The Galloway Family and their “amazing” four year old Ruby
05 November 2019
The Galloway Family and their "amazing" four year old Ruby
Young Ruby Galloway is an extremely brave and courageous girl who has NF1. At 4 years old she has already undergone a year and half worth of chemotherapy but still manages to "just get on with it" and in doing so is an inspiration to both her Mum Katie and Dad Tom.
– Mum Katie"She's such a little character, always full of mischief."
– Dad Tom"Everyone loves her - it's not because of what she’s got, it's her personality."
The family hosted their own Masquerade Ball which took place at the New Continental Hotel on October 25th, in support of their amazing daughter Ruby. The event itself was enjoyed thoroughly by the many in attendance.
Everyone was dressed up in their smartest attire for a night full of dancing, eating, drinking and even a fantastic raffle. Our own NF Specialist Advisor Helen Tomkins was even in attendance!
Helen Tomkins, one of our Specialist Neurofibromatosis Nurses, represented the charity at the event. Helen who is based at Derriford Hospital in Plymouth supports those diagnosed with both NF1 and NF2 in the counties of Devon and Cornwall
– Helen"What a wonderful evening, A well organised, well attended and successful event. A big thank you to Ruby’s parents for organising, you truly did an amazing job. The Ball was a great fun – an entertaining evening and on top of that you raised crucial funds for Nerve Tumours UK. A BIG Thank you "
We at Nerve Tumours UK would like to thank the Galloway family for not just their wonderful Masquerade Ball but all their continued efforts in supporting the chariy and work in helping to spread awareness for Neurofibromatosis!
Credit Images: SmileOnTheTiles.co.uk
The family also recently held a "bare it bold" event in which people turned up at the Ker street social club in Plymouth to have their heads shaved or legs waxed in honour of their incredible Ruby, who will be losing her hair due to her treatment.
On top of everything the Galloway's last year even undertook a sponsored 5k inflatable run fun, again portraying the fantastic work they do to help support our charity!
Filter News
First Diagnosis Survey
A survey to improve NF diagnosis support by gathering feedback on early experiences and concerns from those affected.
Read More_800_600_s_c1.jpg)
Working with the hospitality industry & creating safe spaces for everyone
Read More
Visible Differences: Changing The Narrative
Nerve Tumours UK joins multi-organisational workshop to enhance support for those with a visible difference
Read More
Repurposing anti-retroviral drugs to treat NF2 related tumours Retreat Study
Join a brand new study treating tumours in NF2 patients.
Read More_800_600_s_c1.png)
Nerve Tumours UK joins the Neurological Alliance of Scotland
Nerve Tumours UK joins the Neurological Alliance of Scotland.
Read More_800_600_s_c1.png)
Brain scans to give crucial insight into childhood genetic disease
New funding secured for exciting new global research initiative.
Read More
Looking Back, Moving Forward: A Message from Our Charity Director
Read More
Oliver’s Blog
Oliver Bromley shares some personal experiences of visible difference, and how education and kindness can reduce stigma.
Read More
Ellen’s Story
Read Ellen's story, how she recovered from 'radical surgery' and why she's raising funds for NTUK.
Read More