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Matthew Chapman Appeal

£3,810 of £20,000 goal

Raised by 65 people in 1 month
Created June 4, 2019
Matthews condition is called Infantile Neuroaxonal Dystrophy which is a terminal condition as it slowly makes the body weaker and daily functions become so regressed it cannot sustain life. The prognosis is between 5 -10 years old and unfortunately there is no way of knowing how quick the disease will progress. It is extremely rare as there are only around 100 cases worldwide. Matthew has a full time peg feeding tube, he also has an artificial airway to help keep his airway open as it is now partially collapsed. He also has a ventilator at night time as well as oxygen during the day. Much adaptation is needed to the family home in order to make Matthew's quality of life more comfortable and less stressful for however much time is remaining to him. Most recent estimates are put at £24000 to achieve this aim. This campaign is to help with this as much as possible.
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Joseph Verney, a journalist from the Lincolnite sent a request to Jason Manfords Charity Ninjas on our behalf:

https://mobile.twitter.com/Verney21/status/1139183377339342848?s=19
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THIS IS A GLIMPSE OF WHAT THIS YOUNG FAMILY ARE FACING AND WHY WE NEED TO RAISE THE FUNDING!
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£3,810 of £20,000 goal

Raised by 65 people in 1 month
Created June 4, 2019
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CH
£10
Carol Hudson
11 days ago
JL
£10
Jennifer Lloyd
13 days ago
JM
£10
John Murphy
14 days ago
PB
£1,000
Partyman's Magic Makers Bowerman
14 days ago
£20
Anonymous
20 days ago
£100
Anonymous
25 days ago
£25
Anonymous
26 days ago
£50
Philippa Creasey
29 days ago
LH
£20
Laura Holmes
1 month ago
SW
£10
Sarah Woolven
1 month ago
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