Check out this news story on BRP and the Alliance

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News

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November 2020 Letter to Members

Letter from Co-Chairs outlining vision, seeking volunteers. 

Media Coverage

Here's a story on BRP and the formation of the BRP Alliance

Alliance Invited to Present to World's Top Itch Scientists

The International Forum for the Study of Itch have invited us to speak at their next conference!  Their President, Dr. Elke Weisshaar, writes to us: “I am impressed by your alliance. I know that BRP is not rare, it is underdiagnosed. I am also suffering when taking care of my BRP patients because other physicians like orthopedics and radiologists tell my patients that this disease does not exist. There is so much ignorance”.

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  • Letter Nov 2020