A A A Accessibility A A A A
Thursday, 01 January 2015 00:00

Let's Get it Straight - A Mother's rant

What is Multi Sensory Impairment?

"Persons are regarded as deafblind if they have a severe degree of combined visual and auditory impairment resulting in problems of communication, information and mobility".

One severe impairment e.g. severe hearing loss, accompanied by partial sight or moderate sight loss still constitutes deafblindness. The reason the later or secondary loss only requires to be moderate before compounding effects are felt, is that the second sense has been relied on to compensate for the first loss. Normally a profoundly deaf sign language user who becomes partially sighted will have inherent problems with communication, access to information and mobility. In a similar manner, a hard-of-hearing person who has always lipread, when vision deteriorates at all will have problems. Equally a blind person who has relied upon sharp hearing will have real problems if hearing substantially deteriorates.

So how should somebody of school age with this condition be supported?

A teacher of the deaf or teacher of the visually impaired is not enough, there must be a multi sensory impairment specialist involved. 

In our area we found support for deaf children outstanding. At the beginning it was very full on, literally bombarded with information, weekly visits from a teacher of the deaf, meeting with speech therapist, groups to attend to meet other parents and deaf children, audiology appointments regularly, details about claiming Disability Living Allowance, details about our local Deaf Children's Society and the Charity DELTA (Deaf Education through Listening and Talking) who's ethos I absolutely recommend and details about SEN (Special Educational Need) and Statementing.

It was daunting but looking back how lucky we were to have so much support and input from the Hearing Impairment Team and particularly the Teacher of the Deaf (TOD) and great input from the Speech Therapist.

We also had consistency and accept for two or three visits Molly had the same TOD from pre-school through to almost 14 years old.

Lots of hard work went into supporting Molly on her journey as a deaf youngster and the results are clear.

Molly caught up with her peers, her speech developed beautifully and she often describes her happiest times where at nursery and primary school.

Then came the "Usher Diagnosis" at senior school.

Confusion best describes the next chapter:

Deafblind, no qualified teacher to work with the deafblind but there are Visual Impairment Specialist (VIS) teachers, Molly will have a senior one!

All well and good but a TOD and a VIS do not add up to a Multi Sensory Impairment (MSI) Specialist.

There was the honesty that neither the Deaf nor VI teams were familiar or experienced in supporting somebody with Usher Syndrome - somebody needed to be trained' it would take 3 years for somebody to be qualified!

In the meantime MSI support had to be bought in from Sense to support not just Molly but the team around her and that was to include teachers and teaching assistants at the school as well as advise the TOD and VIS.

The one thing that became ever obvious was the sheer exhaustion deafblindness brings along with mobility issues and acceptance.

Acceptance made ever harder by the ignorance surrounding the condition.

For us there was a grieving period, which was very painful, particularly when there is continuous questioning "You're not blind" "You're not deaf" even by those who should know better.

The cruelty of an invisible disability makes acceptance all the harder, the continuous questioning often leads to a very unhealthy and unacceptable denial which again has its problems.

The desire to just "fit in" never goes away and then the need for acceptance from all.

Acceptance and understanding in education, acceptance and understanding in the work place and acceptace in general is required and it really isn't a big deal to know the basics.

I cannot and nor would I want to speak for the entire Usher Community but where my own daughter is concerned she wants to get on with her life, to achieve what she can and more important than anything she wants and deserves to be happy.

In order for her to have those few things all she needs is to be accepted as the person she is and to be understood and what is more she is the expert on herself!

At this stage direct support can be achieved by simply asking!

In the workplace potential employers should be aware of the diversity and unique skill set people with usher syndrome can have, how much value they can bring to any workforce.

Like us all they just want that chance.

I think they call it "Thinking outside of the box".

Thursday, 27 November 2014 00:00

When Denial Becomes Reality

Retinitis Pigmentosa (RP) has always been something that I've denied but this year as I turned 39 it became clear I couldn't deny it anymore.

I was 7 years old when the news came that there was RP in my family.  My sister was the first of us to be officially diagnosed it was the early 1980's and there was very little information around then she recently told me that back then she was informed by the specialist at Moorfields that there was no cure or treatment, she would most likely go blind and not to have any children!  However, she now lives in San Francisco with her husband and two amazing children Lauren and James both in their early twenties and both unfortunately have RP.

My memories of that appointment are vague all I remember is having eye drops that made me unable to see for a few hours which I remember was scary especially at 7 years old. From there on I didn't think about it, RP was just an occasional conversation piece that we had an uncurable eye disease in the family that might make me blind but probably not until I was very old!

