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AffloVest Patient Testimonials2019-06-12T15:40:15+00:00

AffloVest Patient Testimonials

Want to review some AffloVest Patient Testimonials? See what cystic fibrosis patients and bronchiectasis patients and their care providers are saying about AffloVest HFCWO airway clearance therapy! The only way others can know how it works them is to share their experiences. Join the many Afflovest family members and share your experience with others. If you see a testimonial that hits home and you want to share it on your Facebook feed, please feel free to do so. Our goal is to make the treatment available to everyone that can benefit from our vest therapy. Thanks to our patients for sharing their AffloVest Patient Testimonials! You can read more reviews on Facebook.

Breathing Deeper

“I am 61 years old. I have Bronchiectasis & have horrible mucus secretions. I started my treatments yesterday. I can breathe deeper & haven’t noticed more coughing. I am so happy this is portable because I can use it at work. Looking forward to breathing better.”

Clarice L

Bronchiectasis Patient

A CF student’s best friend

“My daughter is in college just got an Afflovest and she loves it. A total game changer for cf patients that need to be mobile.”

Margie

Cystic Fibrosis Patient

The Best Vest

What’s not to like…it’s got everything over the competition. Fit to size, lightweight, portable, easy to use remote control, 2 hr battery life, use twice a day for half hour at a time, 3 cycle therapy. It IS the GOLD STANDARD for percussion therapy. There is nothing better!!!!

Tom B

Bronchiectasis Patient

Mucus is on the move

I just received my Afflovest and I love it. I like how it moves from different places of your lungs. I have a hill-rom vest but it only focus’s on one spot. It doesn’t move to different areas. I do find myself coughing a lot more with the Afflovest which is a good thing.  By the way its moving my mucus around should be a great thing.

Cynthia

Cystic Fibrosis Patient

Less constricted treatments

“It can get pretty boring sitting in the same place 3 times a day for the time being for treatments. This makes me feel less constricted and like I can live a little more. I’m so happy I got this!

Jennifer

Cystic Fibrosis Patient

Normal kid again

“Nathan doesn’t let doing the AffloVest stop him from having fun with his friends. In fact, our house is the local hang-out for 6 kids in the neighborhood. None of them bat an eye at his treatments.”

Cynthia

Cystic Fibrosis Parent
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