The Fibroid Foundation Announces the 2021 Fibroid Awareness Month Event Schedule

The Fibroid Foundation announces the Fibroid Awareness Month event schedule for July 2021.
This year’s Fibroid Awareness Month Theme is “Living Your Best Life.”
Featured events are:
Registration for all events can be found here.
Women* with symptomatic uterine fibroids often experience a diminished quality of life. During Fibroid Awareness Month, the programming will focus on helping the fibroid community to Live Their Best Life by featuring virtual segments on exercise, nutrition, legislation, research and peer-to-peer support provided by The Fibroid Foundation’s chapters.
The Stephanie Tubbs Jones Fibroid Research and Education Act — H.R. 2007, introduced in The House of Representatives by Representative Yvette D. Clarke (NY-9) in March, will provide long-overdue fibroid research funding. A vote on the bill in the fall of this year is anticipated. Community support is requested by residents in each state to achieve the Congressional sponsorship required for H.R. 2007 to become law. Letters of support can be downloaded to send to congressional representatives via this template.
The Stephanie Tubbs Jones Uterine Fibroid Research and Education Act of 2021 will provide $150 million to the National Institutes of Health. Legislative benefits of the Uterine Fibroid Act include:
In the United States, an estimated 26 million 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.
The “Uterine Fibroids: Burden and Unmet Medical Need” 2017 study found that “using ultrasound screening, the 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, which creates a significant multi-billion dollar annual economic burden.4  Data has shown that there are significant cardiovascular risk factors associated with hysterectomy.5 
The Fibroid Foundation is encouraged to see introduction of meaningful legislation aimed at addressing the uterine fibroid public health crisis in the U.S. which is impacting women* and their families.
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 global support to address the disparities from a unique patient perspective. 
The Fibroid Foundation Mission:
As a strong, supportive and empowered community, we are elevating menstrual health and fibroid treatment by:
About The Fibroid Foundation
The Fibroid Foundation is an organization founded by fibroid patient Sateria Venable in 2013.  
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!” ~Sateria, Founder
*We use an inclusive definition of “women” and we welcome trans women, genderqueer women, and non-binary people who are significantly female-identified.
1 Management of Uterine Fibroids
2 The Health Disparities of Uterine Fibroids for African American Women: A Public Health Issue
3 Uterine Fibroids: Burden and Unmet Medical Need
4 The Estimated Annual Cost of Uterine Leiomyomata in the United States
5 Clinical practice and research yields valuable data for management of uterine fibroids
For Media Inquiries:Emma JasperPhone: 844.484.7698 (IT-IS-MY-U)
For anyone interested in partnering with The Fibroid Foundation, please visit
Source: The Fibroid Foundation