I continued to live my life and was lucky enough to have an amazing one with many extreme highs and lows enough to write a pretty good book but that's for another time. I travelled the world working as a singer beginning my career as a Bluecoat at Pontin's and eventually becoming a touring cabaret act performing at holiday parks and hotels all over Europe. My travels eventually took me to Glasgow where I began to settle and build a new life. RP was still very much at the back of my mind even though I knew I was struggling with going from light to dark places, by this time I was in my mid twenties. I was building a career in car sales was in a relationship and the years began to fly by without much thought of my eyes.

By the time I reached my 30's my thoughts turned to becoming a father, I never entertained the idea before, nothing to do with RP just down to having too much fun working in entertainment. On November 4th 2007 my life changed when Ellie was born, I took to being a dad as naturally as I take to the stage and as the tattoo says on my right forearm "It's like a song I've never heard I've never sung but know the words" a line from one of my favourite songs which describes becoming a father.

The bond between Ellie and I was so strong unfortunately the same couldn't be said for the one between myself and her mum and the relationship came to an end by the time Ellie turned 3.

At that time I had gone back to singing again driving all over the uk performing as a cabaret again. I made the hardest decision of my life to move back to manchester to be near family and to give up singing again so I could regularly make the long drive to bring Ellie down from Glasgow. By this time even though my eyes would struggle in darkened rooms I could still drive with no problem. As hard as it was trying to start again being so far away from my little girl I knew it was something I had to do, I had a gut feeling that it would eventually work out and that's when I met Amy.

Amy came in to my life and brought with her the promise of a love filled life I thought I'd never find. Amy had two boys Harvey and Louie, Ellie and I slipped into their world like it was just meant to be.

Within 2 years together I had gone back to car sales trying to build our life we were blessed with the arrival of the cutest baby boy you will ever see Austin, he arrived in June 2013 and on Xmas day that year I asked Amy to marry me and she said yes!

We then started to plan our wedding for New Year's Eve 2014. The following year everything changed!

By May this year my eye started to get worse and a check up at the local opticians confirmed my worst most denied fear my RP had started to rapidly progress and my driving days were over. My first thoughts were of Ellie and how was I going to be able to see my little girl? My second was what was I going to tell work?

I told work straight away and they let me go on the spot as I could no longer continue my role without a driving licence.

My little families world began to unravel, I went to the specialist who confirmed me as legally blind and gave no other answers. I then went to the job centre and asked for help. From there on it has been a constant battle to try and get the help we so desperately needed but were plunged into extreme poverty falling behind with bills and just finding it extremely hard to survive due to the horrendous waiting times for PIP etc never mind not being able to see Ellie due to the cost of collecting her from Glasgow.

As the months have passed this year my eyesight has rapidly declined to the point where I have now started long cane training and am on the list for a guide dog to try and get back the independence I have lost as I now suffer with anxiety due to my vision loss my confidence has all but gone and I very rarely go out alone.

The things that have kept me going is getting married to the love of my life on New Year's Eve as planned and meeting an amazing friend in Simon who I met through one of the facebook RP support sites on the advice of my sister in San Francisco.

Simon has Usher Syndrome Type 2 and it was obvious from the start we had so much in common other than our crap eyes. We shared a love of music and the same sense of humour. He is my best man for the wedding. When simon and I became friends he invited me to come round to his house as he had a mini recording studio so I could sing and let off some steam. Here began the start of a little confidence returning and the idea for my RP project.

Simon and I had held a couple of informal meetings with other RPers and that's where we met Colin who also has Usher Syndrome Type 3, a very special person who was equally passionate about connecting those who felt alone.

As time and eye sight went by I became more vocal and passionate about the injustices visually impaired/blind people were going through all over the world and that's where "Stand By Me RP" was born.

I was asked to perform at a meeting for people with RP and Ushers in the north and decided to created a theme song for us that I could share worldwide, I decided to use "Stand by me" http://youtu.be/qxFdmqZoceo because everyone knows it and then I re-wrote the lyrics around the fears a lot of us have. Through the support of the VI community and the amazing people who have responded to the video and continue to keep sharing it the message has reached place and people I never thought I would reach.

