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

Questions And A Tiny Vent.


JosieToxic

Recommended Posts

JosieToxic Newbie

Few things:

  1. This is my first post so, Hi!
  2. I have only been dealing with all this stuff for a short time, was confirmed Celiac July 9th, been gluten-free for less than a month (started gluten-free after my EGD on June 25th).
  3. My brain fog is pretty terrible right now and I am sorry if this is as much of a hot mess as it feels like to me.
  4. I know there are threads about changing symptoms after being gluten-free for a while, but I am having a heck of a time finding them, so my apologies if the answers I seek are they I was unable to find them.
  5. Up to this point I have not had obvious Digestive symptoms (Cramps, bloating, Diarrhea) 

 

Alrighty, Sister-in-Law is getting married tomorrow rehearsal was today and we all went to a Mexican place for dinner. Long story short I got gluttened cause I didn't stick to my guns and not order food, and my mother-in-law was starting to spaz out that I wasn't going to be able to eat anything. Ultimately my fault, I really knew better, and did it anyway. Maybe now they will be more aware of what is going on and not make things harder for me if I don't order anything.

 

So this is the second time since going gluten-free that I have been gluttened, the first time was only a few days after starting and my symptoms were pretty much what I was used to. This time things are very different, a lot of the same stuff is there: Brain Fog (did not miss that let me tell you!), irritability, joint pain, attention issues, super tired, and a rocking headache. Then there are some new things: I keep coughing for no reason (maybe unrelated but not sure), and stomach pain, like muscle pain not really what I expect cramps to feel like. Kind of like someone punched me in the stomach a couple times. Oh and my skin is super itchy.

 

The stomach pain started about the time the food was probably hitting my small intestine from what we (me and the hubs) can tell. I know this stuff is different for everyone but does this ring bells for anyone else?

 

Thank you all so much, this forum has been SUPER helpful for me so far even though I haven't posted before now.


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



Celiac.com Sponsor (A8-M):



Georgia-guy Enthusiast

Josie, welcome to the cool peeps club!

I have not heard of cough directly being associated with celaic (so maybe unrelated?). The other symptoms you list, I have heard them all associated (and I have experienced them all). I have not heard the stomach pain described as being punched in the stomach, but it does kinda fit to be described that way. I'm going on the assumption (yeah, I know what happens when we ass-u-me) that you are female, and I will say someone I spoke with described her stomach pains as a "higher up menstral cramp". (Which on that description mean when a woman says I don't know what menstral cramps feel like, I can say I do

user001 Contributor

I really hate when families are like that. I also have some in my family that are very not-understanding. It is really hard but I always bring at least a quest bar in case. They are under 200 calories but have a ton of protein so it keeps you really full and they gluten free. Chocolate chip cookie dough is the best. When I accidentally have gluten or just make a bad choice, my symptoms aren't so much gastro either. The biggest symptom I have is brain fog, followed by flushing face, fever, irritability, extreme fatigue, and headache. I also discovered that I still cannot eat oatmeal, even certified gluten free oatmeal because I have alot of the same symptoms.

 

The stomach pain.I have this, no matter what I eat. I have been struggling with this since january. I have brought it up to my doctor several times, but he seems to not want to properly address the problem. For me it starts to feel almost like a hunger pain, so I first thought I had an ulcer but my endo revealed no ulcers. Then it may get a little worse and start to feel like a cramp or like someone is kicking me in the gut, almost takes the wind out of me! If I pay attention it is more so to the left side and I can sort of feel it in my back. For me, It starts between 1-2 hours after eating, sometimes 1-3 hours. I have determined this to be a pancreas issue. From the little that I have read, it has something to do with the small intestine not producing enough enzymes for digestion and things get all crazy with the pancreas causing a lot of pain during digestion. I could be wrong, but I am sure there is a veteran who would be better educated on this.

 

Things that have helped. I just recently have started figuring out what helps. I bought some digest gold at the vitamin store and I take 2 at each meal. I tend to eat larger breakfasts so sometimes I will take 3 in the morning. This confirmed what the problem was for me, because the enzymes worked. If I have more food than I anticipated or just don't take enough enzyme pills I end up having the pain. The only thing that seems to help is if I lay on a heating pad for awhile or just drink my meals in the form of a protein shake instead.

 

Edited to add- BTW I have had a little nasal drip since I had a cold in october/november. It sometimes causes me to cough.

w8in4dave Community Regular

Yup I remember when I started the gluten-free diet. Felt like I was hit by a Mac truck when I got Glutened. It did feel like I got socked in the gut and I also threw uo was on the floor because I couldn't get up. I layed there for hrs. It was just crazy! I feel so bad that you didn't get support. I tell the waitress I have Celiac and have them help for a choice. I am also Corn intolerant it is had on me at a Mexican restaurant but is do able. Don't be afraid to ask a waitress or talk to a manager and see what they say. I was always shy about that kind of stuff. And the 1st time I asked a waitress what was a good gluten-free selection my friend said she doesn't have to know your problem I said yes she does so she can help me. And they will. Good luck! I hope you feel better soon. 

cyclinglady Grand Master

My stomach twinges, I burp and I feel like a rock is in it when I first get glutened. I hope you feel better soon.

Mexican restaurants are no safer than others. Sure, you can order tacos, but be sure they are 100% corn soft (not fried) tortillas as some are now adding wheat to make them more appealing to gringos (and pliable). Ask to see packaging. No corn chips or fried taco shells due to cross contamination issues (chimichungas or flautas are often thrown into the same fryer.) Enchilada sauces are often thickened with wheat flour.

The bottom line is that you have to ask and I am not talking about a waiter, but a manager or chef. If you get a "deer in the headlight" look then do not order! Listen to your "gut" feelings and do not discount them. I try to check reviews from other folks who have celiac before trying a new restaurant or use a celiac disease website.

I always travel with some safe food. You can just order a drink and enjoy the company.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • 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.