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[email protected]

Resource Centre
Level 2, 210 Lonsdale Street, Melbourne
Open 10am – 5pm Mon, Wed, Thurs
(closed public holidays)

Time we talk about bowel cancer

June is Bowel Cancer Awareness Month. 

Bowel cancer (also called colorectal cancer) is cancer of a lower part of the bowel – the colon or the rectum. 

  • 1 in 15 Australian women will develop bowel cancer is their lifetime.
  • Bowel cancer is the second-most common cancer in Victorian women.  
  • In January 2021, there were around 6367 women living in Victoria who had been diagnosed with bowel cancer in the last 5 years. 

The risk of bowel cancer increases with age, and it can also be genetic. Two genetic conditions that can increase the risk are Familial Adenomatous Polyposis (FAP) and Hereditary Non-Polyposis Colon Cancer (HNPCC), also known as Lynch Syndrome. 

The good news is that, if it is found early, it is one of the most treatable types of cancer. With an early diagnosis there is a 5-year survival rate of around 98%. 

Screening for bowel cancer

In Australia, we are lucky to have a screening program that allows bowel cancer to be found before symptoms are seen. This means treatment is far more likely to be successful. 

If you are between 50 and 75 years old, you will have been sent a screening test in the mail. All you need to do is collect 2 tiny poo samples, in the privacy of your own bathroom. Mail them back in the post bag provided. The samples will be tested for blood.  

If blood is found, it might not be cancer. Your doctor will follow up quickly to find out what has caused the bleeding. They will make sure you get the care you need. 

Some people feel squeamish about doing the test, but it is quick, easy and clean.  Watch this video from the Australian Department of Health and Aged Care to see what you need to do. 

Prevention 

Of course, avoiding cancer is even better than catching it early. 

Cancer Council Victoria gives these tips for lowering your risk of colorectal cancer:  

  • Be active 
  • Stay at a healthy weight 
  • Don’t eat processed meat 
  • Cut down on red meat 
  • Drink less alcohol 
  • Don’t smoke 
  • Eat wholegrains, dietary fibre and dairy foods. 

You could speak with your doctor about whether aspirin might reduce your risk.

Bowel cancer treatment  

Treating and managing bowel/colorectal cancer will depend on each person’s diagnosis and situation. Here are 4 great places where you can find out more: 

  • Bowel cancer: your guide to best cancer care is a fact sheet that steps you through each stage of diagnosis, treatment and management. It explains some medical words you might hear, a list of questions you might like to ask your treating team, and links to more information.  
  • Bowel Cancer Australia explains how the cancer is diagnosed and treated. You can also read stories from people who have had bowel cancer.  
  • The Bottom Line  – podcast from Bowel Cancer Australia. A monthly chat sharing stories and information. 
  • Cancer Council Victoria has lots of information on diagnosis, treatment and management. Includes a link to download the booklet ‘Understanding bowel cancer’. 

Peer support 

Talking to someone who has had a similar condition can be reassuring. This is called peer support.  


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.

What’s new –April 2024

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


April is Oesophageal Cancer Awareness Month 

Pancare Foundation Oesophageal Cancer Awareness Month graphic. Features Pancare logo.

Pancare Foundation provides in-depth information on various aspects of oesophageal cancer from symptoms, diagnosis and beyond. They also offer supportive resources and practical guidance to help patients and their loved ones navigate the challenges associated with this type of cancer.

Visit the Pancare Foundation website or download their Oesophageal cancer patient handbook.


Inquiry into Women’s Pain

text: Have your say, Inquiry into women's pain with Victoria government logo and words 'department of health'.

The Inquiry into Women’s Pain provides a platform for individuals to share their experiences, assess barriers to care, describe the impact of current service delivery, explore opportunities for improvement, and consider models of care and workforce adjustments. Additionally, it aims to translate research to address gender disparities and improve equity in pain management outcomes.

To read more, make a submission or complete a survey visit the Department of Health website.


World Cancer Rehab Week: 15–21 April

Text reads '15-21 April, world cancer rehab week.' with graphic an arm holding a dumbell.

Cancer rehabilitation involves a range of therapies that aid in recovery and assist with regaining optimal physical, emotional, and functional wellbeing. It can include exercises, physical therapy, occupational therapy, speech therapy, nutritional support, pain management, counselling, and other supportive services. The goal of cancer rehabilitation is to improve quality of life, alleviate symptoms, and promote overall recovery and wellbeing throughout an individuals cancer experience.

