Foley catheter?
Hi guys. My dad failed his voiding trial and is still retaining 50% of his urine so the plan is to discharge him with a Foley. My mom is a very, very reluctant caregiver (horrible marriage for my whole life) and I doubt his ability to manage the Foley on his own and watch for signs of infection. He has historically been very unhygienic and it's only gotten worse since the PD diagnosis. I highly doubt he will manage it properly on his own and will end up back in the hospital with an infection.
He seems convinced that just "drinking water" and "trying harder" will solve all his problems. Realistically, how difficult is at-home Foley management? How often will he need to go to the urologist for management? What are the biggest things to look out for? Has anyone seen their family member with PD and a Foley regain bladder function or is this just how it's gonna be from now on? Thanks for any at-home tips you can provide.