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Our idea of success is annihilating the nonsense that stands between someone & their best health.

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WE ARE THE VOICE
of the rare-disease community.
Excuse us while we drop some names...
Here are Some cool people we partner with




Our leadership
Normally this is where you’d see some people with fancy titles and expensive headshots that show how important and creative they are… That’s just not us.
Everyone at Purplemoon has a voice. Everyone has a say. So “leadership” is more of a logistical thing. If that sounds like your kind of place, drop us a line.
Ask us what we did today and we’ll tell you we worked hard TO CHANGE SOMEONE’S LIFE
More than a company.
A CALLING.
“Alee just ate, slept, and seized.”
Alee was born with a devastating rare disease. By age 5, she had progressed to more than 200 seizures a day. She couldn’t walk and her only word was “mama.”
Alee then began a novel medicine that changed everything. Within 5 years, she was walking, talking, and even back at school. She was experiencing no more than one seizure a year.
In 2015, we brought her story to life in an HCP/DTP campaign to raise disease awareness and drive growth. The campaign received multiple business and creative awards, and OUR PURPOSE WAS BORN.
WE EXIST TO IMPROVE THE LIVES OF PEOPLE LIKE ALEE, by furthering education, raising awareness, and improving the overall patient experience. Rare disease isn’t just our focus—it’s our passion, our purpose, and our reason for being.
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Our spot
We’ve got a pretty sweet space in Jersey. Check it out!