To learn more about cancer rehabilitation visit the Cancer Council Website.


Ovarian Cancer Australia (OCA) launches Psychosocial Research Centre

The Ovarian Cancer Psychosocial Research Centre is dedicated to advancing research on the psychological and social aspects of ovarian cancer, and translating findings into practical strategies. Through collaboration with experts, including its Advisory Committee composed of academics and health professionals, the centre prioritises research efforts, establishes new projects, and ensures effective support for those impacted by ovarian cancer. The goal of the centre is to improve the quality of life for patients by addressing their diverse needs and bridging the gap between research and real-world support.

Read more about the centre on the OCA website.


Lecture: Hope and Resilience in Women after Cancer through Music and Arts Therapy

Music and Imagery Association Australia presents – Creating Hope and Resilience in Women after Cancer through Music and Arts Therapy. Presented by Dr Margareta Wärja, this lecture focuses on the results of a clinical study about the impacts of music therapy after gynecological cancer treatment. This event is taking place on 1 May at the Dax Centre & online.

Visit the Eventbrite listing for full details.


New app helps GPs support patients with palliative & end of life care

The CareSearch GP app assists GPs in delivering quality palliative care by bringing together guidance and evidence-based information on crucial care topics such as advance care planning, recognising deterioration, engaging in palliative care case conferences, caring for dying patients, and assisting families through bereavement stages.

Visit the CareSearch website for details on downloading the app.

What’s new – March 2024

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


March is Lymphoedema Awareness Month 

Lymphoedema awareness month. Stylised illustration of a group of women walking together. One wears a compression sleeve on her arm,

If the lymphatic system isn’t working properly, lymphoedema can occur at any time. For people diagnosed with cancer this can happen during initial treatment, after treatment is completed or when in remission. Usually it develops slowly, over many months or even years. Visit Lymphoedema: what you need to know for more information.


New cancer story published 

Robyn's story, photo of a woman sitting at her desk looking at her computer.

Everyone’s experience of cancer is different, but the support, comfort and connection we gain from sharing stories and experiences is powerful.

Robyn, in her tenth and final year of cancer treatment shares her experience with us. Read Robyn’s story.


Help develop a resource for gynaecological cancer nurses

Gynaecological cancer study: Optimising specialised nursing care. Illustration of a nurse in scrubs,

This project aims to create a helpful guide for specialised nurses caring for women with gynaecological cancers. Nurses and people who have experience of a gynaecological cancer diagnosis are invited to join an online focus group to provide their input.

Read more on this information sheet (includes a link to the online form).


18–24 March is Advance Care Planning Week

Two people sit with their arms linked. Banner overlay says 'share what matters most'.

Advance care planning helps to ensure that your loved ones and your doctors know your preferences for future health care. Find out why it’s important to organize a plan when you are healthy and how you can get the process started via the Advance Care Planning Australia website or watch our recorded webinar.


Have your say on the draft National Optimal Care Pathways (OCP) Framework 

White text on black: Have your say
White text on purple: Draft national optimal care pathways framework,
Australian Government seal in black on a white strip across the bottom.

This framework will assist health professionals and health services to deliver optimal care that is consistent, safe, high-quality, evidence-based and also culturally appropriate.

Visit the Cancer Australia Engagement Hub for full details.
Consultation will close on 8 April 2024.

Lymphoedema: what you need to know

March is Lymphoedema Awareness Month, so we are sharing information for people who have had treatment for cancer and may be at risk of developing this condition.

What is lymphoedema?

Lymphoedema is swelling (oedema) that occurs when fluid (lymph) builds up in tissues, under the skin, or sometimes more deeply in the chest, abdomen or neck. Your arms and legs are most commonly affected after cancer treatment.

When this swelling is caused by damage to the lymphatic system (for example, by surgery or radiotherapy), it is called secondary lymphoedema. In rare cases, people may develop primary lymphoedema, but we are only discussing secondary lymphoedema here.

What is the lymphatic system?

