Lōvu Health的动态

How true! Companies and individuals within those organizations must learn to walk the talk!

All-new insights on your biggest #diversity in clinical trials challenges will be explored on May 15-16! DGE releases the OFFICIAL AGENDA for the 3rd Diversity in Clinical Trials Summit. View the agenda: https://ow.ly/RBuB50QuSpf Register to save $400 with super early bird: https://ow.ly/fjZF50QuSpg #DGEvents #diversityinclinicaltrials

Improving diversity among clinical research study participants starts by building trust and awareness across patient communities. Join our Patient Diversity media campaign that spreads awareness about the critical need for more diverse representation directly to underrepresented communities. Learn more about getting involved: https://lnkd.in/e7Ptf-8

???????? ?? ??????????????:?The healthcare and research establishment is hard enough to navigate, but when your child is sick, it can be particularly daunting. Cure Mito Foundation is a patient advocacy organization that advances #LeighSyndrome research and supports affected families worldwide. By implementing the Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard (MRCT Center) Clinical Research Glossary on their website, they empower families with critical, plain language resources to make informed decisions about the care of their loved ones. Learn more about how to implement this free resource in your patient/participant materials at our June 4 webinar: ???????????? ?????? ??????????????????: ???????????????????????? ?????? Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard (MRCT Center) ???????????????? ???????????????? ???????????????? ?????? ???????? ???????? ???? ???????????? ????????????. Register here:?https://bit.ly/3VmbhOe Sophia Zilber ?? is dedicated to supporting and empowering families that #LeighSyndrome impacts. Join us on June 4th as she shares her personal experience and why Cure Mito Foundation includes the Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard (MRCT Center) Center’s Clinical Research Glossary as part of its educational resources. #PatientAdvocacy #LeighSyndrome #HealthcareResources

Looking forward to participating as a panelist at the upcoming Healthcare Leadership Quorum, discussing Human Capital and People Strategy! We will be diving into critical conversations on how health systems are addressing the growing challenges of workforce vacancies, innovative approaches to retention, and the impact of leadership on fostering a resilient workforce. This is an important opportunity to share insights, learn from industry peers, and collectively tackle the evolving dynamics of healthcare. #workforcedevelopment #HealthcareLeadership #PeopleStrategy #HumanCapital #WorkforceInnovation #HealthcareTransformation

IgG4ward!'s Director of Patient Advocacy, Katharine M. Provencher, MSW, is counting down the days to The JAM and shares a few reasons why you should be too. ?? The JAM is all about patients. We are fortunate to have key opinion leaders from all over the world participating in The JAM, sharing patient-centric information. ?? The JAM is about access. The schedule not only builds in ample time for questions after each talk, it also includes smaller “Breakout Sessions” during which attendees can interact with faculty and with each other. ?? The JAM is about outreach, including networking opportunities like the cocktail hour, morning yoga, and more. Learn more about The JAM: #IgG4RD #IgG4relateddisease #IgG4wardJAM

We've been advocating for a seat at the table for People of Color. But we recognize that one seat represents only a single voice. To enact the meaningful change, the Global PAD Association's DEI Patient Advisory Committee aspires to achieve, they have determined it requires more than one-off, token representation. A chorus of diverse voices, reflecting varied backgrounds and socioeconomic perspectives, is essential for authentic and effective change. Designing for a community, demands the collective input of that community. Therefore, instead of inviting only one or two patients to come to you, DEI Committee Chairman Charles Winters and his team of nearly two dozen Patients of Color (and growing), invite ?????? to "???????? ???? ?????? ??????????", where we can amplify the ???????????????????? voice of the community, fostering true inclusivity and the change we all want to see. "???????? ???? ?????? ??????????" ??????: ???????????????? Bring your opportunities for a diverse ???????????????????? of Patients of Color to review your research projects and trials to offer guidance, support, and feedback throughout the entire process. ???????????????? Seeking effective outreach to communities of color and impactful messaging for heightened awareness and engagement? Share your projects and objectives with us and receive real-time feedback from our DEI Advisory Board. ?????????????????????????? Are you seeking to amplify the voices of patients of color, drive awareness, and foster tangible change, ultimately leading to a reduction in amputations? "???????? ???? ?????? ??????????" and present opportunities for patient involvement in seminars, media, and conferences (virtual or in-person), empowering us to elevate the narratives and experiences of people of color impacted by PAD. For More information on how to get GPAD DEI Certified, go to www.ComeToOurTable.org

Please join us in welcoming our newest member We Want Life (WWL). WWL was founded by Esraa, a cancer patient advocate who has worked with thousands of patients since 2011. She gained in-depth experience in five years and learned valuable insights that led to the establishment of WWL. Patients have something to say, patients have useful input for the policy makers. Patients need guidance to say their insights in a useful way. Patients are the end users of the health care system. Patients need a chair at the table where decisions are made. Patients need training and inspiration to be able to earn the chair. Patients need this chair because they need life to be more precious, they need a quality life, so it is time to start our patient advocacy group, because we all want a life! Empowering patients to positively impact the healthcare system in the best possible way. Learn more:?https://lnkd.in/eGAhf8cp

Join us for an upcoming webinar on September 10th to hear from patient community-based organizations as they give an inside look into best practices and strategies for clinical trial communications and awareness. More specifically, the panelists discuss: ?? The obstacles and limitations experienced by diverse patient groups in accessing clinical trials ?? Suggestions on fostering meaningful connections at the community level ?? Tailoring strategies for approaching communities accordingly ?? Tips on disseminating crucial information within diverse communities ?? Promoting general awareness about clinical trials Learn more: https://lnkd.in/ekqbKx2e #PatientVoice #PatientAdvocacy #Diversity #PatientsasPartners #clinicalresearch #clinicaltrials