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Fife family’s £100k appeal to give Cammy, 4, life-changing surgery

Four-year-old Fife youngster Cameron Gilmour with dad, Jim and brother, Scott,11.
Four-year-old Fife youngster Cameron Gilmour with dad, Jim and brother, Scott,11.

The parents of a Fife youngster have launched an appeal to raise £100,000 to provide life-changing surgery for their four-year-old son.

Anstruther parents Jim and Eleanor Gilmour, whose son, Cameron, was diagnosed with quadriplegic cerebral palsy shortly after he was born, said they are overwhelmed after receiving more than £13,000 in public donations just two weeks since the campaign was launched.

The family hope to raise enough to provide surgery for Cameron only available in the United States, that would ease his suffering and may eventually allow him to walk.

The family are trying to raise £100,000 for surgery that will ease Cameron’s pain and possibly enable him to walk.

Cameron, or Cammy as he likes to be known, was born in December 2015, 15 weeks premature and weighing just 1lb 13oz.

After a four month struggle to survive, brave Cammy was finally allowed to go home but was later diagnosed quadriplegic cerebral palsy which seriously affects his muscle control and coordination.

The family say thy have been overwhelmed by the level of support after more than £13,000 was donated in the first two weeks of the fundraiser.

He was also found to have spasticity in his limbs which means Cammy cannot do the things other children take for granted like crawling, standing and walking.

The family is campaigning to raise the funds to give their son the quality of life he deserves but Jim admits, while it is a fantastic start, there’s still a long way to go to secure that trip to America.

He said: “We are astounded that people have donated so much in just the first few weeks but there is till much to do so we are urging people to dig deep if they can, as every single donation, regardless of how small, will make all the difference to Cammy.”

The £100,000 will enable Cammy to have intensive therapy and secure potentially life-changing Selective Dorsal Rhizotomy (SDR) surgery.

Because of the severity of his condition the treatment is not available on the NHS but is available at The St Louis Children’s Hospital in the USA.

“This comes at a considerable cost not only for the surgery itself but also for pre and post-op therapy along with specialist equipment that will be required to get the full benefits of the surgery,” Jim explained.

“While the NHS do carry out the surgery in the UK, it’s geared around a success rate basis and Cammy is ineligible. That’s why we are looking towards America for our son.”

With the ongoing Covid-19 restrictions hampering the family’s ability to fundraise, Jim is urging those who can make a donation to do so online.

“For obvious reasons, we can’t do the normal fundraising events you would expect but we do have a number of thing planned in the months ahead including auctions and the like and so we are appealing for the public to help us take away the pain and give Cammy the chance he deserves.”

To learn more about the Team Cammy G fundraising and to make a donation, go to www.justgiving.com/campaign/teamcammyg