WELCOME TO MANDY SELLARS.COM.
Me at Downton Abbey 2012
SOME OF YOU MAY KNOW ME FROM NEWSPAPERS YOU HAVE READ, PICTURES YOU HAVE SEEN & DOCUMENTARIES YOU HAVE WATCHED. THIS HOWEVER, IS THE ONLY PLACE YOU CAN LEARN UP TO DATE INFORMATION!
**** NEWS FLASH ****
I finally have a diagnosis for my condition,
it is a mutation in the PIK3CA gene,
this has caused the overgrowth in my legs & foot.
I was the first person in the world to be discovered with
this particular type of gene mutation.
So now I can say that I have
All this was down to two amazing doctors who took the
time to research my condition. Subsequently they were
able to offer me treatment in the form of
a tablet that has amazingly started to
shrink the fatty tissue in my legs & foot.
Me with my new 'magic pill'
Despite my condition not being Proteus Syndrome.
I wholeheartedly support the Proteus Syndrome Foundation. Please see the link below for more information or to help by making a donation. Every little helps as Tesco say :-)
HELP FOR OTHERS:
If you or anyone you know would like any help
in finding out more about any overgrowth condition you or they maybe living with then please contact me on this email address:
My amazing doctors in Cambridge are wanting
to try & help as many of you as possible.
Me with my amazing doctors, Robert Semple & Vicki Parker
**My recent fundraiser (EBay auction) for the Proteus Syndrome Foundaton (June 2013) raised: £657.39 Thank you to everyone who shared the information, placed bids & of course those who kindly donated prizes, Simone Lahbib, Eamonn Holmes,
Dr Pam Spurr & my lovely friend Diane.**
Me on my lastest appearance on This Morning
with Stephen Mullern & Emma Willis