A year ago, David Fenton was lying in a hospital bed after his blood pressure reached dangerous levels
29.02.2024 - 06:27 / manchestereveningnews.co.uk
A midwife with more than 40 years of service in the NHS is being forced to pay hundreds of the medication keeping her in work. The medication for her incurable, life-limiting condition is available for free in Wales and Scotland, but not in England.
Annie Taylor-Edwards spent three years struggling to get a multiple sclerosis (MS) diagnosis, a condition that can affect the brain and spinal cord and lead to serious disability. When she was finally told she had the condition she says an NHS consultant recommended a medication to ease her symptoms.
She then found out the drug was not available on the NHS in England and would cost her £200-a-month privately. Annie, 61, said the situation was 'insulting', adding: I have an incurable, life-limiting neurological condition, but if I lived a few miles up the road I wouldn't have to spend hundreds. It's so divisive, so wrong."
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Annie, who lives in Bury, works as a senior midwife at the Royal Bolton Hospital. She has been a midwife for 20 years, having spent the 20 years prior as an NHS nurse. She says she began suffering some of the typical symptoms of MS - including a deterioration in her walking and mobility - around three years ago.
Despite several rounds of hospital tests and having cared for patients with MS herself, Annie did not get her diagnosis until the start of last year. "I was walking like I was drunk," Annie told the Manchester Evening News.
"Even though I have nursed people with MS, it just didn't click. I had a scan on the top of my neck and the consultant said 'I'm really sorry, you've got MS'. The same as a lot of people with MS, I have some really bad days, some alright days. My consultant
A year ago, David Fenton was lying in a hospital bed after his blood pressure reached dangerous levels
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