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

Very Low Vitamin D!


Rockgurl

Recommended Posts

Rockgurl Rookie

Hi folks. I am new and this is virtually my first post here. I got my celiac panel results today and as I suspected they were "within normal limits" but my Vitamin D came back very low. I have been avoiding wheat for quite a while because I also have Endometriosis and my nutritionist told me that wheat can effect the pain of that disease so I have hardly touched it for about a year. I haven't been gluten-free though, so I'm mildly surprised that the lab results were negative. I've not eaten much with gluten in it but I haven't really paid attention to labels and have been eating out with sensible choices.

However, I am still very much having symptoms of Celiac Disease...the bloating, constipation, nausea, heartburn etc. The fact that I have low Vit D is quite concerning to me as it would appear to suggest malabsorption at a serious rate. I have been referred to a gastroenterologist but I'm not sure if he'll want to do an endoscopy based on the lab results but I sat down and wrote down my symptoms and got as far as 19! :( I am considering doing the gene test through Enterolab. I decided to start eating wheat again in order to take the lab test but I only lasted 4 days because it made me so ill. I don't think I can do it for a month or two in order to get the endoscopy. I was very positive to the gluten challenge. I would just like to have a diagnosis but in my heart I'm pretty sure I'm celiac because all the pieces are beginning to fit. Now I realize that all my nausea and other symptoms is indicative of malabsorption and I couldn't possibly eat healthier than I do. I eat fresh food everyday, goats yoghurt, cheeses, fruits and vegetables, organic meats. How can I be deficient in Vit D? I know gluten free is the way to go and I'm starting the change already but I just wish I could tolerate gluten long enough to get a diagnosis!


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



Celiac.com Sponsor (A8-M):



missy'smom Collaborator

I just found out about and started taking a liquid vit. D supplement that costs around $15-$20 for a year's supply(if you take 1,000 IU a day) depending on where you get it. Carlson's is the brand. They also have a higher dose available. It's a drop so no pills to swallow!

mushroom Proficient

You're between a rock and a hard place on diagnosis. :( Some of us just have to be content with self-diagnosis, knowing what we know and what the doctors don't know. :P Some doctors will give a diagnosis based upon positive response to the diet and to the gluten challenge (if you have a history of GI symptoms with that doctor).

Your low Vitamin D is very indicative to me. Before either of us knew we were gluten intolerant (neither of us have a diagnosis) Dh and I had DEXA scans which showed a remarkable drop in bone density over a fairly short time for both of us. Unbeknown to me, this was a good warning to go gluten free. I did not know at the time about the connection between celiac and Vit D--in fact knew very little about celiac, period. When i decided to stop eating gluten (to see if it made any diffference to my RA) Dh decided to go along with it too since it would be easier and he had some GI issues. It was only after that, and finding this forum, that I started putting two and two together and we both got tested for nutrient deficiencies (both had multiple including Vit D).

If you have 19 symptoms that could be associated with celiac disease, I would say go with your gut instincts--you probably have it. Do you think he would order a bone density scan??

Rockgurl Rookie
You're between a rock and a hard place on diagnosis. :( Some of us just have to be content with self-diagnosis, knowing what we know and what the doctors don't know. :P Some doctors will give a diagnosis based upon positive response to the diet and to the gluten challenge (if you have a history of GI symptoms with that doctor).

Your low Vitamin D is very indicative to me. Before either of us knew we were gluten intolerant (neither of us have a diagnosis) Dh and I had DEXA scans which showed a remarkable drop in bone density over a fairly short time for both of us. Unbeknown to me, this was a good warning to go gluten free. I did not know at the time about the connection between celiac and Vit D--in fact knew very little about celiac, period. When i decided to stop eating gluten (to see if it made any diffference to my RA) Dh decided to go along with it too since it would be easier and he had some GI issues. It was only after that, and finding this forum, that I started putting two and two together and we both got tested for nutrient deficiencies (both had multiple including Vit D).

If you have 19 symptoms that could be associated with celiac disease, I would say go with your gut instincts--you probably have it. Do you think he would order a bone density scan??

