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  • Yesterday we learned a great deal more about Mommy’s left arm.

     

    Finally…the stitches are out on Hillary’s left elbow and though Steri-Strips had to be placed on the incision, they won’t last more than about a week.  Her “torture device” was adjusted and we learned Hillary’s prognosis on the arm had been quite guarded.  If Dr. Tressler told me the details of his concern that evening after her surgery I did not really hear him.  We now know Hillary’s ulnar nerve had been completely encapsulated in the new (and unwanted) bone growth.  The ulnar nerve is important for movement in the upper arm which not only engages the upper arm to move, but offers control to keep the arm from gravity drop with her lack of muscle use.  This brilliant doctor “removed” the nerve and repositioned it in another location in hopes it could reroute and reengage her arm for movement and control.  It wasn’t until Hillary demonstrated new movement in other parts of her arm and hand as well as information shared about conversations with Occupational Therapist, Catherine, that Dr. Tressler felt we could expect great recovery of the arm. Perhaps full recovery….but of course, he continues to be a bit guarded.  As Sammie said today, “We will make it happen and now we have even more reason to ‘show our stuff’”.  In any case, Hillary’s willingness to work the schedule planned for her uncomfortable “torture” device is going to be a challenge.  We recognize it is painful but of course none of us can determine just how painful…except Hillary.   (And she is ready to inform you of that at any moment!)  How can anyone argue with her, and particularly in light of the happiness we feel every time she shows increased cognitive development…which she does every day around most any subject.  But the painful challenges she deals with and how every painful step in her journey is hers and not ours, brings on extremely enlightened and cognitive discussions.  She wants us to be the extremely enlightened ones, if you catch my drift.  .

     

    Paul and I talked last evening about how careful we were when our children were young to avoid the annoying parental habit of bragging on our kids.  And, to a fault, I was guilty of not supporting our children when controversy would arise that might place child against authoritarian such as a teacher.  I still believed in the principles my parents taught me that the world is made up of authorities and each and every one of them had to receive our respect, even if we didn’t always feel they were right.  Their motto was much like John Mellencamp’s :  “…Authority always wins.”   So I would usually take the side of authority and rarely “believe” my children’s side trying perhaps to hard not be one of “those parents” (Quotation marks clearly demonstrated by two fingers from each hand as I say, “those parents”  of course)

     

    Last night we realized I have thrown all the old behavior out and completely and shamelessly have become a bragging Mom.  My kids would say I have become a bragging “Paducah Mom” (A name I now cherish instead of bristle upon hearing that I deserve the name.  But that’s a whole bunch of other stories and a lifetime ago.  Just know Alex Coltharp, I consider that title a fine honor and don’t your forget it!)  But I digress:  It’s true….we have become shamelessly bragging parents and we just can’t help ourselves. When so many of our friends were able to share the joyous news of their children’s scholastic achievements or brilliant accomplishments, we used to laugh at ourselves and say there needs to be a bumper sticker for parents like us that says, “My __(insert school)__ student is fun at parties.”  And oh to be sure the Coltharp kids were!   But after yesterday’s trip to the Trauma Clinic and watching Hillary speak to the women who were around us in the waiting area….watching how deeply she holds the heart of her doctor’s and other’s on that medical team…. I realized it’s impossible not to brag on her.   She’s special in every way. And if she never improves beyond this level, she has gifts to offer beyond anything (or anyone) we have ever met.  She held every single patient and caregiver in that clinic in the palm of her hand.  They couldn’t stay away, even when their individual work for her was completed.  I tell her every day how proud I am to be her Mom and I mean it in every way.  And as Dr. John said to her, “Hillary, you are a better parent in all of this than some on their best days.” 

     

    And the same goes for the rest of our crazy fun kids.  We are so proud to be their parents.  In trying to determine Hillary’s Rancho Level (Coma Stage) today, I remember long ago setting on a bed in Hillary’s hospital room in Vanderbilt reading out the descriptions of each level.  As I read aloud, Paul and I were surrounded by our children who hung on every word -- supporting their sister (and us) all the way.  Looking back on that time, Ashley was often at Hillarys side--swamped with trying to coordinate an army of her “Nashville Girls” who were feeding us and offering respite as we lived through each difficult day. All the while our first born kept a perfect house, excelled in her busy career and dealt with her first pregnancy.   And Alex was driving in from school every possible weekend to help in his own way leaving fun college weekend life behind—offering to help in transportation with her son if a visit was possible, as well as spending the night with his sister.  And Brittany was there to help us in her own way as well, and through the challenges of a six day a week new career.  And it hasn’t stopped.  This weekend our children have decided they are taking over and giving us a chance to be alone and “off duty”… and they aren’t taking “No” for an answer.  They are very special kids and without a doubt, still very fun at parties!

