Hannah's road to recovery
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The O'Donoghue's 2018 London Landmarks Half Marathon fundraising page - Helping Hannah on her journey.
We are hoping to emulate Hannah’s determination and as a family complete the London Landmark Half Marathon to raise funds to support Hannah and her family during her recovery process.
Hannah was born on Valentines Day in 2001 with a rare genetic condition called Apert Syndrome which causes fusion of bones prenatally and prevents normal growth of the skull and face. Over the last 17 years, Hannah's health has been extremely inconsistent and she has had in excess of 40 operations and skin graphs - all of which she has faced without fear.
Her love for life, combined with her determination and will to live, has inspired us to challenge ourselves and raise money on her behalf. We’d really appreciate any financial support you can give and also if you would share this with your friends so we can raise as much as possible. All funds raised go entirely to support Hannah.
We are hoping to emulate Hannah’s determination and as a family complete the London Landmark Half Marathon to raise funds to support Hannah and her family during her recovery process.
Hannah was born on Valentines Day in 2001 with a rare genetic condition called Apert Syndrome which causes fusion of bones prenatally and prevents normal growth of the skull and face. Over the last 17 years, Hannah's health has been extremely inconsistent and she has had in excess of 40 operations and skin graphs - all of which she has faced without fear.
Her love for life, combined with her determination and will to live, has inspired us to challenge ourselves and raise money on her behalf. We’d really appreciate any financial support you can give and also if you would share this with your friends so we can raise as much as possible. All funds raised go entirely to support Hannah.
Organizer
Sophie O'Donoghue
Organizer
