Jump to content
  • 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

What Is Normal?


raesue

Recommended Posts

raesue Rookie

I'm not sure of the correct place to pose a question about everyone else.

Kind of gross question:

Is it "normal" to have frequent, almost daily, constipation with cramps that rapidly transforms into extreme urgency and diarrhea?

Is it "normal" for this diarrhea to involve such things as undigested food, malabsorbed fat, mucus, and blood?

Do these things happen when there is nothing wrong with a person?

Was I lying when I told my daughter that she had to have blood work because most peoples tummies do NOT hurt everyday and diarrhea is NOT supposed to be the normal form of bowel movement.

Seriously, can we have all these issues without there being anything wrong with us?


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

No, what you describe is not what I would consider normal.

kareng Grand Master

I suppose you could have these things if they are a normal response to something like eating potato chips and soda all day. With a reasonablly healthy diet, this is not normal. Its not how the parts were made to function.

Judy3 Contributor

I'm not sure of the correct place to pose a question about everyone else.

Kind of gross question:

Is it "normal" to have frequent, almost daily, constipation with cramps that rapidly transforms into extreme urgency and diarrhea?

Is it "normal" for this diarrhea to involve such things as undigested food, malabsorbed fat, mucus, and blood?

Do these things happen when there is nothing wrong with a person?

Was I lying when I told my daughter that she had to have blood work because most peoples tummies do NOT hurt everyday and diarrhea is NOT supposed to be the normal form of bowel movement.

Seriously, can we have all these issues without there being anything wrong with us?

What you have described is me before I was diagnosed with Celiac and went gluten free.. :unsure:

IrishHeart Veteran

I think you already know this is not how a normal GI system works...perhaps you want us to tell you that you are doing the right thing by having your daughter tested?

You are doing the right thing by having your daughter tested. ;)

No one should have that going on every single day. (well, I did... but now I know WHY) And now, it doesn't happen anymore.

raesue Rookie

I'm wanting to be told something other than "its all in your head". i was even straight called crazy yesterday. my incredibly supportive boyfriend/father of the five year old child occasionally doubled over in pain from cramps thinks a negative blood test is sufficient reason to forget all of this. he even suggested I let him support us and.go back to school or at least begin socializing more with friends to get myself to stop creating health problems for myself and dragging our daughter into it. I'm making sure I'm not just missing something here in that my experiences are lesser or different than those of you who can actually prove something is really going on with you.

raesue Rookie

What I really want is scientific proof to throw in his face and scream STFU! or maybe I just want to rant. In his mind, no tangible evidence = nothing there


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

I'm wanting to be told something other than "its all in your head". i was even straight called crazy yesterday. my incredibly supportive boyfriend/father of the five year old child occasionally doubled over in pain from cramps thinks a negative blood test is sufficient reason to forget all of this. he even suggested I let him support us and.go back to school or at least begin socializing more with friends to get myself to stop creating health problems for myself and dragging our daughter into it. I'm making sure I'm not just missing something here in that my experiences are lesser or different than those of you who can actually prove something is really going on with you.

Many people have negative test results. If you want statistics to present to him--I am sure it's on this site somewhere. My doctor told me it was almost 30% of the time.

That's why so many people remain sick and in pain--reliance on a test that renders false negatives all the time. I am one of dozens on here who will tell you horror stories of what happened to us because our tests were negative and people said it wasn't the gluten. But we knew better.

Some of the people who are seriously ill from gluten intolerance never get "proof"--i.e. any test results that shows positive--but ALL of us know that symptoms such as the ones you describe are NOT NORMAL--in a child or in an adult.

Do not listen to what others say to you. If you think your child is ill from gluten (or you, for that matter--I do not know your health situation) and you feel she may do well without gluten in her diet, then take it out and see if she starts to feel better.

That's all the proof you need.

I know you want the piece of paper with positive test results on it so you can say "I told you so!"...I felt that way once, too....and even WITH that proof, it did not change a thing. No doctor has ever "apologized to me" (except one) or said "Oh wow--you were right all those years and you're not crazy..gee, sorry!..." Seriously, who gives a rat's butt what others think?

Your daughter's health is all that matters. Proof or no proof--recovery from illness is the best "revenge"....then you can say "I told you so" if you want.

Do what's best for you and for her.

raesue Rookie

My daughter's symptoms aren't that bad.... yet. She sounds like I did at her age, though, and I'm pretty miserable at this point. By experimentation with diet, we both seem much better gluten free. When our results came in, I gave her the choice whether to adhere to the diet or not. She chose chicken nuggets from burger king. It was the first gluten meal for both of us in 4 days. She decided to go gluten free after her first trip to the bathroom. The next morning she still wanted gluten food the next morning, and we both had frosted mini wheats. The evening, we lined up at the bathroom at the same time. That night, she complained of hemorrhoid like symptoms. This was two days ago. She has since been with my parents for the weekend, and my mom is to be keeping a food journal for me.

I don't think she's seriously ill at this point, but I believe she is headed that direction. It's just so much easier to be angry and defensive over your child than yourself. I'm afraid it does seem necessary to have her diagnosed to be taken seriously by the school. I realise I could just pack her lunch in future years and be good, but she's starting kindergarten where I know there will be daily snacks in the classroom.

IrishHeart Veteran

There are chicken nuggets that are gluten-free. There are cereals that are gluten-free. You can eat the foods you love. As for snacks, there are Mommies on here that deal with these easily on a daily basis and I am sure they would be more than happy to share their ideas with you. Read under the sections on children, baking and cooking, and recipes, etc. and get yourself a few good books on living gluten free.

School administrators and teachers are used to dealing with kids with food allergies and food intolerances. They don't need a certificate or proof.YOU JUST TELL THEM SHE CANNOT HAVE GLUTEN. PERIOD. They HAVE to take you seriously!

Anyone she stays with? Just tell them the same the thing. You're in charge of her health.

It's not a big deal, really. Just tell them your daughter is on a gluten free diet and that you can send gluten-free cupcakes or whatever other snacks with her to school--for her and to share. I believe that play-doh is an issue as well.

This is not a difficult lifestyle. Fast food is an absolute gluten-filled landmine, however and you really have to stop eating at burger king.

You sound as if you have been living with illness yourself for quite some time, hon. Yet you keep eating foods that send you to the bathroom?...well, frankly, asking her what she wants and then watching her--and you--- race for the bathroom--is a lot like hitting yourself over the head with a giant hammer. Soon, you will realize that it feels good when you stop. ;)

Best wishes.

cahill Collaborator
I'm making sure I'm not just missing something here in that my experiences are lesser or different than those of you who can actually prove something is really going on with you.

It took me 40+ years of testing,unnecessary procedures, unnecessary drugs,unnecessary suffering and pain, 40 +years of doctors suggesting I was making things up.Some of the docs actually telling me I was crazy, a hypochondriac BEFORE I was FINALLY officially diagnosed by a wonderful,open minded GI doc.

Many here do not have a "official" diagnoses.That does not stop them from doing what they need to do to be well.

A gluten free diet does not need a doctors order nor do you need a prescription.

I would encourage you to have all the testing done on your daughter before she goes gluten free though,, it is much better to have all the testing done before she goes gluten free than having to do a gluten challenge later on

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,947
    • Most Online (within 30 mins)
      7,748

    Sinch23
    Newest Member
    Sinch23
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.