EB Research Partnership
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The Padres and Mariners will be pursuing more than their respective division titles when they meet this year, as beginning this season, they will join rock star Eddie Vedder in creating the real Vedder Cup, the prize for the victor in their six-game season series!

Fans have playfully referred to the Padres vs. Mariners series as the Vedder Cup for years, in honor of the Rock & Roll Hall of Famer and multi-Grammy Award winner, a one-time resident of both San Diego and Seattle. The winner of the season series will take home the Vedder Cup trophy, featuring a guitar provided by Vedder.

​As part of the annual series, both teams will come together to support our mission of funding critical research to discover treatments and cures for Epidermolysis Bullosa (EB), a rare and life-threatening genetic condition that causes fragile skin to blister and tear. Co-founded by Eddie and Jill Vedder, EB Research Partnership is committed to advancing treatments and ultimately, finding a cure for EB, and we are grateful for the support of the Padres, Mariners, and their fans to accelerate this mission. 
The Vedder Cup poster with event details for the Padres vs. Mariners series, supporting EB Research Partnership and raising awareness for Epidermolysis Bullosa.
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 At EBRP, we know that in order to do things that haven’t been done you need to be willing to break the mold.

With this innovative business model we’re pioneering a new path forward that will not only revolutionize the way nonprofits operate, but also show the world how cures are found. We don’t just write checks and hope for the best. Instead, we operate like a venture capitalist with a focus on a different kind of ROI, return on impact. We create venture agreements with each project we fund. When those projects succeed, the returns are reinvested back into other promising
research and development projects.

Did we mention the science we fund is also scalable across thousands of other rare diseases? That's right. The impact of every dollar invested at EBRP is multiplied many times over.
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​​Our Venture Philanthropy Model has been highlighted for its leadership by Harvard, Yale, MIT, the Milken Institute,  Stanford Social Innovation Review, and more.
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With this business model we are actively transforming the EB landscape while creating scalable impact. These projects, this work, and the way we operate will create a butterfly effect for the 400M+ globally impacted by a rare disease.

Download our Impact Booklet to explore the Harvard Business School and Yale School of Management case studies on EBRP's innovative model and transformative impact.
Download Impact Booklet

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Children with EB are often called “Butterfly Children” because their skin is as fragile as the wings of a butterfly. With skin this fragile, everyday activities that many take for granted like eating, sleeping, walking and playing can become monumental tasks.

​The harsh reality is that rare diseases affect more people than HIV and Cancer combined.

EB is one of over 10,000 rare diseases, 95% of which have no approved treatments or cures. We are focused on finding a cure for EB, but for us that’s just the beginning.
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Founded in 2010 by a group of dedicated parents, Jill Vedder, and Eddie Vedder of Pearl Jam, EB Research Partnership (EBRP) is the largest nonprofit funding research aimed at finding a cure for Epidermolysis Bullosa (EB).

Over the last decade, we have made remarkable strides, including raising +$60M for life-saving research, contributing to a 20x growth in EB clinical trials, helping to fund the first-ever FDA approved topical gene therapy and treatment for EB families.

The progress we’ve made in EB is undeniable, however, we are only scratching the surface. 

​Our Venture Philanthropy Model is actively transforming the EB landscape while creating scalable impact. These projects, this work, and the way we operate will create a butterfly effect for the 400M+ globally impacted by a rare disease.
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646-844-0902
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COPYRIGHT @2025 EB RESEARCH PARTNERSHIP. ALL RIGHTS RESERVED. EB RESEARCH PARTNERSHIP IS A 501(C)(3) NON PROFIT.

  • Epidermolysis Bullosa
    • What is EB?
    • Life with EB
    • Resources
  • Research
    • Our Impact
    • Scientific Advisory Board
    • Clinical Trials >
      • Filsuvez
      • Vyjuvek
      • ZEVASKYN
    • Town Halls
    • Apply for a Grant
  • Get Involved
    • Donate
    • Sponsor
    • EB Active
    • Events
    • The Effect
    • Shop
    • Give Cryptocurrency
    • Give Stocks
    • Give through Donor Advised Funds (DAF)
    • Accelerator Fund
  • Media
    • Matter of Time Film
    • Press
    • Videos
  • About Us
    • Our Mission
    • Financials
    • Venture Philanthropy
    • Supporter Spotlights
    • Leadership >
      • Board of Directors
      • Staff
  • Donate