From Michele: I’ve said it many times on my blog and my Instagram, but you never truly know what someone is dealing with by what they look like in real life. I mean, looking at my feed, you see a girl smiling, but you can’t see the struggles that I’ve had to fight. The same is true for the majority of those who share their story. And today, I want to share Gaby’s story on what it’s like living with Ulcerative Colitis. Maybe it’s just the inspiration that you need in order to keep going.
I was diagnosed with Ulcerative Colitis, a form of Inflammable Bowel Disease in September of 2017. I was initially relieved to know there was a physical cause for my symptoms (e.g. cramping, bloody mucousy stools, fatigue, etc.) and it wasn’t just something I was doing wrong.
I didn’t expect my life to change – I figured by taking medication everyday I could keep things at bay and life would go on as I expected (similar to how my acid reflex medication works).
In April 2018, my symptoms took a turn for the worse and I ended up as an inpatient at a local Chicago hospital for 8 days, treating a severe flare-up. My doctor explained to me that I was misdiagnosed and my inflammation spread further up the large intestine. She adjusted my treatment plan and I started to feel better, but wound up back in the hospital a few months later. After that second visit, I’m happy to say we found a treatment that works for me (monthly remicade infusions coupled with a compounded suppository) and I’ve been hospital free for just over a year!
Some of the toughest parts about having IBD is hearing people tell me that I don’t look sick or I’m too young to have this many doctors appointments or “problems”.
IBD is an invisible disease but the symptoms and side effects are 100% real. It can also be tough going out with friends or having to cancel plans at the last minute and be that friend, but most people who matter in my life understand. I wouldn’t be able to do any of what I’m doing without the incredible support of my boyfriend, family and friends.
Ironically, the best part about my diagnosis is it helped me find my passion for healthcare.
Right after getting out of the hospital the second time last year, I quit my corporate job to pursue a career in medicine. I’m currently working as a trauma tech at a Level I trauma hospital with the end goal of being a Physician Assistant.
While my days can be tough sometimes – chronic fatigue, random stomach pains, other bleeding problems, hormonal imbalances,etc. I am so grateful that my disease led me here. I’ve connected with so many people on social media (and in real life), have been advocating for myself, have (hopefully) helped inspire others on their own journey and truly found my career passion!
Gaby
Connect With Her:
Instagram: http://Instagram.com/fitfourtitude
Twitter: twitter.com/gabroniNcheese
