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

Blood Type


cat3883

Recommended Posts

mushroom Proficient

A+


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



Celiac.com Sponsor (A8-M):



  • Replies 84
  • Created
  • Last Reply
cahill Collaborator

AB+

My grandmother came to the US from Scotland when she was 5. I had red hair( it is now mostly white-gray ) hazel eyes and have very light skin.

bartfull Rising Star

A-

MJ-S Contributor

O+

beebs Enthusiast

O positive I think? Which is the common one? Hazel eyes/brown hair, Irish descent

Marilyn R Community Regular

O+

O+ and Dutch descent, inherited (I believe) by A+ Mom. Biopsy negative, but delayed several months while on gluten-free diet.

Googles Community Regular

I am O+ brown and hazel. I am also a Western Euromutt (sorry had to steal that) with some Native American ancestry.


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



Celiac.com Sponsor (A8-M):



cahill Collaborator

I would wonder if hazel eyes or being an euromutt are more of a common denominator (if there is one) than blood type .

Roda Rising Star

I posted earlier but I'm O+ with med brown hair and green eyes. My youngest son is O+ also with medium brown hair and dark brown eyes. My oldest son is A+ light brown hair and the deepest blue eyes you ever saw. My dad and brother(whom I think have celiac) have B+. They were both toe heads when they were little and their hair eventually turned light brown. They have hazel eyes. As for my dad, brother and I mostly german/european decent with a touch of native american(my great grandmother was half). As for my boys, they have what I have plus from their dad's father's side is pretty much all irish decent and some native american(my husband's grandfather was half). From their dad's mother's side I know that they were german Jews that emmigrated to the US.

DonnaMM Explorer

I too am A positive

AVR1962 Collaborator

A+ here! Sounds like I am reporting a grade!! Oddly enough I have looked at my blood type diet, Swedish decent, and the foods I have been forced to eat to get my vits levels where they need to be are the exact foods on the blood type diet and the diet of the Swedish.....lots of fish!

sa1937 Community Regular

I am A negative. Blonde hair, blue eyes, maternal grandparents were from Denmark and paternal grandparents were from Norway so I'm about as Scandinavian as I can get.

My celiac daughter is also A negative, blonde hair, blue eyes, 3/4 Scandinavian and 1/4 Heinz 57. :lol:

I've never given a thought to checking into the blood type diet.

kitgordon Explorer

B positive. Brown hair and eyes. "Euromutt" (love that!) with a smidge of Native American.

navigator Apprentice

A+, I'm Scottish with brown hair but red highlight/tones in it. Eyes grey/blue.

bartfull Rising Star

OK, I forgot to give my background and coloring. I have grey hair that used to be brown, blue/grey eyes, and I am German, English, Polish, and Lakota Sioux. (What a combination!)

yorkieluv Newbie

O+ Sandy blonde hair and hazel eyes.

RVluvin Apprentice

O+, Hispanic with 1/8 Irish, Brown hair with red and blond mixed in (and some white now). My mother was a natural red. Eyes are brown. Undocumented, but very likely some native american from my fathers side.

Austin Guy Contributor

0+, CMV-. Light brown hair, blue eyes. Grandfather of Irish descent and mom's side has Danish roots.

If you don't know what CMV negative is, I have never been exposed to the Cytomegalovirus, a flu-like virus most people are exposed to at some point. CMV can be dangerous to individuals with weakened immune systems, newborns and people undergoing organ transplants. For these individuals, having a blood donor who is CMV- (someone who has never been exposed to cytomegalovirus) is very important.

I used to donate a lot, but thanks to gluten (I know this now), my pulse and blood pressure got too high to donate. Getting off gluten has it back where it needs to be and I can donate again.

kareng Grand Master

I think we are all over the place with blood types!

I'm 0+. Reddish brown hair & freckles! No one asks where my ancestors come from, they just assume Irish or Scottish. Actually, only about 25% Irish, mostly German and some shady areas we are not sure of.

saintmaybe Collaborator

AB- here, with mostly Irish, Lebanese, and Eastern European ancestry. Hazel eyes, brown hair.

skyloft Newbie

O+, blue eyes, Irish, German

  • 4 weeks later...
Kimberly888 Newbie

A+ brownish red hair scottish

chai Newbie

I'm B+, black hair, Brazilian and Italian descent.

So far i've been the only one diagnosed in my family but I suspect people on both my mothers and father's side could be celiac.

Judy3 Contributor

A+ Reddish Brown hair, Green eyes. Polish,German, Swedish, French, Indian (several tribes)... Apparently, my family never heard of borders!!! LOL

ciamarie Rookie

I'll play, since it was the blood-type diet that had me eating spelt and rye and very occasionally wheat for several years when I should have been gluten-free. :angry:

O+ American (Scottish and Canadian French and who knows what else).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,901
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    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

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.