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

What's Your Blood Type?

FoxersArtist

Recommended Posts

munkee41182 Explorer
munkee41182
Posted

I'm O+, and my fiance is A+ (though he's not celiac or gluten/wheat intollerant). I love red meats and they make me feel so much better if I haven't eaten them in a while. I try to eat it one every week/every other week. He on the other hand can't handle red meats as well. I know both of my parents are O+ and the celiac comes from my dad's side. I'm trying to talk my dad into getting tested as he now has diabetes and his mother and myself have celiac. He's just too damn stubborn though.

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

Celiac.com Sponsor (A8-M):


Krystens mummy Enthusiast
Krystens mummy
Posted

I am O+ my daughter is A+ we both have symptoms. my dad is A+ gene comes from his side

rsm Newbie
rsm
Posted

B+ looks like the B's are in the minority here!

Kaycee Collaborator
Kaycee
Posted

A+ here.

Yes it looks like the B's are in the minority.

Cathy

Lukalovescats Rookie
Lukalovescats
Posted

I'm O+ but am a vegetarian. Never handled meat well and now it just grosses me out. Of course I haven't had it since I gave up gluten, but I sure do enjoy my veggies! Not sure about my girls blood type, the older one loves meat and the younger could care less. Interesting theory.

Crimson Rookie
Crimson
Posted

My husband, Daughter and I are all O+.

I've actually looked in on this. Dr. D'Adamo has written several books based on blood type diets.

I found the diet to be rather helpful to me. He does have a website: Open Original Shared Link

He says that those that are non secreters (meaning you do not secrete your blood antigen into other body fluids

such as saliva the like) are 200% more likely to develop Celiac disease.

There's been a good bit of research. But it, like most ideas that are not mainstream are looked down upon.

I think he has a point.

My Natropath (sp?) says that it's still quite "one size fits all". My thoughts are that it's a great place to start.

The B blood type minority does not surprise me a bit. They're supposed to handle grains well.

Those that have Celiac may very well be non secreters.

I find the topic quite fascinating.

That's my ramble. :D

fedora Enthusiast
fedora
Posted

U.S. Blood-type Distribution

O+ 38 percent of population

A+ 34 percent of population

B+ 9 percent of population

O- 7 percent of population

A- 6 percent of population

AB+ 3 percent of population

B- 2 percent of population

AB- 1 percent of population

There are way more Os and As out there

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

Celiac.com Sponsor (A8-M):


rsm Newbie
rsm
Posted
U.S. Blood-type Distribution

O+ 38 percent of population

A+ 34 percent of population

B+ 9 percent of population

O- 7 percent of population

A- 6 percent of population

AB+ 3 percent of population

B- 2 percent of population

AB- 1 percent of population

There are way more Os and As out there

No wonder we B's are in the minority!

torontosue Rookie
torontosue
Posted

O neg here......as are both mykids, though one has allergies he seems ok on gluten so far.

JNBunnie1 Community Regular
JNBunnie1
Posted
O neg here......as are both mykids, though one has allergies he seems ok on gluten so far.

I'm O+, but I love (looove) meat. Always have. Dairy too. Might be a holdover from the 'I'm too skinny' days when I was trying to fatten myself up, but I just feel like crap if I go 36 hours without animal meat. Eggs and cheese don't even quite do it. We have lots of fish and chicken and cow and buffalo and lamb even. I hate shellfish though, not allergic, I just think it's slimy and squishy and ew. I used to like fried shrimp, but good luck finding that gluten free.

Munkee- good luck with your dad.

ShayFL Enthusiast
ShayFL
Posted

Seems like a pretty even split between O's and A's which make up most of the population. So I dont see a specific connection to type O.

luvs2eat Collaborator
luvs2eat
Posted

Both my ex and I are A+ so I assumed all our kids are too... Celiac kid surprised me... she's O+.

neesee Apprentice
neesee
Posted

I'm o+ and my gluten-free son is o-

neesee

FoxersArtist Contributor
FoxersArtist
Posted
  • Author

Well shoot. If 72% of the population are O+ and A+ and that's the majority of blood types here, this tells us nothing. LOL. Oh well, back to the drawing board.

-Anna

U.S. Blood-type Distribution

O+ 38 percent of population

A+ 34 percent of population

B+ 9 percent of population

O- 7 percent of population

A- 6 percent of population

AB+ 3 percent of population

B- 2 percent of population

AB- 1 percent of population

There are way more Os and As out there

  • 4 years later...
surviormom Rookie
surviormom
Posted

O- and  2 kids that appear to need to be gluten-free too, both O-.  

DistressedNewbie Newbie
DistressedNewbie
Posted

My entire family and I are O -

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      132,916
    • Most Online (within 30 mins)
      7,748
    Ykat
    Newest Member
    Ykat
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):

  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):

  • Upcoming Events

  • Posts

    • xxnonamexx
      Fermented foods, Kefir, Kombucha?

      By xxnonamexx · Posted

      very interesting thanks for the info  
    • Florence Lillian
      gluten free cookie recipes

      By Florence Lillian · Posted

      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Severe severe mouth pain

      By Russ H · Posted

      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Severe severe mouth pain

      By cristiana · Posted

      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      gluten free cookie recipes

      By Scott Adams · Posted

      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.