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Muscle Pain


Bigbread

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Bigbread Rookie

Do you guys get a lot of muscle pain when you eat wheat?

I'm not specifically only talking about joint pain, more all over muscle pain or in a certain part of you body?

Thanks

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aeraen Apprentice

That was the surprise benefit of going gluten-free for me.

I was begining to walk like an old lady, and I was only 50. I thought it was the result of being old, fat and out of shape.

About a month of going gluten-free, it suddenly occured to me that I was walking normally, not walking like Frankenstein's monster the first 20 steps after getting out of the car, and getting up off the sofa w/o groaning. I had no idea that celiac caused these symptoms.

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rosetapper23 Explorer

Yes, when I'm accidentally glutened, I get horrible bone, joint, and muscle pain. The medical community is finally beginning to understand that muscle pain can be a symptom of celiac (also tendon and ligament problems). I also suffer from muscle weakness after eating gluten.

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IrishHeart Veteran

Oh yes! Muscle pain, joint pain, bone pain, lost muscle mass and tendon and ligaments sore, too---I have it all. :unsure: (MRIs and blood tests say I am "normal", no RA, etc. "just" osteoarthritis <_< )

A PT told me I can't even get relief until the gut clears from the gluten inflammation. (at least NOW I know why I am in so much pain after years of seeing several specialists, PTs, Chiros,Massage therapists, acupuncturists..THOUSANDS of $$$$ for no relief whatsoever)

I have been in constant agony for several years and I cannot take anything for it. Rips my stomach!!

Boy, I look forward to seeing some of it resolve. So many on here tell me they have improved greatly. Hope yours does too! Fingers crossed!! :)

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nmthommy Rookie

I sometimes feel like I've been hit by a truck. I have to get a massage before getting an adjustment at the chiropractor.

I was also walking like an old lady and having to watch the ground so I wouldn't trip. I just thought it was due to my fast weight gain and that I didn't know where my "new" body center of gravity was.

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rosetapper23 Explorer

IrishHeart,

Have you looked into taking Curamin? It's a natural pain reliever that has helped a lot of people. Their Website is www.curamin.com .

I also take Dr. Christopher's Joint Formula and his Tissue and Bone Formula for the joint and bone pain. I can really tell the difference when I run out.

For the muscle pain, I follow Brian Peskin's protocol of taking 1/2 teaspoon of organic flaxseed oil and 3/4 teaspoon of either grapeseed oil or safflower oil--simply mix the oils into juice or a smoothie. This combination gives you the correct ratio of parent essential oils to fully oxygenate all your cells. It really helps my muscles, particularly after I've exercised.

Just some natural ideas that seem to help...

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Luddie Newbie

I started having lots of aches and pains last summer even though I was on gluten free everything! I have struggled through until now and have been on an elimination diet through doc/nutritionist for the past 3 weeks to see if we can figure out what's happening. My pains are lessening considerably, so I'm hoping tomorrow's blood test will show some really good news. I, too, have had acupuncture and physical therapy and they have helped keep me sane. There were mornings I couldn't even get myself dressed.

I do have another question, though. I never had intestinal symptoms before I was diagnosed, but since I've been on the gluten-free diet and taking supplements (including magnesium) I do have intestinal symptoms, not really the big D, but very close to it.

And lots of stomach gurgling. I'm wondering if I can tell when/if I get "glutened" by my hurting or by my bowels....or both. Anybody else have that situation?

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YoloGx Rookie

I have found that when I get cross contaminated with gluten it often messes up my intestines as well as my joints not to speak of migraines. I also tend to get easily upset or anxious at first, and later depressed with no or little energy.

It is at these times I have to be much more careful about my health because I am in fact run down, unable to fully make use of the vitamins, minerals and oils from the foods I eat. I have noticed too that during these times even my hair suffers --it gets dull and limp plus my fingernails get weaker--not to mention back and hip aches and tender elbows plus jerking nerves at night.

Finally if I have been CC'd a lot (as I was recently helping take care of my mother) I also have to be very careful to not get either a bladder or kidney infection from systemic inflammation, as well as lung congestion. Needless to say, I stopped doing personal care for my gluten eating mother...

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ravenwoodglass Mentor

I started having lots of aches and pains last summer even though I was on gluten free everything! I have struggled through until now and have been on an elimination diet through doc/nutritionist for the past 3 weeks to see if we can figure out what's happening. My pains are lessening considerably, so I'm hoping tomorrow's blood test will show some really good news. I, too, have had acupuncture and physical therapy and they have helped keep me sane. There were mornings I couldn't even get myself dressed.

