Thursday, March 22, 2012

7 years ago today...

...Glenn and I were sitting in a room listening to a "genetic counselor" tell us that our baby boy had Spina Bifida and Hydrocephalus.  It's funny how my perspective of that day has changed over the years.  It's not that I can't remember how devastated I was, or how I cried so much that I truly had no tears left, or how I curled up on the couch telling God that there was no way I could do this.  I remember all of that.  I remember the doctor telling us that our baby boy might not survive and if he did, he would have no quality of life.  I remember the doctor informing me that termination was an option but that I had to do it quickly because I was already 18 weeks pregnant.  I remember walking out of the doctor's office and seeing a nurse playing "Solitaire" on her computer.  I remember calling my mom and telling her about her first grandson.  I remember the paralyzing fear I felt.  The absolute despair.  And while I remember all of that and the memory is vivid, I don't dwell on Tuesday, March 22, 2005 very often.  

What I do dwell on is how blessed I am to have Caleb, and how I am a better person because of him.  I dwell on the fact that he is smart, funny, loving, and absolutely the most handsome 6 1/2 year old on the planet.  I dwell on the fact that I have found an amazing online community that has truly blessed me in ways that I can't even begin to express.  These people are family to me.  I dwell on the absolute peace that God has given me over the years.  I dwell on today and try not to get consumed by the worries of tomorrow.  I dwell on the fact that Caleb is so much more like every other 6 year old than he is different.  I dwell on the joy of being his mom.  It truly is a privilege.
I dwell on the silliness that is Caleb.


And I dwell on his killer dance moves.


This kid brings me joy.  I wish I had only a glimpse of this joy when I was pregnant with him.  If I had only known what God had in store, I wouldn't have been so scared.  Spina Bifida isn't easy and it isn't always pretty.  But as my dear friend Jill (Kingsley's mom) says:  "It's not that bad".




4 comments:

HennHouse said...

I love the things you dwell on!

Great post.

Anonymous said...

My son was born with SB just 4 days before you found out about Caleb. I didn't know til he was born so I just know that March 18, 2005 was the happiest and scariest and worst day of my whole life. At least that's what I used to say. Now I know it's not the worst day but just the day of infinite change. We love our boy so much! And, I'm now pretty glad to not have a day like you had with the genetic counselor. So glad.

Love your blog! Jennifer Stewart

Anonymous said...

My son was born with SB just 4 days before you found out about Caleb. I didn't know til he was born so I just know that March 18, 2005 was the happiest and scariest and worst day of my whole life. At least that's what I used to say. Now I know it's not the worst day but just the day of infinite change. We love our boy so much! And, I'm now pretty glad to not have a day like you had with the genetic counselor. So glad.

Love your blog! Jennifer Stewart

Kat Curlee said...

You can definitely tell by this video that he is a complete HAM! Oh my! I giggled through the whole thing! What precious boys you have!!