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Sara Pot

Featured in: Favicon christiancourier.ca

Articles

  • Dec 11, 2024 | christiancourier.ca | Sara Pot

    What do you want for Christmas? I remember this question from my childhood, part of recess-time chatter. In January, the question would shift: What did you get for Christmas? In my family, we’d make a big deal of writing our names on a piece of paper and then each choosing a name randomly, meaning we were to buy one gift for just one person in our family.

  • Nov 25, 2024 | christiancourier.ca | Sara Pot

    “The volcano room will be here.”The architect indicated the spot with his cursor on the shared screen and continued describing the blueprint for what will be a children’s hospice home in Dundas, Ontario. I was part of a Zoom call with others who were invited to offer feedback in the design stage. The children’s hospice home will be called Keaton’s House – Paul Paletta Children’s Hospice, inspired by the life of a young boy named Keaton who died at seven years of age from stage 4 Rhabdomyosarcoma.

  • Oct 23, 2024 | christiancourier.ca | Sara Pot

    In 1998, I was teaching middle school students in Minnesota. I wasn’t aware that Australian sociologist Judy Singer and American journalist Harvey Blume were discussing the idea of individual differences in brain variation and neurodiversity. What I did know at that time was Parker Palmer’s book The Courage to Teach.

  • Sep 2, 2024 | christiancourier.ca | Sara Pot

    When I started my post-secondary schooling You Can’t Say ‘You Can’t Play’, written by Vivian Gussin Paley, was on the syllabus for my first education class. Paley was an American primary school teacher and early childhood education researcher who took a special interest in observing the non-directed experiences in the classroom and the corresponding conversations that took place among small children.

  • Jul 22, 2024 | christiancourier.ca | Sara Pot

    Back in May of this year, journalist Meagan Gillmore wrote the article “What one man needed for a second chance at life.” The story features an update on Michal Kaliszan, an individual born with spinal muscular atrophy (SMA). Michal first caught public attention through his GoFundMe campaign in 2022 when he tried to raise money for his own home care. SMA is a rare genetic condition in which the muscles throughout the body weaken over time.

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