The Fibroid Foundation is Proud to Support the ‘Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021’

The Fibroid Foundation is proud to endorse the ‘Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021’. This important legislation was introduced on March 18, 2021, by Representative Yvette D. Clarke (NY-9). 
In the United States, an estimated 26,000,000 women between the ages of 15 and 50 have uterine fibroids.1  Uterine fibroids are the most common gynecologic condition in women2 , however, treatment options and medical research funding have yet to match the enormity of the affected community. 
Sateria Venable, Founder & CEO of The Fibroid Foundation, responded to yesterday’s introduction of the Fibroid Bill by saying, “Consistent fibroid research funding will transform the quality of life for millions of women in the United States.”
Ultrasound screenings were used in the 2017, ‘Uterine Fibroids: Burden and Unmet Medical Need’ study.  The tests revealed an “estimated cumulative incidence rate of UF (uterine fibroids) by the age of 50 is significantly higher in black women (80%) compared with white women (nearly 70%).”3 Annually, uterine fibroids account for approximately half of hysterectomies performed in the United States.4  Data has shown that there are cardiovascular risk factors associated with hysterectomy.5 
According to The Fibroid Foundation, patients are suffering in silence. Community members express concerns about limited treatment options, the high cost of treatment, insurance coverage, and difficulty finding fibroid specialists. The organization recognizes the significant health disparities which impact its community and provides support with a unique patient perspective. To aid in the correction of those disparities, the Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021 will provide $150M to the National Institutes of Health. Legislative benefits of the Uterine Fibroid Act include: 
The Fibroid Foundation, with members in most U.S. states, and 48 countries, develops annual programming centered on education, advocacy and access to treatment. This month, the organization announced the #askHER initiative, aimed at encouraging conversation about uterine fibroids. The initiative addresses the stigma surrounding menstrual awareness by promoting dialogue in support of those diagnosed with fibroids.
The Fibroid Foundation is proud to support the ‘Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021’. Uterine fibroids disproportionately impact those of African descent. The Fibroid Foundation is encouraged to see meaningful legislation aimed at addressing the public health crisis in the U.S. which is impacting patients and their families. We thank Representative Clarke and the Congressional Black Caucus on Women & Girls for their leadership and look forward to working in partnership with Congress, and the many supporting organizations of the ‘Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021’.
About The Fibroid Foundation
The Fibroid Foundation is an organization founded by fibroid patient Sateria Venable in 2013 after her third of four fibroid surgeries. As the premier global community of fibroids patients, their mission is to:
The Foundation has 25 chapters and a readership of 29,000 people around the world. The Foundation is published in Obstetrics and Gynecology, The Green Journal and other medical journals.
‘One woman at a time, we are showing the world that we are empowered and that we are driven to change our story!’
1Management of Uterine Fibroids
2The Health Disparities of Uterine Fibroids for African American Women: A Public Health Issue
3Uterine Fibroids: Burden and Unmet Medical Need
4The Estimated Annual Cost of Uterine Leiomyomata in the United States
5Clinical practice and research yields valuable data for management of uterine fibroids
For Media Inquiries: 
Emma Jasper
Phone: 240.621.0020 
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Source: The Fibroid Foundation