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

Corn Too?


wystearya

Recommended Posts

wystearya Rookie

I've not been very active here in a while, and I am still a little new to handling my gluten sensitivity.   A few weeks ago I 'poisoned' myself with gluten.  Badly. (I ate some homemade rolls my Dad offered me... stupid I know!)  I'm actually now turned off eating it, which is a good thing for me!

 

Anyway, on to my current question.

 

I know that in some people corn is also an issue.  I'm wondering if I might also have this.  I've had raccoon eyes as long as I can remember, but apparently this can be a symptom of corn allergies.  I've also noticed sometimes in the past getting tiny fluid filled bumps on my fingers, and I think this is also something to do with corn..? 

 

I'm just concerned since several gluten free items still contain corn.  I love corn chips and salsa..  But if I have a problem with it I don't want to make myself sick anymore.

 

Is there a way I can test this?   I guess the only way is to eat some corn and see how I feel??  *ugh*

 

I do eat corn, but I am not sure if I react to it.  This is because I wasn't being as careful at avoiding gluten as I should be.   My recent glutening was a wake up call for me.  I cannot let myself eat any, especially on purpose!  I'm not celiac, and I thought 'a little won't hurt' but it does.  And I am now being much more careful.

 

Can anyone here tell me how common it is for those who are gluten sensitive to also react to corn?

Should I try a bit and see how I feel?  Or..?

 

Thank you very much!

~Wystearya


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

A good test would be to sit down and eat some corn on the cob.

 

Another good idea would be to keep a food diary.

wystearya Rookie

I had some corn on the cob a few months ago and don't remember having any negative affects. 

 

Maybe I'll just have to test myself and see if there are corn products and I can and some I cannot.

bartfull Rising Star

The best way (and I say this from experience), is to avoid ALL corn for about three months, then eat some processed corn - something like your corn chips or some gluten-free cornbread.

 

Corn is in just about all processed foods so it's really hard to avoid. And it isn't labeled if it is "used in processing". That means you need to buy your salad fixings whole because those bagged salads are washed in a veggie wash that contains corn. Just about anything that has cirtic acid, they get that citric acid from corn. Most gluten-free breads have corn starch so if you want bread you will have to go with Against the Grain. The good news is, their stuff is really good. They even make a frozen pizza that is good.  

 

Almost all pills have corn starch as filler. If you take medications, you may have to have them made at a compounding pharmacy. If you take supplements you can buy SOME at a healthfood store without corn, but vitamin C is going to be hard to find. I eat lots of sweet potatoes instead. They are full of vitamins.

 

Those fluid filled bumps on your fingers - are they clear fluid or kind of whitish? My palmoplantar pustular psoriasis gives me the whitish kind. They look like whitehead pimples and they hurt like a pimple if you put any pressure on them. Then after a few days they become a non-raised red spot. Then the red spot turns into peeling skin. They don't really itch a lot, but they hurt. If I stay away from corn (and gluten of course), I don't get them, but if I get "corned", they flare BADLY. I also get them on my feet.

 

If yours are filled with clear liquid and if they itch, you might have DH. If that is the case, you most likely DO have celiac instead of NCGI.

 

So my advice is to go on a whole foods diet for three months. Nothing but meat, fresh veggies, fresh fruit, and rice. As I said, if you need baked goodies, get Against the Grain. And if you need ice cream, look for one sweetened with sugar instead of corn syrup. Hagen Daz vanilla and chocolate are good, and if you're lucky enough to live someplace that carries Blue Bunny ice cream, their ALL NATURAL vanilla has only milk, cream, eggs, sugar, and vanilla, and it is SO GOOD!

 

If you need more advice, PM me. I'll be glad to help. Oh, and I'm glad to hear you have learned your lesson about gluten. :)

wystearya Rookie

The bumps I get (used to be every summer, now just rarely) are tiny and clear.  The first time I got them they did itch like crazy.  Once they break the surface the skin there gets dry. 

Is this DH?  What is DH? 

 

I was not tested for celiac, it was assumed I didn't have it.   I guess people with celiac react more and are more sensitive to the gluten and cross contamination?   I know when I finally went to the doctor I was very ill.  Digestive issues were every day.   It was awful.   I can say that since limiting gluten I also don't get migraines like I used to either.  More energy too.

 

I might request to be tested, even though I have been limiting gluten for a long time.  I am fairly certain my digestive tract was in bad shape.  It took me a long time before I could eat spicy foods again and not be ill.

 

Thank you so much for the replies!   I just recently have tried some gluten free bread.  I was reluctant to pay $5 per loaf, but it is worth it not to be sick!   I'll just go without for a while, though if I need a fix it is good to know a trusted brand.   Do they sell online?   I'm not sure I have any stores near me that carry Against the Grain, but I will check!

