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hi everyone,

i need some advice and sage words from you, if at all possible!

i have been diagnosed with RA,  it's early and mild.  I have seen 3 Rhematologists and they all agree that I have RA but without the MRI I probably would not have been diagnosed.

To give you a quick summary:
- i have joint pain, but NO stiffness in morning or visible swelling
- My RF is 37
- Sed rate is near normal, CCP is negative, C-Reactive Protein was a bit elevated in November but has come down now
- my symptoms are very sore joints, migratory joint pain and fatigue

The radiologist who wrote the report from the MRI wrote: "multiple small enhancing erosions within the capitate bilaterally with mild synovitis of the carpus and MCP joints.  Findings are consistent with and concerning for mild inflammatory arthropathy".  Also, mild to moderate tendonopathy of both carpus extensor ulnaris tendons in both hands/wrists.

My white blood cell counts are low (2.4) and one RD says I'm not a candidate for methotrexate because of it.  She suggests I go on Enbrel immediately.  I asked her about minocycline and she thought that with my joint damage it was not advisable.

Next RD says I could try many things and suggested:
a) enbrel
b) minocycline
c) triple therapy (meth, plaquenil and sulfasalazine)
d) methotrexate (and watch my WBC frequently)
e) sulfasalazine

The next RD thought "If you start with the milder drugs and they do not work, you can proceed to the stronger ones rapidly; the damage described is early.  However,  that damage has happened fairly rapidly, and may not be reversible.  There is accumulating data suggesting that very early aggressive treatment has a better outcome, and may be worth the little bit of extra risk associated with the treatment."

So.... the opinions are a bit different and I'm trying to figure out next steps.

I am toying with the idea of trying the antibiotics first, for 3 months, and if that does not work, going on Enbrel.  I'm not too jazzed up about the idea of trying Methotrexate and I refuse to go on Prednisone.

I am 38 year old white female with 2 children under the age of 3, so I need to get my life and energy back.  Any sage advice appreciated.

I am currently taking Vitamin D, Diflofenac, Turmeric, Fish Oil & Evening Primrose Oil.

I forgot to mention... right now I'm trying to decide between Enbrel now, or antibiotics first and Enbrel later....  or maybe the "triple therapy" option.... I have heard that triple therapy can work very well.  I have only been on MTX a little while, and am having to wait to add other drugs.  Ugh.  So far MTX alone isn't doing anything. 

 
I don't know a lot about Enbrel, I'm sure others will chime in.  But from a bird's eye view it looks like all 3 RD's have suggested Enbrel, that's they only thing they agree on. 
hi cdndream welcome to you.. all of my joints were ruined in the first 4yrs
even though i was on mtx and prednisone..  tough desision on these meds.
i was never given a choice just got given the meds.. i hope you find the
right meds for you

Boney
I'm no expert, but you could consider NSAIDs as a first line of defense. Naproxen or Nabumetone would deal well with the inflammation and discomfort and they are inexpensive. If they don't work or you can't tolerate them, switch to something more potent like Enbrel. Chances are you will switch regimens over the course of your illness anyway. I have tried Mobic and am currently on Diclofenac, both are NSAIDs.  Neither help at all.
 
 
NSAIDS are not a suitable treatment for someone with early joint damage. I don't know if you are aware but it is possible to use minocycline with Enbrel. While I think AP is a GREAT long term therapy it can take a while to kick in (some people have reported several years). What you want to do is get the RA under control rapidly and then get a maintainance program going. Many people use Enbrel in conjunction with AP, then later stop the Enbrel.

My vote?

Minocin first.  Run for 3 months and keep a diary.  Record any Ah-ha moments so you can decide if it's working. 
 
Second choice - sulphasalazine - it's a really, really, really almost removed from being, but still has some, antiobiotic properties. 
 
Third choice - Plaq - yes, I know it's not on your list.  ;-)
 
Triple therapy
 
MTX
 
Enbrel. 
 
My reasoning is I have some damage on my left foot - it will or it won't repair - but if you're trying to delay the ladder - exhaust all options first. 
 
