Courtney Update - Thursday, February 13, 2014

All things considered, Courtney had a very good day today.  She was holding her eyes open for several seconds at a time and she is much more consistently responding to all our voices, but especially to Kelsey.

We have to make sure that Kelsey is on Courtney's left side of the bed when talking to her because once today Courtney tried to turn her head toward Kelsey when she was on the other side.  While connected to the ECMO machine, Courtney has two tubes that look like clear garden hoses with flowing red blood that go through her neck (right jugular) and connect to the machine.  Sudden movements to that side are not necessarily a good thing.

This morning the doctors performed a TEE test (Trans Esophageal Echocardiogram) - which is basically an ultrasound through her throat to provide a closer look at the heart's valves and chambers without interference from the ribs or lungs.  They discovered that her valve is obstructed, which at some point, will require intervention, but they now hope it can wait while she continues to recover from this NASTY sepsis.  The left side of her heart has regained its function, but the right side has not recovered as fast.

Her health has improved enough that the plan (as of Thursday night) is to clamp off her ECMO tubes on Friday morning somewhere around 7:30 for about an hour or so and see how she does.  If it goes well, they will try to take her off the ECMO machine sometime on Friday.  She will remain on the ventilator, the dialysis machine, multiple IV pumps, and occasionally the Apheresis machine (plasma pheresis and exchange).

Overall, it was a very encouraging day....more steps forward than backwards.

Thank you again for your continued prayer support.

Courtney Update - Wednesday, February 12, 2014

The last 24 hours have been a mixed bag of reactions, emotions, and opinions on Courtney's health status.

Last night (Tuesday) at midnight, Courtney had reached a stage that Jennifer called the worst she had seen her have since being admitted to the PICU on Saturday night.  However, by 6:00 AM this morning, she was looking the best that Jennifer had seen her during this stay in the PICU.  She continued to look pretty good (relatively speaking) throughout the day.

She remains connected to several machines (ECMO, dialysis, ventilator, apheresis) and mulitple IV pumps and monitors.  However, on a positive note, for a couple of times today she was able to tolerate some weaning off complete dependency of the ECMO machine.  She was doing 50% of the work and the machine was doing 50% of the work.

Even with aggressive treatment, she continues to test positive for the staph infection.  The infection has definitely affected her heart valve and its ability to work properly.  A more invasive test of the heart valve will be performed some time on Thursday.  The test will better evaluate her heart valve status and allow the doctors to begin formulating a plan.

One other positive note:  This afternoon on multiple occasions, Courtney intentionally and successfully tried to open her eyes on Kelsey's command.  If you know their relationship, it is no surprise since Kelsey has always been able to get Courtney to do things that other people could not.  :-)  To a lesser extent, she also opened her eyes for me, albeit was after they were moving her over and aroused her some.  She opened them up a couple of times after that when I talked to her.

When the doctors were asked today "assuming the best possible outcome, how long should we expect to be in the PICU?", the answer was a consistent "weeks".  Obviously, there is no answer to to how long it will be for all other possible outcomes.

We continue to request your prayer support.  I have always believed in the power of prayer and I would love to have all 50 states represented when praying for her.  If you have friends and family in other states, please feel free to outstretch our prayer chain to other states.

God bless you for your support and thank you to everyone who has left comments here, texted your support, or left us messages on Facebook.

Courtney Update - Tuesday, February 11, 2014

Around 2:00 AM this morning, Courtney's body started tolerating some fluid removal from her body.  They have added a new machine to Courtney's regimen that will be used a couple of hours per day for the next few days.  This machine piggybacks off the dialysis and ECMO machines and is used for Plasma Pheresis and Plasma Exchange.  You may not know what these terms mean, so in simple language, the machine removes the plasma from Courtney's blood after going through the other machines and replaces her plasma with "new" plasma from donors.

By late morning, her skin coloration was much better, the swelling was going down, and she was making small improvements elsewhere as well.  Unfortunately, as the day progressed, her color worsened in some areas and her skin has started to blister.  Her right lung now has much more fluid, which was to be expected.

The infection in her blood has been identified as Staph MSSA and they will now find the best fit for an antibiotic to fight this bug.  We also learned that the likelihood of this infection attaching to her heart valve has gone from possible to probable.

We have had family and friends with us throughout this process.  We also have prayer warriors represented across at least 7 states and have numerous friends asking what they can do for us.

