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Every morning begins with a negotiation.
You open your eyes and take stock. How do my legs feel today? Is the fatigue already settling in, or do I have a window? Can I manage the school run, or do I need to ask for help again?
This is what living with multiple sclerosis actually looks like. Not a steady decline, but a daily renegotiation with a body that refuses to follow the same rules two days running.
More than 130,000 people across the UK understand this reality intimately. The unpredictability that makes planning feel pointless. The exhaustion that arrives without warning. The grief of cancelling plans you desperately wanted to keep. The frustration of explaining, again, why yesterday you could manage something that today feels impossible.
Traditional mobility aids were designed for consistent conditions. A wheelchair assumes you need it all the time. A walking stick helps with balance but does nothing for the crushing fatigue that makes every step feel like wading through treacle.
For people with MS, these options create an impossible choice. Accept equipment that signals permanence you haven’t reached, or push through without support and pay the price in exhaustion, cancelled plans, and shrinking horizons.
The space between “walking fine” and “needing a wheelchair” is vast. Most people with MS live in that space for years or decades. But until recently, there was nothing designed specifically for it.
James Morrison was diagnosed with primary progressive MS at 52. A former rugby player from Cardiff, he’d always defined himself by physical capability. The diagnosis felt like losing his identity piece by piece.
When his daughter Emma announced her engagement, his first thought wasn’t celebration. It was calculation. The church in Bath. The reception venue with its gravel paths. The first dance. Walking her down the aisle.
“I sat down with a calendar,” James remembers, “and tried to work out if I could make it. How far was the aisle? How long would I need to stand? What if my legs gave out in front of everyone?”
He considered a wheelchair. But he could still walk on good days. Sometimes he could walk for an hour before the fatigue hit. A wheelchair felt like giving up on the good days to prepare for the bad ones.
“My wife found the ATTO online. I was sceptical. I thought mobility scooters were for people who couldn’t walk at all. That wasn’t me. Not yet, anyway.”
But desperation made him curious. He booked a home demonstration at their house in Milton Keynes. Within five minutes of trying it, something shifted.
“It folded up smaller than my golf bag. I could keep it in the boot and only use it when I needed to. Suddenly I wasn’t choosing between walking and not walking. I had options.”
On Emma’s wedding day, James walked her down the aisle. He stood for the photographs. When his legs started to tire during the reception, he slipped away, unfolded his ATTO from the car, and returned to the party. He stayed until midnight.
“Emma said it was the best gift I could have given her. Not the walking. The staying. Being there for all of it, not just the bits I could manage without help.”
James’s experience reflects broader patterns. Research from the UK MS Register found that over 55% of people with MS experience clinically significant fatigue, which has a direct negative impact on walking ability, psychological wellbeing, and quality of life. The study, drawing on data from nearly 21,000 UK participants, confirmed what patients already know: fatigue doesn’t follow predictable patterns, and its effects extend far beyond physical tiredness.
A separate survey found that 70% of people with MS identify mobility impairment as the most challenging aspect of their condition. Yet the fluctuating nature of MS symptoms means that standard assessments often fail to capture the daily reality. You might score well on a walking test in a neurology clinic and still be unable to make it around Tesco three hours later.
This disconnect between measured capability and lived experience creates particular difficulties. It can affect PIP assessments, workplace adjustments, and even how family members understand your needs. Invisible symptoms create invisible struggles.
The ATTO SPORT was engineered specifically for this reality. It folds in ten seconds, fits in any car boot, and weighs little enough that even on difficult days, deployment doesn’t drain your limited energy reserves. The design acknowledges that your needs at 9am might differ entirely from your needs at 3pm.
What rarely gets discussed is the mental burden of unpredictability. The constant calculations. The preemptive disappointment of assuming you’ll need to cancel. The guilt of asking for help again. The loneliness of a condition that others can’t see and often don’t understand.
Many ATTO users describe an unexpected psychological shift. They expected to feel diminished. Instead, they felt liberated.
“I keep it in the boot like you’d keep an umbrella,” one Movinglife customer explains. “I hope I won’t need it. But knowing it’s there changes everything. I say yes to invitations now. I used to say no by default.”
The option exists without requiring commitment. Good morning? Walk into the shop. Energy crashes halfway through? Unfold the scooter and finish your errands. No drama. No defeat. Just a tool, used when useful.
This flexibility matters because MS affects the mind as well as the body. The constant vigilance. The fear of being stranded somewhere public when your legs stop cooperating. The exhaustion of performing wellness when you’re anything but well.
The MS Society acknowledges that using a stick or other walking aid can help, particularly in open spaces or unfamiliar places. But they also recognise that MS mobility needs extend beyond what traditional aids address. When fatigue is the primary limiting factor, the solution needs to eliminate exertion, not just provide balance support.
