When
Candice went into labor with her first child, she never dreamed that
she would soon be saying "good bye." She has written about her journey
of love and loss of her son Alex in the hopes to raise awareness for
Hyplo-plastic Left Heart Syndrome. On Monday, she shared her story. Today she talks about coping with life after the loss of a child.
Read the entire series here.
Read the entire series here.
A Guest Series By Candice DeLeeuw
Many people ask me how I did it. How I was able to survive
losing a child. I will tell you this: it was not easy. I will also tell you
that I didn’t survive it, God carried me through it.
You see even when I was pregnant I had this overwhelming
feeling that something was wrong, but nothing was detected. I kept having odd
dreams that there was something wrong with him. I also got intensive care
insurance that would protect both me and my unborn son while I was
pregnant.
While visiting West Virginia,
my husband and I stayed in a hotel that was next to a beautiful cemetery. We
were told that it was a place many take walks because it is so beautifully
landscaped. We decided to give it a try. Where we cut across the cemetery to
enter; there were hundreds of graves of children who had passed away. At this
time I was seven months pregnant and I told my husband I could never imagine
burying my child. I believe God was preparing me with each one of these
moments.
The night before I was induced I looked at my mom and
husband and told them that I felt like I was having a baby the next day, but
that I wasn’t bringing him home. The next morning when we went to be induced I
started sobbing before we got out of the car and told my husband we needed to
pray. My prayer was simple. Over and over again I cried, “Whatever it is You
are about to do, just prepare our hearts.” I believe he was doing just that.
Throughout our time at Duke I felt God’s presence. I somehow
knew that our time was short with Alex. This for some reason didn’t freak me
out, but made me enjoy every minute with him. I prayed many times on my knees
sobbing in an empty hallway of the hospital praying for a miracle, praying for
Him to change His mind. But I always felt His answer was, “no.” He made me okay
with this answer. He put blessing after blessing in front of us. We met amazing
people and made forever friends. We were able to be a part of a new surgery
program where they removed Alex’s thymus tissue and used it to correct DiGeorge
anomaly. Duke is the only Medical Center that performs this procedure. In the
summer of 2007 we received a letter from Dr. Market telling us that the child
who received Alex’s thymus tissue was alive and well because of him. We believe that although God didn’t answer
our prayer of healing for Alex on earth, He did answer many other prayers, and
ultimately He healed him.
Although I felt God’s presence when Alex was sick. I pushed
Him away months after losing him. I was angry and honestly going a little
crazy. I can’t even begin to count the
number of times I paced the house not knowing what to do, or how many nights I
laid in my bed unable to close my eyes despite how tired I was. When the
morning would finally come I wouldn’t want to get out of bed.
Doing the day to
day things was even hard. I can’t even begin to fathom what the water bill was
like at that time because I would sit in the shower sobbing until the water
turned cold. I would sit in his untouched nursery and rock in the glider
smelling the only outfit he ever wore alive. I would sleep on the rug in his
nursery. I would wake up to a baby crying; only to realize there was no way it
was possible. I was alone. I didn’t want to laugh or show happiness because did
that mean my heart was cold and I was moving on so quickly? I couldn’t talk to
my friends and family about it because no one really understood how I felt and
besides, I was supposed to be getting better.
I didn’t want to burden my
friends and family with all my pain, when I knew it just made them feel
helpless. My husband and I were grieving completely differently and I couldn’t
talk to him either because he didn’t want to talk about it. I was spiraling out
of control in my own mind and was angry that everyone else could move forward
and I couldn’t.
I can’t pin point exactly when things started getting better
for me, but one thing I did that was so helpful was read. I read book after
book of other mothers who lost their children. For me this was comforting. I
knew that I wasn’t alone. I could read about someone else’s experiences and
know that although I felt like I was losing it, I was okay and other people go
through this too in their grief. I read about how couples grieve differently
and that because of this there was a high percentage of marriages that end in
divorce (although statistics are stating otherwise now). This forced my husband
and me to communicate and to “make it.”
We also began several traditions that first year. At the
first Christmas we got the grandparents gifts that incorporated Alex, knowing
they were grieving as well. The first year was a silver booty ornament engraved
with his name, the second was a plate with the footprints of our second son in
which one footprint was made into a
reindeer and the other an angel, and one of the more recent a Yankee Candle
with a picture of my two children holding Alex’s picture.
For Alex’s birthday we celebrate, this has
gotten easier over the years and with the help of our children. Together we
bake a cake or cupcakes and have a celebration. In the past we have gone to different
kids museums or play places. This year we even had a close family come and
celebrate with us. We also remember his “Angel Day.” We do this by releasing
balloons. The number of balloons represents the number of years he has been
gone. We each write him a note, including the kids, attach it to the balloons
and release them. We feel this is a great representation of him leaving this
Earth and reaching farther than we can see.
Some other things we do are: plant
flowers each year in our “memory garden,” give hospital “goody bags” of the hospital
stay essential to families we know in the hospital, we have provided hotel
stays for friends whose children were in a hospital a good distance away, as
well as financial support to other families in the same situation. Although we
have created many little traditions over the years, the most important thing we
do is talk about Alex. We share with our children who their brother is. We do
not hide pictures, even the “bad” ones. We are honest with them about how he
was born with a bad heart and was really sick. They often will talk about him
themselves as if they know him, especially our second born, Xavier.
Here is what I know about grief. I know that it is different
for everyone and that everyone has to find a way to handle their emotions and
all that surrounds their child’s life. I also know that at some point you have
to make a conscious decision: will I get out of bed today? Once you have
decided to get out of bed, you have to decide how you will LIVE.
For my husband
and me, we decided to live each day remembering our little man with good
memories. We don’t mourn the loss of his life (although you may catch a few
tears or sobs once in a while) but celebrate his life. We believe that God
could have chosen anyone to be his parents, but He chose us. He chose us to
love him, help him fight, and to ultimately achieve his purpose in life. We may
not be clear on what his purpose was but we know that such a tiny little soul
has completely changed our lives. Because of his life, we are able to talk to
other parents who are dealing with loss. We are able to share with others the
positives in life.
We are not scarred by his death, but blessed by his life.
We are not scarred by his death, but blessed by his life.
Candice is a mother of 3 and wife to 1. Her children are
Alexander (would be 6- deceased), Xavier (4), and Irelyn (2). Originally from
Michigan, her husband, Brandon, and she moved to North Carolina in February of
2005 for a teaching offer. Within a few months they were surprised with the
blessing of the news of their first born. Alexander arrived in January 2006
with an undetected congenital heart defect. After fighting for his life, he was
released to heaven in March 2006. She is a guest blogger sharing her story of
loss and living. If you would like to contact Candice, send an email to mumblingmommy@mumblingmommy.com.





1 comment:
Candice,
I could hardly breathe thru my tears. Your courage and faith are incredible. I truly loved your honesty regarding the grieving process, the moments of lost sanity, and your ability to put all this into beautiful words of hope and comfort.
Many blessings to you and your wonderful family.
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