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

Ovarian Cysts?


mimommy

Recommended Posts

mimommy Contributor

Hello all. I was just wondering if anyone else has had ovarian cysts? I'm curious about the symptoms.

I went to my GYN in the Spring because I had been having so much pain on my ovaries (mostly the right, but occassionally the left, too). The exam showed nothing, but they were visible on the TVUltrasound. My doc said that they should NOT be causing me pain, but everything I've read says that they can be very painful. I left there feeling pretty well 'dismissed' as my doc never even came back in the room to discuss a treatment plan/options or educate me on the subject <_<

Any advice on this from you ladies out there?


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Hi Minimom :)

I had ovarian cysts that also showed up on ultrasound. I had horrible pain on the same side, but was told that unless a cyst ruptured, it wouldn't cause the type of pain I was experiencing. At one point, the pain was so intense I came close to passing out. (scary)

I ended up choosing to have a hysterectomy, since I had other issues (fibroids) and was frankly tired of dealing with it all. It turns out that I also had endometriosis and adenomyosis (where the endo infiltrates the uterus). At my post operative appointment, the doctor told me that it was the endometriosis that was causing the pain. I never knew I had it, since I'd never had a laproscopy, and it doesn't show up on ultrasound.

If I had it to do over, I would have avoided years of pain by insisting on being tested for endometriosis. In my subsiquent research, I read about a possible autoimmune link which would make sense. At any rate, unfortunately sometimes you have to keep at them. <_<

Fiddle-Faddle Community Regular

I had a terrible episode of ovarian pain a few months ago. I was told by the ER doctor that my experience was typical of a burst ovarian cyst, and that by the time they burst, they no longer show up on the ultrasound. I had been having ovulatin pain for several months before that, on the right side, but that seems to have calmed down. I am exercising much more now--I don't know if that is directly responsible for the improvement or not.

Also, I was taking prednisone at the time of the terrible episode. The doctors insist that that had nothing to do with the pain--but they don't really know for sure. Prednisone can have all kinds of crazy effects on your body.

Rondar2001 Apprentice

I had a couple burst when I was in college. After the first one I ended up in an ambulance because the pain was so sudden and severe. The pain passed in about 4 hours. I didn't have any pain or warning that I had any cysts before they burst.

If you have steady ongoing pain, I would have your doctor keep investigating.

mindyandy420 Apprentice

A few years back I had an ovarian cyst rupture. I remember waking up in the middle of the night with severe pain. I thought my appedix was rupturing. I got into my dr first thing in the morning and got sent to the hospital for CT. Thats when they told me I had an ovarian cyst rupture. They told me to take tylenol and wait for the pain to go away. It did. Oh boy it was painful tho.

Mtndog Collaborator

I don't have cysts but I do have a fibroid and THAT causes pain so I would imagine (and have heard from friends with cysts) that they DO hurt quite a bit. I would either bug your OB/GYN or find a new one who will listen to you goshdarnitall!

Angels~Exist Newbie

I'm only 16 but I've had an ovarian cyst...more than one actually. Mine didn't show up on the ultrasound or CT. My gyn did laparoscopy and during the surgery found a cyst but he also found scar tissue that was binding my abdominal organs together so I really couldn't tell you which one was causing the pain or if it was a combination of the two. Either way if your doctor is ignoring your pain you need to find a better one that will take your concerns seriously.


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



Celiac.com Sponsor (A8-M):



mimommy Contributor

Thanks guys gals, for the responses.

My pain was growing slowly worse over a years time before it throbbed so bad I couldn't stand it anymore (we need throbbing ovaries like we need a hole in the head, right?). My GYN is a decent professional and knew enough to do the T V U, and that's when they saw the cysts. Although the doctor just wasn't concerned or convinced that they should be hurting, she also never mentioned a lapro and didn't seem too keen on the idea when I asked her if I could have scar tissue (had a verryyy bad c-section 9 years ago).

What they found on my labs was that I was vit-D deficient and prescribed D-3 and for me to come back for another T V U and re-test on vit in 5 weeks. Bad me, I haven't gone back. The D didn't make a bit of difference in how I feel, and in fact bothered my stomach. The cyst pain almost disappeared for a little while, but is back now, so I guess I need to call.

