Newly Diagnosed Afternoon Tea 2018

Registrations are closed

Thank you for RSVPing for our Newly Diagnosed Afternoon tea. We're looking forward to catching up with you on Saturday 2 June 2018. If you need to cancel your RSVP or if you have any questions please email us at support@cfcc.org.au or phone (03) 9686 1811.

Newly Diagnosed Afternoon Tea 2018

By Cystic Fibrosis Community Care

Date and time

Sat, 2 Jun 2018 2:30 PM - 4:30 PM AEST

Location

Melbourne Marriott Hotel

Cnr Lonsdale & Exhibition Streets Melbourne, Vic 3000 Australia

Description

Cystic Fibrosis Community Care (CFCC) would love you to join us for our Newly Diagnosed Afternoon Tea

This event provides an opportunity for family members to meet other families who have recently been diagnosed with CF.

View other family support events at https://www.cysticfibrosis.org.au/get-involved/events/events-listing/vic or contact us on (03) 9686 1811.

Book your place

Afternoon tea will be provided for CFCC Members. Please book your tickets to let us know if you will be joining us (as well as any dietary requirements) by Thursday 24th May 2018.

Infection control policy

Events conducted by CFCC are open to all members of the CF community, including people with CF, family members of people with CF, and CF community supporters. These events are intended to provide enjoyment, recreation, education and the opportunity for people from the CF community to meet.

By RSVPing for the dinner you agree to our policy regarding infection control.

Organised by

Cystic Fibrosis Victoria (CFV) was founded in 1974 by a group of parents of children with cystic fibrosis and became an Incorporated Association in 1984. Today, CFV is known as Cystic Fibrosis Community Care (CFCC) through its integration of CFV and CFNSW into one organisation.

We provide advocacy, support and information services to people living with cystic fibrosis and their families. We also conduct awareness programs for the general public and fundraise to support service provision to families and adults living with cystic fibrosis and to promote cystic fibrosis research. As a not-for-profit charitable organisation CFCC relies heavily upon the generosity of the Victorian public as well as private philanthropic sources.

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