Megan’s Story
28 May 2020
My name is Megan. I'm 19 and I was diagnosed with NF1 and mild Scoliosis when I was 11. My NF1 was discovered when I was seeing my paediatrician for something completely different. I'm forever greatful to him for knowing about the condition and recognising it as otherwise, I still may not have known about it to this day.
Since my diagnosis, they've discovered through MRI scans some fibromas in my brain, which are being closely monitored by the amazing neurosurgery team at The Queen Elizabeth hospital. I'm always grateful for everything my doctors have done for me- they've kept me informed, reassured me and made sure that everything was explained to me in regards to treatment options.
Despite my NF1, I am living life to the full and doing the things that I love. I have a scary acting job, I'm studying to be a children's nurse and I'm making the best out of every day. NF1 is a part of who I am, but it doesn't define or control me and I hope that one day we will #EndNF
Filter News

First Specialist Neurofibromatosis (NF) Nurse for Wales
We're delighted to announce the first ever Specialist NF Nurse for Wales, find out more
Read More
2020 A Review
2020 was hard for everyone but our NF community is stronger & more resilient than ever. Read our reflections on 2020
Read More
Geena’s Story
James Harkness talks about his late mother Geena Andrews & what Nerve Tumours UK meant to her.
Read More
Xmas Party Superheroes
Had your Xmas party cancelled? Find out how you can save the day & become instant #XmasPartyHeroes
Read More
Lee’s Santa Dash
Check out Lee's Festive Santa Dash for NF and see how you can get involved
Read More
Thinking Forward to 2021 - A Message from our Charity Director
A message from Karen our Charity Director on looking forward to the year ahead
Read More
Rarefest 2020
RAREfest20: a free virtual, interactive science, technology, advocacy & arts exhibition with a rare twist. Visit exhibition
Read More