Why the Cystic Fibrosis Foundation?

When I first started my business 3 years ago, I wanted to be sure that my business was one that was operated with integrity and that people knew that I cared about the community. Just before I started my business my niece was born with a life altering genetic lung disease called cystic fibrosis (CF) This disease not only affects her lungs, it also effects her digestive track, her ability to socialize with other kids, and her quality of life. Finding a cure for this disease has become an important goal for our entire extended family. We fundraise on social media, we participate in walks in Manchester, CT and Norwich, CT, my daughter has an annual lemonade stand...

With this mission in mind, the first mini sessions I ever did were to raise money for the Cystic Fibrosis foundation and this March 2021 I am hosting my 3rd annual mini sessions to raise money to fund research that we hope ultimately leads to a cure. As we've gotten more involved with the Cystic Fibrosis Foundation Connecticut chapter, we've met families in our own town of Coventry, Ct, in the Hartford area, and in the state of Connecticut who have been affected by this horrible disease.

When I say that 100% of the proceeds from this event go directly to the Cystic Fibrosis Foundation, what I mean is that I don't even handle any of the money, payments are made directly to our fundraising account and are tax deductible to our clients.

If you are looking for spring and Easter photos in Hartford, CT, please contact me to book your session and help us support this valuable mission.