North West Metro Melbourne 2020 Support Dinner

Registrations are closed

Thank you for RSVPing for our dinner. We're looking forward to catching up with you on Wednesday 26 February at 6.30pm at the Victoria Hotel (43 Victoria St Footscray VIC 3011) If you need to cancel your RSVP or if you have any questions please email us at socialworkvic@cfcc.org.au or phone (03) 9686 1811 (or 0438 082 553 outside business hours).

North West Metro Melbourne 2020 Support Dinner

By Cystic Fibrosis Community Care

Date and time

Wed, 26 Feb 2020 6:30 PM - 9:30 PM AEDT

Location

Victoria Hotel Footscray

43 Victoria St Footscray, Vic 3011 Australia

Refund Policy

Refunds up to 1 day before event
Eventbrite's fee is nonrefundable.

Description

Cystic Fibrosis Community Care would love you to join us for our next support dinner in Footscray.

These dinners provide an opportunity for family members to meet others who are, or have been in a similar situation, and to share stories, experiences and resources. They are also a great chance to meet new people and catch up with old friends.

Dinner will be provided for 2020 members, drinks will be at bar prices.

Book your place

Please book your tickets to let us know if you will be joining us (as well as any dietary requirements) by Monday 17 February 2020.

Infection control policy

Events conducted by CF Community Care 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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