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

Origin Of Celiacs?


C'smum

Recommended Posts

SacGFGirl Explorer

I'm Polish and German and the only one in my family who has celiac, although my sister seems to be developing a gluten intolerance.


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



Celiac.com Sponsor (A8-M):



  • Replies 97
  • Created
  • Last Reply
Jenny (AZ via TX) Enthusiast

Wow, it looks like there's a little of everything here. I'm mostly French, then Spanish and a little Irish and Welsh(sp). My gastro asked me if I was Irish.

I reside in Ontario but grew up with my family in England.My family believed themselves to be true English.Recently we found out that we are of Irish decent through my fathers side the same side that has passed on Celiacs to me.There is some belief that Celiacs originate from Ireland.Whats your background?
  • 2 weeks later...
raen Apprentice

i am inclined to beleive celiac is dominantly european/"white" based on everything ive read to date.

i am only three things - my mom is cherokee and i got celiac from my dad who is a combo english-scottish.

i read somewhere that the first (assumed) celiacs were roman, though.

  • 2 weeks later...
Maryellen Newbie

I am of Irish, English and Scottish descent but I don't think it has to do with "nationality" per say. When I remember back to my childhood some of the elders from Europe knew that bread, cakes, cookies and gravies were not for "our type of people". My paternal grandmother was absolutely firm about it and I remember a pretty heated moment between my grandmother and my father one holiday about barring bakery cookies from the house. They always said that we should "stick to the old ways" and that our "mother lineage" had a particular style of cookery that kept us well. This was why so many of them wouldn't change from Cahtolicism because the explanation was that the Church had the only continuous written records internationally of births, deaths and marriages thereby tying one back to their original mother lineage. We were all supposed to stick to something called the "strict code of names" which ties this together. It really is quite fascinating to me and the more I research it the more it becomes understood that you could live in the NW of Ireland and be of the same mother tribe as someone in the Southern tip of Italy. My Dad's parents were from Ireland and Scotland, most were of a tribe called D'Anu. Every firstborn girl was named a derivation of Anna; Maryann, Oona, Enya and when they became the elder of the clan they put the "N" in front of the name, hence, the title "Nana" or "Nanny" in English. In Italy it would be Nona or Nonni, Anglo Norman is Nancy. Every first born son was supposed to be William but as years went on the names were jumbled around a bit. My mom's people were from England and Scotland and were Brigends and they have almost the same name sequencing. I later found out all Brigends are a direct descendant tribe of D'Anu. I believe now that many of them had Celiac in one form or another and consequently had horrible disease and suffering in their lives and ultimately died young.

MauriceReed Newbie
The first description of childhood and adult coeliac disease was written in the second half of the second century A.D. by a contemporary of the ancient Roman Physician, Galen. He is known as Aretaeus of Cappadocia and his writings which have survived to more recent times were edited and translated by Francis Adams and printed for the Sydenham Society in 1856. The original Greek Text of the sections on "The Coeliac Affection" suggests that Aretaeus may possibly have understood a remarkable amount about the coeliac condition.

So, the Romans were aware of this some 1,800 years ago which show that the condition is not as recent as some may think. Take a look at the following article which makes interesting reading:

Open Original Shared Link

samcarter Contributor

Heinz 57. :D

Seriously, all I know about my ancestry for sure is that my dad is 1/2 German, 1/4 Irish, 1/4 Hungarian. My mom's ancestry is pretty much a mystery, since her people were so busy making the farms produce something that they were too busy to write down where everybody came from. :huh: So I have no idea what my ancestry is on my maternal side.

mslee Apprentice

Wow!

Interesting!

I am also a German, Irish, Scottish, Welsh, Swedish, Choctaw, Black Foot Mutt!

I wonder if those of pure Native American (both North and South) blood have a better tolerance to nightshades? Or do they just make everyone feel cruddy?

oooh, yeah on second thought ... probably none of those left

....but in theory :huh: ?


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



Celiac.com Sponsor (A8-M):



hawaiimama Apprentice

I am 1/4 Irish 1/4 English, 1/4 from the Channel Islands and 1/4 scottish.

