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

Vitamins?


Tigercat17

Recommended Posts

Tigercat17 Enthusiast

Hi everyone,

I really hope someone help me figure this out. I've been gluten free for about a year and a half now. I was wondering if anyone else had reactions to vitamins that are supposed to be gluten free? To make a long story short, I just had a larparoscopy done for enlarged lymph nodes in my stomach a month ago and I really think it was all because of the vitamins I was taking. I also had dizziness, headaches, fatigue, stomach tenderness, lost weight, night sweats and low grade fevers daily. My symptoms started in Feb and continued for two months. The doctors had to rule out lymphoma and performed a lymph node biopsy. Luckily the path report came back reactive lymph node. So they sent me to a rheumatologist to check me for other autoimmune diseases since they supected that it was an autoimmune reaction. All the tests came back negative. I was always studying my food journal to look for any patterns that might point to my symptoms being a gluten issues but I really didn't see any until I noticed that on the days that I didn't take two of my vitamins, I didn't have a fever that day. And it was always at night that I got the fevers and I always take my vitamins in the evening.

I stopped all my vitamins a little over two weeks ago and I'm starting to feel so much better. The fevers and night sweats stopped the day after I stopped taking them and I'm slowly starting to get my energy back. And I'm not losing weight anymore. (Also, I didn't change anything else with my diet, I don't eat out much if at all and I always had a gluten free kitchen)

Here's what I was taking:

1.Slow Fe Iron-I started this on back up and so far I haven't had any reactions to them and I really need iron.

I really suspect it was one or two of these but I'm really too afraid to try them again to find out:

2.GNC vitamins Utra Womens Multi vitamins - I just started these in Jan so I really suspect one of these.

3.GNC fish oil triple strength

4. Vitafusion Gummy Vitamins Calcium 500 - I was taking these for the last ten months with no problems, but I noticed they did change their labeling and product in the last three months and these two bottles were the newer venison. I also seen a strong pattern with this brand so I really don't want to start these up again at all.

5. Vitafusion Gummy Vitamins C 250

I did just call the Vitafusion company to see if there were any changes made to the product, but they told me no, but I think the rep. herself really didn't know that information. Blah-Blah-Blah... They are going to send me a refund and I have to mail them the vitamins to them so they can check them.

I am really wondering if maybe I am just too sensitive to take vitamins even if they do say gluten free. I've tried others- Country Life, Megafoods, Members Mark, Giant Eagle Brand, and now GNC, Vitafusion and I always end up having reactions to them. These last three months were the worst. I'm really ready to give up on all vitamins but I do have ostopenia, anemia, vitamin D deficiency, so I really need to take iron, calcium and vitamin D.

Does anyone have any ideas or suggestions? Has anyone had similar problems with vitamins? I just feel like I'm the only one...

Thanks everyone!


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Nope, you are not the only one! ;)

I have deficiencies & osteopenia too and need to take them as well.

Okay, let's figure this out...step by step.

My first thought was the fish oil.

Do you have a problem with fish?

I had to hunt around and find ones that do not bother me. I found that some of the gummy ones have all kinds of sugars and citric acid and dyes in them. They made my tummy and mouth burn and I flushed hot and pink. Very strange.

Also, many vitamins contain SOY LECITHIN and that may be the culprit. It is for me.

Ones that are top- 8 allergen free are made by NOW and they are not very expensive and I have never had a reaction whatsoever. I use sublingual methyl B-12, D-3, calcium Citrate (with Mag and D--make sure they are the V caps--they are the only ones that are soy-free) and the B-complex from them. CHECK the LABELS, of course. They do not make a multi without soy though, so I use Pioneer ...in fact, I bought them from this website's gluten-free mall.

The fish oil without soy I use is Jarrow. It is hard to find a fish oil NOT infused with soy oil.

If you want to know where I buy them inexpensively, PM me and I will tell you. i think they have to edit it out if I put it here.

But, before you buy all these, I would say just try ONE and see if you react.

Hope this helps!

