I Karaseva

Dream Big for Emily - CAN 2023

Fundraising for FAST UK (Foundation for Angelman Syndrome Therapeutics)
£2,515
raised of £12,000 target
by 23 supporters
Celebrating the birthday of Emily
The 2023 Cure Angelman Now (CAN) Campaign is now open. FAST UK's goal this year is to double what we raised in last year's campaign. We cant do this without your help so why don't you set yourself a target and help us smash our goal for CAN 2023.

Story

Hello there!

We'd like to invite you to be a part of our mission to make a real difference in the life of our almost 3-year-old daughter, Emily. 

Emily lives with Angelman Syndrome, a rare genetic condition that affects her cognitive abilities, gross and fine motor skills, and sleep. 

We're raising funds for FAST UK to support research and the Natural History Study, which will help find a life-changing therapeutic and improve the lives of those affected by this condition.

Last year's FAST Gala theme was "Dream Big," and we believe that with your support, we can help Emily expand her dreams

She's making great strides, too! Emily has been working hard to develop her walking and motor skills, and she's even started eating with a spoon. We couldn't be more proud of her! She loves pushing her bike around, and we're hopeful that she'll be able to ride it soon.

We're also working on helping Emily communicate with us more effectively. It's a long journey as Emily doesn’t have any spoken words, but we're committed to seeing it through. We've been working on her individual support plan for over a year now, and we're hoping she'll get the support she needs at the nursery and through therapy soon.

As a parent of a child with additional needs, I can tell you that we have to fight for every little thing for Emily. The needs of those who can't advocate for themselves are often overlooked by policymakers and budget allocators. That's why every donation, big or small, makes a meaningful difference in the lives of those affected by Angelman Syndrome.

Your donations go directly to the Natural History Study in Oxford, which costs £250k per year to run. We're also doing everything we can to support the community and raise awareness for Angelman Syndrome through FAST UK.

If you'd like to follow Emily's journey, you can check out my Instagram page. I also help run the FAST UK account, so please give us a follow and see what we're up to!

Thank you for your support. Let's dream big for Emily and help advance the research towards a cure.

A kind reminder… If you are a UK taxpayer, please don’t forget to select Gift Aid. Also, it’s worth checking if your employer can match your donation, as this would practically mean doubling your donation in some cases - which is amazing.

About the campaign

The 2023 Cure Angelman Now (CAN) Campaign is now open. FAST UK's goal this year is to double what we raised in last year's campaign. We cant do this without your help so why don't you set yourself a target and help us smash our goal for CAN 2023.

About the charity

The Foundation for Angelman Syndrome Therapeutics UK (FAST UK) is an organisation of families and professionals dedicated to raising awareness and finding a cure for Angelman Syndrome through the funding of an aggressive research agenda. We are also committed to helping individuals with AS.

Donation summary

Total raised
£2,514.15
+ £417.50 Gift Aid
Online donations
£2,514.15
Offline donations
£0.00

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