As told to Shannon Shelton Miller
July is Fibroid Awareness Month.
Experiencing debilitating period cramps and heavy bleeding, I was repeatedly told it was normal. Growing up, the healthcare system overlooked my symptoms, attributing them to adolescence. It wasn’t until after giving birth to my twins in 2006 that I was diagnosed with fibroids. Despite managing the condition temporarily, it eventually led to a myomectomy and, later, a hysterectomy in 2023. The journey was taxing, but the support from organizations like MusiCares and The White Dress Project, as well as the advocacy of my sister-in-law, helped me through. Uterine fibroids are not just a women’s issue; more research, clinics, and support are needed to ensure better quality of life for those affected.
Gabbie with her husband, twins Elijah and Evelyn, and Ella, 2022 (Photo/Patricia Kelly)
Gabbie performing, 2015 (Photo/George Kelly, Jr.)
Life with fibroids affected every aspect, from work to intimacy. After exhausting all options, a hysterectomy became the last resort for survival. With a strong support system and access to necessary resources, I was able to navigate this challenging journey. Uterine fibroids demand more attention, care, and research for the well-being of those impacted.
Hysterectomy selfie, November 18, 2023.
Grateful for the unwavering support received, I advocate for increased awareness and support for those dealing with uterine fibroids. Encouraging women to find reliable healthcare providers and seek the care they deserve is crucial. With dedication to research and resources, we can improve the lives of those affected by fibroids.
Resources
The White Dress Project
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