"My wish, for you, is that this life becomes all that you want it to,
Your dreams stay big, and your worries stay small,
You never need to carry more than you can hold "
Well I cant believe yesterday marked the 2 year anniversary since we received Westins
diagnosis. It feels like it was just yesterday. Ill always remember,
we were sitting in the cold Sioux Falls Ultra Sound room..... and
hearing the words.. Spina Bifida
While those are no words any expectant couple wants to hear, they are a part of life... our life.
Its
funny the things that stick out in your mind, the things that you
remember. After going though months of infertility treatments to be
told we were pregnant was the best thing we could have ever heard....
and at my first Dr visit in Wahpeton
the Dr. told Travis and I to close our eyes and to think to ourselves
about the following question. If we were told we were having a child
with Down Syndrome or Spina Bifida,
would it change our minds if we would keep the pregnancy or not. We
both at the same time said No way, this is our baby he was given to us
for a reason. How I still remember the words Spina Bifida coming out of his mouth, at the time I didn't even know what that meant. Funny how things change.
Fast forward to today.. and we have a son who is wonderful, happy, smart, cute and soo
full of life. He has a smile that can light up a room and a laugh that
is contagious. While I know god has a plan for all of us, I believe my
plan was to be Westins Mom. While I have days that are tough, I know things can always be worse.
I'm
thankful for my different support groups. I am a part of several
online groups that know exactly what its like in my shoes... which is
nice. We also have a great support group with family and friends.
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