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Female Founders in Health & Wellbeing - Candid Conversations

I’ve been thinking a lot about how many brilliant women are building things that make other women’s lives better. Apps. Devices. Clinics. Communities. Products. Platforms. Entire companies. And yet, too often, we’re all building in parallel. So I’m starting something new with Veya. Veya Voices — informal conversations over coffee with female founders in health, wellbeing and beyond. No panel jargon. No “tell us about your journey” followed by 47 minutes of corporate polish. Just real conversations about what we’re building, what’s gone wrong, what’s worked, what nobody warned us about, and what we wish more women knew before starting. Because I’d love to create more than content. I want to build a community where women share introductions, opportunities, lessons, contacts, encouragement and the occasional “please tell me this is normal” voice note. Less gatekeeping. More opening doors for each other. Less pretending we have it all figured out. More “here’s what I learned the hard way so maybe you don’t have to.” I’ll be starting with female founders across health and wellbeing — digital, physical products, hardware, services, the lot — and sharing the conversations across LinkedIn, Instagram and YouTube. So, if you’re a woman building something interesting in this space — or you know someone I absolutely need to meet — comment, DM me or tag her below - let’s take over the world together woman at a time 🌹 Coffee is on me. Well… virtually. I’m not funding everyone’s flat whites just yet. ☕️ #VeyaVoices #FemaleFounders #WomensHealth #WomenInBusiness #WomenSupportingWomen

Recruitment & Hiring Experts - Candidate Mistakes & Standout Traits

Who wants to have coffee with me? Virtually, of course! I’m lining up some upcoming episodes for https://lnkd.in/gBDsF_jE and I’m looking for some great people to have real, honest conversations with. I’m looking for experts in a few different areas, including: 🔹 Recruitment & Hiring Someone who lives and breathes hiring — what employers are looking for, what candidates get wrong, and what actually makes someone stand out. 🔹 Mental Health A psychologist or mental health professional who can help us have a practical conversation about mental health, business, leadership and the workplace. 🔹 Career Development Someone who helps people figure out what comes next — career choices, skills, finding your direction and navigating the world of work. 🔹 Youth & the Workforce For one episode, I want to talk specifically about teenagers entering the workforce — what they should be doing, what they definitely should NOT be doing 😂, what employers expect, and how we can better prepare young people for that first job. 🔹 Employment & Special Needs I’d also love to talk with someone who specializes in helping people with disabilities or special needs find meaningful employment and helping businesses create opportunities where they can succeed. The format is simple. ☕️ Virtual coffee chat 🎙️ Casual interview 💬 Real conversation 💡 Practical insights 😂 Probably a few laughs I’m not looking for someone who wants to give me a 45-minute corporate presentation. I want to talk. 🔹Tell me your stories. 🔹Tell me what you’ve learned. 🔹Tell me what people get wrong. 🔹Tell me what you wish more business owners, employees, parents or young people understood. If you are one of these people — or you know someone who would be fantastic on the podcast — I’d love an introduction. Tag them below or send me a message! Let’s have a coffee and talk business. It’s Time for Success: The Business Insights Podcast Listen on Apple Podcasts #ItsTimeForSuccess #BusinessPodcast #PodcastGuest #Recruiting #MentalHealth #CareerDevelopment #YouthEmployment #WorkplaceCulture #Entrepreneurship

Physicians Recovered From Burnout - Resilience & Career Reinvention

🎙️ Want to Be a Guest? Want to Share Your Story? I’ve shared my story on the Mindful Practice Podcast—my story of burnout, recovery, resilience, and transformation. I’ve shared what it has meant to experience healthcare from both sides: as a physician and as a patient. I’ve talked about rebuilding my life and career and finding a more sustainable way to practice medicine while creating a life that reflects who I am and what matters most to me. Now, I want to hear your story. The Mindful Practice Podcast is looking for guests who are ready to have meaningful, authentic conversations about the experiences that shape us personally and professionally. We’re especially interested in conversations about: ✨ Burnout and recovery ✨ Resilience and transformation ✨ Being both a patient and a physician ✨ Trauma and recovery ✨ Entrepreneurship ✨ Alternative streams of income ✨ Non-clinical careers ✨ Utilization management ✨ Locums and alternative ways to practice medicine ✨ Career transitions and reinvention ✨ Creating a sustainable medical career and life Whether you have a personal story, professional expertise, a unique career journey, or lessons that could help another physician, healthcare professional, or patient—we’d love to hear from you. 🎧 Ready to share your story? Apply to be a guest on the Mindful Practice Podcast: 👉 https://lnkd.in/gtS2Cwn4 Your story may be exactly what someone else needs to hear. #MindfulPracticePodcast #PodcastGuest #ShareYourStory #PhysicianWellness #PhysicianBurnout #BurnoutRecovery #PhysicianEntrepreneur #NonClinicalCareers #HealthcareLeadership #PhysicianLife #Resilience #CareerTransformation