My kids have half chinese thrown in for good mix of the breeding gene pool ;)

suett Newbie

Hi,

I am Norwegian and Kroacian, Scottish, and Italian

aorona Rookie

I am 1/2 swedish, from my mother's side (the side celiac came from), part german, & french from my father's side. The fair skin has nothing to do with gluten. I have an olive skin tone and my mom tan's pretty good too.

dogle Apprentice

Mother: Asturian ancestry (Northern Spain) and Portuguese ancestry. She is white, blue eyes and strawberry hair.

Father: Spain ancestry and Native American (Aztec). My father is browned-skinned with brown hair but his family is a mix of aztec apparience people and red-hair white people.

I have green-hazel eyes, fair skin and freckles all over my face, chest, back, arms. I was blonde as a kid but my hair now is brown.

angieInCA Apprentice

another mutt here. Mother's side- Lakota Sioux and Irish. Father's side - Northern Italian and Irish.

So, not only did I get a double wammy of Irish but I get to be Native American Indian lactose intollerent too :rolleyes:

Chrissyb Enthusiast

German, Polish and Irish. My kids are German, Polish, Irish and Spanish they have the Spanish look dark hair, eyes and skin where I am fair skin, blue green eyes and dark blonde hair. Nobody ever believes they are my kids. Works well when the misbehave :lol:

healthiernow Newbie

Irish/English/Mohegan/Swiss

I see a lot of Irish on here

nasalady Contributor

Sounds like the luck of the Irish to me! :lol:

My background is mostly Irish and English, but I'm 1/4 Austrian because of my maternal grandfather from Salzburg.

Blueberry Newbie

My mother's side is mostly Irish (they came over here on the ships in 1862 from Ireland) and some English on her mother's side. My father is Scottish through and through. I think I got more of the Irish side though... I have fair skin, hazel eyes, and the lightest hair out of all my family. The other thing, my mother is also celiac. We also think my brother and sister may have it, but refuse to acknowledge it. I think that other people are right in thinking their may be an Irish connection, since alot of poeple seem to have Irish ancestory...

land-turtle Newbie
I agree. I think it is no longer an issue with where your family is from. The fact of the matter is that our food suppliers are poisioning us! Too many hormones, too many fillers, too many additives etc... Our Government is allowing this to happen. (We should start a new post.) Let me ask everyone here a question (30 and older) When you were growing up did you kow anyone that had cancer? If you did wasn't it a BIG deal? How many people do you know that have it or have had it now? Big difference right? How many new diseases and ailments have you read about/heard about? It's our food and the toxic chemicals that we use everyday.The US is now poisioning other countries. I will say this to all of you that may say something negative to what I posted: I have only been gluten-free for 6 days. I was never worried about what I ate etc... although I did try to eat somewhat healthier foods. I was aware of some of the chemicals in my food, but I had no idea the affects that it had until this happened to me. The population isn't educated enough. I know that I wasn't. I just rolled with "the times." I figured I would probably die of a heart realted disease,but I just didn't GEt how bad all of this stuff was. I had never even heard of celiac disease even through my medical training. We now have tons of cancer, autism, thyroid diseases, ADHD, ADD, OCD, RLS, celiac disease, Chronic Fatigue (not spelled right lol) IBS, Addisons, Parkinsons, allergies, COPD, mad cow disease, avian flu, SARS, AIDS, HIV, Hepatitis through the roof (and a new addition to it every 5 years or so), drug addiction, seziures, depression, ulcers, diabetes is skyrocketing, we have CFS oh my goodness I could go on forever. The sad part is this: there is no cure for most of these. It is sad. Please educate people about what they are putting into their bodies and allowing their children to eat. It's scary. We have done this to ourselves unknowingly. I know that I also did it to my children unknowingly and that hurts me. I always bought what was cheap because of funds, but when I look back I could've done better. We ate out a lot. I could've bought healthier foods instead of eating out, and probably had money left over. I know I am devestated by celiac disease, and the affects it has had on my family. I am ranting in the wrong place, I'm sorry. :) My point is that no one is "safe" anymore. I'm sure at one time there was a link, but it would be impossible to track now due to US food CC.
land-turtle Newbie
I agree. I think it is no longer an issue with where your family is from. The fact of the matter is that our food suppliers are poisioning us! Too many hormones, too many fillers, too many additives etc... Our Government is allowing this to happen. (We should start a new post.) Let me ask everyone here a question (30 and older) When you were growing up did you kow anyone that had cancer? If you did wasn't it a BIG deal? How many people do you know that have it or have had it now? Big difference right? How many new diseases and ailments have you read about/heard about? It's our food and the toxic chemicals that we use everyday.The US is now poisioning other countries. I will say this to all of you that may say something negative to what I posted: I have only been gluten-free for 6 days. I was never worried about what I ate etc... although I did try to eat somewhat healthier foods. I was aware of some of the chemicals in my food, but I had no idea the affects that it had until this happened to me. The population isn't educated enough. I know that I wasn't. I just rolled with "the times." I figured I would probably die of a heart realted disease,but I just didn't GEt how bad all of this stuff was. I had never even heard of celiac disease even through my medical training. We now have tons of cancer, autism, thyroid diseases, ADHD, ADD, OCD, RLS, celiac disease, Chronic Fatigue (not spelled right lol) IBS, Addisons, Parkinsons, allergies, COPD, mad cow disease, avian flu, SARS, AIDS, HIV, Hepatitis through the roof (and a new addition to it every 5 years or so), drug addiction, seziures, depression, ulcers, diabetes is skyrocketing, we have CFS oh my goodness I could go on forever. The sad part is this: there is no cure for most of these. It is sad. Please educate people about what they are putting into their bodies and allowing their children to eat. It's scary. We have done this to ourselves unknowingly. I know that I also did it to my children unknowingly and that hurts me. I always bought what was cheap because of funds, but when I look back I could've done better. We ate out a lot. I could've bought healthier foods instead of eating out, and probably had money left over. I know I am devestated by celiac disease, and the affects it has had on my family. I am ranting in the wrong place, I'm sorry. :) My point is that no one is "safe" anymore. I'm sure at one time there was a link, but it would be impossible to track now due to US food CC.
slmprofesseur Apprentice

