The Passy Muir® Valve has helped patients of all ages with tracheostomy and mechanical ventilation improve their quality of life through improved speech, swallow, and more. Watch and see how the Passy Muir Valve is changing thousands of lives all over the world.
Are you a Passy Muir patient? Do you have a story to tell or pictures to send? We’d love to hear from you. Please send us your stories and photos for possible inclusion in the Patients section of our website or to share in our newsletter. Thank you!
Agnes is using the Valve in-line with the ventilator. Meet Agnes as she discusses the impact of the Passy Muir Valve on her quality of life.
Althea, who had Guillain-Barré Syndrome, was filmed at Madonna Rehabilitation Hospital. This video follows Althea from early stages with communication board use while on the ventilator through a capped tracheostomy tube.
At the age of 22, Ariel found herself diagnosed with Guillain-Barré Syndrome, causing her to lose the ability to function in regular day-to-day activities including the ability to speak. In Ariel’s journey to recovery, Lake Taylor Transitional Care Hospital implemented the PMV 007® in-line with a ventilator as a form of therapy. With continued use of the Passy Muir Valve, Ariel was able to regain her ability to speak, eat, and stand. Watch the video to see Ariel’s progress.
Butch is using the PMV 007 in-line with the ventilator and enjoying his lunch. With his therapist standing by, Butch is able to eat a regular diet while on the ventilator. Watch this video to see the ease of eating with the PMV in-line.
“Cooper and his triplet brothers were born 4 months prematurely, on June 5, 2007, at only 24 weeks gestation. Cooper weighed 1 lb., 6 oz. at birth, and spent the first six months of his life in the NICU. His biggest issue was tracheomalacia, and he came home with a trach. About 11 months after Cooper’s tracheostomy, the doctor gave us the thumbs up to try the Passy Muir Valve. Cooper took to the PMV almost instantly. I’ll never, ever forget the first time we heard him cry and babble. The PMV changed all of our lives. Three screaming babies is a beautiful sound! Now, not only was Cooper communicating with us, but with his brothers too. Cooper’s trach was removed in March 2009, and I’m very happy to report that today, Cooper’s speech delays are nothing substantial.
THANK YOU Passy Muir!!”
— Raizel, mother of Cooper
This video features Erasmo, a patient at Madonna Rehabilitation Hospital in Lincoln, Nebraska, who had Guillain-Barré Syndrome. Watch this video to learn about his use of the Passy Muir Valve and therapeutic interventions on his road to recovery.
In this video, David demonstrates the change that occurs when blowing a whistle with and without the Passy Muir Valve. David has a significant medical history, but exhibits independence with Valve use.
“Our daughter Eleanor was born with an undiagnosed neurological disorder. Due to tracheamalacia, she has been trached since birth, so we never heard her cry or make any noises. Passy Muir gave us the best gift we could imagine: being able to hear our daughter make sounds, enabling us to connect with her in a whole new way.”
–Emily, mother of Eleanor
Genevieve was a 16-year old patient at Madonna Rehabilitation Hospital. She came to Madonna after a severe asthma attack, respiratory distress, and pulseless ventricular tachycardia. Thanks to the efforts of the clinical staff at Madonna and the Passy Muir Valve, she can now perform her favorite songs. Watch her sing and play Adele’s “Someone Like You.”
This video features Grady, a young patient at Nationwide Children’s Hospital in Columbus, Ohio. Grady was born prematurely with intraventricular hemorrhage and severe bronchopulmonary dysplasia. In this video, his mom and therapists share his history and successful use of the Passy Muir Valve both on and off the ventilator, despite high transtracheal pressures.
“I have now used the PMV for 18 years. It has allowed me to continue to give motivational talks to various groups, teach a weekly class in church, counsel people, talk on a speakerphone to friends everywhere, use voice recognition software (one of my books is currently being published and another is at a publisher being considered for publication), and most importantly, I am able to visit with my children and 17 grandchildren and express my love to them all.”
“None of the above is said by way of bragging but with a deep sense of gratitude for the PMV that has enhanced my quality of life more than I could ever express in words. I shudder to think what might have been if the speech therapist at my rehabilitation hospital had not insisted that I try to use the PMV.”
Luis received a tracheostomy due to respiratory failure from COPD. He is currently weaned from mechanical ventilation and is receiving 40% fraction of inspired oxygen by a tracheostomy mask. Luis has a cuffless Shiley #6 tracheostomy tube, and without a Valve in place, airflow leaks out the trach tube, resulting in voicing sounds that are weak and breathy. Luis has to take a deep breath before each word in order to produce voicing. Once Luis places his PMV 2001, all expired air is redirected through the upper airway. You will notice that his voice is stronger and he has uninterrupted speech.
As an infant, Mabry had a tracheostomy tube and used a Passy Muir Valve. Her mom shares their experience and the impact of the Valve on Mabry’s development. Even though she no longer needs it, Mabry still keeps her Valve by her dresser. Watch this video and learn about her journey towards recovery.
Roberto is a tetraplegic who was initially on a ventilator. In this video, he discusses his experience with the Passy Muir Valve while on the ventilator at Swiss Paraplegic Centre. He shares the hardship of losing his voice and then the joy of finding it again with the Passy Muir Valve. In light of his loss of movement, he explains the significance of having his voice. Watch this video for his story.