September 24, 2023
This article explores the life of Dustin, a young man living with a rare disease called chronic granulomatous disease. It features an investigative journalism piece, a personal essay by Dustin, a medical research article, a news piece, and a narrative nonfiction piece, offering readers unique perspectives into the challenges of living with a serious illness.


Dustin is young, ambitious, and determined. He never thought that he would have to deal with a serious illness in his prime. Unfortunately, Dustin was diagnosed with a rare disease that has changed his life in ways he never imagined. In this article, we will explore Dustin’s journey living with this condition, and offer insights into how this disease impacts his life.

Investigative journalism piece

Dustin’s disease is a rare autoimmune disorder that affects only a small number of people worldwide. Some of the symptoms of the disease include chronic fatigue, joint pain, and increased susceptibility to infections. To better understand Dustin’s condition, we spoke to several medical professionals who have treated him over the years.

According to Dr. Kurt, Dustin’s attending physician, the disease he is suffering from is called chronic granulomatous disease or CGD. This is a rare genetic disorder that affects the immune system, causing recurring infections that can become life-threatening. Dustin was diagnosed with the disease at age 13, and Dr. Kurt has been treating him ever since. He says that while there is no cure for the disease, it can be managed through regular monitoring, medication, and in extreme cases, bone marrow transplantation.

Aside from the medical perspective, we also spoke to Dustin’s close friends and family members to gain insights into his struggles with the disease. His sister Amy says that Dustin is one of the strongest people she knows, carrying on with his life to the best of his abilities, despite the challenges put before him. “His tenacity is amazing,” she says. “He never gives up and always tries to find a way to overcome whatever is thrown his way.”

Personal essay by Dustin

Living with a rare disease is not easy. It’s like walking on a tightrope where the only way to survive is to keep moving forward. For me, the emotional toll of the disease is almost as bad as the physical symptoms. I often feel isolated from the rest of society, and worry that I might never achieve the things in life that I’ve always wanted.

But I’ve also learned to cope with my illness on a daily basis. I try to stay positive and focus on the things that I can control, even when it feels like everything else is out of my hands. I’ve also learned to rely on the support of my loved ones, who have been there for me through thick and thin. They remind me that I am not alone in this, and that there are always people who care about me.

Medical research article

Currently, there is no known cure for Chronic Granulomatous Disease. However, there are various treatment options available that focus on managing the symptoms of the disease. The most common treatments involve taking prophylactic antibiotics, antifungal, or antiviral medications to prevent infections.

In extreme cases, a bone marrow transplant may be considered as a potential cure. Although it is a risky procedure with potential complications, it has the potential to cure some patients of the disease entirely.

Research on the disease is ongoing, and new treatment options and therapies are being explored regularly. Scientists hope that a better understanding of the disease’s underlying causes will lead to more effective treatments in the future.

News piece

Despite the challenges he has faced, Dustin has worked hard to maintain his professional career. He currently works as a software developer, a job that allows him to work from home and adjust his schedule to accommodate the needs of his health. He admits that working from home can feel isolating at times, but he tries to stay connected with his colleagues and maintain a positive outlook.

Dustin uses his platform to raise awareness about the disease and advocate for more research into potential treatments or cures. He wants to ensure that others living with this condition in the future can have a better quality of life than he has had.

Narrative nonfiction piece

While Dustin may be the one with the disease, it’s important to recognize the toll that caregiving can take on loved ones as well. Megan, Dustin’s girlfriend, has been a pillar of strength and support throughout his journey with the disease. Despite the emotional stress of being a caregiver, she says that it has also brought them even closer together.

“It’s been hard at times,” she admits. “But I wouldn’t trade it for anything. I love Dustin so much and I’m grateful to be able to support him through anything.”


Living with a rare disease is a challenging and often isolating experience. However, as Dustin’s story shows, it’s also possible to find resilience and hope in the face of adversity. Those who struggle with similar conditions can benefit greatly from a supportive community, medical care, and the knowledge that they are not alone.

Beyond raising awareness about rare diseases and the need for more research and treatment options, it’s important for us to remember the power of empathy and compassion. By being a source of support and positivity, we can all make a difference in the lives of those who are affected by these conditions.

Leave a Reply

Your email address will not be published. Required fields are marked *