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A
BLUE
PURPLE
MOON
IS
EXCEEDINGLY
RARE
A
BLUE
PURPLE
MOON
IS
EXCEEDINGLY
RARE
(About once every 2 years)
(About once a lifetime)
Rare HAS ARRIVED
A rare-disease-focused, client-minded, patient-centric, end-to-end agency is finally here.

What makes us

end-to-end?

If there’s a sales team that needs training, a product that needs launching, or a congress that needs to be f’ing sweet,WE GOT YOU.
Purplemoon provides full-service marketing and sales training capabilities along with customized, cutting-edge production and event experiences—all with the same commitment to being awesome.
Yup. We do all three. Which means a consistent and cohesive brand journey—start to finish—and a more efficient experience for our clients. We’re rare like that.

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

Here’s what END-TO-END looks like

MARKETING

Marketing that moves people and the needle.
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LEARNING

Sales training as engaging as it is educational.
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PRODUCTIONS

Conventions, events, and experiences that truly engage.
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LEARNING

MARKETING

PRODUCTIONS

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.”
Then Alee began a novel medicine that changed everything. Within 5 years, Alee 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.

Our spot

We’ve got a pretty sweet space in Jersey. Check it out!