Improving your research
We can help you to improve your research (proposal) by incorporating and/or feedback on the patients’ perspective of your research, from start to finish.
The Women’s cancers research theme greatly values the partnership with patients. We formed a patient advisory board (PAB) at the start of our theme, and since then it has resulted in a meaningful and successful cooperation, providing valuable insight into the patient experience. We consider our patients as important partners in various aspects of research, and are actively exploring different ways to involve patients in our research strategy. These patient volunteers are equipped to participate in the PAB, attending training courses, meetings, and conferences. PAB members are very willing to further professionalize and actively participate in the 6-monthly Research Rounds (seminar sessions) of the theme.
Theme researchers have the opportunity to discuss project ideas with PAB members, and get their advice in the early stage of writing grant applications. At the same time, PAB members get an overview of the research being performed in our theme by setting up meetings with junior researchers every 6 weeks.
In the coming years the procedures for reflection and advice will become more systematic and professional in accordance with the standards as set by, for example, the Dutch Cancer Society (KWF). To obtain grants, it is also important to involve patients in your research proposal.
How to involve patients in your research?
- Share research ideas
It is important to involve the PAB as early as possible in the research process. Also if your research idea is not yet concrete! At start you can plan a meeting to get to know each other.
- Project proposal
PAB members can comment on (the summary of) your grant proposal, focusing on the clarity of the proposal for ‘non-medics’, the consequences of the research for the patients in the research and benefiting from the research, and the attention to patient participation.
- Interim feedback on current research
The PAB would like to stay informed about the state of affairs. Especially when the process/results involve a different view on the patients’ perspective/interests.
- Completed research
What happens after the research has been completed? Was the research considered successful? Why (not)? What did you learn; in general, but also considering the patients’ perspective? To reflect on this together, means we can learn from each other, which is important for future developments. Does the project lead to follow-up research questions?
Patient members and their stories
- Geralda's story
I am Geralda Brus, I work as an administrative assistant at Webton. At the age of 35 I went to the doctor because I felt a lump in my chest. In the hospital in Hengelo breast cancer was detected with metastasis in the axillary nodes. A mastectomy and removal of axillary nodes followed. Of the 36 glands, 26 glands were affected. Further treatment consisted of first 6 TAC chemotherapy and then 25 more in the hospital in Enschede.
As far as I knew, there was no breast cancer in our family. On my father’s side, other types of cancer did occur. My father had already had prostate cancer. Because I was so young, I was eligible for hereditary research. For this research I had to go to the Radboudumc. At the beginning of 2007 I received the results of the hereditary research and I was found to be a carrier of the BRCA1 gene mutation. In June 2007 I therefore preventively removed my other breast, my ovaries and my uterus in Hengelo, and immediately a reconstruction of both breasts was performed.
After the results of the heredity test, my parents and 2 sisters were also tested. My father and both sisters also have a BRCA1 gene mutation. My youngest sister has undergone a preventive breast surgery with direct reconstruction after the birth of her youngest child. Later she had her ovaries removed. My other sister wanted children and therefore did not opt for preventive operations, but she was under control. To make a long story short, she was operated during her pregnancy and treated for breast cancer in the Radboudumc. After the birth of my niece, she also preventively removed her other breast and ovaries.
Bad luck aside, we have had a lot of luck in our family. We are all there! I realize very well that a number of years ago, we probably would not have survived this disease. Thanks to medical science, great doctors and researchers, we survived cancer. I am very grateful for this. By participating in the Patient Advisory Board of the research theme Women’s Cancers, I hope to make a small contribution to cancer research and I hope that I can do a little bit for medical science. I also hope that in this way I will help other people who will have to deal with cancer in the future.
- Claudia's story
I am Claudia Soede, I have been working at the Radboud campus since 2000: first as a researcher at the Radboudumc (prostate cancer research 2000-2002), then as a researcher at Radboud University (rheumatism research 2002- 2007) and since 2007 as a grant advisor at the Radboudumc.
I knew the Radboudumc practically solely as an employee, until in November 2015 (at the age of 46 years) a nodule in my breast turned out to be a tumor, which had also spread to my armpit glands. After intensive treatment (chemotherapy, surgery and radiotherapy), I had enough energy to gradually pick up my work again during radiotherapy sessions. Something that really helped me with my recovery. After the radiotherapy I had hormone therapy for another 7 years.
