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Immune Disease Runs In Families
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Started by SharonF,

6 posts in this topic

Posted

2004 was a crazy year for my family. First I was diagnosed with celiac, then my mom with hypothyroidism, then my sister wtih hyPERthyroidism. My sister's doctor says that immune diseases can show up in different forms in families. This is fascinating to me.

Does anyone else have experience with different autoimmune diseases in your families?

I worry I'll pass something along to my kids.

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Posted

My sister has Type 1 diabetes. A cousin has celiac disease, and I suspect her brother does, too. Another cousin has Crohns. ( That looks misspelle.) I wonder if she is really a celiac.

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Posted

I have hypothyroidism and chronic hives (5 months now), my son (12) has the thyroid antibodies and is on synthroid too. My 16 yr old has vitiligo, an autoimmune skin disease. My oldest son is gluten intolerant, he had positive blood IgG and tested positive with enterolab. Three of my 4 sons have thyroid antibodies. They have to be watched for Hashimotos thyroiditis.

The funny thing is neither of my parents or to our knowledge my grandparents have any autoimmune diseases! I don't know where it came from. The doctor said I inherited my lovely autoimmune diseases but I have no idea from who.

Lisa :blink:

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Posted

Since you have Celiac Disease you can pass it on to your children.

My Mother, brother, and I all have Celiacs.

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Posted

I have Celiac and Hashimotos Throiditis. My son has Celiac. My mother has Crohns and my brother has Diabetes. We are not in the process of getting my daughter, sister and her daughter tested for Celiac. They all have symptoms and have had them for a while now.

I was told that Celiac is known to be passed on in families. Our family does seem to have quite a bit of autoimmune problems.

Hope this info helps.

Kathy B

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Posted

I have celiac, my dad has thyroid issues along with my mom. My mom has a severe allergy to wheat but tested negative for celiac. Crohns runs in my dads family, thryoid disease runs in my moms family. My uncle, grandma, and 2 cousins we think need to get tested for celiac because they have alot of the symptoms.

I think that many people in my family have celiac, some are willing to get tested, others I don't think would really follow the diet correctly

I think it def. does run in families though

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Go To Topic Listing Celiac Disease - Related Disorders & Research

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    • psawyer
      Taking Advil to cope with pain?

      By psawyer · Posted

      Advil (ibuprofen) is gluten-free, but can be a stomach irritant, especially if taken on an empty stomach. That said, I will also place my bet on the garlic and onions. As Raven said, eating more than once a day may also help. An empty stomach is likely to be an irritable stomach.
    • ch88
      Mental Trauma

      By ch88 · Posted

      Another link: http://naldc.nal.usda.gov/download/7351/PDF
    • ch88
      Mental Trauma

      By ch88 · Posted

      Thanks for posting.  I know it is difficult to talk about these sorts of things even on a webforum.  It is good thing for people to be aware though about celiac disease and that it can cause mental problems.  Gluten can cause brain damage and it can cause anxiety. If the brain does heal it may take a long time. I know that gluten can cause anxiety and obsessive thoughts.  My experience has been similar to your experience. When I first quit eating gluten I had a similar constant loop and strong negative feelings. There are lots of people on this forum who get anxiety when they eat gluten. Some people also experience gluten withdrawl where they experience anxiety after giving up gluten. It can take a long time for the body to heal and for obsessive thoughts to go away.
       It is normal for people to socialize with each other and to be comfortable about it. You said you have problems still socializing and being around people. It might be a depressing thought but it sounds to me like you still have problems with anxiety.  I would recommend considering what options you have available to treat the anxiety. When I quit eating Gluten I still had some symptoms, even though I felt much better. I have been slowly recovering over a period of about three years. I had obsessive thoughts even after I quit eating gluten.  Now I very rarely if at all think about those things. My experience is that my mind would latch on to certain things that caused me anxiety and focus on those things. Sometimes my focus would shift and I would latch onto other things. My ability to socialize has also improved greatly with time. I have made some dietary changes which I believe have helped greatly. It sounds to me like you have obsessive thoughts about things and maybe some brain damage. My experience has been that my obsessive thoughts about different things went away with time. I feel my obsessive thoughts were caused by gluten and not by what people did around me or any events. As my brain healed I became more self aware and things became less stressful.  I can't give medical advice on this forum but I can talk about my current diet and my experience with celiac disease. My experience with gluten is different from a lot of other people so it is a good idea to ask other people and to talk to a doctor.  I avoid oats and avoid almost all processed foods. I buy certified gluten free food. I eat healthy and I exercise every day. I take st John's Wort as I have read studies that say it may be as effective as some other anti-depressants for treating certain types of anxiety. It is available over the counter. I started with a small dosage and then stepped it up over time. I think it helps a lot.  This is also something that you should talk to a doctor about first. https://www.researchgate.net/profile/Martin_Mahoney2/publication/7426926_St._John's_wort/links/540d8acc0cf2f2b29a386673.pdf A lot of people with celiac disease have vitamin deficiencies.  Vitamin b deficiency can cause anxiety. Some people do not process the synthetic form of vitamin b (from normal pills)  very well, and do better on an activated form of vitamin b. I take:
      1 activated vitamin b12 daily
      1 activated vitamin b6 every once in a while. 1 regular vitamin b multivitamin
      1 magnesium pill every day.
      St Johns Wort daily.
      1 zinc vitamin daily
      I drink lots of Chamomile tea and decaf coffee. I avoid most caffeine. 
      I think each of these helps lower my anxiety level.  I eat fruit with every meal. Canned fruit from walmart is cheap and good for you. I eat salad and and vegetables and avoid dairy.  I eat frozen fish often as it has healthy proteins. Eating healthy is very important. I eat potatoes and rice. http://www.livestrong.com/article/454179-what-is-methyl-b12/ I avoid eating soy sauce, soy, cheese, aged meats and fermented foods (I do drink certain types of alcohol in moderate amounts.) These foods contain lots of Tyramine. I might (or might not) have "monoaine oxidase deficiency" and if so high Tyramine foods should be avoided.  I thought I might have problems with elevated ammonia in my blood, but I am not convinced of that anymore. I limited my consumption of meat for a while as well as dairy but I am not sure if i helped.  I have heard that Celiac disease can effect other organs besides the brain and those organs can have an effect on the brain.  My current diet is working so I am going to stick with it for now. I try not to worry about things that are outside of my control. Be patient as it took me a long time to recover.  Let me know if you have any questions. There is a lot of information on this site and people who are willing to help.
       
    • ironictruth
      other food allergy testing

      By ironictruth · Posted

      Thank you. This is really helpful. I will call around next week.  I just want to heal! 
    • kkgirl
      endoscopy showed damage

      By kkgirl · Posted

      My endoscopy showed i had decreased folds in my duodenum. The biopsy came back and showed that my villi were fine... i have been on a gluten free diet for 6 years because i was just told i was intolerant but never had any testing before. when i eat gluten i get sick for 2 weeks. i came down with issues of other foods in march so they were trying to figure out why and wanted to know if i had celiac are not because that would explain why dairy and fructose are a problem.. both intolerant test for both were negative but the fructose test made me extremely sick but it was negative...      Im trying to figure out why i have decreased  folds in the first place. my Gi doctor is stumped on that to why the endoscopy would show damage but the under the microscope are fine. She is going to call the dr who did my scope and then is supposed to get back to  me..    would being gluten free for 6 year make it so there was damage and then my vili are now fine but still cant be seen in the endoscope?

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