Weighing six stone and on the brink of organ failure, Charlotte Chapman-Hart is admitted to hospital in excruciating pain.<\/p>\n
It’s assumed the former model and dancer has an eating disorder.<\/p>\n
But Charlotte, who repeatedly denies she’s starving herself, has a rare disease.<\/p>\n
She’s been prescribed a new pain relief medication, which should have been monitored by her GP and wasn’t. A side effect is rapid weight loss – but it’s been overlooked by those treating her.<\/p>\n
Charlotte’s experience over the next three months would leave her adding post-traumatic stress disorder (PTSD) to the list of her symptoms. She now fears the care that she needs to stay alive.<\/p>\n
\u00ab\u00a0I think the hardest thing I’ve ever had to face is trying to convince people that I am of sound mind, and that what I’m telling you is the absolute truth,\u00a0\u00bb says Charlotte, sitting in the garden of her home in Cuckney in Nottinghamshire.<\/p>\n
\u00ab\u00a0I told them that I’ve never had an issue with eating. I’m just not hungry. Things don’t taste the same.<\/p>\n
\u00ab\u00a0But rather than think differently, I was put into a diagnosis box that was wrong.\u00a0\u00bb<\/p>\n
Charlotte, who is now 32, has always lived in the same rented house with her mum and dad, who she relies on to look after her.<\/p>\n
Since a young age, she’s loved dancing, starting classes when she was two.<\/p>\n
Charlotte performed with the English Youth Ballet three times, between the age of eight and 16 after successfully auditioning.<\/p>\n
\u00ab\u00a0Dancing was my life, I was always known as Charlotte the dancer,\u00a0\u00bb she says.<\/p>\n
When she was 13, she started experiencing chronic head and back pain. She said doctors blamed her training schedule and hormones.<\/p>\n
\u00ab\u00a0My mum took me to all these appointments explaining, ‘Charlotte will only complain if she’s really, really in pain’,\u00a0\u00bb she says.<\/p>\n
\u00ab\u00a0But none of that was enough for people to do some diagnostic investigation.\u00a0\u00bb<\/p>\n
She continued dancing despite the pain, taking dance as one of her GCSEs at school and training with the Northern Ballet.<\/p>\n
\u00ab\u00a0Any time that I was in pain it was like, ‘it’s because you dance, it’s because of what you put your body through’,\u00a0\u00bb she says.<\/p>\n
By the time Charlotte graduated from university with a health and human sciences degree, she remembers being in physical agony almost constantly.<\/p>\n
\u00ab\u00a0It felt like an axe down the middle of my head,\u00a0\u00bb she says.<\/p>\n
\u00ab\u00a0Sneezing and coughing created a huge amount of pain, I felt like my head was going to explode.\u00a0\u00bb<\/p>\n
At the age of 21, in 2014, Charlotte was diagnosed with chiari malformation type 1 – a condition in which part of the brain pushes down into the spinal canal – and syringomyelia, a rare neurological disorder.<\/p>\n
She remembers the shock of hearing the results.<\/p>\n
\u00ab\u00a0He [the doctor] turned the monitor round and showed us the scans,\u00a0\u00bb says Charlotte.<\/p>\n
\u00ab\u00a0It was like, ‘this is what you’ve got, this is how you spell it, this is what we’ve got to do’, and having just graduated, it was just like, ‘right, park that for a moment, we’re going to cut your head open’.\u00a0\u00bb<\/p>\n
According to the NHS, there are four types of chiari malformation, with type 1 the most common.<\/p>\n
It is thought to affect one in 1,000 births, and can cause painful headaches, movement problems, dizziness and muscle weakness.<\/p>\n
She also developed syringomyelia, which affects roughly eight in 100,000 people, in which cysts form on the spinal column.<\/p>\n
Syringomyelia is one of an estimated 7,000 rare diseases under the UK Rare Diseases Framework.<\/p>\n
Charlotte’s dreams of dancing were put on hold while she had emergency brain surgery.<\/p>\n
She added: \u00ab\u00a0I was really scared about the nature of it and I did genuinely have a fear of, am I going to survive this?\u00a0\u00bb<\/p>\n
Although no-one could have predicted what was to happen, she says there was no time to acknowledge that this was a significant moment in her life.<\/p>\n
\u00ab\u00a0Just to have a human kind of conversation with somebody would’ve been invaluable,\u00a0\u00bb she says. \u00ab\u00a0Because it does impact your sense of identity and nobody ever talks to you about that.\u00a0\u00bb<\/p>\n
Surgery in 2015 to remove the base of her skull was successful. It alleviated the pressure and unblocked the cerebral spinal fluid so it could flow from the brain to her spine.<\/p>\n
After recovering from surgery, Charlotte briefly returned to teaching dance, but had to stop completely due to worsening head and neck pain because of the surgery.<\/p>\n
In November 2018, Charlotte unexpectedly started losing weight. By January, she’d lost a third of her body weight and was admitted to hospital with organ failure.<\/p>\n
She didn’t know the new drug she’d been prescribed – which is used to treat epilepsy and migraine – could cause rapid weight loss, nor that it should have been monitored by her GP.<\/p>\n
But when she was admitted to hospital in early 2019, doctors misdiagnosed her with an eating disorder.<\/p>\n
