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

Randomly Sick


123glldd

Recommended Posts

123glldd Collaborator

So every so often for a few years I got upper abdominal pain. Upper stomach right between the ribs. It happened so infrequent that I left it alone. I found it increasing and many times waking me up from my sleep for a little while...taking an anxiety pill or chewing gum or eating a little sometimes helped but sometimes it felt so achey i thought i'd be sick but it would subside. So fast foreward to me finding out i have celiac disease..i have UTI test strips that I use from time to time to make sure i don't have something when i feel sick as i have a history of them. Bilirubin is on these strips as well. It was elevated. However in november 2011 i had blood tests and they were pretty normal levels. Though I had had water within 4 hours of the test so that could have messed it up. Anyhow..at first i was scared about this as bilirubin isn't suppose to be in urine and so I went to the doctor and he sent me for an abdominal ultrasound. Liver, pancreas, spleen. kidneys...i might be forgetting something. All turned out perfectly normal looking apparently. So the doctors theory was Gilbert's Syndrome. Later I found out leaky gut can cause it as well. So I don't really know for sure what causes it with me yet.

.I did fine for the first 2 months or so gluten free then had a reaction..gluten or otherwise to something in the beginning of august. Lots of mucus etc. Since then I've been on a pretty limited diet and trying to re-introduce things. The upper stomach pain has continued..but it's not as severe as it use to be...and i seem to get it primarily during the middle of my cycle. I am currently working on keeping track of that on a calendar because I SUPPOSE it could be SOMETHING hormonal? Well anyhow...fast foreward december 29th 2012...I woke up nauseous. Never had anything different to eat other than what I have been eating the past few months. My temperature while up and walking around was 99.2 which is technically not a fever but i'm usually between 98 and 98.5 and rarely do i get above that from just walking around the house. So my temps were elevated a bit. This was not the same kind of sick feeling that i got from the tummy aches..this was full blown nauseous. So I was nauseated for a couple days. Then the last couple days I'm waking up with really loose bowels. No mucus. I have had a stressful month so i suppose it could just be that? But it's not completely watery but like a step away from it...tons of little bits of stool rather than water or full pieces. Very small tiny bits. And yellow. Now over the years when I'd have "irritable bowel" (most likely i was celiac then tho) I'd have yellowish stool. My mom said she'd had it before and she doesn't even have what i have that we know of. Just when she'd have diarrhea sometimes it was that color. Right now...no tummy aches but i've been checking my bilirubin in urine again since the 29th and it's been elevated. Did I get glutened? Does anyone else just get randomly sick for no reason while healing? Not sure what could be causing the elevated bilirubin right now as it had started to get a bit better for a while...but i haven't been getting my usual 8 glasses of water and have not eaten as much as i'd like and i know dehydration and starvation can cause it to happen as well. Past two days I've eaten a lot of ore ida fries it's all my tummy goes for as well as broccoli. I know the fries have annatto food coloring..could that be why my stool is yellowish?

So many factors...really cranky about it all right now...just wanna feel normal and go DO something lol Thoughts?


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



Celiac.com Sponsor (A8-M):



GFreeMO Proficient

I had elevated liver enzymes when I was diagnosed. It's a hallmark symptom of celiac. The fevers I run when glutened same thing with your stool issues. It sounds to me like you were glutened!! I would lay off of those fries and make your own. Just peel some potatoes cut into pieces and put in a bag with some oil and shake it up then just bake at 425 until they are done like you like. You can broil the last few minutes to get them brown and crispy.

Hope you feel better.

123glldd Collaborator

Ore Ida are gluten free though and they've never bothered me before?

123glldd Collaborator

Still trying to figure out where the heck gluten could have gotten me....

123glldd Collaborator

My diet the day before this started was:ore ida fries, goya black beans and chick peas, kettle sea salt chips, and rice chex. None of which have been bothering me. My husband is worried that i might be eating beans too much. Almost every meal every day for a while now.

GFreeMO Proficient

Sometimes we just don't know what could have gotten us since reactions can be delayed. When you have been glutened, sometimes it helps to eat nothing processed until you start feeling better.