I am the true mutt:

I am african-american. I am unsure of my african ancestors, however, my great grand mother was the daughter of her slave owner. My mother has a Scottish last name and father has a Welsh last name. (both are african-american).

My husband has a Ukranian/German background.

I think I have more European blood than anyone wants to admit. Many relatives have had stomach cancer, diabetes, gout, etc. etc. I am the first to go Gluten-free.

As for the proof of this blood...

Our first son has blonde hair and light brown eyes! (No one thinks I am his mother!)

I can tolerate nightshades- no problem.

mftnchn Explorer

So interesting! Gene pool mixing just has increased with all the increased moving around in the world.

What I know is German, English, Norwegian, but nobody really knows what all is in the mix. My grandfather had the bright red hair...

I'm the only celiac I know of in the family but suspect many others; both parents have DQ2 because I have a double dose of it. Means all 5 of my siblings have at least one DQ2 gene and so do my two kids.

one more mile Contributor

My grandma advises me not shake a stick at anyone.

I have Irish, prussian, German, English, welsh, black, American Indian.

and enough "randy gals" that any thing is possible.

one more mile

mysty Newbie

im german/hungarian...blonde and blue eyes...both of my grandmothers died of complications related to the disease...and there are plenty of allergies in the family tree.

i married a scotsman...and my kids seem to be no better for that lol

all my children are intolerant to wheat in some way...and my nephew is allergic to peanuts and wheat and gluten...while his sister is not.

my husband isnt allergic to a thing ...but he does have diabetes and arthritis...so obviously some immune disfunction on his side that he doesnt feel inclined to go further into lol.

MollyBeth Contributor

Italian, Iraish and English!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Ibuprofen

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

      My only proof

    3. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings

    4. - Scott Adams replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Oh my goodness medication causing pain !!!!

    5. - Scott Adams replied to Me,Sue's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Knowing what to do when feeling unwell.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,869
    • Most Online (within 30 mins)
      7,748

    Stacy W
    Newest Member
    Stacy W
    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

    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
    • Scott Adams
      I am so sorry you're going through this. It's bad enough to fight for a diagnosis and manage this disease, but to have your partner use it as a weapon against you is truly devastating. What you're describing isn't just a lack of support; it's abuse, full stop. Controlling your food and money is cruel, and his pleasure in your misery is chilling. Please hear this: the kindness from that woman at the food pantry is what you deserve. It's a glimpse of the real world, where people care. You deserve to eat, to heal, and to have peace. His actions are the biggest barrier to your health right now, and you are not broken—you are surviving in an impossible situation. Don't give up on that lifeline you've found.
×
×
  • 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.