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If you would like to make a donation towards
Billee's ongoing therapy and medical costs please click on the
'donate online' button in the left hand
menu.
Thank You!
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We are
currently trying to raise money to pay for Billee's next 6 month
MAPS programme.
Please visit
their website for more info on what MAPS
does
www.multisensorytherapy.org
A message from Billee’s Godparents…..
Welcome to this website which is dedicated to Billee Alysse
.This site has been created to help Billee who suffers from a very
rare genetic brain disorder called Lissencephaly.
In order for Billee to live a life to her best potential she
requires constant, continuous care and attention along with
intensive physiotherapy, speech therapy and further down the line -
treatment overseas.
This website has been designed for the family & friends of
Billee’s parents (Kerri & Glenn) who want to help but don’t
know what they can do!!!
Please read the site and look at what YOU can do to help
not only with the financial strain of bringing up a child with a
severe disability but with also raising the awareness of a very
rare and extremely severe condition. With the hope that more
awareness will bring a better understanding of Lisscencephaly and
other rare brain disorders.
Please take the time to register on the site so that you can
receive the monthly updates from Billee’s mother Kerri. This will
inform you of the progress that can and will be made through
very hard work and funding from friends, family and other people
concerned with the plight of Billee.
We have made a list of suggestions of ways that you can help to
raise money. Remember, every little bit helps and we need you
all to get behind this website. Visit it regularly and please
remember to forward the website address to at least two different
people every month. Between us all we CAN make a difference
to Billee’s life and how she will live it.
Thank you for taking the time to read this and Happy
Fundraising!!!!
Tony & Bobbi Conway
Click here to
contact us
  
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