Why I Write . . .

I have spent the past three weeks utilizing this blog space to provide updates concerning Kimberly and Angie’s kidney transplant surgeries.  Social media (like blogs, Twitter, and Facebook) are an interesting animal.  They allow a level of interaction (albeit selective and managed) that would have been impossible just 10 years ago.  Over the past few weeks, thousands of people have read at least one of the posts I have attached to this blog detailing our saga.  I never thought that many people would ever read this . . . I have not written these posts to promote my blog, make a name for ourselves, or generate sympathy.  However, I have been writing these posts for a reason.  Tonight, I wanted to put up a post letting you know what those reasons are.

I think I have been writing these posts for three primary reasons:   Me.  You.  Jesus.

  •  I have been writing these updates for Kimberly and myself . . . as a journal record for us of what all has happened . . . and someday as a testament for Joshua of what God did in our family.
  • I have also been writing this to help facilitate updates and prayer requests to so many of you who have expressed interest in this transplant.  We are so thankful for your help, prayers, and words of encouragement.  We have NEVER felt alone in this trial.
  • Finally, we have also been writing this to help shine a spotlight on our beautiful Savior through all this.  Our lives are a canvas on which God paints a revelation of Himself for a watching world.  I wanted to encourage all of us to see Him, not just hospitals at this time.  Think of this blog like a flashlight shining on His handiwork.

So, that is why I have been writing: for me, you, and Jesus . . . Hopefully these three purposes intertwine like a cord of three strands . . . allowing us to fellowship together around His work.

Two Week Follow Up

Kimberly and Angie today in the transplant clinic after their check-ups!

Hello friends.  I wanted to post a quick update this afternoon to let you know how things are going around the Robinson household now 15 days after transplant . . .

We spent the morning at the hospital today doing lab work, a CT scan, and meeting with the doctor for our routine two week follow-up appointment.  The news we got today was very good.  Kimberly’s new kidney is doing great.  She still has the hematoma behind her new kidney (from the internal bleeding right after surgery), but the CT today confirmed that it has not really grown since it was drained by needle ten days ago.  She has a pool of fluid about two-thirds the size of her fist that is sitting behind the new kidney, but it is not putting pressure on her new kidney or causing distress.  They think this fluid will just absorb into her body over the next 4-6 weeks.  This is the source of the tenderness she has experienced, but they are confident that additional surgery will not be needed to correct it.  This is a major praise!  Also, the blood she experienced in her urine over the weekend has stopped.  Another praise!

Also, Angie had her first check-up since leaving the hospital.  Things looked good and she was released to return home!  After 20 days in the Sooner state she is boarding a plane in a few hours and headed back to her husband and kids.  We are praising God with them and looking forward to their reunion tonight.

Thanks for joining us in prayer.  Please continue to pray for recovery and lack of complications.  Things are looking good.

Josh spent some time this morning reading the paper (financial section), drinking some coffee, and eating a fruit cup. Looks like he has spent too much time with grandparents the past couple of weeks 🙂

A Little Man to Man

This sign hung on Josh’s door when he got home tonight.

They say a picture is worth 1,000 words.  I am not sure if that quip is actually true, but tonight we had the joy of testing it out.  After 15 days of fun with his cousins, aunt and uncle, and grandparents, Josh returned home.

I met my parents at a local hotel around 4PM today to pick Josh up.  I wanted to take him to get ice cream, just the two of us, to talk about what was going on with Mommy before I brought him home.  For his entire life, Josh has accompanied Kimberly to doctor’s appointments.  Over the past 8 months, especially, Josh knew that Mommy’s kidneys were getting tired, and needed some help.  Before Josh left town, we told him that God had designed our bodies in such a way that someone could give Mommy one of their kidneys to help her’s since they had gotten tired.  When we told him this, Josh’s eyes got huge.  “Not mine!,” he exclaimed.  We reassured him by letting him know that Aunt Angie would be giving Kimberly one of hers.  He cheered.

