Julie Ann Evans
13 July 2020
Guidance on Disability Benefits Claims Related to Neurofibromatosis
Julie Ann Evans is a welfare rights consultant, who has been assisting people who have NF to navigate the benefits system. She explains how to approach a Personal Independence Payments (PIP) assessment.
For PIP, you are required to have a medical assessment. The assessor might be a nurse, or a paramedic or a physiotherapist, and when they’re good they’re good, and when they’re bad, they’re shockingly bad. It is very hard for the assessor to understand when the symptoms are hidden. With NF1, when someone walks in, it is not always immediately obvious – they may have tumours under the skin, or on the spine. And people can be inclined to put on a brave front when they are asked about pain, and say ‘oh, I’m fine’.
It can be difficult to get across the struggles you’re going through. If you have some good days and some bad days, this can be challenging for the assessor
to understand.
The PIP form is about 50 ages long. When you make a claim, you need to provide as much information as you possibly can. You need to gather supporting medical evidence – from doctors, nurses, Nerve Tumours UK – so the assessor has some information. If you suffer from weakness and fatigue, you need to get that over on the form and in the assessment. If you have good days and bad days, a good day might be one without severe pain, but not pain-free. There can be a tendency to under-estimate problems, and also to find work-arounds – but they still count. One way to overcome this tendency can be to keep a daily diary for a week. The process can make you miserable, but it is important.
You need to prepare yourself for the assessment. There are useful guides provided by Turn2Us (turn2us.org.uk), the national charity for welfare rights, and by the Citizens Advice Bureau (citizensadvice.org.uk) – search for “PIP”. Make sure you are receiving all your benefits. As well as PIP, you may also qualify for a severe disability premium. You may also be entitled to Jobseekers Allowance, Council Tax reduction, Universal Credit and Housing Benefit among others.
Filter News
Nimo’s NF1 Story
Read Nimo's incredible journey of coming to terms living with NF1 & how Nerve Tumours UK has changed her life for the better
Read MoreGeorgia’s Schwannoma Story
Read Georgia's inspirational Schwannoma story and how she had to fight for her diagnosis
Read MoreVoices of Visible Difference #YoureNotAlone Men’s Campaign
Two-thirds of men with visible difference are affected in their day to day life. Read more
Read MoreChildhood Neurological Conditions Survey
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read MoreWe’re Here for You, Our NF Community.
A big thank you from Karen our Charity Director - your support has been amazing!
Read MoreGlobal Genes LIVE!
Join Global Genes September 15-25, 2020 at Global Genes LIVE! A RARE Patient Advocacy (un)Summit.
Read MoreShine A Light on Neurofibromatosis now streaming on The Disorder Channel
Find out how we are bringing NF Awareness to people's homes
Read MoreBest Film Nomination “Shine A Light on Neurofibromatosis” PM Society Digital Awards
Join the awards ceremony virtually this Wednesday 16th September
Read More