Pulmonary Fibrosis News Forums | Bill Rotureau | Activity https://pulmonaryfibrosisnews.com/forums/members/brotureau/activity/ Activity feed for Bill Rotureau. Sat, 18 Apr 2026 02:22:38 -0500 https://buddypress.org/?v=2.20.0 en-US 30 hourly 2 100ce449d4c87ccb8dd410a64467679d Bill Rotureau replied to the discussion Different Types of Fatigue for Patients with PF. in the forum Welcome Lounge https://pulmonaryfibrosisnews.com/forums/forums/topic/different-types-of-fatigue-for-patients-with-pf/#post-19077 Sat, 11 May 2019 17:03:52 -0500 Reply to Different Types of Fatigue for Patients with PF.

3 years in since diagnosis of IPF. Oxygen 24/7 @ 6lpm. Taking Ofev since diagnosis. Age now 74. Fatigue is my new normal. Better some days, don’t want to move on some. Hurt my back and am almost recovered and that stopped my exercise for the last 3 months. When exercising (3+ miles on a recumbent stationary bike, multiple reps with light… Read more

]]> 48fe3cbaf5fbcfe8ed0bb644022368cb Bill Rotureau replied to the discussion Your Most Difficult ADLs as a Patient with Pulmonary Fibrosis. in the forum PF Life: Young Adults https://pulmonaryfibrosisnews.com/forums/forums/topic/your-most-difficult-adls-as-a-patient-with-pulmonary-fibrosis/#post-19040 Thu, 09 May 2019 22:15:36 -0500 Reply to Your Most Difficult ADLs as a Patient with Pulmonary Fibrosis.

Toughest thing for me is taking a shower. Can still do it but only every other day. Standing for prolonged periods like cooking, etc., is also draining. Actually, most daily activities that I used to take for granted before going on oxygen 24/7 are now a chore. But, that is my normal (can’t say new as I have been at this for 3 years now).

]]> 4b2cae65f03c2dbe1f665a7e785edea6 Bill Rotureau became a registered member https://pulmonaryfibrosisnews.com/forums/activity/p/12068/ Thu, 09 May 2019 16:54:20 -0500 1