I've been using Philips Hue lighting for many years now, and it's one of my very favourite bits of tech: I rent my home so Hue enables me to redecorate with light instead of incurring the wrath of my landlord. And as our "Hue mistakes everyone makes" article points out, there's lots of stuff going on that you might not know about and lots of features you might really benefit from.
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If I were starting from scratch today, I'd still go with Hue. I think it's the best smart lighting ecosystem you can have. But there are five things I'd want to know before I bought a single Hue smart bulb.
The Hue app is very good – one of the best smart lighting apps I’ve ever used - but you’re not limited to it. There are some fun third party apps as well as some more geeky ones; I used the latter to get some early IKEA Tradfri bulbs to connect to my Hue Bridge. Speaking of which…
You can cut the cost of a Hue system by skipping buying a Bridge, which is the Hue lighting hub. The most recent Hue bulbs work over Bluetooth – there’s a label on the box so you can be sure when you’re buying – and don’t need to be connected to a dedicated Hue Bridge. However, there’s a big but: you need to use the Philips Hue Bluetooth app, not the normal Hue app, and you won’t be able to use some of the more advanced features that only the Bridge provides.
Hue uses the Zigbee Light Link protocol and that means you can connect non-Hue bulbs to a Hue system; I’ve got some IKEA bulbs in mine, because they’re so much cheaper than Hue’s white bulbs. However you can’t use most third party bulbs with the Hue entertainment features such as music syncing or TV sync via the Play box, and they can be a little fiddly to set up.
Hue has the biggest bulb selection of any smart lighting ecosystem, but there are still some omissions: if your home has halogen downlighters that predate the GU10 fittings, such as MR16 bulbs, there isn’t a direct Hue replacement. And for bathrooms, the only safe Hue lights are the ones with IP44 ratings.
Once you start, you won’t stop. I started with two Hue spotlights in my living room. Today I have three Hues in the hallway (it’s a long hallway), two Hues over my dining table, four Hues, a Hue Play Sync Box and a gradient lightstrip in the living room and a Hue in the bedroom. I had to stop myself from putting Hues in the kitchen, and if I weren’t renting I just know I’d have Hues outdoors too. Like tattoos, once you get Hue you don't see where the Hue lights are; you see where they aren't, and where you could put some more.
From questions about my medical condition to offers of miracle cures and declarations of how ‘brave’ and ‘lucky’ I am, I round up 5 things not to say to a disabled traveller.
Here she is again, that wild-haired, wheelchair-using woman, moaning about all of the things people say that offend her…
I know that, mostly, strangers who say things without thinking are well-meaning. We’re all guilty of saying something daft when we feel a bit awkward, me included!
But when you’re disabled, there are certain things that people say to you time and time again – you get so used to hearing them that you’re almost expecting it. Then there are the questions or statements that are so shocking, you can’t quite believe a stranger just said that. You get flustered and mumble a response, and then spend the next 5 hours mentally coming up with slaying comebacks.
Travel, in particular, seems to magnify these situations, whether it be on a stressful commute when someone projects their irritation on to you, or a relaxed holiday when someone says something so unthinking, you wonder if they’ve left their brain at home.
I travel on my own, for work, usually by train, pretty much every week. It’s not always easy – assistance fails happen, crowded trains happen, luggage and buggies in wheelchair spaces happen. But, honestly, isn’t train travel pretty stressful for everyone, at least some of the time? Public transport can bring out the worst in people, and often we see the more selfish side of others when seats are limited or timetables are delayed.
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None of us can control how other people see us, and if someone admires the independence of a wheelchair user travelling alone, I don’t have a problem with that. But please, don’t tell me I’m brave; I’m just going about my everyday life like everyone else.
The reason I started blogging was to share my travel experiences with others, to show that accessible travel IS possible. If you’re a disabled person who wants to know about the best accessible restaurants I found on a recent trip, or my favourite accessible dog walking routes, or which hotels I recommend with wheelchair accessible rooms, I’ll always be happy to chat.
However, if you’re a stranger asking me how I manage to travel out of morbid curiosity – well you’re just going to piss me off. We’ve come a long way from disabled people appearing in 19th century freak shows, and we shouldn’t be made to feel like some twisted form of entertainment for the ill-mannered non-disabled people among us.
In my experience, this one is favoured by a particular brand of rude taxi driver. Maybe they’re bored, maybe they just don’t know what else to say, maybe they think it’s perfectly acceptable to ask a complete stranger for their medical history? I don’t know. What I do know is, this question is never ok. Never.
My favourite answers range from elaborate stories about thrill-seeking activities gone wrong, to “I have a highly contagious disease”, to “Oh I’m just really hungover today”, and the ultimate conversation shut down “Nothing, what’s wrong with you?”
This one isn’t exclusive to travel, but I have two very vivid memories of people enforcing prayer on me; once, in the supermarket at a train station, and another time in – of all places – a hotel sauna. These conversations have affected me so much that I remember them, years later, word-for-word.
I am, very happily, not a religious person. Those who embrace religion, I’m also very happy for. Some peoples lives are greatly enhanced by the power of prayer; my life is greatly enhanced by the power of gin. The upsetting part for me is the inference that I want to be healed, that my life must be so awful that I’m just waiting for the chance to be miraculously cured in the ready meal aisle at M&S. I LOVE my life – wonky, uncooperative, wheelchair using body and all – I wouldn’t be the person that I am without Cerebral Palsy, and I wouldn’t want to be anyone else.
This is a direct quote from a woman I met on my most recent holiday in Portugal. My response was, “Go and spend 10 minutes with him, then come back and tell me how lucky I am…” (It was a joke, Darren, I love you). It felt particularly intrusive as I was sat in the sunshine, engrossed in a book, sipping a cocktail – not giving off any kind of vibe that said I wanted to speak to a stranger. Still, this woman thought it a good idea to pull up a chair and tell me how fortunate I am that Darren decided to put a ring on it, despite the fact that I use a wheelchair.
I AM lucky to have Darren. He’s (obviously) lucky to have me. Disability just doesn’t come into it. We both have strengths and weaknesses, skills and things we’re not so good at – I make all the travel plans, he puts the bins out. We’re a team, a partnership; just like any other relationship.
You might be reading this thinking, well I’m just never going to speak to another disabled person again, you’re offended by everything! Honestly, we’re not.
By all means, ask me if there’s anything you can do to help me - but don’t be surprised or offended if I say thank you, I’m ok.
Ask me something completely unrelated to my disability – I’m a person too, my thoughts and interests don’t just extend to wheelchair ramps and accessible toilets.
Definitely tell me if my hair looks good – compliments may not get you everywhere in life, but they’ll make the recipient feel great!
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