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This is our daughter Elsie Katie Novell. Elsie suffers from an extremely rare genetic neuromuscular condition called Spinal Muscular Atrophy type II. This means that Elsie will never be able to walk and her muscles will gradually become weaker, eventually wasting due to lack of use. There is currently no cure or treatment for this condition
Elsie's diagnosis did not come until she was 18 months old; this is due to the complex nature of her condition. As a baby, Elsie met all of the milestones that you would expect her to meet. She sat up, crawled, stood up and began to take her first steps all before her first birthday. Unfortunately, at around 11 months, we noticed that Elsie's movements were regressing and decided to seek medical advice. Seven months later, after a plethora of tests and medical appointments, we received the diagnosis.
SMA is a severe, degenerative disease which will, in time, affect the neck, arm, shoulder, hands and most importantly her ability to eat, swallow and breathe. More information about this condition can be found at www.smasupportuk.org.uk Whilst there are currently no treatments or cures available, there are a number of things that can be done to improve Elsie's care and quality of life, ensuring that she is as mobile as she can be for as long as she can be. All of these things are very expensive, which is why we need your help.
As Elsie is now approaching her third birthday we have some very clear fundraising goals. We have very recently committed to buying Elsie her first full size powered wheelchair. The wheelchair (Snapdragon) is designed and made by Dragon mobility. Elsie fell in love with the snapdragon at a recent trial and we could see how much this would improve Elsie's ability to explore and socialise with her friends at nursery. The Snap dragon is £23,600.
We are currently going through the DFG process to have our home adapted in order to provide Elsie with the best quality of care. This will significantly improve Elsie's accessibility at home which will involve installing a wet room, first floor lift, hoists, special bath and storage for all of her equipment. We are able to access £30,000 through this scheme but have been told that the adaptations will cost double this amount. We are trying to raise £30,000 to make up the difference.
The support we have received so far has far exceeded our expectations and we have been overwhelmed by the continued effort people have made to help us.
So far we have raised over £30,000. Our aim is to raise double this amount by the end of 2017. If you think you can help fundraise in anyway or would simply like to offer your support at events please contact us through thus page.
Thank you to everybody for their continued support.
Chris and Charlotte Novell (Team Elsie)
This is our daughter Elsie Katie Novell. Elsie suffers from an extremely rare genetic neuromuscular condition called Spinal Muscular Atrophy type II. This means that Elsie will never be able to walk and her muscles will gradually become weaker, eventually wasting due to lack of use. There is currently no cure or treatment for this condition
Elsie's diagnosis did not come until she was 18 months old; this is due to the complex nature of her condition. As a baby, Elsie met all of the milestones that you would expect her to meet. She sat up, crawled, stood up and began to take her first steps all before her first birthday. Unfortunately, at around 11 months, we noticed that Elsie's movements were regressing and decided to seek medical advice. Seven months later, after a plethora of tests and medical appointments, we received the diagnosis.
SMA is a severe, degenerative disease which will, in time, affect the neck, arm, shoulder, hands and most importantly her ability to eat, swallow and breathe. More information about this condition can be found at www.smasupportuk.org.uk Whilst there are currently no treatments or cures available, there are a number of things that can be done to improve Elsie's care and quality of life, ensuring that she is as mobile as she can be for as long as she can be. All of these things are very expensive, which is why we need your help.
As Elsie is now approaching her third birthday we have some very clear fundraising goals. We have very recently committed to buying Elsie her first full size powered wheelchair. The wheelchair (Snapdragon) is designed and made by Dragon mobility. Elsie fell in love with the snapdragon at a recent trial and we could see how much this would improve Elsie's ability to explore and socialise with her friends at nursery. The Snap dragon is £23,600.
We are currently going through the DFG process to have our home adapted in order to provide Elsie with the best quality of care. This will significantly improve Elsie's accessibility at home which will involve installing a wet room, first floor lift, hoists, special bath and storage for all of her equipment. We are able to access £30,000 through this scheme but have been told that the adaptations will cost double this amount. We are trying to raise £30,000 to make up the difference.
The support we have received so far has far exceeded our expectations and we have been overwhelmed by the continued effort people have made to help us.
So far we have raised over £30,000. Our aim is to raise double this amount by the end of 2017. If you think you can help fundraise in anyway or would simply like to offer your support at events please contact us through thus page.
Thank you to everybody for their continued support.
Chris and Charlotte Novell (Team Elsie)
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Team Elsie
by Chris Novell
This is our daughter Elsie Katie Novell. Elsie suffers from. . . . .
| £4,521 donated |
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