Happy Thanksgiving
For rest and shelter of the night,
For health and food, for love and friends,
For everything Thy goodness sends.
~Ralph Waldo Emerson
Happy Thanksgiving!
Hope is the thing that is willing to take a chance on the future. Hope is the capacity to see something on the horizon that we are willing to move toward. If our hope gets us from today to tomorrow, and in that new day we are ready or able to deal with something we thought we couldn’t face, then hope has done its job. There is a worse thing than false hope. It is no hope.
I'm participating in Love That Max photo carnival by posting my favorite picture of Jack.
As if I need something else to get the tears flowing these days. I downloaded Annie Lennox's new Christmas Album (A Christmas Cornucopia) from iTunes tonight and heard the song "Universal Child" for the first time. I can't imagine that this song won't move every parent to tears, but especially those of us with kids who struggle every day just to live and do those things that too many take for granted - our extraordinary children who are on this earth to teach us all to love unconditionally, appreciate the simple things, accept what we cannot control and to persevere through adversity.
I invite you to join me in a good cry .............
So, I wrote a post on Friday night that I published and then deleted. It was way too "woe is me" that even I couldn't stand it. I should know to NEVER write blog posts on Friday nights. Friday nights have always been the toughest day of the week for me. I could give you all the reasons why, but if you don't live the life, you won't get it and if you do live the life, you already get it, so I'll spare you the explanation.
Things are just really hard for me right now. I miss my mom. It's hard losing your mom. It's exceptionally hard when you didn't get to see her before she died and when you didn't take the opportunity to tell her things you wish you had before she died. I find myself in tears every day.
Jack is 13 years old and was born with a congenital muscular dystrophy. As a result of his disease, Jack has severe muscle weakness and is ventilator dependent 24/7. This blog started out as a way to keep family and friends updated on Jack's spinal fusion surgery in the summer of 2006. It has since become a window into Jack's life and the lives of those who love him. Jack lives with his parents, Mark and Ann and his older sisters, Hilary and Mary and his little brother, Eric.
Thank you for riding along with us on our journey.