© 2015 Nevus Support Australia
PO Box 262, Seacliff Park, South Australia 5049
.
Welcome to
Nevus Support Australia
Australasias’ first registered
Not for Profit, tax deductible
support group and charity,
providing information and
support to individuals and
families affected by (CMN)
Congenital Melanocytic Nevus
Today
Nevus
Support
Australia
has
a
membership
of
over
300
families
incorporating
New
Zealand
and
southern
Asia.
We
are
working
collaboratively
with
support
groups
and
researchers
around
the
world
to
provide
members
with
the
latest
information
and
treatment
options
for
this
very
rare
condition.
Ultimately we are striving to find a cure.
A
Congenital
Melanocytic
Naevus
(spelt
Nevus
or
Naevus)
is
a
skin
growth
present
at
birth,
they
can
range
in
size
from
the
very
small,
up
to
large
rare
forms
that
cover
much
of
the
body
surface.
It
is
a
rare
disorder
that
affects
around
1
in
20,000
newborns
in
some
form
and
as
few
as
1
in
500,000
in
its’
most severe form.
Nevus Support Australia ia a registered Not for Profit, tax deductible charity,
we raise funds to maintain our services and to support research into
pigmented skin conditions and associated conditions including melanoma,
NCM and hydrocephaly.
We rely entirely on donations and sponsorships to maintain services to
families, we are run completely by volunteers, no staff member is paid and
no paid collectors are used.
100% of all donations go directly to supporting our families and research.
This information on this website is for general information purposes only.
It is not intended as a medical reference.
Please talk with your doctor for medical advice.