WOW ! I'm impressed you are already home from the hospital. I was in for 10 days. My surgery went well but due to all the pain meds, I had little appitite and so my bowels wouldn't cooperate...and we all know they won't let you leave the hospital until you pass gas and have a BM. When I did eat, whatever I eat came back up so I couldn't get my digestive system to settle down until day 9....woke up on day 10 and announced to the doctors that i was going home. Several times while in the hospital and after I arrived home I was contacting Pat to calm my fears. My RC was in July 07 but now it seems like ages ago and I feel like a pro...you will also, in time.
Easy to digest foods is key. You really have to be very picky about your choice in foods. Chicken noodle or veggie soups are good. One friend brought me some frozen fruit and a blender with yogurt to make smoothies...that was good for me as long as I didn't get too much citris...even now, too much OJ or pineapple juice will irritate my system. Pat suggested scrambled eggs...good protein. Peanut butter, also an easy and good source of protein...some mornings a spoonful of it was all I could manage. I love brocolli but found the pouch didn't like more than one serving of it at a time. As others have said, you will have to be cautious and carefully test foods to determine what works well for you and what doesn't. I suggest you take it slow and esy for the first couple of months...and forget fast foods if you're inclined to indulge in them.
I feel I must apologize to you because I did tell you earlier about my website and I fully intended to get there earlier this week and add some additional information to be helpful to you. I am going to go there now and work on it in the hope that I can be of better assistance to you. If you want to contact me personally there is a place for that on my website and I would be happy to answer any questions you might have...I have found that the forum offers great information from warriors who have been there and done that...and we relate to some more easily than others....anyway, my site is:
www.bladdercancerwarrior.com I hope to work the site during the next few hours and update it with more details on life with the Indy pouch...check it out if you feel up to it. Melodie