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

2 Months In And Frustrated!


glutenfree015

Recommended Posts

glutenfree015 Rookie

Hey everyone,

I recently posted something like this in the college students forum, but I figured that posting in one of the other forums would reacher a broader audience. I


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



Celiac.com Sponsor (A8-M):



Skysmom03 Newbie

I would have the endoscopy or a colonoscopy done. That way they can look for other things besides just celiac. Could be that you are one of those few people who have to take steroids to see an improvement..... But that will never happen until they can get in there and check things out.

Sweetea888 Newbie

Being a celiac is hard no matter what your age. I really wish I had gone gluten free in college; that was when I first began having problems. I wasn't diagnosed until I was in my fifties. It is MUCH better for you to start now. I got very discouraged at first...after the initial excitement of feeling MUCH better. I can remember almost crying in the grocery store because I had to read every label.

My main advice is stick with it...it gets easier...and to be very careful. There is gluten hidden in all sorts of things..foods and non-foods. I even had to change toilet paper and my favorite shampoo because both had gluten. I have talked to people who really have had problems because they have eaten dressings, spices and herbs, and lots of other things that they thought were gluten free. Make SURE what you eat is gluten-free. Many items are marked...others (like many of Newman's products) are clearly listed on their website.

Hang in there! You will figure it out. And don't get too discouraged. When I was first diagnosed, my teenaged kids didn't want to go to restaurants with me. They were embarrassed because I had to ask so many questions and my choices were so limited. Now, they try to find new places and new dishes for me!

It gets better!

shadowicewolf Proficient

Where do you eat when your at school, in an apartment? A dorm? The food place on campus (so not CC free)?

It could be your body is still trying to get better. If so, then its best just to wait it out i'm afraid.

mushroom Proficient

You say you started feeling bad after you went home for break. Was anyone else preparing food for you during that time? Are your family gluten eaters? You could have been cross-contaminated very easily.

The nausea would be consistent with recovery from a glutening. Don't be discouraged, it happens to us all. Now that I am gluten free nausea is my main glutening symptom. All of us have symptoms that last for different periods of time.

You are doing all the right things. You just have to be super careful when eating food that you have not prepared yourself. Even though I'm sure your mom likes to cook for you, she probably does not know ALL the places where gluten lurks, and I am willing to bet that that's why you are feeling bad this week. Next week should be better :)

Hang tight and give your mom some gluten free lessons :D

Lisa Mentor

Where do you eat when you're at school, in an apartment? A dorm? The food place on campus (so not CC free)?

It could be your body is still trying to get better. If so, then its best just to wait it out i'm afraid.

Yes. Are you in your own place where you can be careful about what you eat and it's preparation?

If you have a clinical diagnosis, the college needs to meet you needs, by either offering you personal, clean space in the cafeteria or supplying you with gluten free options.

It sounds like you're in your own place or a shared apartment. Cross contamination with roomies is a large concern?

Also, as mentioned...it might take a while of 100%attempt at gluten free and dairy free to feel the benefits. Healing takes time, just as damage takes time.

You're smart about a food journal. Do you have a shared toaster, or check your makeup,lipstick, lotions, shampoos...anything that can get into your mouth.

Sounds like you are on a good track, but finding some missing pieces. That's a good thing. :) And be balanced, with fruit, grains, proteins and starches.

AND being home, is another lesson. B) Hope you feel better soon.

GottaSki Mentor

It is common to become more sensitive once gluten has been removed. Many that remove gluten do feel much better at first only to have some symptoms return. I know my digestive symptoms improved first, but there were times when they would return for seemingly no reason. It took months for me to prevent most glutenings and to figure out the difference between accidental glutening and other foods causing problems.

At times your healing system may react to any food which will leave you confused. I found it helped to note positive changes as well as negative. For many months the only positives were that my nails, skin and hair all were healthier. If you have a day that you feel good - take note of what you ate during the past two days - the positives can really help when you are frustrated by negative symptoms.

Try to limit gluten-free processed foods - the advice of sticking with whole foods is repeated here regularly because it really does help to remove processed foods while healing.

The ups and downs are likely to continue for some time - hang in there and come in here to vent - no matter the age, we understand your frustration.


