Orange Gearle

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Saturday, December 01, 2007

it's a kidney!

A short update--

Surgery was at 7:30 Thursday morning. Dad woke up from the surgery perkier and more animated than ever -- even his voice sounded better! Amazing. There's even more spring in his step.

It's really all about pain control at this time for me. We have had several steps forward and backward. I will update more when I am not quite so tired (and on less percocet). :-)

They kicked me out of the hospital today...but we are in the middle of an ice storm so we are at a hotel until it passes. We will head home tomorrow.

peace out

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Wednesday, November 14, 2007

thank you

Today we had our pre-surgical appointments at UIHC. Everything went well. More blood drawn from both of us. Dad had a few re-checks since it had been so long since the first ones. He had to take his clothes off twice...I got to keep mine on the whole day!!!

I don't even want to talk about the three hours that I waited to see the surgeon.

Highlights:

I do NOT have to have an enema.

They are taking my left (for sure)...putting it on his right (I think).

My new (biggest) scar will be in the bikini line area (just in case I decide to wear a bikini someday to show off my belly....and large c-secion scar). There will also be a couple (maybe three) really small scars where they insert the instruments for laparoscopic surgery.

They are gluing me together instead of staples (Shelley thought gluing was appropriate, since I am a teacher).

I got to see the pictures that they took of my kidneys last time. VERY cool.

I was sitting across from Mom and Dad in the waiting room and Dad came over and sat right next to me and said:

I thought I'd come over and sit closer to you so my kidney can get used to your kidney.

Later he said:

Did you feel that? I think my republican kidney is already starting to reject your democrat kidney.

As I got out of the car Dad hugged me and said "Thank you."

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Friday, November 02, 2007

less than a month now

It's November 2nd. The second day of American Diabetes Month. I've now read all of this blog. Kathy's struggle is amazing to me. I am thankful that my father hasn't had nearly the troubles that she has. But it also makes me wonder if he's feeling even worse than he lets on.

Last night when I got home from the jam, I couldn't get to sleep right away. So I decided to do a bit of internet exploration. I was searching for stories about live kidney donors. I want to know a bit more about what I'm in for. :-) I'm not worried about me, or pain or anything....just curious about the process. I stumbled upon this site. Very interesting. Very informative. I even cried some. I haven't read all the stories, but I will. Ed's story was the first one I read. He was back to work after 11 days! He might be a nut, who knows?

It makes complete sense, but I am not thrilled that I have to have an enema. Ick. I hadn't really thought about that. But Ed's story informed me of my impending doom in that area. UPDATE: My friend, Gigantor, said he didn't have to have one...maybe I'll get lucky.

I've been very emotional about this whole thing lately. I can't exactly explain it. Like I said before, I'm not worried about me at all. I'm young and in reasonably good health. And from everything I've read, I will go through a bit of discomfort, pain even, but it will be very short term. I'm not questioning if this is the right decision. I know it is. I've never been more sure about anything. I have but ONE concern, and it's been weighing heavily on my heart lately.

What if I wake up from surgery to find that my father didn't make it through the surgery?

I can't stop thinking about it really. As we are now less than four weeks away from surgery, I am worried that I will only have four weeks left with him. Good grief. I have no idea what is wrong with me. There has got to be some sort of 12 step program for worriers!!! Sign me up, man. I think I could be their poster child.

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Monday, October 29, 2007

kidneys in the news

I found this story this morning...it's worth a read. And here's a link to the author's blog.

A few facts quoted in the story:


  • 20 million Americans - 1 in 9 adults - have Chronic Kidney Disease (CKD) and another 20 million more are at increased risk.
  • Heart disease is the major cause of death for all people with CKD.
  • Hypertension causes CKD and CKD causes hypertension.
  • High risk groups include those with diabetes, hypertension and family history of kidney disease.
  • African Americans, Hispanics, Pacific Islanders, Native Americans and the elderly are at increased risk.
  • About 200,000 Americans suffer from kidney failure and need an artificial kidney machine to stay alive.

