logo
Raise a Glass to New South Wales: Australia's Most Exciting Wine State

Raise a Glass to New South Wales: Australia's Most Exciting Wine State

Independent3 days ago

From the gourmet delights of the historic Hunter Valley to the cool-climate vineyards of Orange and the 19th-century charm of Mudgee, New South Wales is the place to be for life-affirming wining and dining. And if you're flying into the state capital Sydney with Qantas, the experience begins before you even touch down on Aussie terra firma.
From takeoff to touchdown
On board the airline's award-winning A380, which flies from London to Sydney via Singapore, the wine list is already overflowing with sommelier-selected Aussie pours, a rotating list of top labels from regions you're about to set foot in, and a food menu that pays homage to the country's superb produce. But you're just getting started – as soon as you land in Sydney, it's easier than ever to hop between foodie hotspots across New South Wales with Qantas' domestic network and the Qantas Explorer, which makes travel both flexible and affordable.
The historic Hunter Valley
There are few better places to embark on a wine escapade than the Hunter Valley, Australia's oldest and most widely-renowned wine area, just a two-hour drive from Sydney. With more than 150 wineries to choose from, you could easily spend years exploring them all. Sip on semillon in the sun and taste shiraz made from some of the oldest vines in the world, or enjoy a languorous lunch surrounded by endless hills speckled with vineyards. The food isn't an afterthought in the Hunter Valley. Restaurants like Muse and Bistro Molines champion a farm-to-fork ethos, with menus that evolve with the seasons and many wines that travel from vine to glass in less than a mile.
The cool-climate wines of Orange
The high-altitude vineyards of Orange offer a different kind of tasting experience; the cooler climate here results in excellent Chardonnay, Pinot Noir and Sauvignon Blanc. Daily Qantas flights from Sydney get you to Orange in just over an hour, and Oenophiles will be in their element, with cellar doors sandwiched into rolling hills and ancient volcanic soils that give the grapes their full flavour. Despite being one of the newer wine regions, Orange is making waves among Australian wine insiders.
The food scene is equally impressive. Try Sister's Rock Restaurant for produce that celebrates what grows in the Wiradjuri country – the ancestral lands of the Wiradjuri people, one of the largest First Nations groups in New South Wales, whose knowledge of the land stretches back thousands of years. It's located at one of Australia's highest vineyards, Borrodell Vineyard, with glorious views of the Towac Valley and beyond. The region is also flecked with bakeries, cafes and farmers' markets that spotlight Orange's ever-evolving food scene.
The rustic region of Mudgee
Mudgee is just a few hours northwest of Sydney in the pretty Cudgegong River Valley and is home to more than 40 family-run cellar doors known for full-bodied reds and wines made from Italian grapes. The town is a popular weekend escape for Sydneysiders, with Qantas operating regular flights from Sydney to Mudgee in under an hour. The area offers a snapshot of the past, with lots of colonial-era architecture, gold rush history, and Aboriginal rock art sites. The food is also something to shout home about; paddock-to-plate is hot here, and restaurants like Zin House craft their menu around what's grown on-site – if they don't grow it, they don't serve it. Tuck into plates of handmade pasta laden with veggies grown a mere 50 metres away, and sip on organic and biodynamic bottles from Mudgee's award-winning winery, Lowe Family Wine Co.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

‘Bored of being your sidegirl' – Boxer from ‘battle of the boobs' retires as she posts emotional farewell
‘Bored of being your sidegirl' – Boxer from ‘battle of the boobs' retires as she posts emotional farewell

The Sun

time42 minutes ago

  • The Sun

‘Bored of being your sidegirl' – Boxer from ‘battle of the boobs' retires as she posts emotional farewell