Hugs,
 
Pip
P.S.  My reason against Enbrel WITH Mino is we 'herx' to get better.  If you take the pain away, it's really hard to say, "OK, give me a little pain now that I'm ready!"  I'm not convinced that people eventually wean - it's used more as a holding action.  That being said, I'm more for mixing Enbrel and Mino than not Mino.  Does that make sense?
Do the Minocin, and look at your diet. The sooner you get onto the diet the better.
Like Pip say's you need to experience the 'herx' - feeling crappy before you feel better. This has been many peoples experience with this disease. With you sed rate at 0, i believe it means you don't have inflammation, being that the test is what they go by on me for inflammation.
 
I understand why they wouldn't want to put you on these drugs if inflammation is not there.
 
Have you talked with doctors about fibro?
My sed rate isn't at 0, it's just not as high as it was. I will find my latest bloodwork and let you know what it is. Hello. Welcome to the board, sorry you had to find us though.

I am a 40 year old female with a six year old daughter who I am a single parent to. I have been diagnosed for three years and they are yet to find a medication to stabilise my symptoms. As a result, I have tried every medication except one, so I have had a bit of experience.

My advice would be this...triple therapy plus add a probiotic.

It's a good, solid combination that has worked well for many people and a good place to start.

In my opinion, MTX is a no more dangerous or scary than anything else and Enbrel won't necessarily do a better job because it's a biologic.

Also, I'm afraid that there is 'no getting your life back'. I have been looking for three years and wanting that can cause you a lot of disappointment. What you have to do is create a new life from what you have now. I have done much crying and screaming in the last three years...wanting my life back but I can't have it. Better to look at what you can have now. I know what it's like to feel desperate to get your energy back to cope with young children, it's awful but work with what you have, find new ways of doing things. This means there will be lots of change and loss for you and your family. It isn't easy.

I hope that whatever therapy you choose goes well for you.


I am also on Mobic.  My RD (and what I have read) says that NSAIDs CAN drastically reduce pain & inflammation.  It has for me, pain when I am resting is gone, as is most of the inflammation.  However it does NOT stop the disease process-damage to cartlidge and bone will continue even if pain is gone.

I'm glad you are being offered triple therapy.  I've read recent reports that it is much more effective than any one DMARD alone, and no more toxic.  But my RD is making me go one at a time, in case I have a side effect, so I don't have to go off of all of them to figure it out.  But I feel like it's also wasting precious time.
 
I agree with Cordella. Triple therapy is starting to be standard treatment. Now a days, they recommend aggressive treatment to start as a lot of damage happens the first two years. Think about how important your hands are, even if just your pinkies are damaged that can limit how you hold a cup. You are talking about your hands. Your hands. MTX has been around for at least 20 years and works for more people more often than any other medication. That is why it is the first line drug. Try taping two fingers on both hands together that might show you what it can be like. Remember, once you have damage it isn't easily repaired so it is much better to not have damage.

MTX takes 2 to 3 months to start working, antibiotics can take a year to start working and Enbrel starts almost immediately. Time is not on your side, it is on the arthritis side. You can all normal bloodwork and still have a lot of rapid damage.

This doctor said it best>>>The next RD thought "If you start with the milder drugs and they do not work, you can proceed to the stronger ones rapidly; the damage described is early. However, that damage has happened fairly rapidly, and may not be reversible. There is accumulating data suggesting that very early aggressive treatment has a better outcome, and may be worth the little bit of extra risk associated with the treatment." <<

I'm surprised that any RD would suggest mtx with your white blood cell count so low.  I suppose though it would depend on how much you'd be taking and then really watching your WBC count.  I know that the few times I've had to stop my mtx for a few weeks was when my WBC count got down to 2.4  I'd have to go off until it worked it's way back up to 3.0 I believe.

 
I was surprised about RD #2 suggesting mtx with my WBC being so low too.  He really doesn't think that the mtx would make them drop further - RD #1 did though, she ruled MTX out entirely.  I told each of them what the other has said (they know each other) and they stand by their opinions.

