Launch goes down a treat

A NEW family-run restaurant in Knaphill threw a fine Italian feast to celebrate opening their doors.

Former professional golfer and commentator Peter Alliss, along with the Mayor and Mayoress of Woking Tony and Mary Branagan, shared food, drink and laughter with the many other visitors to La Bella Amalfi in the High Street.

THE BEST IN THE BUSINESS – Veronica Lanzetta (far right) with mum Antonietta, dad Nino and uncle Salvatori, plus special guests Mayor Tony Branagan and Mayoress Mary and former pro golfer commentator Peter Alliss

THE BEST IN THE BUSINESS – Veronica Lanzetta (far right) with mum Antonietta, dad Nino and uncle Salvatori, plus special guests Mayor Tony Branagan and Mayoress Mary and former pro golfer commentator Peter Alliss

But there was a more tender side to the family-run occasion. While friends and guests tucked into the delicious culinary delights of the plentiful spread laid on by the venue owners, brothers Salvatori and Nino Lanzetta, they were invited to make a donation to the Cystic Fibrosis Trust.

Nino’s daughter Veronica, who is 28, was born with the debilitating genetic disease. She was diagnosed at eight months and has been blighted by hospital visits all her life.

Both parents have to be carriers of the gene. Veronica’s sister Sofia, who’s 32, and 27-year-old brother Alfonso are also both carriers but neither have cystic fibrosis.

It is a cruelly progressive condition in which excessive production of mucous clogs the lungs and pancreas, causing respiratory and digestive problems.

Children are usually diagnosed in the first few years of life, and less than half live beyond the age of 18. For those who do, life expectancy is about 35 years.

However, this figure could improve with more advanced treatment options, which is why it is so important to raise funds for more research.

Veronica’s lungs are now so damaged from degeneration that everyday activities are extremely difficult, if not impossible. She is on antibiotics, inhalers and has to take enzymes with food.

She is also on oxygen 24/7, is virtually housebound in a wheelchair and is dependent on her primary carer, mum Antonietta.

Veronica, who has lived in Woking all her life and went to St John the Baptist School, has a feeding tube or ‘peg’ attached to a hole in her stomach to supplement her diet.

Although she is able to eat a normal meal, she has to intake 3,000 calories a day, which in turn leads to further vulnerabilities and complications. Her second tube was fitted six months ago after she was rushed to London’s Westminster Hospital with peritonitis caused by the first.

Veronica, who lives in Mayford with her parents, has been on the hospital waiting list for a double lung transplant for three-and-a-half months. She doesn’t know how long she will have to wait. She added: “It could happen at any time. Some sufferers wait just a couple of days; some die waiting.”

Despite the hand she’s been dealt, Veronica has a positive outlook and a bravely philosophical take on life. She said: “It’s just one of those things you get on with. It’s no one’s fault and can’t be helped.”

La Bella Amalfi, at 42-44 High Street, raised £375 towards the worthwhile cause.

VISIT ww.cysticfibrosis.org.uk to make a donation or to get involved with the Cystic Fibrosis Trust.

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