Jack Figg, Digital Sports Reporter Published: Invalid Date, AVRIL MATHIE has retired from boxing after posting an emotional farewell - in the form of a love letter to the sport. The Aussie star hangs up her gloves with a record of eight wins, one loss and one draw. 7 7 7 7 She was lined up to face Ebanie Bridges in 2023 in what was dubbed "the battle of the boobs". But Mathie - who has since had her breast implants removed - pulled out from the bout through injury. And now she has called time on her career - taking to Instagram to make the announcement. She posted: 'To the love of my life. Sadly, after 13 years, I must say goodbye. "My heart is broken walking away from you, I still have so much love for you, some may call it addiction in fact. "I had so many dreams for our future, but my body can't take your abuse anymore. 'You gave me the highest of highs. We travelled the world and achieved things most only dream of. "But a year and a half ago, you hurt me so badly. And while I missed you during that time apart healing, I also had the best year of my life. "It opened my eyes to what else is waiting for me beyond you. Still, I tried to come back to you again and again this past 6 months, but you just keep hurting me. "Where I had once believed we'd always work it out, slowly I just became tired of the pain, bored of being your sideline girl and am craving to be again in something like that we once had when I felt like I was growing unstoppably. 'After long chats with friends, I understood that you can no longer fulfil my needs. "I've realised it's me who's the fun and inspiring one, it's not even about you and that will translate into all my future relationships. 'And there's so many other I've been flirting with that you don't even know about yet. So I know I'm going to be just fine. Better in fact. "And I know you'll miss me, but don't worry, I'll find a way to stay connected to you. 'Thanks for everything, boxing, I'll be forever grateful we crossed path." Bridges, a former bantamweight champion, commented: "You'll always be the one that got away to me." She also added: "I love this letter. You are amazing in and out of the ring. Onto the next chapter / new love. which I have no doubt you will succeed in." Mathie - a former OnlyFans star and swimsuit model - revealed on her YouTube channel that undisclosed injuries were the prime reason for retirement. She also suffered a horror injury after falling off a motorbike in 2023 - with her bone gruesomely sticking out of her leg. 7 7 7

Europe's first airport Five Guys is landing at London Heathrow Airport
Europe's first airport Five Guys is landing at London Heathrow Airport

Time Out

time3 hours ago

  • Time Out

Europe's first airport Five Guys is landing at London Heathrow Airport

Heathrow Terminal 5 is one of the best places in the world for airport grub. Yes, really – the restaurant experts at Food & Wine have said so. For fancy fliers, there's Gordon Ramsay Plane Food, the Fortnum and Mason Bar and La Belle Epoque and for the rest of us there are firm favourites like Wagamama, Itsu and good old Wetherspoons. So it only makes sense that T5 will be the very first airport terminal in Europe to get a Five Guys. Soon you'll be able to get your hands on a big fat oozing bacon cheeseburger right before your 6am flight to New York, if you want. The hub has been renamed 'Terminal Five Guys' to mark the momentous occasion. Expected to open late this year, Five Guys will be on the upper level of the terminal with around 90 seats for eating in, plus a takeaway option. It's opening times will align with the first and last flight of each day, so no one misses out, and will have ordering kiosks in six different languages. The American chain's breakfast options (egg, cheese or bacon sandwiches) will be available throughout the day, as will its classic burgers, hotdogs, boardwalk-style fries and milkshakes. It's been more than a decade since Five Guys first landed in the UK, with its first British branch opening in Covent Garden in 2013. John Eckbert, the CEO of Five Guys UK said: 'We are thrilled to be opening a brand new Five Guys at Heathrow Terminal 5 this year. Having opened over 170 restaurants across the UK since we first launched back in 2013, the brand has established itself as one of the nation's favourites for premium burgers. 'Now Five Guys is cementing itself at the UK's busiest travel hub; we are excited to be providing our delicious menu to travellers as part of their journeys.'

NRL cheerleader Savannah had a 'normal' life... Until she made a devastating discovery in Dolly magazine
NRL cheerleader Savannah had a 'normal' life... Until she made a devastating discovery in Dolly magazine

Daily Mail​

time3 hours ago

  • Daily Mail​

NRL cheerleader Savannah had a 'normal' life... Until she made a devastating discovery in Dolly magazine

