Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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:
    Where Your Contribution Counts!
    eNewsletter
    Support Us!

Ultrasound Results. Cysts On Ovaries.


MomGoneRunning

Recommended Posts

MomGoneRunning Rookie

I just spoke with my PCP about the results of my ultrasound. She said that there is a 4cm cyst on my right ovary and another smaller one on my left. My question is has anyone ever had ovarian cysts or heard of them being related to Celiacs? My GI problems are still continuing, and getting worse. Or are they not related and I am just insane? Thank you in advance for any responses!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



birdie22 Enthusiast

Can't comment on whether ovarian cysts are related to Celiac, but I have had one before. It was suspected to have been caused by the mirena IUD. It was deemed a "simple" cyst and went away on it's own about a month after having the IUD removed. My cyst caused lower back aches, pelvic cramps, and general abdominal discomfort. This all resolved once the cyst was gone. Of course my other GI and other symptoms continue.

Link to comment
Share on other sites
BabsV Enthusiast

I have a history of "functional" cysts -- the ones that are related to your cycle and come and go. I've had them since long before being diagnosed with Celiac Disease so have no idea if they are related. My doctors just watch them since I don't usually have any problems or symptoms, and if I have pain issues they check via ultrasound to see what is up -- they probably wouldn't do that except that I had a cyst that no one knew about and it caused torsion of one of my ovaries (OMG! that was like being hit with a sledgehammer, it literally caused me to collapse in a fetal position on the floor!) which led to emergency surgery to remove it (the cyst not the ovary.) But that is not common...and if the doctors know they are there and keep track of how they are growing (if they are growing at all) the cysts are not usually something to fret about. What does your doctor want to do about it?

Link to comment
Share on other sites
SilverClaerity Newbie

I've been wondering this myself!

I'm not diagnosed, but pretty sure I have a problem with gluten. About a month ago, I went for a CT scan and was told that I have a 2.7cm cyst on my left ovary. My ultrasound to check up on it isn't for another month.

I have no idea if this is related to the GI issues I've been experiencing.. but it's definitely food for thought.

Link to comment
Share on other sites
Bubba's Mom Enthusiast

Add me to the list of those with Ovarian cysts. As it was explained to me...in a woman's cycle a little cyst forms on the ovary and bursts when the hormones tell it that it's time to. That sends the egg down the tube to the uterus. Sometimes that cyst doesn't burst when it's supposed to, and continues to grow.

Sometimes they cause symptoms..and sometimes they don't.

I found I got achy pelvic pain on whichever side it was on, and sometimes migraines. When they finally did burst I'd feel a sharp cramping pain.

I had this going happen off and on for years. It was before I was DXed with Celiac. I don't know if there's a link, but I know a lot of Celiac women have fertility issues, so maybe this is what is happening with them?

Link to comment
Share on other sites
MomGoneRunning Rookie

Thank you for the responses ladies. Each day I get more and more frustrated. I feel crazy somedays. My brain fog is getting so bad, I have a hard time getting through the day. I have to keep telling myself that I am much more fortunate than others who have had to suffer like this for years, and sometimes decades. I almost feel selfish for getting so frustrated just because I want to know what is wrong with me.

Link to comment
Share on other sites
Bubba's Mom Enthusiast

I completely understand your frustration! You know yourself better than anyone..and when something isn't right you feel it and want answers. I hope you get things worked out so you feel better.

(((hugs)))

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



GlutenFreeNewB Rookie

I have a problem with cysts. I've had them in my face, breasts, and even had a giant liver cyst that had to be surgically removed (it was fused to my gallbladder, so that had to go too). Dr. said he had no idea why I had so many cysts or how one got to be the size of a soccer ball. Maybe it's related to celiac, I wasn't diagnosed at the time. So many things are related to celiac that I wouldn't be at all surprised :o

Link to comment
Share on other sites
mushroom Proficient

I did not know I had had an ovarian cyst until one time I got my annual intrvaginal ultlrasound which stated "The ovarian cyst present on examination last yearis no longer present." :blink:

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      120,480
    • Most Online (within 30 mins)
      7,748

    EJenkins
    Newest Member
    EJenkins
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Tlbaked13
      Thank you and I am aware that I should be eating a "normal" diet until tested it's kind of been trial and error for my diet or more like just ERROR! I about 1-3 bites a meal I'm to a point that 99 percent of the time I'm having trouble swallowing just about everything occasionally I find either something or a very small window of time that allows me to get very little of something! I am basically getting zero nutrition what so ever because I take one bite of the meal that I usually just slaved over just to end up tossing it when it's all said and done...did anyone else ever experience anything like this?  I am more then open to suggestions! It is taking a very extreme toll on me and my body forsure 
    • JustGemi
    • trents
      No! Do not start the gluten free diet until you know whether or not you will be having an endoscopy/biopsy to verify the blood antibody test results. Starting gluten free eating ahead of either form of diagnostic testing can invalidate the results. You don't want to allow the villous lining of the small bowel to experience healing ahead of testing by removing gluten.
    • Scott Adams
      We offer a ton of recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/ and have done some articles on fast food places, but keep in mind that eating out is a common source of gluten contamination: https://www.celiac.com/search/?q=fast food&quick=1&type=cms_records2 Many colleges now offer allergen-friendly, and sometimes gluten-free options in their student cafeterias: https://www.celiac.com/search/?&q=colleges&type=cms_records2&quick=1&search_and_or=and&sortby=relevancy PS - Look into GliadinX, which is a sponsor here, but many studies have been done on it which show that it may break down small amounts of gluten in the stomach, before it reaches the intestines.
    • JustGemi
      Thank you! What do you recommend in the next 7 weeks until I see my Doctor?  Just start my Gluten free diet?
×
×
  • Create New...