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Darryn Van der Merwe

Kloe Rae born fighting and living her best life!

Fundraising for Nerve Tumours UK
£738
raised of £2,813 target
by 22 supporters
Donations cannot currently be made to this page
Nerve Tumours UK

Verified by JustGiving

RCN 1078790; SC045051
We provide specialist advice & support to reduce the impact of NF.

Story

Kloe Rae was born fighting but it was only when her cafe au lait spots started to develop before she was a year old that her parents started to make the links. Kloe, although under investigation only saw the complex team when her parents started to notice in March 2018 that she was developing a secondary condition, a progressive and severe scoliosis in the lower thoracic and upper lumbar spine. Plexiform neurofibromas we’re identified in MRI scans that followed leading to her diagnosis and surgery at 4 years old. Together the world class Neuro and Spinal team at Manchester Children’s Hospital worked timelessly to come up with a plan that would allow Kloe to have the surgery she required but one that would also not see her having to go back to theatre every six months. Kloe underwent major spinal surgery for the insertion of Magec spinal rods and was fitted with a spinal jacket post-operatively to ensure the safety of the rods. Her follow-up from hospital requires 3 monthly visits for lengthening in clinic, with subsequent surgery around 2 and 5 years independently. With a final fusion when Kloe’s growth is complete.

Since, Kloe has the developments of a left optic pathway glioma which require close monitoring but the changes in the MR scan of the brain remain stable.

Kloe now age 6 still does not let her NF define her. Although she has a magnitude of obstacles to overcome she is a vibrant and determined little girl who doesn’t have time to be sick. She is happy go-getter with a tenacious fighting spirit, one that inspires us to be more like her everyday. Her diagnosis have given us a sense of urgency to make a positive impact in life where we are not only striving to be our best but thrive! Her family and friends take comfort from her strength and hope that by sharing her story that it may become someone else’s survival guide.

As a family we would like to give back where we can, raising the much needed funds for research into NF. Every little helps make a big difference.

https://www.justgiving.com/fundraising/darryn-van-der-merwe2?fbclid=IwAR2DGjasxR4T-yp76k62qprR5GYi_QO0dfouZDexlcN4Zl8Q4WroHqCFJrY


#Kloeraebornfighting #livingherbestlife #endNF


About the charity

Nerve Tumours UK

Verified by JustGiving

RCN 1078790; SC045051
Nerve Tumours UK provides support and information, as well as campaigns and raises awareness on behalf of over 26,500 people in the UK who have NF, the group name for Neurofibromatosis Type 1 (NF1), NF2-related-Schwannomatosis (NF2) and Schwannomatosis (SWN).

Donation summary

Total raised
£738.00
+ £179.50 Gift Aid
Online donations
£738.00
Offline donations
£0.00

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