Ground Zero first responder raises awareness for lung disease


Posted: October 18, 2021 | Word Count: 614

Twenty years after 9/11, some World Trade Center first responders still struggle with long-term health complications brought on by the catastrophic event. For Tom Frey, a former New York City detective, the consequences started with Hodgkin’s Lymphoma — a blood cancer that can be linked back to inhaled dust from his rescue and recovery efforts at Ground Zero.

After his ninth session of chemotherapy, he developed shortness of breath and learned the treatment had led to bleomycin lung toxicity and pulmonary fibrosis (PF), a progressive, debilitating lung disease.

“I was a policeman, and the first three days down there, they didn't give us proper equipment. They gave us paper masks along the way. We worked for months and months digging through debris,” said Frey. “After a while, they gave us hazmat suits, but then 2,000 feet away we would eat our lunch and take the top of our hazmat suits off. The wind blew white dust onto our food, and nobody thought anything of it at the time.”

Now Frey struggles daily to breathe and relies on a portable oxygen device. Despite his health struggles, he works to drive awareness about PF.

“You’d be very surprised how little is known about this disease. I want to help people living with PF, especially the ones who are just starting out,” said Frey. “Having gone through it for so long, I feel confident I can be a resource. I don’t want to see a single person struggle like I did, so I’m going to keep advocating for high-quality care so everyone impacted by this disease can live longer, healthier lives.”

What is pulmonary fibrosis?

In simple terms, pulmonary fibrosis means scarring in the lungs, and it can be seen in many types of interstitial lung disease (ILD). Over time, PF can destroy the normal lung and make it hard for oxygen to get into the blood. More than 250,000 Americans are living with PF and ILD, and more than 50,000 new cases of PF and ILD are diagnosed annually.

Because the disease remains largely unknown, it can be difficult to diagnose. The main symptoms of PF may be hard to pinpoint because they are so common: shortness of breath, a dry, persistent cough and fatigue. It is more likely to occur in those that are 60 years and older with a history of smoking, or those, like Frey, who have used certain types of medications.

Learn more about pulmonary fibrosis

The Pulmonary Fibrosis Foundation (PFF) is dedicated to educating patients and the healthcare community about the disease.

“Understanding the symptoms and risk factors associated with PF is critical to engaging people nationwide in the fight against this lung disease,” said William Schmidt, president and CEO of the PFF. “Raising awareness of the disease is imperative to driving earlier diagnoses, advocating for needed research and ultimately finding a cure.”

The PFF empowers the community to become advocates by promoting disease awareness, sharing the latest information and research, and spreading hope and inspiration to the PF community. The PFF offers numerous helpful resources to support patients, caregivers and family members, including the PFF Help Center, more than 150 nationwide support groups, as well as PFF Care Center Network, which consists of 68 medical centers in 33 states. Medical professionals at these sites understand the disease and provide comprehensive, high-quality care to people living with PF.

“The PFF is a great organization; it’s helped me so much,” said Frey. “I’m going to keep on fighting. I hope that together, we can find better treatments and a cure for this disease.”

For more information about pulmonary fibrosis, visit www.aboutpf.org.

This article is available to download for free use in print and online publications. If you must edit the article, please include at least one brand reference. All articles must retain the (BPT) or Brandpoint byline.
Download this Article