I just can't be impressed by doctors--no matter how nice, intelligent, or caring or educated they are--who don't take my symptoms seriously enough to discuss things with me even when they have definite lab results in their hands. I had to research cysts online and found out that there are many different types, most disappear on their own (but do come back) and that even if they burst internally there is really no treatment. I find this heinously hard to believe.

I guess I'm just looking for real life experience from other women, since my medical pro hasn't been very forthcoming. Thank you for your input and advice :)

mimommy Contributor
I'm only 16 but I've had an ovarian cyst...more than one actually. Mine didn't show up on the ultrasound or CT. My gyn did laparoscopy and during the surgery found a cyst but he also found scar tissue that was binding my abdominal organs together so I really couldn't tell you which one was causing the pain or if it was a combination of the two. Either way if your doctor is ignoring your pain you need to find a better one that will take your concerns seriously.

I'm curious--did you have diarhea or other abdominal issues as a result?

Angels~Exist Newbie

Actually that's another thing the scar tissue affected. It glued my colon to both my sides. Before and even for a while after my surgery I had to have a bunch of fiber.

Angels~Exist Newbie

I did have pain on my right side though. (the side the cyst was on) The inside of my hip also felt kind of hollow if that makes any sense. lol :)

debmidge Rising Star

I had such bad left side pain with my ovarian cysts (3 of them on one ovary) that I needed prescripton pain meds and it was not in any danger of rupturing. The pain came on suddenly and I thought I had diverticulitis - GP ran a CT Scan - saw something on ovary and told me to see my ob/gyn. Ob/gyn did ultrasound and there is was - 3 medium cysts all ganging up on my left ovary. The pain went away as the cysts went down, but they never really went away. A few years later ('08) I had to have surgery to remove my ovaries and I am glad I did - no more cysts and pain!

LeAnne8790 Newbie

First, if you feel your doctor is being dismissive of your symptoms, you need to find another doctor. No matter how good a doctor is, if I'm told I could not be feeling something I'm clearly feeling, I would not trust the doctor after that.

I've had good doctors and I've bad doctors, and you owe it to yourself to find one who will listen to you. When I've had a doctor who was attentive to what I was telling him/her and was not afraid to consider my own "self diagnosis" it has made all the difference. When I went to my GI doc with suspicion of celiac, I was scared he would tell me that it wasn't because I'm overweight. Instead, he said "I think you are on the right track" and ordered the tests among other tests as well - some not GI related.

Have you ever considered that you might have PCOS? Do you have issues with weight, facial hair, thinning hair, infertility or acne? I ask because, I had ovarian cysts and endometriosis discovered in my early 20's and it took me 20 years to find out the true cause, which had nothing to do with ovaries, but my endocrine system. The cysts are just a symptom of the disorder, not the condition itself.

Something to think about.

NicoleAJ Enthusiast

Every time I have ever had an ultrasound for any reason, the doctor has found one or more very large cysts on an ovary. Women frequently get cysts when the ovary releases the egg--it's just that some get bigger than others, and they generally dissolve on their own, unless there's some sort of underlying problem like PCOS. I have never had any symptoms from these cysts except for when they've ruptured. I had a period after a very serious car accident when I was having cysts burst frequently. My doctor gave me vicodin to take when it happened because it really was the most gut wrenching pain, and when I couldn't stand it anymore he put me on birth control to prevent me from ovulating. I stopped getting ruptured cysts when this happened. I've been off bc for 9 months now and have not had any cyst symptoms or burst cysts, but I am also not ovulating regularly for some reason. My 20 year old cousin had an 8 pound ovarian cyst that had wrapped itself up in her fallopian tube--she had some pain and incontinence, so this is when they discovered it. They thought it might be a tumor, but when they removed it, they realized that it was just a cyst. Months after the surgery she still had a giant indentation in her gut from where they'd removed the cyst--but that's the only time I've heard of someone having any symptoms of an ovarian cyst (unless it has burst).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,397
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    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

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.