Holly

“In May of 2008, I had just completed my first year of college and was back home for the summer. My parents had a delicious menu on deck to celebrate Memorial Day. I remember this because it was the last meal I would eat for two weeks. I woke up with an upset stomach and it proceeded to turn into what we thought was a stomach flu, which eventually landed me in the hospital.

Thanks to my dad being diagnosed with Crohn’s Disease a few years prior, the gastroenterologist knew what to look for. I was quickly diagnosed with Crohn’s Disease (later rediagnosed with Ulcerative Colitis!) and set me on a path I could have never expected for myself.

I remember laying in my hospital bed sobbing because my world was just flipped upside down and all I was given was a pamphlet and discharge papers.  Was my life over? I had no idea what life would be like with a chronic illness. 

As a 19 year old, my way of coping was to ignore it altogether. I continued on with life and pretended it wasn’t there, which actually led me to a cycle of denial, pushing my body to its limits, and hospitalizations. I was hospitalized 5 times before I took any responsibility for my own health.

When I was 24, I became sick and tired of feeling sick and tired all the time. My brain fog, pain, and fatigue were nearly unbearable, so I began a deep dive into nutrition and alternative care for IBD and I’ve never looked back.

Whenever I find myself feeling resentful and ‘woe is me’, I have to remember that I was set on this path for a reason. I am here on purpose; nothing happens on accident. Because of my own experience, I am now a health coach and personal trainer for the Crohn’s and Colitis community and get to share knowledge that I wish I had back in 2008.

I do often wonder what the version of me would be like if I was never diagnosed with Ulcerative Colitis. Who would I have become? Looking back on everything I’ve been through, I can say for sure that my experience has gifted me resilience, grit, perseverance, and a deep sense of gratitude for the big and small moments in my life.”

Holly

Similar Posts

  • Sergio

    “I was 35 years old when I was diagnosed with type 1 diabetes. When I found out, I thought my life was over. I was so scared. The first person I contacted was a good friend of mine. He calmed me down and explained to me that there is nothing I can do but to…

  • Daniela

    “My story is of a girl who lost everything and is now gaining back more than she ever had.  I was fourteen when a traumatic event triggered my chronic illnesses. I started experiencing countless symptoms, mostly due to autonomic nervous system dysfunction. The worst symptom of all, was the extreme pain in my chest that…

  • Eliana

    “At a very young age, I was diagnosed with MS, also known as multiple sclerosis. This is a disease that attacks the brain and spinal cord, that could potentially leave you paralyzed. It’s an incurable disease, so when I found out that I had it, I was extremely scared. When the doctor first told me…

  • Roberta

    “On June 16, 2021, I was diagnosed with stage 2 triple negative breast cancer in my right breast at the age of 44 years old. I had 3 opinions from UCLA, Providence in Santa Monica, and finally City of Hope. UCLA found the tumor, Providence removed the tumor, and City of Hope treated me with…

  • Dianna

    “In 2014, I was 25 years old living in Westchester County, NY, which is 35 minutes outside of Manhattan. I am a native New Yorker. I was working in Greenwich, CT when I noticed strange things happening to my body. I am now 34 years old living in Los Angeles and operate 2 businesses birthed…

  • Kayliana

    “I started to get sick when I was around 4 years old, I’m currently 16. This life is all I’ve ever truly known; being in pain everyday. I lost my hearing in my left ear when I was 6, almost 7 years old. I have something called Behcet’s Disease which is rare, fibromyalgia, SVT, chronic…