Fellowship Fund

One of the biggest challenges with undertaking research is funding the actual work itself. 
It's not sexy, it's not particularly tangible, but it is vital to improving the lives of cancer survivors in the future.

The NCCS Fellowship Fund has been developed as a way of enabling philanthropic-minded individuals, families and businesses from across Australia to come together and fund the bright minds who are pioneering cancer survivorship research.
With your commitment, young researchers can gain greater insight to address the physical, emotional, and practical challenges faced by survivors of cancers. Our clinical team develop their projects around three specific research goals that align with gaps in cancer survivorship knowledge. The outcomes from our research underpins provision of best practice survivorship care, both nationally and globally, as well as influence policy and practice in care of cancer survivors. 
The NCCS is looking for Australian individuals, families and businesses to partner with us to help fund the crucial cancer survivorship research positions that will move us forward over the next few years. Contributions to our Fellowship Fund will support a Masters Scholar, a PhD Scholar and a Post-Doctoral Fellow. On average, both a Masters and PhD Scholar will spend three years completing their studies. To correlate with this, and to ensure some stability and continuity to their research, the NCCS intends to engage a Post-Doctoral Fellow for an initial period of three years also. 
We are looking to individuals, families and businesses who are willing to invest $1,000 or more annually, for three years. 
By directly supporting just one researcher through our Fellowship Fund, you can make a difference in the lives of thousands of people.
For more information, please download the NCCS Fellowship Fund proposal here and the accompanying pledge form here.
Alternatively, you can get in touch with our Executive Officer, Roshana Sultan.
     p. 02 9385 1390
     e. Roshana@unsw.edu.au 


"At first a felt a bit funny about talking to a lady about my problems after my cancer treatment, but my doctor is really nice and really understanding.  Plus she is an oncologist so she understands all the medical stuff that goes along with cancer treatment so I didn't have to explain things to her the way I did to my GP.  I felt like she really understood where I was coming from and gave me some good strategies to help with my issues.  And she wrote a care plan and sent a copy to my GP as well, so hopefully now when I go to see him he will feel like he is better able to treat me."

Anthony, prostate cancer survivor
"At 26 I was diagnosed with a rare form of ovarian cancer... having survived this (thanks to a great medical team), I ‘floundered’ for many years with the resulting impact of early menopause, fertility issues and general fatigue. Even worse, I felt extreme guilt that I should be able to overcome these issues easily as I survived when others didn’t, I really didn’t have the right to ever complain again. This impacted directly on my confidence, self esteem and identity. ……I am now 46, have 2 children, a partner, a career and a good life.  However, the struggle I had undergone, in pretty much isolation, has been hard.  Even friends and family who were great during treatment felt I should ‘just move on’.  The establishment of this centre is a great comfort as it shows there is now a greater awareness of cancer survivor issues to hopefully ensure better long term support for people who have had cancer."

Melinda, ovarian cancer survivor 
"I am aware of the National Centre for Cancer Survivorship and support them in their mission to find new and better ways to care for cancer survivors through research. With the high number of Australians now surviving cancer or living with ongoing cancer for many years, we need to better understand the health issues confronting this group and develop interventions to address their unique and often complex needs. As someone who has worked in the medical oncology setting for 20 years, I believe the National Centre for Cancer Survivorship is leading the way in this work."

Dr Elizabeth Hovey, MB BS FRACP MSC - Medical Oncologist, SESIAHS & UNSW, Prince of Wales Hospital
"As Director of the Kids Cancer Centre, Sydney Children’s Hospital and Professor of Paediatrics at the University of NSW, I have watched the development of the National Centre for Cancer Survivorship over the last few years. I strongly support the opportunity the Centre provides to bring together research focusing on survivors of childhood cancer with that focusing on adult survivors. In both areas it is clear that there are many unresolved challenges in understanding the health care needs of cancer survivors, and developing best practice interventions for both prevention and treatment of those problems. I believe wholeheartedly that the work that being undertaken through the Centre will benefit both kids and adult survivors people for many years to come."

Professor Glenn Marshall, AM, MB, BS, FRACP, MD Paediatric Haematologist & Oncologist, Director, Kids Cancer Centre, Sydney Children’s Hospital