During her three-month hospital stay, Charlotte says she experienced \u00ab\u00a0domineering\u00a0\u00bb and \u00ab\u00a0dehumanising\u00a0\u00bb care.<\/p>\n
On one occasion, she says she was threatened with being sectioned if she didn’t admit to having an eating disorder. The whole experience, she says, caused her severe anxiety and PTSD.<\/p>\n
\u00ab\u00a0I felt like I was alone and had a lot of people and things to fear,\u00a0\u00bb she says. \u00ab\u00a0All of which were beyond my control to effect. I just felt very vulnerable.\u00a0\u00bb<\/p>\n
After a brief recovery, a year later – in 2020 – Charlotte discovered that, when she got a Covid-19 jab – her prescribed pain medication had caused her severe weight loss.<\/p>\n
A consultant later confirmed that she should have been closely monitored by her GP.<\/p>\n
\u00ab\u00a0That could have really, really made a difference to my quality of life, acknowledgement of that earlier on,\u00a0\u00bb she says.<\/p>\n
Then, in 2023, Charlotte suffered a sudden respiratory arrest and had to be resuscitated by neighbours.<\/p>\n
She was never told what may or may not have caused it, but she believes things can change if patients like her are listened to.<\/p>\n
\u00ab\u00a0There’s been a lack of accountability,\u00a0\u00bb she says. \u00ab\u00a0I don’t want somebody to hold up their hands so that I can apportion blame.<\/p>\n
\u00ab\u00a0It’s so that we can learn. There’s no funding for research, but we are research. Our lived experience is research – capture it.\u00a0\u00bb<\/p>\n
This year, Charlotte became an ambassador for the charity Medics4RareDiseases, and is helping to raise awareness among health professionals.<\/p>\n
It’s one of four priorities set out in the government’s Rare Diseases Action Plan, which aims to focus on faster diagnoses and better co-ordination of care.<\/p>\n
\u00ab\u00a0To contribute to something that could have the potential to really transform care is an incredible honour,\u00a0\u00bb she says.<\/p>\n
\u00ab\u00a0It really makes all of the challenges, all the pain, absolutely worthwhile.\u00a0\u00bb<\/p>\n
It’s real-life experiences like Charlotte’s that is being captured by Dr Lucy McKay, CEO of the charity.<\/p>\n
\u00ab\u00a0What people are asking for over and over again is to be listened to, is to be believed, is to be involved in their healthcare,\u00a0\u00bb says Dr McKay.<\/p>\n
\u00ab\u00a0If technology, fast diagnosis and treatment alone were going to improve the lives of people with rare conditions, then we would already be fine.\u00a0\u00bb<\/p>\n
According to Medics4RareDisease, more than 3.5 million people in the UK live with rare conditions and often face the burden of constantly explaining themselves.<\/p>\n
She adds Charlotte’s experiences are all too common, and can prove fatal.<\/p>\n
Charlotte now uses her role, as an assistant project manager for the North West Anglia NHS Foundation Trust – which she does from home – to share her experiences with clinicians.<\/p>\n
This saw her recognised by the trust on 3 July as \u00ab\u00a0individual of the year\u00a0\u00bb, during an awards ceremony.<\/p>\n
Despite Charlotte’s unpredictably debilitating symptoms, her ambition is to drive change.<\/p>\n
She adds: \u00ab\u00a0If I go to bed at night, knowing I couldn’t have done any more, then even if I don’t wake up the morning after, I’m content.\u00a0\u00bb<\/p>\n
The government says \u00ab\u00a0it is clear that Ms Chapman-Hart’s care fell far below acceptable standards\u00a0\u00bb.<\/p>\n
\u00ab\u00a0Our Rare Diseases Framework aims to improve awareness of rare diseases among health professionals and help patients get a faster diagnosis,\u00a0\u00bb a Department of Health and Social Care spokesperson says.<\/p>\n
\u00ab\u00a0Our 10-year health plan will give more power and control to the patient.\u00a0\u00bb<\/p>\n
Follow BBC Nottingham on Facebook, on X, or on Instagram. Send your story ideas to eastmidsnews@bbc.co.uk or via WhatsApp on 0808 100 2210.<\/p>\n","protected":false},"excerpt":{"rendered":"
Weighing six stone and on the brink of organ failure, Charlotte Chapman-Hart is admitted to hospital in excruciating pain. It’s assumed the former model and dancer has an eating disorder. But Charlotte, who repeatedly denies she’s starving herself, has a rare disease. She’s been prescribed a new pain relief medication, which should have been monitored […]<\/p>\n","protected":false},"author":0,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":{"0":"post-9096","1":"post","2":"type-post","3":"status-publish","4":"format-standard","6":"category-uncategorized"},"_links":{"self":[{"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/posts\/9096","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/types\/post"}],"replies":[{"embeddable":true,"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/comments?post=9096"}],"version-history":[{"count":0,"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/posts\/9096\/revisions"}],"wp:attachment":[{"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/media?parent=9096"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/categories?post=9096"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/placedesnations.org\/index.php\/wp-json\/wp\/v2\/tags?post=9096"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}