One year after her first relapse, Sarah started experiencing bladder issues. She would go to the toilet, but she felt as if her bladder never really emptied. When she wasn’t on the toilet, she would suddenly urinate, without ever having felt the urge to go.
“I would hide from the world because my bladder was unpredictable.”
At first, she tried to manage the situation using pads, but they couldn’t handle the volume of urine that would come out. At no point did Sarah connect her bladder issues with her MS. Only when attending an MS workshop for children with her daughter, Charlotte, was the connection between her bladder issues and MS apparent.
“They had set up little stations that explained how MS affects the body. We got to one station that had a sports bottle filled with water. The nurse at the station said it represented the bladder, and she squeezed it. Water came out uncontrollably. Then she let go, and it stopped. But there was still water in the bottle, or bladder. At that moment, I thought, “That’s what’s happening to me.” And I realised my MS is linked with my bladder issues. That was four years after my diagnosis.”