Just a note about the toilet for PP patients.
Don’t worry if things stop being as regular as before.
My specialist doctor says that the automatic functions will always work, but I’m here to say: Not without help!
I got very worried when things seemed to be very difficult, with many more minutes spent in there than usual, and a lot of groaning. (My brother found the same thing - he also has MS - and actually gave himself a hernia!)
Now I’m used to the new regime. One has to wait for a bit of a build up, then push quite hard, and sometimes one is rewarded. Don’t be disheartened at first. What was once natural and easy becomes something of an achievement when it happens. But try to relax about it - it WILL happen!