Hi Mushroom and thanks for your reply. Yes, I think my doctor will allow further tests. She knows and understands that I am on the ball medically speaking. She's great. It was actually her that suggested it was celiac disease. I haven't yet spoken with her personally about the blood results but I think I will make another appointment to speak with her. She's written a prescription for strong vit D supplementation but if I'm not absorbing anything then I can assume it won't work. I know this because for the past year I've been taking a Calcium/Mag/Vit D supplement that has 400iu of Vit D, a multivitamin that has a further 100iu plus a Cod Liver Oil capsule! That equates to about 400% RDA! Obviously I'm wasting my money because I'm not getting any of it.

I agree with you about it being indicative. My strong gut feeling was that the low Vit D was more relevant than the normal anti body result considering I've been on a low gluten diet for a year or so. As we know, low gluten is not enough...it has to be NO gluten! I immediately knew when I heard about that vit D result. I will push to get what I can but otherwise I will be tempted to self-diagnose and call myself celiac from now on. Thanks for listening. This is a real learning curve. For so long I put my declining health down to Endometriosis and all the while it was a totally different autoimmune disease!

Back in January I herniated a disk in my neck. Now I'm wondering if this has anything to do with my low Vit D levels. Hmmm....

Foxfire62 Newbie
Hi folks. I am new and this is virtually my first post here. I got my celiac panel results today and as I suspected they were "within normal limits" but my Vitamin D came back very low. I have been avoiding wheat for quite a while because I also have Endometriosis and my nutritionist told me that wheat can effect the pain of that disease so I have hardly touched it for about a year. I haven't been gluten-free though, so I'm mildly surprised that the lab results were negative. I've not eaten much with gluten in it but I haven't really paid attention to labels and have been eating out with sensible choices.

However, I am still very much having symptoms of Celiac Disease...the bloating, constipation, nausea, heartburn etc. The fact that I have low Vit D is quite concerning to me as it would appear to suggest malabsorption at a serious rate. I have been referred to a gastroenterologist but I'm not sure if he'll want to do an endoscopy based on the lab results but I sat down and wrote down my symptoms and got as far as 19! :( I am considering doing the gene test through Enterolab. I decided to start eating wheat again in order to take the lab test but I only lasted 4 days because it made me so ill. I don't think I can do it for a month or two in order to get the endoscopy. I was very positive to the gluten challenge. I would just like to have a diagnosis but in my heart I'm pretty sure I'm celiac because all the pieces are beginning to fit. Now I realize that all my nausea and other symptoms is indicative of malabsorption and I couldn't possibly eat healthier than I do. I eat fresh food everyday, goats yoghurt, cheeses, fruits and vegetables, organic meats. How can I be deficient in Vit D? I know gluten free is the way to go and I'm starting the change already but I just wish I could tolerate gluten long enough to get a diagnosis!

You said you had a panel, and I'm assuming that's a blood panel. The only way to be 100% sure you do or don't have celiac disease is to get scoped and have a biopsy of your intestines. If you have not done this, I would recommend getting an appointment set up and get tested. That would require ingesting gluten. Is there any kind of gluten-containing food that you tolerate better than others? You might want to experiment with that. Otherwise, I would recommend you stay completely away from any gluten and start taking supplements.

Rockgurl Rookie
I just found out about and started taking a liquid vit. D supplement that costs around $15-$20 for a year's supply(if you take 1,000 IU a day) depending on where you get it. Carlson's is the brand. They also have a higher dose available. It's a drop so no pills to swallow!

Thanks. That sounds great! I'll look into it. I hope I can absorb it!

Rockgurl Rookie
You said you had a panel, and I'm assuming that's a blood panel. The only way to be 100% sure you do or don't have celiac disease is to get scoped and have a biopsy of your intestines. If you have not done this, I would recommend getting an appointment set up and get tested. That would require ingesting gluten. Is there any kind of gluten-containing food that you tolerate better than others? You might want to experiment with that. Otherwise, I would recommend you stay completely away from any gluten and start taking supplements.

Right now I am feeling so sick that I dare not return to gluten. I'm not even absorbing healthy food and I don't think I could tolerate a few more months of illness. I am getting weaker and more fatigued all the time. I am not sure if my doctor or my insurance company will authorize an endoscopy with a negative blood panel. I have asked for copies of the actual lab values so I can interpret them. I will do it if they allow but I have been gluten light for a long time. However, due to my symptoms and obvious malabsorption, I presume there is quite a bit of damage to my intestine. I have been referred to a gastroenterologist.