 

~Wystearya

bartfull Rising Star

Oh Hon, I'm sorry, but you DO need to be tested for celiac. It sure sounds to me like you have it. IF you can find a KNOWLEDGABLE dermatologist, you can be tested by biopsy of the possible DH. They have to test a CLEAR spot, right NEXT TO an active lesion. If you do have DH, that is your celiac diagnosis right there. Or you could get the several blood tests and biopsy of your small intestine. You do need to be eating gluten to get accurate testing.

 

Go to the Newbie 101 thread and read. Go to the DH (Dermatitis Herpetiformis) section of this forum and read up on that. There are lots of pictures too, so you can get an idea of what it looks like. Then, come back with any questions you might have. We'll help you all we can.

wystearya Rookie

Thank you again!

 

I looked up some pictures of DH on hands (as this is where I used to get it) and found this image:

http://www.made4ll.com/wp-content/uploads/dermatitis-herpetiformis-hands-dermatology-image-atlas-made4ll.webp

 

This looks just like it!  I have not had this happen in a very long time.  But I will say my cheeks are quite red a lot of the time.  Not itchy and no little bumps, just red.

 

Since I haven't had any DH in a long time, I think blood tests and biopsy is my best bet.  I'll talk to my doctor about it.  She is the one who recommended a gluten free diet to me.  At that time I thought I might have Irratable Bowel Syndrome as I was constantly sick.  Turns out some stress I was having at work seemed to cause my gluten issues to escalate!

 

I don't want to have to get sick (eat gluten) just to take a test that might come back negative (even if I am celiac), then again a firm diagnosis would be good to have.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

Why in the WORLD would a doctor NOT test for celiac, but tell a person to try gluten-free and ASSUME they are NOT celiac???!!! It ticks me off to no end!

 

The problem with going back on gluten in order to be tested is that you risk getting a MAJOR flare of DH that may not go away for TWO YEARS!!! Yet if you don't go back on gluten, your tests will come back negative even if you do have celiac.

 

If it were ME, I would just self-diagnose and go STRICTLY gluten-free for life. Some people feel they need a doctor's diagnosis in order to take it seriously enough to be able to stick to the diet. It's up to you, but if you decide to be tested, take a list of all the tests you want done. And you might want to mention to this doctor that if she recommended a gluten-free diet she must have SUSPECTED celiac, and she should have tested you THEN!! :angry:

wystearya Rookie

Yikes.  I definitely don't want to risk getting DH again.  I know it used to bug me so much when it would flare.  The little bumps got so sore once they burst!

 

I'll probably skip the tests then, as I really don't relish the thought of making myself ill anyway.  I really was very sick this last time.  I don't want to do it again. 

 

It has made me realize that 'just a little bit' is not OK for my body anymore.  Thankfully I do have some grocery and specialty stores here that carry gluten free items.  I also have discovered the joy of cooking.  When I have time, I do love to cook!  I enjoy watching the cooking shows on TV for tips and ideas.  I've been doing good at gluten-free cooking.  It's just hard during the week since I work full time.  :P

 

I do have to say I now wish my doctor had gone ahead and tested me.   She suspected gluten was my problem, so I don't know why she didn't test me at the time.  :/   I'm still thankful that I eventually heeded her advice and went off gluten.  It amazed me how quickly my digestive issues cleared up!  And I do feel better overall when I avoid gluten.   It's just a shame that without the official diagnosis some people will never fully accept my disease. 

 

I appreciate your help so much!   I am going to focus on getting myself 100% off gluten now.  Even the trace amounts.  *ugh*  I know this won't be easy, but my health is worth it.  I just have to remember how sick I was and how much better I can feel.

 

~Wystearya

bartfull Rising Star

Start with the Newbie 101 thread. It'll help you ferret out any gluten you may still be contaminating yourself with. There are also a lot of GREAT gluten-free recipes to be had here. Check out the breakfast/lunch/dinner threads here.

 

And as for your friends or whoever else you fear won't accept your disease, too bad for them! You are the one living in your body, and you are the ONLY one whose "opinion" matters! I am self-diagnosed based on my reaction to the diet and my family history. (It's genetic, and my Mom had it.) Even my doctor accepts it. As for others, I just tell them something along the lines of, "I have been gluten-free since I was diagnosed with celiac disease." It's not a lie - I WAS diagnosed with celiac - by myself! :D

wystearya Rookie

Nice, and your right it's not a lie!

foam Apprentice

Corn is hard of the gut. I avoided it for about a year and now I can tolerate it enough that a few corn chips wouldn't hurt me. I think it's important not to eat it initially though because it's pretty bad news. Second worst after Wheat/Rye/Barely imho.

T.H. Community Regular

Re: testing

 

The one thing that's good/bad about the DH is that IF you get gluten contamination, which is almost certain to happen eventually, then you'll likely get a DH flare up, and THEN you can get tested.

 

I would think it might be useful to find a celiac knowledgeable dermatologist NOW. Go in to see them, talk to them about wanting to get tested eventually, and set up a protocol so that whenever the day comes where you get gluten contamination and have the rash, you can get in ASAP and get that biopsied before it goes away, you know?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    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

    • 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.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.