My Story
Hi, my name is Anusha Gandhi (she/her).
Writing my bio has always been a challenge, because so much of my life has been shaped by chronic illness. Pain has a way of taking centre stage, crowding out memories of who I once was. But I am learning to look at the bigger picture — to accept where I am today, to celebrate the little things, and to remind myself that I am a work in progress.
My story with endometriosis began at 14. Within my first year of menstruation, I was hospitalized for pain so severe I would blackout, and was prescribed birth control, which I remained on for 15 years. It wasn’t until I began exploring the idea of becoming a mother that I was referred to a fertility clinic — and finally, officially diagnosed with endometriosis.
Since then, I’ve undergone one ablation and two excision surgeries, removing disease from my ovaries, bladder, colon, and diaphragm. For me, menstruation meant debilitating cramps, heavy bleeding, and period-related bowel flares. For nearly 20 years, I thought my digestive issues were simply tied to endometriosis. But mere months before my first excision, I was rushed to the hospital by ambulance, believing I had the flu. That day, I was diagnosed with severe ulcerative colitis. I was immediately placed on a biologic (Entyvio), and later learned I also live with other conditions, including pancreatitis and the ongoing possibility of primary sclerosing cholangitis.
My last excision in 2020 brought its own challenges. I developed a prolapse, lost nerve function in my rectosigmoid (meaning I can no longer pass a bowel movement on my own), and eventually required a sacral neurostimulator — a permanent device implanted in my back. The image to the right is taken from that surgery, and the wedding picture - 4 months after that operation.
It has been a long road of surgeries, setbacks, and recovery. And yet, alongside the hospital stays and medical charts, there have been moments of love, joy, and deep resilience.
Through it all, I’ve built a set of tools to help me recover, to bounce back faster each time, and to carve out a meaningful life despite chronic illness. Those are the tools I want to share with you.
Over the years, through the ups and downs of living with endometriosis, I poured my energy into patient advocacy—working to move the needle on women’s health, dismantle misinformation about endometriosis, and help others navigate the healthcare system. What began as a personal quest to find connection and community grew into something much bigger: a shared movement among endo warriors, each of us chipping away at meaningful change.
My own contributions have taken shape under three names you may recognize: CrampMyStyle, Femade, and Anusha Gandhi.
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Cramp My Style Blog
CONTENT CREATOR
Founded in 2018, my Blog (crampmystyleblog) and my Instagram account (@cramp_my_style) have been a safe space for endo warriors and healthcare practitioners alike, spreading awareness and true information to help guide others on their journey, be it with endometriosis or invisible illnesses.
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Femade
FOUNDER AND DIRECTOR
In 2022, I opened Canada’s first multidisciplinary allied healthcare clinic focused on women’s health. Through the counsel of several advisors including women’s health specialists across the country, Femade has become a success story and a safe haven for more than 3000 patients.
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Anusha Gandhi
ENDO WARRIOR AND HEALTH NAVIGATOR
Holding a Masters of Neuroscience, Two decades of Genetics Experience, A certification in both Health Navigation and Peer Support, I began offering Health Consults to Endo Warriors and their family members to provide guidance on navigating various medical systems worldwide.
Contributions over the years
I’ve been there.
My approach is simply to work with you, provide guidance where needed, hold you accountable, and provide you hope.
No lotions. No potions. No cures. Just two people working together to optimize your quality of life.
Contact me
Interested in working together? Fill out some info and I will be in touch shortly. We can’t wait to hear from you!