A Colourful 5K Challenge
29 April 2021
My 9-year-old daughter, Poppy, has recently been diagnosed with NF1. It has turned our world upside down and has been quite a lot to take in. NTUK has been such a supportive tool for us as a family. The nurses are on hand to offer advice and support.
One of the most daunting things about the diagnosis is that almost every person I have spoken to, including some medical professionals, have not heard of NF1. Speaking to someone and being part of the community group and listening to specialists who are involved in research and who know exactly what NF1 is has been a real support.
I work in a primary school and in Liverpool, we have quite a high number of SEND children across the city. It really struck me that after being in education for almost 20 years that I, or a lot of my colleagues, have not heard of this condition, which is more common than cystic fibrosis for example! Because of this, we have managed to get copies of the 'Friends' book into schools in the North Liverpool Learning Network. My aim is to raise awareness. Awareness to parents, especially of SEND children as NF1 is linked so closely to learning difficulties, awareness to children and awareness to staff. For a long time, I believed that my daughter had lots of birthmarks. I had no idea that cafe au lait marks looked like birthmarks.
Now that we have the diagnosis it explains so much. Our daughter has trouble with balance, fine and gross motor skills, and memory. We now understand why. She is an amazing little girl who is the kindest and caring soul. She puts others before herself and lives her life to the full. She has many friends and she does not let her NF hold her back. She loves to sing, swim, climb and enjoys the many adventures we go on as a family. She amazes me every day and I know she will use her condition to teach others how to embrace their differences and stand tall.
World Neurofibromatosis Awareness Day - 5K Colour Challenge
Poppy really wants to raise awareness and even though she is too young to join us in the colour run obstacle dash, she will be there cheering us on. The teachers in the school are really eager to support charity events and we have 19 participants so far. Together we can raise awareness and offer the support that is needed to our NF community.
The colour run will be on Sunday 16 May at Aintree Racecourse, Liverpool.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/samantha-gaden_370x280_800_600_s_c1.png)
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![](https://nervetumours.org.uk/images/made/images/common/melanie-murrell_3_800_600_s_c1.png)
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![](https://nervetumours.org.uk/images/made/images/common/carolyn-smyth_370x280_800_600_s_c1.png)
Statement by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
A Statement on Coronavirus by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
Read More![](https://nervetumours.org.uk/images/made/images/common/martin-sanchez-Tzoe6VCvQYg-unsplash_370x270_800_600_s_c1.png)
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![](https://nervetumours.org.uk/images/made/images/common/NF_Nurses_370x280_800_600_s_c1.jpg)
Working For The NF Community and Helping to Protect and Save The NHS
Coronavirus is impacting the NHS heavily including our Specialist NF Nurses; help us support them, find out how
Read More![](https://nervetumours.org.uk/images/made/images/common/top-header-rotary-logo-and-name370x280_800_600_s_c1.png)
Leighton Linslade Rotary Club hosts Brains of Leighton Buzzard Quiz
Leighton Linslade Rotary Club hosts Quiz in aid of Neurofibromatosis type 2, find out more here
Read More![](https://nervetumours.org.uk/images/made/images/common/Royal_Society_of_Medicine_-_Medicine_and_Me-370x278px_800_600_s_c1.jpg)
Postponed: Medicine and Me: Living with Nerve Tumours at the Royal Society of Medicine
Postponed: Find out more about the event at the Medicine & Me event at the Royal Society of Medicine here:
Read More![](https://nervetumours.org.uk/images/made/images/common/adolscent-nf1-dayDesktop-1600-x-900-px-copy_800_600_s_c1.png)
NF1 Teenager Support Day!
Bridie Windsor is a Deputy Clinical Nurse Specialist who has organised a support day for teenagers with NF1. Read more here:
Read More