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

Irish Heritage And Celiac's


Queen Serenity

Recommended Posts

chgomom Enthusiast

I am 100% Irish on my mother side, and on my father side 50% "right off the boat" to Illinois in 1867, my great great grandmother was a chool teacher in Lemont, IL at St. Patrick's. So yeah...I guess you could say I'm Irish.

Then the other day when I had my big GI appt.....the Dexxa scan lady said...yeah....I see so many people with an Irish background that have this ...and I was like reallly??? Then I saw this...weird.


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



Celiac.com Sponsor (A8-M):



  • Replies 187
  • Created
  • Last Reply
txnmaryann Rookie

Dad's side: German & Irish

Mom's side: English, French, Scottish

My GI asked my "heritage" during the first 5 min of our conversation about my symptoms.

  • 2 years later...
Celi2009 Newbie

My strongest heritage is Irish, my Grandma was born there, the rest of my ancestors have been in Canada for several generations. This week I went for my biopsy and my GI actually told me that there is a proven link between Irish heritage and Celiac disease. I googled it and found a great website: Open Original Shared Link. This source explains that wheat, barley, and rye weren't introduced into Ireland (and Irish people's diet) until a much later date than other countries. Therefore we have more difficulties with gluten and are more susceptible to celiac. Check out the link for a better explanation.

nasalady Contributor
This source explains that wheat, barley, and rye weren't introduced into Ireland (and Irish people's diet) until a much later date than other countries. Therefore we have more difficulties with gluten and are more susceptible to celiac. Check out the link for a better explanation.

Hey everyone....here is an abstract from a medical journal article published in 2001, which is entitled, "Why is celiac disease so common in Ireland?".

Open Original Shared Link

There are concentrated "pockets" of celiacs here and there around the world (Ireland is one hot spot) and archeologists and agrarian historians collaborate to find out why. I believe that Celi2009's explanation (above) is at least approximately correct.

I think that the general idea is that you will find the highest rates of celiac disease in those areas which relied on foods other than wheat, barley, and rye the longest, historically speaking, but which today ingest large quantities of gluten-containing foods.

This is due to the fact that celiac disease kills babies/small children, and frequently leads to infertility in those who survive to adulthood as well, so susceptible people/families are weeded out of the population fairly quickly (i.e., people like us).

Therefore populations in places which have been growing wheat the longest have lower rates of celiac disease...the "weak links" have been mostly eliminated.

P.S. Celi2009, I couldn't get your link to work.

nasalady Contributor

P.P.S. I'm mostly of Irish heritage too.... :lol:

Lisa16 Collaborator

Interesting thread.

On my dad's side (going back to the 15th century) German-- Westphalia, but also part Pomeranian (which now belongs to Poland.) On my mom's side Polish (but from areas that could have been Austria or the present Ukraine) and Scotch-Irish. I have been told this last designation is a specific groups of immigrants who originated in Scotland and were forcibly settled in Ireland before immigrating to the US. That side came over after the battle of Cullodan (sp?) and were very early US settlers. Celiac runs on both sides and both sides have identical DQ genes-- 6 and 7 (well, as far as the accuracy of the test will allow me to say so. I guess Enterolab doesn't tell you the beta part of the gene?)

It just goes to show that Europe was more of a melting pot than most people know. Those borders were actually pretty fluid.

In addition, Polish people will tell you that they have blood from the Mongol hordes which swept through there, giving them slightly asiatic features-- the high cheekbones, the lovely eyes-- in short, the "slavic look". I do not know if this is so, but it certainly seems plausible.

And to make matters more interesting, many of the first year linguistic books I use posit the theory that the Celts actually originated in Northern Italy and were gradually pushed to the extremes of Europe by the expanding Roman Empire. Achaeological evidence seems to support this. They were also in Spain (the so called Celt-Iberians.)

So maybe knowing your ancestry isn't as useful as some people think. But it sure is interesting.

The Fluffy Assassin Enthusiast
I am curious to know how Celiac's is related, in the majority, to people of an Irish background. Everyone I have spoken too, who have the disease, have some Irish background. I just want to know if there is a connection. If you have no Irish background, please let me know what nationalities you are. Thanks in advance, if you choose to take the survey.

Vicki :)

Mostly Swiss, German, Danish and English, but I think it was the Irish that got me. Thanks loads, great-grandma Tighe!:)


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



Celiac.com Sponsor (A8-M):



ranger Enthusiast

Irish on both sides. Maybe a little Norwegian from the Viking Marauders! Thanks a lot, Mom and Dad

  • 3 years later...
surviormom Rookie

Interesting.  Irish on my mom's side, hubby has French and Irish and our kids have issues.

BelleVie Enthusiast

I'm very, very Irish and am fascinated by the connection between that and celiac. I seem to remember reading a hypothesis somewhere that said the Irish diet was always traditionally very heavy in potatoes, and then when wheat was introduced, people just couldn't handle it. 

nvsmom Community Regular

I'm a German and Ukranian/Russian mix and I have celiac disease on both sides of the family. My hubby has a British/Scottosh/Irish background and he's fine... there's some irony in there somewhere.  ;)

  • 1 month later...
dotsdots Newbie

Yes, there is Irish in our background, along with many other European ancestors including Danish, English and German.

I have heard that there are some who think JFK with all his medical problems may have been an undiagnosed Celiac.

Italy is another country that has a high percentage of Celiacs. It may be due to their much more frequent testing for the disease.

DK

Maybe it's because everyone eats pasta - LOL!

dotsdots Newbie

I have an Irish, Scottish, and English background. My husband, who I believe also needs to be tested as he has symptoms, is Irish and German. I've read that people from northern European countries have a higher percentage of celiac disease than other populations. I think there might be an article on this site about that, in fact.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.