New Englanders - Local Good News & Community Wins

Any New Englanders here? I want your good news!! HELLO GOOD NEWS FANATICS Longtime lurker here but this is my first post on this subreddit. A lot of the posts / discourse here focuses on good news with a global perspective, but I'd like this thread to be about things more LOCAL!! I've been really into this world for a while (I am a fanatic subscriber of all the outlets-- Our World in Data, Fix the News, The Progress Network, Human Progress, Good Good Good, etc), and wanted to start contributing to the good news movement, but in a way that was unique. So I began a locally-focused project, where I curate / share good news stories from my region of the world-- New England (northeast United States). My project is called Granite Goodness! It's been really fun because I've gotten to show people that plenty of perfectly impressive good news happens all the time, and it hides in plain sight. We just tend to not see it curated together. Here are some local stories that have brought me some optimism lately. Connecticut farmers are organizing to solve shared problems. The state's 120 farmers markets long operated in relative isolation, each one troubleshooting vendor rules, permits, and slow days on its own. A new statewide coalition is now two years into connecting organizers to share resources and knowledge. (Yonkers Times) Rhode Island is protecting 174 acres of open space. Using $1.23 million in voter-approved Green Bond grants, four projects are being funded from forestland in Glocester to a shoreline property overlooking Mount Hope Bay in Tiverton. The same program has protected more than 13,000 acres since 1985. (RI Dept. of Environmental Management) Vermont just became the 23rd state to pass a consumer privacy law. Governor Phil Scott signed the Vermont Data Privacy Act in June, giving residents new rights over how their personal data is collected, used, and sold. The law includes added protections for health and genetic data and takes effect January 1, 2028. (IAPP) In 2025, Maine exceeded forecasts for ADU construction. ADUs made up roughly 9% of residential building permits across Maine's 183 largest municipalities last year, surprising even housing researchers as small towns exceeded expectations. Windham led with 16 permits, and New Gloucester, a town of under 6,000, matched Portland with 14. (Portland Press Herald) The University of New Hampshire just launched a new Center for Neurodiversity. The center supports all students, staff, and faculty, with resources ranging from internship support to faculty training on neuroinclusive syllabi. UNH's long-term vision is to expand services beyond campus to communities across New Hampshire. (University of New Hampshire) Massachusetts just reduced opioid deaths by 27%. 978 deaths were recorded in 2025, the first year since 2013 when the figure was below 1,000. The drop is credited to expanded treatment, harm reduction, and recovery support. (WBUR) Traditional news matters, but it often highlights a disproportionate share of the worst events, which can leave people feeling burnt out, anxious, or cynical. Note that these summaries are my own words on what I find optimistic from the original stories, not direct quotes from the sources. If you want more detail, I link and credit the original sources on our site. Reddit discourages too many hyperlinks, so I don’t include them here. Please use this thread to share some good news LOCAL to YOU!! especially if you're from or around the northeast USA! If anyone is working on a similar project, I'd love to hear from you too. -Andy

