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Patricia Mulpeter's Fundraising Page

Patricia Mulpeter's Fundraising Page

Fundraising For Angelman Syndrome Ireland
Latest Update !!

I'm running the Dublin City Marathon for Angelman Syndrome Ireland. Hoping to raise funds for this worthy cause which is close to my heart!

Angelman Syndrome Ireland

Every day 18 people are born worldwide with Angelman Syndrome. Between the Republic and Northern Ire...

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My grandniece Sophie was diagnosed with AS. Sophie is now 4 years old, she is a beautiful little girl full of love & happiness, you should see her smile. She is non verbal & cannot walk yet......but I believe she will walk in the near future. Please support this very worthy cause, there is still so little known about Angelman Syndrome, please help me to make a difference......Trish x

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Supporters

18
02-11-2016

Dawn Dempsey

Well done Trish x

20.00
01-11-2016

Donna Jamieson

Well Done Trish x

20.00
30-10-2016

Anne O'Brien

Best of luck Trish great cause Hooe you make a fortune 😉

10.00
30-10-2016

claire Noons

Best of luck this morning xx

20.00
29-10-2016

Valerie O'Kelly

Best of luck Trisha on your run tomorrow.

20.00
15-10-2016

Anita Meenehan

Very best of luck trish X

10.00
14-10-2016

Jamie farrell

20.00
13-10-2016

Paul Guilfoyle

Good luck Trish. Fair play to ya

20.00
13-10-2016

Triona gleeson

10.00
13-10-2016

Anthony kelly

50.00

About the Cause

Angelman Syndrome Ireland
Every day 18 people are born worldwide with Angelman Syndrome. Between the Republic and Northern Ireland there are about 350 people living with this condition.Angelman Syndrome is a genetic disorder and babies are born with a severe learning disability.People with Angelman Syndrome may speak only a few words & most do not speak at all, many have mobility problems or cannot walk, most suffer debilitating seizures and all require 24/7 care throughout their lives. People with Angelman Syndrome ...