Hoping to go to Paris with my son in late February this year. I will be about four weeks out from my last chemo treatment which has taken over the last six months of my life. Hoping by then I will have more firm colostomy output and less diarrhea.
Can anyone help give advice about bathroom and toilet availability while out sightseeing, eating etc? I will take all my supplies with me. Any tips from anyone living there? I have done some trips in the US with no problems, but remember in England last year that I sometimes had difficulty finding public restrooms.
We are still working out where to stay, I would rather rent a place for the week so we can do some of our own meals and shop from the markets. I am very susceptible to cold from the chemo and have bad foot neuropathy too, so interested to see if the heating there will be good as February is a pretty wet month anywhere in Europe!
This is my second recurrence with cancer (2008 and 2010) so this trip is one of my Bucket list items...I am SO excited! Thanks in advance for any help at all...!
Can anyone help give advice about bathroom and toilet availability while out sightseeing, eating etc? I will take all my supplies with me. Any tips from anyone living there? I have done some trips in the US with no problems, but remember in England last year that I sometimes had difficulty finding public restrooms.
We are still working out where to stay, I would rather rent a place for the week so we can do some of our own meals and shop from the markets. I am very susceptible to cold from the chemo and have bad foot neuropathy too, so interested to see if the heating there will be good as February is a pretty wet month anywhere in Europe!
This is my second recurrence with cancer (2008 and 2010) so this trip is one of my Bucket list items...I am SO excited! Thanks in advance for any help at all...!


