Guest guest Posted September 29, 2009 Report Share Posted September 29, 2009 Gee , Thanks for taking the time to send this information. It's good to know if the meds don't work there's another option. PJ in OH, 54, IPF'09, Sjogren's'95 Hi PJ Yea I like the nap thing also----I have never taken a nap, but have always heard about the wonderful feeling of the proverbal "Power Nap"---since this disease thing---I have taken a few power naps and it does do wonders for me. I have a tendency to try to stay up and active and keep on the move---but boy it sure feels good to just veggggg out and do nothing. Hope you are doing O.K.? I do read all the posts but by the time I am done reading I am to tired to respond--- so just bare with me--- I love all the info and attitudes and totally understand about how little all the Pulmodudes know about this disease. I am very lucky with my Doc---his office even calls randomly to see how I am doing. My wife (she is a RN), is always reading about PF and every time she sees something new, she prints it off and gives the Doc a copy and they talk about it during the visit--he even tells us how little the "experts" know and he appreciates the new info. I quit making "to do" lists--that way I don't have to do anything and I am not disappointed at the end of the day. My dog Dakota (yellow Lab) gets up of the floor and just stares at me when he thinks it is time for me "to do" something--like take him to the park and play----so thats what we do. G. Quote Link to comment Share on other sites More sharing options...
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