doctor wants to start me on embrel, but since i had TB in the past im not sure of taking it. My hands, wrist, elbows and feet are the worst,, Most days i cant walk,, or straighten my arm..There are days when i cant open my doors,I used to be a very active person, but since this dieases i can barley do anything,, Any suggestions on how i can make the pain a little more bareable
tim
07 Mar 2010, 20:12
hi I was always in pain unable to use my arms started taking the new drug and I feel great no side effects
sleeee
06 Mar 2010, 07:53
i hope it's side effects is minimum
Kamalika
15 Feb 2010, 00:37
HI,

My husband is suffering from RA from past 1 year. He is taking SAZ and Nucoxia daily. His eyes were affected but he recoverd that stage safely, but now his right leg knee in swollen heavily and his feet also.. He cant walk properly... Apart from doctors suggestion we would like to know if someone knows any other remedy that could relive some pain ...

Thanks
Kamalika
Paul
01 Feb 2010, 16:50
I am 55 and diagnosed with RA in December. So far it has been very aggresive and I am unable to continue working as a nurse. Although I appreciate it has proberbly been lurking in my system for a number of years. The onset of my RA coinsided with a swine flu jab,could this be connected ?
holly
01 Feb 2010, 16:34
i have been recently diagnosed with R.A i seem to have to take pain meds all the time is this normal daily living for me from now on ?
Joe Cocuzza
09 Jan 2010, 00:01
Hey Ricky I am 26 and had arthritis since I was 3 been in a wheel chair and got out and had my knee replaced and getting both hips replaced in Febuary.. So I feel your pain truth is My meds sometimes make my heart feel weird like its beating to fast even with little movement feels like im going to have a heart attack scary.. anyways ask your doctor if you can take baby aspirin 81mg once a day its good for the heart and maybe will releave some of your RA pain GOOD LUCK to you..Joe
Ricky
04 Jan 2010, 20:04
I have RA and have had two heart attacks
I have not been on any kind of anti inflamatory since my attacks I took viox and the doctors believe that is what contributed to my first heart attack. The second was because the stints were to small for the artery in which they were placed. My RA is full blown and I am dealing with a lot of pain is there any thing I can take that is safe for my heart.
Robin
29 Dec 2009, 12:00
Haven't had much luck with all these I.V. treatments and injections. I've taken everyone made...and have had RA since 1991. I DO NOT want to quit teaching, I love my job! My RA has worsened, but I am a fighter. If anyone knows about how to be in the trial tests for this new drug, I am so game!! I will NOT let this disease win!! EVER! Would LOVE info on this, and am printing the above to ask my Dr about. God bless all who suffer from this disease! AND I still pray others who do not have RA will come to the realization that it is not a "take some asprin and you'll feel better" kind of pain!!
linda
27 Dec 2009, 19:10
I have this learned that i have aprticularly aggresive form of RA. I also haveve figured out that a flare up of this is close to Hell on Earth! I am so glad that I am not going there because of Jesus Christ my Lord and Savior!

The Humira (an ethical treatmemnt) only worked a few months. My body won't tolerate the the Methotrexate --now I have a liver problem! I will not take the RA meds,that are derived form Aborted fetal cells! A dooctor lied to me or didn't know it when I asked about where the cells came from! I found I a site online that has a chart of ethical and unethical injections and immunizations. You would be amazed!
I am looking for natural means to get over this toxic congition!

As for the HAIR LOSS, Biotin is supposed to help that condition--- a high amount can be taken daily!
Ryan
21 Dec 2009, 14:48
I'm 29 now. I have had RA since age 24. The medications I take are methotrexate, remicade, and folic acid. The remicade made a huge huge huge difference for me. I took advantage of feeling better and being able to move more easily again. I began eating healthy and exercising. This made a huge difference. Going from 195lbs to 165lbs helps so much. If you need to loose weight try to do it. My ,feet, ankles, hips, and knees don't flare up anymore, only some random wrist/hand irritation a couple times a year(during winter??). I truly feel a healthy life style helps with RA.
Naveenchandra
08 Nov 2009, 11:40
Hi Dear Ones,

