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I recently shared my personal journey with breast implant illness (BII) and expressed my concern for women who have breast implants. Too often, we’re misled into choosing and keeping them, despite countless women having to remove their implants due to severe health issues. After my article was published, I received numerous comments from other women with implants, and the dismissive attitudes were astonishing.
Understanding breast implant illness can be a harsh reality. Before I opted for implants following my breast cancer diagnosis, a friend advised me to thoroughly research the potential risks. Regrettably, I ignored her warning, and as a result, I spent three and a half years suffering from the debilitating symptoms of BII. I share my experience not to shame others but to raise awareness. Yet, despite my efforts, I continue to encounter skepticism from both women and the medical community.
Let me be clear: those of us who reveal our harrowing experiences with BII are driven by one goal—to protect others from facing the same painful and costly consequences. Discussing the risks associated with breast implants is not glamorous; it’s often met with resistance, as many prefer to admire flawless bodies on social media rather than confront the grim realities of breast health and surgery.
These discussions can be uncomfortable. I can almost hear a voice of disapproval every time I write about my struggles with feeling like a frail version of myself, burdened by toxic implants. But the discomfort of medical discussions pales in comparison to the actual suffering endured by those of us living with these implants.
It troubles me to see women quickly dismiss the experiences of others. Each person’s story is valid and deserves to be heard. We share our truths because we believe that women’s health is important, and that every woman deserves to live a fulfilling, healthy life. When personal experiences reveal that breast implants fall short of providing that, it compels us to speak out.
When met with opposition, especially from fellow women, it can be disheartening. We’ve faced enough skepticism from the medical community. Many of us considering explantation have endured years of doubt, stigma, and victim-blaming, which is incredibly damaging.
When we report symptoms like food intolerances, rapid heart rates, insomnia, rashes, and other ailments related to BII, we often undergo exhaustive testing—CT scans, ultrasounds, blood tests—only to be left without a clear diagnosis. Why? Because breast implant illness is not recognized as an official medical condition. It’s a collection of symptoms that can mimic other illnesses, making it almost impossible to receive a proper diagnosis.
Since BII lacks formal recognition, we must advocate for ourselves during medical appointments. Many healthcare providers are unfamiliar with BII, and even after we educate them, some dismiss our experiences as psychological. While breast implants are FDA approved, they come with a black box warning, highlighting their potential dangers.
This contradiction raises critical questions. Some women request to keep their implants after surgery, only to be told they can’t because they’re classified as “medical hazardous waste.” If they’re too hazardous to keep, how can they be deemed safe for insertion into our bodies?
When I share my story, I often hear from women who claim to have implants and feel perfectly fine. However, many of these same women have confided in me about unexplained symptoms their doctors can’t diagnose. If I suggest that their implants could be to blame, they often shut down.
I understand the complexity surrounding breast implants. Many women are reluctant to part with them, even when they may not have been the right choice from the start. I admit, I loved how my implants looked in swimsuits, giving me a sense of confidence I hadn’t felt before. But that confidence crumbled under the weight of my health issues.
Denial of my experiences, especially from other women, is infuriating. I share my story to help others—those considering implants, those who have them but are struggling, and those who might need support after explanting. My motivation isn’t financial gain or recognition; it’s genuine concern for women’s health.
I believe that one day, breast implant illness will be recognized as an official medical diagnosis, leading to greater understanding and acceptance for those of us affected. Until then, I will continue to share my experience, even if it makes others uncomfortable.
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In summary, it’s crucial to acknowledge and listen to the experiences of women facing breast implant illness. Their stories matter and can help others navigate their own journeys with implants.