I have heard and read that a lot of people feel like crap when they are on MTX and with two little rugrats to take care of, I would prefer to feel better rather than worse.  Power of positive thinking???  :-)

I am sooo confused...  triple therapy, enbrel, mtx, plaquenil, sulfasalazine... these were all just cryptic words to me a few short weeks ago. 

I want to figure out what to do first.... like others have said I can always try another if the first doesn't work out.  I really want to nip this in the bud and feel better.  I feel like such a "newbie" writing this.

BTW, my sed rate was 12, now it's down to 1....  But since different labs did the 2 tests  I've been told that they cannot be compared directly.  ANA was negative.  C-reactive was 8.   Vitamin D was low at 26 (supposed to be 30-100).
Before you add in D - make sure they run all 4 D tests to make sure you're not D sensitive.  I suspect a lot of us are - but I haven't completed my research so even tho I'm low too - I'm not doing anything about this until I do.
 
Cdndream - your body is on the fence (or maybe your seronegative) but this is all so new you have a shot to beat this.  Please go for it!
 
Hugs,
 
Pip
PS - Anna/Birdgirl whatever!  You are such a .....
From the way I understand ra, (someone correct me if I am wrong) that the first few years are the most vital because that is when most damage is done and the ra is most aggressive. I have been on enbrel for five months and am doing quite well. I tried all the others, alot I was allergic to and some didn't work. I noticed improvements on enbrel the day after my first injection. My morning stiffness was gone and I now have some energy and my pain has gotten better too. RA is such a personable disease and everyone is different. But IMO I would treat is fast and with aggression!
Good luck and I hope whatever path you take is a good one for you.
Remember Pip doesn't have RA and has no real medical education she just pretends. MTX doesn't really effect WBC's like is Azulfasdine does.

The first couple doses of MTX you might feel nausous. Take it in the evening, with carbs. Many many people take it with kids, a job and a very active life.

The insurance co wiill probably make you take MTX before letting you have Enbrel, Enbrel is expensive. The insurance co knows how well MTX works.

You are talking about your hands. What if you can't make dinner for the little ones? The medical advances are happening rapidly. So far there is no cure, but there might be soon. Protect your hands.This might be helpful. I thought it was very positive and it certainly seems to be a good fit with your situation.

Take care,

Lynn

Early Treatment With Remicade and Methotrexate For Rheumatoid Arthritis Has Led To 1/5 Of Patients In Drug-Free Remission:

Early treatment with a combination of methotrexate and infliximab may be effective as remission induction therapy and alter the course of early rheumatoid arthritis (RA), according to data presented at EULAR 2007, the Annual European Congress of Rheumatology in Barcelona, Spain.

At four year follow up, over half (51%) of the patients who started treatment with a combination of methotrexate and infliximab in the BeSt ('Behandel-Strategieën' or 'treatment strategies') trial had been able to discontinue treatment with infliximab and maintained a good response (Disease Activity Score (DAS) ≤2.4). 41 patients were still taking methotrexate monotherapy at trial end. Almost one in five (17%) of patients had reached clinical remission (DAS <1.6), with minimal joint damage progression, and were no longer receiving any anti-rheumatic drugs,

Study leader Dr Cornelia F. Allaart commented: "Our findings indicate that clinical remission from RA is achievable provided effective treatment - such as the infliximab methotrexate combination we used in the fourth arm of this study - is administered early in the course of the disease."


http://www.medicalnewstoday.com/articles/74289.php
[QUOTE=cdndream]

I have heard and read that a lot of people feel like crap when they are on MTX and with two little rugrats to take care of, I would prefer to feel better rather than worse.  Power of positive thinking???  :-)



[/QUOTE]
Some people yes...but not all.  Just wanted to let you know that other than the occasional low white blood cell count, I've had no problems at all with mtx.  Been taking it for about 16 years now (25 mg) with good results.  Although I do take plaquenil and sulfasalazine with it. 
Good Luck!
Lynn and Anna -
 
I have not hunted the actual study down - but despite the title - these authors make a startling conclusion. 
 