  • I took a walk with my dad yesterday after Sunday family lunch. He said to me, "Now, I can't walk too fast. I just kinda stumble along." He did just fine...and it was nice father-daughter time.....no politics, just life.

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    Wednesday, September 26, 2007

    kidney update

    I received word this morning that I have been approved to donate my kidney to my father. Read on if you’d like a few more details.

    Since Dad isn’t feeling the best, it is possible that he may do some dialysis prior to surgery (beginning in October, probably). This will clean out the toxins, etc. Then we will have pre-op appointments one day in November, and the surgery Nov. 29. (this means I will only miss about 13-14 days with kids). During the pre-op appointments, my dad will need to have some of the same evaluations done that he did last winter/spring — just to make sure that surgery is still safe for him. They will not go through with the surgery if it isn’t safe for us both.

    I am very excited!! This is such good news. When I saw that spectacular moon this morning, I knew it was going to be a good day.

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    Monday, September 17, 2007

    kidney update

    Today I learned a lot about my body. I also had to take my clothes off four times!!!!

    Yesterday I collected my urine all day. I had to be away from home for part of the day, so I had to carry my pee in a cooler. Very odd. Anyway, as part of my tests, they needed a 24-hour collection of my urine. This is to test my creatinine levels. My father has had to do it many times.

    My day started with one last urine collection before leaving my house bright and early and heading to UIHC with my mom to support me. Last spring when we traveled to UIHC we went through a bunch of construction in the building -- it's been through several aesthetic changes -- and now, a few months later, it seems to be complete. Very beautiful. Art everywhere. When we arrived we checked in and headed to the Surgical Specialty Clinic -- which was our home base for many of my dad's appointments, so we know it well. They took several vials of blood out of me, and asked for ANOTHER urine sample!! I met with Shelley, our transplant coordinator. She had a side-kick with her today -- another woman that is learning how to do Shelley's job.

    After the blood was out, a little food went in. I had to fast for my lab work and only had a small window of time before I had to fast for a test later in the day (CT Scan). So I had a Zone Bar, a banana and a Diet Dr. Pepper (of course).

    They took my vitals, I signed a bunch of paperwork, and I met with the social worker. Her job is basically to make sure I am aware of any potential risks, and that I will have a good support system to help me out when I get home from the hospital. Then I met with Dr. Heather Muster about a study that I have an opportunity to participate in. It's called Assessing Long Term Outcome of Living Donation (ALTOLD). I will probably participate in this study....more on that at a later time.

    The first time I had to undress was to be examined by the nephrologist, Dr. Bertolotus. This is the same doctor that saw dad on his first visit to UIHC for the beginning of his evaluation. Dr. Bertolotus examined me and took a look on the computer to see if any of my tests were back. Even though it had only been about 3 hours, there were many complete and already entered in the system. Apparently I'm very healthy. My kidneys are functioning "normal" (whatever that means). My cholesterol is 203, which to me seemed high. But Dr. Bertolotus said that the reason it is so high is because my GOOD cholesterol is about as high as it can be (apparently that's good). My BUN (blood urea nitorgen) and creatinine levels are all good -- low even. Here's some information on that. I have low BUNs....lol.

    The second time I had to undress was for an EKG. And then the third time was for a chest x-ray. Both of these were very quick, and painless.

    The fourth and final time I had to undress was for my CT Scan. This was not my favorite part of the day. It didn't hurt much (IV went in well), but I was uncomfortable....more mentally than physically I suppose. They had to inject "contrast media" into me and take a bunch of pictures. It wasn't bad...just not my favorite. They took pictures of my kidneys. They are checking to make sure I have two, for starters. :-) Then they will be looking at them both to decide which one to take for the transplant.

