Yesterday evening we kicked off the 2024 LBF and Foresight Longevity Workshop with a VIP reception in San Jose with our Speakers, Sponsors, and Fellows. Thank you to our hosts: Longevity Biotech Fellowship, Stanford University School of Medicine, and Media Partners: Lifespan.io (Lifespan Extension Advocacy Foundation). This event wouldn’t have been possible without our sponsors: Protocol Labs, AgingBiotech.info, 100 Capital, NFX Bio, OpenCures, Deep Origin, and THE MICHAEL ANTONOVICH CHARITABLE FOUNDATION. We look forward to exploring new ideas for critical pathways with you at CANOPY and LKSC at Stanford University these next two days.
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Your brain has the potential to be an invaluable gift to research and in recognition of 𝗡𝗮𝘁𝗶𝗼𝗻𝗮𝗹 𝗕𝗿𝗮𝗶𝗻 𝗗𝗼𝗻𝗮𝘁𝗶𝗼𝗻 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗗𝗮𝘆, we want to share about the opportunity to extend your legacy to future generations scientific research through The Brain Donor Project. For the past few years, the RLS Foundation has worked closely with agency leaders to consolidate the process of proper identification of RLS brain donations for research insight that may ultimately lead to developing more effective treatments and potentially a cure. 🔗 𝐑𝐞𝐚𝐝 𝐨𝐮𝐫 𝐛𝐥𝐨𝐠 𝐩𝐨𝐬𝐭 𝐭𝐨 𝐥𝐞𝐚𝐫𝐧 𝐦𝐨𝐫𝐞 𝐚𝐛𝐨𝐮𝐭 𝐭𝐡𝐞 𝐝𝐨𝐧𝐚𝐭𝐢𝐨𝐧 𝐩𝐫𝐨𝐜𝐞𝐬𝐬, 𝐭𝐢𝐩𝐬 𝐟𝐨𝐫 𝐜𝐨𝐧𝐬𝐢𝐝𝐞𝐫𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐝𝐢𝐬𝐜𝐮𝐬𝐬𝐢𝐨𝐧 𝐨𝐟 𝐭𝐡𝐢𝐬 𝐨𝐩𝐩𝐨𝐫𝐭𝐮𝐧𝐢𝐭𝐲, 𝐚𝐧𝐝 𝐦𝐨𝐫𝐞 𝐚𝐛𝐨𝐮𝐭 𝐓𝐡𝐞 𝐁𝐫𝐚𝐢𝐧 𝐃𝐨𝐧𝐨𝐫 𝐏𝐫𝐨𝐣𝐞𝐜𝐭: https://lnkd.in/evrxQcZJ
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For the second year, the NR2F1 Foundation has an incredible team of athletes riding in this years Million Dollar Bike Ride on Saturday June 8. We are very excited that BBSOAS Sidelle and Leo will also be joining the team! Sidelle will ride with her mom, Carlie and Leo will ride with his mom, Megan. We are raising funds to support our mission to empower families living with rare NR2F1 gene variants through education, advocacy, and research. This year we need to raise a minimum of $205,000 to fund our research roadmap projects and operating costs. What's in our research roadmap? 3 Post Doctoral researchers to work alongside our lead scientists to exclusively research NR2F1 and BBSOAS for 3 years, in US, France and Germany A NR2F1 ‘New Investigator’ grant. Attract junior researchers to research the NR2F1 gene Develop a new BBSOAS mouse model Discovery of BBSOAS Biomarkers Who are the dream team riding? Jen and Eric - Mom and Dad to BBSOAS Maggie Peter McCourt - Uncle to BBSOAS Maggie Kim Barrow - Family Friend to BBSOAS Maggie Carlie and Jeff - Mom and Dad to BBSOAS Sidelle Fred and Lickel - Grandfather and Uncle to BBSOAS Sidelle Ross and Megan - Dad and Mom to BBSOAS Leo https://lnkd.in/ebShDDqt
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🌟 Meet SVI Rising Star Award Recipient: Dr Kate Firipis Dr Kate Firipis is a tissue engineer, with extensive cellular and biomaterial experience. Kate is working to bioengineer skin that can be used to heal complex wounds in SVI's Vascular Biology Lab. According to Kate, investigating the unknown is a great challenge. Why does our body work the way it does and how can we improve quality of life? "Chronic wounds impact thousands of people’s daily lives. We’re pursuing a lab grown skin to heal the body with its own cells." "I’m very excited to investigate lab grown human skin that responds to touch. Many patients require replacement skin tissue due to cancer, trauma or chronic wounds. Growing skin in the lab would reduce the need to take skin flaps which create a secondary wound site." #SVI #StVincentsInstitute #Fundraising #Medical #Research #MedicalResearch #Donation #NFP #notforprofit
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As marketers within the biotech space, we often find ourselves filled with wonder as we learn more about innovations and breakthroughs in sequencing technologies, immuno-oncology, targeted therapies, spatial biology, and other realms where our clients are making an impact. We recently connected with SciAll.org, a nonprofit organization that aims to create an inclusive space where individuals can embrace and celebrate their STEM identity. There’s a scientist within each of us, and we’re helping SciAll reach and inspire more young minds. Discover more about SciAll and how Samba is supporting nonprofits: https://hubs.li/Q02JPbQ60 #STEM #Diversity #LifeSciences #Biotechnology #NonProfit #LifeScienceMarketing #Accessibility
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ALS TDI's founder, Jamie Heywood, discusses how his bother Stephen's ALS diagnosis led him to create the first-ever nonprofit biotech – with the ultimate goal of putting the patient first. Learn more about the evolution of ALS TDI at https://lnkd.in/e9KUeQMr.
