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

Ahh! Obsessing About Other Problems Now!


123glldd

Recommended Posts

123glldd Collaborator

Guys I am totally freaking out....

#1 I've had anxiety issues most of my life...just putting that disclaimer out there. I KNOW I am overreacting....I just keep..."what if" ing.

#2 When i got my enterolab results...my fat content was 332..normal was below 300. My husband was about 700-800. It stated that Biliary Cirrhosis and pancreatic problems can cause that..or simply malabsorption due to celiac...or even just a high fat diet.

#3 For a few nights there I was waking up with tummy pain and nausea around the same time every night.

Okay..the past two nights i've been okay. *knock on wood*

So....I've not been feeling great and my husband suggested I do a UTI test. Well, the UTI test strips we have also have bilirubin on it..which of course is to do with the liver. I did 3 tests to be sure of my results. 2 were a color that didn't even match any of the colors on the comparison chart the last one was normal.

Blood tests I had in november 2011 showed all within range results for total bilirubin...albumin....alkaline phosphatase, ALT and AST....

So here's the thing...I'm still freaking out! Thinking about gallstones and blockages of bile ducts....please someone tell me i'm crazy and probably fine? lol *bangs head off the desk*

Yeah I really hate anxiety.... <_<


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



Celiac.com Sponsor (A8-M):



tom Contributor

Well I dunno if you're crazy, but ya REALLY ARE probably fine. :)

lynnelise Apprentice

I wouldn't say your are crazy. All I can say is that I wouldn't worry too much about a blocked bile duct. Symptoms are usually pretty severe. My husband had one and he was doubled over in pain, the whites of his eyes started turning yellow, and his urine was day-glo orange!!!

Couldn't hurt to see your regular doctor and ask for some labs though!

ravenwoodglass Mentor

I agree you should talk to your doctor about your concerns. If your DH hasn't seen a doctor yet to figure out why his FF score was so high it would be a good idea if he did.

123glldd Collaborator

Thanks guys. In the bilirubin topic I created I wrote out my experience with the doctor today..here is what i wrote in that topic:

I just got back from the doc and he felt around my abdomen..didn't feel anything weird and asked me if it hurt....i always feel a little uncomfy having my abdomen pressed on but nothing hurt at all. There was a trace small amount of billirubin in my urine he said but he thinks at worse it's probably gilberts syndrome. He said starvation (i think? and i haven't been eating much the past couple days) and stress (i've been pretty stressed) can cause slightly elevated levels? I mean he said it was apparently VERY slight. So i dunno...he's sending me for a full abdomenal ultrasound which i think should show something even if it's autoimmune as i guess they'd see the damage? i dunno... he and the nurse both felt that damage causing that probably wouldn't come on so quickly...my levels in november 2011 were great. which is why he feels gilberts could be what might be happening if anything which he says is not life threatening and is just something that happens sometimes. I mean..i know i COULD have had this my whole life...i mean..i've never tested billirubin on my own before so i have nothing to compare it to. I'm still a little scared but...i would guess if it was stones he'd prably of felt SOMETHING? hell..i should have if i had them but i didn't feel a thing so who knows.

So I'm gonna try and relax and enjoy memorial day weekend ....hopefully i can get my mind off the worry....i have horrible anxiety.. hopefully the more i stay away from gluten the better my anxiety will get (hopefully non existent). I agree my hubby needs to get checked as well. We have such a limited budget all the tests are killing us. *sighs* AND he just had surgery in march for a pilonidal cyst. Hoorah...isn't life grand? heh

ravenwoodglass Mentor

Thanks guys. In the bilirubin topic I created I wrote out my experience with the doctor today..here is what i wrote in that topic:

I just got back from the doc and he felt around my abdomen..didn't feel anything weird and asked me if it hurt....i always feel a little uncomfy having my abdomen pressed on but nothing hurt at all. There was a trace small amount of billirubin in my urine he said but he thinks at worse it's probably gilberts syndrome. He said starvation (i think? and i haven't been eating much the past couple days) and stress (i've been pretty stressed) can cause slightly elevated levels? I mean he said it was apparently VERY slight. So i dunno...he's sending me for a full abdomenal ultrasound which i think should show something even if it's autoimmune as i guess they'd see the damage? i dunno... he and the nurse both felt that damage causing that probably wouldn't come on so quickly...my levels in november 2011 were great. which is why he feels gilberts could be what might be happening if anything which he says is not life threatening and is just something that happens sometimes. I mean..i know i COULD have had this my whole life...i mean..i've never tested billirubin on my own before so i have nothing to compare it to. I'm still a little scared but...i would guess if it was stones he'd prably of felt SOMETHING? hell..i should have if i had them but i didn't feel a thing so who knows.

