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About RRP
Patients & Caregivers
Find a Doctor
FAQ
- General FAQs
- JORRP FAQs
Research
About RRPF
Contact

Patient Stories

Inspiring stories of strength and hope from people living with RRP

Eden Tansey

Katie Thompson

Emma Sinn

Carter

Keep up to date with the latest research

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We are constantly updating our community on the latest studies, meetings, and developments in the RRP community.

While We Breathe, We Hope
With our voices united, we can and will work to end the burden of this disease on patients and caregivers.

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Disclaimer
Please note that the Recurrent Respiratory Papillomatosis Foundation provides the information on this website for the benefit of the RRP patient and clinician community. Recurrent Respiratory Papillomatosis Foundation is not a medical provider. The Recurrent Respiratory Papillomatosis Foundation offers our MD search as a service to our community and does not specifically endorse any of the clinicians listed. Patients must rely on the personal and individualized medical advice of their qualified health care professionals before they seek any information related to RRP diagnosis and treatment.

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Breaking News!!!

RRPF President, Kim McClellan to speak at the White House Rare Disease Forum

Tonight! February 28th @ 5:30PM EST