News

Letter from Co-Chairs outlining vision, seeking volunteers. 

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

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”.