When Alex Sprackland caught Covid-19 in March 2020, he thought he’d be back to normal in no time. Yet, five years on, the 34-year-old still grapples with the severe, life-limiting effects of the infection.
‘I was diagnosed with long Covid seven months after my initial illness – my life has never been the same,’ Alex, from Tunbridge Wells, tells Metro. ‘I had to leave my flat, I lost my relationship, and I moved back in with my parents. I also dropped out of university when I became too sick to finish the course.
‘I can’t even work, but there’s no support for me. No treatments. Nothing.’
After contracting the virus, Alex developed a series of symptoms that included an irregular heartbeat, breathlessness, ongoing pain and digestive problems. Initially he was misdiagnosed with chronic fatigue syndrome and prescribed ‘graded exercise’ by his GP, which only worsened his symptoms.
Alex bounced between numerous specialists, none of whom could help. ‘It was demoralising, especially when people didn’t believe me about the symptoms,’ he remembers.
Six months later Alex was finally referred to the NHS long Covid service, but says, ‘no one knew what to offer me. I ended up going to a private clinic instead and they started some experimental treatments.’
However, the decision cost him his place at the NHS clinic, as he was pursuing ‘off-label treatments’.
Although 120 specialised long Covid clinics opened in England and Wales in 2021, today there are less than 50 – and Alex is now paying for private healthcare out of his limited savings and Personal Independence Payment (PIP) to find answers.
He is one of approximately 2million people in the United Kingdom with the condition, a chronic, systemic disease that can cause a range of long-term health issues, such as severe fatigue, difficulty breathing, chest pain and memory problems.
‘It’s all a gamble to find trustworthy information; no one knows enough,’ says Alex, who relies on a wheelchair. ‘I spend 99% of the time in my room and haven’t seen most of my friends for five years. I’m watching all their lives pass me by, which is probably the hardest thing to deal with, over the symptoms.’
School became impossible
Avalyn Godfrey, 16, knows the feeling all too well. After catching coronavirus in October 2021 at age 12, she developed long Covid with symptoms of debilitating fatigue, breathlessness, dizziness, sensory issues and brain fog.
Once a super active kid, Avalyn’s energy slowly disappeared, making lessons impossible to keep up with. After transferring to a more understanding school, where a teacher who also had long Covid advocated for her, the teen’s worsening symptoms made homeschooling the safest option.
She has since completed six GCSEs at home, but finds it hard to maintain her social life.
‘When you are not in school as a teenager, there aren’t many ways to keep contact with your friends,’ Avalyn tells Metro from her home in Cheshire.
After fighting for over a year to get an official diagnosis, which was delayed by doctors dismissing the teen as ‘looking for attention’, shewas referred to an NHS long Covid clinic.
However, Avalyn’s mother, Donna McParland, says treatments were limited and the clinic initially insisted she meticulously log every activity, which her daughter didn’t have the energy to do.
Then, they moved on to teaching Avalyn about ‘pacing’ – an activity management technique used amongst people with chronic illness to help people balance symptoms with everyday life – and carrying out numerous tests, which all came back normal.
‘When we have appointments, they tell us about new medical studies or tests they’re doing and for a second, you think, “Oh, that’s great,’ says Avalyn. ‘But then nothing happens.’
Avalyn hopes that her symptoms will improve over time and that one day, better treatments will be discovered. In the meantime, she’s focusing on achieving her dream of becoming a primary school teacher.
‘I’ve always wanted to be a teacher and I love working with kids; it just feels like something I’m good at,’ she says, hopefully.
‘I had to go through an ill-health dismissal’
Mum of two Jenny Sullivan has also navigated the challenges of long Covid support. A dedicated English teacher with boundless energy and a fierce passion for her work; when she caught coronavirus in September 2023, everything changed.
After developing severe long Covid symptoms, Jenny was left unable to stand due to dizziness, while also suffering from frequent fatigue and a marked decline in her overall health. She also lives with MCAS (Mast Cell Activation Syndrome), a rare disease that results in a range of allergy-like symptoms.
After nearly three months of worsening symptoms, Jenny, who lives in Tonbridge, went to the GP for the first time, starting a long journey to diagnosis and treatment for long Covid.
