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DTSTART;TZID=America/Vancouver:20260111T130000
DTEND;TZID=America/Vancouver:20260111T150000
DTSTAMP:20260427T064824
CREATED:20250820T181023Z
LAST-MODIFIED:20251215T182746Z
UID:16215-1768136400-1768143600@cassieandfriends.ca
SUMMARY:Workshop on Writing Effective Scholarship and Bursary Applications
DESCRIPTION:We’re back for part 2! \nCassie + Friends’ youth mentors are back with another workshop for students\, this time about how to write effective scholarship and bursary applications! \nLed by youth mentor\, Ciara Mahaffy (who secured $85\,000+ in scholarships!) and other scholarship recipients\, this session will teach you how to: \n\nUse storytelling\, tone\, and structure to craft stronger applications\nCommunicate your personal story with confidence and professionalism\nApply proven techniques and insider tips from high-achieving applicants\nUnderstand what scholarship committees actually look for\n\nJoin us for part 2 of this FREE online workshop on January 11 at 1 p.m. PST. \nSign up now for the online workshop here! \nRegister here!Ciara Mahaffy is a Cassie + Friends Youth Mentor and a high-achieving student who has secured over $85\,000 in scholarships. She was Valedictorian at the University of Toronto and has served as an application assessor for university programs\, giving her an insider perspective on what makes applications stand out. \nCiara is passionate about helping students tell their personal stories effectively\, and she’s here to share her step-by-step approach to writing compelling scholarship and bursary applications. She knows how to turn application stress into confidence and clarity\, and she’ll provide practical tips to help you showcase your achievements and experiences with professionalism and authenticity.
URL:https://cassieandfriends.ca/event/scholarshipwriting/
LOCATION:Zoom
CATEGORIES:Virtual Education,Youth Leader Network,Youth Mentorship Program
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BEGIN:VEVENT
DTSTART;TZID=America/Vancouver:20250318T160000
DTEND;TZID=America/Vancouver:20250318T173000
DTSTAMP:20260427T064824
CREATED:20250207T223917Z
LAST-MODIFIED:20250219T001254Z
UID:15507-1742313600-1742319000@cassieandfriends.ca
SUMMARY:YMP WORD Day Event: Sharing Your Diagnosis with Friends - Let's Talk About It!
DESCRIPTION:Talking about your rheumatic disease with friends can be tough – but you’re not alone and C+F youth mentors can help! This WORD Day (March 18th at 4pm PST / 7pm EST)\, join us for a real talk on having conversations about your diagnosis. Whether you’ve never told anyone or want to get better at explaining it\, this is a safe\, no-pressure space to connect\, share\, and learn from others who’ve been there. \nWhat to Expect:\n• Hear from YMP mentors who will share their own experiences of deciding when (and how) to open up about their diagnosis.\n• Be a part of an open discussion on the challenges of sharing and the reactions you might get.\n• Get tips & advice on how to start the conversation with friends\, classmates\, and even teachers.\n• Learn more about our 1-1 youth mentorship opportunities where you can continue chatting through topics like this one in a supportive space. \nLet’s talk it out together and help spread the WORD about childhood rheumatic disease.If you’re between the ages of 12-26 and living with a rheumatic disease\, be sure to register here today! 💙💚
URL:https://cassieandfriends.ca/event/ymp-word-day-event-sharing-your-diagnosis-with-friends/
LOCATION:Zoom
CATEGORIES:JA2025Youth,TAG,Youth Leader Network,Youth Mentorship Program
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DTSTART;TZID=America/Vancouver:20240815T150000
DTEND;TZID=America/Vancouver:20240815T170000
DTSTAMP:20260427T064824
CREATED:20240729T212242Z
LAST-MODIFIED:20240730T132549Z
UID:14223-1723734000-1723741200@cassieandfriends.ca
SUMMARY:Summer Refresher
DESCRIPTION:Cassie + Friends Summer Refresher Youth Event We’re so excited to be back with another Youth Mentorship Connection Event\, this time with a summer twist! \nGrab your favourite summer drink and join us for a casual online get-together where we’ll swap summer stories\, share fall plans and chat about anything that’s on your mind. \nOur Youth Mentorship Connection Events (for youth ages 12-26 living with childhood rheumatic diseases)\, are a relaxed environment where you can meet our incredible Youth Mentors\, connect with others who truly understand what it’s like like to navigate a rheumatic disease\, and chat about a variety of topics — all while enjoying a chill atmosphere. \nWe can’t wait to see you there – August 15 at 3 pm PST / 6 pm EST. \nREGISTER HERE!This is a C+F Youth Mentorship Program Event\, learn more about the program here.\n 
