I rarely give up sleep to blog, which is why I am always behind, but tonight I cannot go to bed until I about the important anniversary today is. One year ago was one of the hardest days of my life on earth. My son looked like this:
I wrote in my journal the following:
I
awoke early again Friday, July 15 and prayed that I would accept
whatever God’s will was for our family, that day especially. I walked
into William’s small room to find a plethora of doctors and nurses. It
appeared that his dialysis fluid had stool in it. They had already done
xrays and were waiting for confirmation of a bowel perforation. The
surgical team came in to consent for surgery. Dr. Ford was the surgeon
on call that day. Every person in the room said, “you have ‘the Man’
doing the surgery today.” We met him preop, he was kind and humble with
a soft spoken French accent. Danny came in to me signing the consent
and was livid that it had gone all night undiagnosed. I felt grateful
it was Dr. Ford on call and wasn’t upset with his care. William went
off to surgery and we headed to the chapel to pray, study and cry some
more. We had planned for Hayley to have breakfast with my mom and bring
the kids back, we were so grateful they weren’t there yet. We spent
the morning reading, taking care of business from home and continually
praying. At about 11 am we wondered why he wasn’t out yet and were then
informed that they had completed the surgery and were putting in a
dialysis catheter. The kids and Hayley arrived. Thank goodness she
could stay. We met with Dr. Ford. He explained that approximately half
of William’s lower intestine (the right and transverse colon) were
extremely necrotic and because of that the PC cath tip had poked a 2 mm
hole in the colon. The placed a temporary ileostomy with a mucous
fistula because the rest of his colon was still ischemic and they were
unsure of its viability in time. He told us the ostomy would have to
stay 2-3 months and then we would be “put back together.” When asked
about his future with half a colon Dr. Ford responded “I expect him to
be President of the United States; actually, I expect more from him than
that.” He drew a picture of colon to show us exactly what happened and
also told us people live their whole lives with no colon so even if he
lost it all, he could still have a happy, fulfilled life. So many
emotions went through us. It was the first day I really lost it. I
have never enjoyed ostomies and now my son had one?! Also, William’s
anatomy was forever altered and the future was so uncertain. I went up
to ICU to see him. His dialysis changed to CVVH, a gentle continuous
dialysis. His belly was so swollen and he had a large incision down his
stomach. He was also sedated and on a respirator. It was too much for
me. I left to take the kids out and let Danny and his family spend
time with William. That day was particularly difficult to manage our
emotions. Our family was there and didn’t understand everything, were
suffering themselves and at times were not as sensitive as they could
have been. It taught us we needed to be patient with others no matter
how we were feeling and that we should never focus on ourselves. That
really helped. The kids, Hayley, Wes and April walked to an art park
nearby and walked around. Carter fell going up the steps and for
forty-five minutes proceeded to say that he could not walk because of a
broken leg. I tried everything and Wes did as well. Eventually, I got
him to admit that he could walk, he was just sad everyone was focused on
and talked about William. I felt like it was a normal reaction from a
child and had more patience with him after that.
It was a difficult day a year ago. Today, however, my son looks like this:
and we learned and grew so much through our experiences last summer.
While staying at the Ronald McDonald house, various groups brought in "Happy Meals" to the residents (and often our guests too). One group was a family who had stayed their previously and we realized that it would be great to be able to go back and do the same thing. They had raffles and made it feel like a party so we tried to do the same thing. I have never fed 90 people myself and felt a little overwhelmed at the task but, fortunately, we have great families who helped! We are also very grateful to Fresh and Easy, who donated a ton of chicken and discounted the rest, and to Juan Pollo, who discounted beans and rice for us!
Now, on to the cute pictures. :)
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Grillmaster Papa with a whole lotta chicken! |
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Wes and Danny at the grill |
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The final handsome grill master, Eric :) |
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Claire, Peyton, Will, Ella and Carter all enjoying Ronald |
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The serving area before the food was placed. Sweet Sydnee who is due with our niece in one week can be seen at the back of the photo:) |
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Raffle prizes we all brought |
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Playing at RMDH--he's the only kid who hadn't been there before |
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Looking up at a CHLA hopsital, the same kind he was transported in | |
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The dining room full of guests |
The highlight of the night was definitely meeting the families who are staying there. We aren't sure why this little boys are casted but he sure is sweet.
We also met the family of a 17 year old boy named Brian who is battling leukemia at CHLA right now. They were so kind and skyped him in his room. William said "hi" and "get better soon" to him. Brian's 13 year old sister was his bone marrow donor! It is inspiring to see the hope, courage and optimism of many families.
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Us skyping with Brian | |
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A smiling, happy courageous young man! |
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One of the dining room decorations |
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Our little family after the dinner |
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All of our family who came and helped! Thank you again! | | | | | | | |
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We drove by and waved to CHLA. It is such a wonderful hospital! |
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One final picture of cute blondie cousins! |
I thought more than once tonight of Matthew 25:40 which says "Inasmuch as ye have done it unto one the least of these my brethren, ye have done it unto me." Serving others brings great joy to our lives and we are happiest when we are thinking more of others than ourselves.
William is a
handful but we are so grateful to have him as part of our family. As I reread what Dr. Ford said of his potential for greatness in his life, I feel assured that he is growing and learning and will eventually stop screaming so much. What a difference a year makes!
4 comments:
You are such a great example to take this on! I have found that the greatest experiences we have through service may be uncomfortable, inconvenient or a struggle but the Lord blesses us in our efforts! Looks like he blessed you and your family with a great memory and night! :)
Beautiful Sarah!
WOW how far a year has brought you!
So grateful to have all we do and grateful for the opportunity YOU gave us! THANKS
What a miracle! Thanks for sharing part of your journal entry. That's so fun that you got to volunteer with them- you've come full circle. And thanks for being honest that William is still a handful and screams even after his miraculous healing :)
Wow thanks for sharing. What a difference a year makes. My sister is at the ICU right now as her husband is battling brain cancer. Their hearts have been softened and they too are submitting to the will of the Lord. We are seeing tender mercies in the midst of the trial. We are grateful for them. We are so happy for your family and his miraculous recovery!
My youngest was a screamer too. It took me a long time to take her pacifier away because of it! I used it as a plug in public places more than anything ;) good luck!
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