UK ADHD & Autism Clinicians & Researchers - Rising Assessment Demand

Very excited to announce that I am temporarily hanging up my lab coat in exchange for a blazer! 🥼➡️🧥 I have joined UK Parliament as a Nuffield POST Fellow. Over the next three months, I will be working at POST, UK Parliament to produce a POSTnote on the rising demand for ADHD and autism assessment and support across the UK. Since starting my PhD in 2023, I've been fascinated by the intersection of scientific research and policy, and how evidence can help inform parliamentary decision-making and shape public services. I'm excited to explore this important topic, learn more about how Parliament works from the inside, and gain first-hand experience in translating research for Parliamentarians. My first week did not quite go to plan thanks to an unexpected bout of norovirus, but I'm incredibly grateful to the POST team and my fellow Fellows for their kindness, support and warm welcome while I was out of action. A huge thank you to the Nuffield Foundation for funding this fellowship, the POST team for the opportunity, and my PhD supervisors, Bhuvaneish T.Selvaraj, Siddharthan Chandran and Colin Smith, for their encouragement and support throughout. I also want to thank everyone who offered advice, reviewed application drafts and cheered me on during the application process. I genuinely couldn't have done it without you. As I begin this project, I'd love to hear from people working in ADHD, autism and broader neurodevelopmental research, clinical services, education, policy, public health, or the lived-experience community. Please feel free to get in touch if you'd like to connect or share relevant perspectives and evidence. Looking forward to the next three months! #SciPol #SciencePolicy #UKParliament #POSTNote #ADHD #Autism #Neurodiversity #STEMCareers #PhDLife

parliament.uk logoparliament.uk

University Student Creators & Viewers - Algorithms & Mental Health

Seeking Uni Students & Creators for NCTJ Award Investigation: Social Media Algorithms & Mental Health (15-20 Min Interview) Hi everyone, My name is Janayah, and I am a trainee investigative journalist currently preparing a piece for the NCTJ Awards for Excellence(Top Scoop category). I’m carrying out an investigation looking into the relationship between YouTube and TikTok recommendation algorithms and university student mental well-being. Specifically, the article probes whether social media platforms e.g. YouTube and TikTok are creating a two-sided emotional loop. For Creators (Supply Side):Whether YouTube’s recommendation algorithms amplify users' negative and highly emotional content, thereby potentially incentivising student creators to lean into personal distress for audience reach. For Viewers (Demand Side):Whether TikTok’s feed provides student viewers with disproportionate amounts of negative and highly emotional content, thereby potentially drawing them into a downward emotional spiral that impacts their well-being and mental health. A 2025 study from the University of Iowa mathematically proved that YouTube's algorithm actively forces feeds into emotional ‘grievance’ loops. While the data is clear, the story lacks the vital human element. To complement the University of Iowa's findings on YouTube, this investigation also draws on foundational global research by Amnesty International into TikTok's recommendation algorithm. Their technical testing revealed a rapid "rabbit hole" effect where the 'For You' feed quickly saturates accounts with mental health-related content, reaching over 50% of recommended videos within as little as 3 to 20 minutes when a user shows interest in these topics. By relying on passive viewing habits to drive maximum engagement, the platform risks drawing vulnerable young viewers into downward emotional spirals, creating a demand-side pressure that mirrors the dynamic faced by creators on the supply side. I am looking to speak with: Student Content Creators(YouTube/TikTok) who have felt algorithm-related pressure around the type of content they post. Student Viewerswho have experienced "doomscrolling" or felt their feeds rapidly fill with negative/mental health-related content during stressful periods at uni. What’s involved? A brief, informal15–20 minute chat(via Zoom, Teams, or phone). Anonymity guaranteed:You can be completely anonymised (pseudonym used, uni name withheld) if you prefer. If you’re interested in sharing your perspective or experience to help bring the human side of this research to light, please send me a DM here on Reddit or comment below and I’ll reach out. Thanks so much!

