Wednesday, 25 May 2016
Tuesday, 17 May 2016
How accessible is my blog? #disability #images
This image contains a word
Can you read it?
Most of you will say, yes. But many of those who are visually impaired can not read the word. This is because they need to use screen reader software to "read" for them and this software has enormous trouble reading images.
I am lucky, I can use my zoom software to make the image as large as I like to read the word. And I thought I had made it clear enough that it would be accessible to everyone.
But I was wrong.
We all need to better understand what it means for our websites to be accessible.
Here are some simple tips:
provide a good level of contrast
write in plain English
use a clear font with good spacing
explain all images and videos in text
provide the text for any sound files
I hope this encourages you
(encourage was the word in the image)
Saturday, 14 May 2016
How are your eyes these days? #poetry #DrSeuss
Oh the things
That people say
The words I wish
Would go away
You don't look blind
How are your eyes
What can you see
Can you see the skies
And patiently
I answer them
But very soon
I won't pretend
That it doesn't annoy
And doesn't offend
Because those questions
Will usually send
Me over the edge
Into wondering if
Anyone knows
What it's like to live
With little sight
And lots of pain
And yet they ask
Over and over again
How are you feeling?
You seem OK
I'm glad things are better
Not so bad today?
And what do I say?
Tell me what do I say?
To make you feel better
Coz I think that's it
You want to know
That I'm not so sick
Because that's easier
Than having to see
Really what it's like
Living life as me
And realising
I'm making the best
Of what I've got
I've still got the rest
Of my skills and talents
And beyond the aches
I can use my brain
That's no big shakes
So how are my eyes?
No better, no worse
I'm getting on
I don't feel cursed
In fact I feel blessed
To have technology
And by the way ...
I am still me!
Linked up at Prose 4 Thought
I will still EXPERIENCE the World #travel #disability #spoonie
This morning I read a wonderful article on The Mighty: When I Saw the Adventurous Life I Envisioned Before My Illness Slip Away which spoke a great deal to how I can feel at times. I recommend that you read it for yourself, but in brief, it speaks of a young woman diagnosed with a chronic illness who is having to come to terms with changing her plan for a life travelling the world. There are days when I can let myself think like this, and these were almost every day in the first six months after loosing my eye sight and realising my mobility problems were not a temporary blip; but most days now I think differently.
My Travel Plans (as were)
I will see everything there is to see in the world; all the amazing sights and people and cultures and buildings and natural wonders.
I will stand on Antarctica and walk in colonies of penguins; drive an RV through New Zealand and see the land of giants; watch the sunset over deserts; trek through forests to see orangutans; worry about bears in Alaska and time eruptions in Iceland; see the Northern Lights and watch dolphins and whales time and time again; try disgusting food because it's better to have tried and disliked than never to have tried it at all.
It was all mapped out, every square inch of the planet a place to be seen and explored and captured with my camera and shared with Rachel and Mike. It was a life full of adventure and fun but absolutely no bungee jumping!!
My Travel Plans (as I grieved)
There's no point in even trying to go to any of the places I have always wanted to see, because I can't see. There's no point in expecting to trek through jungles or take a boat up the amazon, because I can't trek or even get on a little boat let alone sit in it for hours. There's no point planning to see the Northern Lights because they're subtle and will not be bright enough for my little sight to pick up, and I will be too tired by the evening to be able to cope with the trips anyway etc etc. A spiral of can nots and will nots and impossibilities for the future.
but......
I have come through the grief (I'll be blogging about how that happened) and now .....
My Travel Plans for life
I will experience everything I possibly can in the world; all the amazing sights and people and cultures and buildings and natural wonders. I will find ways of travelling which make it possible; we are trying cruising this summer to see how that works for me. I will meet people from different cultures and enjoy their company because it's always been more about their stories than about what they look like. I will visit the natural wonders and I will hear through Mike and Rachel what I can not see and we will take photos and I will use technology, there at the place, to see it the very best way I can. I will open my ears and hear the waterfalls; I will touch the rocks and the ice of the glaciers and I will feel the wind and spray from the sea. I will feel the joy of those around me and my own as I travel with loved ones and place memories in my heart.
