Jump to content
  • 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):

Does This Sound Like Celiac?


veggiebite

Recommended Posts

veggiebite Newbie

Okay so I have not been officially diagnosed with celiac (no insurance). I'm 18 years old, vegan, and according to blood work and other tests, I am a very healthy, normal weight person (minus asthma)

So tell me if ANY of these events have happened to you, and some advice you may have please :(

Before I considered a gluten allergy, I was getting heart palpitations, this tearing feeling in my stomach, and muscle spasms everywhere. Not to mention being bloated to the point where I looked pregnant. It was so painful and uncomfortable. It felt as if someone was tearing my stomach in half like a piece of paper. At one point I tested positive for blood in urine but had no UTI. Doctor said it may have been from inflammation? Idk. That never really got cleared up.

So once I thought I may be a celiac, I stopped eating gluten. Which started a week ago. Miraculously, these symptoms are GONE!! I couldn't believe it!

However, I noticed my urine is very cloudy. And I am getting these (my apologies for how gross this sounds) white pieces in my stool and mucus. Also, inside the stool there are light colored chunks of something, idk what it is. I read somewhere that these could be wheat proteins leaving my body.

It has me pretty freaked out but I can't go to a doctor until Jan 1st (when my mom gets insurance)

So, has any of these symptoms happened to you? What were they? What helped?

I would love to hear some personal stories.

feel free to email me at veggiebite@aim.com, too

thanks :)


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



Celiac.com Sponsor (A8-M):



FooGirlsMom Rookie

Hi,

I'm 42 and have been gluten-free for about a month now. The symptoms you described are exactly what I had. As my symptoms worsened I started to have heart palpitations also. (They are gone, by the way :) I had cloudy urine right after starting the diet too and when I googled it a bunch of times it said something about milk causing it (I was still not off dairy yet)

Yes, the - ahem - elimination. I didn't have all that much trouble with it until going Gluten Free. Idk if I'm purging out a bunch of stuff from my intestinal track or what...but it's been odd. Same stuff you mentioned plus times of having undigested food (which is generally not normal for me).

I never had the pain you described unless I had indigestion (used to have it baaad in my 20s and 30s - sometimes so much belching & burping I'd throw up).

The biggest "tell" that you have gluten issues is that by going off the gluten, you recover. Like you I always had a bloated stomach if I ate. Once I was off gluten, it took about a week and no more bloat anywhere. I used to even get it in my ankles & face at various times.

One of my worst symptoms was joint & muscle pain (still not completely gone). The last symptom to develop before going gluten-free were leg spasms when I was at rest. Just sitting and watching TV with my legs up on the couch, they would ache & then start spasming.

I honestly think some of these symptoms are inflammation related -- but also vitamin/mineral related. I became aware last year that I wasn't absorbing vitamins properly. I started to have symptoms of vitamin deficiency.

So when you go to the doc in January, even if you aren't tested for Celiac/gluten, have your vitamin levels etc checked and make sure you aren't anemic etc

Good luck :) This is going to be a journey for both of us.

FooGirlsMom

serenajane Apprentice

Okay so I have not been officially diagnosed with celiac (no insurance). I'm 18 years old, vegan, and according to blood work and other tests, I am a very healthy, normal weight person (minus asthma)

So tell me if ANY of these events have happened to you, and some advice you may have please :(

Before I considered a gluten allergy, I was getting heart palpitations, this tearing feeling in my stomach, and muscle spasms everywhere. Not to mention being bloated to the point where I looked pregnant. It was so painful and uncomfortable. It felt as if someone was tearing my stomach in half like a piece of paper. At one point I tested positive for blood in urine but had no UTI. Doctor said it may have been from inflammation? Idk. That never really got cleared up.

So once I thought I may be a celiac, I stopped eating gluten. Which started a week ago. Miraculously, these symptoms are GONE!! I couldn't believe it!

However, I noticed my urine is very cloudy. And I am getting these (my apologies for how gross this sounds) white pieces in my stool and mucus. Also, inside the stool there are light colored chunks of something, idk what it is. I read somewhere that these could be wheat proteins leaving my body.