    I learned:
    • When the donor kidney is put into the recipient, the recipient's existing kidneys stop working completely in a short time. So, even though they will not take out any of dad's kidneys -- they just hook up the donor kidney-- he will only have one functioning kidney...mine. This is why it is important to wait until just the right time to do the transplant. For example, I was very upset that things were put on hold last spring....and although he went downhill quicker than anticipated...by doing a transplant too soon, we are essentially wasting the good kidney a bit. What I mean is, the donated kidney doesn't last forever...only 15-20 years or so. Had Dad's kidney function remained at a manageable level for several years, we could have been giving him a few extra years with my good kidney down the road. However, he's nearly 73, so.....I think that probably cancels all of that out (in my opinion). As he ages, his health naturally declines, so, in my non-doctor opinion, it would seem to make more sense to do the transplant while he is younger and feeling better. But....he's not younger or feeling better now, so none of that last part really matters....And, although I am wicked smart, I suppose I don't know EVERYTHING...moving on.....
    • The veins connected to the left kidney are longer, so they prefer to take that one....and as long as everything else is equal, that will be the one they take. However, if there are more veins on the left one, or detaching it would be more difficult, they will take the right one. Also, if one kidney is better than the other one -- I get to keep the good one!! So, I wonder....if they take my left kidney, will that make me lean even more to the left, politically? :-)
    • They only do kidney transplants on Thursdays at UIHC.
    • Two healthy kidneys do not work to their full capacity. So, if you donate a kidney, you aren't actually losing 50% of your kidney function. The remaining kidney beefs up and begins to work better (notice I did NOT say harder -- harder implies that there could be undue stress on the remaining kidney). In fact, there are people that live with one kidney their whole life and don't even know it.
    • All of my tests (that were complete when I left today) were good....better than good actually. The nephrologist told me that as long as I continue to exercise and I don't gain a bunch of weight or something....even if I just stay like I am right now....there is no reason to think I will get diabetes. Of course, there are no guarantees. But I've learned that there are no guarantees about ANYTHING in life, no matter how perfect it might seem, it can all come tumbling down at any moment (how's that for positive thinking). Anyway....
    • (I already knew this next part before today, but I'm putting it in here for any of you that think I'm putting myself at too big of a risk in the future). Studies show that a kidney donor is no more at risk for kidney disease than a person with two kidneys. That, along with the VERY thorough exam that I received today, is more than enough to convince me that this is the right thing to do.
    • They will not do the tissue typing until the PRE-OP appointment. That is how certain they are that I will match Dad at LEAST enough for the transplant. It has something to do with me being his daughter. :-) More importantly, Dad has not had a previous transplant, has not had a blood transfusion, and has not given birth to a baby....so he should not have developed any antigens against me. I keep telling them that I'M A LIBERAL and dad is a REPUBLICAN, there is a chance we won't match....but apparently politics has nothing to do with it.
    • Surgery lasts 3-5 hours, and I would go home Saturday or Sunday. Dad would be hospitalized a bit longer, closer to a week.
    So what does that all mean???

    I will know next week for sure...the rest of the tests will be in by this Friday....and then Shelley will "present" my case to the panel of doctors.....but it looks like Shelley will schedule the transplant for November 29, or December 6, 2007!!!

    Here is a bunch more info on organ donation for those interested.

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    Saturday, July 28, 2007

    kidney update

    Friday brought a doctor's appointment for my dad. Although his kidney function didn't decline drasticly, it is apparent that his numbers are fluctuating. He is also either feeling worse (fatigue wise) or he is expressing his feelings to the doctor more effectively, because the doctor is saying we need to move forward with kidney transplant procedures, due, in part, to his feeling poorly. Another factor that the doctor is considering is that his fistula that he had put in several months ago seems to be failing. Now, they haven't even used this fistula, but, it's failing nonetheless. So, if he were to need dialysis, they would have to repeat the fistula procedure first - which is not something we want to deal with if we do not have to.