     

    And by the way, that day so many months ago, as I  sat on the bed reading out the Rancho Level descriptions to my family…(hoping above all hope she was embarking on a Level II or a Level III)…I can remember thinking,  “Oh if only she could someday get to a Level VIII.”.  And then I remember also saying to myself, “Uh oh….I’m pretty sure I’m a Level X!”.  But with joyful news we are beginning to see that day very near.  Hillary is definitely showing firm signs of Level VII and we all see such swift progress we feel Level VIII is just around the corner with perhaps some signs already emerging.  ZOOM ZOOM!

     

    And whatever her Rancho Level, we could never be more proud of anyone.  As we left Dr. Tressler’s office yesterday, we left among “Good bye Honey” and “Thanks for talking to me” and so many well wishes I can’t begin to describe them all. We are very proud!

     

    Thanks for loving our girl!

     

    XOXOX

    --Shawn

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  • Mommy amazes us.

    As Hillary entered the therapy room to begin working with Jerome, her physical therapist, he was warned, “She is going to amaze you!”  Clearly, Jerome didn’t believe it was going to be an amazing day because he said,  “Amaze me?  OK, I would LOVE to be amazed!”  And then he was.  And her therapist never stopped saying, “You’re right…you amazed me.”  Hillary walked beautifully for him and Jerome stated her steps were truly excellently gated and proportional. 

    And that great session followed time with her speech therapist, Rene, who said, “Hillary was able to accomplish things she never could have just a few days ago,” She could list ten items well within a minute on all questions.  She followed three step instructions and continued to do so through her full session.  Rene said, “She was 100 percent on and 100 percent correct in all answers and follow through.” 

    ZOOM ZOOM!

    We've been counting down the day's until Hillary can get her stitches out of her elbow.  The pain from their tight pull on her skin is obstructing her progressive rehab efforts to bend and stretch the arm.  Good news/bad news Hillary's "torture device" will be adjusted for her while she is with her doctor in Nashville tomorrow.  With that behind us, we will begin counting down another couple of upcoming events. Max will return home for another visit on this Friday evening. And then May 1st is marked on our calendar for a couple of additional important opportunities:.1)  Hillary returns to Dr. Konrad on that day to confirm her body has not rejected the bone section he replaced now three weeks ago....though all looks well.  2) May 1st is my mother's birthday and Hillary is working to bring her beautiful voice back so she can sing "Happy Birthday to Maw." 

    Thank you for your visits to this site and your patience with all of us.  We are pushing Hillary very hard right now and it keeps us from being timely with updates.  We are so grateful for your continued push as well.  You continue to help in her race back to her life. It's what she want's more than anything.

     

    XOXOX

    --Shawn

     

  • Monday, March 31, 2008

    HEADING TO SURGERY

     

    Just a quick update for now.

     

    Hillary is heading to the hospital this morning at Vanderbilt to have her surgery. Please say a prayer for Hillary this morning as she prepares for this next step on her road to recovery. Pray also for the staff and doctors at Vanderbilt Medical Center. The surgery is expected to start around 11:00 am and should last for less than 2 hours.

     

    Thankfully her son is in Nashville with all of us and he and his mother are providing great support to each other! We will post a full update after her surgery.

     

    Thank You for keeping Hillary in your thoughts and prayers on such an important day for her.

     

    The Coltharps

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  • Friday, October 5, 2007

    Yesterday was quite a day for Hillary.  She had some very special visitors including “Tweedle” and her son Henry who couldn’t decide whether Hillary was on a bed or a truck.  (Henry wants you to view his pictures (r))  As the day and evening progressed it became obvious Hillary is moving into Level IV a bit more.  

     

    We have decided it is time to share our beautiful girl with you so you can see how much you have helped her progress through your love, prayers, visits and support.  How will we ever be able to explain what you have done for all of us and how much you mean to us?  There are no words.  And none for how happy these two roommates are that Dad is here. 

     

    Thank you for loving our family and sharing in this journey.  We feel you with us in every step.

     

    XOXOXO

    --Shawn

     

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  • Saturday, September 29, 2007

    I can’t keep up.  Things continue to improve so much we are beginning to take some things for granted.  I am never sure what we have already shared as a part of her progress, and what we have not.  Right now, Hillary is probably anticipating a visit from a very important woman in her life and ours—Donna Thomas.  We first met Donna through Hillary a little less than a year ago.  While the introduction was through a gift of massage therapy for my excruciating back pain, the relationship immediately became much more.  My back pain did subside.  Paul’s thirty year college football “parting gifts” of aches and pain as well.  But we have received far more than physical relief from our relationship with Donna.  She has prayed with us, over us and in spite of us, and we have been blessed by our relationship with her in so many ways.  

     

    Today, Donna and Hillary are going to be together and we know good things are going to happen in that room.  She will also be meeting some of our other children and will give Vance’s mommy, Ashley, an “Anointed Touch” pregnancy massage that is long over due.  Please remember Donna and Hillary as they try to cross Hillary over the threshold and back to us this afternoon.  We know God is going to be with them but they need you as well.

