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  • Work with Us
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    • Home
    • Our Mission
      • Founder & Inspiration
      • Financials
      • Contact Us
    • Work with Us
      • Board of Directors
      • Scientific Advisory Board
      • Board of Volunteers
      • Professional Testimonials
      • Family Testimonials
      • SpecialEngagements/Media
    • Support us
      • Donations
      • Shop Merchandise
    • Events
      • Fishing Tournaments
    • Research
      • VAMP2 Syndrome
    • Resources
      • Support Groups
      • Webinars
  • Home
  • Our Mission
    • Founder & Inspiration
    • Financials
    • Contact Us
  • Work with Us
    • Board of Directors
    • Scientific Advisory Board
    • Board of Volunteers
    • Professional Testimonials
    • Family Testimonials
    • SpecialEngagements/Media
  • Support us
    • Donations
    • Shop Merchandise
  • Events
    • Fishing Tournaments
  • Research
    • VAMP2 Syndrome
  • Resources
    • Support Groups
    • Webinars

Raging raymond foundation

Empowering Communities, Changing Lives.

Empowering Communities, Changing Lives.Empowering Communities, Changing Lives.Empowering Communities, Changing Lives.

Welcome to the Raging Raymond Foundation!


 Hello and welcome to our little corner of hope and determination, the Raging Raymond Foundation! We are a passionate community, led by our inspiring founder, Alexandra Gaudlap, a devoted mom and a relentless advocate for children with rare genetic conditions. Our journey began with Alex's son, Raymond, a radiant child who was diagnosed with Cerebral Palsy and a VAMP2 gene mutation, a rare genetic condition.  

Our Mission 


Our mission is to spread awareness about rare genetic conditions impairing brain development and neurological development in children, advocate for the causes, drive research into the disorders, and seek therapeutic interventions. We are here to support families through fundraising events, online support groups, webinars, and by providing resources. We believe in the power of community and aim to be the voice for those who need it the most.

Our Team 


Our foundation is guided by a dedicated Board of Directors, including Alex, our President, Ryan Honick, our Treasurer, and Cheralee Kemp, our Secretary. We are also supported by a brilliant Scientific Advisory Board, consisting of renowned experts like Associate Professor Wendy Gold and Dr. Henry Houlden, who are committed to advancing research in rare genetic disorders.

Our Impact 


We are a volunteer-run organization, maximizing our donors' contributions towards our goal of funding research for rare brain and neurodevelopmental disorders.  We are working tirelessly to support research for many conditions, aiming towards finding a cure. We have obtained  501(c)(3) status in New Jersey, ensuring transparency and integrity in our financial operations. Check out our financials for more details.

Join Us! 


We invite you to join us in our mission to make a difference in the lives of children with rare genetic brain and neurodevelopmental disorders. Whether it's by donating, participating in our events, or simply spreading the word, your support is invaluable. Let's work together to bring hope, support, and a brighter future to these children and their families. Dive into the testimonials from our professional collaborators and see the impact we’re making together!

Final Words 


We are more than just a foundation; we are a family united by love, hope, and a common goal. Alex’s journey, her story, and her unwavering spirit are the driving forces behind our foundation. We believe in the strength of unity, the power of knowledge, and the magic of compassion. So, come along, be a part of our journey, and let’s create a world full of possibilities and smiles for our little warriors!

EIN - 92-0324693

Copyright © 2023 Raging Raymond Foundation  

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