We had told him that while he was gone, the doctors were going to give Mommy one of Angie’s kidneys, but we were unsure how much of that he really grasped.  Therefore, when he got home, I wanted to take him out and have a little man to man conversation with him to update him on what had happened, and to let him know what we could do to help Mommy.  So, over a cup of Braum’s chocolate ice cream, we started talking.

Me:  “Josh, a lot happened while you were gone.”

Josh:  “Yeah?  What?”

Me:  “Mommy got one of Angie’s kidneys.”  (I figured I should just get it out there.  Seems a bit abrupt in print . . .)

Josh:  “Alright!  Now hers won’t be tired anymore.”

Me:  “That’s right Josh.  Now Mommy is resting a lot as she gets better.”

Josh:  “Yeah, she can rest on the couch or in bed while you and I play Legos.”

Me:  “You bet pal.  The main thing we need to remember is that we need to be very gentle with Mommy.  She has a sore tummy and a sore neck, so we need to be very careful and loving to her, and help her out all we can.”

Josh:  “I can do that.  I can help Mommy out while she gets well.  Maybe we can watch some TV together?  That’s what I like to do when I am resting.”

And with that, we loaded up in the car and headed home.  When Josh got home, we heard all about his two weeks in a minimum of 1,000 words.  It was pretty sweet.  The pic of mom and son is also priceless.  So, at the end of the day, I got both a picture and 1,000 words.  I am just praising God that our family is back together again.  It just feels right.

In a side note, please be in prayer for Angie and her family.  She gets to head home on Tuesday after nearly three weeks to see her family again.  Her sacrifice was not just limited to her kidney, or even to her.  Kevin, Angie and the kids all gave deeply to us this past month, and we are forever thankful.

Friday 9:30 PM Prayer Requests

Hey everyone,

Well, tomorrow will be a big day.  We will celebrate our one week anniversary of being out of the hospital by welcoming Josh home from two weeks of fun at “Cousins Camp” (with my sister’s family) and with Grams and Po (my parents).  We can’t wait to see the little guy!

As we get ready for tomorrow, we have a couple of prayer requests and a praise.

First, the praise:  Kimberly had her throat scoped today at Dr. Buyten’s office, and everything looks great . . . no additional swelling in her airway, so she is cleared to have the trach taken out as soon as the transplant team is confident no further surgery is necessary.  Praise God!

Second, the prayer requests:  Kimberly has started to have some blood in her urine.  This started last night, stopped for a while today, but has come back again tonight.  This is not surprising (they told us it was a possibility), because she still has a stint in her ureter connecting her bladder to her new kidney.  During the period this stint is in, some bleeding is possible.  However, we are supposed to monitor this situation and alert the docs if it gets worse.  Thankfully, like every transplant patient at Integris, we have a 24 hour phone number we can call if we have any questions.  Also, thankfully, we all have a 24 hour connection to our Heavenly Father who we can talk to and ask to work to heal Kimberly’s body.  Please join us in praying for this to not turn into anything significant and to calm our hearts and minds.

Also, please join us in praying that everything goes well with Josh coming back home.  We long to see him again and are really looking forward to it!  However, we have to make sure that this active 5 year old does not bounce into mom in either her neck or abdomen while healing is still going on.  Please join us in praying that Josh will understand that he needs to be careful, but that we would also just have some sweet times as a family.

Thanks for joining us in praise and prayer!!!

Top 10 from the past 10

The past 10 days have been filled with a number of memorable moments for us.  Tonight, I am recording a “Top 10” of these moments for us in the form of memorable quotes from the week that was.  So . . .

From our home office in Norman, Oklahoma, here is tonight’s Top 10 things said concerning Kimberly’s kidney transplant in the past 10 days:

10.  “It just didn’t feel right.”  Dr. Samara, the lead surgeon on Kimberly’s transplant was closing her up when he noticed that the transplanted kidney felt a little limp. He trusted his instincts and redid the connection of the kidney to her artery.  When he did this, his instinct was proven accurate.  There was a small blood clot that had already formed.  If he had not caught this it could have been disastrous.  When Dr. Samara was updating me after the surgery, he said “It just didn’t feel right.”  So thankful to God that He allowed Dr. Samara to catch this complication and fix it!

