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

Bad Reaction To Pears


Ursa Major

Recommended Posts

Ursa Major Collaborator

Yuck, my ONLY fruit has just decided to give me an allergic reaction! I get oral allergy syndrome reactions to a lot of things that aren't even on the lists of foods I officially can't tolerate (and which give me systemic reactions). Now pears have joined the ranks of those.

For a while I have thought I was heading this way (tingling on my tongue) when eating pears, so have only eaten one once every few days. It didn't help, apparently, in warding off this allergy.

I just ate a pear, and first got bad burning on my tongue, and then my throat got insanely itchy. Now, after eating some stir fry, it is getting better. My tongue is still burning. I am soooooooooooo mad! What will be next?

I am not looking for any of you to give me any solutions, I am really just venting. I am afraid the only solution is to now stop eating pears.

Okay, now I am getting very dizzy. I guess maybe it IS a systemic reaction after all. From pears, of all things! I think I might be able to eat them cooked, though, I just realize. I don't get this reaction from canned pears.


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Ursula--so sorry about the pears! Definately try them cooked--with Oral Allergy Syndrome, it is possible to have the symptoms with a raw fruit, veggie or nut, but not if the food is cooked. I learned this from my allergist--I thought I had an almond allergy, but it turned out to be OAS--and I can eat roasted almonds fine, but the raw ones are the ones that give me the mouth numbness.

KaitiUSA Enthusiast

I am sorry to hear that. Maybe as your body heals you will be able to introduce more foods? Anyhow, stick with what you know is safe and if you can tolerate canned pears or cooked ones then go for that instead.

kbtoyssni Contributor

Gosh, I have no idea. I know my mum has trouble digesting certain fruits like pears, apples and grapes, but that sounds like a completely different problem.

powderprincess Rookie

Oh no! So sorry to hear about your reaction to pears!

Ursa Major Collaborator

Thanks, guys, for sympathizing. I was still eating banana chips and hazelnuts for snacks, but now I can't tolerate them any more, either. And since yesterday dark chocolate seems to be out, too! That leaves nothing for treats, other than sesame snaps. And they are sort of high in salicylates, and if I eat too many of those, I'll get muscle aches. I guess I can't win.

Okay, I am sort of wallowing in self pity, but it sure sucks.

AndreaB Contributor

I don't know anything about OAS but is it at all possible for stress to cause the body to react to foods?

I'm so sorry Ursula. I know you are limited on your food intake.


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



Celiac.com Sponsor (A8-M):



Green12 Enthusiast
Yuck, my ONLY fruit has just decided to give me an allergic reaction! I get oral allergy syndrome reactions to a lot of things that aren't even on the lists of foods I officially can't tolerate (and which give me systemic reactions). Now pears have joined the ranks of those.

For a while I have thought I was heading this way (tingling on my tongue) when eating pears, so have only eaten one once every few days. It didn't help, apparently, in warding off this allergy.

I just ate a pear, and first got bad burning on my tongue, and then my throat got insanely itchy. Now, after eating some stir fry, it is getting better. My tongue is still burning. I am soooooooooooo mad! What will be next?

I am not looking for any of you to give me any solutions, I am really just venting. I am afraid the only solution is to now stop eating pears.

Okay, now I am getting very dizzy. I guess maybe it IS a systemic reaction after all. From pears, of all things! I think I might be able to eat them cooked, though, I just realize. I don't get this reaction from canned pears.

Had you peeled the pear before you ate it? Or was it from a different grower than the ones you haven't reacted to in the past. Just a thought.

Ursa Major Collaborator
Had you peeled the pear before you ate it? Or was it from a different grower than the ones you haven't reacted to in the past. Just a thought.

Yes, I peeled it. I was only able to eat peeled pears, because the peel has too many salicylates. And I've been having small reactions to many different kinds of pears these past couple of weeks (I tried about five kinds, to see if it was just one). I saw it coming.

And I just ate canned pears, and something is bothering me about them as well. I might have to give up fruits altogether!

So, I guess I'll be truly living on only meat (no pork, I react to that) and about ten kinds of vegetables that I haven't had a problem with (yet).

I find I now even react to buckwheat and arrowroot (they were the last starches left), so no more baking.

Oh well, at least I HAVE food, unlike too many people in this world!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,140
    • Most Online (within 30 mins)
      7,748

    Dorothy Romanczuk
    Newest Member
    Dorothy Romanczuk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      71.5k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      This is such an important discussion! While corn gluten (zein) is structurally different from wheat gluten, emerging research suggests some celiac and gluten-sensitive individuals may still react to it, whether due to cross-reactivity, inflammation, or other factors. For those with non-responsive celiac disease or ongoing symptoms, eliminating corn—especially processed derivatives like corn syrup—might be worth exploring under medical guidance. That said, corn’s broader health impact (GMOs, digestibility, nutritional profile) is a separate but valid concern. Like you mentioned, ‘gluten-free’ doesn’t automatically mean ‘healthy,’ and whole, unprocessed foods are often the safest bet. For those sensitive to corn, alternatives like quinoa, rice, or nutrient-dense starches (e.g., sweet potatoes) can help fill the gap. Always fascinating (and frustrating) how individualized this journey is—thanks for highlighting these nuances! Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful:    
    • Scott Adams
      I’m so sorry your little one is going through this. Celiac recovery can take time (sometimes months for gut healing), but the ongoing leg pain is concerning. Since his anemia was severe, have his doctors checked his other nutrient levels? Deficiencies in magnesium, vitamin D, or B12 could contribute to muscle/joint pain. A pediatric GI or rheumatologist might also explore if there’s concurrent inflammation or autoimmune involvement (like juvenile arthritis, which sometimes overlaps with celiac). Gentle massage, Epsom salt baths (for magnesium absorption), or low-impact activities like swimming could help ease discomfort while he heals. Keep advocating for him—you’re doing an amazing job!
    • Stuartpope
      Thank you for the input. We go back to the GI doctor in June- she wants to do more labs to check vitamin levels( not sure why the didn't check all at once with the iron being so low) and recheck inflammatory levels. Just trying to find him some relief in the meantime.
    • trents
      Welcome to the forum, @Stuartpope! With Marsh 3b damage to the villous lining of the small bowel, your son is likely deficient in a number of vitamin and minerals due to poor absorption, not just iron. B12 and all the other B vitamins are likely low. I would suggest looking into a high quality gluten-free B complex, D3, magnesium glycinate (the form of magnesium is important) and zinc. A children's multivitamin likely will not be potent enough. We commonly recommend this combo of vitamins and minerals to new celiacs as adults. Thing is, you would want to consult with a pediatrician about dosage because of his young age. In time, with the gluten-free diet his villi will rebound but he may need a kick start right now with some high potency supplements.
    • Stuartpope
      Hey yall!  New Celiac mama trying to help my son! My 3 year old was just diagnosed with Marsh 3b by a biopsy. We started this journey due to him being severely anemic (ferritin levels 1.2) He has had  3 iron infusions to help with the anemia. He has also been gluten free for a month. He is still having leg/ joint pain( he described a burning/ hurting) Im trying to help with his leg pain. He has trouble playing ( spending most days on the couch) He tells me 5/6X a day that his legs are hurting. Gets worse when walking or  playing. We have done OTC pain meds/ heating pad/ warm baths. What else can I do to help him be a kid.     Thanks for the help 
×
×
  • Create New...