Welcome to our blog!
About 5 years ago, when I was pregnant with Kennedi, Mark suggested I start a blog but I never did. Two kids later and A LOT of life experiences, I decided NOW is the time.
June of this year (2014) will mark 2 years since Mason was diagnosed with a genetic condition called Joubert Syndrome. These past 2 years have flown by and so many things have happened that I wish I would have started writing things down before, but I was not ready to share our life. Mark and I have thought a lot on what we wanted to share on this blog and in thinking about it, we have decided to share it all. There will be fun and random posts as well as some posts that will be very raw and real. We have felt so alone at many times in our journey with special needs and felt like if this blog, or one post from this blog could help a family, we want to share!
I am going to back date a bit so sorry for the blog over load the next bit. And just a warning, I am a bit of a story teller, so the posts may be long. Let me introduce our family and get this blog up to speed a bit.
Mark and I have been married since November 2005. The first few years of our marriage, we both went to school and worked full time. In 2007 I received my cosmetology license and in 2009 Mark received his Bachelors Degree in Business Management. We are blessed with 2 beautiful children. Princess Kennedi was born in September 2009 and sweet Mason was born in March of 2012… Oh yes, I can’t forget about our 2 Pomeranians Koko and Rocky. We got them in 2007 when they were just 2 months old.
Well there is our intro! I hope you enjoy a peek in on our family, our life and our journey.
Thanks for starting this blog, Dominique. Look forward to reading your story. Mason and Kennedi bring me joy whenever I see them. I am grateful to be part of your life and theirs.
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