RP Gene Research Foundation

RP Gene Research FoundationRP Gene Research FoundationRP Gene Research Foundation

RP Gene Research Foundation

RP Gene Research FoundationRP Gene Research FoundationRP Gene Research Foundation
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    • Home
    • About Us
    • Our Story
    • FAQs
    • Medical Research
    • Blogs
    • Contact Us
    • Privacy Policy
  • Home
  • About Us
  • Our Story
  • FAQs
  • Medical Research
  • Blogs
  • Contact Us
  • Privacy Policy

About RP Gene Research Foundation

Eye testing

Advancing Eye Disease Research

The RP Gene Research Foundation (RPGRF) is a charitable organization dedicated to funding scientific initiatives to combat Retinitis Pigmentosa (RP) and other degenerative eye diseases that can lead to blindness. As one of the most prevalent inherited retinal diseases, RP affects approximately 100,000 individuals in the US and 2 million globally.

Our Mission

Our primary focus is on funding research related to the PRPF 31 gene, a significant contributor to RP, and secondarily, we support studies targeting other RP genes and related degenerative eye conditions. 


PRPF 31 is a dominant autosomal reduced penetrance gene that is a chronic and progressive form of RP. While PRPF 31 is often considered the second most common cause of RP, its true prevalence may be underestimated due to its reduced penetrance. It can silently pass through generations before manifesting unexpectedly, leading to unexpected vision loss. Given its unpredictable nature, extensive research efforts are crucial to uncovering treatments and a cure for PRPF 31 and other RP genes. 

Our Partnerships

We are proud to partner with a variety of organizations to support our goal of curing Retinitis Pigmentosa. Our partnerships enable us to expand our reach and provide even more resources to scientist dedicated to finding a cure.

Our Board of Directors

Founder and President of RP Gene Research Foundation

President

President

President

RPGRF was founded by Martina Manning after both of her children were diagnosed with Retinitis Pigmentosa. When she discovered there was currently no cure for the disease that was stealing her children's vision, it became her mission to fund research to find a cure.


The diagnosis broke her heart, and she hopes that no other person will have to worry that their loved one will go blind from RP. 

Secretary of nonprofit organization

Secretary

President

President

Gayle Guyardo is currently the host of the globally syndicated talk show Bloom Tampa Bay.  Her own family has been affected by blindness and she is passionate about finding a cure.  She also sits on the Foundation Board of Directors for Lions World VIsion Institute. 


She is committed to raising awareness about Retinitis Pigmentosa and has done numerous shows on the topic.

Treasurer of nonprofit organization

Treasurer

President

Treasurer

Neepa Dalal Patel has a background in finance and has dedicated the past seventeen years volunteering with various organizations.  Currently, she serves as a Standardized Patient at the University of South Florida Medical School.  


Inspired by a dear friend whose family has been affected by blindness, Neepa is passionate about raising awareness to find a cure for Retinitis Pigmentosa.  

Please Help Fund Research for Retinitis Pigmentosa

Donate Now

Stay in Touch

Learn more about our upcoming events and fundraisers to help find a cure for Retinitis Pigmentosa!

Connect With Us

Copyright © 2025 RP Gene Research Foundation - All Rights Reserved.


(980) 337-4411

info@rpgene.org


RP Gene Research Foundation is a qualified 501(c)(3) non-profit organization and all donations are tax deductible to the extent of IRS regulations.

Tax ID 99-3640771


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