For the PKD community, it’s a hopeful sign of where rare disease research and regulation may be headed.
Paul Scribner, the PKD Foundation Vice President of Community Programs and Education, said it’s like “putting a flag in the ground and saying, ‘This is important.’”
Paul Scribner, the PKD Foundation Vice President of Community Programs and Education, said it’s like “putting a flag in the ground and saying, ‘This is important.’”
