One mom’s mission to bring awareness to the rare eye disorder Retinitis Pigmentosa.
Hi there, welcome to Never Losing Sight. My name is Melissa and I am the owner/designer of NLS. In early 2014 both of my boys were diagnosed with RP. As a parent, it was heartbreaking. After the initial shock, I realized that people in general do not realize how blessed they are to have their eyesight. In the days & years to come I want to remind not just my boys, but everyone to never lose sight of who you are. Never let memories slip away and enjoy every moment of every day.
As a graphic designer/artist working in the print industry for over 15 years, I decided that I wanted to create a website dedicated to my boys in my own way. I’ve created many websites for fun but NeverLosingSight is by far the most important one to me. Social media is huge now days so what better way to use my design skills and spread awareness, than to create a website that truly has a special meaning.
EVERY single day our boys still have their vision is a gift. This website is my way of spreading positivity, inspiration & most of all awareness to RP.