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

  • Destinee

    Trigger Warning: This story includes topics of rape and sexual harassment. “I was diagnosed with severe generalized anxiety disorder, depression, and PTSD at the age of 19. In the year of 2016, when I thought that this would be the prime year of my life, I was raped by a man I knew from high…

  • 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…

  • Isabella

    “There is a really frightening sense of finality to chronic illness, the term ‘chronic’ seems to serve to soften the impact of the reality that an autoimmune disorder is something I will probably have until I die, that one day I woke up and spontaneously developed something that will stay with me for my entire…

  • Mireille

    “There are things I have to do that are hard to imagine my peers doing. Frequent lab work and speciality visits. Trips to the pharmacy for refills. Filling out my pill container for the week. Then there are the more intimate worries: do I feel sick because I didn’t get enough sleep? Why do my…

  • Bailey

    “It has almost been a lifetime of pain. A lifetime of looking for answers and hoping for a miracle. For as long as I can remember I have been in and out of hospitals desperately searching for answers. Daily bone dislocations, bruising at the slightest touch of a feather, chronic headaches, fainting episodes, and daily…

  • 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…