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



Celiac.com Sponsor (A8-M):



Roda Rising Star
Hi Mushroom and thanks for your reply. Yes, I think my doctor will allow further tests. She knows and understands that I am on the ball medically speaking. She's great. It was actually her that suggested it was celiac disease. I haven't yet spoken with her personally about the blood results but I think I will make another appointment to speak with her. She's written a prescription for strong vit D supplementation but if I'm not absorbing anything then I can assume it won't work. I know this because for the past year I've been taking a Calcium/Mag/Vit D supplement that has 400iu of Vit D, a multivitamin that has a further 100iu plus a Cod Liver Oil capsule! That equates to about 400% RDA! Obviously I'm wasting my money because I'm not getting any of it.

I agree with you about it being indicative. My strong gut feeling was that the low Vit D was more relevant than the normal anti body result considering I've been on a low gluten diet for a year or so. As we know, low gluten is not enough...it has to be NO gluten! I immediately knew when I heard about that vit D result. I will push to get what I can but otherwise I will be tempted to self-diagnose and call myself celiac from now on. Thanks for listening. This is a real learning curve. For so long I put my declining health down to Endometriosis and all the while it was a totally different autoimmune disease!

Back in January I herniated a disk in my neck. Now I'm wondering if this has anything to do with my low Vit D levels. Hmmm....

I personally would follow through with taking the rx vitamin D. It has done miracles for me. I have been taking 50,000 iu rx per week since January of this year. Within about 3 weeks to a month I started feeling great. From what I can gather you have been taking roughly 700 iu a day of vit D. Thats not nearly enough depending how low your level was. There have been numerous studies that the rda for vitamin D is way too low. The Amerian Academy of Pediatrics just upped the rda of vit d for babies and kids to 400 iu/day and there was a study in Brittain that even suggested that this might still be too low for them. You need to build up the stores and then maintain. Once your intestines heal from going gluten free your body will absorb it. You just need to take more and give the diet a go. I am going to finish my high dose for another 6 weeks or so when my pills run out and then supplement with around 2000 iu/day. My level was at 17 before I started supplementing and now it is around 47. I still need to get up some more.

Here are a couple of links for you to look at:

Open Original Shared Link

Open Original Shared Link

and this thread will be helpful to read. There is still alot of misinformation on vit D2 vs. D3. The previous article states that D2 is just as effective as D3.

https://www.celiac.com/gluten-free/index.ph...=56636&st=0

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. - Scott Adams replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Bob red mill gluten free oats

    2. - knitty kitty replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    3. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    4. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    5. - Jsingh replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

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

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

    LMGarrison
    Newest Member
    LMGarrison
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
      @SamAlvi, It's common with anemia to have a lower tTg IgA antibodies than DGP IgG ones, but your high DGP IgG scores still point to Celiac disease.   Since a gluten challenge would pose further health damage, you may want to ask for a DNA test to see if you have any of the commonly known genes for Celiac disease.  Though having the genes for Celiac is not diagnostic in and of itself, taken with the antibody tests, the anemia and your reaction to gluten, it may be a confirmation you have Celiac disease.   Do discuss Gastrointestinal Beriberi with your doctors.  In Celiac disease, Gastrointestinal Beriberi is frequently overlooked by doctors.  The digestive system can be affected by localized Thiamine deficiency which causes symptoms consistent with yours.  Correction of nutritional deficiencies quickly is beneficial.  Benfotiamine, a form of thiamine, helps improve intestinal health.  All eight B vitamins, including Thiamine (Benfotiamine), should be supplemented because they all work together.   The B vitamins are needed in addition to iron to correct anemia.   Hope this helps!  Keep us posted on your progress!
    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
    • Jsingh
      Hi,  My 7 year daughter has complained of this in the past, which I thought were part of her glutening symptom, but more recently I have come to figure out it's part of her histamine overload symptom. This one symptom was part of her broader profile, which included irritability, extreme hunger, confusion, post-nasal drip. You might want to look up "histamine intolerance". I wish I had known of this at the time of her diagnosis, life would have been much easier.  I hope you are able to figure out. 
×
×
  • 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.