For William Eames

For William Eames


Your page address can only contain letters a‑z, numbers 0‑9, hyphens and underscores.

Check address

Your page address must have a minimum of 3 and maximum of 45 characters and can only contain letters a-z, numbers 0-9, hyphens, full stops and underscores

Your chosen address is available

Remember, as soon as you save these changes your existing page address will no longer work.

Sorry, this address is already in use

Please try a different address or choose one from the list of available addresses below.

Total raised so far£0.00

Total plus Gift Aid: £0.00


Raised offline: £0.00


[p]William, our beautiful, caring, funny, articulate little boy was diagnosed with Duchenne Muscular Dystrophy in January 2016 at just 3 years old.[/p][p]Duchenne MD is one of the most common fatal genetic disorders to affect children around the world. 1 in 3500 boys are affected with DMD. It is a devastating, progressive and currently incurable muscle-wasting disease. Duchenne results in progressive loss of strength and is caused by a mutation in the gene that encodes for dystrophin, a protein that plays a key structural role in muscle fibre function. Boys with DMD do not produce dystrophin.[/p][p]Life expectancy is improving as standards of care and knowledge about Duchenne increase however, [b]there is currently no cure for Duchenne.[/b][/p][p]As a family we had never heard about this condition, and we are still learning……we will always be learning, and hoping, for a cure. We want to raise awareness of William and Duchenne – we need a cure, but we also need to ensure a fabulous life for our boy too so we set up Defending William Against Duchenne in January 2018.[/p][p]We have been so grateful to those that have raised money for both William and Duchenne research since his diagnosis in 2016. This is something we will continue to make William’s life unforgettable but also to help fund research for a cure of this horrible condition. [/p][p]Defending William Against Duchenne, DWAD, was set up in 2018 with the hope to raise awareness and funds – we have been overwhelmed with the amazing support of friends near and far. There are some wonderful stories on our [url=]website[/url] of what amazing things have taken place so far. We have raised over £22,000 for charities since diagnosis to go towards research, but we still need more to get a cure. [/p][p]in 2019 we managed, with lots of fundraising and our own SOS from local companies, to totally adapt and renew our house to make it the most wonderful home for us all, with no obstacles for William. He can now enjoy his home like any other regular kid.[/p][p]We want to raise awareness of William and Duchenne – we need a cure, but we also need to ensure a fabulous life for our boy too.…..DWAD will never stop raising funds or awareness. [/p][p][b]So, what’s your forte?[/b] Quiz, raffle, crazy feat, masquerade ball, bake sale, party, fun run, gin tasting evening! Are you in a band, run a shop or part of a sports club – have you thought about bucket collections? Are you part of a sports team that selects local charities for big games? Does your business have a charity of the year? Are you a school that would do a non-uniform day or a charity bake? Would your team like a sponsor?[/p][p]Thank you in advance for all of your help and support.[/p][p]Team William [/p]
For William Eames image 1
For William Eames image 2

Link your personal fundraising challenge

Create or link your personal fundraising challenge to see the total being raised for your loved one.




Sep 18, 2021


Sending you all so much love. Charlotte


plus £5.00 Gift Aid

May 31, 2021


Jan 15, 2021



Dec 27, 2020

Harold and. Jane


Dec 18, 2020

Jill & Al

Hope you have a wonderful Christmas William


plus £6.25 Gift Aid

Dec 14, 2020


Love conquers all- True


plus £12.50 Gift Aid

Dec 7, 2020



Back to Top