    So, what this means...

    Dad has to have a bit of blood drawn and sent to the lab. And I will be going to U of I hospitals to have my complete work over, including tissue typing. Shelley called me within a few hours of Dad's appointment, and we are looking at dates (probably in September) for my mega probing and prodding day. Then, it's a matter of looking into what would be the best time for me to miss work. There is never a good time to miss, especially considering the fact that I am starting a new job this year, but there are times that are better than others. And, in the big picture, work isn't nearly as important. The kids will do just fine with a quality sub.

    I'll admit that when things were put on hold I went into some sort of a mild depression, not that it takes all that much for me to do that, I suppose. I think it's mainly because I could see him feeling worse, and I felt like we weren't doing all we could to change that. So, even though needing a transplant, isn't exactly good news, proceding IS good news, in my opinion. I guess I dealt with the issue of my dad needing a transplant a long time ago...so that's why I can look at this as good news. The transplant was inevitable, now it looks like we are actually going to do something to make him feel better.

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    Wednesday, April 04, 2007

    how was your flow -- a kidney update

    I think nurses are cut out of a special mold. Ok, well, I don’t think that, I know that.

    Today we had another appointment at UIHC. We got to see Shelley and Kaye again. Kaye is the nurse that has taken Dad’s blood, given him shots, etc. Shelley is the nurse that is following our case through to the end. She is the one that does all the organizing with the different doctors and is part of the transplant team.

    All of the nurses that we have worked with so far have been so good with Dad. As anyone that reads this knows, he is ornery! He is always dishing it out…sometimes inappropriately. Well, every nurse that we have been blessed with, dishes it right back…which is EXACTLY what Dad needs. He can laugh with them, and, good or bad, it encourages him to give them a bit more. ☺ But overall, it’s good. It’s very similar to how my sister-in-law (also a nurse, by the way) treats Dad. We are lucky to have her…she’s about the only one that can put him in his place.

    Dad had his second hepatitis shot and met with the urologist, Dr. Wald.

    After Kaye gave Dad his shot, Shelley checked in with us. I gave Shelley my papers from St. Luke’s that included my blood type, and she gave us the good news. As I wrote about here and here, the process is as follows: Dad goes through a bunch of tests, then Shelley presents his information to a panel of doctors. The doctors must approve him before we can move on with the procedure. We were told that this would happen after all the tests were complete. Shelley has already presented Dad, and assuming there is a good report from today’s urologist evaluation, he is approved. What does this mean?

    As soon as Dr. Wald’s report is in, Shelley will call me. I will need to come in for a full day of appointments with many different doctors. Then within a couple of weeks, assuming I am approved, we will set a date for the transplant. This could be as soon as June. This is good news.

    At lunch, after we ordered, I went to the restroom. When I came back Dad said…..

    “How was your flow?”

    We laughed….I bet he does get sick of that question!! And that is exactly my Dad’s sense of humor….here’s another for you….

    On the way out to lunch after the appointments Dad said…..

    “I tried really hard, but I just couldn’t make it happen.”

    Mom and I of course asked what he was talking about…..and he replied….

    “I tried to shit on that doctor for making us wait an hour, but I couldn’t do it.”

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    Friday, March 09, 2007

    o negative

    On Tuesday, March 6, Mom, Dad and I traveled to Iowa City for more tests at UIHC. On the drive there, when we were crossing the Iowa River I saw about eight bald eagles sitting in the trees by the river. Beautiful.