Patients With Medical Billing Errors & Records Issues - Patient Rights

I investigated my bill...it has turned into a Patient led MEDICAL BILLING/PATIENT RIGHTS INVESTIGATION After investigating my bill I have learned A LOT...this system is super complex and I am working on a project to have a single source for ALL the information patients need to know to help investigate and question their own bills..... I found out that it ties directly into patient rights issues. I'm looking to hear from other patients who have had problem with medical records, billing or patient rights issues. Reach out if you have an experience to share....stories can be submitted anonymously on my website I am mostly looking for patterns and to hear stories because the stuff i have been hearing is stuff you literally CAN'T MAKE UP!!!!!!!! My investigation into my own bill is still ongoing after over a year and a half. My questions led to an allegedly false police report (DA dismissed the charges without me having to do anything) and the hospital put a Ex Parte Emergency Temporary Workplace Violence Restraining Order against me...they got multiple continuances for 5 and a half months. I ended up Serving their Witnesses with Subpoenas Duces Tecum ordering them to bring proof of their allegations. Then all of a sudden they dismissed the case 10 days befor our 3 hour evidentiary hearing. Technically they sent me to collections then called the police. I had no idea they called the police on me. I kept disputing my bill. Then they put me on a collections hold then zeroed out my portion of the bill then tried to put the restraining order on me....it didn't work but it is ongoing. I had to defend myself Pro Se in court. The restraining order had a list of 47 names. The entire executive staff and board of trustees of this health system....there were 2 lawyers now there are 3...I think I learned too much! After all that I'm still asking the same questions . I had to learn my patient rights. I am still working on a complete guide on my website. I have found a ton more relevant laws, rules and regulations related to medical billing and patient rights. I am looking to hear stories from other patients to see what kind of patterns exist throughout the broader system......most of the stories I have heard I couldn't have made up myself! You can submit stories anonymously on my website. You are allowed to ask questions. Your supposed to be able to get answers. KNOW YOUR PATIENT RIGHTS!!!!! https://preview.redd.it/behqm6emnqqh1.jpg?width=1224&format=pjpg&auto=webp&s=43f90872e00275c9d9c64487e0ada41517e88a5b

Community Contributors & Pokémon Fans - Heart & Mind Canvas Project

[OC] What started as Pokémon drawings for my community turned into an idea I never expected ❤️🧠🎨 The first few pictures are from a community art project I did recently. It started with me asking my community if they wanted to be part of an art project. I asked people what Pokémon they'd like me to draw, and the community started giving me their requests. I took all of those requests and brought them together on one board. When I finished it, I donated the artwork to a local card shop. Seeing all those individual requests come together into something everyone had a little part in honestly meant a lot to me. And it got me thinking... What if I took this idea even further? What if instead of me being the only person creating the artwork, I could actually bring people together and have the community create it with me? That's where this next project comes in. ❤️🧠🎨 Heart & Mind Canvas Community Art Project 🎨🧠❤️ This project is going to focus on two separate awareness causes: ❤️ Heart Health Awareness 🧠 Mental Health Awareness I'm going to be collecting artwork and contributions from people in the community and bringing them together into one larger collective piece of art. And this time, I want to document the journey from the very beginning. I'm hoping to visit card shops, libraries, mental health facilities and programs, heart health facilities and hospitals, and other places throughout the community. If you know of somewhere you think would be meaningful for me to visit or get involved with, I'd love to hear your suggestions. And if you'd like to contribute, you don't have to be an artist. If you want to draw a Pokémon, I'd absolutely love that. Pokémon are the characters I'd prefer for this project. But you could also draw a heart, create something inspirational, include a cross or something representing faith or hope, or simply write something encouraging that you think another person might need to hear. Something as simple as: "Praying for you." "I hope you're doing okay today." "You are not alone." "Your heart is perfect just the way it is." "Your love is unforgettable." And if you don't feel comfortable drawing something yourself, that's completely okay. If you tell me what you'd like, I can draw something for you and include it in the project. There is no obligation to participate, and you don't have to pay anything. You can even remain anonymous if you'd prefer. I'm also talking with a well-known Christian radio station about possibly expanding the community connection even further. Nothing is guaranteed, but I'm trying to find ways to take this beyond YouTube and into the actual community. That's really important to me. I don't want this to stay inside of a screen. I want to meet people. I want people to create together. I want to hear their stories. I want to document the journey. And most importantly, I want this to be about people, not numbers. This isn't about views. It's about community. I've been praying about this, and I truly believe God has called me to do this and to invite people to be part of it. When the final piece is finished, I want the people who contributed to have a voice in deciding where it goes. Maybe it ends up at a mental health facility. Maybe it ends up at a heart health facility. Maybe somewhere else where people need to see it. We'll figure that out together. I want it to go somewhere that matters — somewhere where someone can see it and maybe find hope, encouragement, or simply a reminder that they're not alone. This is only the beginning. If you have an idea, a suggestion, a place you think I should reach out to, or you just want to be part of creating something, I'd love to hear from you. ❤️🧠🎨 Heart & Mind Canvas Community Art Project 🎨🧠❤️ "May The World Be Your Canvas" — Mr.Mending.Miracles

