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
![](/images/common/masquerade-ballArtboard-1.png)
– 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!
![](/images/common/Masquerade-BallPage-Preview-800-x-500-px.png)
![](/images/common/Masquerade-BallPage-Preview-800-x-500-px-copy.png)
![](/images/common/Masquerade-BallPage-Preview-800-x-500-px-copy-4.png)
![](/images/common/Masquerade-BallPage-Preview-800-x-500-px-copy-2.png)
![](/images/common/Masquerade-BallPage-Preview-800-x-500-px-copy-5.png)
![](/images/made/images/common/SoTTIMG_4846F251019_086_800_600_s_c1.jpg)
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!
![](/images/common/galloway-fam-updated-articlePage-Preview-800-x-500-px.png)
![](/images/common/galloway-fam-updated-articlePage-Preview-800-x-500-px-copy.png)
![](/images/common/galloway-fam-updated-articlePage-Preview-800-x-500-px-copy-2.png)
![](/images/common/galloway-fam-updated-articlePage-Preview-800-x-500-px-copy-3.png)
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Artboard_5_800_600_s_c1.jpg)
Coronavirus and your Mental Health
Mind offers support and advice to help you cope with the impacts of Coronavirus on your mental health and wellbeing.
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen_OneMoreNurse_Mask_Campaign-blackwhite_.37402105_800_600_s_c1.jpg)
2nd Lockdown Announcement
A message from Karen our Charity Director on a 2nd national lockdown - we're here for you
Read More![](https://nervetumours.org.uk/images/made/images/common/Dexter_Parker_370x280_800_600_s_c1.png)
Dexter’s Story
A journey of acceptance with NF1 and understanding that what makes us different from one another is a gift.
Read More![](https://nervetumours.org.uk/images/made/images/common/OneMoreNurse_Mask_Campaign_Website_Header_370x280_800_600_s_c1.png)
#OneMoreNurse
Help support our Campaign, we need your ongoing support now more than ever to continue our vital Specialist NF Network
Read More![](https://nervetumours.org.uk/images/made/images/common/Student_voice_prize_website_header_370x280_800_600_s_c1.png)
#DareToThinkRare
Find out how you can take part in this year's Student Voice Prize 7th annual, international essay competition!
Read More![](https://nervetumours.org.uk/images/made/images/common/global-genes-logo-registered_370x280_800_600_s_c1.png)
RARE Champion of Hope Celebration
Join this years RARE Champion of Hope Awards hosted by Global Genes and be inspired!
Read More![](https://nervetumours.org.uk/images/made/images/common/DSC_0096_London_Marathon_2019_-_Group_photo_preview_website_370x280_800_600_s_c1.png)
A Big “Thanks” for Team Nerve Tumours UK running the London 2020 Marathon!
We want to give a great big thank you to all of you who took part in this year's Virtual London Marathon!
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_video_thumbnail_high_res_370x280_800_600_s_c1.png)
How To Use Lipspeakers – Support For Those Affected By Hearing Loss
Frances Harris at Bridge Lipspeaking shares how lipspeaking can help those with hearing loss or total deafness caused by NF2
Read More![](https://nervetumours.org.uk/images/made/images/common/Oxford_University_(Naomis_photo)_370x280_800_600_s_c1.png)
Living with Neurofibromatosis Type 1: An Anthropological Study
Get involved and share your story to help increase cross-cultural understanding and awareness of NF1
Read More