Lev Facher | February 28, 2017
A young woman whose father founded a biotechnology company in pursuit of a treatment for her rare disease will be front and center on Tuesday night for President Trump’s address to a joint session of Congress.
Megan Crowley, a Notre Dame student who was diagnosed with Pompe disease at 15 months old, will be seated alongside first lady Melania Trump during the address. Beforehand, Crowley and her father, John, will meet with Trump in the Oval Office to discuss rare disease treatments.
“Megan and our family will meet privately in the Oval Office with the President to discuss the needs of people living with rare diseases, and especially advancing medicines for treatments and cures for ALL rare diseases,” John F. Crowley wrote in a Facebook post.
The timing is fortuitous: The visit and Trump’s address come on Rare Disease Day.
Following Megan’s Pompe diagnosis and that of her younger brother Patrick four months later, John Crowley founded Novazyme, which developed protein engineering technologies aimed at treating diseases like Pompe.
Novazyme, which was acquired by Genzyme in 2001, was eventually successful in creating an enzyme replacement therapy for Pompe disease, which Megan and her younger brother are still treated with today.