Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Recently Diagnosed


Guest dlf1021

Recommended Posts

Guest dlf1021

Hello

I was just recently diagnosed (received the call from the doctor with my test results last night, as a matter of fact) with Celiac Disease after over eight years of continuous illness. For years, I've been told that it's Irritable Bowel Syndrome and that I'd have to "live with it" forever...that's great for the doctor who doesn't have to put up with it, but I'm only eighteen years old. I'm hoping that forever is still a mighty long way off for me.

Anyway, my results showed that I have a "mild" allergy, whatever that is classified as and my mother, who hasn't yet done any researching of celiac disease and all things gluten free doesn't understand that when it comes to allergies, there is no such thing as truly mild. It is of her opinion that I should still be able to eat gluten, just in small doses. I'm assuming that this isn't true?

Can anyone suggest any good websites or books I could lead her to in order to help educate her?

My next struggle comes along with school. My doc put me on a gluten-free diet at the time that my blood tests were taken, just in case, and I've found how hard it is to stick to it, especially since my high school cafeteria has absolutely nothing except salad that doesn't contain gluten. I'll be heading off to college in the fall and have yet to decide what to do about housing and meal plans as a result of the dietary restrictions.

Any suggestions, reassurance that it's not as bad as it seems right now, or advice is greatly appreciated :D

Thanks!

Deb


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

One thing to keep in mind - if you have celiac, you are not allergic, you are intolerant. Meaning not that your body goes through an IgE antibody mediated process to produce histamine and inflammation, but that your body goes through an IgG and IgA (if you're not deficient) mediated process that destroys the lining of your intestines. One molecule of any substance your body reacts to is enough to trigger the immune system. In the case of allergies, the majority of the time the reaction is limited enough that a small histamine production is not an issue. In the case of intolerances, the reaction still causes damage.

(And if you're mom thinks that it's just an allergy and you can still have some, ask her to talk to someone who grew up with a mild allergy to something (say, latex, it's notorious for this issue) and then one day ended up in the hospital with anaphylactic shock because the "mild" allergy got major REALLY fast.)

But, more happily, congratulations on being finally diagnosed! Knowing what the problem is can be SO helpful! Search around this site for a LOT of useful information. My MIL got me (per my request) the Gluten-Free Diet: A Resource Guide (Open Original Shared Link .com/exec/obidos/tg/detail/-/1894022793/qid=1075414579//ref=sr_8_xs_ap_i7_xgl14/103-9153272-5155801?v=glance&s=books&n=507846) for Christams, and I find it a good basic reference that is generally useful. I hope that you find yourself feeling better quickly.

As for the food - it gets much easier to stick with it and stay on it without much hassel with practice. You might have to get cooking, but with practice, cooking your own meals can be a simple process that need not take a lot of time or effort. (Plus, if you cook in larger batches, you can keep some in the fridge or freezer for days you REALLY can't cook.) As for college, ask if any of the dorms at the places you're interested in going to have a kitchen. My dorm had a kitchen the whole dorm shared. You'd need some of your own supplies (pots that aren't contaminated, your own food, cutting boards, knives, etc) but I got all that stuff myself even though I wasn't (knowingly or symptomatically) celiac disease during college. And most colleges will allow you to opt out of the dining plan for medically necessary reasons if you present them with a plan to make sure you do get enough food.

Guest jhmom
It is of her opinion that I should still be able to eat gluten, just in small doses. I'm assuming that this isn't true?

Hi Deb, welcome to the board. Absolutely not, you should adhere to a strict gluten-free diet for the rest of your life, even "a little" gluten can and will hurt you.

I know right this seems very overwhelming but it will get easier, I promise. You need to read everything you can get your hands on about this disease and help educate your mom, knowledge is power! I too was diagnosed with IBS as I am sure a lot of people here have been. The good news is after going gluten-free I could feel a difference within a few days.

Here are some links to educate you and your mother and help you find gluten-free foods that you can eat. There is also a "Teenager" section on this message board

that would help you cope. I am sure they would have some suggestions for you as far as school / college goes. Also I would recommend finding a local support group in your area.

Gluten Free Products

List of Support Groups

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

I hope this helps you and your mom learn more about Celiac Disease.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,703
    • Most Online (within 30 mins)
      7,748

    Shenaz
    Newest Member
    Shenaz
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @nanny marley, Have you been taking any vitamins or mineral supplements besides Vitamin D? What are you eating?  Do you eat processed gluten free foods?   You said your symptoms included fatigue, body hair loss, low vitamin d,  Restless Leg Syndrome, Raynaud's Syndrome, contact dermatitis, rhinitis, body aches, TMJ, heart palpitations, sleep issues, vomiting,  dizziness, frequent bowel movements. There's eight B vitamins and Vitamin C that are water soluble.  When one has diarrhea for extended periods of time, those water soluble essential vitamins are flushed out of the body easily, and there's little time to absorb any more water soluble vitamins or fat soluble vitamins from food moving through that fast.   It's easy to become vitamin deficient with diarrhea.   Deficiency in Vitamin B1, Thiamine, can result in Gastrointestinal BeriBeri which can also cause diarrhea, fatigue, and abdominal pain.  Deficiency in Vitamin B3, Niacin, can cause diarrhea as well as skin rashes, and sleep issues.  Deficiency in Vitamin B12, Cobalamine, can cause diarrhea and Restless Leg Syndrome.  Deficiency in Vitamin C can cause diarrhea and skin rashes. Thiamine deficiency can also cause heart palpitations, sleep issues, and vomiting.  Have you had your thyroid checked?  Hypothyroidism can cause body hair loss, as can iron deficiency.   I've experienced serious nutritional deficiencies which my doctors did not recognize as such and blamed me for making stuff up.  I've experienced these nutritional deficiencies.  I earned a degree in Microbiology after studying nutrition because I wanted to know what vitamins were doing inside the body.  Vitamins are special organic compounds that our bodies cannot make, so we must get them from food or supplements.  Without these vitamins, our bodies cannot function well. Talk to your doctor and nutritionist about supplementing with vitamins and minerals that are lacking on the gluten free diet.  Blood tests for deficiencies in the B vitamins are not accurate.  Taking a B Complex and looking for health improvement is best.   I've got serious vision problems and would really appreciate punctuation.  Thanks P.S.  I take a combination of Thiamine, Cobalamine B12 and Pyridoxine B6 for back pain from crushed vertebrae.  I understand back pain.  These vitamins together relieve pain. 
    • nanny marley
      I ment nan not van 🤗
    • nanny marley
      Ii wasn't asked about that she just said if you can't tk the gluten diet have colonoscopy to check for cancer has my van had it and because I'd had naproxen for stomach ulcers but I stopped that a  while back but I've been very ill this week with the back issues so I can't have the colonoscopy too someone said ask for the virtual one it's much easier for people who have body issues too but I'm not sure I can request that if she doesn't think I need that she was basically saying IBS because Ive suffered since age 25 but that's Wen the back started too and I'm sure high calprotein isn't with IBS I've been low in iron Wen I was jounger and I'm always low in vitamin d I take my own supplement for that now there is definitely something going off its been too long a drawn out problem with added symptoms so I i will keep investigating 
    • Sanna King
      King Arthur Gluten-free bread flour contains wheat starch, but has had the gluten removed. According to the FDA, it meets the FDA's gluten-free standard of less than 20 parts per million (ppm) of gluten. Has anyone here tried to bake bread from this? If yes, did you have a reaction? Thank you in advance for your time and attention. 
    • Gliadingoaway
×
×
  • Create New...