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View Full Version : New 29 yr old male diagnosed with IC by default


scott777
01-03-2007, 07:57 AM
I was just diagnosed with IC yesterday. The urologist pretty much told me the diagnosis is due to the fact that everything else was ruled out. I am a 29 yr old male, non smoker, drink rarely, 6'3'', 205lbs, athletic build. For me I first noticed I had an urge about 10 times a day back in Nov 2005. I first went to my PCP who treated me with an antibiotic and checked my prostate. He said the prostate was fine and the antibiotic did not work.

I then went to a uroligist who had a CT scan done to check for stones. He told me I had overactive bladder and my CT Scan and urine tests were fine. I didn't understand how one day I could wake up and have this problem without it being muscular. They put me on Ditropan XL.

I went to a 2nd urologist over the summer who did a cystoscope in office with no anesthesia. Needless to say I wimpered like a dog in trouble the whole time. They said my bladder looked good and told me to stop the ditropan and retrain my bladder. If I feel the need to urinate, hold it as long as I can.

I wasn't happy with this so I called my PCP again and was referred to a surgeon to check for hernia. The disomfort I felt since day one seems to be on more in the lower left quadrant, extending down to the groin and slightly left of my bladder. There is a slight pain that feels muscular or like a tendon strain in my left groin area when I lift my left knee up toward my chest. The surgeon had a MRI done and results were negative.

I next went to a gastroentologist to check my signmoid colon which is on the lower left side. He put me on prozac which is sometimes used for IBS which did nothing for me. I scheduled a sigmoidoscopy for Feb. because pushing on my sigmoid is a feeling of nausea.

While waiting for the sigmoidoscopy appt. I had a really bad flare up around 12/17 where I almost constantly felt an urge or some discomfort even after urinating. I went back to the original urologist who performed urodynamics testing. They said my bladder is definitely overactive. When my bladder feels it's going to explode, it's still 200cc less than a normal bladder telling someone it's needs to go. That's when they told me they think it's IC.

I was prescribed Elmiron 100mg 3 per day, hydroxyzine hcl 25mg 1 per day, and Ditropan 10mg 1 per day.

I am hoping this works. Some days/weeks I feel pretty good. Other times there is a flare up in which the entire day/week I feel an urge or discomfort almost constantly. It's more noticeable when I am walking and especially jogging/running. During flareups I wake up 2-3 times per night to go and each time the urge is really strong and annoying. But, other times when it's feeling better I can make it the entire night without going. During flareups the stream is weak and I feel I need to push harder than I should. I also tend to dribble afterwards which is annoying.

I read about how not drinking water, and drinking a lot of soda/fruit juice, etc... could bring on this condition. I almost never drink/drank water so that certainly could have been the cause. I probably drink about a pt of water every 2-3 days on avg. Normally even before the urges began I would drink 2-3 cups of 1% milk, 2-3 cans of soda or diet soda and maybe 1-2 cups of apple/cranberry juice or gatorade per day.

I don't think I want to change my diet yet. By doing so I won't know if the medication is working or the diet change. I am going to give the medication a try first to see what happens. I will probably replace soda with water a bit more often though.

It's great to see everyone coming together to chat about this, although it be better if there was a quick cure and no such IC forum. I'll make sure to check in weekly and provide updates if something works for me.

Scott

barbour1
01-03-2007, 08:45 AM
Scott,coffee is a no no if you drink it . I have one a day.And i was told any thing with aspratane (diet soda is no good,juice may hurt you.There should be a copy of an ic diet some where on this sight.you might stay away from chineses food that has msg,Chili and spicy foods i can't eat and also anything spicy. There is some thing you can buy called prlief that you sprinkle on your food that may help i think it takes the acid out.Did the Doc give you detrol? That also helped me.I am sorry you have i c but i guess it's not just a female thing..:welcome: and good luck, the peolpe on this sight are just great.

barbour1
01-03-2007, 08:53 AM
Scott go to the IC hand book there is info on foods there..hpoe this info brings you comfort..

scott777
01-03-2007, 08:54 AM
Thanks...I don't drink coffee which I guess is a good thing. I had Chinese for New Years and didn't have any problems. When I have a flare up it's a 1-2 week thing rather than a daily/hourly thing so I really don't feel its food/beverage related. The last flareup I had lasted from 12/17 to about 12/31 and remained constant. I could tell on the 31st the symptoms were getting better...it wasnt an all day 24/7 pressure/tingling feeling like it was the weeks prior. I also went from waking 2-3 times at night to once on the 31st and the last couple days.

theclownster
01-05-2007, 06:45 PM
Welcome to the ICN! It's a great place - a real life saver for me when I was first diagnosed. There are a lot more females with IC - yet it does still effect males. There are other men on this site - hopefully one of them will post and offer you some additional support soon.

A lot of people take Hydroxyzine which helps them tremendously. I'm one of those people. I used to take Ditropan XL but was recently switched to something different (same category med). Ditropan really helped me too.

I would definitely suggest that you stay away from Cranberry juice. It is one of the worst things a person with IC can drink. It often causes pain and discomfort. In terms of drinking beverages, I think the tendency when a person first gets IC is to cut back on how many fluids you drink. Since you have to go to the bathroom so often, it's just natural to think "maybe I'm drinking to much". What I found is that it's actually better to drink lots and lots of water. Drinking more just seemed to limit the severity of my symptoms.

Please post as often as you like. I hope you are feeling much better soon!

Take care,
Jennifer

laurahallie
01-05-2007, 11:03 PM
scott - i know what you mean about the flares being constant and probably not affected by food. when my ic first started, i had the same thing.. fortunately i only had two such flares which both lasted about two weeks. the last one was in july and i havent had that awful feeling since. i hope they stop for you too.

have you heard of/been evaluated for pelvic floor dysfuction? a lot of men diagnosed with ic have it, and also ive read that a lot of people who find that diet doesnt affect their ic have pfd. recently ive been having some other problems and consequently am going to be evaluated for pfd...ive been thinking about it and it would make a lot of sense for me to have it. dont know about you, but when i had the constant urge it wasnt necessarily in the bladder; it felt like it was more in the upper part of the urethra. maybe those flares were the pelvic floor muscles just totally freaking out? just a thought.