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



Celiac.com Sponsor (A8-M):



glutenfree015 Rookie

Thank you everyone for your kind advice! It

ncdave Apprentice

Sounds like your off to a great start, keeping a food log is the only way during healing. I often wish i had started out like you, took me 2 months to remove dairy an 9 months to remove corn. If i had it to do over i think i would have been better to remove gluten,dairy,soy,and corn. Then i could have kept a food log and figured it out from there. Seems that would have been much quicker, and i would have spent many,many, less weeks sick. The dairy and soy symptoms are not so bad but the corn is just as bad if not worse than gluten! (for me)

I would recommend picking out a couple fresh meats some fresh veggies an fruits, live off those a couple weeks an then start adding from there. Stay away from packaged and caned foods right now. Do not let gluten-free labels tempt you (most are not gluten-free)! Rembember your going to have bad days even if you don"t eat anything wrong. Use those days to continue checking non food items for gluten. Don"t go anywhere hungry, if your going to be away from home a while take your gluten-free items with you. If anyone ask if your hungry tell them you just got finished eating :D

Megan- Newbie

Hi,

I certainly understand your concern. You're trying so hard but you still don't feel better. I actually faced the same problems. I followed a gluten-free diet for 2+ years after diagnosis but always seemed to feel worse. After 2 years of suffering, I researched celiac specialists after my GI doctor wrote me off and found Dr. Fasano at the University of Maryland Center for Celiac Disease. He told me that I was "extra sensitive: and even the little bits (less than 20ppm) of gluten I was getting from gluten-free foods was too much. I was prescribed his elemental diet. I was on this diet for 3 months before I could gradually introduce more foods. It essentially reset my immune system and for the first time ever my TTG, etc. scores were in normal range. You may want to consider making an appointment with this center (he isn't seeing patients after December) but there are other good doctors there. My insurance didn't cover my visits there, but trust me it was worth it. This is just my opinion but I hope it helps.

Megan

SMDBill Apprentice

I have not yet heard anyone say whether they have tried, but I have seen Probiotic products that are 7-day regimens for times when the gut gets into bad shape for more reasons than just gluten. I wonder if it would be worth a shot? Today's probiotics contain millions up to 35-70 billion bacteria cells to help get the gut the type and variety of bacteria it needs. Diarrhea and other things flush the good and bad bacteria, so replacement is sometimes necessary for celiacs. Personally, I take VitaCost 10/20 probiotic and I'm doubling up right now each day because I got glutened less than a week ago. The healing was slow without the probiotic, but the symptoms of glutening went away faster after I started the probiotics. Could be coincidental healing, but worth the shot since they're not harmful at all.

I am just throwing it out there in case you get frustrated and look for more immediate help. My 20 billion cells is minimal compared to that 7 day regimen that is something upward of 200billion per day. I think that's why the time period is so short. I read how many trillion bacteria cells are in our gut, but I cannot recall. Hitting it with heavy probiotics is possibly something to help more quickly get the gut in order.

If you are interested in probiotics, without knowing if you take them already, there is a lot of info online. I found that 1) you need more than one probiotic in order to heal the whole gut so look for those that contain multiples. THe one I chose has 10, but there are many types...2) the ones you find in a store seem to be of lower cell count than those at GNC or vitaminshoppe. Amazon also has a lot...3) They are not terribly expensive and you can get a discount for buying multiple bottles at vitamin shoppe, not sure about GNC or others...4) There are some accounts by specialists detailing why they prescribe them for patients with Celiac while others seem to ignore the possibility they can help. Mostly it seems as though those who do not prescribe them are less knowledgeable about what they can do rather than having evidence that they do not work.

Good luck with whatever you find that works. There is also information online from several specialists encouraging people to take a dietary enzyme with every meal in order to aid digestion. It may not be gluten that is now bothering you, but something that just irritates an already tender gut. I don't take an enzyme, and probably should, but perhaps that's another possible avenue to research and decide if it's right for you. Hope you find the answer soon and can really get healing.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,202
    • Most Online (within 30 mins)
      7,748