‘I was signed off work but thought I would be returning soon – then I found out there was a six-month waiting list to see the cardiologist for my symptoms,’ she tells Metro.
‘It was excruciating to realise, over time, that I wasn’t well enough to work and I had to go through an ill-health dismissal – then it was even worse to realise there were no decent treatments to help me.’
Jenny was referred to her local NHS long Covid clinic, but found they couldn’t offer her any advice except pacing and some limited treatments for postural orthostatic tachycardia syndrome (POTS), a condition that causes rapid increases in heart rate and has been diagnosed in many long Covid patients.
Eventually, she decided to seek help privately and now travels to Liverpool to see specialist Dr Binita Kane, who also treats Alex.
‘The problem is, long Covid specialists are so rare and I have to travel so far to see mine to get stabilised just a little,’ says Jenny from her home, having transitioned from a desk to bed to preserve energy while speaking.
‘The lack of NHS treatment means that some people pay thousands to untrained and unqualified individuals promising ‘miracle cures’; it’s easy for opportunists to oversell when there are no alternatives.’
Now unable to work for nearly 18 months, Jenny uses a mobility scooter for outings, which has given her more access to the outside world. However, most of her life is still centred around resting in bed, and she is investing in private care in the hopes of improving her quality of life.
But she is limited by time, cost and distance. A single private consultation can cost up to £500, wait times are still up to six months, and Jenny has to travel for access to care, sapping her already diminished energy.
Do you think the UK government is doing enough to support long Covid patients?
-
Yes, they're doing their best
-
No, more needs to be done
-
I'm not sure
Despite the need for long Covid care still being apparent, many sufferers are facing a dearth of support with doctors who don’t have the funding or knowledge required.
Dr Nikita Kanani, MBE, a GP with extensive experience working with long Covid patients, says that ‘GPs are doing their best, but they’re often working without the tools or capacity they need.
‘There’s been some education and guidance, but it’s not consistent, and many are managing complex cases without access to the specialist support or multidisciplinary pathways they need to refer into.’
While NHS England initially delivered long Covid funding through a centralised national programme, this was passed on to 42 integrated care boards (ICBs) in March 2024. However, many have since shut down clinics or never had one to begin with, according to research by Long Covid Support.
An NHS England spokesperson told Metro: ‘More than 100,000 people have been supported by specialist Long Covid clinics since 2020, with NHS staff helping them deal with the physical, cognitive, and psychological effects of Covid-19.
‘National guidance and funding has been issued to local health leaders to help them create Long-Covid services which best meet the needs of their local area.’
Looking for answers
However, Alex says he has had to become his ‘own doctor in many ways.’
He explains: ‘I am reading the latest research, finding new potential treatments, and then looking for doctors who will prescribe the medications or try the new protocol I recommend. It’s exhausting.’
While energy-draining, Alex admits that being proactive in his treatment helps alleviate some of the frustration. As part of the Long Covid campaign group, Not Recovered UK, he has also helped raised upwards of £12,000 for research.
Avalyn, too, has directed her attention toward raising awareness, working with organisations like Long Covid Kids and writing her own children’s book, called ‘Star Dizzy Lizzy’, to educate young people.
Andrea from Long Covid Support believes the answer lies in improving research and maintaining the precious few clinics that remain.
‘Research is essential; we need it for diagnostics, for treatment, before we even think about rehabilitation,’ she says.
Dr Kanani agrees: ‘the scale of suffering from long Covid should justify faster investment in trials and early access schemes. We need a system that can act with urgency, rather than waiting for absolute certainty before supporting patients.’
Beyond stopping the closure of these much-needed clinics, Alex says, too many people think ‘Coronavirus doesn’t exist anymore’.
He adds: ‘we are the unfortunate aftermath of the pandemic that people don’t want to think about. They just want to put their things in their ears and move on with life. We can’t do that though, because we’re living with long Covid.’
