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Art for the Cure of Cystic Fibrosis

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Tuesday, May 17, 2011

Childrens desk and chair (not pictured) donated by
the interior group
Posted by Art for the Cure of Cystic Fibrosis at 10:27 AM
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Labels: 2011, 5th Annual Art for the Cure of CF

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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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ACCF Past Totals

  • 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

  • ROCK CF
    Join the Rivers Campaign and Win and iPad!
    2 months ago
  • Parenting with CF in a Miltary Family
    Fundraiser in Robyn's Memory
    2 years ago
  • Hunt for a Cure - Targeting Cystic Fibrosis
  • Cystic Fibrosis Foundation - Home
  • Winter Beach Blast – Cystic Fibrosis Benefit – Saline, MI

We ♥♥♥♥ ACCF!

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Blog Archive

  • ►  2012 (1)
    • ►  February (1)
      • Save-the-Date: Art for the Cure of Cystic Fibrosis...
  • ▼  2011 (21)
    • ▼  May (12)
      • A lovely handbag...
      • Childrens desk and chair (not pictured) donated by...
      • Paris at ACCF!
      • Fab prints for YOUR house!
      • Donor that was featured on Skull-A-Day!
      • An artist that has been with us since the beginnin...
      • No greenthumb needed for these garden submissions!...
      • Thankful for lovely donors to our cause!
      • We ♥ this!
      • Hot Dog!
      • Love us some Sloe Gin Fizz!
      • Kids are coming together for ACCF!
    • ►  April (4)
      • Fabric Junkie
      • An invite to ACCF 2011 from Lola!
      • A new submission from da U.P.!
      • New KCCF Submissions!
    • ►  March (3)
      • ACCF 2011 Invitation!
      • ACCF & Conor's Fundraising Day!
      • Call for donations!
    • ►  February (1)
      • Piggy Banks!
    • ►  January (1)
      • Save the date!
  • ►  2010 (17)
    • ►  October (1)
      • Cookies for a Cure!
    • ►  June (9)
      • SUCCESS!
      • Additional Kids for the Cure Submissions!
      • Invite
      • Technical difficulties!
      • Kids for the Cure!
      • Robyn necklaces!
      • Let's Rock CF!
      • More Kids for the Cure Projects!
      • The Power of Two - Trailer
    • ►  May (6)
      • New Kids for the Cure Submission!
      • Kids for the Cure!
      • Art for the Cure of Cystic Fibrosis & Conor O'Neil...
      • Kids for the Cure!
      • Kids for the Cure!
      • 2010 "Robyn" Necklaces!
    • ►  March (1)
      • 4th Annual Art for the Cure of Cystic Fibrosis Inv...
  • ►  2009 (17)
    • ►  December (1)
      • Save-the-Date!!!
    • ►  June (1)
      • THANK YOU!
    • ►  May (11)
      • Kids for the Cure, Robyn Necklace, and Invite/Flye...
      • Kids for the Cure!
      • Another Kids for the Cure submission!
      • Latest Kids for the Cure Submissions
      • Art for the Cure on CTN!
      • The latest submission for Kids for the Cure!
      • "Robyn" necklaces
      • My Fairy Door
      • Another submission for Kids for the Cure!
    • ►  February (2)
    • ►  January (2)
  • ►  2008 (7)
    • ►  August (1)
    • ►  June (1)
    • ►  May (1)
    • ►  April (2)
    • ►  February (2)
 
Because of risks to people with cystic fibrosis (CF), individuals with confirmed positive sputum culture for Burkholderia cepacia complex shall not attend this event. This is because B. Cepacia can be passed between individuals who have CF through close proximity. B. Cepacia infection in a person with CF can cause serious respiratory illness and, in some patients may lead to death. Despite this policy, there might still be some individuals with B. cepacia in attendance. B. Cepacia is not a risk for otherwise healthy individuals. For alternative ways to participate and for information on the CF Foundation call (800) FIGHT-CF or visit our website about this policy at www.cff.org. Consult your CF care center physician with medical questions.