So I'm gonna try and relax and enjoy memorial day weekend ....hopefully i can get my mind off the worry....i have horrible anxiety.. hopefully the more i stay away from gluten the better my anxiety will get (hopefully non existent). I agree my hubby needs to get checked as well. We have such a limited budget all the tests are killing us. *sighs* AND he just had surgery in march for a pilonidal cyst. Hoorah...isn't life grand? heh

It sounds like your doctor isn't really concerned with this. Since you are newly diagnosed and celiac can impact liver function you may want to ask the doctor what he is looking for with the ultrasound and/or if you can hold off on it and recheck when you have been gluten-free for a bit. The liver issues may resolve on their own gluten free and if you are risking finacial difficulties you want to be sure he isn't ordering the test 'just to set your mind at ease'.

GFinDC Veteran

Did you see the part about photo therapy in the link to bilirubin testing in the other thread? It said the treatment for babies is a light blanket and it helps change the bilirubin in to a more easily eliminated form. I thought that was very interesting. So maybe if you get out and enjoy the holiday weekend and get some nice sun time you will reduce your bilirubin score. Maybe. Or at least have a nice weekend. :-)


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



Celiac.com Sponsor (A8-M):



123glldd Collaborator

I actually really want the test as the anxiety is doing more harm to me than anything right now....so i'm going in on tuesday morning.

Also I was told about the light therapy....I am gonna try that this weekend yes :) I always feel better on a sunny day :)

123glldd Collaborator

Well I took another test this morning..it MIGHT have been a bit lighter than it was before the weekend. I'm going for the ultrasound tomorrow morning. A little nervous but..something I noticed was....the weekend i felt great....we got home and within a couple hours i got a bit of a tummy ache...but when i took my anti anxiety meds (clonazepam) it subsided so i think it might be psychological/ stress for the tummy aches..the bilirubin i'm still unsure but the sunlight might have helped that. I'll be doing another urine test in the morning before i go in for the ultrasound. I was outside most of the day today.

GFinDC Veteran

Well good, feeling better is great! :) Getting some sun also helps with vitamin D levels. So that might be something to have checked.

123glldd Collaborator

Well good, feeling better is great! :) Getting some sun also helps with vitamin D levels. So that might be something to have checked.

Oh I was put on nutrimetrix vitamin D3 +k2 last november for a month..every day. Then every other day there after. and YES i felt better. But now that i'm completely gluten free it may be really starting to kick in. But really there is nothing like being outside in the fresh (or semi fresh ? lol) air.

I had my ultrasound today....AND got the results about an hour ago. Everything is perfect. No gallstones...my gallbladder..liver...kidneys..pancreas...apparently they all look perfect. So either the bilirubin was a result of celiac or i have gilbert's syndrome but there is certainly nothing there physically it seems. I cried I was so relieved. No seriously....big weight off my shoulders.

GFinDC Veteran

Great news Krista! :) Celiac can cause a whole lot of symptoms, but the nice thing is usually they resolve on the gluten-free diet. Once we stop poisoning our bodies, things just tend to get better. :)

123glldd Collaborator

Great news Krista! :) Celiac can cause a whole lot of symptoms, but the nice thing is usually they resolve on the gluten-free diet. Once we stop poisoning our bodies, things just tend to get better. :)

For sure. I am guessing I either have Gilbert's Syndrome like my Doctor theorized or maybe I'm not just gluten sensitive but full blown celiac (I think i heard in someone elses thread that's what would possibly cause it?) and had increased bilirubin like some others did. I did another test strip yesterday morning before i went as I had to use the washroom when I woke up and the bilirubin area was much lighter than it was when I first took the test...it probably is to do with the gluten...it seemed to be getting better anyhow. :)

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...