    Between the last UIHC appointment and this one, Dad had his blood drawn for tissue typing. We were looking forward to finding out Dad's blood type. Blood type is the first step. Although it is possible to do an ABO incompatible kidney transplant, it is not our first choice. I've been a bit nervous about all of this because I really want this to work for him. I want him to feel good again. This is how it works:

    Recipient has: Donor must have:
    O blood-type O blood-type
    A blood-type A or O blood-type
    B blood-type B or O blood-type
    AB blood-type Any blood-type

    So I was of course rooting for Dad's blood-type to be AB. :-)

    We checked in at the surgi-care center. As the lady was checking us in, Dad, quite discreetly whispered to my mom that he thought she looked like some character on Grey's Anatomy. My mom, indiscreetly agreed. The woman smiled and said that she heard that a lot, at least once a day. Apparently I am the only one on the planet that doesn't watch Grey's Anatomy.

    After checking in, Kaye (a nurse with Dad's team) lead us back to room six, on the way she weighed and measured Dad. When they started to get his height, Mom made some comment to me like "God forbid Dad shrink during the kidney transplant." It made me laugh, because it does seem kind of silly that they measure his height each time he has an appointment.

    This was the day for us to meet the surgeon, learn Dad's blood type and for him to get his second, and final tissue typing done (labs). Kaye did all the usual routine nurse stuff, then gave Dad a gown and told him to get in it. After she left, Dad said, "I don't know why I have to get naked to talk." But he did anyway.

    The surgeon came in and shook our hands. He was what some might call 'my type'. The dark, kinda curly hair, darker skin, etc. My mother immediately starts looking for a ring on the guy's hand. Poor guy. LOL I thought he was arrogant and that's completely unattractive to me.....so it really didn't matter at all to me that he had a ring.

    He asked Dad a lot of questions. The usual stuff...looked at his chart. When he was asking the smoking questions, my mom said, "But he does chew tobacco." And the way she said it, MADE me say, "Tattle Tale!" The surgeon almost smiled. Then when he asked Dad if he uses intravenous drugs, we all burst out laughing. He looked at Mom and said that if anyone would tell him, it would've been her. :-) Can you picture this man doing intravenous drugs??


    So after Dr. Katz finished asking a zillion questions...he examined Dad. Inside and out, if you know what I mean. He felt something a bit "nodular" which is just a gross word, so now Dad will have to see a urologist before we proceed any further. That kinda stinks because it moves everything back another month. But better safe then sorry I suppose.

    Shelley, another nurse that is taking care of Dad's case, poked her head in several times throughout our time there. She is a riot and handles Dad's orneriness very well. She is the one that told us that Dad's blood type is O.

    The surgeon said that he saw no reason that Dad couldn't have the surgery. So this is about the fourth doctor that has given the ok. Now, it looks like just the urologist and we will be good to go!

    After Dr. Katz left, one of his nurses, Jan came in to talk to us about a study that Dad could be involved in if he so chooses. One of the drugs that Dad will have to take following the surgery is called Cyclosporine. It's an anti-rejection medication, that can cause high blood pressure and kidney damage. Yes, I said KIDNEY DAMAGE. This drug as been around about 35-36 years. They have recently made a new drug that they are testing called Belatacept. This drug is either in Phase Three or Phase Four of testing and Dr. Katz is part of this study. So, Jan came in to tell us about it. The main thing about this drug is that it is not hard on the kidneys. If Dad were to participate in this study, the drug, Belatacept would be covered completely by them...also any extra testing that they require would be covered. The disadvantage is that he would have to go to Iowa City to receive drug intravenously. Every other week at first, then monthly. Dad hasn't made a decision about this study yet.

    There are a lot of drugs that Dad will have to take after this surgery. A LOT. There are drugs to suppress his immune system so that his body doesn't reject the kidney. There are drugs, like antibiotics, to help him stay healthy (some are disease specific). He has to be on these drugs because of the other drugs. You get the picture.

    Mom, Dad and I went out to eat afterwards. I made a quick call to St. Lukes in Cedar Rapids to see if I could get a copy of my blood type (they have it from when I was pregnant with Hollyanne). They said they could get it for me if I came in with proof of identity. I'll admit that I was very nervous when I heard Dad's blood type was O. I was pretty sure that mine wasn't O. And only O can give to O. However, the good news it that Mark is O...so if I wasn't, we had a backup.

