Living with endometriosis isn’t just about painful periods—it’s a daily battle with pain, uncertainty, and resilience. If you’ve ever felt dismissed or misunderstood, you’re not alone. I know because I’ve lived it, and this is why I created this space.
My Journey with Endometriosis
I’ve experienced pain for as long as I can remember.
It started in high school – the kind of pain that wasn’t “just bad cramps” but the type that made me curl up in bed and miss days of school. Back then, I didn’t have a name for it. I was told it was “normal,” that I just had a “low pain tolerance.”
Fast forward through college, and my symptoms became impossible to ignore – blood in my stool before and during my period, constant bloating, and cramps so severe they landed me in the ER.
After nearly 10 years, I finally had answers: Stage 4 Endometriosis. By then, it had spread everywhere – my uterus, ovaries, diaphragm, and colon. I’ve endured surgeries, procedures, and constant battles with pain, but the hardest part was how isolating it felt.
Why I Started This Blog
I want this blog to be more than just my story.
Here, you’ll find:
• Real-life experiences living with endo, adenomyosis, fibroids, and fertility challenges.
• Natural management tips that actually help reduce pain and inflammation.
• Medical insights from trusted sources so you can make informed decisions.
• Community support—because you shouldn’t have to face this alone.
If you’re here searching for answers, hope, or just someone who understands—you’ve found the right place.
Closing:
Endometriosis may be part of my life, but it doesn’t define me. This space is about taking back control, finding relief, and building a community where we’re seen and supported.
Thank you for being here.