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

Well I Need To Change My Signature :(


Guest AutumnE

Recommended Posts

Guest AutumnE

I have been giving my daughter low doses of gluten to see if she seemed to be having a problem after a while of being gluten free and she had a reaction I believe.

Tonight she has a rash on her labia and it is itchy kinda looks dotty. I always keep her dry and put a barrier cream of some sort usually aquaphor. Also at her dentist visit the other day he noticed her enamel looking a bit weak? I told him we do have celiac disease in our family and Im getting her tested and he said there were no cavities yet but it will lead to them possibly.

She had reflux as a baby for six months but seems to be fine with it now. Man, it was hard enough for me as an adult to deal with let alone a little kid whose inlaws do not care if she had a hard time with her diet and would definitely gluten her without thinking :rolleyes: Im fine with me having it, it doesnt bother me at all but the thought of her having it at such a young age breaks my heart :(

My nephew who is six months, my niece who is almost 2 and my older sister all were just diagnosed with celiac disease.


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



Celiac.com Sponsor (A8-M):



Rikki Tikki Explorer

Autum:

I don't mean to seem as if I am coming down on you, but why if you suspect celiac would you give your daughter even low amounts of gluten?

It seems to me that it would be easier to have her grow up being gluten free rather than have her change to gluten-free after she is older.

If it were my daughter and I suspected celiac I would stop the gluten and see of she get's better.

I just don't see the sense in an official diagnosis if she or anyone feels better without gluten.

Best of luck in this

Guest AutumnE

I havent ever had any suspicion that she has celiac problems till now. I kept her off gluten just because I am gluten free with no true diagnosis yet since that is what I cooked. I talked to a gi recently and was told that keeping her off gluten even if she does not have gluten intolerance gene that it would make her body sensitive to it which I dont want to limit her if she truly would never have a problem, but I am nervous that it just wont show up yet.

I dont require an official diagnosis this was enough proof from just a 1/4 cup of regular mac n cheese total over two meals, not alot sorry if it came across that way. This is the first time I questioned it with her since she is a fine totally normal toddler with no problems till now. I also ordered the enterolab tests today to see if she has the gene, even if she doesnt Im still keeping her gluten free. The dentist visit was the first time he saw a problem and we have been going since she was a year old. It may be a coincidence still if the gene test comes back fine but I dont want to take a chance.

I always figured her reflux and was told by dr's it was normal since she was a little early, it may still be only that but I had no idea till research today that it could be related.

CantEvenEatRice Enthusiast

Hi Autumn,

My 19 month old son just tested positive through Enterolab. I was really sad about it, even though I kind of suspected it. He never had any clear symptoms, but my gut told me something was off (occasional bowel issues, sometimes a strange diaper rash and eczema issues). His height and weight are normal and he seems happy and energetic. But I have already noticed that his tummy is less bloated today. I have Celiac myself and hate it so I certainly did not want him to have it. However, I try to look at it as I am helping to prevent a host of illnesses/problems he could develop in the future if left on gluten (that is what happened to me!). I am still suffering the consequences of a delayed diagnosis. But, I am still really sad about it. And I agree that trying to get an "official" diagnosis is very difficult and you will always question either way. In one way I am glad to get a positive from Enterolab, but in another way, I still question that it is 100% accurate. But I think the diet will tell the most. Good luck!

Guest AutumnE

Thats the reason for me too :) It kills me but I would feel bad if I didnt change it even if the test comes back negative. I hate to think of her having the host of things wrong with her that I do. On a mission to become healthier is how I stumbled across celiac disease. I had never heard of it before even though I went through nursing school for two years. I'm glad to have the knowledge to help her that I never had when I was growing up. The only problem we have had is a heart problem with her.

Due to my nephew having seizures I recommended to my sister to have herself and her kids tested through enterolab and their results came back the other day with two gene markers but thankfully no damage they believe due to the antibody not showing up.

Its taking me forever to look up and research things, it is so involved for me but Im getting there.

CarlaB Enthusiast

What I'm confused about is what your doctor said about even people who have no problem with gluten will become sensitive to it if they get off of it. Is this really true? It just doesn't make sense to me. I mean, I can go for months without eating a certain food and I don't become sensitive to it. I'm not asking rhetorically, I really am curious.

eKatherine Apprentice
What I'm confused about is what your doctor said about even people who have no problem with gluten will become sensitive to it if they get off of it. Is this really true? It just doesn't make sense to me. I mean, I can go for months without eating a certain food and I don't become sensitive to it. I'm not asking rhetorically, I really am curious.

