Interstitial Cystitis

Feel free to discuss any topic of general interest, so long as nothing you post here is likely to be interpreted as insulting, and/or inflammatory, nor clearly designed to provoke any individual or group. Please be considerate of others feelings, and they will be considerate of yours.

Moderators: Rosie, Stanz, Jean, CAMary, moremuscle, JFR, Dee, xet, Peggy, Matthew, Gabes-Apg, grannyh, Gloria, Mars, starfire, Polly, Joefnh

Post Reply
amberlink09
Adélie Penguin
Adélie Penguin
Posts: 130
Joined: Sun Jun 24, 2012 5:44 pm
Location: United States

Interstitial Cystitis

Post by amberlink09 »

Hey guys, I just wanted to give you a quick update. So, after I had surgery and my doctor didn't find endometriosis like he 100% expected to he wanted to try a few more things to make sure all of our bases were covered, one of them being a test for interstitial cystitis. Neither of us thought there was too high of a chance of finding it, but lo and behold I had the test today and came back with a positive. I'm still trying to learn about it because I didn't do much research on it beforehand, but he told me some of the treatments for it include low dose anti-depressants (I went on amitriptyline last August and definitely found improvement, but thought this was stomach-related pain) and modifying my diet. There are other drugs too but he wants me to try the diet first, which means I get to cut out more foods including all fruit except for blueberries and cantaloupe, chocolate, all nuts except for almonds and cashews, onions ( :cry: ), spicy food, tomatoes, dairy, coffee and a lot of condiments. I'm trying to be happy that this can be treated through diet but it's really hard to cut even more food out at this point, which I know a lot of you understand!
User avatar
mbeezie
Rockhopper Penguin
Rockhopper Penguin
Posts: 1500
Joined: Fri May 29, 2009 3:14 am
Location: Texas

Post by mbeezie »

Hi Amber,

I don't get on the forum as much as I used to, but I also had IC symptoms at the height of my illness. We talk a lot about mast cells on this forum and IC is just another manifestation of mast cell problems. Here is an article describing the role of mast cells in IC. A low histamine diet might be of some benefit.

http://mastcellmaster.com/documents/Int ... l-2007.pdf


Hugs,

Mary Beth
"If you believe it will work out, you'll see opportunities. If you believe it won't you will see obstacles." - Dr. Wayne Dyer
amberlink09
Adélie Penguin
Adélie Penguin
Posts: 130
Joined: Sun Jun 24, 2012 5:44 pm
Location: United States

Post by amberlink09 »

Thanks Mary Beth! I haven't done too much reading on mast cells at this point, but I do hear them mentioned on here a lot so it's definitely something I want to learn more about. I know that somehow all of my different symptoms and illnesses are related, as my gynecologist told me today the interstitial cystitis diagnosis is only one piece of the puzzle of figuring out what's going on with me. The problem is that at this point I've been through tons of doctors since being diagnosed with Celiac and looking for more answers when I found no relief, my only good doctor has been my gynecologist, and he can only do so much for me. I would be so happy if I could manage to find a great gastroenterologist or GP.
Post Reply

Return to “Main Message Board”