I am caregiver for my husband who has pulmonary fibrosis and COPD. It escalated only 6 weeks ago….he was doing projects and playing golf without oxygen and today his body needs 5-6 liter flow. I have been caregiver for family and friends but this is the first time for this Godly sweet man. Heartbreaking. I have slowed my life down to be with him and consider it my privilege. I know I need to take care of myself and have tried to keep up with swim classes. I think an important thing for both of us is giving him space and encouragement to talk about how this feels. I know he wants to protect me but we can’t pretend. Better we cry it out together and keep going. We are trying to get out once a day for a drive or a meal but are fine having time together at home. This is a hard time of life.