Pulmonary Fibrosis News Forums | Warren | Activity https://pulmonaryfibrosisnews.com/forums/members/wschultz2019/activity/ Activity feed for Warren. Tue, 28 Apr 2026 14:08:11 -0500 https://buddypress.org/?v=2.20.0 en-US 30 hourly 2 bd41ae256140c82a6e98fd77a64efec7 Warren posted an update: I am now in my final stage. I can not generate a […] https://pulmonaryfibrosisnews.com/forums/activity/p/16805/ Tue, 24 Dec 2019 15:55:40 -0600 I am now in my final stage. I can not generate a second breath to even blow clear my nose nor provide push for bowl movements.

]]> 1 d1af5873cee8f418110d4ba2aeaa5c1d Warren posted an update: This is so very true in my case. The higher CO2 […] https://pulmonaryfibrosisnews.com/forums/activity/p/16804/ Tue, 24 Dec 2019 15:52:23 -0600 This is so very true in my case. The higher CO2 production the longer time to recover and increased breathing difficulty. I try to eat fresh fruit and high protein such as eggs and fish and chicken. If i eat a cookie and some ice cream i may not recover for 3 or more hours.

]]> 1 4fa86e4f3884055e65b6357262744708 Warren replied to the discussion The Frequency of Changing Your Nasal Cannula in the forum PF Life: 50+ https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20478 Wed, 24 Jul 2019 03:44:28 -0500 Reply to The Frequency of Changing Your Nasal Cannula

Great question.  I am on high volume (4 to 7 L/min) oxygen 24/7.  I change my cannula at 4 weeks.  I would prefer to change my cannula every 1 to 2 weeks but don’t because it takes so much time an oxygen to purge the cannula of residual ethylene oxide and ethylene chlorohydrin that burn my nose for days and that would otherwise end up in my… Read more

]]> f69f7f39ec701f520737e4a8d97e9c61 Warren replied to the discussion Anxiety and IPF in the forum PF Life: 50+ https://pulmonaryfibrosisnews.com/forums/forums/topic/anxiety-and-ipf/#post-18082 Tue, 02 Apr 2019 15:31:17 -0500 Reply to Anxiety and IPF

Yes and yes.

Different story in that unlike you and over a period of 8 months, I have not been able to return to work or a “normal “ life. I remain on continuous oxygen at 4 to 8 lpm. I have survived, however, the perfect storm of a triple assault of Zoster, pneumonia and upper respiratory virus.

Anxiety remains a constant and breath taking… Read more

]]> ae852e0ae15759ac908089950139bf77 Warren posted a new activity comment https://pulmonaryfibrosisnews.com/forums/activity/p/8340/#acomment-8352 Fri, 01 Feb 2019 21:34:20 -0600 My pleasure. I will be contributing in the near future. I have been an IPF patient for 10 years and still fighting. Will share information based upon my experience.

In reply to - Warren became a registered member ]]> d18fee9f45f643953a5590725dcc0423 Warren joined the group Research and Development https://pulmonaryfibrosisnews.com/forums/activity/p/8351/ Fri, 01 Feb 2019 21:30:59 -0600 0 640d5bc0ccc76b4c81ecc196c8fb59bb Warren became a registered member https://pulmonaryfibrosisnews.com/forums/activity/p/8340/ Fri, 01 Feb 2019 16:30:01 -0600 2