On September 13th, 2011, my husband and I found
out we were expecting our first child. We were absolutely overjoyed! We
immediately began preparing for our new little one and creating a space for him
or her in our hearts and our home. We knew we would love our little baby
forever.
Since the nurse practitioner I saw for my primary health
care would be unable to deliver the baby, she recommended we start looking for
an OBGYN as soon as possible. I found one to try and made an appointment for 13
weeks.
At 11 weeks, we had the opportunity to see our baby for the
first time via ultrasound. I can’t begin to tell you how special that moment
was, watching our tiny, perfect little love bouncing all around, kicking and
even waving hello. With lots of happy tears and full hearts, we carried our
photos home to dream of our new life together.
After a very uneventful first appointment with the new OBGYN
at 13 weeks, she asked if we’d like to take a peek at the baby again. Of course
we would! Once again, our special little one popped up on the screen as we
watched in awe. Then, out of nowhere, the doctor turned the screen away. She
said, “I’m seeing something disconcerting”. Time stopped and my heart felt as
if it did too. She turned the screen back to us and pointed to the baby’s
tummy. “See this black area…that’s not supposed to be there”.
To say we were stunned would be a massive understatement. I
felt as if I was floating as we gathered up our things and headed home to await
further testing. It wouldn’t be until 2 weeks later in the office of a maternal
fetal medicine specialist when we would learn what was going on. Our baby – our
loved and wanted little one – had a fluke condition called Bladder Outlet
Obstruction due to Posterior Urethral Valves and would not be able to live.
Despite the recommendation to end our baby’s life – “Absolutely not!” was our
reply – we chose to love our little one for as long as we could by carrying him
with the condition. With shattered hopes, hearts and
dreams, we went home to try to sort out what on earth we had just heard.
Many, many times during the next five months, we were told
our son (yep, he was a boy!) would not live much longer. We were told to expect
a miscarriage, and then a stillbirth and on and on. Every step of the way, our
little guy – who we named Samuel Evan – proved to be a little fighter and just
kept on growing and living.
At 35 weeks, after a long and crazy labor, our little love
was born into the world and let out a cry. Since he was born alive, they did
all they could to help him. The hospital we were in was not well equipped, so he
was sent to the Mayo Clinic to receive the best care. Due to my c-section, I
was unable to go with him. My husband stayed by his side, held his hand and
spoke love to him for as long as he could. After only four short hours, with
his daddy holding his hand, our little Samuel took his last breath.
Now we are left to pick up the pieces of our shattered
hearts and lives.
It’s been just over a year since he died. I look back on the
time we had with him and I’m so grateful we made the most of our time. I’m so
glad we carried him and met him. We have memories and photos that will help us
make it through each day. If I had the chance, I would do it again. He was
worth it.
Carrying to term doesn’t make the loss easier to bear. It
doesn’t make it okay. I will never, ever, be okay that he was sick, or that he
died. But I will always be glad that we chose life. I will always be proud that
we did all we could. When I looked in his brown eyes, and held his little hand,
I knew in my heart it had been worth it all. I would choose him again, every
time.
I created All That Love Can Do to support and
encourage other families facing the devastating news that their precious baby
will not live. I truly believe there is nothing worse than to hear that news.
It’s like two losses in one; first, at the time of the diagnosis, second at the
time of their death. No one should face that alone. It is my sincere hope that
every family who makes the loving and courageous decision to carry a baby with
a fatal diagnosis will find help, comfort and healing through our page, blog
and support groups.
With Samuel in my heart,
RaeAnne Fredrickson
To read our full story, visit my
blog, TheLoveWeCarry
Find help and resources on our
blog, All That Love Can Do
Support, encouragement at our Facebook Page
And join our groups here:
For Fathers,
For grandparents, Grandparents,
For babyloss families with no living children,
For babyloss families with living children, but no
Rainbow
For babyloss parents who are TTC, carrying, or raising
their Rainbow
*Rainbow is the term used to
describe a baby born after loss.
All That Love Can Do
All Life is Precious, Even a Short
One.
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