Support Specialists Challenges and Ambitions
27 March 2019
Support Specialists
Caroyln Smith
Carolyn Smyth is the new National Lead Nurse at Nerve Tumours UK. She explains her plans for the role.
I have been a Specialist Advisor since 2000. Unbelievably, I will have been in post for 19 years this November!
I had completed a Genetic Counselling course at Great Ormond Street and I remember applying for my current job and thinking I will have a look through my course work and read up on NF.... there was no mention of it! I looked at the charity website and saw the often quoted NF1 strapline
“Most common, least known genetic condition”. Things have improved since then, but there is still plenty of work to be done, raising awareness and improving the lives of those with this condition.
I am very fortunate to have been working with Mel Murrell for the past year (Mel recently featured in the Nerve Tumours UK Magazine). Just to re-cap, I cover Staffordshire, Shropshire and West Midlands, whilst Mel covers Warwickshire, Worcestershire and Herefordshire.
In April, I am looking forward to starting the National Lead Nurse Role at Nerve Tumours UK.
I will split my time between my work as an NF1 Support Specialist based in the West Midlands Clinical Genetics Department, answering the NTUK helpline, and carrying out my role as Lead Nurse.
As with all our jobs, I will be flexible to cover commitments to NF Clinics, school visits and so forth. It’s an exciting time and there is much work to do!
The challenges in this role are as great as the rewards. I have a special interest in education. I have experienced first-hand what it is like to have a child with a diagnosis of ADHD and Asperger’s. This has given me an insight into the difficulties of negotiating the EHCP (Educational Health Care Plan) and a myriad of other issues associated with Special Needs Education.
Working with families and individuals with NF is a privilege, they continue to inspire me after all these years. If you gave me a magic wand, the first thing I would do is provide clinics and support for adults with NF1 who do not fit into the complex NF1 clinic, but desperately need knowledgeable local NF advice.
– Carolyn"Working with families and individuals with NF is a privilege, they continue to inspire me after all these years"
Rachel Beaufort- Jones
Rachel Beaufort-Jones is the Support Specialist for the North East and Cumbria. She writes about its challenges.
My name is Rachel Beaufort-Jones and I am a Neurofibromatosis Nurse Specialist.
On Tuesday to Friday I work in Newcastle, when I support and advise individuals who have the condition within the geographical area of the North East and Cumbria. On Monday, my role as an adviser extends nationally and internationally when I work for the Nerve Tumours UK helpline. This is an incredibly important role to fulfil, as for many areas of the UK who are not so fortunate to have access to a Specialist Nurse, the helpline provides specialist support which people would be otherwise lacking within their geographical area.
During the five years I have worked with individuals who have Neurofibromatosis Type 1, I have found that the condition is not understood by the wider community and this includes many health professionals. As such, specialist support is imperative, which in turn improves health outcomes and the independence of those who would otherwise be struggling with managing their condition.
I feel very fortunate to have been given this role as I have the pleasure of connecting with so many remarkable individuals!
– Rachel"I feel very fortunate to have been given this role as I have the pleasure of connecting with so many remarkable individuals"
Filter News
Jensen’s NF1 story
Stuart describes Jensen's first days post birth, subsequent diagnosis of NF1 plus his & wife Claire's hopes for his future
Read MoreTSL’s Charity of the Year
Specialist Nurse Tracey Kenyon launches TSL’s corporate funding to introduce NTUK & welcome guest of honour, 2 year old Evie
Read MoreOnline – Accessibility – We have the tools to help!
The NTUK website has accessibility tools to give you easier access to online & digital content
Read MoreMy life with Pheo
This story, written by someone with NF1, describes symptoms leading to a phaeochromocytoma diagnosis
Read MoreResources Survey: Initial Diagnosis 2023
We received many responses to our survey asking what would you have found helpful after your initial diagnosis
Read MoreCommunity Fundraising Call Out
Calling all community fundraisers - we need your help, please!
Read MoreOwen family Awareness Event
The event featured guest speaker Prof. Meena Upadhyaya OBE, Member of our Board of Trustees & Medical Advisory Board
Read MoreRunning for Wilbur
Tim is running the Guildford 10k in October, to show support to his son Wilbur who has NF1
Read MoreAlice’s NF studies
Alice is researching healthcare experiences of individuals with NF1 for her Genetic & Genomic Counselling MSc
Read More