PALSONIFY stories

Real stories.

Real courage.

Real possibilities.

Hear from people taking PALSONIFY.

Megan,

PALSONIFY peer

Meet your PALSONIFY peers

Watch David, Megan, and Ashleigh talk about their journeys, their challenges, and the decisions that shaped their treatment paths.

Meet David

Daily joint pain forced David to give up playing piano, and persistent fatigue left him exhausted after work. Hear how starting PALSONIFY made a difference in his acromegaly symptoms and helped him return to the things he loves.

Meet Megan

An active fitness enthusiast, Megan dealt with joint pain and exhaustion. After surgery, she struggled with side effects from several injectable treatments. Find out how switching to once-daily oral PALSONIFY helped her feel more confident in managing her acromegaly.

Meet Ashleigh

After a decade of searching for answers, Ashleigh was finally diagnosed with acromegaly. Watch her story about overcoming uncertainty around switching treatments and finding renewed confidence with PALSONIFY.

Interested in having a conversation with a PALSONIFY peer?

Talk to someone who truly gets it. If you want to talk about symptoms, switching treatments, or what daily life on PALSONIFY is really like, our PALSONIFY peers are here for you. Reach out to have a one-on-one conversation.
David, a PALSONIFY peer, playing guitar alongside another guitarist.

David,

PALSONIFY peer

Megan, a PALSONIFY peer, walking outdoors with another woman.

Megan,

PALSONIFY peer

Become a PALSONIFY peer and inspire others

If you’re taking PALSONIFY, you can share your story to support other people living with acromegaly. As a PALSONIFY peer, you’ll connect with people navigating diagnosis and treatment decisions and share what you’ve learned along the way. Turn your experience into support for someone who needs it.

PALSONIFY peers are compensated for their time and participation.