Jack's Journey and Then Some: Home

Monday, October 13, 2008

Home

We are home! Thanks to all for checking in on us, for thinking of us and for leaving comments during our week in St. Louis.

We are happy we went, we are happy with the results, we are happy to have seen so many of our St. Louis friends and we are most happy to be HOME!

Fading . . . hour 10 of day two in the car

out

Jack upon our arrival at home - one happy kid!

No comments:

Post a Comment

Our son, Jack was born with an unknown subtype of congenital muscular dystrophy. Jack's disease caused him to have severe muscle weakness and he was ventilator dependent from four months of age until his death at the age of 15. This blog started out as a way to keep family and friends updated on Jack's spinal fusion surgery in the summer of 2006. Thereafter, it has become a window into Jack's life and the lives of those who loved him.

Our beautiful son died peacefully in my arms on January 5, 2014. Jack's journey is over. As Jack's mom, I now have to figure out how to live "Ann's Journey". I'm not sure where I go from here, but I know that wherever I go, Jack will always be with me, in my heart and guiding me in all I do.

Thank you for riding along with us on our journey.

Jack's Journey and Then Some

Monday, October 13, 2008

Home

No comments:

StatCounter