Blog
Successful Employment Through Targeted Hiring: A Survivor Experience
What is Targeted Hiring?
Targeted hiring is a type of initiative used by public and private organizations to address employment barriers and help with the under-representation of designated groups to achieve equal employment opportunities. This is accomplished by narrowing the pool of candidates to specific categories of candidates, such as individuals with disabilities.
Q & A With a POGO School and Work Transitions Client
Q: What can you tell me about your recent interview where you were successful in being hired?
Client: I interviewed over the phone, which was nice as travelling can be difficult for me due to my disability. The questions were pretty much what I prepared for because my counsellor and I went through common interview questions and practiced them together over Zoom. We also discussed scenarios and did some mock interview style discussion. Because of this, I was able to answer the real interview questions with confidence.
Plus, the interviewers were very informative about what to expect on an average day.
Q: How is your employer being accommodating to you as a person with a disability in the workplace?
Client: The general attitude of my workplace is genuinely team-oriented! I was asked if I needed a chair, and from day one, I have been greatly encouraged to ask for help. There’s even mental health support, which is quite a relief.
Q: Was your POGO Counsellor a resource in this process? If so, how did they help?
Client: My counsellor was very helpful during the whole process. Finding this job and ensuring my resume was in good shape, practicing for the interview, and ensuring I got placed at a store location I preferred is honestly going above and beyond.
POGO Announces CEO Search
Message from POGO Board Chair James Scongack
The team at the Pediatric Oncology Group of Ontario (POGO), along with our many dedicated partners, continues to work as hard as we can every day to ensure everyone affected by childhood cancer has access to the best care and support. The organization has continued to make substantial progress in many areas and we are committed to building on this going forward.
This progress and passion doesn’t happen without strong leadership and dedication. Jill Ross has served as the CEO of POGO since 2018 and has been instrumental in this progress as a true champion and leader of this important work. Jill has informed us of her intention to step down as the CEO after a very successful tenure. Jill remains wholeheartedly committed to POGO’s mission, and to her ongoing work with you, our partners in childhood cancer care.
The Board has commenced a formal search process for Jill’s successor. This process is being led by a Board-appointed CEO Search Committee and we’ve retained Boyden, given their extensive experience in executive search and the health/not-for-profit sector, to advance this important process in a comprehensive manner. Following consultation and incorporating feedback from the Board, senior staff, partners and other stakeholders, the posting for this role has been made public and can be found here. Questions about the posting can be addressed to Boyden.
Through this process, we will take the time to ensure we find a CEO that meets the needs for the future of POGO and will update you when this process is completed.
In the meantime, it’s business as usual for POGO. We will continue the important work to move the organization forward, advancing the supports, engagement and actions to achieve an excellent childhood cancer care system for children, youth, survivors, and their families and healthcare teams, in Ontario and beyond.
POGO Statement on Childhood Cancer Awareness Month
September is Childhood Cancer Awareness Month and a time to raise awareness and express support for the children and youth with cancer, survivors of childhood cancer, and their families.
The burden of a childhood cancer diagnosis on families is immense, affecting them emotionally, socially, financially and countless other ways. In Ontario, from the time of diagnosis, childhood cancer patients have access to a coordinated system of care in leading hospitals across the province.
Pediatric Oncology Group of Ontario, POGO, is a made-in-Ontario solution, working in partnership with these hospitals and the Ontario government to help ensure everyone affected by childhood cancer has timely access to the best care and support.
This September, we acknowledge the children and youth in treatment or follow up care, the survivors of a childhood cancer diagnosis, the loved ones lost, and their families; and we are grateful to the many incredible organizations and multidisciplinary healthcare teams caring for them, and to those who provide other invaluable supports.
Watch the video statement from Premier Doug Ford, Health Minister Sylvia Jones and POGO Board Chair James Scongack.
Statement from Premier Doug Ford
“September is Childhood Cancer Awareness Month. Throughout this month I encourage everyone across Ontario to help raise awareness for this tragic disease that affects thousands of children and youth in our Province. Not only is cancer devastating to those diagnosed, it also deeply impacts their families in countless ways. I want children and youth, as well as their parents, siblings, friends and loved ones to know that they have a team Ontario on their side as they fight through this terrible disease. I want to thank the Pediatric Oncology Group of Ontario for their support in providing patients and survivors with world class care. I look forward to continued collaboration.”
Statement from Deputy Premier and Minister of Health Sylvia Jones
“This September, I want to recognize children and families across Ontario impacted by childhood cancer. September is a time to recognize the courageous children who are receiving or have received treatment and thank their families for staying strong through their treatment journey. Cancer touches so many lives and I want to thank the dedicated Pediatric Oncology Group of Ontario who advocates for patients and survivors through these difficult times. Our government will continue to work with you and our hospital partners to ensure children in Ontario have access to the care they need and deserve close to home.”
