Survey results for Personal Spirometry and our CF Community

[Imogene]

Recently, 500 members of cysticfibrosis.com on-line social health community responded to our survey investigating the use of mobile spirometers at home.

The results may surprise you.

Watch member LouLou’s video demonstrating this latest FDA approved technology in her home.

http://healthworkscollective.com/je...rsonal-spirometry-and-cystic-fibrosis-patient

Mobile…it’s personal!

Salt and Light,
Jeanne

 

[lilmac1177]

i have several questions, but most importantly to me right now:
1) would a home spirometry device be covered by insurances?
2) how does the data get to my doctor and is it transferred in a secure fashion so that my PFTs are not ultimately visible on the world wide web?
3) would Medrise, or who would, control my data?