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Irish Heritage And Celiac's


Queen Serenity

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armoorefam Newbie

My husband and daughter have celiac. My husband's mom was a MCCoy. Lots of Scotch Irish on her side of the family. She definitely had all the symptoms; though, since my husband was diagnosed a few months after her death from intestinal cancer the connection was never made.


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  • Replies 187
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danikali Enthusiast

Okay, I am 100% Polish!!! I am not dx yet, but I know my problems have something to do with gluten. My fam. came over on the boat 2 generations ago on one side and the other 3 generations. So what are you guys telling me? I'm crazy after all!?? Where are all of my Polaks to prove me right!?!

NYCisTHEplaceTObe Rookie

i have a lot of stuff in me but mostly irish and polish and the irish side has always had digestive problems, very interesting.

jerseyangel Proficient

Never heard about the % of Italians--I'm all Italian, both mom & dad. I think my mother and 1 sister have it but they aren't doing anything about it at the moment.

Lagomom Newbie

Dad is Irish and Cherokee. My mom is all German. Dad had terrible digestion. So did his little sister. Her 2nd son has Celiac. Kind of nice having a cousin to share this with.

Libby.

celiac disease/HH/OA/Hypothyroidism/Lupus B)

Lois23 Newbie

I am Irish,Mimac Indian,English from my Mom's side her last name is O Lawler she also has Celiac. And I am part Finnish from my Dad's side.

danie Newbie

I'm the Celiac in my family. My dad is Scotch-Irish and my mom is a mixture but mostly Scandanavian.

My husband's family is Irish; his sister, 1st cousin and half great aunt have Celiacs.

Dana


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beelzebubble Contributor

i'm first generation scottish on my mom's side and second generation scottish and irish on my dad's. to my knowledge, i am the only person in my family with celiac.

  • 4 months later...
Carolita Rookie

My IgG came back positive last week.

I'm part Irish and part Spanish (probably Mayan as well but not sure). I say I probably have about 25% Irish from my mother's side and 75% Spanish from my father's side.

Carol :unsure:

Rachel .... now there is two of us. I'm also part Spanish :)

schuyler Apprentice

Dad's side: Irish and French. My dad (and some of his family members) has had terrible digestion problems for a long time, but he won't be tested for celiac

Mom's side: Italian, Native American, and possibly English

Green12 Enthusiast

I'm mostly Irish, Scottish, English, and Delaware/Lenape Indian (American Indian).

Rachel--24 Collaborator
Rachel .... now there is two of us. I'm also part Spanish :)

Yeah! I'm not the only one anymore. :D

I think I must be 25% Spanish, 25% Italian, 50% Mexican....or something like that. <_<

JenAnderson Rookie

I am second generation Irish. One set of Grandparents came from County Cork and the others came from Belfast. The only side that had the symptoms were the ones who were from Cork. They were "country people". The other side that was from Belfast didn't have any signs from celiac disease, but there was Diabetes and Colon and Prostate Cancer. I was really happy to claim all this Irish heritage until I got diagnosed. Now I know why we put so much stock in the potato.....

  • 1 month later...
windravyn Newbie

Hi. Just wanted to chime in. Another Irish lass here! I'm gluten sensitive (and I have autoimmune thyroid disease). I suspect my mom, sister, and grandmother are as well. I have Irish heavily on both sides. I also have German heavily on one side.

LKelly8 Rookie

100% Irish and 10% German :blink:

  • 1 month later...
azmom3 Contributor

French from my dad's side, Irish and German from my moms side. I haven't been tested for celiac yet, but have many of the symptoms and just found out my son has it.

beaglemania Rookie

I have gotten Celiac from my dad, who has it also. On my Dad's side from where I got it he is almost 100% Irish. So I got it from my Irish heritage.

On my mom's side I have English, German and Irish.

kb8ogn Rookie

I have really found this interesing.

my dad is 100% irish, my mom is slovak and english.

jayhawkmom Enthusiast

I am also Irish & German - and a little French, Swedish, and English. Fascinating. My father is an English/Nordic mix, my mother is the German, Irish, Frenchwoman.

Vladimir Gluten Newbie

This thread is a monster!!

I am 50% Irish (as my Irish Grandma reminds me) and 50% Pennsylvania Dutch (DEUTSCH).

If anyone is interested in a brief list of the possible reasons for the term "Pennsylvania Dutch" here is a Open Original Shared Link

Rikki Tikki Explorer

German and Dutch

Carriefaith Enthusiast

Scottish, Irish, English, and Norwegian.

Girl Ninja Newbie

Irish and French-Canadian-Indian. That second one is all one. My great grandmother was Indian and lived on a reservation in Canada. She had a tribal name and also a French name.

rinne Apprentice

Irish, Scottish, Ukrainian.

My Irish grandfather died at 65 of stomach cancer.

Nic Collaborator

My son is Irish, Italian, and English and he is a Celiac. But it is passed on in my fathers side of the family who is half Italian, half English, no Irish. I read early on when my son was first diagnosed that this illness is predominant in the northern European counties.

Nicole

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    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
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