RP Advocate Spotlight: David Bammert, Director / President, Relapsing Polychondritis Foundation

Skyhook Interactive
June 10, 2020

[vc_single_image image=”2833″ img_size=”large”]Do you have a friend or loved one suffering from RP? Dave Bammert, a Director and President of the Relapsing Polychondritis Foundation and Race for RP, knows firsthand what that is like. When his longtime friend, Nancy Linn, developed this devastating condition, Dave saw how much she struggled and how difficult it was to get a correct diagnosis and effective treatment.

Today, David is a champion for this rare condition, spearheading an effort towards greater awareness and information about RP. He is optimistic about the effect of current research. Of the recent conference, he said,

“To see a room full of researchers communicating and collaborating on sharing ideas and identifying research in items that they have discovered during their research time and just communicating with each other across disciplines, it’s overwhelming because it shows us that the path we’re on is having some successes.”

To help fund crucial research, please donate by visiting give.polychondritis.org. We are incredibly grateful for your support!David Bammert is an integral voice in the “An Advocates’ View on Driving Relapsing Polychondritis Awareness and Accelerating Research” video, which is available below:[vc_video link=”https://youtu.be/4xRV0mxW2NI” css=”.vc_custom_1591798795089{margin-top: -15px !important;}”]

Facebook-f Instagram Twitter Linkedin-in

Relapsing Polychondritis Foundation
1202 Lexington Avenue, Box 112
New York, NY 10028

Federal Tax ID 46-2458916

admin@polychondritis.org

Subscribe to our newsletter

"*" indicates required fields

Email Address*

Comments

This field is for validation purposes and should be left unchanged.

Privacy Policy
Terms & Conditions

Menu

Privacy Policy
Terms & Conditions

All content of this web site, such as text, graphics, images, or any other material contained in this website are for informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. We do not recommend the self-management of health problems. We cannot and do not give you medical advice. If you think you may have a medical emergency, call your doctor or 911 immediately. The Relapsing Polychondritis Foundation, Inc. is a nonprofit 501(c)3 corporation. Donations are tax deductible as allowed by law.