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

Pelvic Pain


TeachK71

Recommended Posts

TeachK71 Rookie

Hi!

It has almost been two years since I have been diagnosed with Celiac Disease. Last November I woke up and had about one hour of off and on pelvic pain that was very serious (post period, too early to be ovulation). Went to the doctor that day, they did a pevlic exam and urine test and said if it happened again to come back. Almost four months went by and I have been having some pain, but nothing serious.

Just two weeks ago had another morning bout of severe pain. Went to the doctor, she thought it might be a cyst on the ovary and just last week I had a transvaginal and transabdominal ultrasound. I found out today both came back completely normal. They even did some STD tests to rule that out, but my husband and I are monogomous.

So, she said if it returns again, they would bring me back in and check out some gastointestinal stuff and maybe a colonoscopy...which I just had in APril of 2003 when I was diagnosed with celiac.

Could this pelvic pain be a related disorder to celiac disease?

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



Ann1231 Enthusiast

I have that too! I never even thought about it being related to celiac disease. I had it a few months ago for two or three months in a row, then it subsided. I had it again a few days ago. Very sharp and painful. I thought maybe I was having ovarian cysts again but I'm on the pill to help those anyway so maybe that's not what it is....

Sorry I can't help, just wanted you to know you're not alone!

Ann

skbird Contributor

Me three. Similar story, had a doctor check me for cysts, said he didn't think I had any, felt around, etc. No scans or xrays. Was on the pill at the time and he changed it to another kind. Well, I have been off the pill for 4 years now (it never helped in that department) and I still get this from time to time. Still told no cysts. My mom has one that comes and goes.

I dunno. I do have several hormone problems, low progesterone, slow liver, high estrogen. I figure it's related to that. I also figure at this point that maybe all my food sensitivites have given my liver too much to do so that is why I have hormone problems and as I continue on the right diet this may all level out, eventually. I hope. :)

Not alone, don't know if it's related though...

Stephanie

lotusgem Rookie

Hmm. I also have had recurring pelvic pain that can incapacitate me. The pain also includes my "undercarriage" and is just miserable. It is a feeling of swelling in addition to pain. This might only happen a few times in the course of a year. It always seemed to come out of the blue, but I noticed after a while, that it usually follows a time of physical exertion, as in lifting or pushing something that evidently is too heavy for me. I had wondered if it was a prolapsed uterus, since after the birth of my second child at age 32, I had that condition, although at the time, I didn't have any of this pain. Medication set me right again, but the doctor told me that one day, I might have to have a hysterectomy. I never considered Celiac.

Does this ring a bell for any of you?

Paula

gf4life Enthusiast

I have that pain too. I have had multiple ultrasounds to check for cysts and problems. All of them negative. I was told 10 years ago that my uterus was tipped the wrong direction, but none of my doctors since seem to think my uterus is in the wrong position. They tell me it isn't prolapsed, but I swear it feels like it is falling out half the time! I also had problems with stress incontinence. My ureter was sagging (not an actual prolapsed bladder) and I had bladder repair surgery 6 weeks ago to repair that. The incontinence is gone, but I was hoping that would help with the pain, it hasn't. I don't always have the severe pain every month, but at least once every 2-3 months, and I get these sharp stabbing pains in my cervix and near my ovaries fairly often. I worry about it, but my pap tests come back normal and the doctors keep telling me I'm fine. So why do I have these pains! I am thinking about going to a different GYN to see if they can fix me. Maybe I'd feel better if I did have a hysterectomy, but I'm so young that they haven't even considered it yet. And evidently I'm not "sick" enough to warrant the surgery... :( That worries me. How much pain do I have to be in before the doctors will sit up and take notice. I guess I need to become a complainer and run to them for every ache and pain that I have.

God bless,

Mariann

burdee Enthusiast

I'm not sure if my 'pelvic pain' is similar to what all of you have described, but when I get dairy or soy contamination, I experience what feels like severe menstrual cramps. However, I went through menopause 8 years ago and all my gynecological exams are normal. During my last 'contamination' episode I experienced "waves" of that cramping pain. I never figured out what I had eaten, but decided that's as close as I'll ever come to labor pains. :o I ONLY experience those menstrual cramping like pains when I have dairy, soy (or occasionally gluten) contamination.

BURDEE

gf4life Enthusiast

I get cramping in my lower abdomen too when I get gluten. I used to get it from dairy, but not anymore. It feels different that the pelvic pain I get. It feels more like my intestines are so swollen and tender, and the cramping seems to come on more when I have the increased amount of gas from the gluten contamination. I can tell the difference between the two, but they both hurt!

