Ruby Galloway (NF1) is thrown an incredible sleepover!
10 July 2019
Ruby Galloway (NF1) is thrown an incredible sleepover!
At just 4 years old Ruby Galloway has been courageously battling against her NF1.
Recently however she was thrown an incredible sleepover at the hands of Plym TeePee parties run by Claire Shaw and her daughter Nicole.
Ruby received the gift after "nearly half of Plymouth" voted for her to receive the gift, which conveys the respect and love that Ruby's community has for her and brave attitude to dealing with her condition.
Ruby at her sleepover

If you would like to read more about Ruby's sleepover, including Claire and Nicole's reasoning behind their incredibly kind gesture then you can do so by clicking on the link below:
Ruby's family is also set to hold their own Masquerade Ball fundraiser which is set to take place at the New Continental Hotel on October 25th.
– Mum Katie"It has been overwhelming with the many kind hearted people we have met and been in touch with since we planned the charity event that we are holding in October. Us as a family are trying to get as much awareness out there as possible about Neurofibromatosis and have even decide to hold another fundraising event next month where anyone who are are willing to be waxed or have their head shaved will raise money for Nerve Tumours UK"
Everyone at Nerve Tumours UK would like to say thank you to the Galloway family for all their efforts, including putting on what is sure to be a fantastic ball and we would also like to commemorate Ruby for being the incredible young girl that she is!
If you would like to attend the Galloway's ball you can find the link to their event below:
The Galloway Family

Filter News
_370x280_800_600_s_c1.jpg)
Charlotte’s NF1 story
Charlotte and her brother & dad have NF1. She is running the Shine a Light Marathon during May to raise awareness
Read More
Be seen, be counted: #PicsForThe1in6
Be part of the Neurological Alliance's photo collage, representing people with neurological conditions
Read More
Understand the experience of adults living with Neurofibromatosis Type I with Plexiform Neurofibromas (NF1 PN)
Research to understand the reality of the NF1 PN journey from diagnosis to daily life, and the emotional impact that has
Read More
Nerve Tumours UK Art Drop 17 May 2023
White Label Editions & artist Anna van den Hoelden are fundraising by selling unlimited prints of World Strips III on 17 May
Read More
Stand up for Nerve Tumours UK Comedy Fundraiser
Join us on #WorldNFDay for a night of comedy at the Union Chapel, London
Read More
Prof. Meena Upadhyaya, OBE, shares her memories of attending the Coronation
Read more about a special day for Professor Meena Upadhyaya, Trustee & Member of the Nerve Tumours UK MAB
Read More
Teenage Transition Day, Guy’s Hospital NF Centre
Guy's Hospital Neurofibromatosis Centre celebrate the success of their first teenage day since COVID
Read More
India’s NF2 story & Jasmin’s ultramarathon
India describes her NF2 diagnosis & surgery - her older sister Jasmin is fundraising for NTUK with a 50k ultramarathon!
Read More