London woman 'at breaking point' after being unable to wee for 14 months no matter how much she drinks
www.mylondon.news
A London woman unable to wee for more than a year, no matter how much she drank or felt she needed to go says her life "completely changed" when she was finally diagnosed with a rare condition. Elle Adams, 30, woke up in October 2020, unable to urinate and for 14 months she never did.
She went to A&E at St Thomas' Hospital and after explaining her symptoms, doctors discovered Elle had one litre of urine in her bladder. Women's bladders are usually able to hold up to 500ml and men's are usually able to hold 700ml.
Doctors fitted her with an emergency catheter - a tube that's passed into the bladder to drain urine. After visiting the urology centre a week later, Elle was taught how to self-catheter and was sent home.'
Elle's life completely changed and she was diagnosed with Fowlers disease
And after 14 months unable to wee normally, Elle was finally diagnosed with Fowler's syndrome - an inability to pass water normally - in December 2021. Meaning she would have to urinate using a catheter for the rest of her life.
Elle Adams, a content creator, from Bow in East London, said: "I was extremely healthy. I had no other problems. I woke up one day and I wasn't able to wee. I was very concerned. I was at breaking point - my life had completely changed. I wasn't able to complete a simple task like go to the toilet "
Elle was "worried" when she woke up unable to wee. Concerned, she took herself to St Thomas' Hospital, London, where doctors performed an emergency catheter. After four hours in A&E, doctors gave Elle the option to take the catheter out and try to go to the toilet or go home and return to the hospital in three weeks. After waiting for a few hours Elle managed to see a consultant.
Eight months later, Elle went to a urology centre and was told that she was likely suffering from Fowler's syndrome. She underwent a urodynamics test - a procedure that looks at how well parts of the lower urinary tract work to store and release urine - at Guy's Hospital.
Elle woke up in October 2020, unable to urinate, no matter how much fluid she drank
Elle said: "I was told how I was likely suffering from Fowler's. I was talked through the treatment options which were minimal - we did try medication but it just made no difference. The only option for me was to undergo sacral nerve stimulation which acts as a pacemaker for the bladder."
Sacral nerve stimulation delivers gentle electrical impulses through a probe - a thin wire - that is placed near the sacral nerve. Similar to a pacemaker but instead of stimulating someone's heartbeat it stimulates someone's bowel muscles, so they work normally.
Elle underwent an operation in January 2023 and she said: "It is not life-changing, but it can help. I catheterise a lot less around 50 per cent less. It has made my life easier, after two years of hell it is all I can ask for."
Elle added: "I am doing well, I am on the more well side of Fowler's. I am grateful for the difference, I am feeling better than I was. I couldn't have imagined how I was going on before, it was so draining, and it took up my life it was becoming hard to imagine that would have been the case forever.
"Now I can wee on my own, I have cut down my self-catheterisation a lot. It is still difficult, but it is much better than it was."'
https://www.mylondon.news/news/health/london-woman-at-breaking-point-26529675
www.mylondon.news
She went to A&E at St Thomas' Hospital and after explaining her symptoms, doctors discovered Elle had one litre of urine in her bladder. Women's bladders are usually able to hold up to 500ml and men's are usually able to hold 700ml.
Doctors fitted her with an emergency catheter - a tube that's passed into the bladder to drain urine. After visiting the urology centre a week later, Elle was taught how to self-catheter and was sent home.'
And after 14 months unable to wee normally, Elle was finally diagnosed with Fowler's syndrome - an inability to pass water normally - in December 2021. Meaning she would have to urinate using a catheter for the rest of her life.
Elle Adams, a content creator, from Bow in East London, said: "I was extremely healthy. I had no other problems. I woke up one day and I wasn't able to wee. I was very concerned. I was at breaking point - my life had completely changed. I wasn't able to complete a simple task like go to the toilet "
Elle was "worried" when she woke up unable to wee. Concerned, she took herself to St Thomas' Hospital, London, where doctors performed an emergency catheter. After four hours in A&E, doctors gave Elle the option to take the catheter out and try to go to the toilet or go home and return to the hospital in three weeks. After waiting for a few hours Elle managed to see a consultant.
Eight months later, Elle went to a urology centre and was told that she was likely suffering from Fowler's syndrome. She underwent a urodynamics test - a procedure that looks at how well parts of the lower urinary tract work to store and release urine - at Guy's Hospital.
Elle said: "I was told how I was likely suffering from Fowler's. I was talked through the treatment options which were minimal - we did try medication but it just made no difference. The only option for me was to undergo sacral nerve stimulation which acts as a pacemaker for the bladder."
Sacral nerve stimulation delivers gentle electrical impulses through a probe - a thin wire - that is placed near the sacral nerve. Similar to a pacemaker but instead of stimulating someone's heartbeat it stimulates someone's bowel muscles, so they work normally.
Elle underwent an operation in January 2023 and she said: "It is not life-changing, but it can help. I catheterise a lot less around 50 per cent less. It has made my life easier, after two years of hell it is all I can ask for."
Elle added: "I am doing well, I am on the more well side of Fowler's. I am grateful for the difference, I am feeling better than I was. I couldn't have imagined how I was going on before, it was so draining, and it took up my life it was becoming hard to imagine that would have been the case forever.
"Now I can wee on my own, I have cut down my self-catheterisation a lot. It is still difficult, but it is much better than it was."'
https://www.mylondon.news/news/health/london-woman-at-breaking-point-26529675
