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A Message from our President
To all our Members, Friends and Families
As you may be aware, May 15 is International MPS
Awareness Day.
On this day we take an opportunity to remember those
around us who are affected by MPS both directly and indirectly in their
lives.
We also renew our determination to work towards making
treatments available to all those who need them, and to help our
researchers work towards better treatments and cures for MPS and related
disorders.
Please take the opportunity of today to help spread the
word amongst your friends and colleagues about the much needed care and
support that those affected by MPS require.
Today we also remember those who have lost their battle
against MPS and have passed away.
David Oliver
Honourary
President
MPS Australia
The Australian MPS Society
is a non profit organisation formed by parents, relatives and friends of
those suffering from a range of rare genetic disorders known
collectively as the mucopolysaccharide (or MPS) diseases.
The aim of this site is to
support and inform all those who are affected, directly or indirectly,
by a mucopolysaccharide or related disease.
If
you or your family or friends have been affected by MPS, please
contact us and become a part of the MPS family.
If you wish to make a Donation to assist the work of the
Society, please click on this link for details -
Donations |
