Newly Diagnosed Afternoon Tea 2021

Registrations are closed

Thank you for RSVPing for our Newly Diagnosed Afternoon tea. We're looking forward to catching up with you on Saturday 22nd May 2021. If you need to cancel your RSVP or if you have any questions please email us at programs@cfcc.org.au or phone (03) 9686 1811.

Newly Diagnosed Afternoon Tea 2021

Join us for our Newly Diagnosed Afternoon Tea. Meet other parents and families who's child has been recently diagnosed with cystic fibrosis.

By Cystic Fibrosis Community Care

Date and time

Sat, 22 May 2021 12:00 PM - 3:00 PM AEST

Location

Melbourne Marriott Hotel

Corner Exhibition &, Lonsdale Street Melbourne, VIC 3000 Australia

About this event

Cystic Fibrosis Community Care (CFCC) would love you to join us for our Newly Diagnosed Afternoon Tea at the Marriott Hotel.

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

Book your place

Afternoon tea will be provided free of charge for CFCC members. Tickets are capped at 2 per family, but you are welcome to bring along anyone else, you will just have to pay for any additional guests.

Please book your tickets to let us know if you will be joining us (as well as any dietary requirements) by Thursday 13 May 2021.  

If you are unsure as to whether you are a member or not, feel free to call our office on (03) 9686 1811 and someone will check for you.

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.

COVID-19 response

CFCC is committed to delivering our events safely, following Victorian Government guidelines. Please ensure you are healthy and well before attending our events.

Organised by

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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