Beans may cause gas but they wont cause you to be glutened though. I wouldn't worry about that. Maybe try eating some baked chicken and a sweet potato or some fruit or rice or eggs etc.

I hope you feel better soon!

123glldd Collaborator

It's just....I've been so limited....if i didn't eat some of these processed foods i'd be missing on nutrients like for instance..rice chex. I also would NEVER get enough calories into me. But I've been eating them with no issues now for months. Last time I had a reaction (august) it was mucus and diarrhea all the time. I'm only getting it upon waking. And it came days after the nausea...i'm so confused :(


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



Celiac.com Sponsor (A8-M):



123glldd Collaborator

Only thing I'm wondering is ....my husband still has dairy and peppers etc...if I had a casein or nightshade problem that I don't know about...can kissing him be like kissing someone eating gluten? I dunno how casein and nightshade react on people if they are not eating it. Is it as bad as gluten? Cause if so do me and my hubby have to worry about cross contamination? I do distinctly remember a night or two before getting sick he had made homemade queso and i kissed him and could taste the dairy and pepper but...i figured i wasn't EATING it..and i dunno for sure if i have issues with it so i didn't worry about it..then this happened.

123glldd Collaborator

As for sweet potato..haven't reintroduced it and i don't eat chicken after a bad experience getting sick in 2005. I've been worried about POSSIBLE salicylic acid sensitivity and sweet potato is high in that. I tried turnip greens and had a tummy ache mid december and no idea if it was actually them or something else that caused it as it SEEMS it happens middle of my cycle. So you see my dilemma...I have a lot to figure out.

123glldd Collaborator

p.s. what my husband was worried about is that i may be making myself intolerant to the beans by eating them too much. And that that might be why i'm not well. I haven't eaten them in two days now and the nausea is gone. Whether that is coincidence or not I have no idea. But he didn't think I was glutened by them.

kareng Grand Master

I think what your hub is worried aboout is that you don't eat a very balanced diet. Maybe some veggies or fruit? some protein? Fiber? No one will digest well on that limited diet.

123glldd Collaborator

Or maybe it's a virus working it's way through my system i dunno :(

123glldd Collaborator

I do eat broccoli and cabbage and carrot that was just what i was listing from the day before.

123glldd Collaborator

He is worried about the limited diet but i tried to have turnip greens and had a tummy ache. What he's specifically worried about at the moment is the beans being eaten multiple times a day every day.

kareng Grand Master

Wendy, I'm a bit worried about you. You are posting every few minutes, whether you have a comment or not. Stop and take a breath. I think the idea of meditation or Yoga or something might be a very good idea. Get out and find something to do.

Trying turnip greens....try something else. There is no calories or protein in turnip greens.

123glldd Collaborator

I eat salmon and lean ground beef thank you and there is protein in all the beans. I post every few minutes because i just didn't bother to go back and hit edit. As for going out i feel too sick.

What I am severely lacking is calcium which is why turnip greens were a focus.

love2travel Mentor

Wendy, stress is no doubt exacerbating your symptoms in addition to your severely limited diet. Are you able to take calcium supplements? Are you taking any supplements? Probiotics?

GFreeMO Proficient

So Delicious Coconut milk has calcium and is really good. You could try that.

