VHL ALLIANCE INC

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We are a non-profit support organization for patients and families affected by von Hippel-Lindau disease (VHL). Join our group: http://www.facebook.com/groups/VHLawareness/ The VHL Alliance (VHLA) is dedicated to research, education, and support to improve awareness diagnosis, treatment, and quality of life for those affected by VHL.

Founded

1993

Facebook

4800

X (Twitter)

985

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2042047

Address: 1208 VFW Parkway Suite 303, BostonWeb: Sign in to see organisation websiteFacebook: VHLAllianceX (Twitter): VHLAllianceEmployees: 6Revenue: 1537754ICO: 43180414

VHL Alliance | Working To Cure Cancer Through VHL Research Curing Cancer through VHL Research We Bring Heart Soul Science To The Fight. Our Mission Improving quality of life and health outcomes for VHL patients families and caregivers with inclusive community building connections to excellent education and treatment options and advancements in medical research. Backed ByResearch. What is VHL.

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News about from their social media (Facebook and X).

Lucas

1. What strategies can be implemented to increase community awareness and understanding of von Hippel-Lindau disease among the general public?

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Robin

💚 I'm so inspired by the work the VHL Alliance is doing! Together, we can make a difference for those affected by VHL. Let's continue to support each other and spread awareness! 🌟

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James

2. How can we enhance collaboration between patients, families, and researchers to accelerate advancements in VHL-related treatments and therapies?

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Andrew

🙌 Research and community support are key in the fight against VHL! Proud to be a part of this amazing group that brings hope and connection to families dealing with this disease. Keep pushing for progress! 💪✨

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