Bereaved Families from Jehovah's Witness Blood Refusal - Policy Change

Jehovah's Witness Blood Policy 2026: 4 Major Changes Today, September 18, 2026, Jehovah’s Witnesses announced one of the most significant changes to their blood policy in decades. Red blood cells, white blood cells, plasma, and platelets obtained from another person are no longer categorically prohibited. Each Witness may now decide individually whether to accept them. Witnesses may also decide whether to donate blood for the purpose of providing components or fractions. Whole blood from another person remains prohibited. This follows the change announced earlier this year allowing Witnesses to make their own decision about the use of their own stored blood, including preoperative autologous donation. For AJWRB, there are several immediate issues that we believe are especially important. First, this is a significant expansion of individual conscience in medical decision-making, and we welcome that. Second, religious permission is not the same as patient consent. Clinicians can no longer assume that “Jehovah’s Witness” means refusal of red cells, plasma, platelets, or white cells. Each patient’s actual preferences need to be established individually and, whenever possible, privately. Third, many Witnesses are still carrying advance directives that were completed when these treatments were religiously prohibited. Watchtower has announced that a new medical directive is coming and has advised Witnesses that, in the meantime, they may document their current choices through legally recognized forms or directly with healthcare providers. Fourth, there is a transitional information problem. As of today, some clinician-facing information on JW.org still describes red cells, white cells, plasma, platelets, and preoperative autologous donation as refused. That information will presumably be updated, but clinicians need to be aware of the discrepancy now. And finally, we recognize that this announcement may be extremely painful for people who lost a spouse, parent, child, sibling, or friend after blood was refused under the former policy. A policy change today cannot tell us what a particular patient would have chosen under different circumstances, nor does it prove that transfusion would have prevented an individual death. But it can reopen very real grief, anger, and difficult questions. Those experiences should not be minimized. AJWRB has published an initial analysis of the change here: https://www.ajwrb.org/jehovahs-witness-blood-policy-2026-major-change We are now beginning the much larger job of reviewing and updating our website, since a great deal of material that accurately described the former policy is no longer an accurate description of current policy. We also want to preserve the historical record. If you or your family were directly affected by the blood policy, including the loss of a loved one or a serious medical experience involving blood refusal, AJWRB would like to hear from you. Those accounts can be preserved anonymously when necessary. For those who have been personally affected by this policy, particularly families who have lost someone, we recognize that today may be a very complicated day.

ajwrb.org logoajwrb.org

Social Care Changemakers - Community-Led Reform Stories

Something I've noted about the 'social care reform' debate is that 'reform' is framed as something 'done to' the 'social care sector', and yet when I think about the people and organisations that come together under the banner of #SocialCareFuture what I see are social reformers: changemakers not waiting to be led, but leaders seeking to be backed and for barriers in their way to be removed. This morning I went out for a quick stroll around Bermondsey in South East London where I live, and passed the deeply moving statue 'Dr Salters Daydream' on the banks of the Thames. The Salters were a tour de force, not just in this part of London but London as a whole in the early 20th Century, with a public health mission which saw free healthcare brought to Bermondsey years before the NHS, slum clearance, campaigns against air polution and 'beautification' through the planting of trees and designation of parks (hence Ada's spade) all of which characterise Southwark and wider London today. Ada was a social worker at Bermondsey Settlement. So committed were they to the people of Bermondsey and Rotherhithe that they lived among them, and what the statue sadly commemorates is the loss of their daughter, Joyce, who died aged 8 from Scarlet Fever that swept through the slums. In 1922 Alfred was elected as MP for Bermondsey, representing Labour, while Ada in the same year became the first woman mayor in London and the first Labour woman mayor in Britain. I know for a fact there are social reformers across our country today not waiting for government to act when it comes to care, support and wellbeing, and who are creating future possibilities in the present, or 'planting trees under in whose shade they know they might never sit' as Ada did. We don't do enough to tell those stories, and #SocialCareFuture wants to change that so that the debate about the future of adult social care is animated by brilliant stuff that is happening. So we're about to get back to our roots - our early days were very much about spotlighting the good stuff - and will be collating and sharing these over the coming months online and via events, gatherings and meetings. If you've got something you think the world would benefit from hearing and learning about, which can animate the future of social care, drop me a line, and we can talk about how best to capture it.

