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Resource Centre
Level 8, 255 Bourke Street, Melbourne
Open 10am – 5pm Mon, Wed, Thurs
(closed public holidays)

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[email protected]

Resource Centre
Level 8, 255 Bourke Street, Melbourne
Open 10am – 5pm Mon, Wed, Thurs
(closed public holidays)

Volunteers are the heart of Counterpart

What better time to reflect on the importance of our volunteers than National Volunteer Week? We are lucky enough to benefit from volunteer assistance in a range of ways: volunteers provide peer support, help at our events and activities, participate in our Counterpart Advisory Group, review resources and information, and so much more. Thank you to each and every one of you.

Animated text saying 'Thank you' scrolls in, with bright pastel colours in the background and Counterpart's logo in the top right.

Peer Support Volunteers

Our service is founded on the belief that women who have experienced cancer are uniquely placed to help other women going through cancer. Our trained Peer Support Volunteers are available to talk to women diagnosed with any type of cancer who are living or being treated in Victoria.

In 2024, we have been pleased to welcome 14 new trainee Peer Support Volunteers at Counterpart. These women are the first intake to be taking part in our new online training program that consists of self-guided online modules, an in-person orientation session, an online workshop and practical training with more experienced Peer Support Volunteers.

A woman using Counterpart's online volunteer training module on her laptop. On her screen is an orange block with text that says Counterpart Peer Support Volunteer Training part 1.

Online training and extending to regional Victoria

The new training program has taken countless hours over the last 12-months: time spent planning, developing content, uploading and reviewing. We are pleased to see that the feedback we have been given so far has been positive, and the women doing the training are finding the content engaging and the system east to use.

Using technology to assist in mentoring has also been successful. Trainee volunteers can do their on-the-job training in person at our Resource Centre or over Teams, so those who can’t make it into Melbourne can still listen to experienced volunteers provide peer support and debrief afterwards.

This new hybrid training format has meant we could include 4 volunteers from rural and regional Victoria for the first time. We are looking forward to expanding this number in future, as Counterpart develops and creates new opportunities for volunteers.

About the Peer Support Volunteer role

Counterpart Peer Support Volunteers can:

  • listen without judgement to you talk about what is on your mind
  • draw on their own experiences and their training to give you support or encouragement
  • provide emotional support and practical advice (without ever providing medical, legal or financial advice)
  • help you find reliable, evidence-based information or suggestions on where you can go for specialised assistance.

How do I become a Peer Support Volunteer

If you have experienced cancer and want to use your experience to help others, you might consider becoming a Peer Support Volunteer. You can read about the application process and training provided on our Become a Peer Support Volunteer page.

It isn’t a role for everyone. As well as having experienced a cancer diagnosis, you also need to be in the right place within yourself. This is why we generally suggest you wait at least a year between your diagnosis and becoming a Peer Support Volunteer. We are moving towards multiple intakes each year. To find out about the next one, please fill in an expression of interest form, and we will be in touch when we have the next round of applications opens.

Four women of varied ages sitting in Counterpart's resource centre.  The mood is cheerful and casual. Two women hold tea cups and laugh, while the other two have a slightly more earnest conversation.
Counterpart volunteers at a morning tea celebrating National Volunteer Week, May 2023.

Where can I talk to a Peer Support Volunteer?

Our volunteers can talk on the phone, or if you want to talk face-to-face, you can come into our Resource Centre in Melbourne’s CBD (although it is always worth calling first, as our volunteers often work from home).

Some volunteers also take part in our Bridge of Support program, going to the Royal Melbourne, Royal Women’s and Sunshine hospitals, and soon the Peter MacCallum Cancer Centre, to provide peer support to women undergoing treatment or attending appointments in hospital.

Fill out our online peer support request form and we can get in touch with you.

 

What’s new – May 2024

What’s new in May, with links to support, information and other items of interest.


Survey: How many women experience long-term side-effects after cancer and cancer treatment?

'Cancer treatment survey' text in white with a navy overlay on an image of a woman sitting on the couch

If you are a woman who has had cancer, you are invited to take part in a survey about your experiences. The survey is part of a study that aims to understand how women experience long-term side-effects after cancer and cancer treatment. The study also hopes to understand how women’s everyday life is impacted by these side effects. They survey is online and takes about 20-40 mins to complete. It closes 31 May.

For full details and to participate visit the UniMelb survey website.


Melanoma Patients Australia and Melanoma Institute Australia (MIA) webinar series

'webinar series' text over an image of a woman sitting in a wheelchair looking at a laptop.

These free webinars will provide the rare opportunity to hear from MIA experts and a Melanoma Patients Australia community member about different topics of interest each week. They will be held every Tuesday evening for three weeks in June from 7–8pm.

To read more and register visit the MIA website.


Bladder/kidney cancer study: share your story

Asian woman sitting at a laptop

The purpose of the online study is to let those diagnosed with bladder/kidney cancer share their stories including their unmet needs, what is the concern during the treatment, and opinion towards a new treatment to see how they can better supported in the future.

For full information and to take part in this study view the flyer here.


Living with neuro endocrine tumours (NET) program intakes

Living with NETs, register now graphic

This online education program for NET patients and carers provides vital information to help them gain a deeper understanding of NETs, their treatment options and other topics that will support their day-to-day lives. It also offers encourages sharing and discussion in a safe space and build confidence to aid with self-advocating. Spanning over four weeks (session are two hours per week) this program has intakes in July and October.

To learn more and enrol visit the NET website


Managing the financial realities of blood cancer webinar

'Managing finances webinar' white text on dark green overlay with image of woman holding calculator and bills.

Personal and financial security can change after a cancer diagnosis. This webinar, hosted by the Leukaemia Foundation will be live online on Wednesday 29 May at 11am–12.30pm. This session will focus on the unique financial issues related to a blood cancer diagnosis, alternative income streams, the role of financial counselling and information on making a will.  

For full details visit the Leukaemia Foundation website.


Rare Cancers Australia support guide

Image of rare cancers guide booklets on light blue background

The Rare Cancer Support Guide aims to provide patients and their loved ones with thorough guidance to assist them in navigating their individual cancer experience. The guide is split into four separate booklets that can either be downloaded or ordered via their site. Even if your type of cancer is not rare, The support guide is full of useful information.

Find out more and download the guide on the Rare Cancers Australia website.

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