Whilst a lot of people (us included) continue to work remotely, there will be others who need to start returning to work or travelling for other reasons. Whilst we are all still asked not to travel on public transport unless essential, for obvious reasons, a lot of people with vision impairments are unable to drive and are therefore more dependent on public transport than others. There’s a lot of info out there regarding safe travel (which can appear conflicting), so I (Vicky) thought I’d bring some of this information together, as well as us adding some of our own opinions.
 
Social distancing:
Although the 2 metre rule is still in place, this can be reduced to 1 metre plus in situations where 2 metres isn’t possible. If you are sighted, please remember that someone with a vision impairment may not be able to gauge distance and so you may need to move out of their way.
 
On trains and buses, it is advised that people travel side by side or behind other people, rather than facing them, where seating arrangements allow. Again, this might be difficult for a person with a vision impairment to gauge, and so speaking to that person and letting them know where there is a suitable space might be helpful.
 
Wearing masks:
The government guidelines are that masks or face coverings are compulsory on public transport. You should also wear a face covering in other enclosed spaces where it is difficult to maintain social distancing. For example, at stations, interchanges, ports and airports and in taxis and private hire vehicles. A taxi driver or private hire vehicle operator may be entitled to refuse to accept you if you do not wear a face covering.
However, there are exceptions to mask wearing for the following reasons:

• not being able to put on, wear or remove a face covering because of a physical or mental illness or impairment, or disability
• if putting on, wearing or removing a face covering will cause you severe distress
• if you are travelling with or providing assistance to someone who relies on lip reading to communicate
• to avoid harm or injury, or the risk of harm or injury, to yourself or others
• to avoid injury, or to escape a risk of harm, and you do not have a face covering with you
• to eat or drink, but only if you need to
• to take medication
• if a police officer or other official requests you remove your face covering

 
So our message is, if you see someone not wearing a mask they may have their reasons and these may not be obvious to you. Please be considerate with regard to this. If you are concerned for your health, then maintain your 2 metre distance where possible.
 
Guiding:
The rail companies and transport for London have been working on this and have advised their staff that ‘a layer of material may now be used as a barrier between the guide and the customer’. A recent podcast by Kaz, (who is blind), stated that staff have all been provided with plastic ‘sleeves’ that they can use for their ‘guiding arm’, although it seemed to be personal preference as to whether staff used them or not. If you need physical guiding or your route involves an escalator or lift on the London Underground then a taxi will be booked to take you to the next accessible point on your journey.
 
In our last insight (112.  Social distancing and shopping, Part 2: Being aware as a sighted person), I discussed that, as a sighted person, I would be prepared to guide a person, if we both agreed it was necessary. However, it is worth bearing in mind that other ways of assisting may be more practical, such as verbally explaining directions to someone or walking with them and talking through where you are going rather than physically guiding. When doing this, remember to avoid pointing and using such terms as ‘it’s just over there’.
 
#WorldUpsideDown Campaign:
A useful summary of how you might help as a sighted person has been put together by RNIB in their #WorldUpsideDown campaign. There is a video on Twitter (@RNIB) and also an online quiz to help others learn more https://rnib.in/WorldUpsideDownQuiz. Their campaign message is ‘Be aware, be kind and offer help if you can’.
 
I think our message would be simpler – be considerate, and don’t be too quick to judge. These are difficult times for everyone but will have had more of an impact on some people than others. As we all try and return gradually to life as it was before, we need to be aware that this will be harder for some than for others.
 
Other articles used for this Insight:
GOV.UK – Safer travel guidance for passengers: https://www.gov.uk/guidance/coronavirus-covid-19-safer-travel-guidance-for-passengers
 
BBC news ‘The new way to travel if you're disabled and use access’: https://www.bbc.co.uk/news/disability-52927781
 
The ramblings of Kaz -
My first train journey since lockdown - https://podcasts.google.com/feed/aHR0cHM6Ly9hbmNob3IuZm0vcy8yNDRhNjBiOC9wb2RjYXN0L3Jzcw==
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Following on from yesterday’s post (Social distancing and shopping, part 1: What does this mean for someone with a vision impairment?), we thought it might be helpful to write from a sighted person’s perspective and include ways that you might still be able to assist someone with a vision impairment.
 
Vicky: So how does all of this affect those of us with sight? Since lockdown started, my life has altered a fair bit. I am now completely working from home which has its challenges but I have also become involved with several community initiatives supporting people locally. One of these roles has included food shopping regularly for people in my local area who are elderly, shielding or just need support. So, whereas before I would do a bulk food shop online once a month (topped up with regular trips to our amazing local greengrocer often on my way to work), I now find myself shopping twice a week, once in our local Tesco superstore and then once in our local village. Since lockdown, everywhere has altered to some respect. I have to say I’m really impressed with our local Tesco’s – they have marked 2 metre queuing points outside, have hand sanitiser as you enter and a clearly marked one way system on the floor. Even my local greengrocer has risen to the challenge, with them only allowing 2 people in the shop at once (more queuing outside, thank goodness for the amazing weather we’ve had) and hand sanitiser on the wall as you enter.
 
All of these new ways of doing things are a necessity but it takes some getting used to (it still seems strange having to constantly give people a wide berth when out walking) and has raised people’s anxiety levels too. And that’s when you can see.
 
As Dave quite rightly states, lots of shops have signs explaining their specific rules but obviously all of these are visual. And finding the hand sanitiser without sight, even if you knew it was there, would be a challenge. Often people with VI need to pick things up to take a closer look – another ‘no, no’ in this new world of ours!! When I took the photo of the hand sanitiser in the greengrocers and explained what I was writing about, they said they would obviously help someone if they needed it and more local shops have also offered delivery services. There are also lots of local initiatives using volunteers similar to the one I have joined (details of these should be available via your local council), but as Dave said in a previous blog, none of this is the same as shopping yourself.
 
So as a sighted person what can we do?
 
If you are out and about (in shops or elsewhere) and notice a person with an obvious vision impairment (someone using a white cane or guide dog for example), please be the one to observe social distancing. If you are near the person, a cheery hello, would be good and, if necessary, you can let them know verbally that you’re moving out of their way, just as you might visually indicate this to a sighted person.
 
If you do think someone needs support, then the best way to do this is not much different to before. First of all, take time to observe the person rather than rushing in. If out, often the vision impaired person will know where they are going and, even though it may seem that they are walking in to buildings, this might be their strategy for knowing where they are, using building lines as navigational landmarks. If this is the case, then as a sighted person, be the one to move out of the way and maintain social distancing. If the person does genuinely appear to be lost or disorientated, then by all means, double check. This is harder to do whilst maintaining social distance as we would usually recommend a ‘hello’ and maybe a gentle touch to the shoulder, to enable the person to realise you are talking to them, so for now a hello will have to do, but try and make it obvious you are addressing them. If the person does need support, it may be a conversation about exactly where they are will be all that is required, or you may need to verbally re-direct them. If physical guiding is the only way, then you will both need to discuss this and ascertain what you are both comfortable with. If in a shop, again, you may be able to verbally assist them to ensure they can get what they need.
 
However, as before, the main point is to ask the person if they need any help rather than grabbing them and moving them where you think they need to go, or grabbing items for them that you think they want. In this case, maybe social distancing does have its advantages 😊
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

With lots more shops opening today and lockdown starting to unlock, where does this leave people who live with a vision impairment?
 
This is a topic that has been rumbling on across various social media platforms throughout lockdown and we have shared some of these on our Facebook and Twitter pages. It is now generating a bit more pace as lockdown eases and the concerns about social distancing rise amongst many including people living with a vision impairment.
 
