Endometriosis takes 7-10 years to get diagnosed and even then, what do you get?
👉🏽“Take the pill until you’re ready to have a baby”
👉🏽“Have a baby and that will cure it.”
👉🏽“Just suppress your hormones and risk your bone, brain, and heart health.”
👉🏽”We’ll do a hysterectomy or ablation when you’re done having kids.”
Women deserve better
We need more research
We need referrals to actual endometriosis experts
And we need medicine to stop acting like we’re “just being dramatic about some lady parts problems.”
Dr. Patrick Yeung and I just sat down on The @drbrightenshow to discuss surgical options, lab testing, and how to prevent adhesions in surgery.
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#endometriosisawareness #endometriosis #periodpain #infertilityjourney #unexplainedinfertility
Endometriosis is a complex, often misunderstood condition that affects millions of women worldwide but still faces significant challenges in diagnosis and treatment. It can take an average of 7 to 10 years for women to receive a proper diagnosis, during which time many suffer from intense pain and symptoms that are frequently dismissed or minimized by healthcare providers. This delay is not only frustrating but can also lead to worsening of the disease and decreased quality of life. A common misconception is that taking birth control pills or "having a baby" cures endometriosis. However, these approaches do not stop the progression of the disease. Birth control only suppresses symptoms temporarily and does not address the underlying issue. Similarly, pregnancy is not a cure, and women should not be misled into thinking that fertility is the only indication to seek treatment. More alarming is the reliance on hormonal suppression therapies such as Lupron, which acts as a form of chemical castration with potential lifelong side effects affecting bone density, brain function, and heart health. Surgical interventions like hysterectomy or ablation are sometimes proposed as a definitive solution, but these surgeries do not guarantee a cure and should not be considered lightly or used as a first-line treatment. Accurate surgical planning is critical for successful outcomes and requires detailed imaging and consultation with endometriosis experts. Unfortunately, many women do not have access to specialist care and are often gaslit when they report period pain, leading to further delays in receiving appropriate treatment. It is also important to recognize that endometriosis is not only a fertility issue; pain management and holistic care play a vital role. Women with unexplained infertility should be evaluated for endometriosis, as up to 50% of this population may have the condition even without pain symptoms. There is a dire need for more research to understand the disease mechanisms better, improve diagnostic tools, and develop safer, more effective treatment options. Advocacy for raising awareness among healthcare providers and the public can help reduce stigma and ensure women receive timely, compassionate, and evidence-based care. If you or someone you know is living with endometriosis, seek out healthcare professionals specializing in this condition. Educate yourself on the facts and share your experiences to support others in the community. Remember, period pain is not normal, and you deserve better medical attention and respect for your symptoms.