19 Sep, 2025 | Admin | No Comments
'Divorced and it's hard to tell my new man I don't have as much cash as him'
Resident agony aunt Coleen Nolan has advice for a reader who has met a new guy but he has more money than her and she can’t afford to go on the dates he suggests
19 Sep, 2025 | Admin | No Comments
I’m a shopping writer and here’s what I’m buying this week – from Omnes to Benefit
Metro journalists select and curate the products that feature on our site. If you make a purchase via links on this page we will earn commission – learn more
The weather may not be able to make up its mind this week, but our shopping expert is feeling pretty definite on what she’s been loving since last weekend.
Whether it’s a new jumper for the colder weather (because you can never have too many), skincare to keep your complexion from drying up in the cold or homeware upgrades to make your space properly cosy, we’ve found the best of the best this week.
But firstly, housekeeping – because this week has been packed with news and newness you’ll want to hear about.
Bringing together facial health and bodily wellness, FACEGYM, the global leader in facial fitness, has partnered with wellness brand SWIISH to bring functional hydration to all FACEGYM London studios throughout October.
From the 1st to the 31st October, every FACEGYM client will receive a SWIISH electrolyte drink to be enjoyed in-studio or taken away, designed to help supercharge hydration and enhance the results of your ‘face workout’.
The collab is the perfect way to tend to your inner health as FACEGYM’s incredible facialists look after your skin, celebrating a holistic approach to skin and performance.
I mean, you’d neck an electrolyte drink after a workout in the gym, so why not after a face workout at FACEGYM?
In other, more fashion-related news, Omnes, a London-based fashion brand designed with sustainability in mind, has just dropped its autumn range – and it’s absolutely to die for.
Filled with cosy knits, staple denim and even winter wedding guest pieces (currently at the top of my ‘to buy’ list), the collection has everything you could need to give your cold-weather wardrobe a spruce (pardon the pun).
On a different note, England’s women’s rugby team, the Red Roses, play France in the Women’s Rugby World Cup semi-final tomorrow (Saturday 20th September), and we’re pretty darn excited.
If you wanted to score a skincare must-have to commemorate our girls’ spectacular performance thus far, Clinique are selling a Limited-Edition Red Roses iteration of their Dramatically Different Moisturizing Lotion+ – and it’s absolutely iconic.
Finally, Benefit has dropped their newest Christmas gifting collection centered on the joy of playing games with your loved ones during the festive season, and with it three unmissable ‘Beneland’ pop-ups in Selfridges across the UK to celebrate the stunning range.
While their Manchester foray has already come to an end, you can take advantage of glam gifts and huge deals at both the Selfridges London pop-up (11th-24th September 2025) and the Selfridges Birmingham pop-up (1st -28th September 2025) coming up. Trust us, you don’t want to miss it.
Ready to check out our shopping expert’s top picks for the week? Explore below and find the cream of the crop.
This week we’re loving:
Omnes Eugina Cardigan in Merlot
The perfect autumn layer, this adorable Eugina Cardigan from Omnes has everything you need in your staple knitwear. Designed in a rich merlot wool-mix, it features a textured knit that adds depth and warmth to its easy-wearing silhouette, while blue bow details at the shoulders bring an adorable touch.
Clinique Limited-Edition Red Roses Dramatically Different Moisturizing Lotion+ 125ml
To celebrate Clinique's partnership with the England women's rugby team, the Red Roses, you can now shop the brand's iconic Dramatically Different Moisturizing Lotion+ in a limited-edition, rose-printed bottle. This deeply hydrating daily moisturiser delivers instant, soothing moisture for skin in need of comfort.
Kate Somerville HydraKate Pro-Collagen Lip Oil Elixir
My new favourite lip product, the Kate Somerville HydraKate Pro-Collagen Lip Oil Elixir is a hydrating and comforting product I now can't go without. The silky, fragrance-free formula glides on easily, leaving a smooth, glossy finish that feels comfortable and is conditioning from the very first application.
Berghaus Women's Explorer Down Jacket – Red
If you've been after the perfect winter jacket then Berghaus' new Autumn Winter 25 collection is sure to fit the bill. We, personally, can't get enough of the Women's Explorer Down Jacket – perfect for the cold weather with all its squidgy goodness. Made from 650 fill Berghaus Hydrodown®, the jacket keeps you cosy even when wet, while water and wind resistant Pertex® Quantum fabric makes it perfect for any storm.