URL:https://cassieandfriends.ca/event/summer-refresher/
LOCATION:Zoom
CATEGORIES:Youth Leader Network,Youth Mentorship Program
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Vancouver:20240215T160000
DTEND;TZID=America/Vancouver:20240215T170000
DTSTAMP:20260427T064824
CREATED:20240111T183521Z
LAST-MODIFIED:20240613T180509Z
UID:12752-1708012800-1708016400@cassieandfriends.ca
SUMMARY:Cocoa Connect Night: A Youth Mentorship Event
DESCRIPTION:Welcome to our first Cocoa & Connection Night!\nIt can feel isolating to be a youth with JIA\, Lupus or any other rheumatic disease. At times\, it can be difficult to relate to your peers\, and it’s easy to feel misunderstood.  \nThat’s why we’re hosting a Cocoa & Connection Event\, on February 15th\, from 4-5 pm PST. \nPart of our Youth Mentorship program\, we hope you’ll join us for a chance to get to know other youth in our community\, including our very own mentors – over a cup of  hot chocolate. \nThis is a pressure-free way to get comfy\, and get connected to youth who know what you are going through.  \nRegister Today! \nGround Rules: \n\nBe respectful. Inappropriate language or harassment of any kind will not be tolerated and will result in your removal from the event.\nKeep the information shared by mentees\, mentors and staff confidential (i.e. diagnosis\, medical history etc.).\nMust be a teen or young adults with pediatric rheumatic diseases ages 13-22
URL:https://cassieandfriends.ca/event/cocoaconnectnight/
LOCATION:Zoom
CATEGORIES:Youth Leader Network,Youth Mentorship Program
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DTSTART;TZID=America/Vancouver:20230513T110000
DTEND;TZID=America/Vancouver:20230513T130000
DTSTAMP:20260427T064824
CREATED:20230329T230158Z
LAST-MODIFIED:20230512T204700Z
UID:10765-1683975600-1683982800@cassieandfriends.ca
SUMMARY:Cassie + Friends Presents The Future Leaders Showcase
DESCRIPTION:Register Today!\nGet ready to witness an inspiring display of passion\, leadership and hard work at the C+F Future Leaders Showcase – the highly-anticipated finale of the 2022-23 Youth Ambassador program cohort. \nIn 2022\, six exceptional youth/young adults joined the C+F Youth Ambassador Program with their own innovative project ideas aimed at strengthening the juvenile arthritis and other rheumatic diseases community. After a year of dedicated effort\, our Ambassadors have not only sharpened their skills but have also engaged with the community and are now eager to present their progress to you! \nJoin us to hear from community and medical partners about the importance of cultivating future leaders and the impact they can have on our communities. And\, of course\, our Youth Ambassadors will take the stage to showcase their special projects and discuss their next steps. As our esteemed panel of judges provides them with valuable feedback and suggestions\, the stage will be set for selecting the “2023 C+F Youth Ambassador of the Year”! \nLet’s come together to celebrate our Future Leaders and their unwavering passion for the juvenile arthritis and other rheumatic disease community. We can’t wait to see you there. Register here. \nGet to Know our 2022/23 Future Leaders:Sophie FinnChelsea WoolfMatthew SholdiceCiara MahaffyMaryse HendiAlejandra Van DusenSophie Finn\n \nMeet Sophie Finn! \nSophie is a grade 12 student living in Langley\, BC\, and was diagnosed with juvenile dermatomyositis (JDM) – a rare rheumatic disease – in 2017. \nSophie enjoys being engaged in her community; in addition to being a 2022/23 C+F Youth Ambassador\, she also serves as president of her high school’s graduation committee\, is on two leadership committees\, and coaches kids’ soccer (Sophie herself has 10 years of soccer experience under her belt). Sophie is currently working on her university applications and plans to study business or political science which she feels are aligned with her desire to both continue learning and serve as a leader in her community. \nHer work within the Youth Ambassador Program: \nSophie’s project will involve creating resources and tools for newly diagnosed families specifically in the area of preparing for treatment and medication. A component of this work includes organizing a Newly Diagnosed Webinar for spring 2023 alongside medical professionals\, parent/patient leaders and C+F staff. Keep an eye out for session details coming soon! \nSophie hopes her project will positively impact newly diagnosed families and help them to gain the skills and knowledge to prepare for what was the scariest time in her own medical journey. She is grateful for the opportunity to share her story! \nChelsea Woolf\n \nMeet Chelsea Woolf! \nChelsea has a love for medicine and is devoted to learning more about