9.  “I’m so glad we weren’t having this transplant 30 years ago.”  Reflecting on the advances in transplant procedures in recent years, I mentioned to my father-in-law that I was so thankful we were doing this transplant now instead of in the 1970’s or 80’s.  He reminded me that they thought Kimberly would need a transplant in the mid 1980’s.  So thankful to God that her kidneys hung on for 27 years to allow us to benefit from 30 more years of medical advancement.

8.  “I can wear his Captain America shield on my belt for protection.”  Kimberly was thinking about how to protect her surgical site from our very active 5 year old.  She decided that his frisbee like Captain America shield attached to her belt would do the trick.  I reminded her that a Captain America shield to a little boy is a target not a protective pad.

7.  “I was there for her tracheostomy in 2010.”  Dr. Buyten, Kimberly’s ENT acquired special privileges to perform her tracheostomy on the morning of the transplant at Integris Baptist Medical Center.  As the Anesthesiologist was preparing to talk to Kimberly about the plan for sedation during surgery, we overheard him talking to Dr. Buyten just outside our room.  It was so reassuring to us that Dr. Buyten (who really understands Kimberly’s throat) was able to secure her airway and answer relevant questions concerning her anesthesia.

6.  “Grandma is still here.”  One of the first things I told Kimberly in post-op was that her nearly 100 year old Grandmother was still in the waiting room.  She had been there all day.  Hulda Atwater is one of the most amazing women we know.  It was a joy to be with her in the waiting room all day.

5.  “Dad, are you missing me on my trip?”  I called to talk to Josh who was staying at my sisters house in Arkansas.  He said exactly one sentence to me . . . he wanted to know if I was missing him.  He did not even wait for an answer to his question . . . he ran off to play more with his cousins.  I was not offended . . . I was so happy he was having a good time.  Thanks Joe, Debbie, Jenna, and Emma!

4.  “I named him Obi Wan Kenobi Dog Robinson.”  My sister’s family totally wined and dined Josh all week.  They even took him to Build a Bear Workshop where he built a dog dressed like the famous Star Wars Jedi master.  He was all too proud to tell me his name.

3.  “You guys have gone viral on Facebook.”  We were totally blown away by the number of people who followed our saga on Facebook, Twitter, and this blog in the past two weeks.  On the morning of surgery a friend mentioned to me that many were talking, following, and praying.  Thank you!

2.  “Your creatinine is .8”  At Kimberly’s 10 day follow-up appointment today, her new kidney seemed to be working perfectly.  One of the key toxins they look for in your blood that determine if your kidneys are working correctly is your level of creatinine.  Today, Kimberly’s creatinine was .8, well within normal levels.  In fact two physician friends today told me that Kimberly’s creatinine is lower than theirs.  Amazing!

1.  “Cookie Cake?”  Before the transplant, Angie spent a few days with us while they were doing pre-op meetings.  One night, Kimberly, Angie, and myself were sitting around talking.  I said, “How do you thank someone for giving you their kidney?”  We all three sat there pondering this question for a few moments.  Kimberly broke the silence by declaring “With a cookie cake.”  We all got a good laugh at that.  Incidentally, we sent Angie a cookie cake yesterday afternoon.

 

There you go!  A Top 10 List.

Here are a few prayer requests tonight:

  • Though things are looking very good with Kimberly’s transplant, she still has tenderness at the surgical site.  This most likely is due to the added complications that Kimberly had with the internal bleeding following transplant.  They plan to do a CT scan on Tuesday of next week to see how things look.  Pray that they will find nothing wrong, and Kimberly will heal quickly!  Also pray that we will have wisdom to understand if her recovery process is normal, or if we need to alert the doctors that something is wrong.  In light of this, also pray that we will have peace during this healing process.
  • Continue to pray that Kimberly will not have any complications with the trach.  She has had some air that has been trapped under her skin near the trach site.  This is not a major issue, but is a bit uncomfortable.  Pray it does not continue and clears up naturally and quickly.
  • Pray that Kimberly does not catch any illness.  She is on heavy immuno-suppression medications, and is always at risk of catching something.
  • Pray that the surgical transplant team will be able to understand quickly if further surgery is necessary.  If they can determine that soon, we will be able to remove the trach.
  • Continue to pray for Angie’s kids and Joshua as they deal with mom’s who are healing.
  • Pray that Angie’s follow-up appointment goes great next Tuesday.