Benefit BADgal Royalty 2-Piece Mascara Gift Set
The perfect festive gift for the beauty lover in your life (and yes, that can be yourself), the Benefit BADgal Royalty 2-Piece Mascara Gift Set features two full-sized mascaras to help deliver your most gorgeous lashes yet. Inside you'll find the BADgal BANG! and BADgal Bounce mascaras, presented in the most adorable chess piece keepsake tin.
Medik8 Advanced Pro-Collagen+ Peptide Cream 50ml
Medik8's new moisturiser is designed to stop the clock on your skin, featuring a lightweight, pillow-soft finish that's set to leave it instantly quenched. It's been formulated with a next-generation Growth Factor MiniProtein to visibly reduce the appearance of deep-set wrinkles, blended with a unique peptide to restore skin structure and prevent the formation of new lines.
M&S Collection Wool Blend Argyle Crew Neck Relaxed Jumper
Perfect for cold weather styling, this Wool Blend Argyle Crew Neck RelaxedJumper has me totally smitten, made with a wool and alpaca-blend and knitted with brushed yarn for a luxuriously soft feel. The all-over Argyle pattern is to die for, while the relaxed fit and a touch of stretch give that extra comfort.
St Eval Christmas Tealight Advent Calendar
This stunning St Eval Christmas Tealight Advent Calendar has totally captured my heart, featuring a breathtaking scene of the North Cornish coast with all the magical sea creatures that reside there. Behind every numbered door you'll discover a selection of 24 gorgeously scented tealights, as well as a gold-dusted tealight holder.
Abercrombie & Fitch Bra-Free Open-Back Knit Midi Dress
The Abercrombie & Fitch Bra-Free collection has been on my radar for a while, but this dress has me instantly reaching for my Apple Pay. This comfortable midi dress has been made with soft AF cotton-modal fabric and features high neckline, flattering ruching details along the bodice, an open back with a twist detail, plus a seamed-in bra with removable pads.
nere Venture Dual Open Cabin Suitcase
Pack smarter with the stunning Venture Dual Open Cabin Suitcase, the luggage upgrade your collection has been looking for. Lightweight and durable, this 36l suitcase boasts a dual opening system which enables easy access and organisation, letting you pack smarter and find your essentials with ease.
Mafalda Dominic Black Patent Leather Loafer
I only discovered Mafalda and its stunning, hand-made shoes this week, but I'm already totally obsessed. The Dominic loafers are a slingback style made of black patent leather, featuring a square toe and a smooth, structured upper. The result is a shoe that's stable, comfortable and totally chic.
Truly, there’s been so much to love this week.
Follow Metro across our social channels, on Facebook, Twitter and Instagram
Share your views in the comments below
For around a year, my skin was so itchy I would scratch it until I bled – even then, I never managed to satisfy the feeling, and it would often keep me awake at night. It never crossed my mind that it could be a symptom of a life-threatening illness.
At the same time, I was feeling tired, losing weight, sweating at night, and always coming down with a cold or flu. It was only when I found a lump on my neck that I thought it might be something serious.
I often couldn’t take a full breath in – this was because a tumour in my chest was about 30 centimetres – but I’d just assumed that it was probably down to something like glandular fever.
Consultants usually tell patients their diagnoses in person, so when the doctor said over the phone in September 2018, ‘You’ve got cancer’, it was clear time wasn’t on our side.
‘It’s stage 4 Hodgkin Lymphoma in the neck, lung, chest and under the diaphragm. If you’d come to us about a week later, we wouldn’t have been able to do anything for you,’ he added.
The diagnosis left me dumbstruck, like I’d been hit with a freight train. How did this happen? I was only 26.
After I put the phone down to my doctor, I said to my mum and dad, ‘Can you take me to the hospital because I’ve got cancer?’ It was completely unexpected for them, but we didn’t have the space to think about it; I just had to get started on treatment.
24 hours later, I began chemotherapy. I was able to stay surprisingly positive during the six months of treatment and tried to have a lot of fun. I’d fundraise, have chemo parties, and whenever I went out, I was always silly about being bald.
