Teagan Martin’s first day at Canterbury Secondary School
13 September 2019
Teagan Martin's first day at Canterbury Secondary School
Born 15 weeks premature and weighing as much as a box of cereal Teagan was only supposed to have 24 hours to live. Fast forward 11 years later and Teagan's parents are sending her off to her first day of secondary school in Canterbury. It is a truly inspiring story which have left her parents with nothing but pride and admiration for their daughter who despite her struggles with NF continues to defy the odds and uplift those around her on a daily basis
– Teagan's Father Ian"She’s done so well to get this far - she wasn’t meant to be here but she is. We’re well chuffed."
To read the full story then please click on the link below:
Filter News

Hour of Power – Love Yourself Valentine’s Day workout for NF
Thanks to all those that got their hearts pumping this Valentine's Day for our NF community!
Read More
Rare Disease Day 2021 and Rare Reach Festival
Find out how you can get involved in the first ever Rare Reach Festival and make sure the Rare communities voice is heard!
Read More
NF Said
Daisy takes on a 38-mile running challenge for her sister Millie, 1 mile a day for every person diagnosed with NF2 a year
Read More
Love Yourself - Hour of Power in Support of the NF community
Get your sweat on and spread the love this Valentine's day for our NF community!
Read More
Pat’s NF Fundraiser Walk
Read all about Patrick's incredible fundraising efforts to help others affected by NF!
Read More
Laura’s Marathon effort!
Laura beats our 26.5 mile challenge and takes it to the next level - matching miles with donations, find out what she's up to
Read More
Research call: Does neurofibromatosis affect how you feel about your body?
Find out how you can improve self-help methods for people living with neurofibromatosis
Read More
Stitched up by Celia
Get inspired by Celia's creative online haberdashery shop for Nerve Tumours UK!
Read More
NF1 with Plexiform Neurofibromas Study: information for patients and carers
Find out how you can help shape the future of NF1 healthcare
Read More