Healthcommunities.com, Doctors Helping People Online for Over 10 years Healthcommunities.com
Home Search SiteMap Contact Us Forum Store Physician Board

Living with Interstitial Cystitis

This section is a place to share stories about Living with Interstitial Cystitis

Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation.

You may also Help others by sharing your story.

To quickly access health information from your website's browser, download
Healthcommunities.com's healthchannels toolbar.


Kimberley’s Story


by: PD on Tue, Apr 24 2007

My beautiful 24 year old daughter struggled with Interstitial Cystitis for several years before we could find any right path toward handling this painful condition.

She was 15 when she contracted an extremely serious case of tonsilitis, which was resistant to all medications the doctors tried. She literally was ill an entire summer, too ill to even operate to remove her very infected tonsils because they were so afraid of massive bleeding. At one point they had her on a “cocktail” of the strongest available antibiotics to try to handle the infection. Finally, that fall, the doctor did remove her tonsils and she got a little better. But from tonsilitis, she developed numerous digestive tract problems, which I suspected were related to the massive doses of medication; as if all of her bacteria, good and bad, had been destroyed or altered.

Heavy periods and endometriosis run in our family, and when she began experiencing such terrible abdominal pain, I thought it was probably related to her cycle. She also had migraines and weight loss and no energy.

This cycle of pain continued until she graduated from high school in 2001 and that fall she went away to college. She tried everything to feel generally better, including an organic diet, plenty of cranberry juice, exercise, you name it. And nothing got better, only worse. The symptoms, which seemed to be pervasive and also vague, now included what she thought were continuous urinary tract infections. She would call me crying, reporting that the pain was so intense that she could barely sit through class. She had a full ride academic scholarship and was in some very demanding architecture classes, with studio running into late nights and early mornings. I worried that all the stress of grade pressure, little sleep, and her general fragile health would all be too much. Also, she really only had the college’s clinic to go for doctor care, and the specialists we had been seeing in our home town was not an option, unless she actually could literally move back home/quit school.

We finally did get her back home for doctor care and her doctor, a specialist in Reproduction and Urology for Women at a respected university hospital diagnosed her with ICD. Up to that time, she had been told that it was everything from “idiopathic” to mental, with one doctor going into great detail about how she feared sexual activity and needed mental care!

The doctor who finally helped her did a cystoscope and found massive striation and bleeding, along with ulcers in her bladder. It was hard and small, not elastic and able to hold anywhere near a normal amount of urine. He also found endometriosis and lesions in her abdomen, which he removed. These were unrelated to her bladder problems, but a definite additional source of misery.

With a combination of drugs to rebuild the lining of her bladder, the discovery that antidepression drugs actually will also aid in pain management, a doctor who really had an accurate diagnosis and then how to handle that, and a LOT of patience and perserverance on my brave daughter’s part, she slowly got a little better and better.

What we did find out is that ICD is difficult to diagnose accurately and treatment is different for everyone. It is also an autoimmune illness, so paying attention to general good health practices and eradicating any unnecessary stresses is critical to begin to feel better.

Our advice is FIND A COMPASSIONATE DOCTOR and a true specialist. If a doctor doesn’t think you have ICD, visit another one right away. It is NOT in your head. There are also other treatments, such as pain management implants, that can help. But often you have to be informed and ask the healthcare professionals about these things. EDUCATE YOURSELF.

It has been several years since Kim’s pain has been for the most part in remission. She got married last year, after graduating from college on the Dean’s List. She has a wonderful husband who also looks out for her health. She will never be free of pain, but she knows how to take care of herself, including drinking lots of water. Interestingly, cranberry juice, good for bladder infections, is not good for ICD patients, neither is orange juice. The acid is a problem. A bland, easy to digest diet is also helpful, at least while you are having a rough time of it or to maintain the good times. Eliminating right away, and not waiting to go to the bathroom, is important.

This is Kimberley’s story, but mine too, because as her mom there wasn’t a day she was ill that I felt ok either. I am so glad to see her living a normal life. There were many years I wondered if she would be able to.

Comment on this

Comments
    There are currently no comments.

April 2007

  • Dealing with IC one day at a time… - by Beth K - (Mon, Apr 30 2007)
    I was diagnosed with IC after a bladder scope and biopsy in 1999. Before I was referred to my urologist I had seen MANY doctors (and taken many antibiotics) who were convinced I had a UTI or gynecological problem. [more..]
  • Kimberley’s Story - by PD - (Tue, Apr 24 2007)
    My beautiful 24 year old daughter struggled with Interstitial Cystitis for several years before we could find any right path toward handling this painful condition. [more..]
  • ICD - by PSM - (Mon, Apr 23 2007)
    I had frequent bladder pain and doctors kept treating me for an urinary infection with no success. I was going to the doctors once a month for bladder pain. [more..]
  • MY STORY - DIAGNOSING INTERSTITIAL CYSTITIS - by ROBIN - (Fri, Apr 20 2007)
    I WAS HAVING SEVERE PAIN IN MY RIGHT SIDE FOR A YEAR AND A HALF DOCTORS COULD NOT TELL ME WHAT WAS WRONG WITH ME BUT TO TELL ME TO TRY THIS MEDICINE AND THAT MEDICINE AND NOTHING WORKED. [more..]
  • Losing hope. - by N. Martin - (Wed, Apr 18 2007)
    I got diagnosed with Interstitial Cystis three years ago, my senior year of high school. Basically my Dr.s thought I was having recurrent urinary tract infections and after several courses of anitbiotics were unsuccessful, we did the diagnosing for Interstitial Cystitis. [more..]
  • My IC - by Karie - (Fri, Apr 13 2007)
    I was diagnosed with IC about 6 years ago. Just thought I had a really bad bladder infection. Went to the doctor and there was no infection. I thought I was losing my mind. [more..]
  • From urinary tract infection to IC to Overactive bladder - by Suzanne - (Fri, Apr 13 2007)
    At age 30, I was diagnosed with an e-coli urinary tract infection That was after I had taken different antibiotics for four months and they could not find the right one so they finally did a culture and it was e-coli. [more..]
Archives:
  • 2008 January February March April May June July August
  • 2007 April May June July August September October November December

  • The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer)



    Home