Tampa Veterans & First Responders - Mental Health Conversations

How are you REALLY doing? That question is heading to Tampa for MIC 2026! The JMach Experience is bringing real stories, raw conversations, and a whole lot of purpose to the Military Influencer Conference. Here’s where you can find me: ✈️ Wednesday, September 23: Touching down in Tampa! Kicking things off with private podcast recordings and connecting with the military-connected community. 🎤 Thursday, September 24: Moderating the Creator Stage, bringing together voices and conversations that matter. 🎙️ Friday, September 25: The JMach Experience hits TABLE 10 at the inaugural Podcast Row! We’re recording conversations about mental health, resilience, purpose, and community with Veterans, First Responders, and the people making a difference. No scripts. No sugarcoating. Just real people having real conversations. Going to MIC? Pull up a chair at Table 10. I want to hear YOUR story. Not making it to Tampa? Stay tuned. The conversations are coming to you. A huge shoutout to Total Roofing & Construction, West Valley Mavericks Foundation, and FMC for supporting The JMach Experience and helping us bring these conversations to Tampa. Your support means more than you know! 🤝 How are you REALLY doing? Military Influencer West Valley Mavericks Foundation Total Roofing & Construction Services Inc. JW Marriott #MIC2026 #MilitaryInfluencerConference #JMachExperience #PodcastRow #VeteranMentalHealth #FirstResponderMentalHealth #VeteranPodcast

Lichen Planus Patients - Share Lived Experience & Resource Needs

New lichen planus resource Hi everyone! My name is Kathy, and I’m the President and Executive Director of LichenS Support Network (LSSN). We’re a U.S.-based 501(c)(3) nonprofit, but our community and educational work reach people around the world. Some of you may know us from our work in lichen sclerosus. Over the past year, we’ve been expanding our work to better support people living with lichen planus in all of its forms, and we recently launched a dedicated lichen planus site, AboutLichenPlanus.com. I wanted to introduce ourselves and share what we’ve been working on, but more importantly, hear from you about what would actually be useful. We’re slowly building out the site with evidence-based information that is written for patients rather than for medical journals. Right now, you’ll find a general guide to understanding lichen planus, a more detailed cutaneous lichen planus hub, information about why LP can be difficult to diagnose and why people are sometimes misdiagnosed, information comparing vulvar LP and lichen sclerosus, blogs, videos, podcasts, and lived-experience stories. Our content is medically reviewed to ensure evidence-based accuracy. One of those stories is from Melanie, an LP warrior who has lived through a long and complicated journey with both lichen sclerosus and several forms of lichen planus, including cutaneous, esophageal, and vulvovaginal LP. We really want lived experience to sit alongside the medical information on the site, not as an afterthought, but because there are parts of living with LP that clinical information alone simply doesn’t capture. If you would like to share your story via YouTube or a blog, please email [email redacted] – we’d be happy to feature you. We’ve also created an interactive doctor-visit and self-advocacy planner. You can enter your symptoms, medications and treatments you’ve tried, keep track of changes, choose questions you want to ask your healthcare provider, add your own questions, and then print everything as a worksheet to bring to your appointment. The information you enter stays locally in your browser; LSSN does not receive or view what you type into the tool. And there is a lot more we want to build, particularly resources covering the different LP subtypes, diagnosis and treatment, navigating healthcare, self-advocacy, and more patient and caregiver experiences. We’d love for you to check out and explore what we have so far at aboutlichenplanus.com, you’re very welcome to poke around the site. There’s also an option there to join our newsletter if you’d like to hear about new LP resources as we add them. And if you find it helpful, please share with others. But we don’t want to sit behind our computers and guess what people with LP need. So I’d really love to hear from this community: What do you wish someone had explained when you were diagnosed? What has been hardest to find reliable information about? What questions do you still have? And what kinds of resources would genuinely make living with or navigating LP easier for you? Feel free to comment here. We’ll be reading and listening. Thanks for letting us introduce ourselves and, most importantly, for letting us learn from this community.