Statement from POGO Board Chair James Scongack
“Cancer is something that impacts us all, whether it’s ourselves our loved ones our family members, our friends, our neighbours or individuals in our community. At some point or another in all of our lives we will be impacted by cancer. September is Childhood Cancer Awareness Month in Ontario and throughout September it’s a really important opportunity for us as a province to come together to raise awareness around childhood cancer but most importantly come together as a province to do everything we can to be there for those kids and families who are battling childhood cancer. The partnership between the Pediatric Oncology Group of Ontario and the Ontario government and our entire hospital and pediatric oncology sector is a good example of how we can come together as a province and be there for families and kids not only today during Childhood Cancer Awareness Month but every single day of the year. I want to take this opportunity to send a very clear message to the families and kids that are battling childhood cancer, not only today but in the future, that we have your back; that we will continue to work as hard as we can every day to not only raise awareness but to continue to do better. Finally, I want to recognize the frontline healthcare professionals; you do incredible work. We’re proud of you and during September as Childhood Cancer Awareness Month, let’s not only think of the families who are challenged with childhood cancer and battling it today; let’s also thank those frontline workers who come to work every single day under extraordinary circumstances.”
French language Counsellor Builds Trust, Breaks Down Barriers
“I started my working life as a French teacher. From there, I worked for many years with the Ontario Autism Program as a consultant to the school boards helping students on the spectrum successfully transition to school. Last year I was hired by POGO to apply my professional advocacy skills to support brain tumour and childhood cancer survivors in achieving their school, work and life goals. Thanks to funding from the Slaight Family Foundation in 2021, Francophone survivor clients in the POGO School and Work Transitions Program can now receive care in their native language.”
Carol Perry, POGO School and Work Transitions Counsellor
Support to explain the complexities of being a young adult with cancer
The profile of a POGO Transitions client inherently makes communication complex. The age range of most of our clients tends to be from late teens to early twenties. It can be difficult for survivors to express the health difficulties that they have experienced on top of the regular challenges that come with becoming an adult. When you think about the difficult social, emotional and psychological issues survivors deal with, and their personal health challenges (physical and learning), the conversations they need to have with health professionals, colleagues and/or school staff can be very loaded, emotional and complex. Being able to express themselves and receive information in their mother tongue shows respect and helps us get to the root of their issues quicker. It also helps them feel more comfortable and at ease.
Help interpreting technical information critical for a successful future
Sometimes our POGO Transitions clients need an IEP (individual education plan: PEI en français) and unique accommodations to facilitate a smooth transition from high school to post-secondary education and work. A neuropsychological evaluation gives the big picture of a survivor’s cognitive and learning profile. It describes how their brain processes new and novel information, and it outlines their cognitive strengths and weaknesses. The information in the French neuropsychological report is technical and needs to be communicated to our Francophone clients’ French-speaking communities including, their families, school and workplaces. My ability to interpret and relay the information is an asset. I am also able to translate this critical information to unilingual English colleagues
“C’est important pour moi d’avoir une conseillère qui parle français pour que je puisse bien comprendre les stratégies qui me sont données. Ça rend les choses plus simples et plus faciles, ce qui est particulièrement utile lorsque je suis confrontée à de multiples défis.”
“It’s important for me to have a counsellor who speaks French so that I can better understand the strategies she is giving me. It simplifies things and makes it easier for me, which is particularly useful when I am facing multiple challenges.”
Justine is a brain tumour survivor who does well academically but experiences generalized fatigue. Her processing speed is slower because of the radiation treatment she experienced in 2020.
Making delicate conversations easier for students in cancer treatment
The Slaight Family funding helped launch a pilot project that allows me to work with teens who are transitioning from high school to post-secondary education while in active cancer treatment or palliative care. Interacting with these clients requires a different level of compassion, as patients and families face different challenges (including medical disabilities) and can be very emotional. These delicate conversations with Francophone families and school/university/college staff in their native tongue not only makes things simpler but is also a courtesy that these families deserve during a very difficult time in their lives.
Active listening and effective communication are central to every interaction with my clients. Communicating in the preferred language of my client builds trust and breaks down barriers. This also allows me the privilege to be a proactive advocate within the education system for clients and their families.
A grateful merci to the Slaight Family Foundation for supporting our services in French for our Francophone clients and their families.
The Options are Limitless When it Comes to Raising Money for Kids with Cancer!
Our third-party fundraisers have done some amazing things to raise money for childhood cancer care. Hosting an event in support of POGO is only limited by the extent of your imagination. You can throw a themed party, organize a competitive dodgeball tournament, cycle across Ontario, shave your head, create a team challenge at your office, even workout in your PJs to raise awareness about the unique issues young cancer patients face.
At POGO, third-party (individual, community, school and corporate) events are crucial to our annual fundraising goal. The funds you raise provide financial assistance to families so they can pay for out-of-pocket costs associated with their child’s treatment, support survivors with customized school and work counselling when their disease or its treatment has left them with learning challenges, and fund promising research that examines the impact of childhood cancer and its treatment.
Have an idea but don’t know how to get started? Our team and easy-to-use fundraising platform are here to help! We can brainstorm your vision to help maximize your recruitment/attendance/fundraising, and we have pledge forms, videos and marketing materials to help make your event a HUGE success.
Holding an event for POGO is a meaningful way to make a difference in the lives of children and youth with cancer, survivors and their families, and it can also be a fun way to engage your friends, family, classmates and colleagues.
What will you do?
Check out POGO’s easy-to-use fundraising platform for more ideas