August 31, 2009

What has Carter been up to?


.........?


Playing games at Gatti Land with Daddy!


Resting with Daddy on the front porch after working on the house. Daddy is giving him coke, no wonder he is a Daddy's boy! ;)


This is how I found him the other day during nap time. Naked and with all his toys on the bed with him!


Playing in the dirt with rocks!


When I found him like this he said, "Mommy I'm your baby right?" 

August 30, 2009

John 9:1-5

Collin is getting so big and changing so much every day! He is 3 months old and wearing 6-9 month clothes. He is a big boy! He has a sweet, happy spirit and shines his light into my life daily with his sweet smile! These are some pictures I took today as we were spending some time outside on the porch! 








When the doctors told me that Collin was born with Amniotic Band Syndrome millions of thoughts and questions flooded my brain. One of them being "What could I have done to cause this?" or "What could I have done to prevent it?" Our doctors here in M-town as well as our doctors at Scottish Rites Children's Hospital reassured Chris and I that there was nothing we could have done to cause this. As much as I wanted to believe them there has still been a small part of me that was burdened with the thought that maybe this was my fault. Well a week or so ago I had found a few minutes in the chaos of our day to sit down and spend some time in God's word. I have not been in a study or reading any specific chapter so I placed my hands on the cover of my bible and asked the Lord to open it up to where he would want me to read. And when you ask you do receive. I opened my bible up to the book of John. Surprisingly the boys continued to nap so I enjoyed the rare time and continued to read. I came to John chapter 9. 

As he went along, he saw a man blind from birth. His disciples asked him, "Rabbi, who sinned, this man or his parents, that he was born blind?" Neither this man nor his parents sinned," said Jesus, "but this happened so that the work of God might be displayed in his life. As long as it is day, we must do the work of him who sent me. Night is coming, when no one can work, While I am in the world, I am the light of the world."
John 9:1-5

Wow! Collin's ABS wasn't because of something I did, it is so that the work of God might be displayed in his life! God really delivered me from that guilt and worry that some how this was my fault. He replaced those feelings with excitement and anticipation for how God is going to use Collin life to glorify his kingdom. Isn't God amazing! We have questions, He has the answers, and they are right in the pages of his word! 

August 25, 2009

House Update....

House Progress.....

The house is coming along slowly but surely. The leveling, plumbing, electrical, windows, air conditioning and part of the fascia boards are complete. As soon as the fascia boards are done, the roofers can get started on our new roof. I can't wait to start making it look like a house again. So far most of the work has been things you can't see. While I was at my mom's house last week I got a great deal on all of our appliances, so that is exciting.


If we leave a ladder out anywhere, in the blink of an eye, Carter is on top of it. The roofers were at Nana's house last week and next thing we knew Puddin was at the top of their ladder about to step on to the roof! He is a little dare devil!


Chris and Grandpa were working on replacing the fascia board...


Carter got to get on the roof with Daddy.... I almost had a heart attack!


This is our new AC unit!


Our New Windows...


This fantastic tub I found at a garage sale for $35, we are going to refinish it.


My latest find is an old cottage door I found at an antique store in Ft. Worth.
It even has a mail slot.


This will be our new front door, Oh, how I love it!

August 3, 2009

Welcome to Holland


When we took Collin to Scottish Rites in June his doctor gave me a packet of information and this poem was enclosed. I believe it was originally written for a child with downs syndrome but I believe any mother who has had a child with any disability or difference can relate.

Welcome to Holland 

 I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel.

It's like this...... When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

 After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland." "Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in the flight plan. They've landed in Holland and there you must stay. The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place. So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

 It's just a different place. It's slower-paced than Italy, less flashy than Italy.

But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts. But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."  And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

 But... if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things ... about Holland.

 by Emily Perl Kingsley


I read this poem and I wanted to scream "YES"! Yes, that is it, Yes, that is exactly what it feels like. It's not that it is horrible, just unexpected and quite heartbreaking because you love your child so much! So, here we are, settling in Holland. The questions and confused stares have become our new kind of normal. There is the woman who blurts out "Oh my, what happened to his fingers?" to the curious old lady who stares uncontrollably dying inside to ask but doesn't. The ladies who say "Aww..look at those fat rolls on his wrist." and I giggle inside and say "yeah". (there not fat rolls, they are scars from the bands) The child that checks his fingers out every time she sees him and apologizes that he has "owie's" on his hands. I'm learning not to lash out at them in my mother bear kind of reaction but instead to take the opportunity to share with them how much we have felt God's love through this and how we know that God has great plans for Collin despite his hand differences.

Picking the fuzzies out of his creases on his fingers and wrist has become normal. They seem to be great places to collect lint. ;)

Being overjoyed when he grips my finger has become normal. Who knew such a simple task would bring such joy? Those are the little things I would have taken for granted before.

So as crazy as it sounds, his ABS is a blessing. I have met wonderful mothers and precious children through this experience that I would never have met otherwise. I have look forward to everything that God has to teach us through this baby boy of ours.