One person has suggested, if you are able or interested, is to donate blood, plasma, or platelets at an American Red Cross Center and ask that the donation be credited to Courtney's account.  The ECMO process uses lots of blood products, as well as the plasma pheresis and exchange use lots of plasma.  It is not a direct donation, meaning the blood that you donate now will not be available for awhile, so it would not be used by Courtney.  However, it is my understanding that any blood products that are credited to Courtney's account will create a credit for her and not be charged when she uses blood products.

We continue to need your prayer support and can definitely feel the effects and it is very much appreciated.

May God bless you all.

Courtney admitted to Vanderbilt Childrens Hospital PCCU

Monday, February 10, 2014

If you are reading this page, you know that Courtney is in the hospital and you are coming here for updates.  Here is a synopsis of how we got to where we are right now:

When Courtney went to bed on Thursday night, she was complaining about not being able to get comfortable and was shivering.  I put extra blankets on her thinking it was a little colder in her room than it had been, but also told Jennifer she might be coming down with something.

 

She awoke Friday morning a little lethargic and had a small fever in the morning, so she did not go to school and went back to bed.  When Jennifer woke her up later in the morning, her fever had risen and became a very big fever in the afternoon.  Jennifer spoke with doctors at Vandy and had begun giving her Tylenol and Motrin to reduce the fever.  By late Friday afternoon her temperature was back to normal with no other symptoms. 

 

She awoke Saturday morning with a rash and a fever going in the opposite direction, down to 95. We were in contact with doctors at Vandy and by Saturday afternoon Courtney walked herself [holding onto me and walking very slowly] into the ER. Within hours she was going downhill fast. They moved her to the trauma side of the ER and then admitted her into the PCCU about 11:00 PM Saturday night.  They decided to put her on a ventilator at midnight to help sedate her easier and keep her from working so hard.

 

By Sunday morning it was apparent she was essentially in kidney failure and her heart was not 'squeezing' properly [along with other issues].  Her rapidly declining health required her to go onto an ECMO machine which is acting as her temperature control, heart and lungs. They have also connected a dialysis machine to the ECMO to act as her kidneys. They have determined she has a very serious bacterial blood infection but have been unable to determine the origin in order to treat the source.

 

As of late this Monday evening, the ECMO machine is properly filtering her system but Courtney's body will not yet tolerate the removal of all the excess fluid that is accumulating and causing her body to swell all over. However, her skin color is much improved. She is still hour by hour but we are very hopeful.

 

Thank you very much to everyone who has called, texted, posted or commented on Facebook, come by to visit, and most importantly lift up Courtney up in your prayers.  We appreciate all that you have done and have offered to do.  We will be here for several days, possibly weeks, and if things go well, will probably be in for a long recovery.

 

Your continued prayer support is very much appreciated and already felt.  I am comforted by the words in John 14:13 - "Whatever you ask in My name, that will I do, so that the Father may be glorified in the Son".  It may be selfish, but I am asking for God's complete healing for Courtney so that she may continue the good work that Christ has started in her.  Phillipians 1:6

 

March 2013 Update

March was another very busy month for our family.

One small benefit of not working is that I was able to participate in a Titans Fan Forum for season ticket holders at LP Field earlier this year.  The Titans listened to the suggestions and have implemented several ideas to give back and make things better for their loyal season ticket holders.  One of those ideas was to offer a tour of the stadium and provide lunch in the Club area.  Jennifer went with me and we had a great time.  We toured the player/coaches interview room, the Titans locker room, walked out the tunnel onto the field, saw ourselves on the jumbotron, toured the radio and TV booths, the press area, and met with Don MacLachlin (Titans EVP), Ruston Webster (Titans GM), and Mike Keith (Titans announcer & "Voice of the Titans").  We were allowed to take pictures and try on jerseys in the locker room.  Here are some of the pictures:

Courtney's Spring Break was also during March.  She went bowling with me, spent some time at Glen & Peggy's house, and attended her first Day Camp at Camp Widgiwagan.  The camp was hosted by Young Life Capernaum and was for kids with special needs.  Courtney had a blast singing, dancing, creating crafts, meeting new friends, canoeing, & participating in a Talent Show on their last day.  Here are some pictures.

This year Easter was also in March, so we spent the weekend in McMinnville and had a great time with family and friends.  The weather was nice and we were able to play games with the kids outside on Saturday and then we had breakfast at church before the early service and Kelsey sang "O the Blood" by Kari Jobe.  If I do say so myself, she did an excellent job.  :-)  Here are some pictures from the weekend.