Canadian Healthcare Innovators - Voices of Innovation Canada

🍁 Canada is doing remarkable work in healthcare innovation. Now we want to help tell those stories. Submissions are officially open for Voices of Innovation Canada, a new Canadian edition of the Voices of Innovation series, building on Ed Marx’s original 2019 healthcare bestseller. I’m proud to be working on this Canadian edition alongside Edward Marx, Robyn Fulkerson and Sakshika D. with the goal of bringing together voices from across the country who are actually changing how healthcare is delivered. This is not simply a book about technology. It is about the people, organizations and ideas moving Canadian healthcare forward. We want to hear about innovations that solved real problems, created measurable change and produced lessons that other healthcare organizations can learn from. We are looking for stories from healthcare leaders, clinicians, physicians, nurses, researchers, digital health professionals, innovators, entrepreneurs and others working across areas such as: • Artificial intelligence and automation • Data, analytics and learning health systems • Digital health and clinical information systems • Interoperability and connected care • Patient and clinician experience • Virtual care and new models of care • Workflow and clinical transformation • Innovation adoption and scaling • Governance, privacy and responsible innovation • And other examples of meaningful healthcare transformation The book is structured around the HIMSS Innovation Pathways, with contributors sharing practical stories of successful innovation from their organizations. Essays submitted for consideration are 1,500 to 3,000 words, and the Canadian edition is planned for release in 2027. If you have been part of something that changed healthcare for the better, this is an opportunity to document it, share what you learned and add your voice to a broader Canadian story. Visit the dedicated Voices of Innovation Canada page to learn more about the book: Voices of Innovation Canada https://lnkd.in/g8ugVuWR Then, when you are ready, submit your essay here and select VOI: Canada: Submit your essay for Voices of Innovation Canada https://lnkd.in/gUiG4XYn Some of the best innovation stories in Canadian healthcare have never been properly told. We want to change that. What innovation story should Canada be sharing with the world? Digital Health Canada HIMSS HIMSS Eastern Canada Chapter (HIMSS Section de l’Est du Canada) HIMSS Canadian Prairies Chapter HIMSS Global Health Conference & Exhibition HIMSS British Columbia Chapter Canadian Institute for Health Information (CIHI) Canadian Health Information Management Association - CHIMA Michael B. Decter The Hon. Tony Clement TECHNATION Canada Health Infoway Alan John Forster Muhammad Mamdani Ted Scott Jennifer Zelmer Terence Tang André Picard Jerry Zeidenberg Dr. Dante Morra Colin Hung Gary Ryan Chris C. Anderson Elizabeth Toller Anne Snowdon Adalsteinn (Steini) Brown

Community Members in 45 Towns - Loneliness & Connection

Tomorrow, I start walking. Over the next several weeks, The Cost of Loneliness Project will make its way across America. We're visiting 45 towns in 17 states, ending in New York City on November 12, our National Day of Connection. Along the way, we'll walk through communities large and small. We'll meet people where they live, work, learn, gather, eat, and care for one another. We'll sit around tables. We'll talk with community leaders, healthcare professionals, educators, business owners, students, families, and strangers who probably won't stay strangers for long. Mostly, we'll listen. We want to hear about the connection that's already happening in this country, and from the people who are still looking for it. Loneliness is more than a feeling. When it becomes chronic, it takes a real toll on our physical health, our emotional well-being, our workplaces, our families, our communities. This walk isn't about what's wrong with us... it's about what's possible between us. I believe we can build communities where people know they belong and know they matter. Where checking on someone is just what you do. Where gathering is something we plan for, not something that happens by accident. Where we treat connection as essential to our health as anything else we do to take care of ourselves. And where our homes, workplaces, schools, healthcare systems, neighborhoods, and public spaces are built with human connection in mind, not as an afterthought. That kind of cultural shift doesn't happen because one organization wills it into being. It happens because millions of us decide to build it together. So as I lace up my shoes, I'm asking you to come with us. Follow along on our LinkedIn page, our website, and our other social channels: https://lnkd.in/eYDD3Ujm. We'll be sharing the people we meet, the stories we hear, and what we're learning about belonging and connection across America. And do one more thing while you're at it: start planning for November 12 now. Our National Day of Connection isn't something to just observe. Make it yours. Bring people together for a meal. Reach out to someone you've lost touch with. Start something in your workplace, your school, your neighborhood. Invite someone in. Make room at the table. To everyone who's poured into this before the first step, especially Courtney Lewis, Matt Cook, Scott Moody, Ryan Riccordella, Evelyn Lane, Grace Franklin, Bailey Birtchet, Sarah Anderson, Nick Rogers, Kayla Smith, George Nesbitt, and Gracely Murphrey, thank you. We'll share more ways to participate as the date gets closer. For now: follow along, join us when we're near you, and send us your stories. We're walking across America, but building a culture of connection is going to take all of us. Today, we begin. I can't wait to see who we meet."

