Do you just live with the blood?

I have been doing a tapering dose of prednisone since December 29, now i am at 25 mg. and only stopped seeing blood for 5 days then i saw a little blood yesterday.  Anyway, other than that my stools are formed and the urgency is not so bad I usually only go once or twice in the morning and then I am good for the day.  I am still on balsalazide 9 pills a day and using the canasa morning and night because the blood is bright red.  I am at a point of throwing up my hands and surrender and just be happy I am not going multiple times a day and live with the blood.  It is not a lot of blood and only on the tp paper not mixed in.    I have written to my doctor yesterday through the hospital website they have set up, in the hopes he doesn't think I am a pain, to see what he thinks I should do about this.  I have asked him at my appointment a week ago If I should change my oral medication (balsalazide) for something different and he said he wouldn't change it yet maybe wait 3 months after the prednisone.  I really feel that i would have wasted all this time on pred if another medicine would have worked better, but of course, I don't know that, so I will go with what he says.    On a good note the pred has not caused me any side effects at all, except for a little more energy in the morning.

I also started taking bee propolis two days ago, georges aloe vera, cholophyll liquid, turmeric and bromelain, still using vsl#3 ds.  I am eating very well and try to only eat chicken, fish butternut squash, and limit any sugar, although i haven's completed eliminated all sugar, gluten free also. 

So do you think I should just give up and live with the little bit of blood I have each morning?

Thats how I usually feel, but I am at a point where I am so frustrated and don't know where else to turn. I do not want to go on harsher drugs because I don't think I am that bad. I did want to try the sulfalazide (sp) med next because it seems others have had luck with it. I have used the mesalamine enemas also but it seems that when I use them the blood is worse, but maybe only looks worse mixed with the enema.
Again, don't know, and feel really stupid with this disease. It seems that a lot of people here have had luck in controlling the bleeding but no so much the diarrhea, and I seem to be the opposite.

I have a very small amount of blood that comes up every so often. Never any other symptoms, just the occasional blood streak, or after having constipation/hard stool. Still not sure if it is because of UC kicking up or just a fissure/hemmies.

I hope you've talked to your GI about still having a lot of blood, I don't think it's a good idea to just live with it and not let your GI know what's going on. It can take a while to get bleeding under control but the longer it takes the bigger the chances of becoming really anemic goes up so I wouldn't just ignore or live with it.

Do you have hemmies? I ask because you specifically stated that the blood you see is only on the TP. It could be just your hemmies, especially since it is bright red and only on the TP. If that is the case i would use some hemmie meds instead.

yes, I have used the mesalamine enemas at the beginning of the flare but I had a hard time holding them so i would only be able to hold them for like 3 hours and let it out, so I opted to use the canasa instead which seemed to help a little.

I do know what your saying about using too many things all at once but I am at my wits end on this and I do wonder sometimes about hemmies, just not sure.

Thank you everyone for your thoughts I wish I could be less stressed over this.