I do have another question, though. I never had intestinal symptoms before I was diagnosed, but since I've been on the gluten-free diet and taking supplements (including magnesium) I do have intestinal symptoms, not really the big D, but very close to it.

And lots of stomach gurgling. I'm wondering if I can tell when/if I get "glutened" by my hurting or by my bowels....or both. Anybody else have that situation?

Have you tried eliminating soy? That was the last piece of the puzzle for me with joint and muscle pain.

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IrishHeart Veteran

IrishHeart,

Have you looked into taking Curamin? It's a natural pain reliever that has helped a lot of people. Their Website is www.curamin.com .

I also take Dr. Christopher's Joint Formula and his Tissue and Bone Formula for the joint and bone pain. I can really tell the difference when I run out.

For the muscle pain, I follow Brian Peskin's protocol of taking 1/2 teaspoon of organic flaxseed oil and 3/4 teaspoon of either grapeseed oil or safflower oil--simply mix the oils into juice or a smoothie. This combination gives you the correct ratio of parent essential oils to fully oxygenate all your cells. It really helps my muscles, particularly after I've exercised.

Just some natural ideas that seem to help...

RoseT

Thanks for your thoughts.

I am all for the natural approach. I have investigated every protocol there is and I have finally come to the conclusion that I am just not someone who benefits from them.

Right now, I just take flaxseed oil and fish oil, along with a gluten-free/SF/DF multivitamin, D3, B-12, Cal/mag. That's all my stomach can handle.

Since 2006, I have tried them all, spent THOUSANDS of dollars on homeopathic remedies (I saw an ND for 2 years) AND an MD who also recommended things like L-glutamine, probiotics,glucosamine, vitamins, minerals, whey protein powders.....NOTHING helped. I am not kidding when I tell you that I have taken over 100 natural supplements and saw absolutely NO benefit. Can you imagine taking valerian root and still be wide awake? Seriphos? wide awake. These things knock people OUT!6 months of glucosamine? stiff joints...and on and on. I gave them all a long trial period...MY PT had me purchase Curcumin, willow bark, yadda yadda yaadda....I had to stopped trying things. My tummy BURNED and I had no relief. All that money wasted. sigh...

My guess is...my gut is just too messed up right now to benefit from them. No absorption.

I know many people benefit from supplementation. Maybe as I heal, things will work for me too.

It really stinks that I cannot use anything to stop the pain at all. But, I feel that my gut healing is the key. I avoid dairy and soy--the soy for a year now....so, we'll see what happens.

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YoloGx Rookie

I wonder how you are with aspirin?? I discovered recently my "allergy" or intolerance to aspirin was the tip of an iceburg called salicylic acid (SA) intolerance or sensitivity. It can cause a variety of symptoms including muscle and joint aches, ADD like anxiety as well as intestinal distress and eczema etc. Its not clinically an "allergy" even though the symptoms for it can be partly relieved by taking benedryl and/or baking soda.

SA is in the skin of many fruits and vegetables as well as most herbs and nuts--including coconut which is an ingredient in most soaps these days as well as the basis for the charcoal in most water filters. Just a thought...it might be worth investigating. Reason I mentioned it is that for some of these symptoms nothing really worked for me either--especially a lot of things that are healing for most people.

Bea

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IrishHeart Veteran

I wonder how you are with aspirin?? I discovered recently my "allergy" or intolerance to aspirin was the tip of an iceburg called salicylic acid (SA) intolerance or sensitivity. It can cause a variety of symptoms including muscle and joint aches, ADD like anxiety as well as intestinal distress and eczema etc. Its not clinically an "allergy" even though the symptoms for it can be partly relieved by taking benedryl and/or baking soda.

SA is in the skin of many fruits and vegetables as well as most herbs and nuts--including coconut which is an ingredient in most soaps these days as well as the basis for the charcoal in most water filters. Just a thought...it might be worth investigating. Reason I mentioned it is that for some of these symptoms nothing really worked for me either--especially a lot of things that are healing for most people.

Bea

Hi Bea,

Thanks for the thoughts!

I do not take aspirin so I do not know how I react. I only tried the white willow bark a few weeks ago at the suggestion of my PT/ND. She said it worked as well as pain medication. um, nope, it didn't for me!

I looked up foods with salicylics at your suggestion.

Here's the thing. My mouth,throat BURN 24/7 and I eat a LOT of the veggies, fruits, dried fruits, nuts that are on the list for SA intolerance. UH-OH...

