May is Cystic Fibrosis Awareness Month. A month that holds huge significance in my life. My dear friend Lauren Martin and her husband Cole have a beautiful little girl, Harper, born January 1st, 2016. Not even 20 days after she was born, she was diagnosed with the fatal genetic disease, Cystic Fibrosis.
In the 1960s, most children with Cystic Fibrosis did not live long enough to attend kindergarten. Today, 50% of Canadians with cystic fibrosis are expected to live into their early 50s and beyond, and nearly 60% of all people with cystic fibrosis in Canada are adults.
These numbers are promising for our Little Harper, but at present there is still no cure.
Please help me, help Harper <3
50% of all proceeds made will go directly to Cystic Fibrosis Canada & Harper’s fight against CF.
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