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

Research Question


Guest CD_Surviver

Recommended Posts

Guest CD_Surviver

Hi,

My Name is Lauren and I have to write a research paper for Biology. I chose to do Celiac Disease because i have and have had it for 10 years. I need a question that I can research that has little information and that will give me a good topic. If anyone has any ideas it would be much appriciated. Thank you!


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



Celiac.com Sponsor (A8-M):



  • Replies 55
  • Created
  • Last Reply
Carriefaith Enthusiast

How about, "The effects of gluten on the brain". I think this would be a very interesting topic.

Guest CD_Surviver

thank for the idea i will definately consider it! :)

Carriefaith Enthusiast

Here are some interesting articles to look into if you like this topic:

Frontal cortical perfusion abnormalities related to gluten intake and associated autoimmune disease in adult coeliac disease: 99mTc-ECD brain SPECT study • ARTICLE

Digestive and Liver Disease, Volume 36, Issue 8, August 2004, Pages 513-518

P. Usai, A. Serra, B. Marini, S. Mariotti, L. Satta, M. F. Boi, A. Spanu, G. Loi and M. Piga

Open Original Shared Link

Neurologic presentation of celiac disease • ARTICLE

Gastroenterology, Volume 128, Issue 4, Supplement 1, April 2005, Pages S92-S97

Khalafalla O. Bushara

Open Original Shared Link

Sorry if the links don't work.

kevsmom Contributor

Whatever topic you choose, you may find the University of Maryland Celiac Center site very helpful. You can contact them at www.celiaccenter.org/.

Guest CD_Surviver

thank you for the site i think it will help alot. :D

Guest Viola

Good Luck on your paper! It would really be interesting to see what you come up with :D


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



Celiac.com Sponsor (A8-M):



Guest CD_Surviver

If anyone else hase any other ideas i have to have question turned in by monday to my biology teacher. i looking for anything new that maybe doens't have mush info about it yet. our teacher wants us to choose topics that are hare to write on to see what we can do and it is apart of our final grade in the class.

Guest Viola

The brain fog is really a major issue that isn't addressed much. I would expect that those of us that drive with it are likely impaired even though there wouldn't be a test such as acohol level testing. I also get the shakes along with the brain fog, and have at least once scared myself driving enough to pull into a garage and call my husband to come and get both me and the van. Keeping in mind that I was 20 miles from home at the time on a fairly high speed highway.

I for one, would like to know how something as common as gluten could cause such drastic changes in the thought process. :rolleyes:

Guest CD_Surviver

Viola

thanks for the info its is really helpful. i will seriuoslly concider this topic for my paper and if i do end up doing it i will post any info that i find and will make sure that you some how recieve the info.

Lauren

ianm Apprentice

Brain fog gets my vote. The brain fog would be unbelievably crippling for me.

angel-jd1 Community Regular

Brain Lesions caused by Celiac is something that I would like to know more about.

-Jessica :rolleyes:

Carriefaith Enthusiast
I would expect that those of us that drive with it are likely impaired even though there wouldn't be a test such as acohol level testing.
I'm with you on that one! I don't trust myself to drive when I get brain fog.
cornbread Explorer

Another vote for brain fog. It's the first sign that I've had gluten/casein (kicks in within 10 minutes), and it is the longest lasting - about 6 days. It really is incredibly debilitating. Before I knew about my gluten problem, I used to just tell people I had days where I felt 'underwater'.

Guest Viola

Cornbread .. That's a good discription .. it is kinda like being underwater :lol:

Guest CD_Surviver

for those of you who get brain fogs could you please discribe them and tell me all that you know about them so i have a few different things to search in metacrawler.

Much Thanks

Lauren

Carriefaith Enthusiast

When I have brain fog I feel impaired, like I am being partially sedated or something. I also get really stupid and forgetful. And I feel like I am in "LaLa land". Hopefully someone can relate to that ;)

ianm Apprentice

It is like an out-of-body experience. I can see and hear everything going on around me but I cannot connect or respond to any of it. Another description is like having my head wrapped in an airtight box. Nothing can get in or out.

Carriefaith Enthusiast
It is like an out-of-body experience.
:lol: That is the best description yet! I can so relate. lol.
elisabet Contributor

is it supposed to be in molecular biology or cell biology.?

best of luck

Guest CD_Surviver

i am just in biology at school and she wants us to do some thing with life so both subjects would have to do with life. so idon't think it really matters just as long as i have my question turned in by tomorrow.

Guest Viola

With brain fog, concentration is almost impossible. Which is what makes it difficult to drive. I find I have to really try hard to concentrate just to figure out where I am, let alone what the traffic is doing. Very scary when you have an hours drive either home or to town.

My hands are shaky and you look at something and try to figure out what it is, and what you were going to do with it. It sounds funny :lol: But it really can get very scary. And it is everytime I get glutenized. My daughter has the same problems with driving. She is of course, also Celiac.

Rachel--24 Collaborator

Brainfog is one of my worst symptoms. With brainfog I cant focus on anything. My thoughts leave my mind quickly and then I cant remember what I was thinking. I feel spaced out like I'm not really "all there". Driving is difficult and I get confused easily...have ran red lights before...not responding fast enough like my brain didnt get the message to stop. If someone is in the car with me I find that I cant drive and talk at the same time. With brainfog its hard for me to focus on one thing let alone 2...simple things like driving and having a conversation are lost to me if I have brainfog.

Guest CD_Surviver

Thank you all for your help and am still looking for more info even though my question is due tomorrow i have to revise it so that it is very specific so i will be using you guys alot for my paper. :)

Guest Viola

:lol: I don't think most of us are going anywhere. :lol:

If we can help ... ask away :rolleyes:

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    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.