Tigercat17 Enthusiast

Hi Irish heart,

Thanks for all your help once again! I'm still have a hard time believing these vitamins made me that sick, but I know they were... It's really crazy. I know I'm feeling so much better since I stopped them, but I'm still not 100%. I feel like I got glutened for two months, but at the time I didn't know what it was since I usually have acid reflux. I wonder if it was just a small amount. But now my acid reflux is back. It started about a month ago and my hair is thinning again like it did when I got really sick before I was diagnosed with celiac.

I don't have any problems with fish, but I also wondered if it was the soy in the GNC fish oil and GNC Multi vitamins that I was causing all my reactions. I started them a month before I started having the night sweats and fevers. I'm not sure if it would take me that long to have a reaction to them? But it is interesting.

Also, though out this even though I felt like I was getting gluten, my Tissue Transglutaminase IgA blood work continued to stay normal. My GI doctor tested me twice during this time. But my sed rate was up to 66 last month and now it's 43- it's starting to slowly come down since I stopped the vitamins.

Do you think I could get cross containmented with gluten and still have normal IgA blood work? I wonder if I have to get a good amount of gluten now since my intestines are healed from the celiac? :unsure:

Thanks so much for the info about the Pioneer and the NOW vitamins. I did check them out. I was thinking about trying the GNC vitamins next week to see if I have a reaction again, but I'm not sure if I should try it or not. :unsure:

Thanks so much Irish Heart! You're such a big help! :)

BTW -I Love your avatar picture! I have two cats myself -I white & black one and a gray cat. They're my babies!

ravenwoodglass Mentor

I have a problem with soy in some vitamins that are gluten free. I started taking one for my hair and nails to help with hair loss that said gluten free. They really didn't seem to help at all. The new label on the vitamin stated it contained soy and I had missed that. I now take almost all NOW brand and Nature Made for Cod Liver Oil (that was the only one I could find without soy).

Glad to hear you are feeling better now that you have stopped the brands you were taking. You could try adding them back one at a time for a month or so and see if you react to an individual one but not some others.

IrishHeart Veteran

Do you think I could get cross containmented with gluten and still have normal IgA blood work? I wonder if I have to get a good amount of gluten now since my intestines are healed from the celiac? :unsure:

I am not sure. Perhaps someone with more knowledge regarding testing would be able to answer this question for you.

ravenwoodglass Mentor

Do you think I could get cross containmented with gluten and still have normal IgA blood work? I wonder if I have to get a good amount of gluten now since my intestines are healed from the celiac? :unsure:

Since we have to heavily gluten load for at least a couple of months for tests to have a chance to be positive after we have been gluten free, and some of us test negative even on a full gluten diet before diagnosis then I do think that you could be getting CC'd and still have normal blood tests.

IrishHeart Veteran

Since we have to heavily gluten load for at least a couple of months for tests to have a chance to be positive after we have been gluten free, and some of us test negative even on a full gluten diet before diagnosis then I do think that you could be getting CC'd and still have normal blood tests.

Makes sense to me! ;) I knew Raven could help us clarify things. :)

Just try adding one vitamin back in at a time --wait a week in between---and see how you do. Sometimes, too many supps/vits at once can complicate the method of isolating what's causing what.

Good luck, hon!


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



Celiac.com Sponsor (A8-M):



Chad Sines Rising Star

Hi Irish heart,

Thanks for all your help once again! I'm still have a hard time believing these vitamins made me that sick, but I know they were... It's really crazy. I know I'm feeling so much better since I stopped them, but I'm still not 100%. I feel like I got glutened for two months, but at the time I didn't know what it was since I usually have acid reflux. I wonder if it was just a small amount. But now my acid reflux is back. It started about a month ago and my hair is thinning again like it did when I got really sick before I was diagnosed with celiac.

I don't have any problems with fish, but I also wondered if it was the soy in the GNC fish oil and GNC Multi vitamins that I was causing all my reactions. I started them a month before I started having the night sweats and fevers. I'm not sure if it would take me that long to have a reaction to them? But it is interesting.

