Founder of a non-profit patient organisation whose MS has robbed her of being able to do the things she feels a mother should do is backing a charity’s call to urge the Government to establish a Neuro Task force.
Mother-of-two Natalie Busari, 36, of London, was at the height of her career in web design in 2015, when she began experiencing horrific eye pains, blindness and muscle weakness throughout her body.
She was referred to neurology just before discovering she was pregnant and was finally diagnosed months later with the neurological condition relapsing-remitting MS in November 2016.
She said: “We had to move quickly and choose highly effective treatment because my MS lesions were spreading.
“I even had to stop breastfeeding my son because the medical treatment would harm him.”
Natalie recently underwent a successful stem cell transplant which essentially means she has a new immune system and, although she must receive all childhood vaccinations again, the transplant has given her body some time to heal.
Unfortunately, stem cell transplants do not work for everyone with MS.
As a founder of a non-profit patient organisation, The Nerve of My Multiple Sclerosis, Natalie is supporting The Neurological Alliance’s campaign to bring about much needed change for people affected by neurological conditions like MS.
She added: “I’ve had to come to terms with using a Zimmer frame and different aids to get me through the day. I rely on family to support me, like helping me to get dressed in the morning and my mum even batch makes my food.
“It has really affected my self-esteem and my confidence. I’m not able to do things that I feel like a mother should do – it just makes me feel bad.”
The Neurological Alliance handed over a 19,000-strong petition to the Department of Health and Social Care on Monday, June 5. It called on the government to back the one in six people affected by neurological conditions in the UK and calls for a UK-wide Neuro Taskforce to spearhead vital improvements in care and support.
The petition was a result of The Neurological Alliance’s 2022 ‘My Neuro Survey’ completed by more than 8,500 people affected by neurological conditions. It exposed significant shortfalls in mental wellbeing support, delays to accessing vital treatment and care and a lack of information and support at diagnosis.
Georgina Carr, Chief Executive of The Neurological Alliance, said: “Despite affecting millions of people and costing billions of pounds, neurological conditions are too often at the back of the queue. More than half of people who shared their experiences had experienced delays to routine specialist appointments in the last year and a majority hadn’t been asked about their mental wellbeing by a healthcare professional in the past three years. The message from people affected by neurological conditions is clear – this must change.”
Together with the petition, the Neurological Alliance exhibited a brand-new artwork in Parliament, which featured pictures from hundreds of people affected by neurological conditions across the country. It is hoped the artwork will help to raise awareness amongst MPs of the realities of living with a neurological condition.
Georgina added: “We must not ignore the fact that one in six people live with a neurological condition and many are not receiving the care and support they need.
“We stand united with over 100 organisations and 19,000 people to take immediate action. We urge governments across the UK to establish a Neuro Taskforce to address these unacceptable gaps in care and support for people with neurological conditions and deliver real change.”
A UK-wide Neuro Taskforce would make a real difference by making sure everyone affected by neurological conditions has access to the right care at the right time and the workforce to support them. It would provide a framework to support greater collaboration and sharing of best practice in the approaches taken to tackle common problems. Fundamentally, and most importantly, it would help to show that governments across the UK are listening to people affected by neurological conditions.
Dr Arani Nitkunan, Consultant Neurologist, said: “My colleagues and I see the devastating impact neurological conditions can have every day. Despite our best efforts to provide the best support for everyone, we are overstretched and overlooked by commissioners. Ensuring neurological conditions are tackled through a Neuro Taskforce would help us go further and mean that people with neurological conditions and services like mine are listened to at the highest forms of Government.”
The Neurological Alliance is a coalition of over 90 organisations working together to improve services for the 1 in 6 people in the UK who live with a neurological condition and their families and loved ones. Its vision is for every person affected by a neurological condition to be able to access the right treatment, care and support at the right time.
It defines a neurological condition as any condition that affects the brain, spinal cord and/or nerves. Because these systems control your mind and body, neurological conditions can affect the way you think and feel and interact with the world.
There are over 600 neurological conditions, including dementia, ataxia, migraine, epilepsy, Tourette syndrome, Parkinson’s, multiple sclerosis, motor neurone disease and cerebral palsy.
If you need support, Neurological Alliance members may be able to help. Visit www.neural.org.uk to find out more.