    Maroney
    Newest Member
    Maroney
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • kopiq
      I also have food particles left on toiet paper when i wipe and my stool is light yellow not absorbing fats. I urinate about 15 times a day and have very sticky snot,dry throat.
    • kopiq
      Hi all, I was diagnosed by blood work about 2 months ago and have since went on a strict gluten free diet. I have an endoscopy in January and the GI dr said nothing about staying on gluten for it; hes aware i went no gluten. starting to heal symptoms include: (this is huge) sensation coming back to genitals and when having a bowl movement. everything has been numb for a long time down there including lower belly button area. good size (not abnormal) bowel movements once a day or every two days. small dot size wart just fell off my finger that was there for years. have not broke out with a cold sore this winter (every winter prior for years i would develop a cold sore on my lip) Ongoing issues I don't sweat. not from my hands, or armpits or feet. I do not get butterflys in stomach. my hands have been so dry for years ive been using a crack cream as they crack and bleed very severely in the fall and winter.  (since going gluten free ive not used crack cream but they are still very very dry and chapped/flaky, no sweat or moisture in palms of hands at all. I dont crave food. i have no cravings at all, not for pizza, ice cream , nothing. my cravings are dead. smell of foods kinda make me hungry, but my stomach blocks it. pins needles in feet get weak legs standing up from sitting and dizzy, things almost turn black. i cannot tolerate veggies or vitamins. Iam vitamin D deficient according to my Dr and Ive tried vitamin D pills. they give me a massive migraine for 8 hours and upset my stomach. the heat from the direct sun make me extremely tired to the point of wanting to pass out. again i don't sweat. broccoli gives me a migraine headache as well. mushrooms, bell peppers burn my stomach. fruits burn my stomach, fats (peanut butter, any oil or fat from meats make me sick to my stomach for a couple hours or longer. salt and pepper burns my stomach. all these issues cause pain at my belly button area and expand to the rest of my upper stomach and sides the more i ingest through out the day. I currently eat bland basmati rice, chicken, pork chops (fat trim), boiled russet potatoes no skin for three meals a day. my snacks are gluten free ground buckwheat flour pancakes. (just water, no oil , salt, dairy.) how am i to get vitamins in my system if i cannot tolerate them in my stomach? i mentioned epidermal vitamin patchs but dr said no. why cant i stand the heat from the sun ? why cant i sweat? thanks for any info.                
    • trents
      Because you have significantly reduced your gluten intake over a considerable amount of time, it is likely that you will test negative on the antibody tests. However, if the $112 for the Quest test is not a burden, it wouldn't hurt to try. It tests for total IGA (to ascertain if you are IGA deficient) and tTG-IGA. If total IGA is deficient, it can result in false negatives in other IGA tests. The tTG-IGA is the single most popular test ordered by physicians. The Quest test is not a complete celiac panel by any means (refer to the linked article above) but it might be a good place to start. Personally, I think you know enough to conclude that you need to get serious about avoiding gluten, whether you have celiac disease or NCGS. Human nature being what it is, however, many people seem to need an official diagnosis of celiac disease in order to stay on the bandwagon. Otherwise, they seem to rationalize cheating on the gluten-free diet. And there is this misconception out there that NCGS is inconvenient and uncomfortable but not harmful so it's okay to cheat. The more we learn about gluten-related disorders the more they seem to not fit into our neat little black and white categories. By the way, celiac disease is not a food allergy. It is classified as an autoimmune disorder.
    • More2Learn
      These responses are all extremely helpful, ty.  Really good reminder about omega 6.  I also know I'm low in zinc; I took the zinc test where I drank it on a spoon and couldn't taste it.  To that end, I try to eat a lot of oysters.  I do think it would be a good idea to get the blood test.  Two questions: 1-  Is there any reason you wouldn't recommend that I just buy and take a test like this as a first step? 2- I've been somewhat gluten free since ~Jan 2023 (technically organic, gluten free, soy free, light on dairy).  I eat a lot of meat, vegetables, rice -- a common breakfast for me is three eggs and a sausage link, and I can't remember the last time I had a sandwich or bread.  However, because in my mind I didn't think I had an allergy, and I more was doing gluten free to avoid artificially iron-enriched foods, I do make exceptions.  I'll eat breaded calamari.  When my Dad visits, I split mozzarella sticks with him because he loves them so much.  I'll eat the "gluten sensitive" items at a restaurant and if they asked, "is cross contamination ok?",  I always said yes.  Based on that, since I never probably fully eliminated gluten, but it was significantly reduced... is that good enough to take the blood test?  Because the pain in my side gets SO bad (really sometimes I can't function, and I absolutely thought I was dying), I am hesitant to do the gluten challenge.  Would it make sense to take the test, and if it's negative, then consider doing the challenge and seeing if I can deal with eating the bread every day? Thanks again!
    • Yaya
      For me, with osteoporosis, Celiac and more than 1 heart condition, the slower, safer route is preferable.  I'm on 5 meds per day.  Too much of anything can disturb absorption of this or that. Have a Happy Thanksgiving.  I'm gone for a few days.  
×
×
  • Create New...