What is Cystic Fibrosis (CF)?
Cystic Fibrosis, or CF, is a severe, progressive genetic disease that causes persistent lung infections and limits the ability to breathe over time. The disease is caused by a defective gene that produces a faulty protein, known as the cystic fibrosis transmembrane conductance regulator (CFTR). This protein is responsible for regulating the flow of salt and water in and out of cells. When the protein is not working correctly, it causes thick, sticky mucus to build up in various parts of the body, most notably the lungs, pancreas, and other organs.
The Impact on the Lungs
The most commonly known aspect of CF is its effect on the respiratory system. The thick mucus in the lungs can clog airways and trap germs, leading to chronic infections, inflammation, and eventual respiratory failure. For patients like the characters in Five Feet Apart, this necessitates a grueling daily routine of treatments, including airway clearance techniques and nebulized medications, to help clear the mucus and maintain lung function. The risk of cross-infection between CF patients is particularly high and dangerous, as they can carry different antibiotic-resistant bacteria that are especially virulent to others with CF. This reality is the foundation for the famous "six-foot rule" that dictates the plot of the film.
The Impact Beyond the Lungs
CF is a multi-system disease that affects more than just the lungs. The buildup of thick mucus also impacts the digestive system and other parts of the body.
Here are some of the ways CF affects other organ systems:
- Digestive System: The mucus can block ducts in the pancreas, preventing digestive enzymes from reaching the intestines. This leads to poor absorption of nutrients, requiring many patients to take enzyme supplements with every meal.
- Liver: Blocked bile ducts in the liver can cause liver disease.
- Reproductive System: In men, CF can cause infertility due to blocked tubes that connect the testes and prostate gland.
- Sweat Glands: A common symptom of CF is unusually salty sweat, which is often used in the initial diagnostic 'sweat test'.
The “Six-Foot Rule” and the Movie's Plot
Central to the narrative of Five Feet Apart is the "six-foot rule," a real-life infection control guideline that dictates the distance CF patients must maintain from one another. In the film, Stella and Will, both CF patients, decide to "take back a foot," reducing the distance to five feet as a symbol of their rebellion against the disease that dictates their lives.
The reasoning behind this rule is crucial to understanding the characters' dilemma. While a healthy immune system can typically fight off various airborne bacteria, CF patients' compromised respiratory systems are especially vulnerable. They can carry different strains of bacteria in their lungs, and swapping these germs through close contact poses a life-threatening risk. The film effectively captures the emotional weight of this physical separation, making the characters' longing for touch both heart-wrenching and medically precarious.
Fact vs. Fiction in Five Feet Apart
While Five Feet Apart brought much-needed attention to cystic fibrosis, its portrayal drew mixed reviews from the CF community. Many appreciated the heightened awareness, while others pointed out medical inaccuracies and the romanticization of the disease.
Feature | Film's Portrayal | Real-Life Experience | Accuracy Verdict | Comments |
---|---|---|---|---|
The 'Six-Foot Rule' | A central, dramatic premise that the main characters deliberately break. | A critical, non-negotiable safety guideline for patients. Breaking it is extremely dangerous and not common. | Romanticized | Emphasizes romance over medical reality. |
Daily Treatment Regimen | Depicts characters adhering to rigorous daily treatments, like the vibrating vest. | Daily treatment is a constant, exhausting reality for many, involving nebulizers, vests, and a large number of pills. | Mostly Accurate | Captures the physical burden of the disease well. |
Hospital Environment | Shows CF patients congregating freely in hospital hallways. | Hospitals have strict protocols to prevent cross-infection, with CF patients often having to remain in their rooms or use separate wings. | Inaccurate | Exaggerates hospital procedures for dramatic effect. |
Life Expectancy | Can portray characters as being gravely ill at a young age. | While CF is a serious illness, advancements in treatment have significantly improved life expectancy. Many patients live into their 40s and beyond, leading full lives. | Slightly Outdated | Focuses on a worst-case scenario that doesn't reflect the majority of cases today. |
Mental Health | Touches on the depression and anxiety associated with chronic illness. | Many with CF experience significant mental health challenges due to the constant treatment burden, hospital stays, and limitations. | Accurate | Acknowledges the emotional toll of living with CF. |
The film's creators did consult with real CF patients, including the late CF activist Claire Wineland, who sadly passed away from complications after a lung transplant following the film's completion. Her input helped ground some of the medical realities, even if the central romantic premise remained a point of contention for many within the CF community. The film's primary strength is raising awareness for a condition that remains relatively invisible to the general public.
Conclusion
In the movie Five Feet Apart, CF stands for Cystic Fibrosis, a life-altering genetic disease that necessitates strict infection control, such as the six-foot rule, for patient safety. While the film successfully brought this often-misunderstood condition to the mainstream, it also took creative liberties that romanticized the dangers of cross-infection. For those seeking to learn more about the realities of living with CF, it's important to recognize that the movie is a dramatization and that real-life experiences can vary significantly. By understanding the true meaning of CF, viewers can gain a deeper appreciation for the daily challenges and incredible resilience of people living with this chronic illness.
Learn more about the latest research and support for cystic fibrosis by visiting the Cystic Fibrosis Foundation.