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

Polly’s Story (as told by Mum Emily)
"Despite being on weekly chemotherapy she is a happy child and never fails to inspire us all"
Read More
EDEN Study Progress Report
The EDEN study has enrolled 30 babies and toddlers to understand how infants with NF1 develop.
Read More
Ella’s story
Have a read of Ella's story here. An uphill battle which we know she will turn around!
Read More
Grace’s Story
Have a read of Grace's story and she overcame her insecurites surrounding her NF
Read More
Helpful Charities
Find some of the other helpful charities that may be able to support you here
Read More
Sophia and Harvey’s story
"Despite all that, Harvie is a happy little boy who enjoys nursery and loves his favourite things"
Read More
Lucy’s Story
"I love him, and I couldn't be without him, regardless of whether he was sick or healthy."
Read More
Jaycee’s Story
Have a read of Jaycee's incredible story and how she has overcome some major difficulties in her life.
Read More