We were thrilled to host the Craig Foundation Peer Mentor Dinner recently, an inspiring event where inpatients, outpatients, and former patients come together over a meal. These dinners, initiated in 2018 with the support of Erik Hjeltnes, who experienced a spinal cord injury at 23, offer a unique opportunity for connection and support. The Peer Mentor Dinner program aims to help new patients gain perspective on their current situation and future possibilities while providing a platform for former patients to reflect on their progress and share their journeys. Being surrounded by such resilient individuals was truly an honor for us. A heartfelt thank you to Craig Hospital, the foundation, and the team for allowing us to be part of this incredible gathering! If you’re interested in learning more about the Peer Mentor Dinners or wish to sponsor one, please visit https://lnkd.in/ghMS6MWU to learn more.
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📣📣In recognition of Chronic Disease Awareness Month, we are thrilled to share a success story from a dedicated care team in Houston, Texas. 💪Despite being lean and mighty, Sweetwater Medical faced ongoing staffing challenges and a lack of resources. Like many practices, time constraints made monitoring their patients with chronic conditions even more challenging. 💡They knew there had to be a better way. ➡️Discover how AI-enabled RPM helped them streamline clinical workflows, reduce administrative burden and, most importantly, improve patient outcomes. Check out the full case study@ https://hubs.li/Q02DSBzm0
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What does Scleroderma Awareness Month mean to you? We asked Erion Moore, a Scleroderma Warrior, why Scleroderma Awareness Month is important and what this month means to him. And this is what he said: "Scleroderma Awareness Month to me is a time for patients and caregivers to bring attention to our condition and share our experiences with the world. With so many other illnesses, conditions, and other ailments, it could be difficult to find a good time to advocate for Scleroderma. Many of us put in more effort than normal to educate the public including walks, educational events, fundraising and also bring awareness to medical practitioners or researchers in hopes of better treatment or a cure." Find out what you can do and take action with us for Scleroderma Awareness Month: https://bit.ly/34FLWDE
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⚠️ 4 DAYS LEFT TO GRAB YOUR SPOT FOR THIS LIVE VIRTUAL WORKSHOP! 🗓️ Start treating more wear patients with confidence by joining my CPR for the Worn Dentition LIVE hands-on virtual workshop on May 9 & 10. Earn 14 hours of hands-on participation CE credits, ask questions and master the management of worn dentition cases. In this workshop, you’ll: ✅ Identify the etiology of the disease ✅ Discover how to safely transition patients from prototype bonding to definitive therapy ✅ Learn expert smile design and layering tips for creating beautiful smiles ✅ Develop strategies to safely rebuild your patient’s smile and open VDO (if necessary) Ditch the travel and take this course stress-free — this workshop is 100% virtual. 🚫 Stop leaving money on the table by avoiding these types of cases! Enhance your skills and case confidence with this live virtual workshop. Reserve your spot and kit now, only 4 days left to register! 🔗 https://loom.ly/TII8DQs I hope to see you there!
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No one understands the patient experience better than families who have walked that road themselves. In December 2023, we launched the Patient and Family Seal of Collaboration, a program to identify and celebrate projects that incorporate direct input from families. In the first 6 months, we’ve already awarded the Seal of Collaboration to 8 projects – and there are more in the works! These include: • A Family Viewing Screen to see your spot in line for walk-in lab or radiology services. 🖥️ • A Roadmap to Discharge for heart patients. 🗺️ • A Rare Disease Research Agenda to prioritize projects that matter to families of kids with genetic conditions. 🧬 Learn more or share your idea here: https://cmkc.link/3VR5Bff
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This webinar is coming up fast! See you soon!
We want to build YOUR dream practice 🏥 Don't just take our word for it, tune in to our LIVE webinar with Dr. Rachael Jeffrey & Christina Johnson, a DVM/Practice Manager duo who opened a brand-new hospital with VPP in 2023! Join VPP & WVLDI (https://lnkd.in/ge_vmEeW) on 5/30 to learn more about the path to practice ownership and how VPP can help ❤️🐾 REGISTER NOW ➡️ https://lnkd.in/g3Udx_dr
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For those looking to learn more about the Lymphedema Treatment Act, consider listening in to this informational call
🔦Shining Light on the Lymphedema Treatment Act! We invite you to join this webinar hosted by the Lighthouse Lymphedema Network with Shelley Smith DiCecco Featuring our very own Bethanie Noll, MOT, OTR/L, CLT , Clinical Specialist and Hope 4 Healing's Owner and CFO, Terri McClanahan Register here for the webinar on April 17th, 6pm EST: https://lnkd.in/ekTaGn-G
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Some interesting stats for IWD2024 When surveyed, 50% of women thought they would be most likely to die from breast cancer but in reality only 6% will die from breast cancer and 35% will die from cardiovascular disease. And when women present to ED with heart attack it takes them 90minutes longer to get assessed for heart attack than men. Every minute is critical, as time is muscle, so women are more likely to suffer worse outcomes than men following heart attacks.
Happy International Women’s Day! 🎉 I’m privileged to work alongside brilliant women who inspire me everyday. We celebrated this week by hearing from an incredible panel of speakers about their experience with cardiovascular disease! 👏🏻 Rowena Newman, Sarah Zaman, Charlene Bordley, Vicki Wade Heart Foundation David Lloyd Vanessa Poulsen Simon Cowie Lyn Davies Mariam Mukaty Dean Watson Angie Shum Moana Wood
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Watch the first episode in PHA Support Group 101, a series designed to help answer questions about PHA support groups. Abby Sickles, manager of patient and caregiver programs at PHA, shares the importance of PHA support groups and insights about what support groups offer to patients, caregivers and parents of children with PH. Support group leaders of local communities share their favorite part about being a support group leader. Watch now to learn more about support groups and how to become a support group leader. https://ow.ly/MujI50RmHJE
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Business Development Manager - Immunexpress / SeptiCyte RAPID - 1st FDA cleared host-response, Gene Expression, for Sepsis, that aids clinicians to make time sensitive decisions for improved patient outcomes & compliance
If you missed this latest Sepsis Alliance Webinar with Dr. Miller from FirstHealth, sharing his teams practical use and experience, using the SeptiCyte RAPID FDA cleared test in a clinical emergency medicine setting, no problem, DM me and I'll share a copy of the presentation with you to review. #sepsis #emergencymedicine #patientcare #moleculardiagnostics
Save the Date! Dr. Russell R. Miller, Medical Director of Critical Care at FirstHealth of the Carolinas, will be discussing his experience with SeptiCyte® RAPID in a Sepsis Alliance webinar entitled “The Role of Host Response Test, SeptiCyte RAPID, To Improve Sepsis Bundle Compliance and Address Diagnostic Uncertainty” on February 15, 2024, from 2-3pm ET.
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