From the outside, Savannah McKell seemed to have a picture-perfect life. But behind closed doors, the former Newcastle Knights cheerleader was secretly battling a life-shortening condition. 'People often looked at my life and saw a fairytale - I was cheerleading, modelling and taking glamorous Instagram pictures... What they didn't see was me coughing up blood between cheering, managing life-threatening lung infections, and silently battling cystic fibrosis,' Savannah told FEMAIL. When she was born, her parents were given the devastating news that she might not live past her teens - and if she did, she would likely only reach her early 20s. Her parents kept her life relatively normal, shifting the focus away from her illness so she could simply enjoy being a kid. From the age of 20, she began experiencing more frequent infections and health complications. But it wasn't until she was 24 that her condition took a terrifying turn - after she suffered an episode of hemoptysis, just hours before her engagement party. 'The day I started coughing up cups full of blood was the scariest day of my life,' Savannah recalled. 'As I was rushed to the emergency room, all I could think was I'm not going to get to say goodbye or 'I love you' to my parents or make it to my wedding and marry my husband... The party was at the back of my mind and I just went into survival mode.' Savannah has been living with the incurable disease since she was six weeks old. Growing up, she remembers having a 'beautiful' childhood, even as she navigated life with cystic fibrosis (CF) - a genetic disorder that causes an abnormal build-up of thick mucus in the lungs, airways and digestive system. 'My family kept my diagnosis very positive and almost pretended it didn't exist to me as I was so young and unable to comprehend,' she said. 'I had an amazing family, and we'd spend as many days as we could by the beach to soak up the salt, which helped my CF. I had a lot of extra hospital visits and treatment I had to do but my mum always tried to make them as enjoyable as possible.' Dolly discovery Savannah was never fazed by her diagnosis - until she came across a confronting detail in the teen magazine Dolly that revealed the soul-crushing reality of her life expectancy. 'It was devastating. I knew I was "more prone to getting a cold, cough and flu" but I didn't know my CF came with a very dire life expectancy,' she recalled. 'Finding out at 12 years old - from reading Dolly magazine - that I was nearly "halfway" through my life had a profound effect on me.' After reading the article, she made the decision to keep her condition a secret. 'I chose to keep my CF private in the early 2000s. With the life expectancy being what it was, I didn't want the stigma of being "the sick girl" or that "she was going to die soon",' she said. 'I wasn't ashamed of having CF but I never wanted it to be the talking point to my friends, peers, classmates and just everyone around me. 'Growing up is hard enough without already being labelled as 'different'. I just wanted to be Savannah, not Savannah who has CF.' Her childhood with CF was so normal that she didn't really worry about her diagnosis until she read something about the life expectancy of someone living with CF in Dolly magazine As a child, Savannah knew she was 'different' because of the number of hospital visits she had compared to her school friends and other kids her age. 'Some of them said they'd never been to hospital before, yet I was going once a month for clinics and yearly needles, and needing antibiotics all the time for a "cold",' she recalled. 'The clinic visits when I was young were very traumatic with tubes being shoved down my throat and multiple blood tests, and antibiotics... no five-year-old should have to endure stuff like that so young.' Defying odds As she got older, the life expectancy for people with cystic fibrosis gradually increased to around 30 years. However, Savannah, now 29, has received promising news after defying all odds - thanks to medical advancements, research and a breakthrough prescription drug called Trikafta. 'Life expectancy has increased drastically and continues to increase every day. While it's in no way a cure, it's a big step for cystic fibrosis sufferers. It's now almost double the life expectancy to 60,' she said. What many people didn't see was that Savannah was struggling behind closed doors -coughing up blood between cheerleading and managing life-threatening lung infections How you can help make a difference May is the month of Cystic Fibrosis Awareness. Savannah is sharing her story in support of CF Together. She is hoping to help raise awareness and funds for Cystic Fibrosis research. You can donate here. 'Trikafta has completely changed my life. I can now go months, if not years between antibiotics, IVs, hospital stays and clinic visits. Something that used to occur monthly. 'I'm not constantly clearing my throat or coughing up thick mucus, I can now take deep breaths and have clear lungs. It also allowed me to fall pregnant naturally which never happened before Trikafta.' Before discovering the life-extending drug, Savannah experienced fertility issues while trying to get pregnant - likely due to her condition. Baby joy She and her husband conceived their first son Elijah via IVF. 