Kaelyn

“My journey is complex, with layers and a non-linear storyline. As it often is in this crazy and wonderful life. However, I live with endometriosis, fibromyalgia, pelvic floor myalgia, IBS (irritable bowel syndrome), vulvar vestibulitis, migraine with aura, and symptoms that often put me in a place of survival mode. Somehow, I always find the silver lining in the end.

When I think of my chronic illnesses, I can’t help but think about what I have lost over the years, such as my time, money, relationships, friendships, happiness, and self-esteem. Whether that was from my own actions or the cards I was dealt with. I grew up in a household with an abusive father that told me not to cry. Who referred to me as, ‘dramatic’ and ‘ugly.’ One perceived mistake from him and out came the flyswatter. He painted a different picture to the world. He was charming, funny, smart, resourceful and could light up a room, but behind closed doors he was an abuser.

In the year of 2006, my family and I found out on Father’s Day that my dad died from vehicular manslaughter. I was ten years old and my brother, eight. The years of court from this horrific event led to additional mental and physical trauma. It did a number on my family and the people that surrounded us. I was confused and lost in a world where the title I now had was ‘fatherless’. I must add though, that without the love and support from my mom, family and friends, I might have been a different person.

This may come as no surprise, but my mental health took an immense amount of work from me in order to be what it is today. Which, let’s face it, is still a work in progress. I think we are all works of art, where the artist is never satisfied. Needless to say, trauma, suffering, and potential play of genetics has ailed my mental health and in particular my physical health. First, my symptoms started with severe stomach pain, cramping, bloating, digestive issues, awful periods, pelvic floor pain, bladder infections, and migraines with visual disturbances. I was diagnosed with migraines that have aura (visual disturbances), in 2015, but that diagnosis didn’t explain the list of symptoms that was affecting every area of my life.

Every year it seemed like I was getting worse, with new symptoms such as dizziness, chronic fatigue, increased heart beat, tremors, muscle spasms, muscle weakness, mood swings, brain fog, etc. I tried various diets and therapy, but doctors would still tell me I’m just clumsy. That there is nothing wrong with me. That it’s all in my head. I’ve gotten that response more times than I can even remember. I believe mental health can play a role in our bodies, but I know my body, much like the millions of chronic illness warriors who are told this exact phrase on a daily basis.

It wasn’t until these last few years that I was finally diagnosed with endometriosis, fibromyalgia, pelvic floor myalgia, IBS, and an auto-immune disorder called vulvar vestibulitis. It took many specialists, ER visits, therapy, advocating, breakdowns, anger, labs, surgery and begging for an answer, where I could finally identify and have validation to my experience. In 2021, I had surgery for endometriosis and vulvar vestibulitis. This included a laparoscopy to remove the scar tissue in my body. It was a traumatic surgery, due to the fact that I had lost a great amount of blood from a knick in my artery during the procedure. My lips were blue and cold. My mom cried deeply, as she saw me lying in the hospital bed in severe pain. This led to needing a blood transfusion. Mind you, I had a flight the next morning back to California, since I was living in Utah at the time of me needing this procedure.

I am still on this journey with the hope of exploration and success. I have many dreams and passions. I love music, singing, traveling, hiking, nature, sculpting, exercise, family, friends, art, culture, love, and finally, myself. I’ve had to learn to love myself with a body that has endured many trials and tribulations. My long term plans include making music, traveling, and getting a master’s degree in counseling, where I can truly inspire others and help people unravel their stories.

Life is messy and fragile. With this understanding, I try to live my life deeply and with intention. Appreciating my hardships and giving time to the people who want the best for me, is essential to my happiness. I may not always be down for events or hangouts on my bad days, but I do have my good days and even great days. My story is a myriad of adjectives and my future is filled with an infinite amount of opportunity, joy, and adventure.”

Kaelyn

Similar Posts

  • Lauren

    “Looking back at my younger years with Crohn’s Disease, I can’t help but feel robbed. If I could go back and meet my childhood self I would hug her and tell her it would all be okay. Overall, my childhood was great! My parents were amazing and took us to all the fun places and…

  • 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…

  • Meesa

    “I was 22 years old when I started testing for cancer. I was so young that reflecting back I realize how I didn’t even really know it at the time. Doctors would tell me let’s do this test, then this type of test, choosing very carefully in words what we were actually testing for. I…

  • 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…

  • Max

    “On the morning of November 1st, 2016, I had my first seizure. I was seventeen years old at the time, it was the beginning of my senior year of high school. When I woke up, I was in the hospital surrounded by family members and some of my football coaches. I had no clue what…

  • 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…