Dave: As we’ve covered in our past couple of VIDA Insights, things haven’t changed a great deal for me other than having to work remotely and not getting out on my own mainly due to my fears of not being able to ensure a safe distance from other people. I don’t tend to use public transport that much as I prefer to walk where I can and, when not working remotely, have Vicky as a driver, but for people who rely on using public transport for getting to and from work or to do some essential shopping, it’s a different story.
 
Using public transport is a regular challenge at the best of times for people with a vision impairment but trying to navigate bus stops, train stations, ticket offices, etc. all whilst maintaining social distancing is almost impossible. Vision impaired people can usually request assistance on the rail network through National Rail’s ‘Passenger Assist’ scheme but currently they are asking that assistance is only booked for essential travel. Transport for London (TFL) have put their assistance for blind and partially sighted travellers on hold due to social distancing and staff safety which is understandable but will no doubt impact on travellers that rely on this excellent service.
 
Such issues are discussed in the article ‘Will it be worth it? The re-opening barriers facing visually impaired people’ that was recently published on ArtsProfessional.co.uk. Key extracts from the article read:
A “major barrier is getting to a cultural venue in the first place, given that public transport is effectively a no-go for most people with a visual impairment at the moment. Social distancing is too often compromised, and as the rules on this soften, local streets are becoming increasingly crowded. These concerns have a basis in hard statistics. Using measurements from Ordnance Survey, Esri UK has mapped and analysed pavement widths in Great Britain: only 30% are at least 3 metres wide, 36% are between 2 and 3 metres and 34% are less than 2 metres wide.”
 
The article also said:
“Practical support has been made even more necessary since the start of the pandemic, with a proliferation of visual signage about social distancing (distance markers, capacity restrictions and other changes to normal practices) and temporary changes to routes both on the streets and indoors. For those with some sight, and those able to move around independently, a venue should make any temporary signs or floor markings large, clear, and high contrast. Floor markings should also be tactile for cane users as well.”
 
But if you have no vision or not enough to see signage; what then? I read a Facebook post this week from my local shopping centre, @redhillbelfry,  regarding the changes they’ve put in place for when the shopping centre opens fully today (Monday 15 June). It read:
“For those of you who have not visited the Centre recently, please be assured that we have taken lots of steps to keep all our shoppers safe within the Centre. We ask that social distancing is maintained, you keep to the left throughout the Centre, wear a face covering, wash hands regularly (sanitiser stations available) and of course stay home if you have any symptoms.” The post also included the photo of the escalators as used above.
 
Again, I understand the need for social distancing and keeping 2m apart from other people but that is really difficult when you can’t see. I also suspect that the rules aren’t consistent in every shop so trying to do the right thing will end in tears! It just means that, for the foreseeable future, it will be safer for me to stay at home.
 
It’s not just me and my views; these are replicated across the country and likely the world. It is summarised nicely in an article and video published on BBC.co.uk of Louis Moorhouse, an 18 year old guy from Bradford. Louis explains the problems he is experiencing with his guide dog and what sighted people can do to help.
 
Ultimately, all whilst social distancing is required, getting around or accessing services is going to be really difficult for people with a vision impairment or who have a disability that requires an element of support from someone else. I suspect that, like me, that they will remain at home much more, only venturing out when it is really necessary and just hope that other people understand the problems that we face.
 
Part 2 of this blog will be out tomorrow – giving Vicky’s thoughts as a  sighted person and including ways that you might still be able to assist someone with a vision impairment.
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

So we’re in week 8 of lockdown and our Prime minister, Boris Johnson, announced on Sunday (10th May) that we can now take unlimited exercise each day, sunbathe in the park and meet 1 person from another household providing that we can maintain social distancing. Some industries are now allowed to re-open providing that it is safe for their employees but those that can continue to work from home should do so.
 
But what has it been like for people with a vision impairment during these times?
 
So lockdown itself and staying at home is actually quite normal for lots of blind and partially sighted people.
 
For me, Dave, I have a part time job that I do alongside running VIDA Training and the Disability Equipment Service with Vicky and this work gets me out of my house for part of the week, but on other days I work from home anyway. When I’m not working, I might walk in to town, pop to the local shop or meet up with friends for a beer but, on the whole, I would spend lots of time at home so lockdown hasn’t been too bad for me.
 
With regards to work, I have been lucky enough that I can continue to do my work from home with Vicky supporting me remotely, so although a change that’s taken some adjustments on both sides, we have been able to continue working.
 
However, the thing that’s had the biggest impact has been staying safe when going out and trying to maintain a social distance.
 
Even answering the door has become tricky. In the past I would have just opened the door and, if needed, explained to the person in front of me that I can’t see (that’s the phrase that I find works quickest in getting the message across), then taken the parcel, signed the PDA, etc. However, now, when the doorbell rings, I open the door to, if I’m lucky, a delivery driver stood at the bottom of the path shouting instructions on where the parcel has been left. If I’m unlucky, the driver is already driving off and I’m left feeling around until I find the parcel (although to be fair that did also happen sometimes before lockdown too!!). I’m guessing that this will be the same when we have drones dropping parcels off in the middle of the lawn! 😊 (smiley face)
 
Maintaining a 2 metre gap from other people is really tricky when you can’t see; you should try it. I find queuing difficult at the best of times but when everyone is supposed to stay 2 metres apart and no-one wants to touch you or you to touch them then it creates a massive problem. I’m fortunate that I’m married to Kelly who is sighted so she has been able to get out to the shops. However, for many people who live on their own, this option just isn’t available.
 
With supermarket online delivery slots getting booked weeks in advance and people with a vision impairment not classified as ‘vulnerable’ (so not on the supermarket’s priority customer list), food shopping became a real issue for people with vision impairments. Campaigning by the sight loss charities did help highlight this problem but getting through to the supermarkets on the phone to be recognised as a priority for online bookings was taking days. Some blind people were also refused support at supermarkets. Volunteer groups were available in some locations to help, and for others neighbours/friends or family stepped in, but this isn’t available for everyone and certainly isn’t the same as choosing your own shopping so takes away an element of independence.
 
And then there’s going out in general. Again, we’ve walked together as a family and therefore I’ve been guided around people to maintain social distancing – perfect. This has also meant I’ve been guided around objects too and therefore haven’t has to use my sense of touch that I often rely on heavily and which is also a big ‘no’ at the moment. However, if I had been living alone, this would have been another story and I quite possibly wouldn’t have ventured out at all. And again, it has also meant that I don’t currently go out on my own as I would have done before, again taking away another level of independence.
 
So, in conclusion, the actual lockdown and staying at home hasn’t been such a problem for me. It’s the social distancing measures that have had the biggest impact on my life as a person living with a vision impairment and I expect many other blind people will feel the same.  Oh, and for me, not being able to get my hair cut!!!! ((although that one probably applies to many people, vision impaired or sighted 😊 (smiley face)).
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information. 

With the UK in lockdown and all of us being asked to ‘Stay at Home’ other than for essential reasons (to buy food, visit a GP, collect medicine and, at the time of writing this, for daily exercise), what better time to catch up on some podcasts.
 
With our focus on vision impairment and disability, I (Dave) have selected a few podcasts that I subscribe too that I think you might find interesting. Obviously, they’re not all going to be to everyone’s taste (and are slightly skewed towards vision impairment as I am blind myself) but there should be something that is of interest to you.
 
So, in no particular order, have a search and listen to the following podcasts; they’re available on most podcast apps including Apple Podcasts, Google Podcasts, BBC Sounds, AudioBoom, Spotify and Stitcher to name but a few.

• Double Tap Canada

Double Tap Canada is the show where blind people talk tech! If you’re blind or partially sighted and have an interest in technology, this is the show for you. Everyone is welcome no matter how old you are or how much or how little experience you have with technology. Each week the team will help you better understand how technology can help your everyday life, even if you have little or no sight.

