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!
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
Luke’s Story
Luke had NF1 since childhood. Now an adult, surgery last year has enabled him to play football and do whatever he wants
Read MoreCharlotte’s Story
When Charlotte was 6, she was diagnosed with NF1, along with her brother & dad. Now she is on a mission to raise awareness
Read MoreEden P for healthcare professionals
Healthcare professionals, who provide support to expectant parents with NF1 are invited to take part in the Eden P study
Read MoreNicole’s story
Nicole has NF2, she describes the preparations and the absolute joyful experience of the birth of her son Lewis
Read MoreCAR Research - exploring family planning decisions
Research Advisors required to help explore what influences decisions about having children and what support would be helpful
Read MoreCorporate Fundraising 2024
Find out some of the different ways your company can support Nerve Tumours UK
Read MoreMatthew’s story
Matthew, who has NF2 and is a dedicated Scout, has been awarded the prestigious Cornwell Scout Badge
Read MoreElla’s editorial
Have a read of Ella's editorial as she shares her brave journey against NF1 with us!
Read MoreConnected Recovery - Tackling Loneliness
A report from the All-Party Parliamentary Group (APPG) on Tackling Loneliness and Connected Communities
Read More