Tuesday Night Prayer Meeting (8/7/12)

Hello friends.  Tonight, I want to try something different.  I know that many of you are reading these updates and faithfully praying for the requests placed herein.  We are so thankful for that!  Tonight, however, I wonder (if you are comfortable) if you would comment on this post by typing out a short prayer to God regarding this situation.  I say this in order to have a virtual prayer meeting with all who are still up this evening.

In my life, I learned to pray largely through prayer meetings held in David and Hazel Kirchman’s living room, prayer meetings in the Lambda Chi house in college, and Wednesday night prayer meetings at Wildwood.  Hearing my brothers and sisters in Christ pray has taught me so much about how to communicate with our heavenly Father.  I know so many are praying on their own . . . let’s try it collectively this evening.

Some specific prayer requests:

  • Pray for continued kidney function for Kimberly and Angie with no set-backs.  Things are going well in this area now, pray that they continue.
  • Pray for both Kimberly and Angie’s digestive tracks to get back in order after major surgeries last week.
  • Pray for no infections or complications.
  • Pray that Kimberly would not experience any rejection of the new kidney.
  • Pray for Kimberly’s trach, that there would be no problems with it and that it would be able to be removed soon.
  • Pray for Kimberly’s overall health.  She is on heavy immuno-suppression medication.  Pray that she does not catch any illnesses.
  • Pray for full healing for both Kimberly and Angie from surgery.
  • Pray for Angie’s children and our Josh that they would do well during the time of their mommy’s recovery.
  • Pray for Kevin and I as we help our wives through the recovery.
  • Pray for Kimberly’s parents and my parents who are at work helping us in big ways through the recovery.
  • Pray for God to receive glory and praise through this endeavor and that we would all know Him more as a result of this season of life.

There you go!  Thanks for praying!

Dear Lord, thank you for all You are doing at this time in our lives.  We pray your continued work in protecting Kimberly and Angie during their recoveries . . . In Jesus name, Amen.

The Body is Amazing

Science does not kill my faith in God, it inspires it. I realize that the presuppositions I bring to the table because of my faith in Jesus point me to certain conclusions about the existence and nature of God, but as I hear doctors describe the human body, I can’t help but praise God for His intelligent design.

Today, we went to the doctor for our first of many post-surgical follow-ups to make sure Kimberly’s transplanted kidney is working well and her body is not rejecting it. All blood work came back great! As a friend of mine reminded me today, it has been probably 30 years since Kimberly had a blood work score that came back “good” and within “normal” ranges. The transplant seems to be working perfectly! As we got this info from the incredible team of docs serving us up at Integris, we also dialogued a bit with them about what to expect over the next few months. One of the issues Kimberly is dealing with right now is a low level of Phosphorus. This was a surprise to us because for the past eight months, we have been trying our best to limit Kimberly’s Phosphorus intake because her failing kidneys could not process it well. The doctors told us that when a person’s kidneys are not doing well, and someone’s phosphorus levels get high, the para-thyroid kicks in and works overtime, telling the body to eliminate the extra phosphorus. This is a safety valve God built into our bodies as a backup if our kidneys begin to fail. After someone has a transplant, it takes as long as 4-6 months for the para-thyroid to calm down . . . therefore, with a fully functioning kidney and a hyper active para-thyroid, your body does more than eliminate excess phosphorus, it begins to eliminate needed levels as well! Therefore, a high phosphorus diet or supplements are required during this “reset” period. That may sound like medical mumbo jumbo to some, but it reminded me of the greatness of our God and the perfection of His design. Truly we are fearfully and wonderfully made. I did not even know I had a para-thyroid, yet it serves a very important job in my long term health!