• Mosen At Large

Jonathan Mosen MNZM is a Chief Executive, advocate, entrepreneur, technology expert and broadcaster. Direct from his studio in Wellington New Zealand, Jonathan talks about anything that takes his fancy, from technology to music to politics to disability issues and much more. And listeners love to talk back. It's a captivating listen in which you can be informed, entertained, amused, in strong agreement and strong frustration all in one episode.

• Life After Blindness

Tim Schwartz presents a blog and podcast dedicated to the exploration of an enabled life with blindness.

• RNIB Tech Talk

Tech Talk is a podcast and radio show for blind and partially sighted people who are interested in accessible technology. Find out about the latest from specialist equipment to off the shelf solutions.

• Dot to Dot

A daily 5min Echo demo from Alexa. These short top tips and skills for the Amazon Echo are for everyone who’s simply dotty about Alexa.

• Blind Bargains Audio

The biggest names, the latest news, and leading insights from the field. Weekly Podcasts, interviews, technology demonstrations, and commentary from industry experts.

• BBC Ouch

The place where the real disability talk happens. Interviews, life hacks and things you don't say out loud. With Simon Minty, Kate Monaghan and the Ouch team.

• AppleVIS

AppleVis offers a wide range of podcasts covering topics of interest to blind and low-vision users of Apple Devices. Featured topics include walk-throughs and demonstrations of apps, tips on using iOS and Mac OS X, and accessory reviews.
 
If there are other vision impairment or disability related podcasts that you like and we’ve not mentioned, then please let us know; we’re always keen to learn about podcasts that we’ve not heard about or know of.
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Everyday words are easy to remember and spell, right? But when you’re asked to spell a slightly unusual word, a word that you always struggle with or a word that you’ve not had to spell for a while such as definitely, deteriorated or physiotherapist, do you find it easier to write it down? I would expect most of you reading this would say ‘Yes’.
 
I, Dave, have been meaning to write this Insight for a while now but to be honest, just haven’t got round to it. However, I have recently upgraded my screen reading software, Jaws, to the latest version which has lots of new features including announcing and playing sounds when I’ve spelled words incorrectly. Since this upgrade, I’ve realised that I make more spelling errors than I thought or I’m noticing them more now that Jaws is announcing them as I type!
 
I used to be a reasonable speller but as my sight has deteriorated I’m definitely finding spelling harder or I’m having to concentrate a lot more on spelling words that I might have quickly written down to visually check the spelling. Do you know what I mean? Writing down a word would just look right or wrong.  – I guess this is how we learn as a child? I now picture the word in my head and then spell it character by character as I type it. It is easy though to misspell a word or spell a word phonetically. This subject was also covered on a podcast that I regularly listen to called RNIB Tech Talk. The host, Steven Scott, is vision impaired and he spoke about how his spelling has deteriorated since losing his vision (RNIB Tech Talk link - https://audioboom.com/posts/7020255-amazon-apple-and-accessible-technology).
 
It is really common for people that have very little or no sight to spell words phonetically. This is usually because they’ve never seen the word and therefore have had to learn to spell that word by memorising it. Like most people, if you don’t use it you lose it.
 
I usually trip up on people’s names, especially if they’re not spelt in the usual way or have different ways of spelling them. For example, Martin/Martyn, Lee/Leigh, Shaun/Sean, Vikki/Vicky and there is always the names that aren’t spelt the way they are pronounced like Siobhan, Phoebe and Yvonne to name just a few.
 
It’s not all so bad though as we live in an era where the computer autocorrects mistakes as we type and, as I mentioned earlier, even my screen reader, Jaws, will announce when a word is misspelt! This is all fine when you’re in a word processor like Microsoft Word but isn’t as helpful when you’re in a programme that doesn’t autocorrect like Facebook! 
 
There is also the complication of knowing if you’re using the correct homophone and how you would know without spelling each word character by character. This is particularly the case when using dictation to input text. Dictation has come a long way but it still gets the grammar wrong occasionally so I, as a blind person, have to understand when to use the correct spelling – your/you’re, where/wear, by/buy, wait/weight, etc. Problems with dictation come up lots on social media posts and forums but there is no real solution to the problem other than to dictate clearly and, if it’s really important, to double check your entry.
 
I did do a quick Google on this subject to see if there had been any study carried out but drew a blank on this. However, I did find another blog called Spelling Inside Out: Developing visual memory. This wasn’t vision impairment related but was interesting nevertheless as it covered how we learn to spell and how children nowadays aren’t using their visual memory as well as they used to probably due to computers and technology. (Link to the blog ‘Spelling Inside Out: Developing Visual Memory’ - https://sis4teachers.org/2018/08/5123/).
 
Vicky: This is an interesting one, and I think Dave’s quite right in that spelling is quite visual, or at least getting spellings correct is quite visual. By that I mean that not only might we write words down to see if they ‘look right’ when we want to check how to spell them but also we see words regularly when we read them and therefore have a regular reminder of how they are spelt. When we’re working together Dave will quite often ask me how to spell a word. My spelling’s usually ok (apart from sociable – what a weird word that is, I always want to spell it out loud as socialable), so usually I can just answer but on the odd occasion when I need to write it down to double check, he tells me I’m cheating, not entirely fair as he’s asked me how to spell it – 😊 (smiley face)!!
 
However, it’s not always the case that seeing a word makes it easier to spell. My daughter’s dyslexic and we were told to encourage her to read more as a young child to enhance her spelling, (again the reason being that the more you see different words the more likely you are to have a visual memory of them) but that’s not an easy task if reading is hard in the first place and also if you mistake some letters for others!
So, although she can see the words, she still struggles to recreate them as to her they look different once she’s written them, or else she can’t see where they’re wrong. Having just read the article Dave mentions above, ‘Spelling Inside Out’, I have to confess that I personally think this would have just sent her head spinning as a child and I can’t imagine how it could have done anything other than confuse her but if it helps some kids then obviously that’s great.
 
And believe me Dave, you’re probably much more conscious about name spelling than most sighted people I know, and trust me with a name like Vicky, I know what I’m talking about (Vicki, Vikki, Vickie, Vickey to list but a few of the variations I’ve received, and that’s after I’ve spelt my name or they’ve seen it written down!).
 
What Dave has missed from this (unlike you Dave not to point out your positives 😊 (smiley face)) is that Dave is excellent at noticing typos. So, as he says, although he might not pick up on the where and wear type errors, he’ll certainly notice a typo which visually a lot of people will miss. This is because, visually, we will read what we expect to be there, but when listneing to Jaws, it will of course, read out exactly what’s written and therefore typos become more obvious. So he’ll have noticed (and hopefully not corrected when proof reading this!) that listening is spelt incorrectly in the last sentence.
 
What does all this mean? Well for us, if we’re producing documents, it means we make a pretty good tag team!!
 
Leave us a comment telling us how you manage. Do you write down words that you find tricky to spell? And if you’re vision impaired, what coping strategies do you have for spelling correctly?
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

I know, an interesting title to choose isn’t it. Its actually a modern day adaptation of Shakespeare’s Richard III, set in an American high school when they are choosing senior election candidates.
 
I, Vicky went to see this recently with a good friend and colleague of mine who had seen it advertised via Disability Rights UK (https://www.disabilityrightsuk.org/). It was playing (until recently) at the Donmar Warehouse (https://www.donmarwarehouse.com), a theatre just outside Covent Garden.  I think the description of the play on their website as ‘darkly comic’ is pretty accurate – the play was really funny in parts (although I think I missed some of the less common Shakespeare references), but also quite disturbing in others and definitely dark! The acting was truly superb, with Daniel Monks certainly portraying a dark and disturbed Richard to the full. In the play, Richard has hemiplegia, as does Daniel himself and the play explores how people perceive and behave towards Richard (and how Richard thinks they perceive him) maybe as a result of this.
 
