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WELCOME TO MY NEW LOOK WEBSITE!
MY NAME IS MELISSA ADAMS, I DECIDED TO LAUNCH MY OWN WEBSITE WHEN IN 2006 I WAS DIAGNOSED WITH A RARE GENETIC CONDITION CALLED ANGELMAN SYNDROME.I HOPE YOU ENJOY MEETING MY FAMILY AND SHARING IN OUR LIVES AND ADVENTURES.
THIS NEW SITE IS DEDICATED TO ALL THE MANY FRIENDS I HAVE MADE OVER THE YEARS AND TO THE MANY MORE I HOPE TO MAKE LOTS OF LOVE
Melissa x
We shed many tears in the begining but now we take each day one at a time and overcome new obstacles in turn. It is not an easy path we tread, our lives are organised around hospital appointments, we survive on very little sleep, our homes are thrown into chaos. At the end of each day we are exhausted often we cry when we think of the future. But what we have that many don't is the smile of our Angel, the laughter , the hugs and the realisation that together we can handle all of the problems that come with a diagnosis of AS. We are truly blessed to have Melissa in our lives and we hope you all enjoy this site and have a little laugh as you share her way of looking at life. xxxx Melissa's PA
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