Today is one filled with mixed emotions, concerns and thoughts. Today, 18th January 2015 is the last working day for my guide dog Vicky. We have been working together as a qualified team since 18th November 2009, and it has been an amazing 5
Today is one filled with mixed emotions, concerns and thoughts. Today, 18th January 2015 is the last working day for my guide dog Vicky. We have been working together as a qualified team since 18th November 2009, and it has been an amazing 5
It’s almost 11.00 o’clock, 12 hours after this crazy day started. The climbing arena was nothing like I had ever seen before and no matter how much I had researched and looked at photo after photo I was not prepared for the quarry that I
Well, this is something new……. I am sat in the passenger seat of my friends car doing 70+ MPH on the M6 Motorway travelling on my way to Edinburgh; while typing this blog. My iPad is tethered to my phone for 4G and my voiceover
While with a group of friends today we were talking about faith. Discussing it and questioning what our understanding of it is. One comment made about one way to look at faith was If you’re sat on a chair, you hold faith that THAT chair
So, tomorrow is St George’s Day and at 2.40 this afternoon my daughters school sent out a text message to say that any Beavers, Rainbows, Brownies etc are free to wear their uniforms instead of school uniform… With full badges! This created 2 panics…. 1)
There is no witty title for this one, no sarcasm and no humour; I am without.
This is one of those few blogs where I just open my heart up.
This weekend has been full of emotion. It was a weekend that had been planned to be fun, full of laughter and enjoyment with my daughter, my best friend and his son; thankfully they appeared to enjoy it, although maybe by the end of the time away my upset began to show.
It would appear; if only to me that by hearing less I am actually not able to see as much either!
My sight has not changed by any great degree, but when I find myself struggling to hear in a situation, I also find seeing more of a struggle too.
Maybe it is because I am not getting the sound clues that I rely so heavily on to fill in the gaps that I miss with my vision. Maybe it is totally in my head (as some have suggested)
All I know, is that which ever it is. It has completely thrown my idea of the world upside down and has left me feeling RAW and unable to cope.
I have cried, I have screamed and I have hidden it all from my daughter. She doesn’t understand, mostly because I am not sure that I even do.
How do you explain RAW to a child?
And if you do know, can you please explain it to me ?
Yesterday a chance meeting with someone suddenly enabled me to put together the mess of a jigsaw I have been living for many months.
A polite, kind and welcoming woman who was absolutley besotted by Fizz, asked me a question I have never been asked before, there was no malice in her words or ulterior motive for asking what she did, in the way she did; she asked me one very simple question.
How do you feel about having a disability?
I can imagine as I type these words that several of you will be taking an inhale of breathe through your gritted teeth!! Maybe even muttering “you can’t ask that!”
Honestly though ….. YOU CAN.
Why can’t you?
I grew up with the saying “there is no such thing as a silly question.” A phrase that I stand by even now as a parent, a friend and most of all as ME.
The answer to this question was out of my mouth and I could hear my own words as if I were listening to someone else say them.
My answer was simple;
I feel guilty.
I feel as a parent I am holding my children back,
I feel like I am a burden to my friends.
Rationally I know the answer to my own guilt is me, I have just never put it into words. And WOW didn’t those words hit me like a 500 tonne truck!
Not because my own words shocked me, not because they upset me, not I was cross with myself for saying it; rather because hearing the words made me realise my irrational and unfounded fears and how they held me hostage in my own thoughts.
I have no need to feel guilt; I did not cause my eye condition and hearing loss. My disability isn’t the result of anyone’s actions. It just is.
So, if I know rationally I have no need to feel guilt, doesn’t just stop me feeling it. Nor does it stop me thinking these thoughts. It just gives me the realisation that to move forward I need to understand it. Work through it, and most of all admit it.
After all, isn’t there a plagiarised quote on Facebook, Pinterest and Intagram that says:
LIFE IS 10% OF WHAT HAPPENS TO YOU AND 90% OF HOW YOU REACT TO IT
Or more to the point; how did people cope before assisted technology?