Also, though out this even though I felt like I was getting gluten, my Tissue Transglutaminase IgA blood work continued to stay normal. My GI doctor tested me twice during this time. But my sed rate was up to 66 last month and now it's 43- it's starting to slowly come down since I stopped the vitamins.

Do you think I could get cross containmented with gluten and still have normal IgA blood work? I wonder if I have to get a good amount of gluten now since my intestines are healed from the celiac? :unsure:

Thanks so much for the info about the Pioneer and the NOW vitamins. I did check them out. I was thinking about trying the GNC vitamins next week to see if I have a reaction again, but I'm not sure if I should try it or not. :unsure:

Thanks so much Irish Heart! You're such a big help! :)

BTW -I Love your avatar picture! I have two cats myself -I white & black one and a gray cat. They're my babies!

What struck me in your reply is the reflux vs celiac symptoms. I do think for a lot of us this is a point of confusion when it comes to figuring ourselves out. Many of my reflux symptoms feel like celiac and vice versa. And as we all know, too much acid reduction from meds causes all sorts of issues.

Tigercat17 Enthusiast

Thanks everyone for your replies! It's very informative and it helped a lot!

Thank-you Ravenwoodglass! This does make a lot of sense to me! I do really think this was gluten related. It would explain all of my symptoms. I'm really not sure if it was soy or not since I'm still eating small amounts of soy and I'm still getting better. It's been slowly, but I think if I was getting CC for two months, it's going to take me about 1-2 months to be 100%.

My doctor even called off the capsule endoscopy for me since I'm feeling better. I think he suspects, too, that this was my celiac disease reacting to CC from the vitamins.I haven't talked to him since, but I'm due to see him again in two weeks, so I'll have a lot of questions for him.

I also think my symptoms for reacting to CC are changing since I've been gluten free for about 20 months now. I think the only good thing that came out of this is at least now I know that if I'm ever feeling dizzy, headaches, tried, chills and a fever that I'll have to look for CC from gluten.

I think I will try the GNC vitamins first since I really suspect it was the Vitafusion. I'll let you all know how it goes and I won't add anything else for a month. :)

Thanks Chad - I'm not taking anything at all for my acid reflux. It's very mild, but I do notice that my throat gets a little sore and it's sometimes will be uncomfortable to talk. The only meds I take are Levoxyl for my thyroid. I was taking Percocet for two weeks after the surgery. I'm not sure not sure if that would cause some acid reflux or not.

Thanks again everyone! :)

Chad Sines Rising Star

Thanks everyone for your replies! It's very informative and it helped a lot!

Thank-you Ravenwoodglass! This does make a lot of sense to me! I do really think this was gluten related. It would explain all of my symptoms. I'm really not sure if it was soy or not since I'm still eating small amounts of soy and I'm still getting better. It's been slowly, but I think if I was getting CC for two months, it's going to take me about 1-2 months to be 100%.

My doctor even called off the capsule endoscopy for me since I'm feeling better. I think he suspects, too, that this was my celiac disease reacting to CC from the vitamins.I haven't talked to him since, but I'm due to see him again in two weeks, so I'll have a lot of questions for him.

I also think my symptoms for reacting to CC are changing since I've been gluten free for about 20 months now. I think the only good thing that came out of this is at least now I know that if I'm ever feeling dizzy, headaches, tried, chills and a fever that I'll have to look for CC from gluten.

I think I will try the GNC vitamins first since I really suspect it was the Vitafusion. I'll let you all know how it goes and I won't add anything else for a month. :)

Thanks Chad - I'm not taking anything at all for my acid reflux. It's very mild, but I do notice that my throat gets a little sore and it's sometimes will be uncomfortable to talk. The only meds I take are Levoxyl for my thyroid. I was taking Percocet for two weeks after the surgery. I'm not sure not sure if that would cause some acid reflux or not.

