A Magical Weekend
21 February 2020
Each year Blackpool Magic Convention welcomes a line-up of international, award winning magicians, illusionists and acts who are some of the biggest names in the world of Magic and this year as well Nerve Tumours UK as there chosen charity.
With 5,000+ people attending the convention, our main aim was raising awareness.
![](/images/common/BMC_2020_Convention_Hall_-_1024_x_768.jpg)
One of the people we met was John Baird, who posted on Facebook: “I never knew about this charity, even though I have NF1. It came as a surprise while attending the Convention, and the information given to me was a big help.” This shows how important the task of raising awareness is.
We had amazing support from the Convention organisers and from the magicians themselves.
One magician, Phileas Flash invited us to his balloon workshop as he made a life size model of one of the organisers who is affected by NF1, giving us a platform to directly present the charity on stage.
![](/images/common/BMC_Mike_Brenan-_Stand_with_Balloon.jpg)
We were also honoured by a visit to our stand by Uri Geller.
Our community had special guest tickets for the UK Family Entertainer of the Year Event, which was attended by the Paterson family, who have been phenomenal supporters of Nerve Tumours UK. Also attending were St Vincent's School for Sensory Impairment and Other Needs, so this was another opportunity to recognise the importance of issues surrounding Neurofibromatosis and other genetic conditions.
![](/images/made/images/common/BMC_2020_Kids_on_stage_800_600_s_c1.jpg)
Our main fundraising activity was a raffle for a Golden Ticket for the 2021 Blackpool Magic Convention and we sold a total of 501 Raffle tickets.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/adam-buxton-comedy-night-Page-Preview-800-x-500-px_800_600_s_c1.png)
Adam Buxton Comedy Night in aid of Nerve Tumours UK
Our charity comedy night was certainly nothing short of a success. Find out exactly what went down here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Megan-Crews--meet-meganPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Megan
Megan Crews is a 30 year-old special needs tutor in Salisbury. She recently spoke out in The Sun.
Read More![](https://nervetumours.org.uk/images/made/images/common/Fabio-researchPage-Preview-800-x-500-px_800_600_s_c1.png)
How does your visible difference affect you?
Researchers would love to understand your experience of how a visible difference affects your daily life
Read More![](https://nervetumours.org.uk/images/made/images/common/GABYPage-Preview-800-x-500-px_800_600_s_c1.png)
Gabriella’s Story
"I believe everyone should think the same and be kind to people however they look and whatever condition they have."
Read More![](https://nervetumours.org.uk/images/made/images/common/OMN!!Page-Preview-800-x-500-px_800_600_s_c1.png)
One More Nurse Appeal Press Release
Have a read of our #OneMoreNurse appeal press release here:
Read More![](https://nervetumours.org.uk/images/made/images/common/EDEN_study_image_800_600_s_c1.png)
Recent Research from DR Shruti Garg
Find out more about some of the recent research carried out by DR Shruti Garag
Read More![](https://nervetumours.org.uk/images/made/images/common/Research-UWEPage-Preview-800-x-500-px_800_600_s_c1.png)
Advisory group of parents needed to help shape future research
Maia Thornton is a PhD student looking for an advisory group of parents who's child has an appearance altering condition
Read More![](https://nervetumours.org.uk/images/made/images/common/Olivia-Community-Spirit-Page-Preview-800-x-500-px_800_600_s_c1.png)
Olivia’s Story
Olivia is an enthusiastic and determined young girl. Have a read of her inspiring story here!
Read More![](https://nervetumours.org.uk/images/made/images/common/Lottery-fundingPage-Preview-800-x-500-px_800_600_s_c1.png)
The Big Lottery Fund pays for 2 Patient Info Days
Nerve Tumours UK receives Lottery funding
Read More