In a perfect world, I would have been able to call and share this news individually with all that I am close with, but that is not possible. Over the last 14 months, this blog has served as a great way to keep our family/friends updated on my bed rest progress and then new wonderful life with Hope and Jack, so it seems the perfect forum to share the latest update, albeit not the news I would prefer to be posting.
We have been watching Hope closely for the last few months as she has been behind Jack in her developmental milestones (head control, rolling, sitting, etc.) We were told that she was low tone and needed physical/occupational therapy to help her catch up. So that is what we've been doing all the while hoping she would do exactly that. However at her 10 month check up with the neurologist, we were encouraged to do some further testing as they felt her progress was not enough. Genetic testing showed that she has a deletion in chromosome 15 causing a genetic disease called Angelman's Syndrome.
In short, Hope will require life long care, will probably never speak, and will likely have seizures starting by age 2 (which we hope are controllable with medicine). On a more positive note, she will live a full life, will walk (though it may take her longer to get there than Jack), and will remain the sweet happy girl, she has always been. Angelman's children are known to be very social and prone to excessive laughter. It is taking me awhile to internalize and process all of this and I have not done a ton of reading about the disease. I recommend that you all check out (www.angelman.org) for more information. We have been encouraged to not focus too far down the road or on all the statistics, but instead to treat Hope as Hope and face each challenge as it presents itself.
It is sad news and we are all dealing with it in our own way. I am lucky to have Kevin who still tries to make me laugh even with tears in his eyes. As has seemed to be a theme in my life, every time I think I know what the future holds, a new wrench is thrown in the mix to twist everything up. But as I have done in the past, I will face this new reality head on and try to make the best of it - for Hope, for Jack, for Kevin, and for our wonderful family.
I am sure I have made at least a few of you cry (as I indeed am!) so I will stop with all this sadness. :-) We are doing ok, - better than okay really. Our parents have been great as have everyone else who has found out the news. I thank you in advance for all of the prayers, support, love, and kind thoughts, you will have for Hope and for all of us.
The blog will continue (though I make no promises on my update frequency) and will be a mix of photos, happy updates, and news about our challenges. At times I feel very presumptuous that anyone really wants to know all these details about my life, but then I remember that you don't have to read if you don't want to and I know there are a few avid fans out there who truly enjoy my posts.
XOXO,
Kate

This time just a couple photos of our Hopester. My next update will have with extra shots of Jack to keep everything equal. :-)


















