by Laura Bonnell | Mar 1, 2022 | Media/Press
Laura Bonnell, the founder of a foundation bearing her family’s name, is working to make sure people with rare diseases get representation in Michigan. Read the story here
by Laura Bonnell | Feb 28, 2022 | Media/Press
By Institute for Patient Access The 30 million Americans diagnosed with a rare disease represent a large, underserved patient population. Their complex conditions are often poorly understood, and most have no approved treatment. Nevertheless, rare disease patients and...
by Laura Bonnell | Feb 12, 2022 | Media/Press, Uncategorized
BioMatters – Winter 2022, Patient Advocate Issue by MichBio – Issuu Read the story here
by Laura Bonnell | Jan 26, 2022 | Media/Press
Bonnell was interviewed by Tia Graham and on the Morning Edition show with Pat Batchelor. Listen to the interview:
by Laura Bonnell | Nov 28, 2021 | Media/Press
By Vladislava Sukhanovskaya – Capital News Service About a million Michiganders with rare diseases could receive better treatment if legislators establish a Rare Disease Advisory Council. Read the story here
by Laura Bonnell | Aug 24, 2021 | Media/Press
By Amy Lange and David Komer online producer, FOX 2 Detroit FOX 2 – A local family has made it their mission to help those living with cystic fibrosis and this year — their annual fundraiser will return to in-person for their “Night of Hope.”...