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Banbury mother dies after raising £40,000 for sons Banbury mother dies after raising £40,000 for sons
(35 minutes later)
A woman with motor neurone disease who raised more than £40,000 to enable her sons to live with her sister in Australia has died.A woman with motor neurone disease who raised more than £40,000 to enable her sons to live with her sister in Australia has died.
Sam Kyme, 34, from Banbury, could no longer talk, but made the plea through her friends on a crowdfunding website.Sam Kyme, 34, from Banbury, could no longer talk, but made the plea through her friends on a crowdfunding website.
The cash will be used to fund the funeral, plane tickets, and legal and school fees.The cash will be used to fund the funeral, plane tickets, and legal and school fees.
Friend Susanna Howard said she passed away on Thursday morning "peacefully with her family around her". Sister Pippa Hughes said she passed away on Thursday "knowing everything is sorted for her kids".
She added: "The family are deeply saddened but also relieved that she is no longer suffering. 'No warning'
"It's amazing how life can change in a year," she added.
"This time last year it was Christmas and we were all together and this year it's completely changed.
"There was no warning, you just never know what's going to happen.
"We've got a few days now to scream and shout and cry, but Christmas, we're going to make it for Sam."
Friend Susanna Howard said Ms Kyme died "peacefully with her family around her".
"The family are deeply saddened but also relieved that she is no longer suffering," she said.
"Thank you to everyone for the incredible generosity and support during these difficult and devastating months."Thank you to everyone for the incredible generosity and support during these difficult and devastating months.
"We know that Sam would like everyone to celebrate her life by raising a glass to her and her family at this festive time."We know that Sam would like everyone to celebrate her life by raising a glass to her and her family at this festive time.
"Sam will always be dancing in the sky with a drink in her hand. We love you.""Sam will always be dancing in the sky with a drink in her hand. We love you."
Ms Kyme was diagnosed in April and told she had months to live. Within two months she could no longer speak.Ms Kyme was diagnosed in April and told she had months to live. Within two months she could no longer speak.
Earlier in the month she had been "battling to be here for Christmas so that she can spend it with her boys and family", Ms Howard said. Ms Howard said she had been "battling to be here for Christmas" so she could "spend it with her boys and family".
"My greatest fear is not that I am dying - it is the welfare of my boys," Ms Kyme's message had said on her crowdfunding page."My greatest fear is not that I am dying - it is the welfare of my boys," Ms Kyme's message had said on her crowdfunding page.
"I fear that Joey and Harry will go into care," it continued."I fear that Joey and Harry will go into care," it continued.
In November, Ms Kyme's sister Pippa Hughes said the funds meant the family, when the time came, could "all move to Oz, start a new life together, while never forgetting Sam". Ms Hughes said the funds meant the family could "all move to Oz, start a new life together, while never forgetting Sam".
Motor neurone diseaseMotor neurone disease
Source: NHS ChoicesSource: NHS Choices