When I finally got the all-clear a few months later, I couldn’t wait to enjoy my life again.
Why can be itchy skin a sign of Hodgkin Lymphoma?
‘Skin irritations and problems such as dry, sore and itchy skin can be a symptom of lymphoma,’ the Lymphoma Action charity explains.
‘Scientists think that itching as a symptom of lymphoma might develop because of cytokines. These are proteins released by your immune system when your body is fighting an infection or an illness, like lymphoma. It’s thought that cytokines cause itching by irritating the nerves in your skin.
‘Skin problems often start to go away once treatment for lymphoma starts.’
Itchy skin is not always a sign of anything serious. You can often treat it yourself, and it will usually go away after a few weeks, but see a GP if you’re worried or the problem persists.
A step backwards
My parents and I were so confident I would be fine when I went for a routine check-up scan in June 2019 that we dressed up nicely for a celebratory lunch afterwards.
Then the doctor told me: ‘I’m afraid it’s back.’
It was shocking news, but we kept our restaurant reservation as I’d already learnt that you must enjoy life whenever you can. I knew I might not be well enough to go out soon. I enjoyed a few drinks and saw Jude Law, so that was fun!
The severity of my new cancer meant I needed a stem cell transplant, which replaces damaged or diseased blood-forming cells with healthy ones. When I had it in October 2019, I couldn’t leave the hospital – even to go outside – for nearly five weeks. I was also more unwell and didn’t have any energy to make it a fun experience, like last time.
When it came to shaving my head again, I remember my mum’s tearful face in the corner of the bathroom, and snapping at her because I didn’t want to see or feel any emotion.
In some ways, my illness was even harder for my parents. Some days, I was in so much pain it felt like there were little shards of glass floating around my body, and all they could do was sit and watch. Their lives were put on hold every day, not knowing if their daughter would make it.
Going through the menopause
Three months after my stem cell transplant, I had a scan which showed the cancer had gone. My procedure meant that my chances of having kids became around 0.1%, but I had no choice – what’s the point in being fertile if I wasn’t going to be alive?
However, when I started feeling better, reality hit. I always wanted to be a mum, and began grieving for the kids I’ll never get to have.
The transplant also put me through menopause at just 29, which was tough as the doctors didn’t explain it to me, and I didn’t realise what was happening.
At first, I thought I was having a mental breakdown. My emotions were all over the place, my anxiety was crazy, and I was so low. I was also suffering from night sweats, sore joints and brain fog. Once I put my iron in the fridge.
I was lucky to have a therapist who helped me through these life changes and eventually made the connection for me.
I was put back on the pill for oestrogen, but it was suggested I come off because I had strokes. The pill can lead to an increased risk of blood clots and further strokes.
So now, age 32, I’ve been hit by another wave of menopause symptoms, which can be difficult because none of my friends are at this stage and, as lovely and supportive as they are, they don’t entirely understand it.
A new chapter
A few months after the stem cell transplant, I went back to my job as an executive assistant at a recruitment company. They’d been so brilliant with me while I was ill, but in the end, I left so I could concentrate on my social media.
I’d used it as a way to let people know how I was getting on with the diagnosis and treatment, but I also wanted to share my experience in case it could help someone else feel less alone.
I hadn’t known anyone my age who had been sick, so I had no one I could ask about little things, such as how to tie a headscarf or protect my nails in chemo, or talk about the big stuff, like fears. I wanted to change that and now I have nearly 100k followers and the most wonderful community who are all kind, empowering, encouraging and understanding.
It’s also spurred me to start my own business, Life’s for Living, a travel company that takes women on adventure trips. Everyone’s there for a reason, whether they’ve had a health issue, they’re going through a divorce, they’ve struggled mentally, or they’ve been feeling insecure in their bodies. It’s so incredible to bring everyone together. We bond, and it becomes beautiful.
Having cancer means time feels like a precious thing, and now I want to do as much as I can. But my mum reminds me I can say ‘no’ sometimes. For a while, I’d give a panicked yes to everything and get burned out.
