EndoFound's online magazine.
The federal government gave only $13 million to endometriosis research in 2019, despite 1 in 10 US women having the disease. This equates to less than $1 per year for each diagnosed patient. Although…
In 2016 Kianna Scott, endo patient and founder of EndoArmy, moved across the country to Virginia not knowing a single person in pursuit of her life-long dream of working in the veterinary industry with…
From virtual puzzles to endo-friendly recipes, Jessica has shared an invaluable resource on ways to decompress by doing some things you love while at home.
On Sunday, April 19th, at 2 PM (EDT), EndoFound is hosting its second webinar, "Candidly COVID-19 & Endo." This episode features a panel of expert physicians, including Dr. Joseph Vinetz, an expert…
There has never been a more important time to come together (virtually!) with your endo community and your support system, especially during Endo Awareness Month.
Finkenauer went public with her story after reading statistics and stories from other women with the disease on the Endometriosis Foundation of America (EndoFound) website. She has formed the first-ever…
Few people outside of family and friends knew that Rep. Abby Finkenauer had been living much of her young life with endometriosis
UPDATE (3/6/20) In response to the COVID-19 outbreak in the United States, the Foundation Board and the Chairs of the Conference have decided to postpone the upcoming Medical Conference, Postgraduate…
In the fall of 2018, just seven months after launching Karmela Cosmetics, founder Nechami Tenenbaum wanted to donate some of the proceeds of her lipstick line to organizations that unite, empower, and…
Endometriosis takes an average of twelve years to diagnose. Twelve long years. That means most teenagers who have it suffer into at least their mid-twenties or early thirties before they have any clue…
