State Senator Neil Anderson (R-Andalusia) announced that his legislation, Senate Bill 1814, which establishes support and an educational initiative for amniotic fluid embolism (AFE), has been officially signed into law.
“This marks an important step forward in bringing awareness to a condition that is rare, but too often fatal,” said Senator Anderson. “This new law will ensure Illinois is leading the way in educating the public and medical community about AFE.”
The legislation is deeply personal for Senator Anderson. His District Operations Staffer, Annie Hewitt, experienced AFE following the birth of her son, Dolan, in 2022. After an emergency C-section, Annie went into pulmonary failure and was later airlifted to the University of Iowa, where, against the odds, she survived.
“Because of Annie’s survival, she has committed herself to raising awareness about this devastating condition,” said Senator Anderson. “Her strength and determination inspired this legislation, and I couldn’t be more proud to support her mission.”
Amniotic fluid embolism is an unpredictable and rare complication of childbirth that occurs in about one in every 40,000 deliveries in the United States. Its exact cause remains unknown, and studies suggest the mortality rate can reach as high as 60%.
Under the newly signed law, Illinois will launch an educational initiative to provide medical professionals, patients, and the public with resources and information about AFE. The measure aims to improve awareness, support early recognition, and foster further research into this condition.
“Stories like Annie’s remind us that while AFE is rare, action is necessary,” said Senator Anderson. “This new law will help save lives by ensuring Illinois families and doctors have access to critical information.”