God bless,

Mariann


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to Midwesteaglesfan's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Going for upper endoscopy today

    2. - Midwesteaglesfan posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Going for upper endoscopy today

    3. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,267
    • Most Online (within 30 mins)
      7,748

    Kristine Ryder
    Newest Member
    Kristine Ryder
    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

    • Wheatwacked
      Hello @Midwesteaglesfan and welcome. A result greater than 10 U/mL is considered positive. Some labs use 15 as the cutoff, but 34 is in the positive.  The endoscopy and biopsy is looking for damage to your small intestine.  I don't don't think 5 days is enough to repair the damage. This comment is effectly your answer, regardless of your biopsy results.  The endoscopy has been the Gold Standard diagnostic, and most healthcare providers won't diagnose celiac disease until your intestinal lining Marsh Score reaches stage 3. You don't really want to wait for the damage to get worse, especially since only five days mostly gluten free gave you relief.  Yes, migranes is one of the 200 symptoms that may be caused by Celiac Disease. Malabsorption Syndrome is often comorbid with celiac disease.  The western diet is deficient in many vitamins and minerals.  That's why gluten processed foods are fortified.  Gluten free processed foods are not; Vitamin D deficiency is a virtual given.  40 to 60% of the industrial population is deficient in vitamin D, Damage to the intestinal lining from celiac disease can decrease the number of vitamin D receptors.  So now you get no vitamin D from the sun (skin cancer scare) the major source of vitamin D, plus absorbtion from food is poor because of intestinal damage.   Low iodine intake is getting more of a concern because the major source of iodine used to be bread (dough conditioner with iodine was stopped in the US in the 1970s), dairy (lactose intolerance from eating quick pickles with vinegar instead of fermented pickles which supply lactase excreting lactobacillus to improve Lactose intolerance. Commercial Dairies have wheat, barley and rye added to the cow feed. Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein causing the problem.  And people use less iodized salt.  In the US intake of iodine dropped 50% from 1970 to 1984. Switch to Grass fed only milk and consider supplementing Liquid Iodine drops to your diet.  The omega 6 to omega 3 ratio of commercial milk is 5:1; Organic milk is 3:1 and grass fed milk is 1:1. The typical western diet is around 14:1, optimum for humans is 1:1.  Wheat flour is 22:1 omega 6:3.  Choose vegetables lower in omega 6, it is inflammatory.                               Eat fermented foods and switch to Grass fed only milk.  Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein.   
    • Midwesteaglesfan
      At 41 years old I have been fighting fatigue and joint pain for a couple months.  My family doctor kept saying nothing was wrong but I was insistent that I just didn’t feel right.  Finally after running several blood labs, one came back showing inflammation in my body and I was referred to a rheumatologist.  He was extremely thorough and sat with me and my family for a good hour asking questions and listening. He ordered X-rays of all my joints and more bloodwork.  He suspected some sort of reactive inflammatory arthritis.  My TTG (Tissue Transglutaminase) came back at 34. he told me to try going gluten free and out me on Salfasalzin to help the join inflammation.  Over the next couple days going gluten free and doing a lot of research and talking to people with celiacs,  we found that I should have an upper endoscopy for insurance purposes in the future.  I reached back out to my rheumatologist and expressed this concern and he got back to me stating I was correct and resume regular gluten diet and stop the medication until after that scope.     They were able to schedule me in for 2 days later.  I had been gluten free, or as close to it as I could be for about 5 days.  I know I ate some brats with it but wanted to use them up.  My symptoms had gotten slightly better in those 5 days.  I felt less fatigue and joint pain was slightly better(it had gotten really bad) so for these last 2 days I’ve gone crazy with wheat bread, pasta and such.  I’m hoping those 5 days didn’t screw this endoscopy up.  I can’t imagine after a life of gluten, my intestines healed in 5 days and after eating gluten again for these couple days,  my stomach hurts, joint pain is coming back up so I know the inflammation is there.   Hinesight after this diagnosis, I have had chronic migraines since my late teens.  Has that been a lingering symptom of celiacs all these years?  I’ve never really had the stomach issues, for me it came in heavy these last couple months as the fatigue, just always feeling tired and exhausted.  And the joint pain.     So getting in the car for the 2 hour drive to the hospital for this scope now.     Wish me luck!
    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
×
×
  • 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.