Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

I'm New Here And Need Advice!


Violet

Recommended Posts

Violet Rookie

Hi everyone. I'm feeling a bit at the end of my rope at the moment. I was told I should stop eating gluten by an energy worker a few years ago. I know that sounds wacko..but at the time I was feeling so poorly that I agree'd to try it. I have felt better and better from it. I was already eating a natural, organic "health food" diet, so it wasn't all that difficult. However, I have now given up sugar and find it quite difficult to come across decent tasting bread that is gluten AND sugar free. When this woman told me I shouldn't eat gluten, she did say I was able to tolerate spelt. I didn't eat it tho. Recently, I had some spelt bread and pretzels and it was like heaven. Have you ever heard of spelt being ok? I was starting to think maybe I could get away w/eating gluten again but then I got a blood test back saying I was extremeley low in iron and b12. I poked around and found that people w/celiac are often lacking in those due to an inability to absorb them. If that is the case, will the iron pills I'm taking even help? I have EVERY symptom of iron deficiency and its not fun. The most recent is irregular heartbeat. I'm sorry if this a jumbled...I'm in a rush and trying to get it all out. So..any thoughts on iron? B12? Spelt? TIA!!


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

Spelt is for sure not ok. It's just like eating wheat. Spelt is a form of wheat.

Celiacs can have a problem with absorbing nutrients (if untreated) and that may be the cause of you being low in b12 and iron.

If you are in fact a celiac, have you eliminated all of gluten? Obviously you are still on some gluten because you are eating spelt so you should eliminate that.Gluten is hidden in many things like flavorings, modified food starch, etc. Gluten is not only found in food but in products like makeups, shampoos, soaps, etc and can easily get into your mouth.

The iron supplements and b vitamins would not help if you are not absorbing it. After being completely gluten free I think then you would benefit from them to help your body get those nutrients.

Do you still have symptoms being gluten free?

Violet Rookie

Thank you for the quick reply.

I did have lots of symptoms even when I wasn't eating spelt (its new for me, just in the past weeks). Most of my symptoms are that of iron deficiency. I can't figure out why, when I was totally gluten free ( I use totally pure soap etc..) I was still so low in iron? Maybe I was getting it w/out knowing. I dont know tho, I don't go out to eat often, cook in cast iron. Most of the gluten freel things out there are based w/rice. Perhaps rice effects me? I want to have a baby, so I really need to get this figured out, at least how to absorb iron! I'm not usually such a whiner, but I feel like just giving up today.

Carriefaith Enthusiast

If you have low iron, celiac disease is a possibility. If you really want to follow the gluten-free diet and see if it improves your iron levels, I would eliminate all sources of gluten. That includes reading labels and looking for gluten on every product that goes in or near your mouth. I would check shampoo, conditioner, make-up, suncreen, toothpaste, ect.

There is a safe and forbidden food and ingredient list on this web site, https://www.celiac.com/st_main.html?p_catid...-16105622901.3e. Also, if you need help determining what is and isn't, gluten-free feel free to ask us. There are many companies that will not hide gluten in their ingredient list, meaning they will come out and say wheat, rye, barley, or oats. Kaiti has that list if you are interested.

And Kaiti is right, spelt =gluten

Guest gfinnebraska

Just an additional note to the excellent info you have already received. I noticed you said you cook in an iron skillet. That skillet can contain particles of gluten in it. You should really buy a new pan and try that for a while as well. Make sure you aren't using any old wooden spoons that are contaminated, etc. It really takes a while to narrow down all the gluten/contamination issues. You will also need a new toaster ~ if you are using one. Gluten is in so many items that you would never think about. Reading the "safe" lists is an excellent way to start as well.

Good luck and good health!! :)

jenvan Collaborator

Also... It is a possibility that you will need an iron infusion for your anemia. I had to get one this spring b/c my iron would not go up. I am getting a follow-up test this week to see if I have to have another infusion as well. Sometimes it can take a while, and take several of these procedures to get someone's iron up to normal levels.

Violet Rookie

Wow..so much to think about! Thanks everyone!!

How is the iron infusion differnet from iron pills?

I'm confused about the cast iron pan...it has gluten, or holds onto old gluten? Sorry, that one really confuses me, lol.


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

An iron infusion will directly put it into your bloodstream. This would be beneficial if you are not absorbing nutrients. IV's are a good idea to. Supplements just won't cut it if you are not absorbing anything because they will go right through you, so that's where those things become beneficial

As for the pan, what she was saying is if before you made gluten containing foods on it then residue from that stays on it.

Merika Contributor

Hi Violet,

If you are not completely gluten-free right now, and are eating the equivalent of a slice of bread a day (I think), you should get a blood test for celiac. You may have celiac, you may just be gluten-intolerant. Spelt is an ancient form of wheat that has very low gluten levels.

It seems you are unsure what level of gluten-avoidance you should be doing, and a test could give you the firm answer you need.

Before being diagnosed, I had switched to spelt bread and did much better on it than regular bread. I wouldn't eat it now though! If you are merely gluten-intolerant, maybe spelt would be ok? I don't know that much about gluten-intolerance though, just that your insides don't get damaged like with celiac.

Merika

Violet Rookie

I really appreciate everyone taking the time to reply.

What kind of test? Is it as simple as a blood test? The only gluten I have eaten has been the spelt. Is that enough for the test? Probably yes huh?

I used to be able to get some really yummy pizza crust at Whole Foods that was gluten-free. Does anyone have a good brand of pizza crust?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,184
    • Most Online (within 30 mins)
      7,748

    Valerie Mink
    Newest Member
    Valerie Mink
    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

    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
×
×
  • Create New...