In conclusion, researchers advised against starting treatment with TNF blockers until there is evidence that methotrexate is an inadequate treatment for an individual patient.
 
http://arthritis.about.com/b/2008/05/02/tnf-blockers-equally-effective-for-rheumatoid-arthritis.htm
 
Pip

Because RA can do a ton of damage early on, as apparently is happening with you, I personally wouldn't fool around with it.  I wouldn't wait a year for minocin to work, possibly causing further damage to my joints.  Especially at your age with your young children.  If mtx does make you nauseous you can always switch to injectable, that seems to take care of it for many.  But what if 5 years from now you're looking at a knee relacement because you weren't aggressive enough now?  I'm not saying don't try minocin, I just don't think you should try it alone.  In my opinion their is just too much at stake.

Also, don't discount MTX. It works very well in undifferentiated RA....

Rheumatoid Arthritis May Be Prevented with Early Treatment

Results of a study presented at the Annual European Congress of Rheumatology by Henrike Van Dongen, MD, Leiden University Medical Center, Netherlands, and her colleagues on June 21, 2006, suggests that people diagnosed with undifferentiated rheumatoid arthritis could have their disease outlook changed significantly if the proper treatment is given at the right time.

The PROMPT-study (Probable rheumatoid arthritis: Methotrexate versus Placebo Treatment-study), a double-blind, placebo controlled, randomized, multicenter trial in 110 participants with undifferentiated (having an undetermined diagnosis) rheumatoid arthritis (RA), was conducted to determine whether participants would benefit from treatment with methotrexate.

The study concluded that the methotrexate group had fewer patients develop RA during the observed time and more participants reached remission than in the group receiving placebo. “This data is excellent news as it shows that methotrexate appears to delay or even prevent progression to rheumatoid arthritis amongst patients," said another member of the study Tom Huizinga, MD, Leiden University Medical Center, Netherlands.

Methotrexate is a disease modifying anti-rheumatic drug (DMARD) and is well established in the treatment of cancer and autoimmune diseases such as RA. In rheumatoid arthritis, methotrexate seems to work, in part, by altering aspects of immune function which may play a role in causing the disease.

“One of the most interesting findings from the study was that the patients who benefited the most were the ones showing a positive anti-CCP test, which would in general terms show that a patient has a very high likelihood to develop full-blown RA. However, this study indicates that the progression to a full-blown disease amongst these patients could be influenced,” noted Dr. Dongen.

"This is an important study," said John H. Klippel, MD, President and CEO, Arthritis Foundation, "which suggests that there may be a window very early in the development of rheumatoid arthritis in which treatment significantly alters the course of the disease. Identifying patients in this phase of the disease and instituting treatment is an important public health goal."

Linda-
 
What if she needs a knee replacement in 5 years on the biologics?  As we see here every day - they aren't all that.  There was just a post on AF about an RA person whose MD told her the new thought in rheumatology is to have the patient 'cycle-thru' the meds.  Cycle thru?  Until when?  Until you're out of options?  Until something new comes out of the pipeline with even less of a safety profile?
 
Minocin takes longer to work the MORE meds you've been on.  She's on (basically) nothing right now.  I'd bet the farm - and her ability to play with her children - that Minocin will show her its working within 3 months.  Enough of an improvement so that she'll feel empowered to fight her rheumies for more.  It's the same risk I took - for my daughter - when I was reduced to a walker in only 4 months after diagnosis. 
 
She's a young mother.  When is she going to try this?  After she's 'cycled' thru everything and it's failed?  She doesn't have time to mess around looking for a cocktail that covers up symptoms and lets the disease progress in the back ground. 
 
IF, and I really mean IF - the disease IS most aggressive in the beginning - doesn't it make sense to take it out with the most benign med option out there?  By the logic of the other two - the disease calms down later.  Heck, my ARC traditional rheumy told me the same thing.  So, if the traditional doc was right - and I brought my 'severe early onset' to it's knee's with a med I only take 3 times a week - what does that say about how necessary the other meds are?
 
