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minibabe Contributor

100% Female :D

Amanda NY


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  • Replies 63
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DragonQueen Explorer

female...girl power!!!! Wow celiac3270! I saw your new avatar and you look just like my older cousin!! :o youre like twins or something.

  • 4 weeks later...
Ashley Enthusiast

I'm a female. :lol:

sasha1234 Newbie

hey i'm new to this board and i'm 19 and female

  • 9 months later...
TeenCeliac Rookie

hey you guyz..well i am a 13(almost 14) year old girl...and have had celiac disease since i was about 2 so i wanna meet more people like me... please e-mail or aim me aim-spongebobfan888 e-mail-hunterhalverson@hotmail.com

just tell me your name and where you live...and that you are from here(or just say you have celiac disease too) lol and i will talk to you

thanx,

Hunter

  • 2 months later...
Liz92 Rookie

Any teenage males besides ben???? I'm female and 14, almost 15 :PB)

Liz92 Rookie

Actually, Im the ONLY female Celiac I know, and my Uncle, Dad, Cousin(male) and @ brothers of mine are Celiac... wierd

Ya, I wish more guys would talk on stuff like this... They're fun to talk to


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  • 2 weeks later...
Kara B. Newbie

Hey I'm a girl. 15 almost 16. I'm new 2 the site and I've had Celiac for about a year. How many of u guys have friends or know people in your towns w/ Celiac?

  • 1 year later...
Stoyns619 Newbie

Ya im a dude!!! :lol:

  • 8 months later...
Angels~Exist Newbie

Hey! I'm a girl. 16 years old, diagnosed 2 months. There are way more girls on here than guys. <_<

  • 2 weeks later...
RideAllWays Enthusiast

I'm Devon, 18 yo female :D Feel free to add me to msn

d.hoholuk@Hotmail.com

spanish-road Newbie

Im a guy and have been WF for 5 years. :D

ScottyB Newbie

Quarter century (25) year old guy here who just found out that i could have celiac disease. I cant tell you how long i've been dealing with GI tract problems (atleast 13 years). i thought everybody had an upset stomach after they ate, or a heavy feeling after slamming beers, so i got used to all the discomfort that i would experience. i found out after a female cousin of mine was having stomach problems for past 5 years and just recently had the 3rd intestine biopsy, which came back positive for celiac disease. our grandmother has the same stomach problems (her stomach 'talks to her' after she eats her bowl of cream-o-wheat in the morning) and her mother has similar problems. uncle has had severe colitis and other stomach problems.

have been 99% gluten free for the past 3-4 weeks and have seen drastic health improvements. cooking and taking food with me when i go out or bringing my own beer (redbridge is all i can find right now) is something i'm still getting used to. being in austin texas really helps out because its filled with restaurants that cater to vegans, so many of my favorite restaurants are aware of gluten and have menus for people with celiac disease. going out downtown or to 6th street is hard because i love the taste of beer and i cant have it anymore (but i'm fine with it cause i know for a fact that its bad and messes with my GI tract) so i try and find ciders or not drink at all.

is it possible to grow out of celiac disease and become gluten tolerant? there is so much cajun cooking i'm missing like bread pudding....pound cake....mmhmmm.... :D

IChaseFrisbees Explorer

I was just reading the first page about how many women post here vs. men, not realizing it was from 2005. In my health care class last quarter we just discussed how insurance companies prefer young men to young women because we never go to the doctor!

Anyway, I'm a man. Well, male anyway, I'm not sure I'm ready for all the responsibilities that come with using the grown-up terms yet, 19 isn't that old! :P

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    • 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.
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