Our Team

The Red Blood Cell Disorders Hub’s Editorial Committee is made up of patients and healthcare workers. We have common goals of creating a place to share experiences, provide a hub for resources, and build community.

THE RBCD HUB // ABOUT // OUR TEAM

  • Vanessa Ferguson

    SHE/HER

    Vanessa Ferguson is a Health Policy & Health Equity Ph.D. student at York University living with Sickle Cell Disease (SCD). Through her research, Vanessa aims to unveil and challenge both new and old barriers to adequate and deserved care for Black and other racialized people living with SCD.

  • Sogand Jalali-AD

    SHE/HER

    TMU journalism graduate.

  • Bethany Morris

    SHE/HER

    Bethany is 30 years old. In her spare time, she enjoys listening to music and doing word searches. Bethany has her ECE Diploma and BA in Sociology. Bethany also enjoys working out and going to dinner with her friends. Bethany blogs about living with sickle cell disease at The Banana Shaped Blood Cell.

  • Sinthu Srikanthan

    SHE/HER

    Sinthu is a social worker in the Red Blood Disorders Clinic. She is passionate about supporting and advocating on behalf of people with Sickle Cell Disease, Thalassemia, and other hemoglobinopathies using Anti-Racist and social justice frameworks. Outside of work, Sinthu really enjoys watching musicals and theatre. Some of Sinthu’s hobbies and interests include learning how to play the guitar, reading sociology, writing, and spending time with friends.

  • Shirin Taki

    SHE/HER

    Shirin was diagnosed with Beta Thalassemia at six months. She was a patient at the Hospital for Sick Children up until the age of 18, after which she transferred to the Toronto General Hospital. Shirin receives monthly blood transfusions. Her hobbies include playing volleyball and softball, listening to podcasts, and spending time with friends. Shirin is a Registered Nurse and is working in Business Development with Salesforce (Health Care and Life Sciences). Shirin is also pursuing a Master’s of Business Administration. Finally, Shirin sits on the Board of Directors for the Thalassemia Foundation of Canada.

  • James Bradley

    HE/HIM

    James is the transition navigator with the Hemoglobinopathy program working between the Hospital for Sick Children and Toronto General Hospital. He supports adolescents and young adults with hemoglobinopathies with their transition from pediatric to adult care including transition readiness, psychosocial support, resource navigation, goal setting, and ensuring a seamless overall transition to adult care.

    James graduated from the University of British Columbia Master of Occupational Therapy program in 2013.

  • Colleen Johnson

    SHE/HER

    Colleen was a nurse practitioner with the Red Blood Cell Disorders for 10 years and will be retired by the end of 2022. She will continue to donate her time to the RBCD Hub, as needed.

  • Oluwayemisi Abatan

    SHE/HER

    Oluwayemisi is a trained nurse in Nigeria who has suffered and survived devastating consequences of sickle cell disease. Her goal is to become licenced to practice as a nurse in Canada and help other sickle cell anemia patients to accomplish their goals and desires in life.

  • Pratip Aditya

    HE/HIM

    Pratip is a Customer Success Manager working for a Boston based startup called solo.io. He has an MBA in Information Management and an engineering degree in Computer Science. He has been working for over 8 years in different management and business-oriented roles in India and recently moved to Toronto. He takes a keen interest in history, philosophy and finance. He's passionate about supporting and advocating for thalassemia patients and inclusive healthcare without barriers.

  • Kathy Raufi

    SHE/HER

    Kathy Raufi is a Registered Psychotherapist and a Canadian Certified Counsellor. She graduated with a Bachelor of Science and a Masters in Counselling Psychology from the University of Toronto. Kathy has been a counsellor in post-secondary for over 15 years in Toronto and Ottawa. She has worked closely with young/mid age adults in the areas of Accessibility, Mental Health, and Career Counselling. Kathy continues to work as a patient advocate in the Thalassemia community, as a speaker, writer, and a contributing member of the Patient Working Group for the Red Blood Cell Disorders Hub at TGH. Kathy welcomes new connections with others, across the globe. Kathy enjoys time with her family, pilates, and the outdoors. You can follow Kathy’s writing on the Blog here!

I want to join the Editorial Committee!

At this time, we are inviting patients of the University Health Network’s RBCD Clinic to participate in the Hub’s Editorial Team. You can speak with any member of your RBCD care team to get connected.

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