Finally - I have one toe with damage.  I consider that a blessing considering posts here.
 
Pip
Pip, I'm so surprized you don't agree with me!  LOL
 
I know for you traditional meds left you with a walker, for me they restored my ability to walk.  For Cdndream, considering that RA is fairly new for her and she already has damage, I think she should cover all her bases.
 
Personally, I would consider minocin if traditional meds failed me, I guess that's what brought you to minocin, right?  She might not have to cycle through all the meds.  MTX might do the trick by itself. Or Enbrel might.  Or minocin might.  But, if mtx or enbrel isn't working you find that our in a reletively short time, but if minocin isn't working she might go a year of joint erosion before that's realized.   The result of that could be pretty bad for her. That's why I think a combo if she wants minocin is better than minocin alone.
Ah, Linda, you do my heart good.  LOL  Remind me to show you my errant toe when I'm back there so you can 'vouch' for me.  That will be fun, no?  Taking my shoes and socks off in a restauant.
 
No, the only traditional med I was on was Pred.  I still can't understand how most of you guys love that stuff.  It made me worse - enough so my hubby bit one of the docs (and he's not a biter) telling him 'no more'.
 
No what brought me to Minocin was they were the only people talking about 'going for the source'.  As I was feverously researching, I was only researching the first tier meds.  I freaked at Plaq and said 'there has to be another way'.  It wasn't until I was on the Roadback that I even heard about the biologics and that was ...um...er...in a rather disparaging way.  I still didn't know what they were until I got here - so - maybe 4 months after starting AP. 
 
Not trying to offend anybody - but what I'm seeing here freaks me out.  Not only that the meds don't seem to work long, but docs that take people off things that are sort of working, maybe needing tweaking, and moving them up.  And, maybe I'm wrong, but I see more 'reactions' from people who've been on multiple biologics.  To me, and I ADMIT it's not everybody, it seems that a lot of people are getting sicker.  And the thing that creeps me out the most - if you look at the studies, they have some great, pro-biologic titles - but if you look at the numbers, and some of these meds work only a smidge better than placebos.  And it always seems to work better with MTX.  If those meds were 'all that' they shouldn't need the MTX, right?  SOMETHING is going on behind the mechanism of action of the meds - what is it?  Why can't we get efficacy studies?  Serious 'I've not been paid off by Pharma' studies that tell us what the real effects are? 
 
That being said - I've learned a lot here.  Plaq???  If AP fails, that's probably first up in my book.  MTX - bring it on!!!  The first tier fails - I'm gonna be first in line for a biologic.  No way am I living my life with the level of pain I had prior to starting AP. 
 
So, while AP will work for people who've been on everything else - it's a MUCH shorter road back for those who haven't done all the traditionals?  Why is that?  Could it be that maybe suppressing the immune system isn't such a good idea? 
 
She's not been on the other meds - she'll have her proof relatively soon.  And I now advocate getting regular X-rays to be sure you're not getting any damage until you hit remission.  Real remission.  Not just wishful thinking.  I like wishful thinking as well as the next guy - but I'm not in remission yet - and I'm watching my labs and Xrays like a hawk.
 
So far - no damage.
 
Hugs,
 
Pip
[QUOTE=Bird Girrl] Remember Pip doesn't have RA and has no real medical education she just pretends. MTX doesn't really effect WBC's like is Azulfasdine does.

The insurance co wiill probably make you take MTX before letting you have Enbrel, Enbrel is expensive. The insurance co knows how well MTX works.

.[/QUOTE]

Anna, are you some kind of a long distance doctor that knows more than Pip's and CdNDream's doctor? Pip has RA and CDNdream is Canadian, so CDNdream doesn't have to deal with insurance companies, you moron.

Grow up.Thought I saw a post here that she has paladron arthritis, not RA. I did not see her denounce that.