This weekend just gone, I attended a conference with colleagues, part of the presentation was a show, bright lights, loud music, all contained in a large conference centre, with about 1700 other people.
Enough to put anyone with anxiety off! So add to that my sight issues and ever changing hearing and I was in a total panic mode. I had my faithful Fizz with me and some fabulous friends, so knew I would be well liked after. But having been to a similar (yet different) event with the company in the summer, knowing more wasn’t helping to make me feel better.
This was a BIG event, there were lots of whispers about information that was going to be shared, I knew o had to be alert and listen, while also taking notes.
And this is where the assistive tech came into play……
Out of my bag came my iPad and headphones, just one placed inside my left ear and my voice over switched on and I was all set.
Since I was 6, I have been able to touch type, so could happily type as the various speaker talked, using the camera on my phone to photograph the PowerPoint slides I thought would be relevant …. Even though I couldn’t actually see them at the time!
I have said it before that “I am a Mac” but over the weekend it became so clear just how much of one I am.
I have many a ‘shortcut’ set up on both my phone (iPhone SE) and my IPad, so with certain finger taps or multiply finger movements I can easily move around.
The one that got a lot of whispers was the ‘screen curtain’. For those who don’t need it, I guess it is a feature you don’t know about.
The screen curtain does exactly as it suggests, it puts a black curtain over the screen, or an easier way to explain it; it turns the screen off, without turning off or stopping you using the iPad.
This feature works hand in hand with Voice over as I have no need to see what I am doing as I am able to hear it all. Also in a conference setting, where the lights are dimmed and others are sat behind writing notes, it saves the light from my screen being of a distraction or glare to them while allowing me to conserve battery.
It did cause no less than three people gently tapping me on the arm and explaining that my laptop seemed to be switched off. So, with a quick three finger triple-tap the screen curtain was turned off and they could see my document, which often then led to “wow” or “aren’t you clever?” But like I said above, it’s all just part of the tech and my ability to get the most out of such a conference as others.
Over the weekend I wrote pages and pages of notes, which I have since edited and corrected the odd predictive text issue and been able to recap on my learning.
The conference was much more tricky than I had anticipated, I didn’t realise just how much my hearing had changed from the previous 6 months. I didn’t anticipate the eye atrain, ear ache and headache that I would suffer after four hours. So much so, that in the evening instead of putting on my new posh frock, I got into my pj’s and curled up instead. Knowing that Sunday’s training was almost twice as long!
The team around me were concerned about my struggles from the previous day, so arranged for me, Fizz and a friend to sit in a better position, much closer to the screens, yet further away from the speaker, so the presentation was clearer, and not as loud.
I felt very emotional and suppressed my tears at this act of kindness, they did not need to do this, yet they did and it became clear when I returned to the conference just the extent hey had gone to. A member of staff met us at the door and walked us in moving us through the crowds and seating us, checking if Fizz needed any water or if I needed a drink or anything. This biggest part with them making these adjustments for me was that they allowed me to have a friend with me, my colleague who I was sharing a room with, who was more than happy to take Fizz out for a walk and a wee or get me anything I needed or showing me where the toilets were. This simple act allowed me to relax, to know that I was with someone I knew and trusted and that didn’t have to worry about a thing.
So at our next conference in February I shall be keeping a tally on how many comments and ‘gentle nudges’ I shall get about typing or pretending to type on a switched off iPad ….. Watch this space !!
The one thing that this weekend has shown me is how much I am loosing my control on my disability, how much it has changed and thankfully how much I am now surrounded by people that are happy to support me.
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As a girl with a visual impairment, having tech on bus journeys or train journeys are key to my ability to be independent. If such an option isn’t available then I will set myself up to use another method of knowing my location and when or where I am to get off.
so imagine my surprise and upset when half way through a bus journey yesterday evening, I find that the audio has stopped?
I was travelling to an poorly lit area, I had Fizz with me and as I got on the bus I checked with the driver that audio was on. And as we set off, the audio read out the next stop, confirming what the driver had told me. All good, I could feel safe and secure that I could just sit enjoying the ride and await my stop to be read out.
