Beth’s “Novaspers Online Dog Show”
20 January 2020
Novaspers Online Dog Show
A fun online pet show for all pets big and small. The show name is named after Beth's two dogs Nova and Jasper. Most of the money raised will go towards Nerve Tumours UK.
All you have to do is join Beth's Facebook group, and as soon as the show opens you can message Beth with photos of your pets and what classes they would like to enter. If you wish to enter the video class you can send Beth a video of their pet/pets.
The cost of entry will be £2 per photo. The THEME is Bows and Feathers! You can enter as many photos of your pets as you want! The pageant will stay OPEN until March 3rd! Please send photos to Beth via the Facebook group and make all payments via the link below (this can also be found on the Facebook group):
Beth is also looking for a number of people to sponsor her classes. The sponsor for each class will cost £10 and will cover the cost of both trophy and Rosettes for each class.
The prizes for each class will be as follows:
1st place will receive a medal and a Rosette
2-6th will receive a Rosette
7-10th will receive specials.
For more information on the show please visit Beth's Facebook group
We would like to encourage everyone to get involved with Beth's wonderfully unique idea, which we are sure will go a long way to helping support those affected by NF across the UK. 😊






Filter News

Sian & Connor’s story
Sian & Connor describe the invaluable support from NTUK during her pregnancy with baby Reuben
Read More
Anita, aka Fat Lady Slim, is running the London Marathon for NTUK
Anita is fundraising on behalf of niece Sophie & great-niece Lexie who have NF2 by running the London Marathon
Read More
Neurofibromatosis 1 in the 21st Century
Professor Rosalie Ferner delivers key speech “Neurofibromatosis 1 in the 21st Century” to the BPNA 2022 Annual Conference
Read More_370x280_800_600_s_c1.jpg)
The International Rare Disease Showcase 1st – 3rd February 2022
The International Showcase is a unique & important event, with interactive sessions taking place from 1st-3rd February 2022
Read More
Grace’s NF1 story - Nothing stops me
Grace tells us how her NF1 hasn't stopped her from being active and achieving her goals
Read More
Mia’s NF1 story
Bridie & Warren describe their 17 month old daughter Mia's diagnosis with NF1
Read More
Richard & Diana’s 1,000,000 metre new rowing challenge
Diana & Richard have taken on a 1,000,000 metre rowing challenge in 100 days to raise funds & awareness
Read More
A Message from our Charity Director
A message from Karen, our Charity Director, on looking forward to a special 2022
Read More
Childhood Neurological Conditions Survey Part 2
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read More