Tuesday, January 25, 2011

Back from Cincinnati

I know there are a lot of you wondering how things went last week in Cincinnati so I thought I would post here, in one spot, so that everyone can keep up to speed.  We drove down on Wednesday for a Thursday afternoon appointment.  In order to save Paul’s time off from work, he worked the morning so we didn’t leave until around 12:30.  I didn’t tell Keyan about going until that morning because she doesn’t usually like to be away from the family but she was SUPER excited to see Hans the dog and to have a sleepover at Aunt Bonnie and Uncle Alan’s house.  She could not wait to get out of here!  Anyhow, the trip was non-eventful and we arrived in time for a little play time and then she was off to bed. 

Thursday morning brought a snow storm to Cincinnati…not necessarily a snow storm by Michigan standards, but everyone was on edge on Ohio!  It ended up being a little slippery by the late afternoon but as long as we went slow, everything was fine.  Paul and I had spent hours hashing out what may happen at this appointment and making sure that the two of us were on the same page as to how we wanted things to progress.  Those conversations were not easy ones..rather heart wrenching actually, but I am glad that we could present ourselves as a united front.  So, the appointment did not bring any earth shattering news, but it was a very important appointment that helped everyone get onto the same page.
In a nutshell, she has continued to loose weight which now needs to stop.  She NEEDED to loose the first 10 pounds but we don’t want her to loose any more so the doctors will tweak her TPN and hope to keep her weight stable.  The other topic of discussion was a plan to get her off of the TPN.  TPN is the IV nutrition and unfortunately it is not a long term solution as it does damage to the liver and kidneys and is a breeding ground for infections.  However, the past three months were the first time in Keyan’s entire life that we did not work on advancing her intestinal feeds…and by far these past few months have been the best quality of life she has ever had.  The proof is in the data!  We have always said the Keyan’s body is happiest when she is not being fed, but we have never done a long term test of that and the last three months showed us quite a bit.  She did have a lung infection when we increased from 7 to 8 mls an hour which could be circumstantial…although I tend not to lean that way.  So, we talked at great length about what all this means and came up with a VERY SLOW plan to increase her feeds…and I mean REALLY slow.  I won’t go into the details because it is a lot of medical jargon, but they have worked out some ideas to deal with her intolerance, depending on the symptoms, and we will go from there.  The overall message from the docs was that while we would all love to get her off of TPN next week,  her very complicated body is not going to allow that.  She is in control of what happens and her body will direct our path. Furthermore the doctors stated the while TPN is by no means an ideal therapy, in some kids, it is all they have.  You deal with what you have!  We still have no root cause for this intestinal failure so to push forward with the same things we have been doing in the past would be negligent.  None of us are willing to sacrifice the quality of life that she has right now, so that means that the plan is a work in progress.  It is one that Paul and I are pleased with, and one that does in fact keep Keyan’s wellbeing in mind.

As we were leaving the hospital hours later, our minds were trying to keep everything straight and our hearts were trying to absorb the impact of the decisions that had been made when we came across a sign.  It read..
“Cincinnati Children’s Medical Center has been ranked by U.S. News and World Report #1 in the nation for their Gastrointestinal department”
I really felt like God was talking to me at that moment.  You see, the further we get down this road of unknown issues, the more I begin to question if we are doing all that we can for our daughter.  We said Cincinnati would be it…we would not drag her from doctor to doctor, or half way around the globe to continue to search for answers.  This is it for us right now and we feel very strongly about it.  However, that does not mean that in the stillness of the night, doubts don’t come knocking at our hearts.  “Have we done the very best for Keyan?  Is there someone else who could help her?  What about a more alternative approach?  Are we missing something?  Are we giving up?”…I could go on and on.  When I read that sign aloud to Paul, I had a peace wash over me that I will cling to from here on out.  “This is it…there is no one better…we are doing everything that we can, and we are doing it to the best of our abilities.”  I know that some would argue with our decision, and that is alright.  It still comes back to the fact that we have been commissioned to carry this very heavy burden and we will be the ones held accountable for her life.  It is up to us, and after our time in Cincinnati this past week, I can lay my head on my pillow at night knowing that all is well.

Sunday, January 9, 2011

Ice Sculptures

For the last few years, Holland has hosted an ice sculpting competition on the main drag of our downtown.  Some of the kids and I went two years ago, but this year we decided to all venture out and see the very fascinating works of art.  Keyan doesn’t typically spend much time out in the cold weather but the sun was shining and the wind was virtually nonexistent so we bundled her up and away we went.  The sculptures were really amazing to see and the kids had a blast trying to figure out what they all were.  For some reason, Keyan thought that the sculpted fish were hilarious and we all enjoyed watching her face light up every time she spotted another fish.  While warming up at home over some hot chocolate, we asked the kids what they would sculpt is they were in the competition.  Jamahl said he would chisel out a Star Wars scene (no surprise to anyone!) McKenzy would cut out a Mickey Mouse, Abby would create the Mickey symbol from the Disney Channel, Keyan would sculpt an Elmo, and Sidney said she would need Jamahl’s help to do a dragon.  How fun to see their imaginations at work!