'Carrying a pregnancy was the hardest challenge physically, as the strain on my body and health was incredibly hard,' the young mum said. 'The only thing that got me through was the beautiful baby boy I was fighting so hard for.' Three months postpartum, Savannah contracted an infection called B. cepacia, often referred to as a 'death sentence' for people with cystic fibrosis. This scare prompted her to start Trikafta after a year of hesitation. Savannah kept her CF a secret from most people for many years due to stigma and a desire to be seen as 'normal' but she has become more open about her condition - especially after having her son 'The thinning of mucus from Trikafta not only cleared my lungs but cervical mucus too, allowing to conceive naturally, something we had tried for many years with no success without IVF,' she said. Thanks to advocacy by CF Together, she now has access to the life-saving medication - something she attributes to giving her the best years of her adult life. Highs and lows Savannah said her condition is now 'very stable'. 'I live 99 per cent of the time a somewhat normal life minus the pills every day and extra precautionary clinic visits. My new life expectancy is promising and I can look to the future without as much fear,' she said. Despite thriving at 29 with a second baby on the way after conceiving naturally, she still struggles with the 'constant mental noise and fear of decline'. 'While we have advancements and fancy new drugs, it still only takes catching one bad bug to completely bring your whole body and life down, as well as the mental side,' she explained. 'CF means taking pills every day, with every meal, since the day I was born - and that hasn't stopped.' What is cystic fibrosis carrier testing? Cystic fibrosis carrier testing is a genetic test that will help to identify if you have changes to the CF gene. The test involves providing a blood or saliva sample and requires a referral from your GP, obstetrician, geneticist, or gynaecologist. There are around 2,000 gene changes that cause CF, and a typical CF screening will identify the most common CF gene changes in Australia. However, there is still a small risk that you may be a carrier of a rare CF gene change. If you have a family history of CF, it is important to tell your GP, obstetrician or gynaecologist before providing your sample for screening. This will ensure that you are being tested for the most common CF gene changes as well as the specific gene change relevant to your family. Making the decision to know your CF carrier status through genetic testing is a choice only you can make. Knowing whether you are a carrier can help inform you of your reproductive options. You can discuss your CF carrier screening options with your GP, obstetrician or a genetic counsellor. On November 1, 2023, reproductive carrier testing for cystic fibrosis, fragile X syndrome and spinal muscular atrophy was made available for every eligible Australian, thanks to two new Medicare item numbers, allowing people to make more informed choices regarding family planning. The test can be ordered before pregnancy or early in pregnancy. Savannah said she's now enjoying living a 'slow, nature-filled life'. 'I'm raising my family without any fear for the future. Something as small as going for a swim at the beach is such a blessing for me and I want to spend the rest of my life just appreciating every second,' she said. For couples looking to start a family, Savannah urges them to get a genetic blood test before trying to conceive. 'CF is genetic but I advise couples looking to start a family to please do a genetic blood test before falling pregnant. My parents had no idea they were carriers and it's surprisingly more common in Australia than you think to be a carrier,' she said. By sharing her story, Savannah wants every young person living with cystic fibrosis to know that their diagnosis does not define them. 'It should never stop you from chasing the life you dream of. Never listen to any one that doubt you or wrap you in cotton wool because of your disease,' Savannah said. 'I chose to keep my illness private growing up, but I've learned that strength doesn't come from pretending everything's ok... it's from being honest and proving people you can do all of this while fighting something so horrific. 'I share my story now because I wish, as a little girl, I had seen someone like me thriving despite their diagnosis. Appearances don't always reflect reality. 'You truly never know what someone is going through behind the scenes. You should always prioritise your health for those who weren't as blessed.' According to CF Together, nine out of 10 children diagnosed with cystic fibrosis are born into families without any prior history of the condition. In cases where there is no family history, both parents of the child who is born with CF must be carriers of the gene change that causes CF. One in 25 people are estimated to carry the gene changes that can cause CF, and most people are completely unaware they are a carrier. CF carrier screening testing is available to help you and your partner find out whether you are among the one million Australians who carry the CF gene change.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store