On non-trip news....as my Facebook friends on here already saw - Monday was my 6 month anniversary for my kidney transplant!


I am still so amazed at how much of a difference that one little organ can make.
On Tuesday I had an appointment with my surgeon. I only have to do labs once a month now!

When I first came home it was twice a week, after a couple months or so it got lowered to once a week, then to every 2 weeks, now it's monthly.
We also talked about having my "original" kidneys removed. She explained that for some people whose kidneys just don't work she will leave them in. In my case, I have polycystic kidneys and they are many times the size of a normal kidney. Since they are so large they crowd everything else in there. I know when I was doing dialysis and had 2 liters of fluid in my abdomen along with extra big kidneys, I just felt like there was no room for anything else. I ate very little...I just didn't feel like I had room to put anything. If I knew we were going out for supper I wouldn't eat anything all day so I could enjoy the majority of my meal. Now I feel better, and eat more (which probably isn't a really good thing

) She said once she gets them out of there that a lot of her patients talk about how much better their digestion is and sometimes even their breathing - less shortness of breath.
I can't tell you how long my kidneys have been big, but I do know when I was pregnant (and my youngest is 18) that when I would go in for my doctor visits, when Doc was feeling my belly, when he would get over to my left side he would always feel around and asked me if I was...uh...constipated. Well, i wasn't, but evidently he was feeling my kidney somewhere where it shouldn't have been. I wasn't diagnosed until a couple years later.
But anyway, since this is a non-emergency she said we could just schedule it when it was convenient. We have some trips and things coming up, but figured a good time would either be the last week of September/first week of October. Or the week of the 14th of November. The sept/Oct dates would give me about 3-4 weeks before Danny goes out west for a week or so. He gets back Nov 5, and then the following week-end is the local college's play. Danny records them, and this year Mark will be involved in it. He is going to that school with a Talent Grant in theater, so if he isn't in it for some reason, he will be doing lights or sound or something. Once that is over we have nothing for the rest of the year except holidays.
She (my surgeon) is scheduled in the OR on Mondays, so she has me written in for Monday, Nov 14th. That will be 10 days before Thanksgiving. She said I will still be sore than, but that I should be healed enough to enjoy the holiday, but not to prepare the meal.

That is totally ok with me because Mom does it all every year anyway....I was only ever offered "Jello" as an item to bring and that was with a "if you think you need to bring something"

. So I decided that I didn't think I needed to bring anything and just let her do it all. It gives her something to complain about - and that is when she is happiest

so it is a win-win.
I am looking forward to getting them out. It should be about a 4 day hospital stay and recovery time should be less than my transplant (only because I had that 2nd surgery the following week). We will get it done in this calendar year when the co-pays and out of pockets have all been met. Then I can start 2012 healed up and with (mostly) working parts!
And just a little bit of trip news......while I was typing this up Danny came in and got my phone to download the pictures off of it - hopefully that means he is getting everything downloaded in one place so I can get to it!