When I go to toilet I rarely manage a lot out. I feel like I am going to wet myself somedays and all you get is 150mls.I did start a fluid chart to get an idea how much I was actually passing.The most was 250mls
I can be up to toilet up to 5 times during the night which makes you tired next day which in turn make my MS play up- if I get that tired I get the shakes and flu like symptoms.During day its obviously easier as can get to a toilet but you do plan ahead and work out where your toilets are!!
I also get problems with fluid retention (is this linked?) but am unsure what to do. Have seen dr who tbh was a much good as the proverbial chocolate watch. Told me it was fluid retention didn’t offer diuretic in fact wasn’t keen when I asked about them and I am unsure if would help or make it worse as in would be running to toilet 10 times with liitle pees rather than the 5 times lol.
I am overweight so agree that that doesn’t help.
Drs just seem to fob you off and understand they may not be able to do anything it the 'oh its fluid retention Bye ’ that irritates
Has anyone else had this and what did they do to sort/manage it?