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

What Nutrients/vitamins Am I Lacking?


Thewiseguy

Recommended Posts

Thewiseguy Newbie

So I am not celiac but I have a slight gluten intolerance. I've been gluten-free for about 8 months and I've been trying to find information on which vitamins and or nutrients are required or recommended as a supplement to my gluten-free diet. Any info is appreciated.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Welcome to the forum, wiseguy.

It is always best to check for nutrient deficiencies before supplementing on a large scale such as some of us have to do. However, if you are not celiac and have no intestinal damage (were you tested by biopsy?) you may not be grossly deficient in the usual nutrients associated with celiac intestinal damage like B12, D, iron/ferritin.

You can either get tested for your current levels or take a good gluten free multivitamin and multimineral to cover all the bases, That will you will not O.D. on anything.

Juliebove Rising Star

Here's what I do! Go here:

Open Original Shared Link

Get youself a free account. Then enter in everything you have had to eat and drink in a day, including water. You will need to know your portion sizes so you may have to weigh and measure what you eat.

Check each day to see what nutrients you took in and where you are lacking. I do not personally believe that it is possible to eat a totally balance diet each and every day. But... You can see patterns there. For instance, I am always lacking in vitamin E and usually in the B vitamins, often B12 because I don't eat a lot of meat.

Now keep in mind that this will only show you what is lacking from what you eat. You could have other issues. For instance, I take Metformin, a diabetes medicine that causes the body to lose vitamin B12. And some sources say that diabetes in and of itself causes the body not to metabolize B vitamins properly. So my Endocrinologist had me take more B12. I already take a B Complex supplement and a multiple vitamin. And I am now taking extra B1 and B5.

I have psoriasis and have been suffering with really itchy, dry, thick skin on my knees lately. I read that taking extra vitamin C can help with this. Vitamin C is one vitamin that it doesn't hurt to take extra of because you will pee it away. Note that I am not recommending mega doses of anything. That in and of itself is controversial and can be dangerous for some vitamins because they can build up in the body to toxic levels. Vitamin C can also boost your immunity. I also gave extra to my daughter who caught a cold. She got over her cold more quickly than she usually does and my skin seems not as dry.

I do take a lot of other vitamins, herbs and supplements based on various things. I read a lot of books on nutrition and holistic type medicine. If I see something that looks like it will help one of my various medical conditions, I will try it for two months. If I see no improvement, I will stop taking it.

You can also have blood tests done at the Dr. for various things like vitamin D (which I also take more of per my Dr.), vitamin B12, potassium, magnesium, etc. If you are having any other medical problems, those could cause deficiencies. When I was diagnosed with diabetes, I had the big D for many months. This caused a potassium deficieny.

It probably wouldn't hurt to take a multi vitamin. Just check the ingredients first. The one I give my daughter has fish in it and I am intolerant to fish! But beyond that, you don't want to start taking things unless a Dr. tells you to or you see a reason for it. Like a medical condition that could be helped by taking extra or if you find your diet to be lacking in things.

CeliacShack Rookie

Now keep in mind that this will only show you what is lacking from what you eat. You could have other issues. For instance, I take Metformin, a diabetes medicine that causes the body to lose vitamin B12. And some sources say that diabetes in and of itself causes the body not to metabolize B vitamins properly. So my Endocrinologist had me take more B12. I already take a B Complex supplement and a multiple vitamin. And I am now taking extra B1 and B5.

I also take Metformin, and have never heard that, thanks for the info! I am not diabetic, I take it for PCOS (Polycycstic Ovarian Syndrome). All the info I am discovering on these forums is convincing me to call my doc and get in for addtional testing.

archaeo in FL Apprentice

thewiseguy, Juliebove's tool looks like it may be helpful to you - I'd try to look at what you consume over several weeks, though.

The reason many of us take so many vitamins and supplements isn't because we are missing something from eating gluten-free, necessarily, it's because we aren't absorbing the nutrients from what we do eat.

That said, a lot of wheat-based products, especially cereals and breads, are supplemented, at least in the U.S. (think Total cereal), so by removing those products we are also removing some of those supplements.

You might do just as well with a good multivitamin.

Of course, if you can get to a GP and ask for a vitamin panel that'd be best, so you can target any deficiencies with a supplement but more importantly by tweaking your diet.

mommida Enthusiast

I always suggest Biotin. High doses can not cause a "toxic" level. It would naturally be in food, in animal LIVER. I don't know about you, but I don't like liver and won't eat it.

Vitamin B12 does not have a known toxic level. Most Americans are assumend to have B defiencies.

You can start with a daily multivitamin and probiotics. Always do some research on what you are planning to take. I would even double check if a doctor prescribed a vitamin for me.

My dad's cancer was diagnosed because he was at a toxic level of Calcium. (Not pretty, and he was hours away from death. It had the symptoms of a stroke.)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,898
    • Most Online (within 30 mins)
      7,748

    MLucia
    Newest Member
    MLucia
    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

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.