Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Magnesium


bny06

Recommended Posts

bny06 Apprentice

So i'm awaiting my biopsy results which I should get this week, however I have been wracking my brain trying to think why am I overall feeling better (3.5 weeks or so on gluten free diet) but my muscles seem weaker when I use them a lot.. then I started thinking, the only day that I have felt better as far as my muscle weakness/twitching goes was the day I got scoped- after drinking Magnesium prep! Maybe I finally figured out what is causing this!! Anyone take a magnesium supplement, and if so what kind and how much do you take? can you take too much? Thanks so much for ANY advice!!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



AVR1962 Collaborator

Yep, we generally are low in the magnesium department. You can take supplements and may have to to start with until you can get your diet figured out. Look up magnesium rich fruits and foods and try to incorporate them into your diet and you'll find the twitches will go away completely!

gfreelady Newbie

Vitamin deficiancy is an issue with all of us. A one a day should be fine but I also take magnesium. My dr told me that without enough of it, you dont poop

bny06 Apprentice

Thanks yall!! I started taking magnesium malate supplements two days ago and I have to say that my muscle twitches do seem to be better already, though my muscle weakness in my hands is defintely not changed, which freaks me out!!!! gfreelady- I wish constipation was my issue! I'm not quite 4 weeks out on my gluten free diet and unfortuntely have to use the facilities up to 8-10 times a day ughh..so i want the muscle stuff gone like yesterday, but I don't want it to cause me to have to use the restroom anymore than I already am thats for sure!!

mushroom Proficient

If I don't take magnesium supplements I always end up with calf cramps.

Lori2 Contributor

If I don't take magnesium supplements I always end up with calf cramps.

Me too. Without a magnesium supplement I get leg cramps and twitches. But if I take enough of a regular magnesium supplement to stop the cramps, I get diarrhea--most magnesium supplements are 10% absorbed. I found a magnesium product that is advertised to be 99% absorbable. It works for me, I can use as much as I need to stop my cramps without any diarrhea problems. Google Angstrom Minerals.

Cinnamongirl Rookie

Ive been taking Cal-Citrate for several years which contains both calcium and magnesium and it has an overall relaxing effect on me. It helps keep me regular and calms me down when I feel anxious.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



AVR1962 Collaborator

Thanks yall!! I started taking magnesium malate supplements two days ago and I have to say that my muscle twitches do seem to be better already, though my muscle weakness in my hands is defintely not changed, which freaks me out!!!! gfreelady- I wish constipation was my issue! I'm not quite 4 weeks out on my gluten free diet and unfortuntely have to use the facilities up to 8-10 times a day ughh..so i want the muscle stuff gone like yesterday, but I don't want it to cause me to have to use the restroom anymore than I already am thats for sure!!

BNY06, at 4 weeks on a gluten-free diet and still making 8-10 trips to the bathroom, I am wondering if it is not just gluten effecting you. If your diet has been tight you might want to explore going off dairy as well just to see if it too could be causing you issues.

bny06 Apprentice

thanks yall... avr- I have stayed off dairy for about three weeks now- I realized after eating a huge bowl of ice cream a couple of times about 4 weeks ago to try and ingest calories and then my tummy getting REALLY mad at me, that diary must also be an issue! Do the bathroom trips usually slow by almost 4 weeks?? I have just figured I had so much damage that it would take more time.. but I'm SOO ready for more improvement! I am overall feeling better (with the exception of the worsening hand weakness- again freaking me out completely) I am not feeling like my blood sugars are tanking throughout the day like they were, overall my genearlized weakness and icky feeling feels better... it's defintely starting to mentally wear me down a little that My hnads aren't getting better

color-me-confused Explorer

For some reason if I take a magnesium tablet (Mg oxide, I think it is) at night I sleep very deeply.

Reba32 Rookie

magnesium is a relaxant. It can help with the twitches, but too much can cause diarrhea, so be careful.

Potassium can also help with the twitches. Half an avocado should help.

bny06 Apprentice

thanks!!! Yea, i was taking too much and unfortuantely was causing more GI issues.. but did help the muscles.. I eat at least an avacado a day or so.. and about three bananas ha! Sooo.. i'll ask my dr if they can rx any magnesium that doesn't cause any GI upset, i'm not a fan of the twitches, though I can totally live with it of course!

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,553
    • Most Online (within 30 mins)
      7,748

    Jennifer CCC
    Newest Member
    Jennifer CCC
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.