Although the play was 1 hour and 45 minutes without a break, the time flew by, all credit to the intensity of the acting.
 
Prior to the performance we were lucky enough to have a touch tour organised in conjunction with VocalEyes (https://vocaleyes.co.uk/) a charity providing audio description to ensure plays are accessible for people with vision impairments (my friend has a vision impairment). We were able to wander around the set, getting a sense of the location of different items and also feel some of the costumes that the characters would later be wearing.
 
On this occasion the touch tour also included an opportunity to meet some of the main characters, who gave an introduction as to who they were, described their physical characteristics and also spoke in the accents they would use in the play so people could associate those voices with the characters when they came on stage. My friend and I chatted for a while to Ruth Madeley who plays Bucks in the show. Bucks is in a wheelchair as is Ruth herself. I recognised her from her role in the TV show ‘Years and Years’ and also ‘The Accident’. It was lovely to meet her and also hear about future projects she is involved in. She told us that when they were looking for actors for this play, the playwright had specified that hers and Richard’s parts must be played by disabled actors stating ‘They are out there, you just have to find them.’
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

I’m sure that this is a question that people mutter to themselves when they see me walking along in the rain. And just recently we’ve been having a lot of torrential downpours which I’ve been caught out in that have soaked me!
 
Back in November 2017 we wrote an Insight called “Rain… a sensory landscape…” (https://vidatraining.weebly.com/blog/34-rain-a-sensory-landscape) which touched on my experiences of rain. This insight covered all aspects of rain including the sounds it makes, the sensory landscape that it gives me and the reason why I don’t put my hood up. What it didn’t cover is why I don’t use an umbrella.
 
As a blind person, I rely heavily on my hearing to navigate and orientate myself. If I put a hood up then this muffles the sound and removes lots of the directional sounds that I rely on. For this reason, I prefer to hear and get wet than restrict my hearing and remain dry.
 
So the umbrella… Yes, using an umbrella would be a solution to my problem – hooray!
But no, I find using an umbrella just as difficult. Yes, it does mean that I can still use my hearing effectively but it causes other problems.
 
I use a white stick (or long cane to use its correct name) to navigate and get around safely. Obviously this takes up one hand and the other hand I like to have free so that I can use it to help identify objects if I need to or be able to protect my face if I walk through overgrown trees etc. If I had to hold an umbrella then I wouldn’t be able to do this. The other problem with using an umbrella when you can’t see is that you are forever getting it caught on trees or hedges, knocking it against walls, lamp posts or vehicles or worse still poking people with it. Ultimately they’re more of a hindrance and danger to others than a help.
 
However, I recently received a gift from my children that solves this problem… a hands-free umbrella! J Yes folks, this is an umbrella, as demonstrated in the video clip, that pops up and attaches to your head using an elastic headband – no hands!
 
Not only does it make me feel like Inspector Gadget and want to say ‘Go go gadget umbrella’ when I put it on, it makes me look a tiny bit sillier than I already do. Practically it solves one of my problems by not having to hold the umbrella but I still would have the same issues with brushing it against trees and branches or catching it on lamp posts and other objects.
 
Ultimately it was a fun present that I’ll use on our training or for embarrassing the children in the school playground but not something you’ll see me wearing sensibly when it’s raining. 
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Dave: “If you could see for 1 minute, what would you look at?” This was a question posed to me late one evening by a friend when we were talking about my vision impairment. It took me a bit by surprise as I’ve never been asked this question before and I didn’t know how to answer it.
 
My answer at the time was “probably my family; seeing my wife again and also what my kids actually look like”. However, we then went on to discuss perhaps scenery; looking at the horizon again, etc.
 
I wanted to write an Insight about this question as it’s really got under my skin. I’ve thought about the question long and hard and I still can’t think of what exactly I would do or look at in that minute. I’ve also thought about what I would look at if I could choose how to use the minute; for example, what if I could have 6 x 10 seconds of clear vision or 12 x 5 second windows of clarity… and have these over a period of time.
 
Ultimately I would want to see my family; my wife, kids, parents and extended family. But would a minute be enough? Perhaps a few photos so that I could scan them quickly rather than seeing them in person as I’m sure this would cause delays or take up valuable time somehow. But what else? I would be interested to see what the graphics are like on new game consoles, what HD TV is like, try a virtual headset, see what cars actually look like and see my house in a way that I’ve not seen it before. To be able to see the leaves on trees again, blades of grass, ants on the pavement and birds in the sky… and what about watching a firework display, seeing the moon and stars in a dark sky or watching a sunrise or sunset over a horizon? What do my friends and work colleagues look like and how much has changed from what I remember from the past (road signs, new buildings, etc). There are so many things that, when I really think about it, I would want to see…
 
So I can think about the question and plan my minute of clarity but, unless there is some kind of breakthrough in medicine or technology that restores my vision, it’s never going to happen… and that’s a bit depressing! :-(

So, put yourself in my shoes (I’m a size 10) and think about the question. What would you do with that minute?
 
Vicky: Gosh, your shoes are way too big for me Dave (I’m only a size 4!). And, although my feet clearly fit inside them, its always hard to put yourself in anyone else’s shoes isn’t it. And I’m conscious that as a sighted person, do I have the right to answer this question? However, Dave and I have discussed this question and he’s asked me to comment.
 
So, what would I want to see if I hadn’t seen for a long time and only had a minute? I’ve thought long and hard about it. Funnily enough – seeing the latest tech (as Dave mentioned) never entered my head (it’s just not my thing) but I do love sunrises and sunsets, and also wondered if I would like to see the beach again at Polzeath in Cornwall – a place that I love and where we have spent many happy family holidays.

However, I have my visual memories of these (would I still if I hadn’t had sight for a long time?) so maybe I would rather not waste my minute on these. So then I wondered about things I hope to see at some point in the future and, if I lost my sight before I saw them, would I want to use my minute to see them? Things like the Grand Canyon, the pyramids, and Meteora – possibly not possible to see all these in one minute :-)
 
So back to the reality of just one minute, and I have to ask myself, is seeing these places really what is important to me?
 
So, I think what I would spend my minute doing is gazing at my loved ones and how they’d changed since I lost my sight – how my kids had grown up etc. and just drink that in for a full minute to try and capture it all in my memory.
 
My only concern about all of this is, would having just one minute be almost more painful when it was snatched away at the end?? And I don’t profess to know the answer to that one.
 
What about other people, what are your thoughts? 
 
Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

We, Dave and Vicky, took ourselves up to Sight Village South East last week, along with a friend, Gary who works at Sight for Surrey as their Assistive Technology Trainer.
 
Sight Village is the name given to the exhibitions that are organised and run by Queen Alexandra College. There are 5 ‘Sight Village’ exhibitions held throughout the year (South-West, Central, West Midlands, North-West and South-East) and are described as “The UK's leading exhibitions for blind and partially sighted people and for those experiencing sight problems”.
 
To be honest, Dave and I had discussed whether we would go again this year as we’ve been for the last few years, but we decided that we should – and we’re really glad we did.
 
Having fuelled up with breakfast en route, we made our way to High Street Kensington Tube. There were Sight Village volunteers at the tube ready to sight guide or support people to the venue itself, we declined their offer of assistance though as the 3 of us were managing okay. A guy called Steve also asked if he could just walk with us, which was fine, we joked about us all getting lost together and me not having another guiding arm available but Steve was ok just to follow us and as it’s only a brief distance we all got there ok.
 
Once we arrived, following the obligatory photo to prove our attendance, Dave, Gary and I went straight into the main hall. Many of the stands were familiar and focussed on CCTV and OCR technologies. We took the opportunity to head to the Sight and Sound Technology stand and, at Gary’s suggestion, managed to get our hands on and explore their MiniVision and SmartVision 2 mobile phones.
 
