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

Possible Celiac


bluesea84

Recommended Posts

bluesea84 Newbie

I'm 25 years old and think I might have Celiac disease, I know no one can tell me definitively whether I have it or not just based on some symptoms, but I guess I wanted to ask does it sound like it could be a possible case based on these symptoms. Some of these symptoms are embarrassing, but I'm just going to lay it all on the line.

I know this symptom is a Celiac symptom, basically I've been having the runs (loose stool) for over a year on and off. Sorry to get graphic but I have to for the same of explaining the symptom. It ranges from being normal, to being a half formed stool that kind of sticks to the bowl and requires me to open all the windows of the house afterward if you get my drift, and then sometimes I get just all out diarrhea. I can't remember exactly when it started, but it's been at least a year. I know I should have seen a doctor but I really can't afford it, and this problem comes and goes. Sometimes it's normal for a week and then it's weird for another week. I figured it might have been coffee because I read coffee is the number one cause of bowel problems. I cut coffee out for three weeks and it seemed to be getting a better, but at the end of the 21st day I had explosive diarrhea, so that pretty much ruled out coffee. My stomach has a burning sensation after I drink coffee, and yet I now know coffee isn't the actual cause even though it isn't good for me either.

Some other symptoms I've been having which may or may not relate to Celiac.

My bottom lip is constantly drying up and I can peel off an entire layer of skin every couple of days.

My wrists are incredibly thin, to the point where I look like a starving Ethiopian.

My endurance has always been crap, and I remember this symptom from when I was a kid. I was always lean and fit as a kid because I rode my bike frequently, but when I would start running a mile in P.E. I would hit a brick wall and crap out after about 30 seconds. I would finish the mile heaving and panting, and literally the only kids slower than me were 2 or 3 obese students. It never made any sense and always frustrated the hell out of me.

I was always very tired in the morning, could barely keep my eyes open.

I read delayed puberty is a symptom. Well I didn't stop growing taller until I was 22 years old. I look unusually young for my age, I'm 25 and I look about 18 years old and that's being generous. I was always skinny and underweight and under height, which could be a symptom. Presently I'm 5'8" and weight about 145, which isn't really that underweight but I just never seem to gain weight no matter how much I eat. I can eat an entire pizza and gorge myself for a week and I'll lose a pound. I also have a incomplete facial hair that's still coming in combined with skin problems, whiteheads on my face and red bumps all over my back, it doesn't itch like Dermatitis Hepaformis, but instead just hurts like hell.

I also have intense anxiety, depression, and insomnia. Of course, that might just be because of all the symptoms I'm experiencing. But the anxiety is real bad and uncontrollable, it's gotten real bad in the past year or two.

This last one is embarrassing but I have to mention it because I read this may be associated with Celiac. In the past few years before I started to get the runs, I would have Large stools, really large, a foot long at times. I had to get the plunger on different occasions.

I can't honestly say I get bad symptoms right after I eat gluten. Sometimes I'll eat 6 slices of pizza and I wont get diarrhea. I just feel lousy all the time, and the bowel problems always come back.

So does that sound like it might be Celiac? I really can't afford to see a Doctor as I don't have Insurance and I'm broke. I ordered the Biocard at home test kit for $42, even though I live in the USA and it hasn't been approved by the FDA, I ordered it from some online place in Australia and paid $12.50 for international shipping. By the way, why in the world can't I order this kit in the USA? I mean it obviously works as it's for sale in every European country, in Canada, and in Australia. The FDA's going to sit on it for a whole bunch of time to "confirm that it works" when everybody around the world already knows that it works? There are thousands of people who could use this test in the states.

So hopefully that kit will get here but if doesn't I'll just try and find some other place to obtain it. I figure if it tells me no, I may still have Celiac, but if it tells me yes I'll definitely know I have it, so the possibility of obtaining that yes is worth the $42 in my mind.

Anyway, thanks in advance for any replies to this.

Edit: Forgot to mention two symptoms, I burp like hell constantly, especially after a meal, sometimes little small belches and sometimes big roaring belches. Also I used to have constantly have bloating and gas in the evening after dinner, but that doesn't seem to be as bad lately, for whatever reason. Dunno how I forgot to mention those symptoms.


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

I'm sure you've come to the right place for answers, even if you don't have trouble with gluten. Many people here can relate to your symptoms, and will likely be able to guide you in the right direction, Celiac or not. But, based on the symptoms you've detailed, it could certainly be Celiac or gluten intolerance. Either way it means avoiding gluten.

There is a very easy and basically free way that you can get a much better idea if gluten bothers you, than anyone here can tell you. Simply avoid all gluten for a few weeks or so, and see if there is any change. If your symptoms significantly reduce or clear up completely, then you have your answer. Note that some people need much longer than others to feel better though. For me it was six months before there was any noticeable change.

The only possible downside to going gluten-free without having tests done, is that it makes the accuracy of any tests you may wish to have done later all-the-more unreliable. Since antibodies generally hang around for about two weeks, I'd guess it wouldn't impact test results so much if you tried gluten-free for less than that. The longer you remain gluten-free, the more the antibodies and intestinal damage are expected to diminish. The best tests are not very accurate though, so regardless of what they say, you'd be wise to try the gluten-free diet anyway.

If you ever decide to get tests done, you'd have to go back to eating gluten for at least six weeks first, to have any chance of accurate results. Many members here have reported that once gluten-free, and symptoms go away, accidental ingestion means much more pronounced symptoms, and even new symptoms. So basically, if you do have Celiac, there's no turning back for testing unless you are prepared to deal with a lot of suffering. If you don't have Celiac (or gluten intolerance), you'll be fine on a gluten-free diet, and returning to eating gluten won't bother you at all.

Welcome to the board! I hope you get the answers you need.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,189
    • Most Online (within 30 mins)
      7,748

    Eric bell
    Newest Member
    Eric bell
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • 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.
×
×
  • Create New...