The lymphatic system protects the body against infection. It is made up of a network of fine tubes across the body. It carries lymph fluid from tissues and organs and takes this to lymph nodes. The lymph nodes filter the lymph fluid removing bacteria and viruses. Then the filtered lymph fluid passes out of the lymph nodes into the bloodstream.

Diagram of the lymphatic system showing the lympatic vessels spreading throughout the body bringing lymph from the limbs to the thoracic duct in the centre of the chest, above the heart.
SGUL lymres, CC BY-SA 4.0, via Wikimedia Commons

Who gets lymphoedema?

If the lymphatic system isn’t working properly, lymphoedema can occur at any time. For people diagnosed with cancer this can happen during initial treatment, after treatment is completed or when you’re in remission. It may develop if you’re experiencing advanced cancer. Usually it develops slowly, over many months or even years.

Lymphoedema affects 1 in 5 women after cancer. 
Source: Cancer Australia
Black text on light orange. Illustration of a woman sitting, wearing a compression sleeve on one arn.

 

More than one in 5 people with cancer develop lymphoedema to some degree. Most don’t and it depends on the type of cancer you have, where it is, what treatment you’ve had and other health conditions you experience.

Risk factors include (from the Cancer Council, 2023):

  • surgery that removes lymph nodes
  • radiation therapy that damages the lymphatic system (scarring and thickening the vessels so they’re not carrying the lymph fluid as well as before)
  • Taxane-based chemotherapy (speak with your oncologist about this association)
  • an infection in the limb where lymph nodes were removed/damaged
  • an injury to the lymphatic vessels
  • obesity
  • not being able to move around easily
  • rheumatoid arthritis
  • older age.

 

The table shows areas that may be affected by lymphoedema depending on the type of cancer:

Cancer type Commonly affected areas
Bladder Genitals and legs
Breast Arm, hand, breast, chest, trunk
Cervical Genitals and legs
Head and neck Face, below chin and/or neck
Melanoma Any part of the body such as face, neck, hand, forearm, upper arm or whole arm, breast and/or chest wall, legs
Ovarian Genitals, abdomen/trunk and legs
Uterine Legs
Vulvar/vaginal Genitals and legs

 

How do I know I have lymphoedema?

Diagnosing lymphoedema early gives you the best chance of reducing how it affects you.

Early signs include:

  • swelling that is soft to the touch and is usually not painful at first
  • swelling and a heavy or achy feeling in your arms or legs that may spread to your fingers and toes
  • swelling and a tight uncomfortable feeling on your face, neck, or under your chin
  • difficulty moving your head or neck
  • a dent when you press on the swollen area
  • tight watches, jewellery or clothes.

 

Warning signs of LYMPHOEDEMA include: 
* swelling, especially at night
* recurrent cellulitis
* area feels heavy or stiff.
Source: Australasian Lymphology Association. 
Black text on light teal. Illustration of a woman with moderate lymphoedema in her right leg.

 

Later signs include:

  • swelling that doesn’t go down after elevation (overnight)
  • swelling that is firmer and more difficult to dent
  • infection – cellulitis (redness, heat and pain) of the skin over the swollen area
  • nail changes to the affected limb.

 

What help can I get?

Treatment improves the lymphatic fluid’s flow through the affected area. This helps reduce swelling and improves the health of the swollen tissue. Reducing the swelling will lower your risk of infection, make movement easier and more comfortable, and improve your wellbeing. A range of health professionals may be involved in your care including a lymphoedema practitioner, your doctor, a podiatrist and dietitian.

Treatment can include:

  • skin care, especially preventing infection, including nail care
  • exercise, moving the affected area helps move the lymphatic fluid
  • maintaining a healthy weight
  • massage therapy (manual lymphatic drainage, if needed)
  • compression therapy (if advised).

 

Lentpjuve, CC BY-SA 4.0 https://creativecommons.org/licenses/by-sa/4.0, via Wikimedia Commons

If you talk to your doctor about getting a Management Plan, you can be referred to an Accredited Lymphoedema Practitioner and may be eligible for Medicare rebates for up to five sessions from approved allied health professionals. You can also ask your oncology team about what services are available.

 

More information

Australasian Lymphology Association (ALA) (lymphoedema.org.au) The ALA is a professional association for lymphoedema practitioners and those working in or interested in lymphoedema. Their website includes information and a look-up tool to help you find an accredited practitioner near you.