Also, today I was reminded again about the beauty of the Body of Christ and God’s intelligent design of how His people work together on this earth. Over the past few weeks, we have been blessed in so many ways by so many fellow believers . . . members of His Body. The love shown us has been a visible demonstration of the hands and feet of Christ to us. Some big thank yous go out to:

  • Friends who helped us take a fun vacation last spring before all this started, and other friends who helped Kimberly and I spend a night in OKC the week before transplant. Thank you!
  • Angie donating her kidney to save Kimberly’s life. Thank you!
  • My sister/brother-in-law/nieces and parents who have been watching Josh during the past week and through this next week allowing our house to be quiet and Josh to have fun during this surgery season. This has been a tremendous blessing. Thank you!
  • Kimberly’s mom and step-dad who have been helping care for Angie during her recovery. Thank you!
  • Kevin’s (Angie’s husband) support throughout this entire process. So generous and helpful. Thank you!
  • Kevin’s sister and brother-in-law, and their next door neighbor who helped watch Kevin and Angie’s kids while they were in OKC for surgery. Thank you!
  • Dozens of family and friends who sat with us at the hospital during surgery, checked in with us afterwards, and have offered to help in so many way. Thank you!
  • Dr. Williams and his great staff for taking care of Kimberly for so many years and referring her on to transplant in time.  Thank you!
  • Dr. Buyten who has gone the extra mile in helping us through the trach process . . . twice now.  Thank you!
  • The many, many people around the world who have been praying for us over the past two weeks. It has blown us away. Thank you!

And many, many other things we could be thankful for. Heavy loads are easily lifted by either very strong people, or many helping hands. In this case, we have had both: the strong back of our Savior lifting the load and His hands and feet (you all) adding your support. We are very blessed. His Body is truly beautiful and intelligently designed. Trials do not kill my faith in God, they inspire it.

Father/Son

A few days before Kimberly’s transplant, Kimberly, Joshua, and myself had a “family fun day.”  We went swimming, ate ice cream, played video games, mini golf, and more.  It was awesome.  Knowing we had a a few weeks of hard road ahead of us, we wanted to kick-back and enjoy a day as a family before it all began.

One of our last stops on this family fun tour was a place called Andy Alligator’s Fun Park.  If you are not from Norman and have never seen this place, it looks exactly like it sounds:  arcade, mini-golf, bowling, go karts . . . the works.  This place is one country music show away from Branson.  We spent most of our time in the arcade.  We played a bunch of games that Josh really enjoyed.  After a while playing the “kiddie games,” Josh wanted to go for broke and hunt deer on one of the “big boy games.”  Thankfully, there were two guns that came with this game, so we each grabbed one to play together.  When I looked at the cost of the game, however, I saw that it was $1 per game.  Knowing that Josh would not be able to hit the targets, I paid for only one game . . . mine.  I did not tell Josh, though.  When the game started, we both fired our fake weapons at the screen.  Josh (of course) took credit for each big elk shot.  Because I love him, I never told him otherwise.  Someday, when he gets older, he will understand more of what was going on.  For now, I loved watching him enjoy his part in the game.

I mention this story tonight because I am having somewhat of a hard day.  We have certainly had a hard week, and that has contributed to my feelings tonight, but my anxiousness tonight goes somewhat deeper.  Like many “type a” people, I revel in getting things done.  I excel in giving my time and energy to accomplishing something.  In many of the key areas of my life, however, I currently feel totally out of control . . . and that is bothersome to me.

On a macro level, Kimberly’s transplant is going great.  The new kidney seems to be working great, every day we see small progress, and we have just spent our first 24 hours out of the hospital.  However, as I have transitioned into the “nurse” role at the Robinson house, I have found myself unable to be able to do what I most want done . . . help my wife feel better.  No matter what I do, I can’t help her sleep, cough, breath, or feel better.  The combo of the trach (which makes her cough) and the incisions (which hurt when she coughs) makes parts of her day miserable . . . and I can do nothing to change that.  Her stomach is rumbly but no food I bring to the table can make her stomach accept it well.  These are normal issues following the kinds of surgeries Kimberly had last week, but it is hard to see those situations play out and not be able to do anything about it.

