Hello,
I read somewhere (not sure where!) that humidity below 50% is best for CF'ers. Is that true? Is that why my daughter (at age 20) had a terrible time with uncontrollable coughing while we were in Mexico for a week? Does the severity of the CF have a bearing on whether or not humidity affects you? (she's ~40% lung function). We have had a particularly wet summer/fall in our area, and wonder if we should be using a dehumidifier all the time. Amber says it makes no difference in the way she feels. I think she sleeps better. Hard to tell. Any advice? thanks
I read somewhere (not sure where!) that humidity below 50% is best for CF'ers. Is that true? Is that why my daughter (at age 20) had a terrible time with uncontrollable coughing while we were in Mexico for a week? Does the severity of the CF have a bearing on whether or not humidity affects you? (she's ~40% lung function). We have had a particularly wet summer/fall in our area, and wonder if we should be using a dehumidifier all the time. Amber says it makes no difference in the way she feels. I think she sleeps better. Hard to tell. Any advice? thanks