     

    And one more thing…..my mantra…always “One more thing”:

    I realize how intensely personal these writings have been.  I want to say “…it just happened”. But those of you who know me, (and still love me even though you do), know that is just me.  Our lives have always been “out there” on the streets, wide open for all to see.  That has not been easy for my husband Paul over the years who is an intensely personal and private man.  He should have been writing these updates all along because he is MUCH more open behind written words than he is in face to face situations.  One thing is certain; through this experience, Paul has learned to let people who care about his big ole’ crazy family reach out to him… and him to them.

     

    These writings—this experience—has not been easy for some people very close to what we are living right now.  To the Gholson/Wicks/Davis family...to the Gwinn/McKnight/Fowler/Black family…to the Barker family and so many more:  We are so sorry for the flashback of memories these writings have thrust upon you.  But on another level, we hope you are reminded of how much people care about you and have held you in the palm of their hands and hearts along your forever difficult journey.  You were and are further along the road than us, but no less important to the people who love you…especially to us.  

     

    And speaking of hands… (I know, I know…I said, “One more thing a second ago.”)

    Paul had anticipated a long and welcome night with his “injured angel”.  After all, Hillary has been mixing her days and nights up in tiny rooms while we sleep on chairs that are welcome, but not particularly comfortable.  Of course in Hillary’s NEW room and Paul’s first slumber party with her, he had his own bed in what we now call the Grand Ballroom-- complete with what could be turned into a GREAT bar and media room while she slept through the night.  More than anything he wanted her to stay awake with him and it didn’t happen.  She had been no doubt been “partying” with her girlfriends and was worn out. But this morning he asked her to let go of the bed rail and hold his hand.  And she did it!  A little later this morning as she awakened from a nap he told her it was time to hold his hand again; and she reached for him again.  It was well worth the wait for both of them.

     

    Thank you for your prayers and love.  You are shouldering so many “pieces” of this for us and we are eternally grateful to each and every one of you.

     

    XOXOXO

    --Shawn

  • Friday, September 27, 2007

    Much to tell tomorrow, but this evening I'll keep it very short.  When I returned to Hillary after two days away I was thrilled to see her progress.  Tonight I left her with four of her forever childhood friends who are laughing and crying and reminding her of all the things they did (and shouldn't have) as young girls. 

    Hillary is more awake (almost all day) and is doing many of the things necessary for rehab.  Her team plans on keeping her very busy this weekend as they push her closer to level four.  Please keep Hillary and her Vandy team in your prayers.

    More to come tomorrow.   Thank you for every prayer...they are carrying her and our family every step of the way.

    XOXOXO

    --Shawn

     

  • Hillary is RAPIDLY improving!!!!

    Hello everyone....this is NOT a "Coltharp exaggeration!"  Your eyes are reading the title for today's update correctly.....this statement was told to me by someone assessing Hillary tonight at Vanderbilt. 

    This is Ashley and as many of you know my mom is in Paducah getting organized and planning Hillary's next move.  I know you must be thinking.....Shawn getting organized?  Now THIS I have to see!  To tell you the truth I can hardly believe it either!

    With that said allow me to tell you what was told to me tonight by Hillary's Healthcare TEAM.  They explained to me that Hillary was at a Rancho Level 2-3 yesterday and today she is at a FULL BLOWN Level 3 with a few steps of Level 4 being complete.  I am THRILLED!  WE are thrilled!  YOU should be thrilled!  It is truly because of each of your prayers that she is rapidly improving (I just love saying that.....rapidly improving)  GOD IS GOOD and he is listening to all of your prayers.   

    We all know that Hillary will have a long road ahead of her but as our bracelets read "one day at a time" let me tell you today......

    She made it to a full 3 and on her way to 4.  The nurses say if she progresses the rest of the weekend the way she has these last few days then she WILL be at a 4.  To be at a 4 gets her into Stallworth and that is a GREAT thing. 

    She was swinging her right leg back and forth and putting it on the bed when I was on the phone with my parents telling them this story.  It made me laugh because it was like she was saying...."seriously I am bored here!"

    She is almost off of the catheter and the trach is getting closer and closer to coming out completely

    She is hugging me DAILY and even turning her head to kiss me!!!!  I promise I will never get mad or fight with her again when this is finally over.  Each of you are my witness :)

    Today when asked by a nurse what a particular tube does.....Hillary knew the answer and lifted it to her mouth (which is where the tube goes for mouth care)

    ABSOLUTELY AMAZING!!!!!

    Thank you to everyone a million times over.  I don't know how those words, a thank you card, or anything else we can say or do would ever show each of you how humbled we are by your love and support.

    I love you all and I know we are getting closer every day to throwing that big HILLARY'S BETTER AND THANK YOU FOR EVERYTHING Party :)    Enjoy your weekend, wear your seatbelts and don't forget to hug those you love and tell them what they mean to you everyday xoxoxoo

  • MASS SCHEDULED FOR WEDNESDAY

    A Mass for Hillary has been rescheduled for Wednesday September 26 at 8:00 am at St Edwards Church in Nashville. For those in Nashville who can attend please join us for a moment of prayer for Hillary. If you can not attend, please take a moment in the morning to say a quick prayer as we ask God to heal our broken angel.

     

    St Edward Church