Founders & Investors - Book On Building Startup In Real Time

I’m the founder of Enerium Health, and I’m also an author. Until recently, those two parts of my life existed almost separately. I’m a professional nutritionist, so I know how to write about nutrition and turn complex physiology into something people actually want to read. I’ve also written a children’s book, where the challenge was completely different: talking to children about health through a story rather than a lecture. Now Enerium is going through the Health Founders Estonia accelerator, and somewhere during the first sessions those two parts of my life unexpectedly came together. I found myself wanting to write a book I had never planned to write: a book about what it actually looks like to build a company while you are still building it. I don’t want to reconstruct this story years later, if everything works out, when mistakes have become lessons and hindsight has arranged the chaos into a convincing strategy. Enerium is still at an early stage. We have a working product, users, our first paying subscribers, a team, and ambitious plans, but I genuinely don’t know whether we will build a global company, raise a major investment round, or what Enerium will look like several years from now. That uncertainty is exactly what makes me want to write now. I want to capture the journey as it happens: what we believe today and may discover was wrong tomorrow, how mentors change the way we see the company, which questions from investors force us to rethink our assumptions, how the team evolves, and how a product gradually becomes a business. The working title came to me while writing the first chapter: Conceiving a Unicorn. There is something fascinating about writing a business story without knowing whether it will ever become a success story. I don’t have the luxury of hindsight. I’m writing from inside the process. I would also love to bring other perspectives into the book. If you are an investor, founder, or entrepreneur who has seen companies grow, pivot, scale, raise, fail, or start again, and you would like to contribute your experience, please write to me. The first chapter, “A Good Product Still Isn’t Enough,” is already written, and I’m sharing it here for anyone who would like to read it. And a special thank you to John Collins. His first lecture at Health Founders Estonia made me question things I had taken for granted about Enerium and unexpectedly became the starting point for this first chapter. I have no idea where this story will end. For now, I’m building the company and writing the story at the same time. https://lnkd.in/ezZpFeWn

Parents/Carers & Practitioners - Pica & Polydipsia Joined-Up Support

PICA and POLYDIPSIA - Calling All Voices: SOCIAL CARE, HEALTH, PARENTS/CARERS, EDUCATION I’m looking to hear from people across health, social care and education, as well as parents/carers and people with lived experience of pica and/or polydipsia. When a child or young person has pica or polydipsia behaviours, what does good joined-up support look like in real life?: What should each service be doing? What should they be doing together? What support should parents/carers receive? Where are the gaps? What has worked, helped or shown promise? Of particular interested is real-life experience and practical approaches, not just published research. There is very little research on what joined-up practical support looks like, so professional experience, lived experience and parents’ experiences are all really valuable. The responses will contribute to a blog and a pica and polydipsia training module for school leaders, looking at how health, education, social care and families can work together to understand and meet underlying needs, while supporting safety and quality of life. There are no right or wrong answers just different perspectives and insight. Feel free to comment or message me. Contributions will be attributed unless you would prefer otherwise. Please share with colleagues, SEND charities, advocacy organisations and parent/carer groups, particularly those working with children and young people affected by pica and polydipsia behaviours.

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