Thanks for taking the time to visit one of William’s tree of hope #BeMoreWilliam original JustGiving pages!

Thanks to everyone who has donated so far!

The current fundraiser and activities are now on Williams hundreds of miles for hundreds of smiles fundraising page.

https://justgiving.com/fundraising/hom4hos

Again…

Thanks to everyone who has donated so far!

So far donations have gone towards in no particular order:

1) The garden wetpour (6k)

2) A hi lo bath (12k)

3) Therapy (2k)

4) An ot sensory toy from smirthwaites (circa £300)

5) A cup to try to see if it would work for drinking independence (sadly it didn’t work) (£60)

6) The urZone safe travel bed (6k)

7) towards adapting our solar to give us grid independence for his equipment and warmth in a power cut £960

8) swim spa (we paid £20k, fundraised £4k)

9) off road wheelchair (funded by other charities - thank you - Jack O’Donnell foundation and nhs voucher)

10) trike (supported by local masons, and children today)

11) running buggy £600 solely off the page

Please note we say “gone towards” as we have part funded some of this ourselves also, or other charities have also helped - such as Wipe away those tears (4k towards the bath) and the AAron Lewis foundation (3k towards the urZone bed);

Williams BACK STORY brief version:

William has had over 50 -60 ambulances in his short Life for epileptic seizures or for respiratory issues and takes nebulisers and twice daily medications to stay alive. He’s such a brave boy and always bounces back so we started a hash tag due to his bravery!

#BeMoreWilliam;

If the world was more William it would be a better place!

He’s won a highly commended child of courage award at the Pride of Essex 2019 awards;

You can donate on the page or by text:

text:

Bemorewilliam 5 to 70085 to donate £5.

This costs £5 plus a std rate msg. Alternatively, you can opt to give any whole amount up to £20. Thanks!

Williams Facebook blog:

https://www.facebook.com/emsjg/

detailed Back History:

William was born in 2016 and it was quickly apparent he had significant health issues;However at the time there was no reason to believe he was neurologically impaired. We have always been a couple to raise funds for charities, we never had a realisation that we were about to become a family ourselves in significant need (a hard transition to face).

From conception William suffered seizures and respiratory issues. However we did not realise that some of his odd behaviours / movements were seizures until he had a 3.5 hour long tonic clonic convulsive seizure including stopping breathing at 7.5 months old. This was on London marathon day 2017 - an event we watch as both of us (his parents) are runners.

Investigations started and a monthly cycle (or more frequent) began of life threatening seizures, ambulance blue light rides, high dependency stays, hours getting lines in and bloods.

Every time he gets ill, it triggers seizures. He often stops breathing. He has refractory epilepsy (uncontrollable with medicines).

Along the way he picked up a life limiting condition called pseudomonas auregenosa (a super bug if you like), which lives in his lungs and attacks his respiratory system.

On June 2017 on daddy’s first father’s day, William suffered 12 hours of cluster seizures, using up all rescue medicine options and required intubation onto life support to stop the seizures.

During this week in St Mary’s picu, William was diagnosed at 9 months old with a neuro-genetic condition called Angelman syndrome.

This is a chromosome 15 deletion (impairment for other individuals) which leaves him facing a life of therapy to learn to walk, even just sit properly and communicate.;

He has, amongst other things, sleep disorder (imagine new born stage... FOR LIFE), ataxia (movement disorder), apraxia (coordination and motor issues), dysphasia (communication impairment in brain- he is non verbal),;dysphagia (difficulty co-ordinating swallowing), a slow brain wave pattern (encetholopathy), a small head (microcephalic) a flat backed head (brachecephaly), albinism, strabismus (a bilateral squint causing vision and depth issues) and epilepsy, all attributed to Angelman Syndrome.;

William has severe complex life threatening epilepsy (7 known seizure types) that has put him in hospital every couple of weeks and even intensive care on life support. He has as a result brain damage due to the seizures.

He also has laryngomalacia bronchiomalacia, tracheomalacia, sleep apnoea, severe reflux disease, pseudomonas auregenosa (a super bug in his lungs) and low muscle tone everywhere leaving him with breathing and oxygen issues and general issues doing things we take for granted.

He is a brave boy with all he’s been through and always bounces back with a giggle and a smile. Even after a seizure If he can!

He will never lead an independent life and move out and have his own family.

We may never hear him say mummy and daddy or I love you.

William did the ketogenic diet for 2.5 years to try to control his seizures. Without a doubt this saved his life.

He has amongst nhs therapies, numerous private therapies that just don’t exist or aren’t accessible on the nhs.

He goes to/has been to:

Reach for hippotherapy (physio on a horse not just horse riding)

jumpstart centre for occupational sensory integration therapy

Kids therapy works for private physio

All the above cost around £80-100 per hour.

Please help us!

You have no idea how hard it is for us to ask.

Every penny counts!

The legal bit:

As I said above this just giving page is to allow us through a charity tree of hope to raise VITAL funds for Williams needs and improve his motor function, give him the ability to use his digital Voice and improve his quality of life.

Why through a charity? Well it allows us to approach companies that can only donate to registered charities and ask for donations for Williams cause. We can apply for gift aid and even with the small fee the charity take (which are less than direct jg fees), we get more money per pound than doing our own crowdfunding page as we have in the past.

They can also set up payments on our behalf to the therapies saving me vital time and hassle!!! They can also help negotiate vat discounts from companies, something we will need when we do the house modifications.

7.5% of all donations to Tree of Hope in relation to this appeal will be allocated to the general charitable purposes of Tree of Hope to cover core operating costs.;If we raise insufficient funds, or surplus funds, then the funds will be used, if appropriate, to fund support for our child’s needs in accordance with Tree of Hope’s charitable objects.  If in those circumstances we are unable to use all or part of the funds for the benefit of our child in accordance with Tree of Hope’s charitable objects, then any funds that cannot be used will be transferred to be used for the general charitable purposes of Tree of Hope. If you have any questions at all please do not hesitate to call the family support team on ;01892 535525.

Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving - they'll never sell them on or send unwanted emails. Once you donate, they'll send your money directly to the charity. So it's the most efficient way to donate - saving time and cutting costs for the charity.