What do we do?
We support children who suffer from Perthes disease and Associated conditions.
We Are a Voluntary Organisation!
Fund raising events have enabled the association to buy such things as
Major buggies, wheelchairs and moveable seats, which are loaned
entirely free to members. They have also bought almost 100 hand
propelled trikes which they loan to children in splints or plaster, to
enable them to play with their friends. Currently they are raising
money to buy more of these and also additional reclining wheelchairs
for children to use whilst in an immobilising plaster following
surgery. They have a long-term aim to raise sufficient funds to be able
to contribute to research programmes into the cause and possible cure
of Perthes' disease and other forms of osteochondritis.
A
contact register has been established of families / members who are
willing to speak to new members in their locality and is run within the
guide lines of the Data Protection Act .
Membership of the
Perthes Association entitles you to a free Handbook and Layman’s Guide
to Osteochondritis, plus you will receive 4 newsletters on a quarterly
basis along with access to the equipment library and helpline.
If you do not wish to join the Perthes Association but require further information the Handbook and Layman’s Guide are currently available at £7.50 (Incl. P&P). Adults suffering from Multiple Epiphyseal Dysplasia or from long term effects of Perthes or other forms of osteochondritis are welcome members of the Association.
We currently have a database which enables us to put them in touch with others who are experiencing difficulties related to their condition. We support claims for benefits where appropriate and are currently compiling a booklet specifically for adults.