My wife is suffering from severe RA. She likes to know any new drug is available now in the market for RA so that she can be relieved of pain. Another point which I would like to mention here is that Meditation, for at least 20 minutes, daily gives a lot of relief.
Carolina
07 Nov 2009, 00:32
Hi Friends,
A neurologist gave me this suggestion for RA flareups and/or neuralgia. It really does work. (Don't use on an open wound.) It's practically free and you can avoid taking more medication when you have a flareup. Put about 10 aspirin in a small container and just cover with warm to hot water. When aspirin has dissolved completely, add hand lotion (I use Vaseline Intensive Care or unscented Aveeno)and stir until it reaches a consistency of thick cream. Spread thinly on hot, inflamed, painful areas (wrists, knees, etc.) Repeat after i/2 to one hour if needed. Keep mixture covered and stir each time you use it.
Betty
06 Oct 2009, 17:46
I was not able to see my doctor or take lab work because of past due bill. so I am on my own now. I was taking methotrexate but I have
not taken it in about a month, I have not had
any problems in fact I feel better without
the shots. I don't know if this is going to
have some effect on me later.
Joe Cocuzza
04 Oct 2009, 14:06
Hello everyone I am 26 I was diagnosed with Juvenile RA at age 3 and was placed in a wheel chair from 3-8..The meds I have taken over the years are Methotrexate, Enbrel injection,Humira injection, Orencia IV,Remicade IV, Prednisone,Relafen,Ultracet,Percoset, Oxycontin,Imitrex,Arava,about 6 advil a day when needed about 4 tylenol a day when needed many cortizone shots in several joints, NOTE: not all taken at once! just thru the years they all worked great at first then ware off..
I just had my 18th surgery June 23 09 I had a total knee replacement and am struggling with recovery. They then had to munipulate under anestesia in sept. I go to therapy 5 days a week 3 hours a day.. I have been on disability since June and now my job benefits run out as of November and have to return to work.. I now been having severe hip pain so I went to the Dr. he mentions I have avascular nacrosis where the hips don't get enough blood supply then the tissue and bone dies I will become paralyzed from the waist down if I dont get my hips replaced and at 26 replaceing my body parts isn't exactly what I want to do. I'm in a new marraige and im sure it takes a tole on my wife. although she very supportive, but its just hard because we dont go out as we use to my friends start doing there own thing singling me out because they do things I can't par take..Its sad when you see friends drift away, thats what should make us apprieciate our spouse. I know we can relate on here. we are all going thru tough times.. but by writing on this you never know who you will inspire! Its hard when you go from having alot and being able to do so much to almost losing everything and almost being able to do nothing.. I feel like im going backwards! But trust me people we have to stay as possitive as possible and believe me I know its hard! Its funny because Im sure you've heard "oh it could be worse theres people out there that are really bad or have cancer or whatever" and you feel like your being selfish because in your mind you dont care what anyone else has or going through. all you know is the pain you suffer from! Anyways Even though its hard! try to smile thru the pain keep possitive and know that there will be a better day! Take your meds, excercise,use heating pads, ice, go for a soft relaxing massage whatever it takes to help you get thru the day! talk to your Dr about everything. dont hold anything back get second opinions make smart decisions. work hard!. the funny thing is us with problems work harder then people without problems its like we have to prove something to ourselves! or you know those people on welfare that dont need it but get it anyways rather then those who really need it!! I just lost medicade that I had since I was 3 because I got married isnt that something? they combined your income well NJ does anyways.. oh well
ENJOY LIFE GOD BLESS!
Nick Palmieri
16 Sep 2009, 13:18
Lisa our daughter was diagnosed w/JRA age 4, now 17 yrs old. We started w/ Metho. (varying doseages, oral and subQ)together with Naprosyn and Folic Acid. Later progressed to Enbrael (alone)worked ok about 9-12 mos, then Humira alone w/no relief- (under Humira alone JRA progressed far back to orignal untreated diagnosis state). A blow up w/our Pediatric Rheum. to get back to Metho. due to near remission 3x over 12 yrs, we began Metho. and Enbrael with folic. OUr daughter did wonderfully w/ near imediate results. However, today we're dealing with Osteopenia inaddition to JRA, unsure whether disease, drugs long term or combo of both has created this. Either way, our point - Metho and Enbrael combo worked for us even though last appt. was her first time for Aspiration of fluid in knee. Weigh the long term saftey studies, (many published by Arthritis Foundation) and start treatment. Experimentation w/combo's and dosage is normal. JRA has no set table for all. Each person and progression appears to be different. Excersise and keep healthy diet. Not starting treatment can seriously effect ability of remission the older a patient gets.
Dani it
05 Aug 2009, 12:47
Hi everyone I was diagnose a year ago with RA but I had the first sintoms one year prior. The Reumatologist put me on Metotraxate and also on Humira.
Since I started the injection I had a noticeble improvment, but yet months later I am still in pain,and my quality of life is not that great.
