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Leg Pain


DonaldandAlanda Evans

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DonaldandAlanda Evans Apprentice

I've been getting pretty bad bilateral leg pain/weakness off and on for a long time. It seems to be worse in the morning, and is sometimes accompanied by tingling in my feet or hands. Is this something that is Celiac related? I've had my thyroid levels checked as many family members have Hashimotos , but i'm fine. I also had normal calcium, magnesium and b12 levels.......I do have a slight D deficiency.

Does anyone else get this? I've been gluten free for a couple months......will this go away?


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Wolicki Enthusiast

yes, I think it is related. Mine started after going gluten free, and lasted for about 6 months. I would get sharp shooting pains across my shins, and had tingling in my feet and ankles. Thank goodness, it stopped for me.

lizzers Newbie

I've been getting pretty bad bilateral leg pain/weakness off and on for a long time. It seems to be worse in the morning, and is sometimes accompanied by tingling in my feet or hands. Is this something that is Celiac related? I've had my thyroid levels checked as many family members have Hashimotos , but i'm fine. I also had normal calcium, magnesium and b12 levels.......I do have a slight D deficiency.

Does anyone else get this? I've been gluten free for a couple months......will this go away?

I have this as well - i think it comes from a combination of too many carbohydrates (sugar/ etc) and a lower b12 even though your b12 came back "normal" you still may need more and/or an injection every once in a while. I've been told by my doc that I *don't need* b12, but when I stop for more than 6 weeks, I have more inflammation etc. The theory is when I'm gluten free for two years or so, I shouldn't need it by injection any more.. but until then I still get it.

The tingling can be diabetic neuropathy, b12 related, magnesium, zinc and/or related to high blood pressure, high levels of plaque/ cholesterol, inflammation generally or heavy metal deposits. So it could be a few things - if you go gluten free for 6 months and aren't noticing a difference, I'd get another opinion... but maybe in the meantime just focus on eating meat/veg/fruit diet and keep all the refined carbs until you know you are feeling better?

Amyleigh0007 Enthusiast

I've been getting pretty bad bilateral leg pain/weakness off and on for a long time. It seems to be worse in the morning, and is sometimes accompanied by tingling in my feet or hands. Is this something that is Celiac related? I've had my thyroid levels checked as many family members have Hashimotos , but i'm fine. I also had normal calcium, magnesium and b12 levels.......I do have a slight D deficiency.

Does anyone else get this? I've been gluten free for a couple months......will this go away?

I get leg pain when I eat gluten. It's more like restless leg symdrome. They ache (especially at night) and I feel like I must move them in order to feel better. I was glutenated last week and my legs have been bothering me for the past few nights.

nyctexangal Rookie

I get leg/hand pain/numbness if I don't take all my vitamins/minerals/calcium/and EFA's. I'm newly diagnosed Celaic, gluten-free for 7 weeks, and pain the in my hands/feet is getting less and less as I move forward and take the supplements. For me it has all been Celiac related. Hope you get to feeling better so soon!

newgfcali Rookie

I had bilateral peripheral neuropathy before going gluten free. (That's in fact why I went gluten free, hoping to make it better.) Neuropathy can be very painful, and can cause tingling in feet and hands as well. Ataxia can cause weakness in limbs. If you google "gluten neuropathy" and "gluten ataxia" you'll come up with some links on new research being done by Dr. Hadjivassiliou. He's researching the connection between gluten and nerve/brain disorders.

Maybe what you're experiencing is nerve damage caused by years of eating gluten. Nerves are very slow to heal, so perhaps in a few more months they'll start to get better.

masterjen Explorer

I was having significant problems with episodes of muscle weakness, although I've always taken a multi-vitamin, along with extra calcium and vit. D. The weakness was fairly constant, but I would have episodes where i would suddenly be almost unable to stand or if I was carrying something that wasn't necessarily that heavy I would have to put it down. Through a bit of online research I learned that potassium supplements can help with muscle weakness. Potassium levels in my blood were at normal early on after being diagnosed with celiac, but I've since learned that this doesn't mean the muscles necessarily have their needed supply of potassium in those with our condition. So, on a hunch, I decided to try the extra potassium. By day 4 of taking them, the episodes of weakness had improved by 50%, and now, about day 7, the episodes are much fewer and are about 75% less in intensity. The supplements I take are only 50 mg, plus I eat a banana every day (along with lots of other fruits and veggies), and I am now thinking of taking 2 supplements a day to see if taking more will completely reverse this annoying weakness.


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  • 2 weeks later...
ellie-lynn Newbie

I was having leg pain and occasional weakness before I got diagnosed -- some of it was bone pain (ache) and some was more neurological. My vitamin D was low/low-normal, and my rheumatologist put me on mega-doses of D. The bone pain started to go away, even before I knew about the celiac and went gluten-free. The gluten-free diet has resolved the weakness and neurological symptoms.

  • 1 year later...
Cora Newbie

I was just diagnosed with celiac via biopsy about a week ago. I haven't seen the nutritionist (scheduled for late Nov) and am trying to be gluten-free while waiting. Since dx, I have also started to have leg pain and severe knee pain, bad enough to side-track any exercise. Any recommendations for tests on vitamin levels the Drs should be running? I have already scheduled an appt with a Rheumotologist due to issues resembling Sjorgrens?

Cora, 51 and just learning about this...

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    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
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