The same principles apply to other fluctuating conditions. ME/CFS. Fibromyalgia. Long COVID. Lupus flares. Ehlers-Danlos syndrome. These conditions share a common thread: good days and bad days arrive without warning, and the ability to participate in life shouldn’t depend on which type of day you’re having.
A mobility device that adapts to variability gives you something medication can’t: control over participation. Not control over symptoms, but control over whether symptoms get to decide which parts of life you access.
The ATTO’s compact design specifically serves this need. Small enough to forget it’s in your boot until you need it. Quick enough to deploy that you’re not standing in a car park struggling whilst your energy drains. Stylish enough that you don’t feel like you’re hauling medical equipment. You’re simply carrying a solution.
Professional life particularly benefits from this flexibility. ATTO users report managing conferences, corporate campuses, and business travel with a confidence they’d lost. The device signals competence and preparation, not limitation. The meeting happens. The presentation gets delivered. The career continues.
Social life transforms too. The National Trust property you’d given up on? Accessible. The Christmas markets that span half a city centre? Manageable. Your grandchild’s sports day across a sprawling school field? Attendable.
Family dynamics shift in quieter ways. When you can handle errands independently, relationships stay balanced. Your partner remains your partner, not your carer. Your children remain your children, not your support team. The boundaries that keep relationships healthy stay intact.
For comprehensive resources on travelling with MS, including airline policies, cruise ship accessibility, and travel preparation guides, visit our travel mobility solutions page.
Living with variable mobility means making choices constantly. Will you bring the scooter today? Use it at this venue? Fold it and walk this section? Each decision requires reading your body honestly and responding to what is, not what you wish were true.
The people who report highest satisfaction with mobility assistance share a common trait: they made the decision proactively rather than reactively. They chose function over symbolism. They refused to let pride cost them participation.
Energy management with MS requires accepting a truth that ‘push through’ culture refuses to acknowledge: you cannot willpower your way past physiology. You can exhaust yourself trying. You can pay for it in days of recovery. Or you can use tools that extend your functional capacity and preserve your energy for what matters.
James still has difficult days. MS didn’t disappear because he bought a scooter. But last month, he took his granddaughter to Legoland. Next week, he’s flying to Portugal for a family holiday. He’s planning a trip to Edinburgh for the Fringe Festival.
“I stopped waiting for my body to cooperate,” he says. “I found something that works with the unpredictability. And now I have my life back.”
Your condition changes daily. Your mobility solution should adapt with you.
The ATTO was designed with input from MS patients and healthcare professionals. It features enhanced suspension to minimise jarring on sensitive bodies, higher ground clearance for varied terrain, and a comfortable seat for extended use. The ten-second folding mechanism requires minimal hand strength or energy, which is crucial when fatigue or weakness affects dexterity. Most importantly, its variable-use design matches the unpredictable nature of MS symptoms.
Absolutely. This is one of the ATTO’s primary design advantages. The compact folded size means you can keep it in your car boot as insurance and only deploy it when symptoms require it. Many users with MS and chronic fatigue conditions report using their scooter two or three days per week when symptoms flare, and walking on better days. Having the option available often reduces anxiety about outings, even on days you don’t end up using it.
ATTO scooters preserve energy by eliminating the physical exertion of walking whilst still allowing full participation in activities. For conditions where energy is the limiting factor, the scooter prevents the post-exertional crashes that can trigger symptom flares. Users consistently report completing full days of activities without the exhaustion that previously forced early departures or multi-day recovery periods.
Yes. ATTO scooters work across the spectrum of mobility needs. As conditions progress, the same scooter that works for occasional use transitions seamlessly to daily use. You’re not investing in equipment that will become inadequate as symptoms change. Models range from the compact ATTO Classic for occasional use to the ATTO SPORT for more demanding daily requirements.
Yes. Movinglife offers free home demonstrations across the UK, as well as showroom visits at locations including Milton Keynes. A mobility specialist will bring the ATTO to your home, answer your questions, and let you test it in your own environment. There’s no obligation to purchase, and many customers find that experiencing the scooter firsthand resolves uncertainties about whether it’s right for them.
This is one of the most common concerns we hear. You don’t need to reach a certain level of disability to benefit from a tool that preserves your energy and expands your participation. If you’re declining invitations, leaving events early, or spending days recovering from activities, a mobility scooter can help. The question isn’t whether you’re disabled enough. It’s whether this tool would improve your life.
The holidays have passed, but the year hasn't quite begun. These quiet days between Christmas and New Year offer something increasingly rare: time without urgency. This is the moment to create resolutions that mean something—simple commitments you'll actually keep. Discover why mobility solutions enable the connections and experiences that matter most in 2026.
This holiday season, consider giving a gift that expands possibilities rather than just adding to what they already have. When chosen thoughtfully, ATTO accessories become tools for maintaining the independence your loved one values most.