    After we ate we went to St. Luke's to pick up a copy of my records. Mom dropped me off and went around the block while I ran in. I couldn't believe it when I saw it. I am type O negative. This is the first step toward a match. :-) We are part way there...with many more tests to go, but at least I'm in the running. :-)

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    Monday, February 05, 2007

    here a kidney there a kidney

    Friday morning my alarm went off at 5:00, no different than any other morning.

    I got up and got ready for the day, as usual. Talked to my mom on the phone, they planned to arrive by 6:30. For once, they weren’t early! As 6:30 arrived they pulled in the driveway ready to go. Hollyanne woke long enough to hug her grandma, grandpa and me -- then back to bed for her.

    The drive to University of Iowa Hospitals and Clinics was uneventful, other than the bitter cold. As we turned off the interstate onto Melrose Avenue memories of the seven years I spent in Iowa City flooded back. We passed where I worked, where I lived, where John lived, and were I spent many, many football Saturdays. Rich called as we were approaching the hospital, warned us of a accident (to make sure it wasn’t us), checked to see if we were ok, and indicated he may join us for a while at the hospital if he can. We pulled into the parking ramp, parked and took the skywalk into the hospital.

    I directed us to the registration where dad gave all his information, reluctantly. We were only forty minutes early. ☺ The lady at the desk, I cannot remember her name, gave us directions to the UI Heart Care Center, our first stop of the day. Dad was forced to give out much of his information again (annoying but necessary, I suppose). Mom began filling out paper work. She had to list each of Dad’s nine siblings, ages, and if deceased, cause of death. There were also the usual questions designed to provide the doctors with the background information required to best help him.

    Before Mom had even finished the two pages of paperwork, Dad was called back to the room. I went with him. Brenda started to take his blood pressure, in the wrong arm. Dad had a fistula put in a few months ago, and as a result nothing is supposed to be done on his right side. Dad promised he wouldn’t tell if she didn’t! So she took his blood pressure again in the left arm and took five vials of blood.

    Side note: Dad loves Seinfeld. He didn’t watch it much when it originally aired, however he has enjoyed nearly every episode since syndication. He frequently references Seinfeld to fit situations in his/our lives. The Seinfeld episode that has been referenced as of late is one that centers around Elaine. In this episode, the sponge form of contraception is about to be taken off the market. Elaine purchases as many as she can because this is her birth control of choice. So when she meets a guy, before she has sex with him she has to decide if the man is “sponge worthy”. Dad, of course, finds this hilarious. He says to all that will listen -- today’s appointments are to find out if he is “sponge worthy”, corrects himself and says “kidney worthy”. When Brenda was taking his labs, he made no exceptions and indicated that he was here to see if he was sponge worthy.

    After his blood was drawn, Dad had an EKG. Then he was allowed to have a little bit of food. He is diabetic, but was forced to fast for 12 hours before his labs, so he was quite hungry. They allowed just a bit of fruit, due to the tests yet to come.

    We waited for a while…during this time I went downstairs and turned in my paperwork for my portion of this whole thing. I also went upstairs and got myself a veggie sandwich. Never mind that it was not even 9:00. I was hungry! And a Diet Pepsi would have to do, no Diet Dr. Pepper, of course.

    Dr. Theresa Brennan, cardiologist, came in examine Dad. She did the usual, listened to his heart, made him take deep breaths to listen to his lungs, etc. She indicated that his heart rate is really low, which is actually a good thing. She also said that her husband had a kidney transplant 4 years ago…and that he is doing very well. She checked the strength of his right and left side, and thought it was pretty good considering he had a stroke 10 years ago.

    Dr. Brennan was a bit concerned with the noises she was hearing when she listened to his carotid artery and ordered an unltrasound of that area. They were able to get the appointment in today.

