RAO Network

Recurrent Respiratory Papillomatosis Foundation

A group of adults and children in a conference room pose for a group shot at a Recurrent Respiratory Papillomatosis Foundation gathering.
An RRPF gathering for a patient education and support event in Atlanta, GA in 2018. Photo courtesy of Recurrent Respiratory Papillomatosis Foundation.
An RRPF gathering for a patient education and support event in Atlanta, GA in 2018. Photo courtesy of Recurrent Respiratory Papillomatosis Foundation.

Recurrent Respiratory Papillomatosis (RRP), also known as laryngeal papillomatosis and tracheal papillomatosis, is a rare disease that causes benign tumor growth in the aerodigestive tract. RRP is caused by the HPV virus, typically HPV 6 or HPV 11. There is no cure and patients can have surgical intervention counts into the hundreds.

So many of those living with a rare disease, such as RRP, often feel isolated, discouraged, and it is organizations such as the RRPF that are often the lifeline to patient support and disease education. Several years ago, patient leader Kim McClellan became an active advocate for RRP and other RRP warriors, bringing the patient voice and the need for treatment options to a broader audience.

As part of the Rare As One Network, the RRPF aims to elevate the non-surgical treatment options patients desperately long for, as well as galvanize research into a centralized location to help guide a research agenda and elevate the patient voice.

Learn How We Support Science

Science Funding

Learn more about funding apportunities.

Hear Rare Disease Stories

Hear Rare Disease Stories

Listen to The Story Collider podcast featuring stories about patients who are driving progress against rare disease.