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

Help. Servre Cronic Canker Sores


hwmom

Recommended Posts

hwmom Newbie

HI I am new to the board. My son is being tested next week. My son is 7 years old and has debilitating canker sores. I was wondering if anyone noticed a differance in canker sores when they took their child off Gluten.

Also, does anyone know of any good snacks that are dairy free and glutten free?

Thank you so much.


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



Celiac.com Sponsor (A8-M):



hwmom Newbie

Hi I am new to this board. My son is being tested next week. Has anybody's child had servre canker sores? If so, did taking your child off Glutten make a difference?

Also, does anyone know of any dairy free and glutten free snacks that kids like?

THank you.

aorona Rookie

My children did not have canker sores, but I had geographic tongue. This is basically many open sores on your tongue that never seem to heal. It is very painful. Going gluten free for almost one year has almost cured this problem. It comes & goes, but is getting better.

As far as snacks. My kids love air popped popcorn with butter; cheese crisps made with corn tortillas; rice pudding; corn chips with salsa; gluten-free rice crispy treats; just to name a few. Basically anything your child liked before going gluten free can be modified to be gluten free. My kids also like "sandwiches" made with a corn tortilla toasted in the toaster. Just be sure to buy a new toaster, since the old toaster will have gluten on it. (we have 2 toasters in our kitchen) You can put anything in these "sandwiches". My kids like peanut-butter & jelly; and turkey with ranch dressing.

jmengert Enthusiast

I'm not a child, but I, too, had chronic canker sores before going gluten free. Now I don't get them at all unless I get glutened. Hopefully, your son's will clear up, too.

Ursa Major Collaborator

Hi, well, I am certainly no child either :D , but I used to get canker sores while consuming gluten, and haven't had any since going gluten-free.

kabowman Explorer

I have problems with canker sores and have had SINCE I went gluten-free. My pcp thought it was a vitamin B deficiency so now I take mega doses and but no effect...they just come (up to 10+ at a time) and go in waves (about a month at a time) but in the last few months have actually finally gotten better.

My dentist just prescribed me a mouthwash to use that is supposed to help but I haven't tried it yet - it is waiting for me to pick up at the Rx as we speak.

My son, dairy free, likes corn chips and chocolate sorbet as a treat (this is what he gets for easter and christmas now instead of chocolate).

Oh, I also have a geographic tongue and have had since I was young - mine doesn't hurt and I never notice changes but I don't spend a lot of time looking at my tongue. My DF son also has a geographic tongue.

Ursa Major Collaborator

Sorry about the double initial post, that ocurred because I merged two duplicate posts, because they had both gotten responses.


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



Celiac.com Sponsor (A8-M):



lindalee Enthusiast
I have problems with canker sores and have had SINCE I went gluten-free. My pcp thought it was a vitamin B deficiency so now I take mega doses and but no effect...they just come (up to 10+ at a time) and go in waves (about a month at a time) but in the last few months have actually finally gotten better.

My dentist just prescribed me a mouthwash to use that is supposed to help but I haven't tried it yet - it is waiting for me to pick up at the Rx as we speak.

My son, dairy free, likes corn chips and chocolate sorbet as a treat (this is what he gets for easter and christmas now instead of chocolate).

Oh, I also have a geographic tongue and have had since I was young - mine doesn't hurt and I never notice changes but I don't spend a lot of time looking at my tongue. My DF son also has a geographic tongue.

I had a bad cold sore before my big glutten outbreak(rash and D) Never had one before that. That was about 4 or 6 months ago. I'll find out what vit. I took. Can't remember right now. (brain fog) What's a geographic tongue? LindaLee

2kids4me Contributor

Prior to going gluten-free, my daughter would have severe canker sores - she would refuse to eat cause it hurt. They always seemed to be clearing up then a new bunch would arrive. We aave had ZERO canker sores since going gluten-free!

DeeTee33 Newbie

I stick to Crest Toothpaste and haven't had a Canker Sore in years. I forget which exact one but Colgate Toothpaste gave me horrible ulcers or Canker Sores in my mouth!

My mother's cure for Canker Sores was to put Baking Soda directly on them. You would make a paste and pat it on and had to hold your mouth funny for a few minutes though. Do it a couple times in a day. Kinda stung, but it did get rid of them much quicker. Curious if anybody else heard of this?

jerseyangel Proficient

I used to get canker sores frequently--since gluten-free, I have not had one :)

flagbabyds Collaborator

My sister used to get canker cores all the time and she took Lysine tablets, they really helped her.

lindalee Enthusiast
My sister used to get canker cores all the time and she took Lysine tablets, they really helped her.

That was it - Lysine. LLee

BRUMI1968 Collaborator
HI I am new to the board. My son is being tested next week. My son is 7 years old and has debilitating canker sores. I was wondering if anyone noticed a differance in canker sores when they took their child off Gluten.

Also, does anyone know of any good snacks that are dairy free and glutten free?

Thank you so much.

I haven't read through other answers, but I'll tell you that I immediately stopped getting canker sores when I quit gluten. I might've also quit citrus (trying to calm my gut down)...but the gluten definitely put an end to the canker sores.

