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​VENTURE INTO CURES: LIVE IN NYC
NOVEMBER 10 | 583 PARK AVE | 6:00PM ET
TICKETS AND SPONSORSHIPs
DOWNLOAD SPONSORSHIP PACKET
​VENTURE INTO CURES: A DIGITAL SHOW
www.ventureintocures.org | 4:00PM ET
fundraising
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ABOUT VENTURE INTO CURES: THE LIVE EVENT IN NEW YORK
 Join us for EB Research Partnership's 13th Annual Benefit on Thursday, November 10th, 2022 at 583 Park Avenue in New York, NY. The event will raise awareness and funds for critical research to treat and cure Epidermolysis Bullosa (EB), a life-threatening genetic disorder that affects children from birth. More details will be announced soon! 
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To purchase tickets or a sponsorship, click the button below and for additional sponsorship information, please reach out to  info@ebresearch.org. 

More details
TICKETS
DOWNLOAD SPONSOR PACKET
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ABOUT VENTURE INTO CURES: DIGITAL
For the past two years, Venture Into Cures has shared inspirational stories of EB families alongside celebrity friends including Jill & Eddie Vedder, Tom Holland, Selena Gomez, and many more. Combined, the 2020 and 2021 shows have raised nearly $5M for critical EB research, and has been seen by millions of people worldwide. 

This free, family-friendly, one-hour digital show will be broadcast on Sunday, November 20th, 2022. 
Details on how to watch this year's show will be released soon. If you'd like to sponsor the digital show, or inquire about packages for both the in-person event and digital show combined, please email info@ebresearch.org.


FUNDRAISE IN YOUR COMMUNITY
Help EBRP raise funds for critical research by creating or joining a fundraising team for Venture Into Cures! Whether you're a business, a school, or a family looking to support our mission, your fundraising dollars will give you the opportunity to be listed as a sponsor for this world-class show featuring your favorite actors, musicians, and other stars. To create or join a team, please visit https://give.ebresearch.org/vic2022.


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WATCH THE 2020 SHOW
WATCH THE 2021 SHOW
ABOUT EB RESEARCH PARTNERSHIP

Epidermolysis Bullosa Research Partnership (EBRP) was founded in 2010 by Jamie and Alex Silver along with Jill and Eddie Vedder (Pearl Jam) with one bold audacious goal: treat and cure the devastating and life-threatening genetic rare skin disease epidermolysis bullosa and in the process pioneer an innovative business and technology model to lead the way for 400 million people with a are disease. As EB is typically caused by a single genetic mutation and treatments are observable on the surface of the skin, EB is first off the runway for impactful and curative medicine such as gene, stem cell, and immune therapies. Leading researchers believe a meaningful treatment or a cure is achievable before the end of this decade. While EB is a rare disease, there are 7,000 rare diseases that affect 1 in 10 people in the world, 95% which have no treatments, that can benefit from the research EBRP funds and its innovative venture philanthropy model - both of which are scalable to all rare diseases. 
To learn more, visit ebresearch.org​
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EB Research Partnership

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COPYRIGHT @2022 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
    • Community Council
    • Apply for a Grant
  • Get Involved
    • Donate
    • Sponsor
    • EB Active
    • Events >
      • Venture Into Cures
    • The Effect
    • Shop
    • Accelerator Fund
  • Media
    • Press
    • Videos
  • About Us
    • Our Mission
    • Financials
    • Venture Philanthropy
    • Supporter Spotlight
    • Leadership >
      • Board of Directors
      • Staff
      • Founders
  • Donate