In the summer of 2016, I was approached by a researcher if I wanted to take part in the Patient Advisory Board of the research theme Women’s Cancers, because at the time there were not many women with a breast cancer past in the PAB. After having gathered more information, I agreed. From both my perspective as a patient and as a grant advisor, I hope to make a positive contribution to (funding) cancer research.
- Nicoline's story
I am Nicoline Soede, I work with great pleasure as an associate professor at Wageningen University. In 2014, when I was 50 years of age, I had what appeared to be an easy removable myoma, but turned out to be ovarian cancer with metastases. Fortunately, the chemo worked well (hospital Gelderse Vallei in Ede) and the debulking operation (Radboudumc) was successful although a metastasis was found in my head in August 2016. However, the metastasis was also successfully removed (UMC-Utrecht) and no further signs of the cancer have appeared.
In March 2017 I attended a meeting of the Radboud Research Round of the research theme Women’s Cancer. I did not have to think twice about my participation in the Patient Advisory Board of the research theme Women’s Cancers; it combines my interest in research with the ability to mean something for future patients. An important role of the board is assessing new research proposals from the patient perspective; is there, for example, attention to the burden of research for the participants? Does the research contribute to a better quality of life? Fortunately, we also get the opportunity to take courses to be able to do that assessment properly and we are regularly updated about current research. Interesting and informative!
- Bouwien's story
I am Bouwien Oosting, I have worked as a social worker in which I specialized in mourning and loss counseling. I stopped working in 2017 when womb cancer was diagnosed with metastasis in the lymph nodes.
After surgery at the Radboudumc, chemotherapy and radiation therapy followed. During this entire process I experienced the importance of being in control of my disease process and my quality of life. Good communication with doctors and nurses is essential, but unfortunately this is not always obvious. Therefore I've joined the Patient Advisory Board of the research theme Women’s Cancers.
Doorlene van Tienoven
- Doorlene's story
I am Doorleene van Tienoven, I have been working as an analyst in the laboratory at the Radboudumc for quite a few years. When an innocent-seeming cyst turned out to be breast cancer in October 2014, I got to know the Radboudumc as a patient.
An intensive treatment program followed until April 2016. Where I thought beforehand that a lot would not be possible, partly due to the many research studies for the treatment of breast cancer, it has become a time in which I have been able to do a lot.
Then, in June, when the question came whether I would be interested in participating in the Patient Advisory Board of the research theme Women’s Cancers, I didn’t have to think twice. I wanted to look forward again after all that had happened and participating in the PAB was perhaps the way to do something in a positive way with all the experiences unintentionally made richer. By attending meetings, thinking about a research choice or, for example, assessing research proposals, I hope to contribute to cancer research through the PAB.
- Ineke's story
I am Ineke Runneboom. In February 2002, I was diagnosed with breast cancer at the age of 31 and a year later I was told that I have the BRCA1 gene mutation. This was not a complete surprise to me because several of my family members have been diagnosed with breast cancer at a young age.
In 2015, I was approached to take part in the Patient Advisory Board of the research theme Women’s Cancers. I have been appointed as the chairman of this board. I find it interesting to be in conversation with researchers and doctors together with other experience experts. This is to contribute to research and communication between doctors and patients from my own expertise.
- Patricia's story
I am Patricia Evers, I work as a carer in community care. I also work in a residential care center for the elderly, where well-being is my official focus of attention and where I am also coordinator of the volunteers. Through my work I regularly come into contact with women who have cancer or are cured from cancer. I see what an impact this has on their well-being but also what this means for their loved ones.
In August 2016, I was diagnosed with cancer for the first time. I had a melanoma on my right arm (stage 1b.) Shortly after that operation I was told for the second time that I needed surgery and this time it was vulva cancer. I myself had never heard of this rare form of cancer and neither had many people in my area. Partly due to research, I have been fortunate that my quality of life is good and that I am not physically restricted by my illness. I am very grateful to science and my doctor!
Through my participation in the Patient Advisory Board of the research theme Women’s Cancers, I hope and wish to make a difference for other women for their well-being and life expectancy. I want to share my own experiences with vulva cancer. I would also like to see more awareness of this form of cancer, unfortunately many women are still ignorant.