There seemed to be a long pause in the audio. I checked with another passenger sat near me and he confirmed that the screen (as the audio on buses is teamed with a visual; just like on the train) was reading the next stop, but he hadn’t been paying attention and didn’t know where we were as he was getting off at the last stop, so didn’t need to know.
it was then moments later that the audio returned, only to read out a destination that was much further along the route, a good 45 minute walk back to where I needed to be if I had got off then!
so instead I travelled back to the bus station and started the journey again.
This time, when I got on the bus I asked the driver for my specific stop and asked him to ensure that he stopped there for me, he said the bus had audio, but understood my concern following my previous journey.
The audio on this bus was on, it also continued to detail each and every stop, so I was aware of where I was and when I was due to get off.
I put it down to a glitch and having safely arrived at my destination all be it an hour later, I forgot all about it.
That was until this evening. This time I was travelling with my son home after a shopping trip. Again, it was dark but I was more aware of my surroundings as it is a journey I have done thousands of times.
Again, the bus left the station and the audio announced the next stop. This continued until just before we were due to get off the bus, we were literally around the corner and the audio stopped. I could work out roughly were we were, and having stopped at several stops to let people in and off of the bus, there were no further announcements.
Thankfully a block of flats lit the way to enable me to work out that we were approaching our stop. But again, the audio had let me down.
Memtioning it to the driver as we got off the bus he simple said “I don’t pay any attention, I couldn’t tell you it had stopped.”
So, what is a gal to do?
I shall be sending this blog to the bus company, is it just really bad luck that I have encountered this issue? Is it a relay issue with the bus audio?
I know that my hearing is going, but to hear the audio and then to not hear the audio….., that isn’t me?
I feel that I am not able to trust the audio on my bus journeys anymore, and with the dark early evenings. This is making me feel that going out after dark isn’t an option. Or do I just walk?
Lots of questions. But I am totally stuck with whatever I do.
All the climbing of 2016 has taught me so much more about myself as a climber, I am going to need to work on my technique dramatically if I am to turn my 1st place into a Team GB place.
This doesn’t mean that I am giving up on my fundraising, now more than ever I want to show my worth and EARN my Resound Hearing Aids, but with my climbing partner currently our of action, as the post title suggests ‘The Cheesegrater is going to have to wait’
Just days before Christmas, my climbing partner in crime underwent an operation for a hernia, one that has left him unable to train for a minimum of six weeks. So with him not even being able to go to the gym until mid-February, let alone climb. I have made the decision to postpone my climb.
Yes, I can climb with another partner.
No, I am not sharing my climb with ‘climbing partner in crime’.
But…… He is my motivator, my muse and my forceful “not let me down until I have reached the top” coach. It wouldn’t be right to climb without him as my belay.
The new date is looking like late March, early April. But no date is being set until the whole of ‘Team T’ is fit enough.
First a gherkin; Next a Cheesegrater !! is where I wrote about my challenge back in October, it was hoped that the climb would happen later this month, but health comes first and so, I am going to be cheeky and link you to the Crowdfunding page that has been set up for me, ‘HelpTeeHear’ where you can see why I am doing all of this.
My world is getting quieter in addition to darker and I’m not happy with it, not one little bit. I want to be able to keep me, my independence and my love of technology that helps me to do all this.
So, my shameless plug is above, please take a moment to have a look.
And in the meantime, follow me for more updates on the climb and my other adventures.
January First, a day for the 3 R’s; Resolutions, Reflections and *the most important of them all) Rum !!!
This isn’t going to be a slurred hiccup fuelled post…. It is a small, little tradition. Raising a glass to those who lived life to the fullest, but that never made it out of last year alive.
And this year I am having it as a long drink of Captain Morgans Spiced Rum and Crabbies Ginger Beer. It is during this time of reflection that I think of those happy times with those I miss, I also raise my glass in celebration of those who have taken the decision to leave my life.
Regardless of what lead to their leaving, the initial sadness their departures caused, I am glad they did. We learn from all that cross our path, those who are born family, yet don’t act like it, those that start as strangers and become family….. They all count.
Cheers…….. Here is to an action packed 2017 !!