Also, I am the kind of person who always carries the responsibility I feel given to me, so I have struggled with being gone from my post at the church during the “fall kickoff” that is August.  Especially in a season where we have a lot of things we are trying to launch for this fall, and our staff team has been scattered for most of the summer.  I feel the inner (not external, but internal) pressure to reengage at the church to push things forward.  (Don’t worry . . . I am taking time off, but I still feel the tension.)

As I was getting dinner ready tonight, I found myself tensing up over these feelings of being out of control.  That’s when God reminded me of my time with Josh at Andy Alligator’s two weeks ago.  It was as if God was whispering in my ear, reminding me that in all the areas of my life, he is the One who is always pulling the trigger.  Though I spend much of my time with my “weapon” in hand firing at the screen, ultimately, it is always only God who is hitting the target.  He allows me to stand beside Him and play because He loves the Father/son time it brings . . . however, He does not need me to accomplish His work at home or at church.  I feel as though in this season God has taken the gun out of my hand and asked me to watch Him work . . . in my wife and at church.  These are tough lessons to learn, but important ones nonetheless.  It is a humbling but important reminder . . . a push to trust in Him.  Someday soon, I will be asked to pick the gun back up.  When I do, I need to remember that it is my Father who bought the game, and it is my Father who takes aim and does the work in every area that really matters.  He wants us in the game, but without His work, we can accomplish nothing.  Sometimes, we have to have the gun taken out of hands to remind us of that.  It is a tough, but beautiful reminder.

I don’t know if any of you can relate to this.  The experiences you are going through are probably different . . . but the principle still holds true.  We are all less important than we think . . . but we all get to stand beside our Father who equips us and invites us to watch Him work around us and through us to accomplish His will.

Saturday, 6 PM – Home Again (8/4/12)

The medicines and equipment they sent us home with today . . . yikes.

As Jon Bon Jovi says, “Who says you can’t go home?”  The good people at Integris Hospital certainly did not say that today, therefore, we are home sweet home (another 80’s rock anthem for those of you keeping track at home).  Great to be back home tonight.  Kimberly is totally wiped out, but is resting on the couch.  I am trying to organize our new life.  The picture attached to this post shows only the medicines, equipment, etc. that we came home from the hospital with today.  Kimberly has more meds, etc. that she was taking before.  Needless to say, it is a bit overwhelming.  You can pray for us as we transition back home.

One other thing you can pray for concerning Kimberly has to do with her digestive track.  As with many who undergo abdominal surgeries, she is having a little harder time getting back on track.  Please pray that everything starts working normally there.

Angie made it to Darrell and Kaye’s house today without major problems.  Thanks for praying for her!  The text I saw said that her pain was less today.  Praising God for that!

I’ll share some more thoughts later, but wanted to update you on the trip home for those of you who were praying today.  Thanks for lifting us up!  We are truly “livin’ on a prayer” and hope we don’t get any “bad medicine” . . . ok, I’ll stop.  (For those of you who didn’t listen to the hot new Z104.5 in high school in the 80’s, this post probably was a bit confusing.)

Saturday, 11:30 Update (8/4/12)

Hey everyone.  Hope your weekend is going well.  I wanted to drop you an update and specifically ask for prayer for Angie today.  She is headed to her parents house for a few days to recover more.  This will require a bit of a drive, so please pray that Angie does well in the car ride, does not have too much pain, and continues to recover on schedule.

Kimberly is still in the hospital, but should be released a little later today.

I’ll update more as things develop.  Thanks for lifting up Kimberly and Angie in prayer!  Also please pray that Kimberly and Angie’s new nursing staffs (me for Kimberly and Darrell and Kaye for Angie) are up to the task 🙂