We then chatted to Barclays, mainly about the current issue Dave has regarding the recent App update not reading transaction dates on the statement correctly. As always they were keen to know about this and Dave gave them a demo of what’s wrong. They promised to pass it on to their Digital Access Manager the following day – let’s hope it gets corrected soon!
 
As the Amazon stand was quiet, we took the opportunity to have a quick listen to the new Amazon Echo Studio, a beefy smart speaker that will play streamed HD audio quality music. This sounded lovely but we were informed that presales were more than 700% greater than expected so, even though it goes on sale this month, they’ll not be available to purchase until at least February 2020, although currently showing on Amazon as retailing at £189.99 and available from 25th December 2019 – probably not one for this year’s Christmas list though.
 
We had a brief chat with Kevin at the Look UK stand and found out about the charity, the support and information they provide to young vision impaired people and their families and their peer mentoring service for vision impaired students aged between 11 and 29.
 
Gary was keen for us to have a look at the Synapptic TV Box. We had a demo of this from Ken at their stand. If you’re looking for a fully accessible way of watching live or catch up TV, catching up with box sets, keeping up with your emails or doing some online shopping, then this might be the ideal solution for you!
 
Our next stop was at the En-Vision America stand where we met and had a long and interesting chat with David. He demonstrated the audible prescription service called ScripTalk, a service that has been available across the USA and Canada for several years. En-Vision are keen to bring ScripTalk to the UK and David was at the exhibition trying to raise the awareness of the product and to engage with vision impaired people and get their views on the service. We all agreed that this is a great product and a service that should be available in the UK. Its definitely something that we’ll be shouting about, demonstrating on our training and raising awareness of over the coming months.
 
The traditional white cane has been around for years and companies have tried to bring it in to the 20th century by adding GPS and motion sensors but no-one has yet put lights in it… until now! Lighting up the exhibition halls was Dave from ‘Gizahand’ with their new illuminating long cane. This was a cool product that was designed to help a person using the long cane be more visible to other pedestrians, cyclists and drivers. Basically the bottom quarter of the traditional folding cane has been replaced with a durable opaque section that is filled with LED lights. It’s powered by a USB power bank that fits in to the top of the handle and provides over 3 hours of light from a 2 hour charge. Although a fun idea, at £129.95 + delivery, it’s another item that won’t be finding its way on to Dave’s Christmas list this year!
 
During our rounds, we stopped off and had a long chat with Andrew from TravelEyes. It’s always great to catch up with him and we chatted loads about Amir Latif’s recent TV programme Travelling Blind and all the other things he’s now up to. Dave and Gary both entered their competition to win a trip to Burma (the offer was only available for VI people otherwise I (Vicky) would’ve been straight in there too!!). Going on one of their holidays is still something I’d love to do, but it’s just not feasible at the moment with family commitments etc.
 
We bumped into Stella from the Macular Society, a friend and previous work colleague of both Dave and Gary’s and as well as taking the opportunity to wish her a happy birthday, we also caught up with the work they are doing.
 
And finally we took the opportunity to sit in on the ATW Solutions seminar where we met and heard from Colin Fowler, the founder of ATW Solutions. He discussed how they can help with Access to Work (ATW) applications, propose reasonable adjustments within the workplace and provide recruitment services for employment support workers.
 
One thing we did all notice was that the exhibition was less busy this year and that there is definitely a lack of organisations with ‘daily living’ products now exhibiting. Let’s hope that this is a blip and that next year there will be more exhibitors with a wider range of products for us to have a look and feel of! J
 
That said we found out about some interesting products and services, enjoyed catching up with several people and will definitely be making the effort to attend again next year.
 
Direct links to products and organisations we visited:
 
QAC Sight Village - https://www.qac.ac.uk/exhibitions.htm
 
Sight and Sound Mobile Phones - http://www.sightandsound.co.uk/hardware/mobile-phones.html
 
Barclays Accessibility (Sight) - https://www.barclays.co.uk/accessibility/sight/
 
Amazon Echo Studio - https://www.amazon.co.uk/amazon-echo-studio-high-fidelity-smart-speaker-with-3d-audio-and-alexa/dp/B07NQCKJSH/ref=sr_1_1?keywords=amazon+studio&qid=1573214695&sr=8-1
 
Look-UK - https://www.look-uk.org/
 
Synapptic TV Box - http://www.synapptic.com/products-tvbox.aspx
 
En-Vision America (ScripTalk) – https://www.envisionamerica.com/products/scriptability/scriptalk/
 
Gizahand Illuminated long cane - http://www.gizahand.co.uk/illuminated-mobility-long-cane/
 
Traveleyes - https://www.traveleyes-international.com/
 
Macular Society - https://www.macularsociety.org/
 
ATW Solutions - https://www.atwsolutions.co.uk/
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Why are lamp-posts not soft and bendy? This is a question that I, Dave, seem to be asking myself on a regular basis at the moment.
 
Over the past few weeks I have come in to contact with a few metal posts whilst walking in to town. You know the type; they are the thick metal ones that usually are holding up road signs or a street lamp; the hard metal, non-forgiving ones.
 
My assumption is that they haven’t been breeding or the council haven’t spent more money erecting new ones and that they’ve always been there and that I’ve always managed to navigate around them, be that with Errol, my old guide dog, or with my white stick.
 
So, something has changed and, discussing this with Vicky, I can only conclude that I’m hitting these posts now due to my sight deteriorating to a point that I now don’t receive any indication that they’re there. Its weird because, if asked, I would have said that I haven’t been able to see them for ages, but whilst they haven’t been clear, we can only assume that I was getting some sense that they were there and therefore managing to avoid them whereas now I don’t even get that.
 
No doubt that there are many people reading this and wondering what my stick is for if it’s not to help identify these posts so that I don’t walk in to them and you would be right. The white stick is designed to be swept from left to right, going just beyond the width of my shoulders, and therefore should make contact with and alert me to objects that are in my path. I would then be able to identify the object and navigate safely around it. Well that’s the theory! In practise, even when sweeping the white stick correctly, it is easy to just miss an object as you sweep and, especially if it’s just off centre and not very big (like a lamp post), not  know about it until you hit it with your knee and/or shoulder or sometimes head.
 
A few weeks ago I bounced off the post in the photo. This is a particularly hefty post situated near a bridge on the busy A23, my route to Redhill town centre. I was walking home, had just gone under the bridge and, as I came out from under the bridge I was thinking about a car on the pavement that I had had to navigate on my way in. Right at that point, I was also overwhelmed with the noise from a train passing overhead, a large lorry passing on the road creating an echo under the bridge and also the noise of a crane or mechanical equipment operating nearby and then boom… the noise of a metal pole hitting my head!! I’ve no doubt that someone in a car or walking near me would have seen it and I wouldn’t blame them if they had a small chuckle at my expense but I can tell you that it hurt… it also bent my sunglasses and split the skin above my eyebrow!
 
So I have put this in the memory bank and haven’t hit this post since. I had also put hitting this down to the noise and nothing more. However, just this morning it happened again. It wasn’t the same post but it was on the same road!
 
