CYSTIC FIBROSIS

Cystic Fibrosis affects the cells that produce mucus, sweat and digestive juices, causing these fluids to become thick and sticky, and resulting in symptoms that include coughing and repeated lung infections. The Cambridge Mask provides the benefit of blocking an array of microbes including bacteria like pseudomonas, fungus, and fungal spores.  

BESTSELLERS

Sold out
Sold out
Sold out
Sold out

Fitted correctly, the Cambridge Mask blocks particles down to size PM0.3 and provide users with the following benefits:

  • Lightweight & breathable fabric
  • Filters 99.6% of all viruses and 99.7% of bacteria
  • Filters PM10, PM2.5, PM0.3
  • Lasts up to 340 hours of active use (3 – 6 months)

PRO Mask Use for Lung Disease

The Cambridge Mask PRO is infused with a three-layer filtration system that blocks particulates, viruses, and bacteria from entering the respiratory tract. Due to the mask’s ability to reduce the chance of contracting respiratory infections, it will be of benefit to people with COPD and Cystic Fibrosis.

WHAT OUR CUSTOMERS SAYS

“Love love love these masks! Our daughter is 2 1/2 and has cystic fibrosis. We ordered 2 of the 65 Roses masks for her and we all love it including our girl”
- KC Bettes
“We have now bought 4 masks from Cambridge Mask co, as we bought one for my young son a few years ago, he has Cystic Fibrosis and after seeing recommendations from the CF community I purchased one for a flight and it was great.”
- Sophie Moore
“My wife has Cystic Fibrosis so I can't risk bringing any viruses home to her. I feel confident wearing my Cambridge Mask that we will both be protected in these challenging times!”
- Eric Wolf

SIZE GUIDE

NEWS FROM OUR BLOG

FIVE YEARS AND 42 MILLION BREATHS LATER – AN IN-DEPTH CATCH-UP WITH ROB & JEN

The couple discovered our products a few years ago and have not only used them but have also promoted them, with Jen having played a significant role in the design of our now famous 65Roses PRO mask.

WHAT IS THE BEST MASK FOR CYSTIC FIBROSIS PATIENTS?

Over the last year, masks have become an essential part of any outing for people worldwide. However, it’s important to recognize that for people with respiratory or autoimmune diseases, masks have long been a permanent part of their lives. This is particularly true for people with Cystic Fibrosis (CF).

INTERVIEW WITH JENNIFER RONNENBERG: LIVING WITH CYSTIC FIBROSIS

A close member of the Cambridge Mask Co extended family, Jennifer Ronnenberg has played a huge role in raising awareness for the cystic fibrosis community over the years. We have followed Jen’s journey closely since her lung transplant back in 2017.

THE UNIVERSE OF CYSTIC FIBROSIS

Cystic Fibrosis (CF) affects more than 30,000 people in the United States alone, including children and adults. In order to live with CF, a person must take medication every day, perform chest physical therapy twice a day, and follow a special diet.

CERTIFICATIONS

OUR PARTNERS

CONTACT US