When Pippa Dungey went to her public year, he suffers from numbness in her legs last year, she was told that she faced a waiting list From 10 months for specialized nerve services.
Two months later, the 25 -year -old trainee lawyer from southeast London ended, A & E. Unable to walk.
Mrs. Dungey went for the first time to see her doctor in September last year and she was referred to a neurologist, but she warned against expecting a long date.
She also waited for her symptoms She worsened, and in the end they became so bad that he was unable to raise her right leg and forced to pull it.
Pepa Dingy, 25, left London unable to walk for a week after waiting for months to make the NHS date. (MS community)
I asked for help from A & E. And GP for it, but it was She turned away and told that she would have to wait for her nerves.
But in the end she was forced to return to A & E.Where it was accepted for a week and is unable to walk and was diagnosed later Multiple stiffness (Ms).
There are about 150,000 people who live with multiple sclerosis, a condition that affects the nerves in the brain and spinal love. It can affect people in different ways, including influencing vision, balance, memory and emotions.
“By November, I was really worried. I could not raise my right leg and I only waged it, which is really scary. I felt as if I was stuck to dry and did not know who I went to. Everyone was telling me that they could not do anything. I even tried to go separately, and I was exhausted every dam and did not know what to do.
“After that I had an emergency date with my doctor, and they referred me to A & E again. Thank God, this time the doctor confessed me and I was finally diagnosed with me and I was diagnosed with the end [with MS] But I spent a week in the hospital unable to walk because I couldn’t get a date for neuroscience. “
Dungey was one of the hundreds of thousands of people waiting for neuroscience in NHS – 6175 of them waiting for more than a year.
Charitable, which the MS Association has warned people who live with multiple sclerosis on average five-month to obtain a date for the first neuroscience in 2023-24, an increase of 65 percent in the average waiting time in 2019-20.
The Charitable Society warned that multiple sclerosis patients were letting them awaiting the risk of “irreversible disability” and they said government Neurological conditions have been overlooked so far in its ten -year plan.
Since she came out of A& E, Mrs. Dungey said she is still working to restore her ability to walk.
According to a survey conducted by the MS Association, which includes 600 patients in England, one in seven unplanned acceptance in the hospital, which could have been prevented. Almost one in every five travel warned more than 20 miles for hospital appointments.
“This report draws a realistic photo of hospitalization for people with multiple sclerosis – whose repercussions can be huge,” said Peter Lloyd, MS, Director of Policy at the MS Association.
“Neuroscientists and numerical nerve nurses face tremendous stress, and there is no simply enough of them to keep pace with the increasing demand. This means that people are waiting for a longer period and longer to obtain basic support such as initial diagnosis or planned care – which leads to emergency situations that can be prevented below.
“The 10 -year NHS plan aims to address some of these issues, which is encouraging. But it is worrisome that there is no specific plan for one person in every six people in England who live with a nervous condition. That is why we call for a national neuroscience plan, so that people with multiple sclerosis and other conditions can obtain the care they need without delay.”
The Ministry of Health and Social Welfare was dealt with for comment.
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