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of so many people.

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You are not alone, read words of
encouragement and hope from
families dealing with Alport
Syndrome. Read Here

Volunteer

One person can make a difference and you can be that person! Volunteers are vital to the success of the Alport Syndrome Foundation. We welcome volunteers with a wide range of talent and skills. There is only one requirement – your desire to make a difference in the lives of patients and families dealing with Alport Syndrome. Here are some examples of where we might need help:

  • Host a Fundraiser
  • Develop Fundraising events
  • Develop the Newsletter
  • Write articles for the Newsletter
  • Develop educational materials to post on the website
  • Advertise the Foundation
  • Contact kidney and related health organizations about the Foundation
  • Assist in developing future family conferences
  • Monitor websites for Alport Syndrome related research.

Please join us! To be a volunteer you must Register and you can contact us at info@alportsyndrome.org.

Thank you!

The 501(c)(3) non-profit Alport Syndrome Foundation is dedicated to educating and supporting patients and families with this genetic kidney disease.
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