Thanks again everyone! :)

I really think our GI systems are so wonky that many issues are so multifaceted that it is nearly impossible to figure out. Reducing gluten reduces many issues but maybe a dairy issue is causing nausea and then the soy and then the corn. So in the end we get no complete relief from anything so it is a constant struggle. So nice that there are a group of people who understand these issues.

GFinDC Veteran

I've had problems with vitamins. Especially the multi-vitamins. I have tried various brands that are supposed to be GFCFSF but none has ever worked for me. I have some of the Pioneer multi-vit too, but don't take them anymore. What I do take is calcium, D and zinc pills. And a B-12 pill sometimes, or a B-complex. I don't take any vitamin pills every day. And the ones I take are not grandiose fix everything pills with everything but the kitchen sink in them. Those kind always cause me problems. I suspect the retinal palmitate (vit-A) in the Pioneer multi-vits is a problem but that is just a think on my part. It doesn't really matter since I get sick if I take them, so I don't take them. When I have done elimination diets in the past that is always one of the first things I have eliminated, vitamin pills. When I went off soy completely it took a couple weeks to start feeling better, and a month and a half to really feel pretty ok. Some of these things can take some time.

etta694 Explorer

I was going to ask about the source of the vit E in the multi but I guess if they say gluten free... then that shouldn't be an issue.

Cattknap Rookie

I don't have any sage advice other than this general statement - most people take too many vitamins. Based on doctor and nutritionist advice I take only vitamin E, C, calcium, D, and iron complex - that is it. Both my doctor and my nutritionist advised me only to take those supplements that my blood tests show I need and both stated that many people take too many unneeded vitamins.

IrishHeart Veteran

I was going to ask about the source of the vit E in the multi but I guess if they say gluten free... then that shouldn't be an issue.

Vit E "mixed tocopherols" are often derived from SOYBEAN OIL, so it needs to state they are SOY -free for me as well.

IrishHeart Veteran

I've had problems with vitamins. Especially the multi-vitamins. I have tried various brands that are supposed to be GFCFSF but none has ever worked for me. I have some of the Pioneer multi-vit too, but don't take them anymore. What I do take is calcium, D and zinc pills. And a B-12 pill sometimes, or a B-complex. I don't take any vitamin pills every day. And the ones I take are not grandiose fix everything pills with everything but the kitchen sink in them. Those kind always cause me problems. I suspect the retinal palmitate (vit-A) in the Pioneer multi-vits is a problem but that is just a think on my part. It doesn't really matter since I get sick if I take them, so I don't take them. When I have done elimination diets in the past that is always one of the first things I have eliminated, vitamin pills. When I went off soy completely it took a couple weeks to start feeling better, and a month and a half to really feel pretty ok. Some of these things can take some time.

that's interesting!...what do you think is the problem with Vitamin A for you? just makes you feel ill? I am just curious as I too have to be cautious with what I take...and I researched Pioneer brand to make sure it was okay for me. You've got me thinking now.... :unsure:

IrishHeart Veteran

I don't have any sage advice other than this general statement - most people take too many vitamins. Based on doctor and nutritionist advice I take only vitamin E, C, calcium, D, and iron complex - that is it. Both my doctor and my nutritionist advised me only to take those supplements that my blood tests show I need and both stated that many people take too many unneeded vitamins.

I agree completely!!!

I only take the ones I need too, based on what's deficient in me (Folic acid (B9), D-3, cal/ mag-for osteopenia, and an anti-oxidant formula for E,C and A)

I took so many supplements during the last 3 years, on advice from others, and think it made me feel WORSE! My gut wasn't absorbing anything anyway.

I might as well have lit that money on fire for all the good they did. :blink:

In the end, a healed gut will solve most vitamin deficiencies anyway. :)

Marilyn R Community Regular

I've tried a number of calcium supplements. My doctors kept telling me that calcium couldn't make me sick! :P But they did!

I've been doing fine with Citracal with D, even though this is the (cover their rear-end) response they sent me when I inquired about gluten-free/SF/DF status:

"Thank you for taking the time to contact Bayer HealthCare. We appreciate your

interest in Citracal.

