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North West Metro Melbourne 2020 Support Dinner

Cystic Fibrosis Community Care

Wednesday, 26 February 2020 from 6:30 pm to 9:30 pm (AEDT)

North West Metro Melbourne 2020 Support Dinner

Registration Information

Registration Type Sales End Price * Fee Quantity
Dinner RSVP for 2020 CF Community Care members   more info Ended Free $0.00
Dinner RSVP 2020 for non-members   more info Ended $35.00 $0.00
* Prices include GST

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Event Details

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.

Have questions about North West Metro Melbourne 2020 Support Dinner? Contact Cystic Fibrosis Community Care

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When & Where


Victoria Hotel Footscray
43 Victoria St
Footscray, Vic 3011
Australia

Wednesday, 26 February 2020 from 6:30 pm to 9:30 pm (AEDT)


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Organiser

Cystic Fibrosis Community Care

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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