Tuesday, October 1, 2013

Our walk

Julianna woke up on Sunday morning and we heard her (through the monitor) say to Tyler, "Today is your heart walk day Tyler". My heart melted and even though she doesn't know what it really is about, at least she knows about the walk and was excited to go and she knew it had something to do with him.

Sunday was our CHD (Congenital Heart Defect) Coalition walk that I talked about in previous posts. Here is the link to my CHD Coalition page if you want to check it out. Technically it's not a "walk", it's a fundraiser & gathering for an amazing cause.  Yes you walk around the 'duck pond' but it's really about CHD warriors (survivors) and sadly in some cases, it's angels. The money raised was for Congenital Heart Defect Research & Awareness... Brian and I we raised $920! That was way more than I ever thought we would do. I am so thankful & blessed that we received the support & donations from our friends and family. It amazes me how fabulous other people can be when they know how important something like this is to you!

After spending most of the day at this event, my mind was spinning as to how much 'more' we could do for next year. We were part of the (Goryeb Children's) Hospital's team this year, but next year, I think I want to create our own CHD team for Tyler! We can do great things with this and I think I really want to go all out and recruit everyone I know to be part of this special event. It was such an emotional day to see all the CHD babies & children running around healthy and happy & it was so inspiring for Tyler's future and the future of CHD research. I think this needs to be something bigger for us and for our family next year. Brian and I already have ideas for team names, fundraising, sponsorship, etc!

Most of the teams made posters for the warrior they were walking for, and they were hung up for everyone to read. We did not make a poster this year, but I will totally make that a priority next year. I read story after story of each child, looked at all of the photos, and I broke down crying because it reminded me of Tyler's surgery and hospital stay... and all the emotion that went along with that horrific experience. It exposed a nerve for sure. I stood there holding Tyler in my arms, reading the posters, crying because everyone there today shared similar stories. We are all connected in a very special way and had pieces of our hearts broken when our little warriors were sick. We all had a CHD rockstar with a unique story to share. The CHD Coalition released butterflies to honor the children who lost their battle and turned into Angels. The whole event was very emotional and overwhelming to me.

Some of the parents from our CHD support group were there Sunday walking with their little warriors & families. It was nice to meet their families and of course their blessed little heart children! I feel like I will be even closer with some of these parents as time goes on especially since I got to meet their beautiful little heart babies!

It's so weird to think just 5 short months ago, Congenital Heart Defects weren't a thought in my head and never in my life. Now I'm completely immersed in Congenital Heart stuff up to my neck & I want to be as involved with it as I can. I want to make sure my son has the best possible outcome and healthy future, so I feel like I need to stay on top of everything. There is a group called "Little Mended Hearts" which has local chapters all over the country - except there isn't a local chapter in New Jersey - so of course the website asks if you want to start a local group in your area. I actually would LOVE to do that, but I know I am not physically & mentally able to take on that challenge right now since it requires a major time commitment, however I might think about doing that in the future if no one else does it for New Jersey.

Oh and wouldn't you know it? I completely left my big girl camera at home. I was SO bummed out & had planned on taking a ton of pictures Sunday. So instead, I took a few with my iPhone. Not the same... but it's better than nothing.

Our "Team Heart Throbs" shirt - Brian & Julianna 


 Me & Brian 


All of us 


 All of the CHD warrior posters hung up - Amazing stories!


Daddy & Julianna blowing bubbles (Brian put his other CHD walk shirt on - it fit better)


Me & my boy :) 


Julianna got a butterfly tattoo


Julianna painted a pumpkin - there was so much for the kids to do! 





 Drying pumpkins








Seriously, does it get cuter than this? 
He is very proud of his scar too! 


Tribute to all the Angels


Tyler's shirt (He'll fit into it in a couple years!)


Saturday, September 28, 2013

Boardwalk - Part 2 Pictures

I took too many pictures at the boardwalk and I needed to break them into 2 parts. First part was HERE. That day was perfect. Perfect weather. Perfect family day. The type of day you wish would never end. We didn't go on vacation this year, so I cherished the days we got to spend the day doing something so great! Our vacation this year was having Tyler and spending weekends on our boat. (Real Vacation - Next year! I want to go to Ocean City Maryland again!)

Julianna on the motorcycle ride


Eating ice-cream on the boardwalk is the best 


Me and my boy (in hindsight, I probably shouldn't have blinded him by facing the sun)


Julianna enjoyed collecting rocks and shells on the beach 





Cheesy toothy smile 


She put too much sand in the bottle and tried to empty some out... and out came her rocks








 I love my little girl 


My pretty girl


Had to show this .... Naptime on the boat... 
Brian and I got to relax and enjoy some time while anchored... while the kiddies slept soundly. 
(No life jackets required while boat isn't underway)




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