Here is a post about early aggressive treatment. It even mentions mincen (as a MILD DMARD).

http://arthritis.about.com/od/rheumatoidarthritis/f/earlytreatment.htm
Anna/BrrdGrll/BeeBee/TrollNameOfTheWeek, I know you know Pip has RA, that she has herself told you, and that you've pulled this "Pip doesn't have RA" on other boards. If you're going to try to play innocent and manipulate people, could you at least be clever about it so we can have a crumb of respect for you?

People come here for input and information. Just because you have a chip on your shoulder for whatever reason doesn't excuse your constant throwing in of misinformation. We all have major health issues and your behaviour is damaging.

You need to find another hobby besides looking, or making up, ways to discredit people who's health management choices you don't agree with.
cdn - if you haven't given up on this thread yet LOL, here is some info about minocycline from the Arthritis Foundation site that might be helpful:


  Hey - I just want to be a representative for the early aggressive treatment.  I was diagnosed in Jan.  As you can see below, bad numbers.  The combination of plaquinel and MTX put me in , dare I say, remission in 2 months.  
 
The side effects sound so scary.  I just trust in the frequent blood tests etc.  Life for me is back to normal. OMG, sorry CDNDream, I get so hotheaded sometimes I help the trolls hijack the thread. I'm sooo sorry.

Back to our regularly scheduled program.

(BTW, I just got back from my (non-AP) RD's, and she said what I'm doing is working. I've been kind of stalled in my Minocin therapy but she says she's on board to do whatever the next step is to get it going again. So it can and does work.)Just another of over a hundred options:
 

Urine: Your own perfect medicine

Urine Therapy: Your Own Perfect Medicine "Every one of us ... Multiple sclerosis, colitis, lupus, rheumatoid arthritis ... mentions that a celebrated breeder of cattle and horses ...

levlarry2008-05-07 16:55:06Hey all,

I really do appreciate all of your advice and experience. This is extremely frightening for me. I'm totally pissed off that I have this RA thing in the first place. When I was pregnant 9 months ago with my son, I had PUPPPS, which is an auto-immune rash induced by the male DNA in the placenta (or so they think). I wonder if the RA is somehow correlated.

As my name, CDNDream indicates, I am indeed Canadienne. However, we moved to the USA two years ago for my husband's job. So... I do have to worry about the idiotic american insurance companies, unfortunately.

RD #1 thinks that she can easily convince my insurance to pay for Enbrel b/c of my white counts being so low. I have "neutropenia".   She vehemently believes that taking MTX will be bad for me and my immune system. And to be honest, I'm not too excited about the prospect of going on a chemotherapy drug. As I wrote earlier, I'm not about to go on prednisone either. I have a friend who is a radiologist and her opinion was "Of course prednisone will make you feel better, EVERYONE feels better on a bit of prednisone." She thinks, and I agree, that the side-effects are not worth it. Especially given that i don't have morning stiffness or hot & swollen joints.

My RA is early. My only physical symptoms are achy sore joints, the damage as shown on my MR and the RF factor. My sed rate was up, (now it's down), my C-Reactive was elevated (now it's down)...

I have a good friend who is a chiropractor in Canada and into the holistic-wellness approach (and whose daughter has JRA) and he think I can beat this with minocin, diet, counselling (to relieve stress) and a wellness approach to my life. I am hoping he's right.

I may even go see Dr Mercola - has anyone been to Chicago to see him?

From your posts, I am thinking that minocin alone for 3 months and then if no major improvement, Enbrel with Minocin would be a good combo. I'll ask RD#3 tomorrow what she thinks.

Thanks everyone, and please, if anyone has tried Enbrel in combo with Minocin, please advise.I loudly applaud your decision. The only thing is Dr Mercola doesn't do AP anymore (although he still maintains it works), as he believes you can combat RA on diet alone. There's another lady here, GenaRogers, who sees him. She doesn't come by too much these days but if you PM her maybe she'll tell you more about her experience. Last I heard she was doing quite well.

To find another good AP doctor, try posting on the Roadback Foundation's bulletin board (www.rbfbb.org). The Roadback Foundation's website is also a good place for more information about AP (www.roadback.org). Knowing a lot about the therapy will greatly increase your chance of succes. While there are now many competent AP doctors, your average rheumy doesn't know much about the finer points so unless you have an AP doc you end up kind of steering the ship.