I must admit, I don’t walk in to town as often now as when I had Errol and this is partly due to not having a need to but also a bit of ‘can’t be bothered’. I would consider myself to have good cane technique and be safe with using it, however, these couple of incidences have knocked my confidence and brings home how difficult getting out and about really is. I do find that I’m having to concentrate lots more when out on my own and that I get tense in the shoulders and I’m sure that this is partly due to not really knowing if I’m going to hit anything…
 
I wanted to share this with you all, not for sympathy, but to raise your awareness as to what it is really like for blind people using a white cane. Getting around with a white cane is slow, sometimes frustratingly so, and requires lots of concentration. I have a map of the town in my head that I recall all the time but this map isn’t just where roads are, but references key points/landmarks on a journey, pedestrian or safe road crossing points, particular areas where pavement parking is bad, etc. I also have to remember where particular shops or houses are or obstacles such as trim trail equipment in the school playground! It doesn’t stop there, I then remember where steps are, where doors are and whether they swing in or out and then what’s inside… where the reception or customer service desk is, what other hazards might be waiting, etc. This all requires a certain level of concentration and if this slips or I get distracted (this could be by a car parked on the pavement or a loud noise as in the example above, or one of those pesky A frames, anything really that I’m not expecting) then I could get injured or lost very quickly!
 
A good example of a hazard/obstruction can be read in a Facebook post that I wrote back in June when  I came across a builder’s van parked over a designated safe crossing point at the top of our road - https://www.facebook.com/705702186224015/posts/2160066160787603?s=725461053&sfns=cl
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Vicky: Dave and I have both read and enjoyed books 1 and 2 of this series – The Rosie Project and The Rosie Effect. My book club has also read at least book 1 (we’re a pretty rubbish book club – more a wine and crisps club - so don’t put any store by the fact that many of them won’t have read any further. **Update, one of our members has read all 3 and gave this one a 10/10!!**).
 
The books are described as feel good and they certainly are, leaving you with a warm feeling and hope about humanity (much needed at the moment) but they are deeper than that.
 
The books are narrated by a genetics professor, Don Tillman and the first one is about his quest to find true love. Don has never been on a second date and finds social situations hard to read, therefore he devises a chart to find his suitable match. Things understandably don’t quite go according to plan. The second book continues with his relationship.
 
The books make you smile and even laugh, but only ever with Don the narrator and never at him. His way of describing and relating to the world may not be familiar to many of us but it is intriguing and at times enlightening.
 
Although I would urge everyone to read all 3 books, it’s the third book that I felt was worthy of a mention on this blog as it relates to a lot of discussions held within the wider disability community and touches on subjects that we discuss in our training. Unfortunately, RNIB Talking Books have not yet caught up, so Dave has been unable to read it yet.
 
This third book, ‘The Rosie Result’ is set later in Don’s life when he also has a son, Hudson. The book covers a year in their lives and, with lots of anecdotes along the way, uses situations and other characters to cleverly raise questions about acceptance and fitting in, making the reader consider that maybe this shouldn’t be a one-way street, i.e. it shouldn’t all be about the person in the minority feeling pressurised to fit in with the majority.
 
There’s a great analogy at one point by a speaker talking about the social model of disability – ‘Imagine everyone used wheelchairs except you and society was designed to accommodate them, you’d knock your head on door frames and have to ask for chairs at restaurants.’
 
It’s a great read and one that should have us all questioning how we behave and react in society. I don’t want to ruin the story for you but a few quotes will hopefully give enough of a sense of this book to encourage you to read the series…
 
‘Hudson preferred to wear the summer uniform, with shorts throughout the year. The school rules specified that Years 5 and 6 boys were to wear long trousers in the cold season, other than in exceptional circumstances. Hudson had argued that as he was the only student who wanted to wear shorts, he was exceptional, and therefore should be accommodated. After extensive discussion, the school agreed.’
 
Talking about ABA (Applied Behaviour Analysis) ‘Psychologists and parents love it. Of course they do, because that’s who it’s for – not for the kids being trained like puppies…She’s being trained to spend her life seeking approval from others.’
 
‘…a lot of people think autistic people are weird and uncaring…my parents and teachers tried really hard to help me fit in because they didn’t want people to think I was autistic and then assume those things about me…but it took a lot of work that I could have spent on other things…what I learnt is that autistic people shouldn’t have to do all the changing’
 
‘I’m not a person with autism any more that I’m a person with lesbianism. I’m lesbian, I’m autistic. When I get a cold, I have a cold; I’m a person with a cold and I want to get rid of it. Medical help appreciated. But being autistic and lesbian, that’s who I am, and I’m not interested in anyone trying to cure me of who I am.’
 
‘I would never have the intuitive sense of others’ emotions that supposedly is needed to deal with interpersonal problems, but I had done my best using rationality, experience and hard-won learning about human behaviour and these skills had been sufficient.’
 
And the final word must go to Graeme himself:
‘This series of novels was inspired and informed far more by life experiences – my own and others’ – than research. Thanks to everyone – all of you – who contributed to those.’
 
We urge you to read these books and let us know your thoughts!
 
Dave: Well, all that has done Vicky is make me want to read it; it sounds intriguing and interesting. Come on RNIB… how long will I need to wait until this book is available in an audio format?
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

We’re asked many questions on our training sessions but it’s the first time that I (Dave) have been asked this one – “Did your wife dress you this morning?” Now of course I expect my wife to dress me every morning but the reality is that she is usually still asleep when I’m getting dressed so the answer to this question is “No”.
 
After we had all had a chuckle, we established that the actual question she was asking was “Did you choose your clothes or does your wife choose them for you?” She wanted to know how I, or blind people, choose their clothes because she thought this must be difficult if you can’t see.
 
It is actually a really sensible and good question and my answer was something like:
 
“It is relatively easy for a man to choose what to wear (or me anyway). I tend to wear jeans (blue and black) and then either a polo shirt or a smart casual shirt but pretty much I can put any top with any jeans and it’ll be fine. My VIDA training shirt has an embroidered VIDA Training logo so this makes it easy to identify but I keep my training clothes together in a particular part of my wardrobe so I know where it is when I need it”.
 
However, for women it is likely to be harder due to the array of clothes (basing this fact on my wife’s wardrobe) and the importance of matching colours, styles, etc. Ultimately most vision impaired people will have a very organised wardrobe and be fully aware of what they have in it, what colours the items are and what they go with. 
 
I do get help with pairing my socks after they’ve been washed as I like to wear stripy socks or socks with coloured toes or soles but if I didn’t have help to do this then I would use pegs to pair them when I take them off so that they come out of the washing machine together. I don’t feel it appropriate to talk about my pants… surely that’s taking it too far! :-)
 
In years gone by people used to sew different shaped and sized buttons in to their clothes so that they could then identify what an items colour was and what it went with by the shape or size of the buttons. Obviously you had to remember the relationship of each shape and size button but for some people this really worked and some still use this method today.
 
A few years ago RNIB released a gadget called the Pen Friend. This is a scanning gadget that is used for many purposes including food items, DVDs/CDs, important letters and much more. It is also a great gadget for identifying clothes. It works by reading labels that have a unique bar code that You scan and record a description to and when you re-scan the label it reads out the description. You can get labels that are washable, freezeable, stickable and some that attach with a tie making this a great gadget for so many things.
 
I guess nowadays there are also new apps coming out all the time that will be able to help. The Be My Eyes app could be used to get support with identifying clothes as could the Aira service that is soon to be released in the UK; you would just need to be careful when using one of these video call apps that you had at least your underwear on!! :-)
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information. 

No this is not our combined age (though not far off eh Dave 😊) but equally surprising is that Dave and I (Vicky) can’t believe we’ve written and posted 100 VIDA Insight blogs over the last few years…where did all that time go?
 
We really hope that you’ve enjoyed reading them as much as we’ve enjoyed thinking about topics and writing them. Most of our posts have been based on our own experiences but some have been based on books we’ve read, conversations we’ve had or other articles that have got us thinking. We hope they have provided you with some insight about vision impairments. We also hope that, on occasions, they’ve made you laugh.
 
