Cure NF2 Foundation

Join us in moving research forward. Donate today: US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4

NF2 impacts entire families, and for Lizzie and Alanna, the journey has included surgeries, scans, specialist visits, and constant resilience. Behind every appointment and every procedure are real people fighting to hold onto their health and their futures.

Donate today: US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4 #CureNF2 #NFAwarenessMonth #NF2Day

Every NF2 diagnosis involves a child facing extraordinary challenges. A.J. was diagnosed at 6 and continues to manage multiple tumors and ongoing monitoring, but his strength shines through daily.

In honor of Lyren and every family affected by NF2, help us continue funding research and moving closer to better treatments: US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT

Lyren passed away in 2019, but her courage, strength, and spirit continue to inspire our community and our mission to find a cure for NF2. Her story is a reminder that behind every diagnosis is a person deeply loved by family and friends, and why this fight matters so much.

Donate today: US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4 Mail: Cure NF2 Foundation, P.O. Box 859, West Chester, PA 19381

Behind every diagnosis is a person. A family. A fight. NF2 is not just a condition: it’s a daily reality for children, parents, and loved ones navigating uncertainty, treatment, and hope. Their stories are why we exist. Their strength is why we keep going.

Donate today: US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4 Or mail a check: Cure NF2 Foundation P.O. Box 859 West Chester, PA 19381

Behind every NF2 diagnosis is a story, and a child, a family, a future. Tucker’s journey began with small changes that led to a life-changing diagnosis. Stories like his remind us why this fight matters so much. Help us turn stories like Tucker’s into hope.

Donate today: US: buff.ly/jmoqb59 Facebook: (buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4 Mail: Cure NF2 Foundation, P.O. Box 859, West Chester, PA 19381

NF2 is rare, but it affects real people in every community. Most are diagnosed young. There is still no approved treatment. But there is hope. Gene therapy research is advancing and with your support, we can help move these breakthroughs closer to real treatments for patients.

US: buff.ly/jmoqb59 Facebook: buff.ly/AYASXrP PayPal: buff.ly/iEGJtHY UK: buff.ly/2uWyPkd Canada: buff.ly/tFQgRyT Europe: buff.ly/t1wqsN4 Mail: Cure NF2 Foundation, P.O. Box 859, West Chester, PA 19381 #CureNF2 #NFAwarenessMonth

Before a therapy can be tested in people, it must first be shown to be safe, high-quality, and ready. That’s the work happening now, and it’s what your support makes possible. Closer to clinical trials. Closer to a cure. Donate today and be part of this progress:

Donate today: buff.ly/7nEgMFb Read Laurel's story: buff.ly/AcoB6WJ #CureNF2 #NFAwarenessMonth #NF2Day

Today is NF2 Awareness Day. NF2 is a rare genetic condition that can cause tumors to grow along the nervous system, impacting hearing, balance, vision, and more. But behind every diagnosis is a person, a story, and a community that refuses to give up.

Living with NF2-SWN comes with real, everyday challenges, especially when it comes to mental health. We want to hear from you: what has helped you cope? Share your experience or tips in the comments. Register for our upcoming webinar: buff.ly/qRGkudY

Living with NF2 can bring more than physical challenges. Join our webinar to explore tools and strategies to support your mental health, whether you’re managing appointments, scans, or uncertainty. Friday, May 22 at 11:00 AM ET / 4:00 PM BST Register here: buff.ly/NJxiJxq

As NF Awareness Month begins, we want to share an important milestone. NF2 BioSolutions is now also known as Cure NF2 Foundation. This new name reflects our continued commitment to advancing research and progressing toward better treatments and ultimately a cure for NF2.

May is NF Awareness Month. All month long, we’re raising awareness, sharing stories, and advancing research that brings us closer to a cure for NF2. Join us this May. Help raise awareness. Support the mission. Be part of the movement to #CureNF2.