why and how the body works the way it does. \nChelsea was born in Calgary\, Alberta\, and currently lives in Edmonton where she works as a paramedic. She has also served as a medic in the energy sector and completed firefighter training this past June. She is passionate about supporting people through their healthcare journey and advocating for resources to empower everyone to access the knowledge they need to live healthy lives. Outside of work\, Chelsea loves to ski and sing! \nChelsea became involved with Cassie + Friends when she was 18 when she joined a research group studying the experience of transiting from pediatric to adult rheumatology care. She also presented her story as a youth panelist at the 2021 C+F Virtual Transition Fair. \nHer work within the Youth Ambassador Program: \nUpon reflecting on her experience as a child navigating JA\, Chelsea realized there was a lack of kid-friend information and resources that could help her understand her diagnosis and what was happening inside her body. She remembers going to rheumatology appointments\, eye doctors\, and physical therapists and getting bloodwork done but never understanding why. While talking to her Dad about the opportunity to submit a project idea to the C+F Youth Ambassador program\, he mentioned that he also found it difficult to explain ger JA and the medication world that she now belonged to her as a child which in turn caused stressed and anxiety for the whole family. \nTo fill this gap\, Chelsea project aims to equip parents and kids with a tool that explains the JA journey in an age-appropriate way and enables them to prepare for what is yet to come. Chelsea hopes this book will become widely available for children throughout Canada upon diagnosis and will lead to more books on other rheumatic diseases. \nThe most important part of the project for Chelsea is emphasizing to children that chronic does not mean incapable – her vision is for the book to carry an optimistic voice that both empowers and educates. \nMatthew Sholdice\nMeet Matthew Sholdice! \nMatthew was born and raised in London\, Ontario\, and currently attends McMaster University in Hamilton\, where he studies Health Sciences. Matthew enjoys staying active and watching Netflix when not in school or working. Matthew is a black belt in goju ryu karate and has played volleyball\, hockey\, and soccer! \nHe is a committed advocate for the childhood rheumatic disease community and an active volunteer in both youth-focused and research initiatives. His career goal: to become a rheumatologist and complement his practice with his own lived experience. In the meantime\, he is passionate about creating resources that extend beyond treatment and medication outside of the doctor’s office (i.e. nutrition and yoga classes). \nMatthew first got involved with the community as a camper and then counselor at camp Cambria (later Camp Ontario)\, a camp for kids ages 8-17 diagnosed with rheumatic disease\, where he has also formed lifelong friendships. Matthew also works for The Take a Pain Check Foundation as an outreach coordinator. \nMatthew initially became involved with Cassie + Friends when his rheumatologist passed along a survey from the organization asking for feedback on what makes a good mentorship program. This further fueled his already existing interest in their organization and led him to reach out. Since then\, he’s participated in several youth-focused sessions and share his own story on the C+F website (which you can read here and includes his own thoughts on transitioning to adult care). Now\, Matthew is acting as a Youth Ambassador for Cassie + Friends and getting the chance to create his own project. \nHis work within the Youth Ambassador Program: \nMatthew’s project was inspired by his time volunteering for a program called Project Thrive in Ontario. Project Thrive worked with newly diagnosed families and organized events where they could learn from and connect with other families. Parents had the opportunity to chat with healthcare professionals and\, at the same time\, the kids participated in an activity aimed at learning life skills specific and vital to rheumatic diseases. Unfortunately\, despite the adults saying how valuable this program was\, the program is no longer available. \nMatthew hopes to carry this torch and continue the work with his own spin and experiences; therefore his project is to create a similar event that gives newly diagnosed families the opportunity to join the community and learn about rheumatic diseases. \nIf you live in Ontario\, keep an eye out for event information related to Matthew’s project! \nCiara Mahaffy\n \nMeet Ciara Mahaffy! \nCiara is an ambitious and proactive member of her community – wherever that