    Dr. Brennan also suggested that Dad try the stress test on the treadmill rather than the
    Dobutamine induced kind. Mom was concerned about him walking on a treadmill, because he is a little bit unsteady, but he was assured that he would have a handrail to use while walking.

    After the cardiologist we went downstairs to get a chest x-ray. I ate my sandwich while Dad was getting his x-ray. Then we went down to the first floor and Ashley took him back for an unltrasound on his carotid artery. The entire time my mother was concerned that we were going to get lost. She kept saying, “Now, do you think you know how to get back?” It was good for a laugh or two.

    Our morning was complete when we returned to the fourth floor, cardiology, for Dad’s stress test. We had to wait a whole hour before the stress test was to begin. I used to think that I got my impatience from my mother, but after today, I think it’s more from my dad. Sitting and waiting is definitely not among his favorite things.

    I went back with Dad to hear the instructions prior to the stress test. On the way back they talked about starting an IV and I told them that Dr. Brennan had suggested we NOT do the drug-induced stress test. They had no idea. ☹ So when we got back to the room we waited while they talked it over with people to make a decision. They ended up doing the Dobutamine induced stress test after all. I stayed in the room while they did an ultrasound of his heart. This was very interesting. I could see the walls of the heart, the valves move, etc. Very interesting. They had a difficult time getting the IV started. Once again he was asked all the same questions. Are you allergic to any medications? Have you ever had a heart attack? Etc. Funny though, when I mentioned that he’s had a stroke ten years ago, they had no idea!! Good grief, Charlie Brown!!!!

    One of the ladies asked him for his birth date – again. Dad told her, and then said, “Have you ever heard the one about the guy that didn’t know how old he was?” As she was shaving his chest for the stickies, she said “No.” Dad continued with his joke….

    “He was asked, ‘When is your birthday?’ and so he said, “September 23”. ‘What year?’ “well, every year!”

    The three women laughed politely as if it was actually a funny joke. Dad was pleased.

    I waited in the lobby while Dr. Schmid performed the stress test on my father’s heart.

    I will admit that this was the part I was worried about. The Howe’s notoriously have good hearts. In fact, it seems like sometimes the rest of their body gives out, but that heart just won’t let them die. So, I’m not sure why this was scary for me, but it was. I was very thankful to see him walk into the lobby with the nurse beside him giving me the thumbs up!

    While we waited for Dr. Brennan to return to give us the test results, Rich called, asked where we were, and then came right over. He was there when Dr. Brennan came in to tell us that from a cardiology standpoint, he was at a low risk for any complications.

    The four of us went to lunch.

    After lunch Rich returned to his job and the three of us returned to the Surgery Out Patient Clinic to meet with the Nephrologist, Dr. Bertolatus.

    Once again my dad was poked and prodded, asked all the same questions and then a few more. Dr. Bertolatus completed his medical assessment and then talked to us about the basic risks of kidney transplant. He was very honest with the worst case scenarios and in the end told us that he thought dad was more than healthy enough to have the surgery, and from his standpoint at low risk for complications.

    Next came the social worker. I think basically her job was to find out if dad was nuts and if he would have support after the surgery. ☺ It was nice listening and contributing to this portion of the day because when you list it all out there, we are really lucky to have so many friends and family members around us and supportive of us. This portion of the day was pretty funny. Dad’s sense of humor was obvious. Actually, our whole family’s sense of humor was apparent.

    Finally, the last person that we met with was Shelley, BSN. She walked us through what happens next. Soon, Dad needs to meet with the surgeon and get some more blood drawn. Then Shelley will present Dad’s case to a panel of doctors and the will give the ok to move ahead. It is then that I will be tested. It sounds like there is very little chance that I won’t be a match. That’s good news.

    There are six or seven code matches they look for….three are the most important….but they even do 0 point transplants. So, odds are, I will have one less kidney in a few months, and Dad will be feeling a lot better. ☺

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