Abilis’s Walk in the Park touches Justin Bagnati’s Family

DSCF9872I have had many changes as my life has gone on.  I met an amazing woman who is my partner in everything, my wife Kate. We have traveled and had many interesting adventures. We have two amazing children, our first daughter Raven Snow, now 3.5 years, and our second, Wolf Grace, now 16 months. I am a very lucky man.

Wolf is the tiniest little lady, a smiling, magnetizing girl. How tiny you might ask? She tips the scales at 13 pounds 4 ounces, about half the size of her peers. In addition to her small stature she is developmentally delayed.  She started crawling, more like sliding but I count it as crawling, at 14 months. Wolf has an extremely rare chromosome disorder, making her one of less than 100 in the world. It is called “duplication of 10Q”. The way I look at it is her genes are twice as awesome as everyone else’s!

Wolf was diagnosed at 5 weeks old. Fortunately the early diagnosis has allowed us  to do everything we can to give her all the help she currently needs.  The biggest problem for us is not knowing what is ahead since there are so few cases of 10q, and even fewer similar to hers.

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Abilis is a program in Connecticut that helps people with disabilities. They help families like mine acquire the resources to help raise a child with special needs.They get children like Wolf ready for school and life. Abilis provides most all of the special services we need to help Wolf advance and develop to the best of her ability. The program also helps us keep moving, keep trying and gives us hope. Wolf has physical therapy, occupational therapy, and will eventually have speech therapy.  This is all thanks to Abilis!

This weekend Abilis is putting on a walk at Tods Point to help raise money for their programs. I am walking with my family and I would love for you to come join me. To donate, or for more info on the walk, click here.

Your generosity  would be a great help to this incredible organization, myself, and my family.

Thank you for listening and your support.

-Justin Bagnati

2 comments

  1. I love this, and how you put it ” her genes are twice as awesome as everyone else” you have an amazing little family!!!!! Much love from our tiny little family!!! Jojo, casey, and lil ayla.

    Comment by casey tilton on October 22, 2013 at 5:36 pm

  2. Thank you, Justin, for the opportunity to support your family as you raise money for this fantastic cause. Wolf and Raven are beautiful children.

    Comment by Patty & Paul on October 22, 2013 at 9:52 pm

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