might be and whatever that might require! Ciara lives in Vancouver\, BC\, and is currently studying in Toronto at the University of Toronto. Some of Ciara’s main interests include acting\, English literature\, dancing\, and singing. \nCiara is completing two majors\, one in English literature and one in dramatic literature. She is also working on a minor in creative expression and society. While attending university\, Ciara has become deeply ingrained in her campus community. She is a co-president of the Trinity College Dramatic Society\, a choreographer for a UofT dance club\, a dramaturg for a production with the UofT college St. Mikes\, and a member of the intramurals ultimate frisbee team. Ciara is also a mentor for a specialized first-year program and was an orientation leader for incoming freshmen. In addition\, this year\, she started a new club at UofT directly connected to her Youth Ambassador project! \nCiara was first introduced to Cassie + Friends when she was initially diagnosed but did not become directly involved until 2020. Ciara started by joining their Teen Arthritis + Autoinflammatory Groups (TAG) and attending their virtual education sessions. In 2022\, Ciara also worked as a summer student at Cassie + Friends and organized several projects and fundraisers include the Team C+F Runs and BC Raffle. You can read more about Ciara here. \nHer work within the Youth Ambassador Program: \nCiara’s project aims to raise awareness about the lack of understanding JA when it comes to peers and educators. When assessing her university community at-large\, she noticed that this lack of empathy for those with rheumatic diseases and other chronic illnesses and/or disabilities is far too common. Ciara strongly believes this comes from a lack of knowledge of rheumatic diseases and how they affect the individual rather than a lack of general empathy and kindness. Ciara proposed that if her peers had more knowledge of rheumatic diseases\, they would be better equipped to support those with a rheumatic disease\, like herself. \nTo address this concern\, Ciara’s project aims to make the campus more inclusive and supportive by establishing a student club called the UofT Rheumatic Disease Awareness and Action Organization. The club will provide education and connection opportunities for the campus\, allowing them to learn more about rheumatic disease\, as well as give those living with rheumatic disease the chance to interact with each other. The club will also organize fundraisers in support of Cassie + Friends. \nCiara envisions that project will raise awareness and understanding of invisible/less visible struggles and credits Cassie + Friends as a source that helped her understand more about her disease. She hopes she can do the same for her new community! \nMaryse Hendi\n \nMeet Maryse Hendi! \nMaryse loves to do fiber art like crocheting and needle felting – enjoying the meticulous nature of making 3D art! As a student\, she is currently attending the University of Calgary (UofC)\, majoring in sociology and minoring in health and society. Her choice of study is largely rooted in her own diagnosis and experiences within healthcare. \nMaryse has had many ups and many downs throughout her medical journey and is passionate about contributing to solutions that better overall experiences for everyone. She is enthusiastic about sharing her story of navigating Lupus in hopes that it can help others. Although unsure of her future career\, she generally hopes to have a career where she can positively impact the lives of young children dealing with illness. \nMaryse is already starting to help people where she can. She is the president of The Invisible Disability Education and Advocacy Association (IDEAA) at the U of C\, which supports awareness of invisible disabilities. The club promotes education and advocacy for all invisible disabilities and has raised funds for various organizations. The club’s goal is to encourage open conversations about invisible disabilities and their impact. \nAnother way she is helping her community is through Cassie + Friends. In 2020\, by coincidence\, Maryse connected with a Cassie + Friends employee at an event who encouraged her to join the community. Since then\, Maryse has been involved with various programs\, volunteered for events and runs\, and provided two blog posts. Learn more about Maryse here and here. \nMore recently\, Maryse attended the C+F Youth Vision Session event\, where individuals were invited to discuss solutions to positively transform the lives of youths with rheumatic diseases. Maryse mentioned during the event that it would be valuable to have a place that compiled information for pediatric lupus. Later that year\, Maryse applied for the