It has me pretty freaked out but I can't go to a doctor until Jan 1st (when my mom gets insurance)

So, has any of these symptoms happened to you? What were they? What helped?

I would love to hear some personal stories.

feel free to email me at veggiebite@aim.com, too

thanks :)

Well I had the cloudy urine with no uti too I also tested positive for blood in urine prior to being diagnosed the cloudy urine I have experienced before and after diagnosis.

After being on gluten free diet 4 months or so ( NO CHEATING) I didn't even eat out anywhere during this time I was just trying to wrap my head around the label reading and the phone calls and email to manufacturers with yes or no gluten questions........

I was working out with a friend at the gym pretty regularly for a few weeks normally I drink lots of water at the gym this one night we went after work and I didn't drink as much I only had 1?2 bottle 10 oz or so that night I did notice cloudy urine. I woke @ 4:00 the morning after with bladder spasm and when I went to bathroom my urine was a rusty red color and my bladder continued to spasm I kept laying down and returning to bathroom feeling a strong urge to pee signs of uti.. went to ER and they diagnosed me with uti then mt urine test came back with blood no uti stop meds and off to uroligist had a bladder scope in the days to follow and everything was ok my bladder wasn't emptying all the way so he advised me to slow down when visiting the rest room to stand after peeing tilt forward and then sit back sown to try and finish emptying. I was also put on 2 cranberry pills a day and he wants to see me in a year

prior to being diagnosed with celiac I was spilling proteins into my urine. This was detected at my routine physical ???????

anyone else have anything to add from there experience????

sorry for long winded response

don't ignore your symptoms we are all very different some hospitals or clinics have a sliding fee for uninsured people don't let something that doesn't feel right go unchecked.

Hope things work out well for you:0)

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - HectorConvector replied to HectorConvector's topic in Related Issues & Disorders
      359

      Terrible Neurological Symptoms

    2. - HectorConvector replied to HectorConvector's topic in Related Issues & Disorders
      359

      Terrible Neurological Symptoms

    3. - akebog posted a topic in Gluten-Free Restaurants
      0

      Fusilli Pizzeria, Miller Place, NY

    4. - nancydrewandtheceliacclue replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      12

      Celiac flare years after diagnosis

    5. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      12

      Celiac flare years after diagnosis

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,062
    • Most Online (within 30 mins)
      10,442

    AutomatedGlutenEjector
    Newest Member
    AutomatedGlutenEjector
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • HectorConvector
      Oddly this effect has gone now, just happened yesterday evening, the nerve pain is now back to its usual "unpredictable" random self again - but that was the only time I ever had some mechanical trigger for it, don't know why! There's no (or wasn't) actual pain in my neck - it was inside the leg, but when I looked down, now though, the leg pain just comes and goes randomly as before again.
    • HectorConvector
      I had MRI scan a few years ago showing everything normal, and now it's no longer triggering the nerve pain when I bow my head today - it only seemed to happen yesterday, and that was the only time it happened! Just seemed weird as no movement has caused my usual nerve pain before. It's normally just random.
    • akebog
      Very good pizzeria with small dining room in back of the restaurant. The owner's daughter has celiac & they have gluten free pizza & a gluten free menu. Some items from the regular menu can be made gluten free also. They have a lunch menu which we ordered from & my chicken with spinach & mozzarella over gluten-free penne was delicious. They also have Tuesday night pasta specials & Thursday night chicken pasta specials. We plan on going back for dinner soon.
    • nancydrewandtheceliacclue
      @Aretaeus Cappadocia and @Russ H thank you both for your helpful advice and information. I haven't seen a GI in years. They never helped me aside from my inital diagnosis. All other help has come from my own research, which is why I came here. I will be even more careful in the future. 
    • Aretaeus Cappadocia
      @nancydrewandtheceliacclue, you are welcome. After looking at this thread again, I would like to suggest that some of the other comments from @Russ H are worth following up on. The bird-bread may or may not be contributing to what you are experiencing, but it seems unlikely to be the whole story. If you have access to decent healthcare, I would write down your experiences and questions in outline form and bring this to your Dr. I suggest writing it down so you don't get distracted from telling the Dr everything you want to say while you have their attention.
×
×
  • Create New...