Muscular Dystrophy

This is a site for all who have lost children and adults to muscular dystrophy there are many
different types but its a slow muscle wasting disease to all ...Duchenne md being the most prolific
they go from being able to walk do normal stuff and then its a downward spiral , watching it is
horrible for parents , horrible for the boys themselves they dont live out their lives. Other types
of dystrophy congenital , becker, mytonic to name just a few can go on for years like a time clock
ticking away, depending from person to person how badly affected they are etc.
This site is for anyone who has lost to muscular dystrophy it is a horrible , debilatating illness
with no cure , its not just physical ..its dignity its everything that goes with this illness that
makes it so bad. To all of us parents and carers who know of this disease leave a loved ones memory
here and for all you strangers who come across this site remember the name and give generously to
this charity if you ever come across it , there really is no cure for it at all !!!!!! xxx take
care , please leave a photo of your loved ones in the gallery xx tc
P.s if there is any information that is wrong here please put it right and let me know or make a
tribute xx