As to snacks - you can make trail mix...I'm still looking for a good tortilla chip that is gluten-free.

Vinegar and citrus might also cause canker sores.

DeeTee33 Newbie

Tostitos Tortilla Chips are gluten-free. Tostitos are a product of Frito Lay. Frito Lay has a Gluten-Free list of all it's chips, dips, trail mixes etc. Check it out!

eKatherine Apprentice

I used to get canker sores regularly, but I haven't in years, which is about how long I've been gluten-free.

kaciemarie Contributor

I used to get horrible canker sores before i went gluten-free as well. Now I only get them when I eat something that I shouldn't. Also, I only use toothpaste without Sodium Laurel Sulfate in it. I use Burt's Bees. I hope this helps!

  • 1 month later...
DiPal Newbie

Even though your post is a month old now, I felt that I should reply. I am 46 an have suffered with canker sores all of my life. Neither doctors nor dentists could tell me why I got them. About 1 year ago, I went on one of those low carb diets. For the first several weeks, I could not eat any carbs except veggies. I suddenly realized that my canker sores dissapeared! I thought it was just a coinsidence so I did a little test. I took 1 bite of regular white bread and within hours, I broke out with 3 cankers. Since then I have gone gluten free and I no longer get them.

I have discovered however, that I can tolerate Spelt flour. Spelt flour has gluten in it but it is a different kind of glute than the gluten found in wheat, oats, rye and barley. There are some great breads out there that are made with spelt flour that are delicious. So, it might be worth it to try spelt bread for your son. He may be able to tolerate it too!

Good luck to you and your son!

penguin Community Regular
I have discovered however, that I can tolerate Spelt flour. Spelt flour has gluten in it but it is a different kind of glute than the gluten found in wheat, oats, rye and barley. There are some great breads out there that are made with spelt flour that are delicious. So, it might be worth it to try spelt bread for your son. He may be able to tolerate it too!

Good luck to you and your son!

No no no no no! Spelt has exactly the same kind of gluten that wheat, barley, rye, and oats have! It is definitely not safe for someone that is Celiac or gluten intolerant. Maybe, and a weak maybe at that, is that some people with wheat allergy (not celiac or gluten intolerance) might be able to handle spelt. Spelt is basically an anicient form of wheat.

  • 11 months later...
Sound Guy Newbie
Even though your post is a month old now, I felt that I should reply. I am 46 an have suffered with canker sores all of my life. Neither doctors nor dentists could tell me why I got them. About 1 year ago, I went on one of those low carb diets. For the first several weeks, I could not eat any carbs except veggies. I suddenly realized that my canker sores dissapeared! I thought it was just a coinsidence so I did a little test. I took 1 bite of regular white bread and within hours, I broke out with 3 cankers. Since then I have gone gluten free and I no longer get them.

I have discovered however, that I can tolerate Spelt flour. Spelt flour has gluten in it but it is a different kind of glute than the gluten found in wheat, oats, rye and barley. There are some great breads out there that are made with spelt flour that are delicious. So, it might be worth it to try spelt bread for your son. He may be able to tolerate it too!

Good luck to you and your son!

I just wanted to say as a chronic major ulcer sufferer I intend to take your advise on converting to a Gluten Free diet. I am 37 years old and have been a sufferer of Major ulcerations for years (17+). It is a shame that so little information is available among health practioners in regards to PREVENTING these little but dehabilittaing demons. I don't mean to sound harsh as I realize it's not possible to be an expert on every subject but, who is suppose to know about this area??? Not a GP or a dentist or at least the ones I've experienced. Years ago I tried to seek help on the subject but shortly realized that I already knew the usual remedies/suspects: SLS, Vitamin B-12, Folic Acid, Zinc, Iron, Lysine, Niacin, food triggers, false food triggers... Literally for me, at any given time I would be uncomfortably housing 2-3 major ulcers at a time. I have to say it goes even beyond a minor annoyance or at least in my life. Besides the pain, if I am to get one on my tongue I find it can literally cause me to be incapable of speaking (although may be great for my wife, it's definately not for my business). I literally once reached a point in my early years where I felt like I would rather not even be, then to go through this painful lonely cycle over and over with no end in sight. I say lonely because I always felt the average person could not relate to what the pain actually felt like. However I did come up with a comparison for my wife (who does not suffer from canker sores thankfully) to relate how it makes me feel. It feels as if someone has taken a pair of pliers to the inside of your mouth that is wherever the ulcer decides to take up residency in your mouth (tongue, lip, cheek...). In a perfect world I would like to write a comprehensive book from the understanding of the canker sore sufferer that provides tangible plottable steps to clearly identify the root cause supported with content based on proven facts... All I know is that I would like to figure it out so I can potentially help others PREVENT this from happening to them... Anyway, thanks for reading my input and If you would like to share a remedy with me I would love to hear from you... Thanks. chris_maynard@lycos.com

wowzer Community Regular

I used to get a lot of canker sores as a child. I never would have thought it was caused by gluten.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,186
    • Most Online (within 30 mins)
      7,748

    Kris46
    Newest Member
    Kris46
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • 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.
×
×
  • Create New...