I might be in a wheelchair, or scooter, or perhaps in a funky off-roading contraption and I will find a way. I might need assistance, but we all need assistance from loved ones or experts whenever we travel, it's just a different form of help.
I have it all mapped out and it's the whole world. I will see as much as it's possible to see and I will see it with the whole of me; I will experience it as me and it will be awesome. No disability is going to stop me, my only limitation is money and let's be clear, that was always the limiting factor but it doesn't matter in dreams and plans for the future.
My Travel Plans (as were)
I will see everything there is to see in the world; all the amazing sights and people and cultures and buildings and natural wonders.
I will stand on Antarctica and walk in colonies of penguins; drive an RV through New Zealand and see the land of giants; watch the sunset over deserts; trek through forests to see orangutans; worry about bears in Alaska and time eruptions in Iceland; see the Northern Lights and watch dolphins and whales time and time again; try disgusting food because it's better to have tried and disliked than never to have tried it at all.
It was all mapped out, every square inch of the planet a place to be seen and explored and captured with my camera and shared with Rachel and Mike. It was a life full of adventure and fun but absolutely no bungee jumping!!
My Travel Plans (as I grieved)
There's no point in even trying to go to any of the places I have always wanted to see, because I can't see. There's no point in expecting to trek through jungles or take a boat up the amazon, because I can't trek or even get on a little boat let alone sit in it for hours. There's no point planning to see the Northern Lights because they're subtle and will not be bright enough for my little sight to pick up, and I will be too tired by the evening to be able to cope with the trips anyway etc etc. A spiral of can nots and will nots and impossibilities for the future.
but......
I have come through the grief (I'll be blogging about how that happened) and now .....
My Travel Plans for life
I will experience everything I possibly can in the world; all the amazing sights and people and cultures and buildings and natural wonders. I will find ways of travelling which make it possible; we are trying cruising this summer to see how that works for me. I will meet people from different cultures and enjoy their company because it's always been more about their stories than about what they look like. I will visit the natural wonders and I will hear through Mike and Rachel what I can not see and we will take photos and I will use technology, there at the place, to see it the very best way I can. I will open my ears and hear the waterfalls; I will touch the rocks and the ice of the glaciers and I will feel the wind and spray from the sea. I will feel the joy of those around me and my own as I travel with loved ones and place memories in my heart.
I might be in a wheelchair, or scooter, or perhaps in a funky off-roading contraption and I will find a way. I might need assistance, but we all need assistance from loved ones or experts whenever we travel, it's just a different form of help.
I have it all mapped out and it's the whole world. I will see as much as it's possible to see and I will see it with the whole of me; I will experience it as me and it will be awesome. No disability is going to stop me, my only limitation is money and let's be clear, that was always the limiting factor but it doesn't matter in dreams and plans for the future.
Thursday, 5 May 2016
Spring into Spring with Torch Trust #poetry
Spring into spring
Here new lives begin
Building
Building
Peace in creation
Gardening
Gardening
Therapy with fingers
Growing
Growing
Plants and confidence
Perfection
Linked up at Prose 4thought
A journey through retreat with Torch Trust #poetry
High anxiety
When we all arrive
What will be?
Immediately
Welcoming friendly faces
Put us at ease
No expectations
Come just as we are
Relax for the week
Bedrooms
Comfy and bright
Home from home
Every detail
Thought out with prayer
A holy place
Within a day
Strangers become friends
Sharing stories
Worship
Sustains and renews
Uplifting
Activities
Empower and encourage
New skills
Meal times
Feed body and mind
Fellowship
Now going home
Leaving this holy place
Will return soon
Torch Holiday and Retreat Centre #poetry
Welcomed warmly
Hearts, hands and minds
Completely safe
Completely safe
In Jesus' protection
Everyone valued
Everyone valued
For individual talents
As children of God
As children of God
Supported and cherished
No fear here
No fear here
On retreat with torch trust
Heaven on earth
Heaven on earth
All eternally loved
Welcomed warmly
Tuesday, 26 April 2016
#TreasuredMoments Bloom Linky
Welcome to the #TreasuredMoments link-up.
