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WLS could be a trigger for fibro because anything that stresses the body can be a trigger to get it started, however it's not just WLS that can cause it. Anything that causes stress or trauma to your body can be a trigger. I've had fibro since I was in my late 20's and that's over 35 yrs ago. Your fibro is not apt to get better, unfortunately it tends to get worse as time goes on. This is a chronic condition with no cure. It has caused many of us on here to gain or not lose as well as we could otherwise. I would suggest you do some investigating on the internet and see what books are available on Amazon.com so you can study up on this condition. Knowledge is your key to living the rest of your life with fibro. There are several meds available to treat the symptoms such as Lyrica, Cymbalta and Savella which sometimes help, but everyone is so different it just depends on which meds work for the individual. The best thing you can do to help yourself is stay as active as you can, even if it's just walking. Most of us find heat helps some but you can't spend your life wrapped in a blanket either. Hopefully some of the others here will pop on and give you more advise. If you have specific questions feel free to ask.
Come on this is the 21st century.
Good Luck Dear,
Lady Lin

about to do with my PC whom I've only had since July, my doc left in June, loved her, she cared about me...and that's what we need, someone who genuinally cares.
Praying for you hun, keep me posted...
Lady Lin

I pray that you will get some relief before it gets too bad, don't let it.
Let me know how you make out,
Lady Lin

1) Believing her when she says she is in pain.
2) Not comparing your pain with hers or finding explanations for her pain.
3) Understanding when she does not feel like "doing" anything or going any place.
4) Offering to run errands, cook meals, etc
5) Continuing to be her friend.
The fibro came after my surgery.
Im not trying to say whats wrong or diagnose you by any means.I just wasnt to urge you how important it is to get into a neurologist. I was hesistant about going to ER but I am glad I did it saved my life.Before that day I didnt even have a primary care I was healthy but slightly overweight.
Please feel free to message me.Also if you are having a hard time with doc and refferals, not always but sometimes a call to your insurance can help.I also belong to another support group daily strength.Hope you feel better
and I am going through the same thing with the aches and pain esp the leg cramps in the night.
I had surgery 8/25, so I am too wondering if this has been caused by the surgery.
good luck to you
LILRED
However, for myself, I completely ruled out RNY as a surgical option:
1. The only meds that have every given me consistent control of my fibro are timed released meds. I was told by my surgeon that RNY patients cannot use time released meds.
2. NSAIDS are another staple of my fight against fibro pain. These too are not allowed post RNY,
3. Some vitamin and mineral def can exacerbate fibro and worsen flares. A few of these are Vit D, magnesium and some sources also say selinium. The malabsorptive issues of RNY might make it difficult to control these def.
You might want to read the post today from 22 BAD FIBRO and a mommy too HELP.
She has two posts. It sounds like having limited medicine choices (or not being able to absorb some meds that might've helped) is an issue for her.
You might want to consider a two step process: Have VSG first, see if you lose weight and it works for you, if not, you can convert to the RNY. At least that gives you options. Once you have the RNY you might not be able to reverse.
Please don't think I am a RNY hater.......I am not. I think doing what's best for YOU is the answer and I applaud and support those that have had RNY. It's just that for me, my fibro was one of the reasons I didn't choose RNY.
Hope this helps.