Putting Patients First: The Creation of ALS TDI
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Strong leadership makes a difference! I'm impressed by Dave's initiative to support critical ALS research. Those impacted by this disease, like Dave, have a unique perspective that can guide research in the right direction. Let's help him reach his goal! #ALS #ALSawareness #Research
May is ALS Awareness Month - and the one-year mark of my journey as an ALS patient and advocate. The past year has been about learning - learning to live in the moment, to adapt to new disabilities, and to persevere. I've also learned a lot about ALS - attending conferences, reading medical literature and studying the landscape. I'm often asked: "How can I help?" The biggest thing I need help with is steering resources towards critical but underfunded corners of ALS research. What better way to do this than to fundraise for a lab that is trailblazing the application of CRISPR to treat ALS and FTD: Claire Clelland and her lab at University of California, San Francisco. This research holds the potential of one day preventing / reversing ALS for many with just one shot. This ALS Awareness Month, I'd like your help accelerating progress at Clelland Lab. Over the past few days, close friends from my alma maters (Columbia Business School, London Business School, and Lehigh University) have seeded the fundraiser with over $20,000. With your help (giving and sharing this with your network), amplified by the power of social media, I believe we have a real shot at hitting our $275,000 goal. Thank you – and let's hack ALS together!
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The Dysphagia Research Society is organized exclusively for charitable, educational and scientific purposes.
New teams are in this weeks lineup - will your team be here next Tuesday? Challenge your friends and colleagues to see who can get in the top 5! Support Early Investigators: Funds raised will go towards travel scholarships for Early Investigators from around the world to attend our 2025 Annual Scientific Meeting. Invest in the Future of Dysphagia Research: The DRS Research and Education Fund will benefit from your participation, helping establish future scholarships and grants for our members. How to Participate: • Register for the DRS Dash for Dysphagia (link in bio!) https://bit.ly/4dK4h4Q • Choose your activity • Complete your chosen activity between June 8-15 • Share your photos and achievements using #Dash4Dysphagia #DRSDash24 #dysphagiaresearchsociety #dysphagia #dysphagiaawareness and tag us @DysphagiaResearchSociety Together, let's make a difference for people with dysphagia! See you at the (virtual) finish line!
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The non-profit foundation that owns Medicon Village, "Mats Paulsson's Foundation for Research, Innovation and Societal Development", now announces this year's donations, with the application period ending on 8 May. Since 2019, the foundation has granted SEK 69.2 million in funding to 33 research projects at Lund University and Malmö University. The foundation invites applications from the Faculty of Medicine at Lund University, the Faculty of Engineering at Lund University, and Malmö University within the following project categories: - Innovative research projects within life science. - Innovative research projects specifically within ATMP and/or cancer diseases. - Equipment critical for the implementation of specific innovative research projects. The Mats Paulsson Foundations is the collective name for the foundations initiated by the entrepreneur Mats Paulsson. This includes "Mats Paulsson's Foundation for Research, Innovation and Societal Development", "Mats Paulsson Foundation", and "Stefan Paulsson Cancer Foundation". A common goal of these foundations is to support endeavors that benefit scientific research and innovations, particularly in medicine and life sciences. For more information, visit https://lnkd.in/dD2jWEs9. #donations #lifescience #sustainableownership #sciencepark Lund University | The Faculty of Engineering at Lund University | Malmö University | Region Skåne | Region Skåne – utveckling & innovation | Lunds kommun
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Join the 2024 SRF Research Challenge to support research like Dr. Flynn's! Dr. Ryan Flynn (Harvard University, Boston Children's Hospital) shares information about his SRF-funded research project, Cell Surface GlycoRNAs in Autoimmunity, and how it could help people living with scleroderma. Your support of innovative research like Dr. Flynn's, and other projects funded by the SRF, helps advance our understanding of this disease. By joining this year's Research Challenge, you'll be a part of the next era of breakthroughs that could end scleroderma. Will you help us accelerate the pace of research so that we can one day end this disease? The best part is that when you make a gift to our Research Challenge, you’ll unlock a matching donation dollar-for-dollar*, thanks to the generosity of two families who, like you, are committed to finding a cure. Double your impact today: https://bit.ly/3RWrUOo P. S. Special thanks to our Research Challenge match donors—Board Members Luke Evnin (Chairman) and Deann Wright, and the Schimberg Family Foundation—for doubling the impact of your gift! *Up to $75,000 through July 31, 2024. #srfcure #sayscleroderma #sclerodermaresearch #scleroderma
Dr. Flynn Shares How His Research Could Help Those with Scleroderma
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It's the last day of #Sarcoma month, but the fight to find new and better treatments for one of the deadliest #Cancers primarily affecting #Children continues.🧑🏽🔬 We're excited to announce a new program, #SarcomaAccelerator, funded by the Hofer Muir Philanthropic Organisation together with the Cooper Rice-Brading Foundation. 🙌 For the next two years Prof Ron Firestein, A/Prof Jason Cain and their team will create a collection of #Tumour samples from sarcoma patients and use cutting-edge technology to study these them. “By understanding the unique characteristics of each tumour, we can develop targeted therapies that are more likely to be effective. This approach has the potential to improve survival rates and quality of life for young patients living with sarcoma.” A/Prof Cain Read more about how we expect this new program to be a game-changer in the fight against childhood sarcoma here: https://bit.ly/3AdTU9V L-R; Dr Yuxin (Sally) Sun, A/Prof Jason Cain, Dr Claire Sun, Prof Ron Firestein
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