Did anyone go part time with work for a few weeks to get their pfts back up?
Specifically I am wondering if going half time while I attempt to get my pfts back up with use of oral antibiotics, increased pt, and exercise will have a lasting effect. I realize I'll need to take some of the good habits (darn thought I was already good - I hate cf) from this few week period into full time work lifestyle but have you found this helpful?
My inclination is the 'get back on the horse' and not take a step back from life but I'm thinking it would be a good idea if nothing else to avoid a hospital stay and the big guns - IVs.
My FEV1 dropped from 65% (201L) to 56% (1.75L) from end of Sept. to end of Oct. I'm not dealing with stress the way I usually do. Too many things right on top of each other: leaving my 3 month old to a caretaker, returning to work after being off for 3 months, not resuming full workout schedule for 4.5 months, MRSA culture first time 9/26, son found to have two mutations of the cf gene (genetic diagnosis but not clinical - atypical?), and vasculitis due to unknown reason.
Time to take a step back I think.
Specifically I am wondering if going half time while I attempt to get my pfts back up with use of oral antibiotics, increased pt, and exercise will have a lasting effect. I realize I'll need to take some of the good habits (darn thought I was already good - I hate cf) from this few week period into full time work lifestyle but have you found this helpful?
My inclination is the 'get back on the horse' and not take a step back from life but I'm thinking it would be a good idea if nothing else to avoid a hospital stay and the big guns - IVs.
My FEV1 dropped from 65% (201L) to 56% (1.75L) from end of Sept. to end of Oct. I'm not dealing with stress the way I usually do. Too many things right on top of each other: leaving my 3 month old to a caretaker, returning to work after being off for 3 months, not resuming full workout schedule for 4.5 months, MRSA culture first time 9/26, son found to have two mutations of the cf gene (genetic diagnosis but not clinical - atypical?), and vasculitis due to unknown reason.
Time to take a step back I think.