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

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
      132,021
    • Most Online (within 30 mins)
      7,748

    maltawildcat
    Newest Member
    maltawildcat
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • NanCel
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
×
×
  • 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.