My name is Cheyenne Laurance and I am a student at Florida Gulf Coast University. Growing up, I always had inexplicable pain in my head, which eventually spread to other areas of my body. I also began struggling with fatigue, brain fog, and more. These symptoms began to really interfere with my life in middle school, and I was officially diagnosed at the beginning of high school. I was grateful to have an answer to why I was feeling this way but discouraged to find there was no cure. Years later, as an adult, I have come to accept this condition and I have found ways to manage it. For me, physical activity and keeping busy with a healthy amount of rest is a good balance. I also utilize pain medication as well as support from friends and family. Balance is the key to success and supporting one another in this struggle is very important. Finding this balance and not letting FM hold me back from living my life has allowed me to transform from a caterpillar into a butterfly, flying free as I journey through life
Short Interview:
Do you have any overlapping conditions?
I have several overlapping conditions including vasovagal syncope and autoimmune gastroparesis as well as chronic fatigue and brain fog due to fibro and some of the other conditions. These conditions have impacted my life in so many ways and my quality of life varies greatly each day due to the unpredictability of these conditions. It is difficult for me to strenuous physical activity or be completely comfortable at any given moment. It is also difficult for me to handle extreme warm or cool temperatures as well as other things. On bad days when my pain and/or fatigue is severe, I have to lie down in bed and there’s not much I can do at all. On good days, I’m able to do moderate physical activity, go to school, and spend quality time with friends and family.
What were the reactions of your family members when you were diagnosed?
My family was very supportive when finding out my diagnosis and have been actively pursuing every possible medical treatment and intervention on the market, both holistic and Western. They have taken me to dozens of specialists and tried virtually every method of alternative medicine there is. They are also always there to provide support for me.
How have your family and friends helped you deal with your FM symptoms?
My family and friends have helped me deal with my FM symptoms by financially supporting my medical journey and providing emotional support whenever I need it.
What type of treatments have you tried to feel better?
Pain medications have been helpful in controlling the pain and allowing me to function, generally speaking. Stretching and making sure I have supportive shoes helps with pain and stiffness. Also, getting enough rest is vital.
Describe your exercise routine and how do you stay active?
I believe swimming is one of the best forms of exercise for those with chronic pain.
I swim, I lift weights and do mild cardio. I believe swimming is one of the best forms of exercise for those with chronic pain because it does not put any pressure on joints while allowing for freedom of movement. Exercise is vital for me to prevent pain and stiffness as well as keep my body technically healthy and fit. I do not have a consistent routine, however, because my pain and subsequent physical abilities vary each day and are unpredictable.
