Tuesday, June 11, 2013

menstral flares

By Amber Saturday, December 04, 2010

 

I am now more convinced than ever that my flares are ONLY produced by hormones. 14 days before I start my period, like clockwork my pain starts. it subsides for about two days in the middle of the 14 then flares back up until it starts.Once I start my pain is GONE.

 

Last month it was so bad. I couldn't walk or sleep or eat. then the next day it was like I lied about the whole thing and the pain had moved to my elbow...

 

I didn't think the timing was so exact until I started keeping a pain diary. I thought I had only had RA since the birth of my son. Now I know I have had this since highschool which was over 15 years ago. I've been looking for help for this for over 15 years!!!!

 

Does anyone else suspect hormones? My doctor suggested I try birth control to not get my period. I'm hesitant to throw anything in my body that could alter my hormones until I know what the imbalance is.

 

Any advice or stories to share?

 

pain in one of my toes
12/ 6/10 10:16am

I swear by bc pills!  After each birth of my girls I had bad flares that helped when I returned to birth control, plus my usual drugs.  My Ob has said that it is the pregesterone in them that can help.  It seems like a small price to pay to feel better.  I take Remicade for my RA and exercise and healty eating seem to make a big difference.  It seems like the all these things help me.  I'd take them!  Also talk to your Ob to make sure you are taking the right pill w/the right hormones to make your disease feel better:)

Lene Andersen, Health Guide
12/ 6/10 11:46am

Oh, hormones absolutely play a huge role! It's why a good two thirds of pregnant women go into remission and why so many of us experience a surge in symptoms around PMS time. Exactly which hormones and what influence they have appears to be a bit up in the air. You may want to consider trying the Pill - if it doesn't work, you can always go off it again, right?

 

I checked out your profile and I respect your desire to try the natural approach with RA. For as long as I can remember, I have supplemented my Western allopathic medication with alternative medicine and find that I'm better for it. However, I do want to mention that even when symptoms are mild, the inflammation can cause damage in your joints. The fact that you do flare for about half the month indicates that your RA is not suppressed and those two weeks worth of flares every month can cause damage. I would therefore recommend that you try one of the DMARDs - your doctor will probably suggest Plaquenil, given that you have what appears to be a mild form of RA. Without it, your joints can become damaged, which can affect your ability levels in the future.

 

You have a wonderful attitude and a really healthy outlook on life and I look forward to reading more posts about your life and how you got to the place you're in now.

 

12/ 9/10 6:59am

Thank you for your response. Also for your advise.

 

Its funny that none of my doctors seem to acknowldege the hormone factor. It just seems like common sense! My Rheumy just says it's "interesting"... not sure if I should start looking for a new one. Also when I get my inflamation levels checked they are always Low. This might be a dumb question but does pain= inflamation? My Rheumy is always telling me to just keep doing what I'm doing and that it is working. He has even suggested that my pain is being caused by something else going on in my body. I asked if he thought I was causing more problems for myself in the future by not taking any of the DMARD's and he said " No, if your inflamation levels were high it would tell me that the disease was active. Your levels are normal." I don't want a doctor to throw drugs at me when not needed but, I also don't want to screw myself here.

Lene Andersen, Health Guide
12/ 9/10 7:37pm

I don't think hormones on the radar of an awful lot of rheumatologists. I once mentioned it in passing to my doctor and she perked up and asked me a few questions about it. She said that a lot of her female patients experienced an increase in symptoms around PMS time, but as far as I could tell, she viewed it as an interesting factor in living with RA. There has been some research on it - I did some digging about it a while back and there is probably more than I found that the time. I guess research into the immune system is more likely to result in treatments that can be applied to everyone with RA. Still, you'd think it would be worth looking into.

 

Pain doesn't always equal inflammation. Basically, there are two kinds of pain with RA: pain that results from inflammation and pain that results from damage to the joint that has been caused by inflammation. The best way to describe it is that damage pain feels sharper, less soggy, less like something wrong is going on deep in the joint. Obviously, it still feels wrong, but in a different way - a friend of mine once described pain from active RA as like a butter knife is slowly being squeezed between the bones of the joints and wriggling a space into it. Pretty close to the mark in my experience.

 

If I were you, I'd get a second opinion. As far as I can tell, most rheumatologists - the good ones, anyway - don't rely too much on blood tests. I was at a forum about RA a couple of weeks ago with a keynote speech by Dr. Edward Keystone, one of Canada's prominent rheumatologists (I'll be posting about it in early January, including a link to the webcast). He said that if you have inflammation and swelling, a diagnosis of RA can be made even though your blood tests are normal. The question is whether you have any sort of swelling in your joints and if you do, even just a little, you can risk damage in the long run. When you see your rheumatologist, does he feel your joints? Do you have any joints that are tender if they're pressed? For instance, if you have RA in your fingers and you put the index finger and thumb on the other hand on each side of e.g., the middle joint in a finger and squeeze, it's not supposed to hurt. This was a huge surprise to me when I found out several years ago, because it always hurt with me. Now that I'm on Humira, it no longer hurts. This is where you need a good rheumatologist, because they'll be able to assess the level of "squishyness" in your joints, relying on examination more than they would blood tests. If your doctor is palpating your joints when you see him and basing his advice on medical examination, he may very well be a good rheumatologist. Still, a second opinion wouldn't hurt.

 

12/ 9/10 8:30pm

Hi, No you are not alone..I also experience a flare up during my monthly. It took me a while to identify, because some months are worste than others. But in evaluating my pain journal I noticed the pattern. During my cycle my regular pain meds don't work, I have to upgrade to the "Big Daddy" meds for a few days prior and majority of my time. It drives me crazy because it hurts to even be touched some days.

 

My doctor did state that this is a common occurance for many women. According to him, it is a hormonal change that causes additional inflamation. I found this article, I hope it helps.

 

http://www.medicinenet.com/script/main/art.asp?articlekey=13186

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By Amber— Last Modified: 12/19/10, First Published: 12/04/10