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

Help With My Sister'S Symptoms...


js9798

Recommended Posts

js9798 Newbie

Hi Everyone.... :)

I'm looking for some insight and information on people's symptoms from Celiac Disease. A brief history... my mom had Celiac when she was a child, and I know that it can be passed genetically. One of my sisters has been sick for many years now... and in the beginning, none of were sure what to think, we just kind of thought that was her, but it has progressed into more serious symptoms and I am trying to help come up with information and advice on how to proceed.

My sister is only 34. Three years ago, when she was at a convention, she passed out and was taken to the ER. It was then that she discovered that she had extremely high blood pressure, and the doctor thought she had had a mini stroke. She smoked at the time, but soon after, she quit, and hasn't smoked since. She followed up with her doctor in town, who basically told her she was too young to have high blood pressure, and sent her on her way.... my sister hasn't really been back to the doctor since, she says she's afraid they will think she's stupid and imagining everything.

In addition to this issue, she has suffered for many more years from severe fatigue, headaches, irritable bowel symptoms, and more recently has started to develop excruciating mouth sores. The last outbreak of the sores was the worst, and lasted for 5 days... the inside of her mouth, throat and lips were swollen. She could barely open her mouth to eat or drink or talk, she was in horrible pain.

The one good thing that came of it though was that it made her decide to go to the doctor. The doctor suspected she was experiencing some type of autoimmune disorder,a and referenced a disease called Bichets disease. It apparently affects the smaller blood vessels, which of course can cause high blood pressure and mouth sores as well. I'm not inclined to agree with her doctor, because when I researched Bichets, the first thing listed was that it primarily effected the Mediterrian and Asian populations, and rarely affected other ethnic groups.

So... I guess my question is to all of you.... 1. have any of you or your family members had high blood pressure with celiac disease? 2. Have you experienced the mouth sores? If so, does anyone have any idea how common these symptoms are?

I would appreciate any advice or information any of you are willing to give. I just want to help my sister find some relief and get an answer for all of her health problems.

My sister lives in WA. state, and I live in MN. I told her that if she felt like she wasn't getting the help she needed there, that I would take her to the Mayo hospital. I know there they would be able to figure out what's going on.

Thanks for your time and help.... :)

Jennifer


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

First off your mom didn't outgrow celiac. It used to be thought that children would because many diagnosed in childhood will seem to be able to eat gluten again in adulthood without issues. We now know that doesn't happen but the disease can change presentation.

Your sister does sound like she is one of us. Have they tested her for celiac yet? Has she let her doctors know that her mom was a diagnosed celiac? It is advised that all first degree relatives of a diagnsoed celiac be screened even if they are symptom free. That includes you. It should be the first thing that is looked for in those of us who have family members that are celiac, not the last.

Please make sure that she has let the doctors know and that she is tested. After all the tests are done then a trial of the diet is needed as many of us will show a false negative on testing for a variety of reasons.

You found a good place for info and support ask any questions you need to and if she has access to a computer clue her into the site so she can visit and ask any questions she needs to also.

CDFAMILY Rookie

Hi Jennifer,

What a great sister you are!

High Blood Pressure

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,012
    • Most Online (within 30 mins)
      7,748

    Anna Costa
    Newest Member
    Anna Costa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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!
    • Scott Adams
      Welcome @Martha Mitchell, I too would like to know more about your prior lenses, and especially about the potential of gluten in lenses. In theory this should not harm most celiacs, as the autoimmune reaction normally begins in the gut, however, in those who are super sensitive or have dermatitis herpetiformis it may be a potential issue. 
    • Scott Adams
      It's most likely going to be a celiac disease diagnosis based on your blood test results, but wait for your doctor to give you a green light for going gluten-free, as they may want to do additional testing. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
×
×
  • 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.