Hello, Sweet Charity…
So, there is this sweet litte girl I know named Violet. Violet is four years old and has cystic fibrosis. If you don’t know much about cystic fibrosis, it’s a genetic desease that affects the lungs and digestive system of children. The body produces a thick and sticky mucus that clogs the lungs and obstructs the pancreas. Living with cystic fibrosis has been described as ‘like living under water’. So, when I think of Violet and what she has to go through everyday it simply breaks my heart. This year has been particularly tough for her. Since Violet wasn’t putting on weight and absorbing nutrients, she had to have surgery to have a g-tube inserted in her stomach to administer all of her foods externally. I’m sure you can imagine how having a bulky tube coming out of her stomach would emotionally and physically affect this active four year old.
But, the great news… There’s hope!! The Cystic Fibrosis Foundation is on the brink of an amazing drug discovery that can trick the CF gene! We are so very close to helping find a cure and need to do what we can to push this through! The Cystic Fibrosis Foundation puts 90 cents of every dollar raised directly to medical research. That is one of the highest ratios for a non-profit foundation out there, since they effectively and responsibly manage their operating cost. This is a foundation worth donating to.
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