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

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.


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



Celiac.com Sponsor (A8-M):



  • Replies 187
  • Created
  • Last Reply
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


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



Celiac.com Sponsor (A8-M):



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

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,555
    • Most Online (within 30 mins)
      7,748

    JMF
    Newest Member
    JMF
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA 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
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.