It is very sad that in the year 2009 there is no cure for this condiction.
Anyway my toughs goes to everyone that does not have an insurance willing to pay for the medication or even worse insurance at all.
So I may suggest somenting that brought me some relif: Boswellia serrata (aryuvetic medicine),Tumeric (both for the inflammation) and as probably many knows the combination of glucosamine 1500 mg, chondroitin mg and msm 500mg. that it worked for me for a wile pretty good.
I hope to have been helpfull.
Meanwile i was wondering if anyone have some tips for the hair loss that I am experiencing wile taking metotraxate.
Something natural pheraps?
God bless
Alma
19 Jul 2009, 17:58
I am 45 and have RA in both hands and wrist. I have a job that takes alot of typing on the computer. I am not sure how long I can kept this job; the pain gets worst everyday I am taking every thing the doctor has given me but it just does not get any better.
Elisa
02 Jul 2009, 22:45
I was diognosed a year ago, I'm not on meds just trying alternative meds. Can you provide more info?
olga loera
02 Jul 2009, 19:51
hi im 46 years old and have lived with ra for six years lately ive been in pain and heared about this new medication i dont have insurence and med are very costly if anyone knows about a study in palmdale ca please help
Pam
20 Jun 2009, 08:09
Please tell Filomena that there is a program for Remicade through the manufacturer to help with the payments. she should ask her medical provider about either Remistart, Access 1 or Cecticor; they should be familiar with one of those names.
jane
17 Jun 2009, 17:12
what is the new drug? it was on the news last night and it is in clinical trial at Mass General in Boston. Please help
Carolyn
14 Jun 2009, 13:04
I am on methotrexiate 2.5 X 6 per week. Have been for over 15 years. Doesn't seem to work anymore. I need something fast. What about the new pill R788 ??? Has it been approved and can I now ask my Dr. about it?? I am having pain in both knees and muscle spasm's in my neck and back of head. Could this also be fibromyalgia??
Lisa
01 Jun 2009, 10:41
Hi-I have had JRA/RA since I was 13. I have been fairly well controlled on methotrexate 2.5mg X3 and now my doctor wants me to take Enbrel. Everything I read is scaring me about the drug. I feel fine-rarely have flare ups yet she said I am progressing and the joints will erode. So confused. This new drug looks good-would love to be in a study-also in Ohio.
tony
01 Jun 2009, 07:40
hello ,
i have R.a now for five years i'm 53 now , and sometimes my pain comes and last for two weeks i have heard about this new drug , i;m very interested in trying it if you know of a study in the ohio area please contact me , i would love to try to help all of the 1.3 million others with this desease, to live a better life, thanks tony
frances
08 May 2009, 07:07
my Father is 83 years old and he has RA each time I see him, he is either sitting down on a recliner with a hot water bag or a massager he says it is very painful. I like to help him but he also complaints about stomach pain and blames the medications he is taking..he has gone through CT scan to check his intestine and several test all are normal... is this medication ok to take at his age? we will consult his physican...
T. Lunt
20 Apr 2009, 03:22
I have taken Methotrexate (2.5mg x6 every Tuesday) for about 15years now, and I find that it is keeping th RA in check at the moment, yes I do have flier-ups lasting for about 2/3 days, which are very painful.
I can withstand most off the painful joints, but the only one that brings me down, is when it is in both of my jaw joints, that is very bad, but I thank my God, it only lasts for about 5/6 days.
filomena
18 Apr 2009, 21:26
Please I need help I no have insurance I need my medication is very expense is remecade on i no have de infusion I cant move please some Hospital help me plesae
bin-zayed
12 Apr 2009, 12:25
what is the latest drug for rheumatoid arthritis? can someone help?
Sharon
25 Mar 2009, 18:12
I meant rheumatologist -- I haven't seen two neurologists. But after all tests came back negative, she told me to stop the Botox, so she's clearly suspicious.
Sharon
25 Mar 2009, 18:07
Has anyone every heard of a connection between cervical Botox injections and sudden onset of RA in the hands and wrists? I have seen a terrific neurologist, a hand specialist and now have a highly respected neurologist, but repeated blood tests for everything from RA to ANA show nothing. I have been getting Botox injections in my neck for almost a year -- the hand problem started with the second three-month course -- and no one seems to know what is wrong with me. I'm at the end of my rope.
Veronica
21 Mar 2009, 13:52
This drug seems to have less risk and its oral When can we know more than this new drug?Thanks a lot
Connie
10 Mar 2009, 15:08
Yes i can't take pain meds strong enough to help me because i have a low tolance for morfine. They don't want us to take vicadon now. Pleas i'am on Medicare and Medicaid. I suppose these drugs won't be covered. Do you need people to try out the new drug. Can you help. Thank you Conne

Leave a Comment

Commercial promotion and inappropriate comments will be removed. If you spot one of these, please send an alert.

All fields are required but only your name and comment will be displayed. Your e-mail address will not be used for any other purpose.

Name:
Email:
Text:

ADVERTISEMENT
Arthritis Foundation National Health Council BBB Accredited Charity