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

Getting An Endoscopy Tomorrow..


dreemilyn

Recommended Posts

dreemilyn Newbie

Hi everyone,

I just wanted to try and (as briefly as I can) explain what's been going on with me. I have an endoscopy tomorrow to get tested for Celiac Disease and my sister just got it done and hers was positive (that's how I even thought to get tested myself.) and I guess I just want your input as well....I'm sorry if this ends up being long.

I've been very sick for the past 2 years but when I look back on my life, I can see that I was gradually becoming more and more tired and weaker. As a kid, I had terrible ezcema and medicine never seemed to help it. I still have it on the backs of my knees at times. I was an irritable kid although my mom doesn't remember me having stomach problems (but she had five kids so maybe thats why! lol). I can remember being about 9 and having constipation a lot as well as diarrhea at times. I would also get stomach pain that was so bad once in a blue moon that I'd be doubled over in pain with it. I went through puberty very young but I never had a menstrual cycle ever. I was diagnosed with premature ovarian failure at 16. I was told to take hormone replacement (estrogen) and I've been off and on it for years because I have terrible side effects from it - dizziness, more fatigue, and nightmares. I've been told that due to a lack of estrogen, I now have osteopenia. I am also hypo thyroid which was diagnosed around the same time.

I went to high school normally. In fact I probably felt my best those years but I always had a very hard time waking up in the morning and my whole life I was never able to run or participate in gym class without becoming really short of breath and getting dizzy. When I look back I can remember feeling dizzy in school a handful of times. I also had terrible sinus problems growing up.

At 18 I worked in a pharmacy where I was standing all the time and this is when my real problems started. I began to feel lightheaded and exhausted and I was sleeping a lot. My legs were cramping up and while I had pain in them growing up (the doctor called "growing pains") this was excrutiating to the point where I couldnt sleep because of it.

At 19 I went on a trip to Oklahoma with my niece and I didn't eat or drink much and I became severely dehydrated. That was the first time I passed out but not the last. The hospital said I was dehydrated and gave me IV fluids and said I'd get better but I didn't. Even just getting on the plane was a nightmare because I could barely walk. For that summer I was bedridden and nobody knew why. I was in and out of the hospital. Finally in September I went online and researched my symptoms. I realized my blood pressure was way too low and my heart rate was too high. Thats when I found a website that described me pretty well and got a hold of a cardiologist in Virginia who officially diagnosed me with Postural Orthostatic Tachycardia Syndrome, a form of Dysautonomia where your blood pressure drops and your heart tries to compensate for it by going up. My doctor once told me though...if we could find out the cause of it, I could fix it because right now we're only treating symptoms and so I've been searching for the cause ever since.

Since then it's been 2 years and I'm on medicines to raise my blood pressure. They keep it stable and I don't pass out anymore but the thing is I still feel horrible. I have no energy. I'm weak and dizzy. That trip I took to Oklahoma was to see outdoor concerts and now I can barely listen to loud music because sounds and lights bother me greatly. I ache constantly. I have diarrhea every single day. My appetite differs greatly going back between severely hungry to no appetite at all. I also urinate very frequently.

I guess my question to you is...does any of this sound familiar? I'm afraid I'm going down the wrong route with all of this and as ridiculous as it seems to want to have an illness, I just want a diagnosis so that I can start to feel better....any input is greatly, greatly appreciated.

Thank you so much, Hope you're all doing great.

-Dreem


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



Celiac.com Sponsor (A8-M):



dreemilyn Newbie

Was my story way too long and boring, lol? Or do these symptoms not sound like Celiac at all? I got my endoscopy yesterday and was told I have duodenitis but I'm waiting for the biopsy results now. Too much waiting! :rolleyes:

dlp252 Apprentice

No, not too long or boring, lol...I think just a lot of people on vacation probably.

Anyway, I had a lot of the things you described as a child...constipation, gastric upset, eczema as a child which was caused by wheat (see they KNEW what caused it even then), etc., etc. I didn't have the ovarian thing, but did have menstrual issues and later in life fibroids, etc.

I don't think you're far off, especially if your sister has been diagnosed! You may not have it YET but with a genetic link, you COULD have it someday.

I'm glad your scope went well.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,015
    • Most Online (within 30 mins)
      7,748

    Rockette47
    Newest Member
    Rockette47
    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

    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
    • JoJo0611
    • Martha Mitchell
      Scott I also have different symptoms than most people. It affects me bad. Stomach ache, headache, nauseous, heart racing, whole body shaking, can't walk then my throat starts to close. It attacks my nervous system. The only thing that saves me is a 1/2 of Xanax...it calms down my nervous system 
    • Martha Mitchell
      Scott Adams. I was dealing with a DR that didn't care about me being celiac. I repeatedly told him that I was celiac and is everything gluten-free. He put an acrylic lens from j&j. I called the company to ask about gluten and was told yes that the acrylic they use has gluten....then they back tracked immediately and stopped talking to me. The Dr didn't care that I was having issues. It took me 6 months and a lot of sickness to get it removed.... which can only happen within 6 months. The Dr that took it out said that it was fused and that's why I lost vision. If they would have removed it right away everything would be fine. He put in a silicone one that was gluten-free and I've had no issues at all in the other eye. Do not do acrylic!
×
×
  • 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.