Lymphoedema Association Australia (www.lymphaustralia.org.au) The Lymphoedema Association provides information and support to people living with lymphoedema.

Counterpart webinar recording: Lymphoedema (recorded 6 March 23)

Counterpart webinar recording: Self care for lymphoedema (recorded 9 March 22)

Understanding Lymphoedema (cancervic.org.au) (Cancer Council Victoria)

Physiotherapy and Lymphoedema (headandneckcancer.org.au) Information about lymphoedema as a result of head and neck cancer.

Counterpart’s ovarian cancer Navigator: lymphoedema

Counterpart’s breast cancer Navigator: lymphoedema

What’s new – February 2024

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


February is Ovarian Cancer Awareness Month 

February Ovarian Cancer Awareness Month text and simple graphics in white and teal.

Every February, Counterpart joins others in acknowledging Ovarian Cancer Awareness Month. We support the important work others are doing to educate women about ovarian cancer.  We also use this time to talk about the support and information available to women living with ovarian cancer. Visit our Ovarian Cancer Awareness Month post for details.


New funding to improve metastatic cancer data collection

A collage of dozens black and white photos of women with the words 'I count too' overlaid.

Following advocacy from Breast Cancer Network Australia (BCNA), a new cancer data alliance will be established to improve routine collection of cancer stage and recurrence data.

This advocacy was initiated by BCNA after hearing their consumer representatives with metastatic breast cancer feel invisible due to inconsistent data collection across Australia.

Better data systems means researchers and policy makers will be able to understand how many individuals are living with metastatic breast cancer in Australia for the first time. This will support better care for individuals with this diagnosis, and will provide a way forward for other metastatic cancers.

Read the media release on the BCNA website.


Cancer Council Victoria LGBTQI+ resources updated

Closely cropped photo of two women stand side by side holding rainbow flags and smiling at each other. Text overlay says LGBTI+ people and cancer.

Discrimination and past negative experiences are common reasons why a cancer diagnosis may be challenging for LGBTQI+ people – lesbian, gay, bisexual, transgender, queer, and other diverse sexualities and genders, as well as people with intersex variations.

The Cancer Council Victoria LGBTQI+ webpage provides information on a range of topics, including talking to healthcare providers, cancer in trans and/or gender diverse people, and cancer in intersex people. You can also download or order a free 84-page LGBTQI+ People and Cancer booklet.

Visit LGBTQI+ people and cancer on the Cancer Council Victoria website.


Free VCCC Alliance webinar: Common sense oncology – outcomes that matter

VCCC Alliance logo Overcoming cancer together

Common sense oncology aims to prioritise patients’ needs, advocates for treatments that improve survival and quality-of-life, promotes informed decision making, and ensures these treatments are accessible to all patients. This webinar discusses the need to recalibrate cancer care and research.

View all details and register on the VCCC Alliance website.  


Consumers invited to have their say on genomic testing

VCCC Alliance logo Overcoming cancer together

The VCCC Alliance is gathering responses via a survey about accessing tumour genetic profiling from people who have received cancer treatment in Victoria. Genomics studies DNA errors causing cancer and its response to treatments. Tumor tests involve biopsies to analyse DNA, guiding treatment plans. This differs from genetic tests assessing inherited cancer risks. Genomic testing personalizes cancer care by targeting individual tumor characteristics.

Take the screening survey to see if you are eligible to take part in this study.


Selsus health professional webinars 

Selsus logo with webinar listings that include headshots of presenters and illegible information.

Cancer care 101, 12.30pm-2.30pm, Friday March 15 
Some of the key highlights: pathophysiology, common cancer treatments, trends, and evidence-based practices in cancer care from a health professional perspective and side effects. Visit Try booking for full details.

Managing cancer related fatigue, 3.00pm-5.00pm, Friday March 15.  Some of the key highlights: understanding cancer-related fatigue, evidence-based interventions, and patient centred care. Visit Try booking for full details.  


Webinar: Inclusive Health and Wellbeing Resources for *Women Over 50

In my prime: celebrating older women logo and Women's Health Victoria's logo. Both appear in black against an orange background.

Women’s Health Victoria is pleased to invite you to our upcoming webinar “Inclusive Health and Wellbeing Resources for *Women Over 50”, which will cover the importance of diversity and inclusion when developing resources that focus on women over 50.

