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

Celiacs, Have You Tested Repeatedly For Trace Of Blood In Urine?


1desperateladysaved

Recommended Posts

1desperateladysaved Proficient

When I have had urine tests, I have had a trace of blood in my urine. I think as far back as high school, and perhaps before. That would be more than 30 years.

The MD would always figure it was a trace and not getting worse. It might have to do with my period which was coming or going in a week or so. My anemia was thought perhaps a result of this small amount of consisten blood loss.

Has anyone else experienced this symptom? Did it go away when you went gluten free?

Over the past 5 , when I was testing every month or two, twice my urine tested negative for trace of blood. I am working up my curiousity now, because I have not had it tested since going gluten free.

DT


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



Celiac.com Sponsor (A8-M):



missmellie Newbie

The only thing I can for sure is you're not the only one. I have experienced the same thing and have had multiple tests to find the cause. They finally said "well, some people just have little amounts of blood in their urine and we don't know why." I guess the important thing is to rule out potential serious causes.

1desperateladysaved Proficient

. They finally said "well, some people just have little amounts of blood in their urine and we don't know why."

Yeah, I have heard that too.

ravenwoodglass Mentor

Yes to blood and in my case also protein. Since I had extreme edema before diagnosis I figure it is from some kidney damage. I don't worry about it since it has been a finding for years.

lynnelise Apprentice

Do you take asprin or advil? I was told by my doctor that occassional use can cause traces of blood in your urine.

heather806 Rookie

Yes! For years...was even sent for ultrasounds of the kidneys etc. No cause found. My brother and father have it too. They haven't been tested for celiac though.

1desperateladysaved Proficient

Do you take asprin or advil? I was told by my doctor that occassional use can cause traces of blood in your urine.

I don't think I have since my pregnancies began 24 years ago!


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



Celiac.com Sponsor (A8-M):



tennisman Contributor

I did about 5 urine tests last year and all had traces of blood , my gastro doctor thinks I have kidney stones . I did also read a vitamin k deficiency can cause traces of blood in the urine and my GP doctor told me sometimes celiac's have a vitamin k deficiency .

Finally-45 Contributor

Frequent urinary tract infections and cystitis are problems for women with Celiac.

1desperateladysaved Proficient

I did about 5 urine tests last year and all had traces of blood , my gastro doctor thinks I have kidney stones . I did also read a vitamin k deficiency can cause traces of blood in the urine and my GP doctor told me sometimes celiac's have a vitamin k deficiency .

Interesting. Thanks, I am considering this.

1desperateladysaved Proficient

Frequent urinary tract infections and cystitis are problems for women with Celiac.

I was tested for infections, but it was negative.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    Carol Zimmer
    Newest Member
    Carol Zimmer
    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

    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
×
×
  • 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.