Gillian Donald

Gillian and Margaret's October Fundraiser

Fundraising for Genetic Alliance UK
£1,030
raised of £200 target
by 29 supporters
Donations cannot currently be made to this page
Genetic Alliance UK

Verified by JustGiving

RCN 1114195
We engage, support, research & campaign to improve policy & healthcare outcomes

Story

Thanks for taking the time to visit my JustGiving page.

The above picture is Finlay's happy face the day that he received a special delivery of balloons from his friends at SWAN UK with a note saying how special he is.  

For over two years we have hoped to get a diagnosis for Finlay ... We are sill hoping.   Although, with every test result that comes back negative, that hope fades a little.  Testing is very slow - some tests take over a year.  No diagnosis means no clear prognosis and worst of all - no certainty that you are doing everything you can for your precious child.  

It is estimated around 6,000 children born in the UK every year have a "Syndrome Without A Name" - a genetic condition so rare it is sometimes impossible to diagnose. I am so grateful to have found SWAN UK who provide many families in this situation with support, including me.

Therefore I wish to raise a bit of money as a thank you to them by giving up my biggest treat (a glass .. or two of wine) for a month.   

Mum, Margaret, has agreed to help me by doing the same!

Thank you for supporting us in this, and more importantly for supporting the SWAN family by your donation.

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About the charity

Genetic Alliance UK

Verified by JustGiving

RCN 1114195
We are a national alliance of over 220 charities and patient support groups. Together we advocate and campaign for the 3.5 million people in the UK with a rare, genetic or undiagnosed condition - improving diagnosis, care coordination and treatment options. We run Rare Disease UK and SWAN UK.

Donation summary

Total raised
£1,030.00
+ £221.25 Gift Aid
Online donations
£1,030.00
Offline donations
£0.00

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