It sounds cheesy, but I’ve realised that saying yes isn’t just for the big things. I used to only light candles for nice occasions, but now I light them whenever I want. It’s not feasible to have some big bucket list trip every day, so I try to remind people it’s about the little things too.
Last year, I had a party to raise money for The Royal Marsden Hospital and celebrate being five years cancer-free.
What most people didn’t know was that I was still waiting to find out if it had come back, after an inconclusive scan. I felt as if I was cheating by celebrating, so I’ve never felt such relief when I got the all clear.
I never like to thank cancer for stuff, because I don’t think it deserves the credit, but I also know that without it, I wouldn’t be who I am now.
You can follow Georgie Swallow on Instagram here.
As told to Josie Copson
This article was first published on June 22, 2025.
What is Hodgkin Lymphoma?
Hodgkin lymphoma is an uncommon cancer that develops in the lymphatic system, which is a network of vessels and glands spread throughout your body. It can develop at any age, but it mostly affects people aged between 20-40 and those over 75.
Around 2,100 people are diagnosed with Hodgkin lymphoma in the UK each year. The most common symptom of Hodgkin lymphoma is a painless swelling in a lymph node, usually in the neck, armpit or groin.
Around 8 out of 10 people with Hodgkin lymphoma live at least 5 years, and most of these will be cured. However, there’s a risk of long-term problems after treatment, including infertility and an increased risk of developing another type of cancer in the future.
Information taken from the NHS website
Do you have a story you’d like to share? Get in touch by emailing Josie.Copson@metro.co.uk
Share your views in the comments below.
19 Sep, 2025 | Admin | No Comments
We found a great alternative to Melania’s canary yellow state banquet gown (and it’s only £40!)
Metro journalists select and curate the products that feature on our site. If you make a purchase via links on this page we will earn commission – learn more
President Trump’s official state visit to the UK is in full swing and last night’s glitzy state banquet at Windsor Castle marked the most formal and fashion-filled moment of the two-day affair.
The Princess of Wales looked breathtaking in a couture gold lace gown by British designer Phillipa Lepley, paired with the iconic Lover’s Knot tiara that the late Princess Diana adored.
You’d be forgiven for thinking that with such a sparkling, incredible dress all eyes would be on Catherine, but it was Melania Trump’s bright yellow dress that stole the show.
Love her or loathe her, the First Lady opted for something quite daring for the lavish dinner: an off-the-shoulder, floor-length Carolina Herrera dress in canary yellow, with a pale pink waist belt and turquoise earrings.
ASOS DESIGN Fold Over Bardot Midi Dress in Orange
A sleek off-the-shoulder number, this ASOS DESIGN Fold Over Bardot Midi Dress in Orange features a fold-over Bardot neckline and figure-skimming silhouette. The bold colour is bright and uplifting and works for all seasons. Pair it with a pale pink waist belt as worn by Melania.
It may not have been to everyone’s taste but there’s no arguing that Melania’s dress was eye-catching.
And while Melania’s exact look likely came with a five-figure price tag, we’ve found a high street alternative that delivers all the drama without the cost.
Let’s state the obvious, the ASOS DESIGN Fold Over Bardot Midi Dress isn’t quite as bright as the Carolina Herrera number, but with long sleeves and a fitted waist, this off-the-shoulder dress bears a pretty striking resemblance to its designer counterpart.
Pair it with a chunky light pink waist belt — Lemon Daisy Accessories’ Vasia Women Square Buckle Belt (£25) is perfect for this — and voila! You’ve got the First Lady’s look without spending a small fortune.
Melania’s bold banquet look might not be to everyone’s taste, but it’s proof that colour, confidence, and a strong silhouette can still steal the spotlight.
And with this ASOS version, there’s no designer label or designer budget required.