Sharing our insights and reflections on the first six month of our initiative In My Prime, this insightful and interactive session will be held on Zoom and led by facilitator, writer, podcaster, researcher, and consultant Ruth De Souza.

The webinar will feature a panel of women sharing their professional and lived experiences from organisations including Transgender Victoria, Women with Disabilities Victoria, Monash University and Multicultural Centre for Women’s Health. 

Learn while you lunch and be a part of the conversation to support older women’s health.

Register to attend Inclusive Health and Wellbeing Resources for *Women Over 50

Ovarian Cancer Awareness Month is happening now

Every February, Counterpart joins others in acknowledging Ovarian Cancer Awareness Month. We support the important work others are doing to educate women about ovarian cancer. We also use this time to talk about the support and information available to women living with ovarian cancer.

Women supporting other women with cancer

When you have been diagnosed with cancer, sometimes you need to talk to someone who has been there. Our Peer Support Volunteers have all women with a lived experience of cancer. They also have been trained to listen and provide emotional or practical support. Depending on what you are looking for, they can help you find information or share what they and other women have found helpful.

Request a call from one of our volunteers.

May, a Counterpart volunteer, talks about how the service could have helped her mother, who also had ovarian cancer.

Other ways we support women with ovarian cancer

On our Webinar recordings page, you can watch videos of talks given by experts. These cover a lot of topics, including:

You might find our ovarian cancer Navigator helpful if you have been diagnosed with ovarian cancer. It can help you to find reliable, evidence-based information for each stage in the cancer experience (newly diagnosed, during treatment, after treatment, and if you have a recurrence). You can also get this information using our Counterpart Navigator app.

Know the symptoms

Ovarian cancer symptoms can be very vague. Many of the symptoms can also be caused by other conditions, especially in the early stages. This disease affects hundreds of women in Victoria each year. Still, many take a long time to get a diagnosis. That is why Ovarian Cancer Awareness Month is all about letting women know the symptoms.

Infographic with the symptoms of ovarian cancer displayed around a picture of a woman.
Text: Ovarian Cancer Symptoms: Fatigue/feeling lethargic; Abdominal or pelvic pain; Urinary changes such as frequency and urgency; Changes is bowel habits; Unexplained weight loss or weight gain; Abdominal bloating or increase in size; Appetite loss, feeling full quickly.

According to Cancer Australia, ovarian cancer symptoms can include:

  • feeling bloated
  • pain in your abdomen or pelvic area
  • loss of appetite, feeling full after eating small amounts, or indigestion
  • changes to your toilet habits, such as difficulty urinating, needing to go urgently, or changes in bowel habits
  • unexplained weight loss or gain
  • feeling tired for no reason.

You should speak to your doctor if you are concerned about any of these symptoms. Think about using Ovarian Cancer Australia’s symptom diary. This can help you keep track of symptoms and present them to your doctor.

Find more information

Exercise after cancer

Judy Sammut OAM is an exercise instructor with a lived experience of breast cancer. She is tireless advocate for exercise after cancer, and volunteered for Counterpart for nearly 20 years. In 2013, she was awarded with our inaugral Champion award in recognition of everything she has done for women with cancer. She has kindly shared the story of how she came to be involved in Counterpart.


Judy Sammut

In the beginning, Sue Lockwood declared, ‘I have a dream… we need a drop-in and resource centre for women with breast cancer’, and she sought support from those of us members of the Breast Cancer Action Group with experience in the ever-widening field of breast cancer. ‘Make a list’ she said, ‘of what you would like to see in this centre’.

Having run the gauntlet of breast cancer in 1992, which included a mastectomy and implant reconstruction, TRAM flap reconstruction followed by another mastectomy, followed by six months of chemotherapy, I reckon I’ve experienced many breast cancer challenges.

During the two-year recovery period I discovered the importance of specific exercises to stretch my chest wall, relieve the tightness that resulted from the axillary clearance, regain my range of movement and restore my damaged body to wellness. One of my sons, a physical education student, and I created a series of relevant exercises that provided the ideal recovery outcome.

I then discovered the YWCA Encore program, a land and warm water pool exercise program that was new to Australia, and I was so impressed with the huge benefits to breast cancer sufferers that I trained as one of the first groups of qualified instructors prior to it becoming a national program. I conducted these programs for 20 years.

