We’ve all been there. It’s the end of a long day, everyone’s asleep, and it’s time to thumb through new movies streaming on Netflix or available on iTunes. There’s always that one compelling movie that begs to be clicked on. Still, you pass it by, night after night. Once in a while you may click through for more information, but you never end up watching it. You’re just not feeling the title, promo photo, or subject matter itself. It’s a little too heavy or hits too close to home. Then, one night, something deep inside tells you to go for it, or rather, makes you go for it. You click on the play symbol without even realizing it and the results are life changing. For me, that night was last night and that movie was called 65_RedRoses.
65_RedRoses is a very true story. A documentary. A work of art. A teaching. It’s a very real representation of perhaps the most challenging period in the lives of three special young women, all suffering from Cystic Fibrosis (CF). This is not Reality TV, this is reality. A raw view into the out-of-control chest congestion and lengthy hospital stays that often accompany CF. In 65_RedRoses, Eva Markvoort, part warrior, part sage, exposes her great pain and vulnerability but also her great zest for life. She opens up and extends her creative mind and adventurous heart for us all to experience. We are brought deep within her inner circle to ride a roller coaster of emotions.
Eva, along with her loving and supportive family and two fellow CF fighters Meg Moore (aka megmucus) and Kina Boyce (aka Spirit_of_Kina), helps us to better understand this disease and the organ donation process associated with a skillful but risky double lung transplant. A process full of on-call waiting, waiting and more waiting. Through online journal entries and footage shot during excruciating moments, we share in their struggles, join along in their friendships and cry with relief when they shine. Shine, a good word. Even in her worst condition, Eva couldn't help but shine on family, friends and everyone else who crossed her path.
For those of you who are unfamiliar with CF, in short simple terms, it’s a disease that causes heavy mucus to accumulate in the lungs and other organs, eventually impacting the digestive system. Among other things, this results in severe breathing issues, infections and fatigue. Treatments are improving and the miracle of organ donations and lung transplants may extend a Cystic Fibrosis patient’s life, however, as the American Lung Association puts it, “People with CF have a shorter-than-normal life expectancy.” That means, that as of today, there is no known cure for Cystic Fibrosis.
Through my Standing Cyclist projects and my own Allergic Asthma challenges, I was somewhat familiar with CF, but my understanding was very limited. I only knew that CF patients had trouble breathing. That’s all. But it’s far more than that. During one of my adventure cycling fundraising trips, I had the opportunity to meet a child with Cystic Fibrosis. I chatted, trailside, with his parents. I listened to their story, impressed by their positive attitude and strength. In that moment, I got to know them, but I never really got to know CF first hand. Not until now. Not until I clicked on that one movie I had been passing on for many months.