Hi all
I’m new. My neurologist said last week that the MRI had shown demylination and that I had probable MS. I am now awaiting appointments.
In the meantime, I have been going to the toilet more, and more and more. To the point that I am now going probably 6-8 times a day. I understood that MS tends to cause more constipation.
I wondered if anyone else has had similar experiences (at any point but especially at the start) and any advice on dealing with it whilst I wait to see the MS specialist?