Art for the Cure of Cystic Fibrosis
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Friday, May 11, 2012

Art for the Cure of CF 2012 - tomorrow!




Posted by Art for the Cure of Cystic Fibrosis at 11:56 AM No comments:
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Art for the Cure of Cystic Fibrosis
Ann Arbor, MI, United States
Art for the Cure of Cystic Fibrosis (ACCF) was created in 2007 in honor of our sister, daughter, and friend, Robyn, in hopes of finding a cure or better control for the disease. Sadly, Robyn lost her battle with CF in November 2008. We continue the fight in her memory and to help find a cure for those still battling cystic fibrosis.
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You Are Invited!

You Are Invited!

Fundraising Weekend!

Fundraising Weekend!
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ACCF Past Totals

  • 2012 - $7,376
  • 2011 - $9,000
  • 2010 - $7,608
  • 2009 - $11,180 !!
  • 2008 - $5,835
  • 2007 - $4,976

Publicity

  • Community Television Network - FYI! 2009

ACCF Pics!

  • 2010
  • 2009
  • 2008
  • 2007

Friends of ACCF

  • Parenting with CF in a Miltary Family
    Fundraiser in Robyn's Memory
    15 years ago
  • Hunt for a Cure - Targeting Cystic Fibrosis
  • ROCK CF
  • Cystic Fibrosis Foundation - Home
  • Winter Beach Blast – Cystic Fibrosis Benefit – Saline, MI

We ♥♥♥♥ ACCF!

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      • Art for the Cure of CF 2012 - tomorrow!
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Because of risks to people with cystic fibrosis (CF), only one person with CF may be invited. Also, individuals who have ever had a confirmed positive sputum culture for Burkholderia cepacia (B. cepacia) complex shall not attend any Foundation events/meetings. These requirements are because CF germs can be passed between individuals who have CF. Some germs in a person with CF can cause serious respiratory illness and, in some patients, may lead to death. CF germs are not a risk for otherwise healthy individuals. Despite this policy, individuals with CF might choose to attend events or meetings without informing the CF Foundation or without the Foundation’s knowledge. If so, they do so at their own risk. The Foundation accepts no responsibility for any risk to health involved in attendance, or in any social contact between persons with CF. For more information, please visit www.cff.org.

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