Consider reading The New Arthritis Breakthrough by Henry Scammell (available at your local library). This explains the history and science behind AP, and it's an easy and inspiring read.

My other bit of advice is probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics
probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics probiotics.

And probiotics.

Good luck on your great choice! If you ahve any questions there are quite a few conversant APers here, as well as the Roadback Foundation being an excellent resource.

Gimpy-a-gogo2008-05-07 22:15:48Thank you so much Gimpy!!

As it happens, RD#2, the one who offered me so many treatment/meds options, is on The Road Back website.  He told me that many folks travel long distances to see him b/c he's willing to try AP.  He also told me he's seen severely handicapped RA patients get better on AP. 

My chiro friend told me that he had heard that Dr Mercola has moved to Hawaii.  I wonder if that's true.

I am seeing RD#3 today, she works in the same office as RD#2 and knows RD#1.  I am hoping that she can offer me some guidance, as so far, RD1 and RD2 have been a little too far apart in their recos for my comfort.  I have to choose a doctor and choose a med regimen. 

I woke up this morning with significant morning stiffness, my first time.  It had me in tears and my tears made my 3yr old cry.  I guess I need to toughen up emotionally.  I don't want my kids to see me crying.

merci mes amis.
Someone who posts as Ellen on RB was on Enbrel and added mino, then was able to reduce and drop Enbrel.  You might try to pm her there.

Best wishes (sorry for the bad morning, but good you have an appt. today!)
"Dr Mercola doesn't do AP anymore (although he still maintains it works), as he believes you can combat RA on diet alone"
 
Does anyone have more information on diet?  Links or key words for google searches?  Thanks in advance!
Well, my dx is seronegative RA and the AP therapy has given me my life back. Was on pred. and mtx and the experience was most horrific.  The AP therapy began changing my life within three weeks - not several years.

Agree with Pip - keep a diary!  *Gentle Hugs*
[QUOTE=Cardimom] "Dr Mercola doesn't do AP anymore (although he still maintains it works), as he believes you can combat RA on diet alone"

[/QUOTE]

I think he just has a variation on the leaky gut diet, of which there are many. No dairy, no gluten (sometimes no grains), no sugar (sometimes no fruit), no alcohol etc.

Here's a search on his site for rheumatoid arthritis:
http://search.mercola.com/Results.aspx?q=rheumatoid%20arthritis

Or just visit
www.mecola.comThanks!Hey Cardimom -
 
I have a friend on another board BIG into Diet.  I'll contact her and see if you guys can communicate.  Greeno is our resident expert because earlier in our 'can't we all learn to get along' phase we ran poor Gena off.  I miss her!  I've seen too many diet people with it working for me to discount it.  I just couldn't go that route first as I was so bad off.
 
CndDream -
 
Mercola is not doing AP anymore and he may have darn well moved to Hawaii as all his videos seem to come from there.  While what he does is important; he's too much of a huckster for my tastes.  I don't fault him 'branding' himself - but I do think we can do all the things he suggests for a LOT less money.  I do still get his newsletter - he provided links to all the research (full articles) and some of the research he cites is top notch. 
 
My advice - if you've got a RB rheumy - take that one!  LOL  They're not all perfect (just like in the traditional fields) but, hey, it's a start!
 
Pip

Hi Cdndream, I am sorry to read about your struggles with arthritis. I work for Corbett Accel Healthcare Group in Chicago, IL and my team is conducting a research project (no sales involved) on new therapies for RA. We would like to get the opinions of people who have been diagnosed with Rheumatoid Arthritis or Undifferentiated (Inflammatory) Arthritis in the past year.

I have read through your postings and would like to ask if you would participate in a 1-hour phone interview. If you qualify you would receive for your time.

To find out if you qualify, please call me at 312-475-7857.

The deadline for responses is Friday, October 24.  Thanks for your consideration.

 

Their clients -
 
http://www.corbettaccel.com/clients/
 
Pip

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