As always I have said that no news is good news in the heartland. Much of the first thee year's updates were our day to day lives in order to document our journey - the good, the bad and the ugly.
The original purpose of this blog was to keep family and friends updated on how Jasiu was doing so that friends and family, whomever was interested, would get up to date information. As we have progressed in our journey and our life became more and more "normal" I have failed to update because we were living our lives. At the same time, I began to have more and more time to devote to helping newly diagnosed families and show them hope and the joys that this journey can bring. As I was talking with some of the families I was paired up with, I often pointed them to this blog to give them a glimpse of our day to day lives were in the beginning because that was their #1 worry and they read all about our hospital stay experience and how we dealt with all of this. I now realized how scary that must be to read, even though our journey has been relatively "easy". I know, I did the same when we were diagnosed.
One day at a wedding we attended, I met a woman who came up to me and said these exact words "You don't know me, but I know you very well". This may sound strange at first, but turns out that she heard from a friend of a friend of a friend who had a "child with a heart problem" and I'm not exactly sure if she googled our blog, or someone pointed her to it, but she found my blog. Turns out she had a little girl born with a large VSD and was for lack of a better phrase, heartbroken. Her daughter's heart had to be operated on shortly after birth. She said that during her daughter's hospital stay she read our entire blog and got courage that if we can get through HLHS, they can get through their journey too. She was the nicest lady and we connected right a way. The heartland does that to people, it's the club you hate to be a part of but you are thankful when you find others like you that you can support each other. This scenario is fine if you are thrown into the heartland unknowingly, after birth of the baby. However being prenatally diagnosed, reading the first two years of our journey can be scary. And it's not an easy path to choose, but it can be as good as you can make it. Where there is a will there is a way.
So in the spirit of trying to provide more hope, my goal will be to post more often our everyday accomplishments hopes and dreams. Hopefully seeing all the positives of this journey will give strength and courage to as many families affected by congenital heart defects to choose to walk this path that they were given bravely and with hope to live each day to the fullest.
Not all days will be great, but all days you live to see another day are worth living. No one knows what tomorrow will hold, and we don't know that our or Jasiu's future is certain, but we choose to live and do everything to strive to be better than yesterday and that should suffice.
So anyone starting to read our story starting just now, read all the current good stuff happening now and then the hospital days, because those hospital days will pass with God's grace you will survive it and be thankful each day forward, as we are.
Here we are living our life with HLHS in the last 6 months :)
|Last weekend getaway trip to Wis Dells|
|Being the best big brother|
|Being the goofy brother|
|Loving some monster trucks|
|Loosing your first tooth|
|Skiing and not giving up|
|just plain silly|
|best presents under the tree|
|Being the cutest ring bearer|
|exploring a firetruck engine|
|and some good pontoon rides|