MEDLIFE’s Post

Altarum’s experience ignites innovation. We are at the forefront of behavioral health solutions, collaborating with federal, state, and community partners to implement equitable behavioral health care delivery solutions informed by evidence, powered by technology, and strengthened by coordination. 🔍 Discover how we’re advancing public health by supporting an integrated, sustainable, and equitable crisis care system for Substance Abuse and Mental Health Services Administration’s (SAMHSA) 988 and Behavioral Health Crisis Coordinating Office https://lnkd.in/gYsM3QKz 🔍 Explore how Altarum is leading the way in behavioral health solutions https://lnkd.in/g3H4dkAX 🔍 Learn about our capabilities in building capacity and driving impact through our training and technical assistance services  https://lnkd.in/eDnUxuPW We are a nonprofit organization focused on improving the health of individuals with fewer financial resources and populations disenfranchised by the health care system. Learn more at altarum.org. #AltarumImpact

That's a wrap! Yesterday Sally Devine and I held the final steering group session of Gorton Health Matters. We spoke about, how community engagement models can struggle to be successfully replicated and reflected on the reasons for the projects success and some of its challenges. Here are some of our closing reflections: 1. Relationships have deep histories - it takes time to embed a successful project and thats often overlooked. We reflected on how long each worker and orgnisation had spent building their own relationships in the area of focus? (It was a combined lifetime!) 2. Discomfort is generative - Partnerships need space for disagreement. Do all of the partner feel comfortable airing grievances? 3. The funding doesn't fit out current needs - We desperately need more funding options for strategic and relational work that sits outside of patient involvement in research project. 4. Why isn't patient experience and engagement included in literature reviews? Who gets to decide when a topic is adequately researched? What a conversation! I'm inspired and genuinely in awe of the amazing experts we got to work with on this. Thankyou Toto, Tikhala, Idowu, Fozia, Sarah and Abin for such a brilliantly inspiring close to the work. Watch this space for our co-authored paper! (The image below was the penultimate one)

🗣️ Today and tomorrow: We need your opinions and experiences to create a more quality and exquitable experience for patients living with neuro-related conditions. Context: A group of is academic researchers, entrepreneurs advocates, equity and accessability advocates and community health providers* are working on NEURO360-a systems-change effort to build an inclusive innovation ecosystem building off of our region’s strengths in neuroscience. The ultimate goal is to improve patient outcomes in neuro related conditions and diseases. As someone who is very open about her own diagnoses, while being very aware of my priveldge in being able to access care, this project is incredibly close to my heart. More info here: https://lnkd.in/gVPwEA7y To make sure we are creating a more equitable system, we are centering the voices of patients, providers, and public health practitioners to help us focus areas for our work. We are asking for input through a number of ways, the first is two listening session happening next week. These will be confidential, facilitated small group conversations. Monday, February 19 from 6-7:30 held virtually over zoom Tuesday, February 20 from 6-7:30pm in person at 20. S Sarah Street (dinner will be provided) We know your time is important, and for participating, you will receive a $50 stipend. Please RSVP using this link: https://lnkd.in/gJBmqXzC. If you RSVP to attend either the virtual or in person session, you will receive an email from Katherine at WashU. We would love to see you there. If you can’t make these times, please let me know so we can get you involved in future community sessions. *Partners orgs included BioSTL, WashU Department of Neuroscience, Cortex Innovation District, Forward Through Ferguson, Starkloff Disability Institute

Are you tired of feeling overwhelmed and being controlled by your anxiety? Maybe you’ve begun to notice the important signals your body is showing you, but you’re not sure what to do about it. Compassionate Community Therapy groups are now forming, and you're invited to learn more about joining this supportive community. https://rpb.li/Af39p #Therapy #TherapyGroups

To drive meaningful change in research, we must actively engage with the communities that are often overlooked. Too often, people take progress for granted, but real improvement comes from those willing to step up. By reaching areas with limited education or financial resources, we ensure that those who need the most help are included. Without diverse participation, treatments may not work effectively across all populations. Your involvement can make a difference for you and your children. #VoicesOfInclusiveResearch #InclusiveResearch #ClinicalResearch #HealthEquity #CommunityEngagement #ClinicalResearch #FutureHealth

"I cannot say this enough: If The Source wasn’t there, I would not still be here." Please Share Ashley's Heartfelt Story to Keep the Momentum Going and Increase the Likelihood for Significantly More Funding for Behavioral Healthcare Services in the FY25 State Budget! Click below to read about Ashley and others' uplifting stories, to access NJAMHAA's full campaign brochure, and for more inspiring examples of the value of behavioral healthcare services and the workforce who provides them. https://conta.cc/3SDlQda

The two phases of Saathealth’s learnings that shape our ambitions for the next 5 years. The first, 2019-2021 showed us how the use of infotaining, preventive health content can be used to influence health seeking behaviors in a base of 100-150K families. The second, 2022-2023 demonstrated our ability to effectively reach, engage with and influence the health choices of millions of health consumers. The third phase - 2024 onwards, is when we apply our learnings to help millions of health consumers access health and financial resilience products through our curated marketplace. Looking forward! Aditi Hazra-Ganju Saathealth

🧡 "It helps to talk to someone that understands what we are going through." 🧡 When you're facing a diagnosis of Myeloproliferative Neoplasms (MPNs), it's essential to connect with others who truly understand. Whether it's through support groups, patient communities, or one-on-one conversations, finding a listening ear can make all the difference. Share your story & Let's #MakeSenseOfMPN together. https://lnkd.in/dMEXrKZq #MPN2024 #MPNAN #Support #Community

Happy to read a just published commentary on #community #involvement, with very practical recommendations, such as: 1st) recognise the value that the lived experience brings to projects and services through appropriate #acknowledgment—for example, including a budget line item for community involvement in grant applications and #authorship opportunities where relevant and appropriate. 2nd) keep up to date with current best practice approaches for community involvement, such as the World Health Organization guidelines, and offer capacity-building opportunities for those affected by #diabetes who are seeking to be involved with projects. 3rd) set clear goals and expectations for community #involvement, with clear and regular #communication, including when and how #community contributions have been implemented and the #outcomes of this. 4th) take proactive steps to reduce #stigma and #discrimination surrounding diabetes to foster a safe environment for contribution and collaboration from those with lived experience. 5th) provide #support for those active in the community involvement space, through initiatives such as ensuring that more than one community #representative is present on a project or committee and offering opportunities for #briefing and #debriefing as needed. Congratulations to the authors, including Ashley Ng and Renza Scibilia, for sharing such relevant lessons to the global advancement of community involvement, meaningful engagement, and co-design.

Dr. Schwartz, founder of Total Lipedema Care, shines a spotlight on Lipedema, alongside patient Nancy Guillen, at KCAL News. Together, they share a powerful message about the importance of understanding Lipedema—an often misdiagnosed condition that leaves many feeling a sense of shame and isolation. In this enlightening segment, Dr. Schwartz emphasizes the critical need for education to dispel misconceptions surrounding Lipedema. By fostering understanding and compassion, we can break down barriers, paving the way for a more informed and empathetic society. Join the movement to spread awareness and support those affected by Lipedema. 💜 totallipedemacare.com #lipedema