Anthem

Emergency hormonal contraception will soon be free of charge in all pharmacies in England - a long-overdue step. But why has it taken almost 25 years to reach this point, and will pharmacies be fairly reimbursed? Let us know what you think about this step towards reproductive health equality.

  Jack Panton and Kiashini Sriharan are as distinct as chalk and cheese, striking the perfect yin and yang in our close knit Anthem team. What unites them is their curiosity, tenacity and drive to deliver impactful communications… and their promotions to Account Directors! We are privileged to have them on our team and proud to support them as they take the next step in their health communications careers.

Are you an experienced healthcare communications agency Account Manager looking for a new challenge? If you’re ready to make an impact and grow your career let’s have a conversation! For more information about the role, please reach out to [email protected] with the subject line "Account Manager".

Are you an experienced healthcare communications agency Account Manager looking for a new challenge? If you’re ready to make an impact and grow your career let’s have a conversation! For more information about the role, please reach out to [email protected] with the subject line "Account Manager".

To celebrate Q1, we took ourselves to All Star Lanes where William Rowley bowled us over with a hat-trick of strikes to take the gold medal 🥇 It’s been an exciting start to the year and we’re looking forward to pinning down our priorities for the months ahead.

Who Gets Heard in Healthcare – And Who Doesn’t? For too long, healthcare decisions have been made without truly listening to the people they impact most. Patient voices are often treated as anecdotal rather than essential, but without them, we risk building a system that fails those who need it most. On Monday 24th March at 2:00 PM GMT, Origins - The Patient Focused Specialists and ISPEP are bringing together experts for an important conversation on health equity and the social factors that shape patient experiences. For "Not Just a Number: Making Sure Every Voice Shapes the Future of Medicine", Su Smith will be joined by Alexandra Charge, CEO of ISPEP, and Professor Lara Bloom, CNE, President and CEO of The Ehlers-Danlos Society, to discuss how we can ensure that every patient voice is heard - and acted upon. If you care about the future of medicine, you need to be part of this discussion. Register now: https://lnkd.in/eCbeNxeR

How can addressing long-term conditions boost the economy and build an NHS fit for the future? This week, our Senior Account Manager, Jack Panton attended the New Statesman panel discussion on this vital topic, featuring expert insights from Dr. Amanda Doyle (National Director for Primary Care and Community Services, NHS England), Dr. Beccy Cooper MP (Member of the Health and Social Care Select Committee), Sarah Tilsed (Head of Partnerships and Involvement, Patients Association) and Charlotte Refsum (Director of Health Policy, Tony Blair Institute for Global Change) The discussion reinforced just how critical tackling long-term conditions is for the NHS to achieve the government’s long-term vision for the health of the nation and the economy. The panel highlighted: • The economic potential of delaying frailty • That for many, the biggest barrier to returning to work isn’t the physical symptoms of long-term conditions, but the mental health impact • It doesn’t take a generation to see the economic benefits of prevention interventions • People need to be empowered to self-manage their conditions using digital tools • The potential of the upcoming devolution agenda for Integrated Care Boards (ICBs) in how they allocate resources, with local decision-making playing a bigger role As we look forward to the government’s 10-year plan for the NHS, it will be interesting to see how they set out their vision for managing patients with long-term conditions.

Beyond the Numbers – Why the Patient Voice Must Shape Medicine Medical advancements are transforming healthcare, but there’s one thing technology and data alone can’t replace - the lived experiences of patients. Health equity and social determinants of health are critical factors in patient outcomes, yet they remain some of the most complex challenges in modern medicine. On Monday 24th March at 2:00 PM GMT, Origins - The Patient Focused Specialists and ISPEP are hosting a live discussion that tackles this head-on. Facilitated by Su Smith, with insights from Alexandra Charge, CEO of ISPEP, and Professor Lara Bloom, CNE, President and CEO of The Ehlers-Danlos Society, "Not Just a Number: Making Sure Every Voice Shapes the Future of Medicine" will explore how we can ensure that every patient’s experience shapes the future of healthcare. If you’re passionate about patient-focused innovation, this is a conversation you won’t want to miss. Sign up here: https://lnkd.in/eCbeNxeR

Shining a Light on Rare Diseases – No One Should Be Left Behind   Today, on Rare Disease Day, we stand with the 300 million people worldwide living with a rare condition. Too often, these individuals face delayed diagnoses, limited treatment options, and a healthcare system that isn’t built to meet their unique needs. That has to change.   At Origins - The Patient Focused Specialists, we believe that every voice matters in shaping the future of medicine. Rare diseases may be individually uncommon, but together, they represent a significant and urgent challenge. Progress starts with listening - to patients, caregivers, and advocates who know firsthand what it means to navigate life with a rare condition.   Let’s use today to raise awareness, drive action, and commit to a future where no one is left behind.    If you are interested in how Origins can help to elevate your work in rare diseases, reach out at [email protected] to learn more.    #RareDiseaseDay #PatientFocused #RareDisease

Did you know that over 300 million people worldwide live with a rare disease? Behind each statistic is a personal story of resilience, of navigating the unknown, and of the daily pursuit of health and hope. At Anthem, we believe communication has the power to transform health outcomes. By elevating lived experiences through compelling, evidence-based storytelling, we can inspire empathy, challenge misconceptions, and drive meaningful change. This Rare Disease Day, let's go beyond awareness. Let's provoke conversations that matter, amplify patient voices, and use the power of impactful communication to unite, rouse, and uplift. Because when we listen, engage, and act - we move closer to a future where no one facing a rare disease feels invisible or unheard. If you’re looking for a strategic partner to elevate your work in rare diseases, contact us at [email protected] to learn more.