James Durrant
James's Jump for Tofs
Fundraising for TOFS
Story
Thanks for taking the time to visit my JustGiving page.
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On the 30th September 2017. I will be doing a Tandem Parachute Jump to raise money for a Tofs . A charity that is so close to my heart. As you all know Cadence my granddaughter was born 24th October 2016. She was born with Oesophageal Atresia unable to swallow and Tetralogy of Fallot. The lovely Doctors and nurses at the Rvi hospital in Newcastle put us in touch with support group called Tofs who helped and supported with Cadence condition. As you know Tracheo-Oesophageal fistula / Oesophageal Atresia is a congenital malformation that effects 1 in 3500 babies. Theses babies also have additional problems that can affect heart , spine, kidney, limbs or vertebrates . Tofs provides emotional support and information to enable families to cope with the ongoing difficulties of this poorly-understood and isolating condition. They receive no public sector funding at all.
So I would love you to sponsor me to help me raise money for families out there who's little ones are born with this condition .
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.
On the 30th September 2017. I will be doing a Tandem Parachute Jump to raise money for a Tofs . A charity that is so close to my heart. As you all know Cadence my granddaughter was born 24th October 2016. She was born with Oesophageal Atresia unable to swallow and Tetralogy of Fallot. The lovely Doctors and nurses at the Rvi hospital in Newcastle put us in touch with support group called Tofs who helped and supported with Cadence condition. As you know Tracheo-Oesophageal fistula / Oesophageal Atresia is a congenital malformation that effects 1 in 3500 babies. Theses babies also have additional problems that can affect heart , spine, kidney, limbs or vertebrates . Tofs provides emotional support and information to enable families to cope with the ongoing difficulties of this poorly-understood and isolating condition. They receive no public sector funding at all.
So I would love you to sponsor me to help me raise money for families out there who's little ones are born with this condition .