The place to share treasured moments in poems and blog posts.
This time the linky will last two weeks until 26th April 2016 and I'd especially love to see your posts about Bloom.
The place to share treasured moments in poems and blog posts.
This time the linky will last two weeks until 26th April 2016 and I'd especially love to see your posts about Bloom.

Saturday, 23 April 2016
Tremor #AtoZofMS #AtoZChallenge #poetry
Tremor
About one third of people with multiple sclerosis may have tremor to some degree.
Shaking
Trembling
Tremor
It's MS
Not parkinsons
Ataxia
Didn't know
This was a possible symptom
But it is, for me
For some people it can be a relatively mild problem with coordination (ataxia), but for others it can be one of the most disabling symptoms of MS.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
Find other blogs posting their A to Z this April 2016
Friday, 22 April 2016
Spasticity #AtoZofMS #AtoZChallenge #poetry
Spasticity
Spasticity is a symptom of multiple sclerosis
Spasticity
pretty new to me
started this year
leg locked
couldn't move it at all
terrified
shoulder stopped
is it a heart attack? no
different spasm
have to be ready
pray that it stays rare for me
not my favourite
Spasticity causes your muscles to feel stiff, heavy and difficult to move. A spasm is a sudden stiffening of a muscle which may cause a limb to kick out or jerk towards your body.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
Find other blogs posting their A to Z this April 2016
Thursday, 21 April 2016
Relaxation #AtoZofMS #AtoZChallenge #poetry
Relaxation
Regular relaxation is really important to manage the symptoms of MS.
Stress is a trigger
it makes my MS symptoms
so much worse
Overwork
exhausts me causing
pain and fatigue
I must rest
Take time out regularly
Relax
Not easy for me
I've never liked to rest
But it works
So I'm learning
to relieve tension, chill out
put myself first
Regular relaxation can help you decrease tension in muscles, lower your blood pressure and slow your heart rate. Relaxation can help with fatigue as it promotes good sleep patterns, increases benefit from rest periods during the day and can help to manage stressful situations.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
Stress is a trigger
it makes my MS symptoms
so much worse
Overwork
exhausts me causing
pain and fatigue
I must rest
Take time out regularly
Relax
Not easy for me
I've never liked to rest
But it works
So I'm learning
to relieve tension, chill out
put myself first
Regular relaxation can help you decrease tension in muscles, lower your blood pressure and slow your heart rate. Relaxation can help with fatigue as it promotes good sleep patterns, increases benefit from rest periods during the day and can help to manage stressful situations.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
Find other blogs posting their A to Z this April 2016
Wednesday, 20 April 2016
Questions #AtoZofMS #AtoZChallenge #poetry
Questions
Questions: so many questions.
What is causing this symptom?
Will it improve or get worse?
Will this symptom stay forever?
Are there any treatment options?
Are there likely to be any triggers which set it off?
What can I do myself to manage this symptom?
What shall I do if my symptoms get worse?
What shall I do if I experience new symptoms?
Possibly the hardest thing is dealing with the huge list of questions which pop up between appointments; especially if you turn to the internet and find lots of conflicting information. It is important to find a trusted source of facts, such as the MS Trust, and share what you are reading with a close friend or relative to help them help you understand.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
What is causing this symptom?
Will it improve or get worse?
Will this symptom stay forever?
Are there any treatment options?
Are there likely to be any triggers which set it off?
What can I do myself to manage this symptom?
What shall I do if my symptoms get worse?
What shall I do if I experience new symptoms?
Possibly the hardest thing is dealing with the huge list of questions which pop up between appointments; especially if you turn to the internet and find lots of conflicting information. It is important to find a trusted source of facts, such as the MS Trust, and share what you are reading with a close friend or relative to help them help you understand.
Find out more about MS at
MS Trust A to Z
Donate to MS Trust
I'm also writing an
A to Z of Blessings at LLM Calling
Find other blogs posting their A to Z this April 2016
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