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

Food Allergies


Brandiwine

Recommended Posts

Brandiwine Contributor

Most of us have more food allergies than just wheat, barley, and rye but I feel like one of my allergies is kind of strange and I haven't met anyone outside of my family that has it. I'm allergic to cinnamon, have been since I was 20. I never had a problem with it when I was younger and made a lot of desserts with it because it helps keep away illness. Is any one else allergic to Cinnamon? I wish I wasn't, I have gotten used to not eating it but the smell is so yummy! Even if it does make me sneeze and my face itchy :-/


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



Celiac.com Sponsor (A8-M):



1desperateladysaved Proficient

Two spices that I like are fennel and fenugreek.  Fennel has a light licorice flavor and I use in gluten-free muffins or cookies.  Fenugreek tastes somewhat like maple.  My family likes the flavor.  I also sometimes use peppermint leaves for a light minty flavor.

 

I am missing cinnamon, but I can possibly eat it again one day. I know, one can't help smelling it from afar when it is being baked.   Yet, some other spices are a nice change of pace.

Brandiwine Contributor

Two spices that I like are fennel and fenugreek. Fennel has a light licorice flavor and I use in gluten-free muffins or cookies. Fenugreek tastes somewhat like maple. My family likes the flavor. I also sometimes use peppermint leaves for a light minty flavor.

I am missing cinnamon, but I can possibly eat it again one day. I know, one can't help smelling it from afar when it is being baked. Yet, some other spices are a nice change of pace.

So you are allergic to cinnamon too? When did it develop?

  • 2 months later...
blessedmamaofmany Newbie

I've only met one other person who's allergic to cinnamon.  That must stink.  Especially around Christmas time when everything is all cinnamon-y.  What a drag.  

1desperateladysaved Proficient

I have a food intolerance to cinnamon, but the hope is that as my body calms down and my digestion improves that it won't be a problem anymore.  I have got some other foods back, but since spices are so small, they are not my first priority to get back in.

  • 2 weeks later...
Rowena Rising Star

I know someone allergic to cinnamon, can't remember who it is...  But I've got a weird one too...  Rosemary.  Its so crazy!

 

  • 4 weeks later...
1desperateladysaved Proficient

So you are allergic to cinnamon too? When did it develop?

I found out by being tested for antibodies to cinnamon and tested positive. It registered as an intolerance.  I waited the indicated amount of time and longer before I tried it.  A week or so ago, I tried a supplement that had cinnamon in it.  It caused a unique reaction that I didn't get from anything else  I got aching joints and my usual general swelling. .  Use to get achy joints mysteriously in my gluten life.  This is the first trouble I had trying to add back in foods. 

 

I think that I would rather live without cinnamon than potatoes; I am not quite sure.  I say that because I tried mashed potatoes before I went on the cinnamon riddened supplement.  When My joints ached, I blamed it on the potato trial.  But my joints still hurt 8 days later, so then I noticed the cinnamon in the supplement.  I stopped taking it and my joints stopped aching the next day.

 

Soon, I will enjoy mashed potatoes again, perhaps for the last time.  I can live without the achy joints.

 

 

D


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

 

Most of us have more food allergies than just wheat, barley, and rye but I feel like one of my allergies is kind of strange and I haven't met anyone outside of my family that has it. I'm allergic to cinnamon, have been since I was 20. I never had a problem with it when I was younger and made a lot of desserts with it because it helps keep away illness. Is any one else allergic to Cinnamon? I wish I wasn't, I have gotten used to not eating it but the smell is so yummy! Even if it does make me sneeze and my face itchy :-/

 

I have a diagnosed allergy to nutmeg. Like most of my other delayed reaction allergies, consuming nutmeg gives me days bloating and gut pain and sometimes diarrhea.  Many people have spice allergies.  I'm also allergic to vanilla.  I'm still recovering from my last accidental ingestion, which caused all the above mentioned symptoms.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      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: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.