A flyer in black printed on a light green with Feel Good written across the top in cursive font, and a photo of a woman stretching her arms above her head.
A 2007 flyer for the Feel Good Gentle Exercise program.

My experience led me to joining up with other driven women to improve the lack of services for breast cancer. So when Sue Lockwood said, ‘Make a list’, mine included, among the many other features available today at Counterpart, an exercise program, of course! Staff members Di Missen and Helen Shepherd undertook with enthusiasm many hours of research and hard work and the enormous task of breathing life into Sue’s dream, and then BreaCan became a reality. As the opening date for BreaCan approached, Sue said to me, ‘You wanted the exercise program – well go for it girl, it’s all yours.’ So what else could I do but say OK? But where were we to hold this program? And what do we call it?

It was decided that we’d try out the Feel Good Gentle Exercise Program on a fortnightly basis and following a slow start, the numbers increased noticeably – we had as many as 21 women at some sessions. More recent years have seen us provide a Stepping Into Wellness with many thanks to Teresa Amelio’s Pink Affair‘s generous funding a 6 week exercise program in many different suburbs.

Judy Sammut AM (right), with the Hon Mary Wooldridge MP, Minister for Mental Health and Community Services, after being awarded the inaugral BreaCan Champion Award in 2013.

Over the years many women have participated in the Feel Good and Stepping Into Wellness sessions while coping with the dreaded emotional and physical rigours of breast cancer. It has been very rewarding and gives me so much pleasure watching the camaraderie develop between them and the reassurance they feel of having appropriate exercises tailored to the limitations they experience following surgery. I love watching them move on, return to work, capture and restore their health and their lives, although sadly not all of them do.

I am privileged to be part of this unique service and watching as it continues to develop and expand under the professional and caring guidance of management and staff and, of course, the warmth of the empathetic volunteers.

What’s new – January 2024

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


Expanded listing on the PBS for ovarian cancer treatment

Recently, the Medicines Services Advisory Committee (MSAC) recommended the government subsidise two Homologous Recombination Deficiency (HRD) tests, expanding access to PARP inhibitors in ovarian cancer. The Pharmaceutical Benefits Advisory Committee (PBAC) followed suit, recommending subsidies for two PARP inhibitor medicines for this additional group. The first of these listings has now been formalised with another on track for confirmation in the coming months, paving the way for affordable and equitable treatment access.

Read more about this development on Ovarian Cancer Australia’s website


4 February is World Cancer Day

Create an event, spread the word, or take on the World Cancer Day 5km Challenge! These are just some of the ways you can get involved this World Cancer Day.

For more details visit the take action page of the World Cancer Day website.


The World Indigenous Cancer Conference 2024

The World Indigenous Cancer Conference 2024 presents an opportunity to bring key Indigenous cancer researchers, clinicians, advocates and community to Naarm (Melbourne), Australia. The conference will identify international research priorities, foster new collaboration, enhance capacity and share knowledge and information about Indigenous people living with cancer on a global scale.

The event is hosted by the Victorian Comprehensive Cancer Centre (VCCC) and will take place on 18–24 March at Pullman Melbourne on the park hotel. Visit the World Indigenous Cancer Conference website for full details.


Help deliver a national agenda to support Australia’s unpaid carers

The Department of Social Services are looking for experienced carers to help them develop the National Carer Strategy. The strategy will provide a framework for the coordination of carer policy across Commonwealth portfolios. If you have experience as a carer and would like to apply to be on the National Carer Strategy Advisory Committee visit the Engage website today. 

Applications close on Monday 29 January 2024. 


Nutritional support during cancer treatment webinar

Nutritional support can play a significant role in improving the overall quality of life for people living with cancer. Watch our recent webinar presented by Tanya Wells, an experienced Integrative Oncology Practitioner from Melbourne Integrative Oncology Group.

View the webinar on the Counterpart webinar recordings webpage here.


January is Cervical Cancer Awareness Month

Are you or someone close to you looking for reliable information, relevant to Australian women regarding cervical cancer? The Counterpart Navigator App has a whole section on cervical cancer and covers diagnosis, treatment, after treatment and recurrence. The Navigator can be accessed on the Counterpart website or by downloading the app onto your phone via the App Store or Google play.

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