
Can-SOLVE CKD Network - Le réseau Can-SOLVE CKD
@cansolveckd
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We are a pan-Canadian patient-oriented kidney research network./Nous sommes un réseau pancanadien de recherche sur le rein qui est axé sur les patients.
Joined September 2016
We are pleased to announce that our 2024 Impact Report is now available! This report highlights our activities, projects, achievements, and contributions to #kidneyhealth research. Special thank you to our funding partners for their generous support. Read:
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📢 Call for Patient Partners: #KidneyTransplant Study.Help shape a toolkit to support informed decision-making. 👥 Open to transplant recipients, candidates, caregivers and those from Indigenous or historically marginalized communities. 🔗#KidneyHealth
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RT @cellotonelli: Kidney disease affects 850M people and is projected to be the 5th leading cause of death by 2050, yet it’s absent from th….
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🌞 New summer series from @kidneycanada!.This July, #KidneyCommunityKitchen is sharing weekly tips, recipes, and wellness inspiration to help people living with #kidneydisease enjoy a healthy summer. New content every Wednesday!.Explore the series below👇.#KidneyHealth.
July = a month of kidney-friendly goodness! The #KidneyCommunityKitchen is serving up weekly content from recipes, nutrition tips, & summer inspiration to keep your meals fresh and fun—at home or on the go! Follow us and share your #KidneyKitchen moments!
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RT @CNTN_RCEN: Just launched: #FundingOpportunity via @CIHR_IRSC Fall '25 and Spring '26 Project Grant competitions. Our Scientific Operat….
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RT @SSHRC_CRSH: 📢 NEW FUNDING OPPORTUNITY: Indigenous Innovation and Leadership in Research Network Grants.These grants will fund establish….
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New @CIHR_IRSC #FundingOpportunity now open for Fall 2025 and Spring 2026 Project Grants!.#CIHR #ResearchFunding.
📢 Just launched! #FundingOpportunity for the Fall 2025 and Spring 2026 Project Grant competitions. Details:
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The Storytelling for Impact module is here to guide people with #livedexperience and caregivers in crafting powerful stories that help others understand what it’s truly like to live with #kidneydisease. 🔗Check out this Can-SOLVE CKD resource:
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As June comes to a close, #NationalIndigenousHistoryMonth reminds us that learning, unlearning, and amplifying #Indigenous voices must continue all year long. Start by reading and sharing our latest newsletter with Indigenous-led stories and resources:.🔗
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“Empowering patients through collaboration and community engagement is essential when conducting meaningful research.”.Meet Grace Salomonie, a young #Inuk leader bringing her voice to IPERC and #IndigenousHealth advocacy. 🔗 Meet Grace: #PatientEngagement
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“Half the people don’t have vehicles… But you’re right here. That makes a difference.” .Rita from Katzie First Nation shares how close-to-home access made possible. BC program in partnership with @fnha. 🔗Read: .#kidneyhealth
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📣 Still time to register!.Black Canadians face higher rates of #kidneydisease—but early detection can save lives. Join our free July 2 webinar to learn from Black health care providers how to protect your #kidneyhealth. 🔗#BlackHealth #HealthEquity
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Although commonly referred to collectively as #IndigenousPeoples, First Nations, Inuit and Métis communities hold distinct cultures, histories & relationships to health. New 3-part series challenges assumptions & highlights cultural specificity in care. 🔗
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📝 New publication alert from the APPROACH team!.This @cansolveckd project created a tool that helps people with #CKD make informed cardiac treatment decisions with their care teams. 📖 Read and share: #heartdisease.
Researchers at @UCalgary used #HumanCentredDesign to build helping patients with CKD make informed cardiac treatment decisions with their care teams. Read how they did it: #SharedDecisionMaking #SDM #KidneyHealth #CardioCare #CKD
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📣One Week Away! .Did you know Black Canadians are at higher risk for #kidneydisease—and often face barriers to getting diagnosed early?.Join us for a free webinar designed for Black communities across Canada. In partnership with @BlackHealthCAN & @kidneycanada .Register below 👇.
Black Canadians face higher risks of chronic #kidneydisease. But early action can save lives. Join our FREE webinar on July 2 to learn how to protect your kidney health. Register: #BlackHealth #HealthEquity
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“Move away from learning about Knowledge Keepers and learn from them.” – Dr. Malcolm King.#KnowledgeKeepers in Research is a resource for researchers on respectful, reciprocal engagement. 🔗 Access free resource: #indigenoushealth.
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Ever heard of #medialarterialcalcification? It affects up to 80% of people with #CKD, yet there’s little research on how it impacts men and women differently. 💡 McGill is planning a new study—and they’re inviting patient partners to help shape it!.Learn:
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🧡#NationalIndigenousHistoryMonth newsletter now available!.Featuring powerful voices and stories from First Nation, Inuit and Métis patient partners and Knowledge Keepers across the network. 📬 Read now and share: .#IndigenousHealth #KidneyHealth
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June 21 is #NationalIndigenousPeoplesDay!.Catherine Turner, a proud Red River Métis woman, shares a message of celebration. This #NationalIndigenousHistoryMonth, we invite you to celebrate, learn, and reflect on the distinct cultures of First Nations, Inuit, and Métis Peoples. 🎥
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Stay connected with the us!.Follow us on social media for updates on #kidneyhealth research, patient partner stories, and network activities. 📧Want more? Subscribe to our bi-weekly newsletter: 🔗Visit our website to learn more:
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“I believe telling our stories and sharing our experiences begins to provide hope.”.🎥 Watch Tamara Beardy’s powerful story as a First Nations woman, #kidneydonor, and advocate with IPERC. Hear the power of Indigenous voices in research. #IndigenousHealth #KidneyHealth
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