So, just in case you haven’t been reading them or have come late to the party and only seen a few, here’s some of our highlights (of course you’re welcome to read all 100):

• The first one to mention has to be Dave’s heartfelt blog about Errol, his wonderful guide dog who suddenly and very sadly had to be put to sleep in June 2017. We can’t believe that this is now over 2 years ago – In Memory of Errol (13.06.2009 – 22.06.2017)
• Our Dans le Noir experiences – Dave’s visit in August 2017 described in blog No. 86 Dans Le Noir - Dave’s Experience  & my visit the year previously for my husband’s 50th birthday – No. 19 Celebrating at Dans Le Noir
• Dave’s various posts about his experience of using technology – No. 97. Be My Eyes: My Experience; No. 87. Accessible TVs in honour of #WorldTVDay and his series of 3 starting with No. 42. Blind Tech Part 1
• My posts about the books that we’ve read over the years which relate in some way to vision impairment – our favourite one being Touching the World by Cathy Birchill and Bernard Smith. We would recommend this wonderful book to anyone, about 2 people travelling the world on a motorbike, one of whom happens to have RP (Retinitis Pigmentosa, one of the eye sight conditions Dave has). Our blog about this one was No. 48. Touching the World. In reading various books, we’ve come to realise that we prefer the ones written by people with first hand experience – either by a person who is themselves vision impaired or co-written by one person with a vision impairment and one person who is sighted, so we also wrote a blog about this – No. 75. First hand experiences
• Answers to questions we get asked and interactions we have with people – No. 88. Do you forget Dave is blind?; Our ‘I thought you were blind?’ series starting with post No. 72. I thought you were blind, part 1; No. 90. Anytime, Anywhere…; No. 53. Access All Areas and No. 6. Sorry, who are you - part 1;
• Hints and tips (hopefully) gained by us working together – No. 70. Playing to Our Strengths; No. 50. Help, Hindrance or Interference; No. 49. Stirred not Shaken; the rest of our ‘Sorry, who are you?’ series – No. 7. Sorry who are you? Part 2 and No. 8. I’m just going for a wee! (or Sorry, who are you?... Part 3) and our series on Communication, starting with No. 11. See you tomorrow...(Communication Part 1)
• And finally, mainly here because they cover one of our favourite topics – food!! (But also because they cover everyday experiences and touch upon gadgets and technologies that might be helpful to others) – No.23. Food…#BritishFoodFortnight; No. 27. Blind Baking Part 1 and No. 28. Blind Baking Part 2; No. 30. What’s in that sandwich? #NationalSandwichDay and No. 61 Argh…Where has my burger gone?

 
Please have a read of any of these that catch your interest or as I said before, feel free to read the full 100! And, please do feel free to share your experiences and thoughts by commenting…
 
We will continue writing a monthly blog so please check in on the 15th of each month to read our latest one.
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Dave and I (Vicky) have recently read (Dave in audio format, Vicky in paperback) this book by Nicola Naylor about a woman with a vision impairment travelling around India. Having been enthralled by India from childhood, this was a lifelong dream for Nicola, but also being an aromatherapist in the UK, she wanted to learn more about traditional Indian medicine too.
 
One review I read (courtesy of Good reads) described the book as
“A traveller without sight takes her dream trip, alone and unsupported, learning about alternative healing and unveiling an India few are able to experience.” Whilst the book does provide an insight into Indian medicine, massage techniques and culture, which are in themselves interesting, from our point of view, the most fascinating parts of the book were Nicola’s thoughts about juggling her desire to travel independently with accepting the support offered along the way and accepting that, if offered in the right way, this sometimes enhanced her experiences rather than diminishing them.
 
Below are some quotes that I think demonstrate the above in Nicola’s own words.
 
From the start of the book:
“Ordinary people, all of us, can do extraordinary things but not always. All our stories are individual and personal as are the inner and outer journeys that we make. That is what makes them refreshing and engaging. I hope that my own story offers enough flavour to whet the appetite but leaves people to discover their own recipes. When I was in the early years of coming to terms with having lost my sight, I know I would have chosen to starve rather than to digest other people’s survival triumphs and ways of overcoming disability”.
 
“I had never been able to use my cane at home because of the stark associations with blindness that it stirred up. When I first lost my sight a guide dog was the only acceptable solution. I did not imagine that I would be able to use a cane in India to guide me around: the skill and technique of doing so required training, which I had resisted. However, I had reluctantly accepted that I needed some symbol to identify my disability for those times when I needed help. But when the moment approached to take out my cane, I realised I had underestimated my anxiety.”
 
There is one section in the book where her friend goes to ‘nip out’ of the car to sort out an arrangement without her. “This time I felt that as the purpose of the visit directly concerned me I was not going to be left in the car like a child. People have often just ‘nipped’ to do this or that and left me to wait because they thought it easier and quicker than asking me to come. It makes me feel like an inconvenient appendage, or worse still, a nuisance invalid or child.”
 
And when an air stewardess takes her hand in order to guide her:
“With the stewardess I slipped my hand free of hers and placed my fingers gently but firmly on her elbow…. All at once I felt myself back in control, and the fear subsided.”
 
Later in the book, Nicola discusses her feelings about receiving some assistance:
“I did not want Goutam to feel I was rejecting his generosity and kindness. If I stuck clumsily to the western model of independence and self sufficiency I knew I risked offending my Indian friends. …I was beginning to see that giving and receiving help altruistically, according to need and opportunity was an integral part of Indian culture, a vital interdependence in a country with so many people and so much poverty…. A thought slid round in my head about how the ties of dependence might have a strengthening as well as a restricting pull, while independence could be an isolating straight jacket, I decided I needed to discover a little more about this approach and for a while be a less intrepid, less selfish explorer.”
 
“When I reached town I decided to take a bus to Mr. Atuna’s evening yoga class rather than go back to the club. After another vigorous class, Mr Atuna said to a class member “Arun, please be taking our guest to the bus stop.” There was no sense in which a favour was being granted, or that I was being an inconvenience, and I felt comfortable with my need for help.”
 
To me, this and other instances in the book highlight how we all have to adapt and change to accommodate each other or our circumstances, whether this be to do with assisting or being assisted by others or understanding cultures that differ to our own. I think this is summed up by a quote from another book we have read - ‘Touching the World’ by Cathy Birchall and Bernard Smith - “What you see depends mainly on what you look for”. ‘Touching the World’ is a fascinating account of 2 people's journey around the world on a motorbike, detailing their fantastic adventures and accounts of the generosity of human nature (in general) but also the strength of character required by both of them to undertake such a journey. Cathy has RP (Retinitis Pigmentosa) and whilst the book is much more than about Cathy's blindness, it is part of everyday life for Cathy and Bernard (her sighted partner) and so is an integral part of the book. We have discussed and recommended this book on many of our training courses and wrote an insight about it last February for #WorldBookDay - https://vidatraining.weebly.com/blog/february-28th-2018.
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

I, Dave, know that I have spoken about apps for vision impaired people but I don’t think that I’ve done an actual review of an app for one of our Insights previously. Following a recent experience, I thought that I would share this with you…
 
I currently use an iPhone 8 and access it using the built-in ‘Voiceover’ (https://www.apple.com/accessibility/iphone/vision/) screen reader. Using a range of taps, swipes and gestures, I can access pretty much all of the phones built-in features as well as many apps including banking, shopping and social media apps.
 
I also have a folder that contains several apps specifically created for vision impaired people including Microsoft’s Seeing AI (https://www.microsoft.com/en-us/seeing-ai?SilentAuth=1) and Soundscape (https://www.microsoft.com/en-us/research/product/soundscape/), Be My Eyes (https://www.bemyeyes.com/), KNFB Reader (https://knfbreader.com/) and TapTapSee (https://taptapseeapp.com/) to name just a few.
 
Although I use a couple of these apps frequently (they all do a slightly different job), it was the Be My Eyes app that I used recently and the one that I wanted to share my experience of.
 