Follow Metro across our social channels, on Facebook, Twitter and Instagram
Share your views in the comments below
There are things each star sign should do to prepare themselves for the incoming autumn equinox, from Cancer focusing on their family to Scorpio taking a break
19 Sep, 2025 | Admin | No Comments
'Married men are obsessed with me – I'm paid thousands just to speak to them'
Jolene Dawson, 29, is an influencer and model who has more than 16,000 followers on Instagram. She he admits married men can’t resist her, even going so far as to pay for her attention
19 Sep, 2025 | Admin | No Comments
'Low maintenance' friendships may seem appealing but could be a sign of something worse
It can be exhausting messaging your friends all day – but how infrequent is too infrequent? A relationship expert reveals whether TikTok’s ‘low maintenance friend’ trend can actually be healthy
19 Sep, 2025 | Admin | No Comments
Shoppers call Dunelm’s heated clothes rack ‘essential’ – and it costs just 7p per hour
Metro journalists select and curate the products that feature on our site. If you make a purchase via links on this page we will earn commission – learn more
When autumn/winter hits, the laundry pile can seem like a daunting task.
Piles of wet washing impossible to dry can mount up and if not dried fully, can develop a nasty musty smell.
While tumble dryers can help, they’re often expensive to run, bulky and not always gentle on your clothes.
That’s why a heated clothes airer is nothing short of an absolute must-have for all households.
There’s few on the market but the one we rate is Dunelm’s 3 Tier Heated Airer. Priced at £95, this heated clothes rack features three tiers that hold up to 15kg of washing and gives up to 20m of drying space.
Made from sturdy but lightweight aluminium, the household gadget folds flat for easy storage and is designed to be used with the 3 Tier Heated Airer Cover to speed up drying time.
It’s economical too and costs just 7p per hour to run so there’s no need to panic about high energy bills.
Sharing their rave reviews, one previous shopper said: ‘Great Product, very cheap to run but also gets the job done!’
Another reviewer wrote: ‘Wouldn’t be without this as a family of 4. Can easily have 2 loads of washing on it, dries quicker than a standard airer for much less than the cost of running the tumble dryer! I wouldn’t be without it.’
And another review said: ‘Really very happy with my heated airer. It is so was to use, works really well and speedily dries a whole washing load virtually overnight. It’s so lovely not to have endless damp washing.’
This autumn/winter, don’t dread the laundry pile. Instead, shop Dunelm’s 3 Tier Heated Airer and get the job done for less.
Follow Metro across our social channels, on Facebook, Twitter and Instagram
Share your views in the comments below
18 Sep, 2025 | Admin | No Comments
This £86 suit is the perfect alternative to Princess Catherine’s £1,370 Bella Freud look
Metro journalists select and curate the products that feature on our site. If you make a purchase via links on this page we will earn commission – learn more
Princess Catherine knows how to pull together a look and her latest outfit is proof.
Over the weekend, the royal paid a visit to Sudbury Silk Mills in a sharp grey checked suit that oozed sophistication.
The tailored two-piece, a Bella Freud number, looked chic and put-together and proved the princess has got effortless power dressing down to a tee.
But, if you’re wanting to shop the suit for yourself you will have to fork out a whopping £1,370.
Luckily, the shopping experts at Metro have found a brilliant high street alternative for just £86, saving you a massive £1,284.
Next Grey/Blue Check Single Breasted Sculpting Blazer
Featuring a grey/blue checked pattern and fitted cut, the Next Grey/Blue Check Single Breasted Sculpting Blazer is stylish and chic. Also available is the matching Sculpting Slim Leg Trousers (£32) for a full-on power dressing moment. Both pieces are machine washable and available in a range of sizes with Petite sizing available too.
Next’s Grey/Blue Check Single Breasted Sculpting Blazer and matching Sculpting Slim Leg Trousers (£32) feature a similarly smart check pattern and flattering, tailored fit that echoes Catherine’s designer look without the designer price tag.
Appropriate for the office but versatile enough for dinner or drinks, this suit looks a lot more expensive than it is but is brilliantly practical and suitable for chucking in the washing machine when it gets dirty.
Style it with a black crew neck top like Kate, and finish with minimal jewellery, a black leather belt and a sleek blow-dry to really channel the Princess’s style.
Not quite confident enough to go all-in on the suit? They work just as well as separates. Try the blazer with black wide-leg trousers or jeans and the trousers with a crisp white shirt.
Because, as this look proves, you don’t need a royal budget to dress like a princess.
Follow Metro across our social channels, on Facebook, Twitter and Instagram
Share your views in the comments below







