Sunday, May 7, 2017

May 7th. Sunday evening

Sorry for the delay.  Life started moving again. So Gage’s biopsy results came in at a 1a!!  This means the steroids did the job!  With that news they released the Mr Aurelius from the hospital Saturday afternoon, hopefully for the last time?? Who knows?  There may be something down the road, but not now. 

Going forward we hope things normalize a bit.  Stacy and Gage will go to his normal school at Nixon.  Gage also hopes to attend or even lightly play in his remaining Little League baseball games.  His Cub Scout leader would love to see him on Thursday nights.  Hunter has more playoff baseball games. Sierra has an upcoming band concert and tests, and Lindsey has the 7th grade drama to deal with.  Megan is still in Oregon and excited that she might even have a family to live with soon.  I will be spending quite a bit of time in Oregon as the ranch work heats up and the office and home responsibilities roll on.  Basically, we don’t have time for anymore of this rejection, or heart, or kidney, or blood pressure, or seizures, or whatever else there might be.  We are ready for someone else to take a turn.

Friday night we had Terry and Jennifer Pickeral come by for a visit. Terry is my father's cousin and made a very special trip here to see Gage and the crew.  It was very kind and very uplifting.

Tomorrow is Stacy's birthday. Big four O!  It will be fun day of school, and Hunter's baseball.

We are asked on occasion how we handle the pressure, uncertainty and stress of 3 heart transplant kids.  For the most part we just ‘keep on keepin on’.  Our kids need us to be positive and upbeat.  They need to see us going on with the most normal life as possible.  We have had to change many things about our lives, but we just keep going.  The only time we really feel the stress and start to break down is when there is an acute medical problem and we can’t see the outcome.   The strange and quite unique issue about heart transplant kids is that they usually have an option, there is always a plan B.  There is either a Berlin Heart option, or Heart Ware, or the long awaited transplant.  The times we feel lost, depressed, overwhelmed, or deeply emotional is the times a heart transplant or heart machine does NOT fix the problem.  Those times include (but not limited to) Sierra’s heart failure 10½ year ago (no Berlin back then); Lindsey diagnosed with the same heart disease Sierra had (the thought of going through that again), Sierra’s 2nd transplant (no Berlin option); Sierra, Lindsey and now Gage’s seizures (fear of brain bleed/stroke); Gage’s heart rejection and related kidney failure last week (fear of loosing him); and when Gage contracted RSV /para-influenza when he was only 3 months old (many of you don’t know about that one).   These were times we felt lost and leaned on the strength of others to get through it.  These were times we prayed to God with all the energy of our soul.  These were times many of you gave use support, encouragement, meals, and even joined us in sincere prayer and fasting.  These were times we would break down outside hospital rooms too scared to go back into the room.  But now those times are past.  Hope those days stay in the past.  Unfortunately, statistics tell us there will be more issues, some we may and some we may not have options for.  But for now we are truly blessed to have 5 healthy and recovering kids.   There are many others that are not that fortunate. 

Till next time,
Jason

   



 These are Sierra's awesome PALY friends, Tomer, Dillon, Theo, Nori, 




Gage when he was 3 months old with RSV / Para-influenza.

         

12 comments:

cici said...

no looking back,,,, just forward :)
GODSPEED
xo

Anonymous said...

Great pictures.....and the sun shines on! Love to all of you from High Valley!

anonymous said...

Thank you for sharing your pictures and story with us, and for being a strong and tenacious example of faith personified. Godspeed.

Linda D said...

Thank you for sharing your journey with all of us. We feel like your family. We prayed and held our breath waiting for news. Gage looks so good in such short time. Your faith and grounding inspired us all. God bless you and your family greatly.You have blessed us.

LaVon Hall said...

That is such good news !!!! Continued prayers your way from a cousin who has your family in my thoughts.

The Reading Nook said...

Wonderful that Gage is home! I really enjoy seeing the pictures of your family living life to the fullest! No matter what comes your way you stand united!

Anonymous said...

Gage looks like he had an appetite in the family dinner picture!!!! Can't wait to see him without a feeding tube. Will look for posts with all regular activity, in Oregon!?!?! Far, far away from a hospital. Continued prayers from Colorado. God is good.

Anonymous said...

Prayers and more Prayers have been sent to you and your families from all over the world and they have all been answered by our heavenly father and I know that more prayers are beening given. Thank you for all of your posts and hope that they continue when you all get to your Beuatiful Home In North Powder Gods World Thank you again

Jetta said...

🙏❤️😃!

Unknown said...

Bless you all..your ability to be a " normal " active family has taught us just how important small every day things are, and to value life. Your family is loved all over the world. I hope you truely feel that love..

Karen W said...

Happy Birthday Stacy. So glad Gage is out of the hospital and things are starting to head in a normal direction. Continuing to pray they remain that way and for the donor family who made such a selfless sacrifice. Hope Gage is able to get rid of his feeding tube real soon.

Elkofolks said...

Meredith Trindle here, you guys are so in need of a break and good news from now on. Praying for you and keeping you all in our thoughts.