Sunday, January 2, 2011

Lego project

The girls received “girl” legos from Santa and Jamahl has been more than happy to show them the ropes of lego building.  In case you don’t know, Jamahl has a lego collection that takes up most of the basement and constantly builds and rebuilds, sets them up, plays with them, ect.  He LOVES legos and for Christmas basically only got legos.  So, once we opened the girl ones, he has been showing them how to build for two days.  Today’s project…

IMG_7140

Can I just say that there is NO WAY that I could figure out how to do this?  He has his father’s engineer brain for sure!  What a cool kid!

Tuesday, December 28, 2010

Ice Skating!

I hope that you all had as good of a Christmas as we did and hopefully I will find some time to post some pictures, but Paul is off this week, and we are trying to make some fun family memories.  So, today we headed to the ice arena.  I probably do not need to state the obvious, but I sat on the side lines due to my foot injury but the ret of the family had a blast.  McKenzy and Keyan took right to it and were UNSTOPPABLE.  The only thing that got Keyan to finally take a break is when her trach came out!  Abagayle followed close behind them and once Sidney relaxed a little, she was making it around the ice as well.  Jamahl was very apprehensive as the last time he went ice skating he ended up with stitches….and if you know Jamahl at all, he is a worrier.  However, he did really well and even had some fun too.  I know I probably say this all of the time, but as I was watching my kids faces as they skated beside my parents and Paul, I got a little teary at the fact that my kids have such special grandparents.  We are all so lucky to have each other and are blessed to be able to make fun memories together.  After a warming drink of hot chocolate, they were all asking when we could go again…now that is good family fun!

Monday, December 20, 2010

A Magical Visit

We had a very special guest visit our house this evening!  We had talked about someone special coming, but when Santa arrived, the kids were all stunned!  We took him down near the Christmas tree and each of the kids took turns talking to Santa.  Keyan asked for a teddy bear, McKenzy asked for a surprise, Abagayle told him she wanted jewelry, Sidney asked for a Barbie, and Jamahl asked for Legos…which Santa said was one of his favorite things too!  Santa showed them Rudolph’s jingle bell harness, and his magical keys that help him get into homes that don’t have chimneys.  He told us that Mrs. Claus really likes to pick out special things for each of them and helps him make sure every child has a special Christmas.
Jamahl had LOTS of questions about his toy sack, getting past our nurses, how the reindeer fly, and if he knew our elf on the shelf, Magic Mike.  Santa knew just how to answer his questions and you could see Jamahl’s eyes growing bigger and bigger.
Obviously, we are all feeling so much joy to have Keyan home with us this Christmas season.  Your life is forever changed when you go through a holiday season with a child in the hospital.  The reality for us is that the overall picture of her health has not changed.  The intestinal failure is still present, she is still TPN dependant, and we live constantly walking on egg shells waiting for her to have a medical crisis.  However, her day-to-day life is SOOO improved and we now know that that is really all that matters.  With the help of Cincinnati, Hospice, and several of our doctors here in Grand Rapids, we have given her the quality of life that Paul and I so desperately longed for.  This is what life is all about.  When faced with the mortality of someone you hold so precious, the value of every joyful minute engraves memories on your soul.  The visit from Santa was just that….a magical moment to etch into our hearts and minds.  One that will carry us thru the tough times of the year to come.  A memory to share with each other for years to come and reminisce about the awe that it inspired.  Tonight, our hearts are full, our minds are reeling with questions, and we are so blessed to be together.  I just want to sit very still and savor the fullness of my heart!

Friday, December 17, 2010

Jamahl's letter to Santa

Brace yourself to experience the big heart of this special nine year old!

Dear Santa,
Hi!  This Christmas I want the lego Star Wars "Death Star" and the lego "Slav I".  The last gift I want is to have my sister not be in the hospital this Christmas.

Love,
Jamahl Hogan

(My Dad says that just for that he should get everything on his list....never mind that the "Death Star is $400!!!  Nice thought Dad!!)



Sunday, December 5, 2010

Birthdays 2010

Birthday week always seems like a blur around this house.  Between eating cake for an entire week, making all the school treats and swimming treats, and squeezing Thanksgiving in between the two special days, when it is all said and done, it is a whirlwind filled with good time and memories. 
The girls were thrilled to be turning six although I had done my best to convince them to stay five, they would have none of it!  They all agreed on spaghetti for dinner and got dolls and doll accessories for gifts.  Later in the week, we took a friend of theirs to all go and see "Tangled" as an extended celebration. 
Jamahl turned nine six days later.  He and Paul took a friend of his to see a movie that afternoon and he had requested spaghetti pie for dinner.  His gifts revolved around swimming and Star Wars...big surprise huh?  The boy LOVES to swim and is an expert at Star Wars!
I have a hard time believing that we now have children who are six and nine years old!  Things are changing at our house and change is hard for this mommy.  The kids are becoming more independent, more vocal about their concerns and wishes, and more thoughtful and introspective.  While I have a hard time, it is fun to watch them become little people.  They have dreams, desires, feelings, and fears.  While not always fun to deal with, it means they are thinking and paying attention to the world around them.  While the statement, "bigger kids equals bigger problems" is definitely true, I don't want to miss the steps of the journey that get us all through those times.  I know we are only on the cusp of school dilemmas, friend problems, boyfriends and girlfriends, realizing that the world isn't a fair and just place, and just plain growing up, but all of that stuff encompasses this thing we call life.  We were all so grateful to have Keyan home this year for the birthdays...last year she was in the hospital.  Those tough times are molding and shaping our family for life.  As the kids get older, I realize more and more than it is not about the end result, but rather the process of getting there!  Enjoy the pictures!