Living with Interstitial CystitisThis 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 Interstitial Cystitis changed my life It began after a Myrtle Beach family vacation, 8 years ago. I thought it was kidney infection, as I often had growing up. The antibiotics didn’t relieve it, after 2 months of getting worse was sent to a Urologist who listen and read what they have done. During all this I had already eliminated the foods and drink that made me feel worse. Again more antibiotic’s no relief. He then did a scope which the numbing solution was of no help. It showed evidence of I.C. Started on the medications, my bladder decided it had enough and pain was unbearable, hospital stay. I was going crazy, my body is allergic to alot of pain medication’s. Which I never be a drug addict but then I couldn’t get relief of the pain. Went to a I.C. specialist. He did a bladder distension and confirmed I.C. and told me the truth of what I could expect. It wasn’t easy by no means, but my family has been my support system. I explain my pain like this, riding a boys bike and falling onto the bar. That is my pain level daily 24/7, a level 4. I still go to work, if I didn’t I wouldn’t have health care. I pray daily that all of us would one day I.C. free. Elmiron, Atarax, and Elavil is what I take daily and DMSO treatments now every 6 or 8 months. I miss alot of the foods I use to eat, but I keep hoping maybe one day. I allergic to the spasm medication, so the increased my Elavil, hope it works. If I have a pity party I feel worse, so I don’t do that. Life is but a whisper in time, how we choose to live it is ours. Comments
November 2008
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