I LOVE coconut and when I tried to supplement with teaspoons of the oil? My throat felt like it was on fire....Now you've got me thinking! :unsure:

I'll start watching what happens when I eat those foods and let you know what I find. Thanks!

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YoloGx Rookie

Hi Bea,

Thanks for the thoughts!

I do not take aspirin so I do not know how I react. I only tried the white willow bark a few weeks ago at the suggestion of my PT/ND. She said it worked as well as pain medication. um, nope, it didn't for me!

I looked up foods with salicylics at your suggestion.

Here's the thing. My mouth,throat BURN 24/7 and I eat a LOT of the veggies, fruits, dried fruits, nuts that are on the list for SA intolerance. UH-OH...

I LOVE coconut and when I tried to supplement with teaspoons of the oil? My throat felt like it was on fire....Now you've got me thinking! :unsure:

I'll start watching what happens when I eat those foods and let you know what I find. Thanks!

Do let me know. It was only due to a suggestion from someone here on celiac.com that I finally figured this SA condition out. Ironically now I can tolerate some foods I used to avoid, and now avoid many I used to eat that I thought were "healthy". Go figure!

Filtered water too seems to bother me due to the coconut based charcoal filters. I have to either boil city water or buy spring water. Sheesh!

But the proof is in finally feeling so much better. I still often have to take benedryl however in order to sleep since I haven't entirely figured out all the things to avoid.

My most recent realization was that my beloved bok choy seems to be bothering me. Plus whereas some sources of powdered carob bothers me others do not. It is probably due to CC from the carob being processed on the same equipment as tree nuts...!!

Bea

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IrishHeart Veteran

Do let me know. It was only due to a suggestion from someone here on celiac.com that I finally figured this SA condition out. Ironically now I can tolerate some foods I used to avoid, and now avoid many I used to eat that I thought were "healthy". Go figure!

Filtered water too seems to bother me due to the coconut based charcoal filters. I have to either boil city water or buy spring water. Sheesh!

But the proof is in finally feeling so much better. I still often have to take benedryl however in order to sleep since I haven't entirely figured out all the things to avoid.

My most recent realization was that my beloved bok choy seems to be bothering me. Plus whereas some sources of powdered carob bothers me others do not. It is probably due to CC from the carob being processed on the same equipment as tree nuts...!!

Bea

Thanks again!

I'll see what happens if I take these foods out.

How long before you noticed an improvement?

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YoloGx Rookie

Thanks again!

I'll see what happens if I take these foods out.

How long before you noticed an improvement?

I wish I could be more exact. However it didn't take very long for me to notice some important improvements being off salicylic acid for the most part--I think maybe less than a week when I noticed my tongue color improved and my abdomen wasn't so distended. The fact I could finally tolerate eating brown rice, bananas and ripe peeled pears and peeled cooked golden delicious apples (in moderation) was huge. Previously I thought all grains and fruit gave me this intractable candida.

Now on the SA intolerance diet my tongue color improved and inflammation went away--which also lessened and often removed the pain in my joints unless I ate something I shouldn't have. Nevertheless, some of the symptoms like eczema and the nerve problems have taken longer--although they too improved. I have days without it and days with it depending on my diet. It has also taken its time probably due to SA being built up in my system. They say it takes roughly 6 weeks to flush it all out. It has taken me a little longer than that probably because learning what does and does not have too much SA in it has been a little complicated. I am still learning--but as said much improved.

One good thing now is that I can tell pretty much right away (or at least overnight) if something is not right for me. Thankfully the benedryl comes to the rescue if I can't sleep and/or have eczema symptoms (actually this usually goes together for me). Baking soda also helps.

I like the previous poster's suggestion of keeping a food and symptoms journal. It really is a good idea with this condition since so many things have SA in them.

For me I still need to have foods that either have negligeable amount of SA or the Low rating. Moderate at this point is still too much for me. I also thought using some spices that are high in SA would be OK since I didn't use that much say in a stew, for instance, but it was still too much for me. Fortunately my taste buds are adapting and I am finding just using parsely, garlic, leeks and onions are sufficient for spices.

I also still can't tolerate asparagus or, it seems, bok choy and have to be careful of SA CC (though one does not have to be as careful of SA CC as one does with gluten CC).

Again good luck!

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calidreamin Newbie

Do you guys get a lot of muscle pain when you eat wheat?

I'm not specifically only talking about joint pain, more all over muscle pain or in a certain part of you body?

Thanks

When I eat gluten, I get severe shoulder pain. Several years ago, my right shoulder was pulled, and ever since then, gluten = pain that vicodin can't touch!

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      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
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      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
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