Piggy Banks!

Our first submissions for Kids for the Cure of Cystic Fibrosis (KCCF) comes from Emily and Alex.

The girls painted piggy banks from Piggy Banks USA (Alex's grandma is the owner). 

Notice the banks with the roses...65 Roses is how many children pronounce cystic fibrosis.  Great detail ladies!   

We are proud to add Piggy Banks USA to our list of donors for 2011.  Not only did they donate the banks for this project, they also are donating gift certificates for auction on the big day.  Yahoo!

Great job and THANK YOU!

Save the date!

Please save-the-date for our 5th Annual Art for the Cure of Cystic Fibrosis!

Saturday, May 21, 2011

Conor O'Neill's

Celtic Room

Additional details to follow...

Cookies for a Cure!

A friend and fellow ACCF committee member's son has started Cookies for a Cure to raise funds towards finding a cure for cystic fibrosis.

Kudos go out to this grade schooler for his interest and dedication to help this cause. We salute Dru and support him in his mission to raise $700 by selling cookies at all Michigan home football games (on Main at Pauline).

If you aren't in our area, but would still like to support the cause, please visit Dru's fundraising site.

A great article is currently available with more information on Dru's mission. In addition to his cookie stand, Dru is one of our beloved Kids for the Cure artists at our annual art auction.

Yeah Dru!!

SUCCESS!

Our event on June 19 was a huge success!! We had a wonderful crowd of supporters, fantastic guest speakers, and incredible auction items all in an effort to raise money for a cure of cystic fibrosis.

A final number will come soon, but at a quick glance we raised over $6,000!!!

Some photos have been posted and more are coming...enjoy!

Thank you to all of our supporters!!!

Additional Kids for the Cure Submissions!

Zoe M.

Talia M.

Invite

Technical difficulties!

So sorry if you are receiving multiple updates from us today. Blogger seems to be giving us a run for our money in our final stretch! Sorry!

Dining Flyer for 15% donation to our cause at Conor O'Neill's

Kids for the Cure!

Our newest submission...

Created by Emily H.

Robyn necklaces!

Robyn necklaces are now available for purchase!

They are $15 each with $10 from each sale going to Art for the Cure of Cystic Fibrosis which benefits the Cystic Fibrosis Foundation. Shipping is available with a $2 handling fee.

To order, please send us an email.

Let's Rock CF!

We are thrilled to have Emily Schaller as one of our guest speakers for this year's event!

Emily Schaller

Emily is the founder of the Rock CF Foundation which helps raise funds and awareness for people living with cystic fibrosis. "Just Let Me Breathe" is the organization's annual rock concert benefit featuring artists from the Detroit music scene.

Her excitement about bringing awareness to those living with cystic fibrosis is admirable. She uses the arts, fitness, fashion, and music to help inform the public of this important cause and her personal crusade.

At the event, Emily will also be acting as live auctioneer for an art piece created by fellow CF'er Somer Love. This is super special as Robyn was an avid follower of Somer's blog.

Like all of us at Art for the Cure of Cystic Fibrosis, Emily wants CF to stand for Cure Found!!

We look forward to sharing Emily and her passion for life on June 19!