Welcome to our blog!! Thanks for checking out our journey with 7 crazy kids, including one named Spencer who has achondroplasia, the most commom form of dwarfism. Here you'll find my personal ramblings on raising a child with a physical disability, thoughts on motherhood and faith.



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Sunday, July 5, 2009

Can life get any crazier?

So, I start a blog and then I'm derailed! I'd planned on keeping up on this and not procrastinating (for once!). But then a 8 day hospital stay changed my plans. Yes, a 8 day hospital stay. We were planning on Spencer's first visit to the specialists at the Skeletal Dysplasia Center at Akron Children's hopsital. Spencer was getting fussy after being in the car way longer then we wanted to be. I checked on him and told him to hang in there because we were less than 10 minutes from the hospital. He was fussy, but he was fine.

We arrived at the hospital, parked in the parking deck and got Spencer out of the car. That moment turned out to be the most terrifying, awful moment of my life. I looked down and Spencer was pale, foaming at the mouth, not breathing and totally non-responsive. I starting yelling his name and Scott was pinching his leg, but nothing. Not one single thing to reassure us that our precious little guy was okay.

So, we ran into the hospital, but the floor we parked on actually entered the Professional Building, which is mainly just offices. I shouted to the first person I saw, "Do you work here?" She said no, but that the lady walking down the hall did. I called out to her and said, "We need help now! My son is not breathing and not responding!!" She stepped into one of the offices and called a code blue. Within minutes we had a slew of people surrounding us in response to the code being called. Thank God Spencer had started breathing again by this point. It was shallow and lethargic to say the least, but at least I saw some life in him again.

They rushed us over to the main part of the hospital to the ER. I was on the verge of throwing up or passing out, but I knew I had to keep it together. The details of the next 8 days will be in the next blog. But re-living this, even just to write in here, is almost too much. All I know is holding your lifeless child is an experience I wouldn't wish on even my worst enemy.

7 comments:

  1. I can't even imagine, but I'm so glad that Spencer is ok! My heart was pounding reading this post and picturing what you must have been going through. I hope you guys are home and resting now.

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  2. You have a beautiful family and I hope and pray that Spencer is okay.

    I'm Andrea and my son, Evan, has hypochondroplasia. We also have a son named Jared!

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  3. Oh my gosh! I can't even begin to imagine how terrifying this all was! I'm glad that they were able to assemble a quick team of help at the hospital! I hope that you all are at home and resting and that Spencer is doing well now! Sending you many hugs!

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  4. I'm hope that Spencer is doing well now. I have the same feeling like Jennifer. That must be a tough time for you and Spencer.

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  5. Oh, I am so glad that you were at the hospital, I cannot imagine going through that! I am so glad that Spencer is okay now, and I cannot imagine how hard it is to have one at the hospital and 4 at home to take care of. Hugs!

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  6. Wow, what a scary experience. I had something similar with my sister years ago and its hard to pull yourself together. Good thing you were at the hospital and got immediate assiatance.

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  7. I have been attempting to post a comment. I cannot even imagine the horror that you guys went through-but Spencer is a strong little trooper and the joy he will continue to bring to your lives is immeasureable! Here's hoping that Spencer stays in the best of health and no more scares for Mommy and Daddy!

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