We do not add any gluten to our products. However, we cannot guarantee that our

products are 100% gluten-free as this product is produced in a facility that

manufactures and/or packages other items which may contain gluten.

Milk/Dairy is not used in our formula. Furthermore, our ingredient suppliers

have confirmed that none of the ingredients produced for use in this formula are

derived from milk/dairy.

Regarding Soy, our Bone Density Builder formula contains Genistein, which is

naturally derived from soy. It is synthetically made in this formula, so it is

not called out as an allergen on the label. If you have an allergy to Soy,

please speak with your physician prior to taking the Bone Density Builder

formula.

The phytosterols in the Heart Health formula are derived from highly refined

soybean oil, which does not contain the soy protein that is allergenic. As

such, it is not called out as an allergen on the label.

Soybean is not used in our other formulas. Furthermore, our ingredient suppliers

have confirmed that none of the ingredients produced for use in these formulas

are derived from soybean. The Vitamin D3 does contain highly refined soybean

oil, which FDA does not require to be labeled as an allergen under FALCPA. (Food

Allergen Labeling and Consumer Protection Act).

Comments such as your own help us meet the growing needs of our consumers. I

certainly will share them with our Regulatory, Medical and Marketing departments

for consideration.

In appreciation of your interest, we will be sending you a coupon booklet via

U.S. Mail. You can expect to receive your coupons in the next 7-10 business

days. If I may be of further assistance, please feel free to contact me."

I find the statements about highly refined soybean oil interesting. A dietician friend of mine showed me an article that all commercially available Orange Juice contains soy, but since it is used with standard mfg procedures and is highly refined, it doesn't need to be listed as an allergin on the label.

IrishHeart Veteran

I find the statements about highly refined soybean oil interesting. A dietician friend of mine showed me an article that all commercially available Orange Juice contains soy, but since it is used with standard mfg procedures and is highly refined, it doesn't need to be listed as an allergin on the label.

Really...I'd like to see that article...what the heck is soybean oil doing in OJ??!! :blink:

GlutenFreeManna Rising Star

Hi everyone,

I really hope someone help me figure this out. I've been gluten free for about a year and a half now. I was wondering if anyone else had reactions to vitamins that are supposed to be gluten free? To make a long story short, I just had a larparoscopy done for enlarged lymph nodes in my stomach a month ago and I really think it was all because of the vitamins I was taking. I also had dizziness, headaches, fatigue, stomach tenderness, lost weight, night sweats and low grade fevers daily. My symptoms started in Feb and continued for two months. The doctors had to rule out lymphoma and performed a lymph node biopsy. Luckily the path report came back reactive lymph node. So they sent me to a rheumatologist to check me for other autoimmune diseases since they supected that it was an autoimmune reaction. All the tests came back negative. I was always studying my food journal to look for any patterns that might point to my symptoms being a gluten issues but I really didn't see any until I noticed that on the days that I didn't take two of my vitamins, I didn't have a fever that day. And it was always at night that I got the fevers and I always take my vitamins in the evening.

I stopped all my vitamins a little over two weeks ago and I'm starting to feel so much better. The fevers and night sweats stopped the day after I stopped taking them and I'm slowly starting to get my energy back. And I'm not losing weight anymore. (Also, I didn't change anything else with my diet, I don't eat out much if at all and I always had a gluten free kitchen)

Here's what I was taking:

1.Slow Fe Iron-I started this on back up and so far I haven't had any reactions to them and I really need iron.

I really suspect it was one or two of these but I'm really too afraid to try them again to find out:

2.GNC vitamins Utra Womens Multi vitamins - I just started these in Jan so I really suspect one of these.

3.GNC fish oil triple strength

4. Vitafusion Gummy Vitamins Calcium 500 - I was taking these for the last ten months with no problems, but I noticed they did change their labeling and product in the last three months and these two bottles were the newer venison. I also seen a strong pattern with this brand so I really don't want to start these up again at all.

