Where does the time go? ....
Three years ago today our life came crumbling down around us. We had the diagnosis of the no treatments, no cure and 100% fatal, duchenne muscular dystrophy. We will never forget being told to "go home and love him there is nothing you can do."
Our days are a little brighter and tears are getting lighter as time goes on. It's still the first thing we think of in a morning and last thing at night. It never leaves us with its constant little reminders that it is slowly and gradually taking over Connor's precious little body.
We have fight, we have hope and so much support. One day we will win the war!! ♡xx
Thank you for taking the time to read this and if you would like to join us at one of our events or organise one of your own please get in touch www.caring4connor.com
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