I've heard this before, but I think he is misinterpreting. I think that people who have a subclinical (symptomless) gluten intolerance will find that their health improves generally when they go gluten-free, but when they eat gluten again, they react just as though they had always been intolerant.


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



Celiac.com Sponsor (A8-M):



CantEvenEatRice Enthusiast

Autumn,

Your signature sounds just like me! I have a lot of your problems as well. I was glad to read that your sister and kids tested negative through Enterolab. I actually like to hear about people testing negative because I was getting nervous that so many test positive. But at the same time, most people who test through Enterolab already pretty much know they have it so the high number of positives make sense. I still like to hear about negatives though. I think I will always be a little nervous that I made the right decision going with Enterolab. But I figure someday my son can do a gluten challenge if he wants to. Right now he cannot make such a big decision and the consequences of eating gluten could be huge if his diagnosis is correct. If someday research is published that says Enterolab is completely bogus then I will deal with that then. But from what I have read, it doesn't seem that Dr. Fine is in the business of pure money-making. Plus, I have read so many stories of people who are so ill, but test negative through blood and negative through biopsy. They then go on the diet and a miracle happens! I just don't understand why doctors won't just say, skip the tests and try the diet and see. It is all so very frustrating! I cannot even tell you how many doctors I saw starting at age 13 all the way until my diagnosis at age 25. I am now 28 and still do not feel very well. Just take it one day at a time. My son got a hold of a goldfish yesterday and ate it. So I know there will be some mistakes.

Guest AutumnE

Carla- I was told since it was a toxin that your body will treat it as one if avoided. It wont be the same effects of glutening. He said there were low levels of toxins in vegetables and grains that need to be cooked in order to eat.

canteveneatrice- Actually they tested positive also with a double gene for the kids and a single one with my sister so her dh has a gene also. I do know of one person who tested negative to it on another board.

The gi doctor I saw said that the gene tests have been proven reliable however it does not classify it as celiac disease without the damage shown to the villi. He said gluten intolerance does not always manifest itself as celiac disease, studies still not out yet, but it puts you at great risk for it so he still monitors them and encourages a gluten free diet since it puts them at risk for developing it. When I get the results back he is going to do a biopsy regardless of the antibody showing up or not. He also gave me the name of a pedi gi to take my daughter to if any of her tests come back showing it.

CantEvenEatRice Enthusiast

I must have read your message wrong. Sorry about the positives, that stinks! But it is good to know. I hope you find out soon also.

Guest AutumnE

It does suck but it is best to know before real damage can occur. Even though I wouldnt wish sickness on anyone its comforting to know my daughter will have family that understand instead of feeling odd or left out if she has it. My parents are going gluten free also since we get it from one of them.

My mom has bought only gluten free foods for a few weeks now in suppourt of her grandkids and me and my sister. We wont have to worry about being glutened over there either :)

Im the only one who has very obvious symptoms, I believe I was meant to have this or I wouldnt be able to help my daughter and my niece and nephew.

CarlaB Enthusiast
I've heard this before, but I think he is misinterpreting. I think that people who have a subclinical (symptomless) gluten intolerance will find that their health improves generally when they go gluten-free, but when they eat gluten again, they react just as though they had always been intolerant.

That makes more sense. And the thing is, they should be off it anyway!

prinsessa Contributor

I'm sorry that your DD might have gluten intolerance. I just found out this week that both of my kids have it. I thought for sure DS had it, but I wasn't sure about DD. DS is 3 years old and still only weighs 28 lbs. He also has only had a few solid bowel movements. I was kind of scared of testing the kids because I know how hard being gluten free is since i have been off gluten for 7 months. I knew I had to do it though because of the problems having undiagnosed gluten intolerance can cause. I'm glad I know now and this is their second day 100% gluten free. Good luck!

Guest AutumnE

Hi prinsessa :)

Good luck with the change also, Im glad you have answers for your son and daughter. I do worry about the future with her in more ways than one. Feeling different like I always did growing up with asthma and epilepsy, cheating even when I didnt want too with my allergies just because I didnt want to explain, and feeling deprived from so many things. I hope by doing this so early we can avoid all they yucky intolerances I have that Im dealing with now. I think that has been more difficult than the gluten.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,175
    • Most Online (within 30 mins)
      7,748

    Lizzy W
    Newest Member
    Lizzy W
    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

    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
×
×
  • Create New...