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

Anyone Have A Mom And Dad With Celiac?


Chakra2

Recommended Posts

Chakra2 Contributor

My mom and I are both in the process of getting diagnosed with celiac disease. Just wondering how uncommon it would be for both my mom and my dad to have celiac. Wondering how much info I should try to pass on to him (mom and dad are divorced).

Chakra2


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



Celiac.com Sponsor (A8-M):



GlutenFreeManna Rising Star

Since it's genetic I think they both should get tested. I'm still trying to convince my parents to get tested. I suspect they have it because between them they have several diseases that go hand-in-hand with celiac, but they haven't been sick enough to want to get tested. I will keep working on them, however. I've only been gluten free for 7 months, so they might think this is just some fad I've started to follow. Once they see that this is my lifestyle for good they might start taking me more seriously.

Chakra2 Contributor

It took awhile to get my mom to be open to testing.

I'm about 7 months gluten-free too! How are you feeling? I felt a huge improvement within the first 2-3 weeks, then roller coastered through months 2-5 figuring out the diet and other intolerances, and just in the past 2 months have finally felt back to normal. I love feeling like a human being again!

GlutenFreeManna Rising Star

It took awhile to get my mom to be open to testing.

I'm about 7 months gluten-free too! How are you feeling? I felt a huge improvement within the first 2-3 weeks, then roller coastered through months 2-5 figuring out the diet and other intolerances, and just in the past 2 months have finally felt back to normal. I love feeling like a human being again!

I'm doing great, as long as I don't get glutened. I sort of did things backward, but it worked out for me. I cut out all possible allergens--all grains, all dairy, all sugars, and even most fruit for a month. I ate nothing but grilled meat and veggies then I started to add things in one at a time to see how I reacted. My reaction to wheat led me to suspect celiac and when I looked into it further, I found it matched so many of my symptoms perfectly. It just made sense. So I found myself a few months gluten free (without knowing that that's what it was called) and I couldn't get the testing done at that point. So now I advocate everyone get tested before trying the diet. I wish I had known to get tested first, but there's no way I'm going back on gluten for the testing. It's not worth losing more of my health.

Skylark Collaborator

Mom has non-celiac gluten intolerance. Dad eats wheat fine.

ravenwoodglass Mentor

My kids do. I also have two copies of the same gene and my Mom was not diagnosed but had all the symptoms and my Dad, from what I remember, had some of the neuro ones and had the celiac 'beer gut'.

Roda Rising Star

and my Dad, from what I remember, had some of the neuro ones and had the celiac 'beer gut'.

The "beer gut", oh my gosh, sounds just like my dad. Granted he does drink beer, but no matter how much weight he looses he has this belly that just sticks out and is very disproportionate to the rest of his body. He finaly got tested and his doctor told him everything was fine and he does not have celiac. However when my Mom asked about their actual results the doctor was snooty and would not tell them. He said to her "I wouldn't steer you wrong you are fine." Yeah like I believe every word he tells them. He told my mom that on her last bone density test that she didn't have osteoporosis any more, but she shrank more! :huh: I told her to go get a copy of the reoprt from x-ray, and low and behold it was worse than the last one. GRR! So the point is Dad will believe this guy. He has alot of signs that point to celiac especially the belly thing, very low cholesterol despite being overweight (I had abnormally low triglicerides etc too, all normal now) and alot of what I call neuro things. He is getting problems in his feet that another dr. (neurologist) has him taking and increasing neurotin and B12 for and it is not improving. My dad believes since his tests were negative he is in the clear. I found out last summer that my Dad's great great nephew who is a toddler by now and his full cousin's daughter are both celiac. So it does run in the family. I highly suspect his brother has it too. He has suffered since a child with psorasis and bad skin and I am pretty confident my brother has it also. He has sarcoidosis which thankfully went into remission 6 month after he was diagnosed in 1992, but has had an awful rash since then and LOTS of stomach issues. He won't get tested and probably never will. He said he didn't care if he was because he wasn't ever going to give up the things he loves. I guess he hasn't gotten sick enough yet. He already avoids dairy as much as possible because it bothers him. I don't really bring it up any more in the context that I think they should try the diet or get tested. It's their choice to make. I just focus on me and they are pretty supportive of me.


