Soleno Therapeutics, Inc.

Do you have someone in your life this Halloween season with Prader-Willi syndrome (PWS)? Those living with PWS can experience a multitude of symptoms including hyperphagia, cognitive delays, behavioral challenges, and low muscle tone, making Trick-or-Treating difficult. Read some tips from caregivers to make for an enjoyable and inclusive Halloween: https://bit.ly/4nUjnsS 🎃 Wishing a fun and safe Halloween for all in the PWS community! #PraderWilliSyndrome #CaregiverSupport #RareDisease #PWSCommunity #SafeHalloween

Looking for a career where you can make a difference? The Soleno team is dedicated to bettering the lives of individuals affected by rare diseases, starting with Prader-Willi syndrome (PWS). If you’re ready to drive impact and work with an amazing and resilient community, we have positions available for talented, dedicated, and passionate professionals. Browse our available opportunities: https://bit.ly/4iyQHDE #PWSAwareness #RareDisease #PWSCommunity

Soleno conducted its fourth successful DC Hill Day of 2025 in September! Jill Yersak and Kara Hinkley are always grateful for the support provided by KPM Group DC's Paula Gutierrez! Our trio met with a dozen congressional offices while advocating for policies that support the PWS community and for the re-establishment of critical incentives for R&D in rare disease drug discovery. Did you know that Soleno's government affairs team also advocates for patient access and affordability policies across all 50 states? Stay tuned for exciting updates! #PWSAwareness #RareDisease #PWSCommunity

Soleno Therapeutics is committing up to $5M in grant funding to advance promising genetic research toward a potential cure for Prader-Willi syndrome (PWS). Led by Dr. Neil Cowen and guided by a world-class advisory board, this initiative reflects Soleno's ongoing commitment to the PWS community. More details to follow. #PWSAwareness #RareDisease #SolenoTherapeutics

As we step into a new season, we look back on a September defined by strong community connection and collective advocacy. It is our pleasure to join the Prader-Willi syndrome (PWS) community in celebration and support at these events. Check out a few snapshots from Prader-Willi California Foundation's Long Beach marathon, the Washington/Oregon State Chapter of PWSA | USA's 50th Anniversary celebration, Crafting Hope for Jaxon, One Small Step Avon and Watch Us Farm that provide a small glimpse of this community's big impact. #PWSAwareness #Support4PWS

Each person’s experience with Prader-Willi syndrome (PWS) is unique. Although this is a complex, lifelong condition, having the right support and understanding can make a valuable impact. Here are some ways to foster an inclusive and supportive environment for those with PWS and their caregivers: ✅ Ask thoughtful and respectful questions instead of making broad assumptions ✅ See the person instead of the diagnosis and lead with empathy rather than judgement ✅ Be patient, cultivate a supportive environment, and educate yourself on PWS Don’t know how to support individuals with PWS? Check out our “Understanding PWS: Showing Up with Care,” guide, created in partnership with the PWS community, for helpful tips, information and resources: https://bit.ly/4l4HKSs #PWSAwareness #RareDisease #Support4PWS #Inclusivity

A sense of shared purpose and community underlies everything we do at Soleno. We value the perspectives and contributions each of our employees makes toward advancing solutions that offer real hope and tangible results for the Prader-Willi syndrome (PWS) community. "At Soleno, the commitment to advancing our understanding of complex and often-overlooked rare diseases is truly felt across the organization. I’m grateful to be part of this journey and to have the opportunity to communicate meaningful science, with caregivers and individuals living with rare disease at the heart of it all." - Sarah Juhn, Senior Director - Medical Communications Interested in a career where you can make a difference? We are looking for talented and driven individuals to join our team: https://bit.ly/4iyQHDE #PWSAwareness #RareDisease #Support4PWS

Congratulations to our CEO, Dr. Anish Bhatnagar, who was named the 2025 Champion of Hope in recognition of his leadership and contributions to the #PWS community. It was an impactful evening celebrating with researchers, advocates, families, and industry professionals who helped make this year’s progress possible. Thank you to the Foundation For Prader-Willi Research for the honor and for an evening that highlighted the strength of this community. #PWSAwareness #RareDisease #PWSCommunity

We were honored to participate in Prader-Willi Syndrome Association | USA’s 50 year anniversary celebration as we reflect on their unwavering commitment to the Prader-Willi syndrome (PWS) community. This milestone highlights years of collective activism through early efforts and present progress. Here’s to a bright future for the PWS community! #PWSAwareness #RareDisease #PWSCommunity