Well, that wrapped up our month of March.  I was still working very hard to find a job, but glad to be able to spend valuable family time during this time of year.

Our weekend in Jackson

Our trip to Jackson a couple of weeks ago was filled with excitement and lots of activities.  Glen drove in from McMinnville early Saturday morning and rode with us to Jackson.  We drove straight to a skating rink in Jackson for Tori's birthday party.  They had rented it for two hours so that there were no other parties going on at the same time.  I'm not sure if that was for the benefit of the little kids or for the adults who ventured to see if they could remember how to skate.  :-)  There were a few falls here and there with a few bruises, but for the most part, everyone came out okay.  The important thing was that Tori and her friends had a great time.  Courtney had not skated in a long time, particularly since her back surgery, so she used a trainer device and Kelsey walked with her.  Kelsey could not skate due to her still recovering from her shoulder surgery.

We left the birthday party and went to McAllister's Deli for lunch, then back to Christy and Phillip's for the afternoon.  We went to Trace's basketball game later in the day and then Jennifer and I went to the church celebration dinner at their church.  The theme was based on the Emmy Awards with a lot of Hollywood decorations, the red carpet for award winners to walk down, and movie trivia contest.  Christy played the role of a host, Phillip was in charge of the music, video/picture presentation for award winners, and the movie trivia contest, and Kelsey sang "I Can't Help Falling in Love with You" with Landis playing an acoustic guitar.  The night was a big success and everyone had a great time.  Jenn and I stayed after the dinner and helped clean up and put away chairs, tables, decorations, etc.  Glen and Peggy kept the kids at home so that we could all enjoy the dinner.




Glen and Peggy headed back early Sunday morning and stopped by our house to get Glen's truck.

We headed back home a little later Sunday morning and we all had a safe trip.  Courtney and I went to the awards ceremony for our bowling league and she won an award for the girl with the highest handicap game (245) - (She bowled a 125 with a handicap of 120).

It was a great weekend and everyone had a good time.

Update on Glen and the Queen family - Friday, February 22, 2013

I haven't updated the blog in awhile and since Glen got his PET scan results this week, people are wanting updates.  :-)  So here goes.

Glen had his PET scan last week and went back to the doctor on Tuesday for the results.  The doctor said that the scan was clean and the blood work looked good, which means that he is still cancer free.  PRAISE THE LORD!!!!!!!  He will continue to have checkups every 3 months or so for 2 years, but for now they are not recommending any maintenance doses of chemo or medication.

Kelsey finished up her J term and got Chemistry under her belt.  She celebrated with a trip to New Orleans with a classmate who lives in Slidell and went home for a weekend between semesters.  She has now started the Spring Semester at Union and is taking 17 hours, which means she should be able to start her Nursing classes in the Fall on time.  She is out of the sling from her shoulder surgery and is now toughing it out through her Physical Therapy/Rehab sessions.  She is able to drive now and is back living with Phillip & Christy.

Courtney participated in the Nashville Special Olympics basketball event at Belmont on Tuesday playing with her McGavock High School classmates.  They had 2 teams from McGavock.  The team Courtney was on consisted of her and 5 boys.  LOL  She did not start the 1st game, but came off the bench and scored 10 of their 16 points, however they lost 20 - 16.  The 2nd game she didn't score, but had a blast and they lost 24 - 20.  They had a Fun Day at Ensworth High School on Thursday, so with them being out on Monday for President's Day, she only had 2 days in the classroom this week.  :-)

Courtney and I finished up our Family Fun bowling league last Sunday and the awards will be handed out this week.  She got the girl bowler of the week (most points over average) several times this year and raised her average up to around 90.  We had a great time and she is already asking when we can bowl in a league again.

Peggy came to Nashville on Wednesday for a doctor's appointment and her and Jenn spent some time together before she drove on to Jackson.  She was going to help Christy get ready for a church event they are hosting this weekend.  Glen is driving to Nashville in the morning and then we are all heading to Jackson for a birthday party for Tori and then Jenn and I are going to the dinner hosted at their church tomorrow night.  We will all be heading back on Sunday.

I have been getting a little more activity in the job search, but still no offers.  I appreciate your continued prayer support.  I am clinging to the words of Jeremiah 29:11 where Jesus says "For I know the plans I have for you, plans to prosper you and not harm you, plans to give you hope and a future".  I know He has the plan and I have to be patient and look to Him for guidance to see it when it is ready.

Thank you again for your prayers.