The Be My Eyes website describes the app as: Be My Eyes is a free app that connects blind and low-vision people with sighted volunteers and company representatives for visual assistance through a live video call.
 
And that is exactly what happens… a few days ago, whilst working at home, my laptop started playing up before it stopped responding completely. Similar to my phone, I use a screen reader called Jaws on my laptop but when the screen reader stops talking to me I have no idea what is on the screen or where I am. With no-one else in the house, I tried some of the other apps mentioned above to see if I could work out if there were any error messages on the screen but they just didn’t work. Finally I resorted to the ‘Be My Eyes’ app and called up one of the sighted volunteers.
 
I was quickly connected to a lady (apologies for not getting your name if you ever read this) in Swansea. She was able, using the video connection, to direct me to point the camera to the screen and inform me that there was nothing on my desktop that was obviously causing my Jaws software not to speak. She was then able to escort me through shutting down the laptop using verbal prompts so that I could re-start it and continue with my work. The call took about 2 - 3 minutes and this included a short amount of ‘social’ chat where I found out that I was her first Be My Eyes volunteer experience, joked about her telling me that she had just got out of the shower (she quickly told me that she was dressed - not that I would have seen anything anyway) as well as me thanking her for her help.
 
This wasn’t my first experience of using the app but this was by far the most important time I have had to use it. Previously I have tried to get someone to read the bill in a restaurant or read a label on a tub of herbs but these were really for testing purposes to see how the app worked.
 
Currently there are 2,090,032 sighted volunteers who have downloaded the app and have signed up to be a sighted volunteer and just 124,087 vision impaired people who have signed up and use the app. This means that the chances of a sighted person actually being called up is slight but without the volunteers the app just wouldn’t work at all!
 
If you want to be a volunteer, then just download the app and register. The app is available for the iPhone (https://itunes.apple.com/us/app/be-my-eyes-helping-blind-see/id905177575?mt=8)and Android (https://play.google.com/store/apps/details?id=com.bemyeyes.bemyeyes) platforms.
 
If you have a vision impairment and feel that you would benefit from using this app, then download the app (as above) and follow the steps for registering as a vision impaired person. Once registered you’re just 30 seconds away from getting sighted support! :-)
 
Read more about this amazing app at: https://www.bemyeyes.com/
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.

Having shared the Facebook post about a woman with a guide dog being told by another passenger to get off a bus as her dog couldn’t be a guide dog as it wasn’t yellow (yes I know, unbelievable but sadly true) – I, Vicky, thought it might be a good time to write a blog about assistance dogs and their different roles. It also happens to coincide nicely with the book I’m currently reading called ‘Dogs with Jobs’ by Laura Greaves – about all the different roles dogs undertake.
 
Assistance Dogs UK is an umbrella organisation for 8 Assistance Dogs charities in the UK. Their roles are different and varied – just like the dogs themselves! The 8 organisations are:
·      Canine Partners
·      Dog AID
·      Dogs for Good
·      Guide Dogs
·      Hearing Dogs
·      Medical Detection Dogs
·      Support Dogs
·      The Seeing Dogs Association
 
Canine Partners (www.caninepartners.org.uk) provide dogs who assist people with physical disabilities and impairments with practical day to day tasks that may otherwise be difficult to perform. They also provide increased confidence, independence and social interaction. Their dogs wear a purple coat to identify them.
 
Dog AID (www.dogaid.org.uk) empower people with physical disabilities to train their own pet dog to assist them with daily tasks which are tailored to the individual. These dogs wear a red and fluorescent yellow coat.
 
Dogs for Good (www.dogsforgood.org) assistance dogs support adults and children with a range of disabilities and also younger children with autism. They also provide a Family Dog service that gives advice and support to help families with a child with autism get the most out of their relationship with their pet dog. In addition they train and support community dogs and their specialist handlers to work in activity and therapy in communities and schools. Their trained dogs wear a green coat.
 
Guide Dogs (www.guidedogs.org.uk) provide dogs who will guide adults and young people who are blind or partially sighted. Qualified guide dogs wear a white harness with yellow fluorescent strips.
 
Hearing Dogs (www.hearingdogs.org.uk) provide dogs for adults and children with a hearing impairment. These dogs are trained to alert deaf people to sounds they would otherwise miss, such as doorbells, alarm clocks, fire alarms etc. Qualified hearing dogs wear a burgundy jacket.
 
Medical Detection Dogs (www.medicaldetectiondogs.org.uk) have dogs that are trained to detect the odour of human disease. This is used both for Bio Detection dogs and also Medical Alert Assistance Dogs who support people with complex health conditions and use minute odour changes in a person to alert them to take preventative action. They wear a red coat.
 
Support Dogs (www.supportdogs.org.uk) are dedicated to increasing independence and quality of life for people with various medical conditions. They have 3 specific programmes: Autism Assistance Dogs for young children, Seizure Alert dogs for people with epilepsy and Disability Assistance Dogs. Their trained dogs wear a blue coat.
 
The Seeing Dogs Alliance (www.seeingdogs.org.uk)
Training dogs to guide blind and partially sighted people. Qualified dogs wear a yellow coat.
 
As you can tell from this list, assistance dogs’ breeds and roles are widely different and varied. However, all qualified assistance dogs can be identified by the coats or harnesses they wear when working which, although different colours all have the name of the organisation clearly shown too. These assistance dogs shouldn’t be disturbed when working so please don’t stroke or feed them. If they are relaxing, then you can ask the owner if it’s okay to say hello to the dog.
 
Legally guide dog and assistance dog owners have important rights under the Equality Act 2010 (EA). This Act ensures people with disabilities to have the same right to public services as everyone else.
This includes taxis and minicabs unless the driver has a medical exemptions certificate from their GP. And yes, this law applies whatever the colour of the assistance dog!!
 
In the past there have been negative comments on social media about these dogs being trained to be slaves, all I can say in response to that is that Dave’s guide dog, Errol always looked so proud to wear his harness, standing up straighter whenever the harness was readied for him (and just for the record, Errol was a black dog – a German Shepherd crossed with a Golden Retriever). Also, Guide Dogs and I’m sure all assistance dog charities, regularly monitor the health and well being of the dog and their focus is that it has to be right for the dog, not just the owner.
 
In reading the book ‘Dogs with Jobs’ which covers a whole range of different roles that dogs undertake, from being assistance dogs, pat therapy dogs, a dog who acts (from his own choice) as a guide dog for another dog, dolphin detector dogs and a dog whose role it is to keep the Seagulls away from the Australian National Maritime Museum, I think what struck me most was each owner's immense respect for what their different dogs could do. Some had been trained, but many had a natural instinct for the role they undertook. And when the dog decided it wanted a break or to stop working, then that was respected too.
 
And, just as an aside, in one of the other services Dave and I run, the Disability Equipment Service (www.disabilityequipmentservice.co.uk), we have been proud to sponsor a guide dog (aptly named Des), through the first year of his training. We have just raised enough money to do this again and will then also hope to start supporting Support Dogs too! This money is raised through kind donations of both money and disability equipment, which we then sell on to support the running costs of the website with 25% being donated to an Assistance Dog charity. Find out more about Des on our Disability Equipment Service Facebook page - https://www.facebook.com/disabilityequipmentservice/. And if you want to read more about Dave’s lovely guide dog, Errol, Dave wrote a heartfelt tribute to him when he sadly passed away in June 2017 - https://vidatraining.weebly.com/blog/archives/06-2017
 
We’re always interested to know about other people’s experiences and thoughts. Please share these by commenting…
 
Interested to learn more about VIDA Training? Read about our Training and Consultancy packages, specialising in Vision Impairment and Disability Awareness, Communication and Team Building or contact us for further information.