Humidifiers, Air Purifiers

anonymous

New member
I have noticed that my daughter will have an increase in bloody noses in the winter here in NY. Does anyone use a humidifier, what type, where did you buy it and does it work? Thanks,
 

anonymous

New member
My son is 6 and he has a hard time with bloody noses in the winter... we have a humidifier in his room plus in the living room and it helps out ALOT!!! ours is a GE cool mist humidifer.. bought it at walmart i think... hope this helps


Melissa mom to dylan 6 no cf and caleb 3wcf
 

anonymous

New member
We were told by our cf nurse that a humidifier would be a double edged sword. It has obvious benefits but if it is not cleaned regularly and properly it is a breeding ground for bacteria. We recently moved into a new home with a humidifier system and our inspector suggested that we remove it because of our daughters CF, stating that it would do more harm than good for her.

Love my girl (forgot to sign in)
 

anonymous

New member
I am a 39 year old with cf and have 2 humidifiers in my house, one in my bedroom and one downstairs. I bought warm mist ones with a UV bulb that kills any bacteria. That, in combination with weekly cleaning, kills 99% of bacteria/molds so it is safer for patients with cf. They are made by Slant Fin. I live in New England, and we have very dry winter air here. The humidifiers really help. Good luck!
 
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