
James Hopkins
|
|
![]() |
In September 1989, Vance and Heather Hopkins decided to start The James Hopkins Trust for special children in memory of their son James, in order to help others like him and their parents. The basic principle of their inspired decision was to enable the children to be cared for at home so that families may experience the tremendous love and bonding that they were able to share with James |
Here is what James Paediatrician had to say:- James had a rare condition called myotubular myopathy, which resulted in his muscles being so weak that even swallowing and coughing was difficult for him. His loving parents, Vance and Heather, became experts at nursing him and this meant that he was able to live as normal a life as possible at home and very little of his life was spent in hospital. All movements were difficult for James but he had great courage and determination. He was very popular with everyone who looked after him and had a very definite personality. He understood as much as other children of his age but his condition prevented him speaking. He seemed to be able to reach out to others with the expression in his eyes and it was a great thrill for everyone when he began to put out his arms to explore the world by touch as well as by vision and sound. He seemed to be getting a little stronger all the time and this made it all the harder for everyone when he developed the severe infection which brought his short life to an end. Dr. Stevens
|
|
A CHILD LOANED "Ill lend you for a little while, a child of mine," He
said, anon |
|
| If you know of anyone that would benefit from James' Trust, then please contact us (Tel: 01452 612216) | |