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



Celiac.com Sponsor (A8-M):



T.H. Community Regular

I would definitely pass that info. on. 1 in 22 of that group (1 degree away from a celiac, like sibling, child, parent) are postive as well.

For me, my dad was diagnosed a few years back and told me it was 'like an allergy,' so I didn't look into it much. I slowly started getting illness after illness, worse and worse, and then I found out I had it as well. I went and pestered everyone to get tested, and my brother and daughter came back positive. My son, who we took off gluten anyway, has problems that have resolved since going gluten free.

Now, talking with relatives, we've found many cousins who have physical problems, including many gut symptoms, that their doctors have told them for years are 'just due to stress.' They're thinking of getting tested, now too.

I think it's DEFINITELY worth looking at.

My mom and I are both in the process of getting diagnosed with celiac disease. Just wondering how uncommon it would be for both my mom and my dad to have celiac. Wondering how much info I should try to pass on to him (mom and dad are divorced).

Chakra2

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,847
    • Most Online (within 30 mins)
      7,748

    rossick11
    Newest Member
    rossick11
    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

    • Colleen H
      Do you or anyone know alot about ibuprofen  I wasn't sure if I was eating too much apple sauce.   Something is making my pain so much worse  I'm referring to the intense pins and needles in my feet and lower legs.  Jaw actually has tardive dystonia and muscle spasms throughout my back Almost like an opposite effect that a pain reliever would do. I'm fairly new to this. Whatever is going on seems to be worsening  Do people get a withdrawal effect from gluten?  It's extremely painful 😖  I'll post that question or research on the site  Thank you everyone for responding 
    • Colleen H
    • Colleen H
      I think I found a huge culprit for severe reactions to create worsening of my c symptoms. Do people with celiac have sensitivity and /or have opposite reaction to certain medications Where can I find a list ?  I'm new here I'm.wondering why I am getting worse when I take certain medicine...the burning feet.  Rebound muscle pain so intense  How many people get opposite effects or have a horrible attack after these meds
    • Colleen H
      Does anyone know if that includes scrambled eggs and healthy smart butter (,gluten free) I add a very tiny amount of margarine less than a teaspoon.  I did no't have any bread    It just seems like no matter what I eat my stomach and nerves over fire and here comes a host of horrible symptoms. My lower abdomen feels horrible, my right leg thigh muscle.. very odd. Jaw pain. Burning feet , joint pain , you name it  The anxiety just creeps up into brain fog. I don't think I could explain this to anyone who is unfamiliar.  Also,  I most likely will not remember posting this until I check it.  This is highly unusual for me because I have an excellent memory.  One weekend before I knew anything about celiac I lost an entire weekend from severe brain fog, confusion, pain, etc.  I honestly thought I was losing my mind. When I think back I recall eating a lot of PBJ sandwiches and turkey sandwiches.  Once again did not know about gluten.  I was just too sick to cook. Do people fast during attacks ?? It seems horrible to keep going through this. I hope I'm not causing my own problems... I wonder if I should fast because I'm not eating gluten .  Chicken ,  scrambled eggs no milk , canned carrots,  gluten free low sugar low fat Greek yogurt which I already posted about 😞 Any suggestions I am open... I am bedridden when this happens to me.  Thank you Celiac community. 🙏🏻❤️      
    • Juliane
      Yeah, that sounds super familiar. When inflammation levels are high — especially at the start of changing your diet — the body often develops a fructose and lactose intolerance. Unfortunately, the only thing that really helps is cutting out anything that isn’t lactose-free or that contains sugar. So basically, stick to meat, veggies, fish…
×
×
  • 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.