Youth Ambassador program using that same project idea\, and got into the program! \nHer work with the Youth Ambassador Program: \nMaryse’s project is a continuation of this initial brainstorming idea and is based on her experiences trying to find credible pediatric lupus information to little or no avail. As a child diagnosed with lupus\, Maryse remembers her and her parents being overwhelmed with how easy it was to end up on a website with scary or unreliable sources. In addition\, the information was written for adult lupus – not childhood lupus\, leaving her feeling in the dark. \nTo address this gap\, Maryse wants to create a digital hub on the C+F website where families can easily find and access reliable pediatric lupus information.  Working alongside healthcare professionals\, this new resource will be medically vetted and easy to read and understand empowering both parents and kids to take control of their healthcare journey. \nAlejandra Van Dusen\nMeet Alejandra Van Dusen! \nAlejandra lives in Regina\, Saskatchewan\, where she is an active member of her community. As a student\, she attends the University of Regina and is working towards a Bachelor of Health Studies degree. Her desire to study in this area comes from her life experience in the health system\, which inspired her to pursue a career that could positively shape health systems and policies. While interested in health policy and health-related research\, she has yet to decide on her career path and is remaining flexible. \nAlejandra has recently started working part-time as a program administrator in the public sector. She is also an outreach coordinator for Take a Pain Check\, helping contact stakeholders for the foundation. In addition to her already busy schedule\, Alejandra also volunteers at a student-led community health centre. When not doing all this great work\, Alejandra loves to swim and bike ride – riding up to 60 kilometers on a nice day! She also identifies as a Taylor Swift super fan! \nAlejandra learned about Cassie + Friends through social media and was excited to join a community of young people with rheumatic diseases. Soon after\, she joined the Cassie + Friends Patient and Community Engagement Research (PaCER) program. In PaCER\, she was trained in qualitative research and got to connect with others with rheumatic diseases to perform a research project to help make a difference in the lives of people with JIA. Many participants in the PaCER program talked about their struggle to transition into adulthood with their rheumatic disease – this included the switch from pediatric to adult care\, high school to post-secondary\, entering the workforce\, navigating relationships\, and more! She also experienced this firsthand at the edge of young adulthood – a time when so much is happening all at once. \nHer work with the Youth Ambassador Program: \nThis experience sparked her project idea for the Youth Ambassador program: the creation of a multimedia (video\, graphic\, and/or written form) library that shares various resources and stories of lived experiences from those who have navigated young adulthood with a rheumatic disease. The style of the content will vary from interview/Q+A to advice columns and cover anything from university to jobs\, to love and social life. In addition\, the library will be supplemented with related research articles. \nThe central goal of this project is to provide a level of support\, mentorship\, and community connection that empowers young adulthoods to take the reins of every aspect of their lives – especially their health!
URL:https://cassieandfriends.ca/event/future-leaders-showcase/
LOCATION:Zoom
CATEGORIES:Future Leaders Program,Youth Leader Network
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Vancouver:20200716T173000
DTEND;TZID=America/Vancouver:20200716T203000
DTSTAMP:20260427T064824
CREATED:20200716T230745Z
LAST-MODIFIED:20240613T180911Z
UID:3970-1594920600-1594931400@cassieandfriends.ca
SUMMARY:Virtual Youth Panel
DESCRIPTION:Our virtual youth panel is taking place on July 16\, 2020! You’ll hear real stories from young adults about how rheumatic diseases affected them at school\, sports\, and with friends\,  and learn more about ways to help your child/teen cope with pain\, treatments\, and emotions. \nThis discussion is beneficial for parents\, affected youth\, grandparents/family members\, healthcare professionals\, educators\, coaches and anyone who wants to learn more about what it’s like to be diagnosed with a rheumatic disease and navigate its treatments\, symptoms\, challenges and lessons.
URL:https://cassieandfriends.ca/event/virtual-youth-panel/
LOCATION:Zoom
CATEGORIES:Youth Leader Network
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