Christian’s Story
12 May 2021
When Christian was born, I noticed something on his head but was told it was just from being born and will go away when the skull hardens. As he got older the lump on the back of his head grew larger. I pushed for a second opinion on his 6-week check-up. We went for Scans, MRI scans, blood tests and eventually got the diagnosis. Up until this time we hadn’t heard of NF1 and found it very overwhelming with everything that comes with or associated with NF1.
When we found out about Christian, me and Christians Dad had to get checked to see if we were carriers of the NF1 gene. The results came back negative which means Christian is the first in the family to have it (well of what we know). Our lives have changed a lot since the Diagnosis with regular hospital appointments and check-ups, yearly MRI’s which has been moved up to twice a year due to the tumour behind his right eye which appeared last year. He is currently having eye tests with a specialist every 3 months, the tumour has grown slightly as if it carries on, he may need Chemo to control the tumour. Which is a lot to take in as a parent.
Christian is a very sociable child and is enjoying nursery and making friends, so socially I do not think it has affected him. His cafe au lait marks are getting bigger as he grows and are on his neck and face along with all over his body. Smaller ones are gathered around his armpits and groin area. As a parent, it does worry us on how this May affect him as he gets older and how he feels about his Café Au Lait marks. The NF doctors and specialists Christian is under are amazing and so helpful, they keep us up to date with any changes and we can’t fault them on the care they provide Christian.
After Christian's diagnosis, I found some groups on social media and found Nerve Tumours UK, which gave us more information about NF. We have done some fundraising for Nerve Tumours UK before and raised a substantial amount. This year we have already beaten our previous efforts and would like to try and raise even more!
We have a long journey ahead of us but to know there are people out there to help and talk to definitely makes it that bit easier.
Filter News

No Laughing Matter
Tom is a former journalist, here he describes his journey from music journalism to comedy, & what his NF2 has to do with it
Read More
Shine A Light on Neurofibromatosis 2020
Find out what we're up to for our Shine A Light campaign this year!
Read More
Statement by Michael Fry our Chair of the Board of Trustees
The impact of the corona virus on the charity sector and Nerve Tumours UK's continued support to those affected by NF
Read More
NF1, Plexiform Neurofibromas Market Research Study
Find out more about an NF1, Plexiform Neurofibromas market research survey
Read More
Statement by Rachel Jones & Rebecca Rennison our Specialist Neurofibromatosis Nurses UK
A statement on coronavirus by Rachel Jones & Rebecca Rennison specialist Neurofibromatosis nurses in the North East & Cumbria
Read More
Statement by Samantha Gaden our Specialist Neurofibromatosis Nurse UK
A statement on coronavirus by Samantha Gaden specialist Neurofibromatosis nurse in the North West
Read More
Statement by Melanie Murrell our Specialist Neurofibromatosis Nurse UK
A statement on coronavirus by Melanie Murrell specialist Neurofibromatosis nurse in the West Midlands
Read More
Statement by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
A Statement on Coronavirus by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
Read More
COVID - 19 News from Children’s Tumour Foundation our partners in the US
Covid - 19 News from Children's Tumour Foundation our partners in the US
Read More