Shop And Make a Difference!

 

Boutique on Feet wanted to do something special for a little girl near and dear to our hearts.  Little Olivia is a 3 1/2 year-old Charlotte girl who was diagnosed with Cystic Fibrosis, 2 year ago.  CF is a hereditary disease that affects the lungs and digestive system, and has NO CURE.  The research that goes in to finding a cure for this awful disease is extremely expensive and has no government support.

Right now, the average life span for a person with CF is 35 years-old.  We want Olivia to live a long, healthy and wonderful life, which is why we want to do our part in helping find a cure. 

WILL YOU HELP US AND SHOP FOR A GREAT CAUSE?
 
During the WHOLE month of May, 40% of all our online sales will go towards, "Team Livi" and The Cystic Fibrosis Foundation.  Please Twitter, Share through FB and with all your friends and family.    We love to give back . . . and we would greatly appreciate your support in helping us do so.  


http://www.boutiqueonfeet.com

Comments

In order to comment on BlogHer.com, you'll need to be logged in. You'll be given the option to log in or create an account when you publish your comment. If you do not log in or create an account, your comment will not be displayed.

Recent Posts by boutiquemama