123glldd Collaborator

Supplements don't agree with me much. I was taking vitamin D3+K2 in a liquid supplement form before all this. At some point while visiting my family back home i realized it was tasting funny. So i stopped drinking it for a couple weeks till we got back and i bought more. Next thing i knew it i didn't have the guts to try it after my glluten or whatever it was reaction in august because i MIGHT have a salicylic acid problem and it's a fruity drink it comes in. I'm scared to take normal supplements because my tummy is sensitive even to food right now so supplements are scarier especially in pill form. The company who makes my vitamin I was taking is nutrimetrix and it's apparently gluten free but whether that's certified i have no idea. They just told me it was. But it's not even so much the gluten that worries me about it...well, that's a lie...all of it worries me but...calcium i have never taken..never needed to because i always drank so much milk and ate greens. Since all this in august I've not had much of both only cabbage and broccoli and some turnip greens that may or may not have upset my stomach. I desperately know i want calcium. Which is why I've focused on that. It's also why i eat the rice chex and beans...per serving the beans have 4%...the rice chex 10% etc Even more worrisome about the calcium is that i eat protein ..and protein can block absorption of calcium so even tho i may get 20-30 % my daily intake of calcium a day...i dunno how much of it is being absorbed. I know I need to eat more but i can't very well try something knew after the turnip greens when my tummy ache lasts a week and then it was christmas and i just wanted a merry christmas and i was going to try pumpkin we have in cans here after christmas but now i'm sick again. I can never feel well enough for enough time to be able to experiment. When the sickness lasts a while and then i don't have much time to get something new into me. I'm not going to try something new while i'm still sick otherwise i won't know if it bothers me and it's becoming a huge hinderance to me so I don't like feeling judged by some on here about this. I'm trying as best I can. This is why i brought up the random tummy pains that don't involve diarrhea or anything like that...the part of my original message that is completely different from what i have now...because that has become a hinderance to my being able to experiment. I can't tell for the life of me whether it was the turnip greens or that i get this odd ache randomly mid month because it seemed that way from the last couple months. I'm waiting for mid month this month to see before introducing something else completely new. Otherwise i won't know whether to try the turnip greens again or not. This is all too frustrating. I cry almost every day because I don't know what to do with myself. I wish people on here would ASK me though instead of making me feel judged..assuming i don't eat protein etc. All I said was what I had the day before my getting sick i didn't list off everything i eat :(

123glldd Collaborator

So Delicious Coconut milk has calcium and is really good. You could try that.

I know and i LOVE their chocolate but i was having that and even amy's palak paneer after the original episode in august and was fine but the tummy aches that seem unrelated to this i have now continued so i cut it all out. I was also nervous about the coconut milk because of sugar and i wasn't sure if i had candida and all this..it's all been guess work. I've been wanting the coconut milk so bad again :(

GFreeMO Proficient

I'm sorry and I don't mean to sound rude but you are really wrapped up in counting calcium and protein etc. How about calcium fortified OJ or So Delicious coconut milk or almond milk etc.

You said that you eat ground beef. How about making a hamburger and eating lettuce, tomato, pickles, ketchup etc. Fry some bacon to put on top...so many things to eat to be concentrated on a few foods.

123glldd Collaborator

I do want to say...this past couple months have been extremely hard on me and my husband. And I already had anxiety disorder...specificially about stomach sickness mostly. But I'm very close to my grandfather and he has alzheimers and end of november i was crying all the time thinking about that and i've been cutting toxic people out of my life on facebook...even family who i just know don't really care..we had a falling out with someone who was suppose to be a close friend.....I'm emotional as hell and i'm scared for my health....i go looking for preferably safe frozen food because it's easier to prepare and i can't find safe companies. I generally eat green giant broccoli and use a pressure cooker for carrots and cabbaage which is fine. I want more cauliflower etc and to try frozen spinach but can't find that in green giant and i don't trust bird's eye etc :(

123glldd Collaborator

I'm sorry and I don't mean to sound rude but you are really wrapped up in counting calcium and protein etc. How about calcium fortified OJ or So Delicious coconut milk or almond milk etc.

You said that you eat ground beef. How about making a hamburger and eating lettuce, tomato, pickles, ketchup etc. Fry some bacon to put on top...so many things to eat to be concentrated on a few foods.

And this as i said before is my issue....I'm unsure what caused the reaction in august. I was eating all kinds of things right left and center before that happened without issue. Including dairy. I don't touch almond milk because it's high in salicylic acid...same with tomato and ketchup etc orange juice would be good onlly for the fact the orange would be a nightmare for my stomach right now. It's high in acid content. I'm completely lost :(

123glldd Collaborator

Point being i'm not stupid..and i'm not avoiding this stuff for no reason....i have reasons.

123glldd Collaborator

We have a can of libby's..or is it liddy's? i don't remember...pumpkin out in the cupboard. My stomach grumbles just thinking about taking a spoonful of it but i don't want to do it while already sick. Which seems to happen on and off all month..which was my original question....while healing is it normal to just...get random stomach discomfort without it being a reaction necessarily to anything in particular? I just want those stomach aches to stay away long enough for me to find out. I could try something now but i'm sick either from gluten or a virus of some kind right now.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.