Pauline & Helen Boughen’s PIP Journey
09 June 2020
Navigating the Benefits System
Julie Ann Evans has guided a number of people from the nerve tumours community. One is Helen, who is 33, and was diagnosed with NF1 when she was 15. Her mother, Pauline, describes their recent tortuous PIP journey.
Helen has struggled for an awfully long time with her NF1, has had multiple surgeries and also has Asperger’s.
She was told she had to apply for PIP if she wanted to continue getting the benefit. We struggled through the form. It’s extremely black and white – there’s no flexibility or leeway. About 8 weeks later, the assessor came. Helen has a lot of scarring in her mouth, which can make her hard to understand, and the assessor herself apologised for having difficulty understanding her. But then when the assessment came back, it scored 0 for communication – in other words, that Helen had no difficulties with speech.
Helen explained that she liked to cook, but that she found it difficult. She was asked if she could walk 200 metres. Helen said she was OK on the flat, but it was difficult to walk uphill to town. After all the form-filling, and the assessment, we got back the results of the assessment: 0 points. That means she was not entitled to any PIP at all. This was devastating and ridiculous: Helen has immense daily challenges and obstacles – and though she is fiercely determined and overcomes them as best she can – the difficulties are real.
Nerve Tumours UK put us in touch with Julie Ann Evans, who helped us with the appeal, but after 2 months, we still hadn’t heard anything. It was then I asked our local MP, Jesse Norman, to get involved, and also got the Hereford Times interested in the story. As if by magic, our appeal was successful and Helen was re-assessed at 12 points, which made her eligible for enhanced payments. Her PIP was also backdated.
– Hereford Times"“Anxiety raised in May when Helen was told she would be reassessed – an assessment in September that sounds shambolic, an utterly perverse decision to strip her of all disability payments straight away, a reconsideration that took months to complete and ended with a giant U-turn.”"
Helen was lucky that she had me to help her through this, and we were both lucky to have Julie Ann to guide us, and our MP and local paper’s support. But what sort of system is it that puts vulnerable people through this?
If you have NF and are struggling with a PIP assessment and are looking for some benefits guidance click the link below to read Julie Ann Evans article
Filter News
VTCT Foundation Showcase
Find out about this event which showcases projects and research supported by the VTCT Foundation
Read MoreCrazy Nanna Hazel & Evie
4 year old Evie's NF1 diagnosis impacted the whole family. Hazel shares Evie's story from a grandmother's perspective
Read More2024 Friedrich von Recklinghausen Award
Professor Rosalie Ferner, Trustee and Member of the Nerve Tumours UK Medical Advisory Board receives this year's award
Read MoreBecome a Trustee
Nerve Tumours UK are looking for at least two new trustees to join the Board. Find out more
Read MoreGuy’s Hospital NF Centre Coffee Meetings
Guy's Hospital Neurofibromatosis Centre Coffee Club 2024
Read MoreLiz’s NF1 story: This is the real me
Liz describes growing up with NF1, difficulties at school, spinal surgery and raising awareness by writing a poem about NF.
Read MoreStronger Together Rare Conference
Read this review of the conference and find out where to access further support
Read MoreGisela’s NF2 story
Gisela has NF2 & has a positive outlook on life, she has just completed a 265km walk during World NF Awareness Month
Read More