Miracle Mason: 18 Amazing Months!!

Saturday, May 30, 2009

18 Amazing Months!!

(This is Mason's hand motions for "SO BIG"!)

Happy 18 months Mason!

It has been....

18 amazingly special months

18 amazingly long months

18 amazingly educational months

18 amazingly traumatic months

18 amazingly emotional months

18 amazingly busy months

18 amazingly joyful months

18 amazingly tiring months

18 amazingly crazy months

18 amazingly memorable months

18 amazingly prayerful months

18 amazingly miraculous months.....

since out little Miracle Mason was born!! My Life would be so different without him, less crazy for sure, but definitely not as special and not so full of daily miracles. I wouldn't trade it for anything!

Mason is happy as could be today. He has 16 pearly white teeth, weighs a whole 16 lbs 2 oz, is 29 in long, still doing his bum scooting, still tangling up in the O2 cord, still loves to cuddle and be held, and still thinks he needs to wake up and hangout with me every hour or to throughout the night! That's our Mason!

No new info about his heart, but he is down to 1 liter of O2. Much better than 2!! We will see Cardiology sometime in the next 2 weeks for another ECHO, but I don't have the date yet. We always are grateful for your continued support and prayers!

(Mason is helping us plant some flowers in the yard here.)

4 comments:

Robin said...: He's looking so good and I'm glad he's doing so well. BTW, your yard looks amazing and I don't know where you get the time to do it all!

ballshouse.blogspot.com; June 1, 2009 at 10:37 AM
queenieweenie said...: wow-he looks SO big and SO good. our prayers are always with you.; June 2, 2009 at 10:41 PM
♥ Michele ♥ said...: He looks wonderful!! Here's to many, many, many more months, years, decades with your cutie pie!; June 7, 2009 at 12:17 AM
Em said...: I hope you will be able to find peace through whatever may come your way! Thinking of you guys and miss you!; June 7, 2009 at 10:54 PM

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Mason Andrew Strickland was born on November 30, 2007! He came 3 weeks early at the American Fork Hospital, weighing in at 5 lbs 8 oz . He is the baby brother to 3 brothers and 1 sister. At 3 days old he became very sick at home. After a trip by LifeFlight to Primary Children's Hospital that afternoon he was diagnosed with a variation of Hypoplastic Left Heart Syndrome. Mason will need at least 3 open heart surgeries before he is 3 years old. He had his first surgery when he was 10 days old and spent 7 weeks in the hospital. He had his 2nd surgery at 6 months old and only spent 1 1/2 weeks in the hospital. Mason also has issues with arythmias which has caused him some scary moments, a 2nd trip by Life Flight, and more time back at Primary's PICU. We feel blessed for everyday we have him here with us. We have created this blog to follow our journey through life with our little broken hearted baby, Miracle Mason (with a few tid bits about the rest of the family too).

It's now October 3, 2009 and Mason's story needs be updated. In April 2009 Mason was diagnosed with lowered heart function (or heart failure). From April through now he has been on medications and oxygen to help improve his heart function. In August, with no improvement seen in his echos we began the process to list him for a heart transplant. He is unable to get the 3rd surgery (or Fontan) as planned because of his heart failure. On Sept, 3, 2009 he had his pre-transplant Heart Cath (the last thing needed to list him for a new heart). The results that day have left us heart broken. He was diagnosed with severe pulmonary vein stenosis and is unable to receive a heart transplant. He will now need a heart-lung transplant, if he is a viable candidate. Since Primary's does not have a heart-lung program we are seeking opinions from other hospitals (outside of Utah) at this time. Even though we are extremely saddened with his most recent diagnosis, we continue to find joy in our journey with our special child of God, our sweet Mason.

(In November 2009 we learned of another possible option for Mason. CHOP and Stanford have both talked to us about doing just a heart transplant to his own one healthy lung. At this time we are exploring that option and the possibility of it being another true miracle for "Miracle Mason".)

February 16, 2010 Mason and I (Mom) flew to Palo Alto, California to do a few last tests and get Mason listed for a new heart(heart only!! not heart-lung!!) at Lucille Packard Children's Hospital at Stanford. We are excited and nervous to start this new chapter of our journey.

March 3, 2010 Mason was officially listed on the Heart Transplant waiting list as a 1B status. Mason and I will wait here in Palo Alto until he receives the miraculous gift of a new heart. We miss our family at home very much!

April 4, 2010 (Easter morning) Mason received his new heart. It was the best Easter gift our family could ever be given. We are eternally grateful to his donor family who during their time of loss selflessly gave our Mason a second chance at life.

July 16, 2010 Mason and Mom flew home to Utah to reunite with their family. Mason is still very immunosuppressed in order to avoid rejection of his new heart, but definitely happy to be home playing w/ his brothers and sister!!

January 30, 2012 Mason continues to do well with his new heart. He finally came off of steroids after 18 months in October 2011! Mason is walking with the help of a walker in hopes to walk alone soon. He conitues to have a few episodes of a pneumonia each year, probably due to only having one working lung. He also has a few new issues we are facing .....sleep apnea and severe scoliosis. But, over all he continues to face life with a fight and a big smile!

April 11, 2012 Mason had back surgery because his scoliosis had worsened to a curve of 75% (normal is 0-15%). He had two rods placed in his back, better known as the VEPTR (Vertical Expandable Prosthetic Titanium Rib). It was a rough recovery, but after about 8 weeks he was feeling much better. Every 6 months he will go in for a minor surgery to extend the rods to keep up with his growth.

May 25, 2012 We finally got into a sleep doctor and she diagnosed Mason with sleep hypoxia, rather than actual apnea. Because of narrow airways his sats dip frequently through out the night, but he doesn't completely stop breathing (good news!). So he was perscribed to be on one liter of oxygen at night while asleep.

July 20, 2012 Mason finally walks all on his own!!

Not a day goes by that we don't think about Mason's donor family who has given our little miracle boy the gift of LIFE! Thank you where ever you are!