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

Newly diagnosed and feeling hopeless


Platinum

Recommended Posts

Platinum Rookie

I was hospitalized back in November for alot of different things. While I was there they did a endoscopy, colonoscopy, blood tests, biopsies, blood transfusions, iron infusion , and then basically told me that I was making most of my symptoms up and there was nothing they could do. My biological father finally got in contact with me after talking to my brother about what was going on and he informed me that he has Celiac's disease and that i might want to get tested. I finally got my blood work done about three weeks ago after talking to my primary doctor. He reviewed my biopsy from my hospital visit as well and he said I was definitely right about the Celiac's and was upset that no one said a thing from November. Since being hospitalized I lost my job, my house, and my symptoms seem to never get any better. I've been gluten free since before the blood work got ordered. I'm just scared to think that I will never be able to function again. Im a mom of three beautiful boys and now I can't seem to support them or myself. I can't think straight. I feel awful all the time and now I don't think I can get the treatment I will need to help...

 

Sorry for the long post. I'm just scared and need to vent. 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master
4 hours ago, Platinum said:

I was hospitalized back in November for alot of different things. While I was there they did a endoscopy, colonoscopy, blood tests, biopsies, blood transfusions, iron infusion , and then basically told me that I was making most of my symptoms up and there was nothing they could do. My biological father finally got in contact with me after talking to my brother about what was going on and he informed me that he has Celiac's disease and that i might want to get tested. I finally got my blood work done about three weeks ago after talking to my primary doctor. He reviewed my biopsy from my hospital visit as well and he said I was definitely right about the Celiac's and was upset that no one said a thing from November. Since being hospitalized I lost my job, my house, and my symptoms seem to never get any better. I've been gluten free since before the blood work got ordered. I'm just scared to think that I will never be able to function again. Im a mom of three beautiful boys and now I can't seem to support them or myself. I can't think straight. I feel awful all the time and now I don't think I can get the treatment I will need to help...

 

Sorry for the long post. I'm just scared and need to vent. 

I am confused.  How long were you gluten free before your celiac testing?   Were you diagnosed by your primary?  If a celiac blood test is positive, usually you are referred to a Gastroenterologist for an endoscopy to obtain intestinal biopsies.  

I am sorry that you are sick and struggling.  ?

 

Platinum Rookie

I had the endoscopy in November and was on the brat diet until the beginning of January where I stopped eating gluten and dairy. My primary doctor was the one who ordered blood work after I asked for more information about it. After the blood work came back he took a second look at my endoscopy results and he said there were definitely signs and my GI doctor completely ignored it. 

cyclinglady Grand Master

That is horrible!  The GI should have caught it.  But I get it.  Two months after my celiac disease diagnosis, I got sick, passed out and the paramedics and doctors thought I was having a heart attack.  I could not get off the floor because my back hurt.    I was admitted and they found nothing.  My primary reviewed the hospital records and found two fractures in my vertebrae.  No one read the X-rays as their focu was cardio.  No wonder my back was killing me.  The good news is that my heart is in awesome shape, but what a way to find out.  

Know that it takes most celiacs a year or longer to recover from celiac disease.  Why?  Most of us have system or collateral damage.  The gluten free diet has a steep learning curve.  So, consider reading our Newbie 101 thread found under the “Coping” section of the forum.  Read and learn all you can about celiac disease and tips for keeping you safe.  

Have you had your children tested?  

Soon, you will feel better.  It just takes time.  If you have questions, just ask.    When you are sick it is hard to research on your own.  

Hugs!  

Platinum Rookie

I'm trying to get on a different insurance so I can continue to see my oncologist and find a new GI doctor. Getting my kids checked is next on the list. I'm starting to think my oldest has it as well. I've been trying to to research more but I feel more lost. I will definitely check into that. Thank you for the help.

notme Experienced

deep breaths!  every one of us has been where you are.  this is a good place to vent and ask questions :) once you have been gluten free for awhile, you should see other symptoms (seemingly unrelated) go away.  this disease is a chameleon - i personally had migraines/ headaches/ joint pain/  fatigue/ dh skin rash etc along with the lovely big D and all the other g.i. issues.   so, good news, you should feel better moving forward!  you can get another job, you can get another house, you can't get another you!  so, time to take care of you.  indeed, read the newbie 101 thread -- lots of good info there.

also, don't take any kids off  gluten before testing is complete.  maybe keep a food journal to see if any other foods are aggravating your gut.  almost every thing you ate before can be duplicated to be gluten free.  lots of new/good products out there lately, even flour tortillas!

hang in there.  you can do this!  welcome to the forum :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,790
    • Most Online (within 30 mins)
      7,748

    Anne fritz
    Newest Member
    Anne fritz
    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

    • trents
      Celiac disease is an autoimmune condition with a genetic base. The the potential for developing the disease is inherited. but remains latent until triggered by some stress event. Thus, there is an epigenetic component to celiac disease. Once the genes are awakened from dormancy, celiac reactions are triggered by the ingestion of gluten.
    • Beeroney
      Hi all, just ticked over into my first year gluten-free after being diagnosed last October and feeling a bit rough after a possible glutening. Diagnosed at the ripe age of 38, never been ill in my life before this so safe to say my health anxiety is now borderline unmanageable. I think I may have been glutened a week ago, since then I’ve had that familiar hot/burning feeling in my gut, gas, bloating and all the Bristol Stool chart types in one sitting. I know people are different but does this sound familiar to anyone? Stomach was churning like mad last weekend like it did when I first ill before diagnosis. Acid reflux(which was my first symptom way back when) also reared its ugly head, which I probably the worst symptoms imo. Anxiety is probably up more so as I’m leaving on holiday to USA in 3 weeks time, which would be pretty much ruined if my guts are still messed by the time we leave.  Any words of wisdom appreciated    Bryan 
    • bombier
      This doesn't answer your question but I'm not sure if you know that this intolerance is passed down from mother to child through Cord blood and or breast milk.
    • RMJ
      I’m having this type of MRI this afternoon,  What specifically do you want to know?  From what I’ve read, not all facilities use the same drink prep.
    • nanny marley
      Hi I've been told I need a MRI on my bowels , I was booked for a colonoscopy, but because of my sever back issues and trapped nerve it can't be done , the nurse told me I will have to have a manitol drink a hour before the scan , I'm just a bit worried has I have issues with sweeteners like even a little,  I get a weird throat and ears and I've read it is a similar substance , not sure if anyone has had one of these scans or could give me some advise on the drink prep thanks in advance 😄
×
×
  • 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.