5. Vitafusion Gummy Vitamins C 250

I did just call the Vitafusion company to see if there were any changes made to the product, but they told me no, but I think the rep. herself really didn't know that information. Blah-Blah-Blah... They are going to send me a refund and I have to mail them the vitamins to them so they can check them.

I am really wondering if maybe I am just too sensitive to take vitamins even if they do say gluten free. I've tried others- Country Life, Megafoods, Members Mark, Giant Eagle Brand, and now GNC, Vitafusion and I always end up having reactions to them. These last three months were the worst. I'm really ready to give up on all vitamins but I do have ostopenia, anemia, vitamin D deficiency, so I really need to take iron, calcium and vitamin D.

Does anyone have any ideas or suggestions? Has anyone had similar problems with vitamins? I just feel like I'm the only one...

Thanks everyone!

Soy affects my thyroid and gives me some of the symptoms you listed (unexplained fever, fatigue, etc). I was going to ask if you had your thyroid checked but then I saw that your signature said you had it taken out. Is it possible that these vitamins are interacting with whatever you are taking for your thyroid hormone replacement? You can check possible drug interactions (including vitamin and drug interactions) on drugs.com

SoyBoy Rookie

I react to GNC products and all fish oils I have tried as well.

I now avoid any supplement with tocopherols (or lecithin of course).

GFinDC Veteran

that's interesting!...what do you think is the problem with Vitamin A for you? just makes you feel ill? I am just curious as I too have to be cautious with what I take...and I researched Pioneer brand to make sure it was okay for me. You've got me thinking now.... :unsure:

I am not really sure IH, just guessing. I get some digestive upset with their multi-vits. It is not gluten, it's a different reaction. The vitamin A has a bad rep for causing skin cancer, so I don't think it is good to take it internally. But that may not be what bothers me in them. They are like most multi-vits IMHO, too many ingredients to isolate the problem. That is why I don't take those kinds of pills anymore.

IrishHeart Veteran

I am not really sure IH, just guessing. I get some digestive upset with their multi-vits. It is not gluten, it's a different reaction. The vitamin A has a bad rep for causing skin cancer, so I don't think it is good to take it internally. But that may not be what bothers me in them. They are like most multi-vits IMHO, too many ingredients to isolate the problem. That is why I don't take those kinds of pills anymore.

I agree---the more ingredients, the more trouble, I find! :huh:

T.H. Community Regular

One thing that helped me eliminate many vitamins as a possibility was to change what I said when I called them. I used to just ask if they were gluten free. Now, I ask if they are gluten free, and then I ask if they test for gluten levels, and whether they test every batch, or periodically.

About a third of the time I asked questions in this manner, I got a spiel about how they don't have to test because they KNOW their product is gluten free: they don't add any gluten ingredients.

That means it's gluten free, right? :rolleyes: Jeesh. Ever heard of gluten cc, Mr. vitamin company?

That's kind of like my saying my house is dust free because I don't add any dust to it. :D

IrishHeart Veteran

That's kind of like my saying my house is dust free because I don't add any dust to it. :D

Good one! :D :D

Marilyn R Community Regular

Good one! :D :D

Sorry, Irish, I'm not going to be able to come up with a link for that article. It was written by a registered dietician, posted on a RD website. I had one copy of the article (which was printed by my friend) and gave it to another friend that has Graves Disease. That was a couple of months ago. The letter from Bayer reminded me about that article.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    2. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    3. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Issues before diagnosis

    4. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

    5. - knitty kitty replied to EndlessSummer's topic in Food Intolerance & Leaky Gut
      2

      Dizziness after eating green beans?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,691
    • Most Online (within 30 mins)
      7,748

    4Nic8ion
    Newest Member
    4Nic8ion
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
    • trents
      Welcome to celiac.com, @EndlessSummer! Do you react to all vegetables or just specific kinds or families of them? What you describe with green beans sounds like it has an anaphylaxis component. Like you, walnuts are a problem for me. They will often give me a scratchy throat so I try to avoid them. Does it matter if the vegies are raw or will-cooked in how you react to them?
×
×
  • 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.