Molly and her incredible family and Joanne Milne who's story reduced me to tears in seconds in fact I have written a song about Usher Syndrome for Jo which we will unveil together in the near future. All of a sudden my future looks good again I am determined to take the disease that has stripped me of my confidence and use it with my passion for music to help as many as I can whilst in turn helping me find me again. Amy and I are stronger than ever and our wedding is only weeks away and even the recent trip to the specialist who confirmed that my central vision is deteriorating fast could not dampen my new found spirit. I will begin 2015 a married man and plan to fight to raise awareness for RP and Ushers with your help of course

Monday, 24 November 2014 00:00

Falling Into The Darkness

This was another day in my life when Ushers Syndrome had well and truly won.

I’d had my shop for three years after struggling with the demons in my head after taking my redundancy. I’d started a shop selling wallpapers and soft furnishings, I’d had a huge build up of emotions. I’d ran the shop for three years, but Ushers was taking over.

It was becoming harder and I was now on the waiting list for a guide dog.

The shop landlord wanted me to commit to another three year lease and also to increase my rent. The time had come to sell up and ship out. My heart was heavy, anybody that knows me will be sure to tell you I don’t do things half heartedly, either all or nothing as if i have a massive point to prove. Turns out all my Usher / RP friends feel the same, as if they struggle for acceptance in the normal world. But what is the normal world?

Back to the Thursday 13th of June 2013, I’d managed to sell most of my stock and had a date to be out of the premises, it was in the two weeks time on a Saturday. I’d managed to sell off lots of stock, but had to get rid of the fittings shelvings etc, this had all been made up in the shop and was too big to take out of the front door. I’d sold some of the display boxes I’d had made for my wallpaper. I’d sold two lots of twenty boxes (these were pretty heavy and made from MDF).

My shop closed at 17:30, so i made arrangements for the display boxes to be collected after that- as you can imagine, middle of June it was a lovely night and quite dazzling on my damaged eyes. I told the guy to bring help but he didn’t and if the truth be told, I didn’t feel comfortable about the whole thing from the word go. The only way out was to slide them along the floor, out the rear fire exit door, then lower them off the flat roof the the van below (which was ten and a half feet). My partner and her father arrived. They watched on the ground as me and the other guy slid them along the roof tied ropes around them, then proceeded to lower them down. It wasn’t easy but we did it.

Thank goddness I thought, took one step back and fell ten and a half feet, I hadn’t seen the hole in the corner. It was a rectangle about eight feet long by three feet wide, but someone had bricked up the wall. So not only had I fallene, but I had no way out!

When I fell I guess I was very lucky, as I had landed on my feet and quickly pulled myself together, but when I fell I didn’t feel right,  I’d hit the floor with my hand and elbowed myself in the ribs. Also my glasses had fell off I searched about all the time, all the time I could hear people screaming my name, asking if I was ok. Then as I tried to pick up my glasses with my right hand I felt pain, I’d never felt pain like this in a very long time. I looked again, my right hand had in fact snapped off the end of my arm. I felt physically chlaustrophobic, how the hell can i get out? I thought. I didn’t want to panic anybody, I yelled “I’m ok, I’ve just broken my wrist I think”. Even though I knew I’d done more than just break it. There was lots of panic on the other side of the wall, as they decided to go and get ladders. I should of dialled 999, but I guess it was the Usher /RP that stopped me!

I went for the hard option rather than embarass myself. It felt like an eternity, all the time I was trying to stay awake and talk to my partner’s father on the other side of the wall, I’d even managed to call up A&E and book myself in.

Eventually, the ladders arrived along with a squad of helpers. One thing I didn’t want or need was someone to remind me about RP/Ushers and how I shouldn’t have even attempted this job in the first place. The ladders were now lowered and I was up the ladder before anybody got one foot on the rung, then the ladders were dropped over the other side of the wall. This time they demanded someone went before me, by this time they’d all seen my hand and how yellow i was becoming. They took forever to get me down. I jumped in the car only to be met by a hundred questions. I knew it was bad, because I couldn’t even put the seatbelt on and my partner wanted to throw up. It was a long, very long couple of miles to the hospital. I even called A&E again: “Hi it’s Colin, we are on our way”.

We arrived in A&E only to be met with a glowing, friendly smile and a wheelchair. It was Mark, a guy who used to work for me many years ago. He was brilliant. He took me to A&E and got me x-rayed and scanned, he then told me it wasn’t looking good and would have to reset, but there was splinters. So now I had everybody off the ward as an audience. He injected my hand twice, held my shoulders, and popped my wrist back on the end of my arm. Next I got a million questions about the incident and what did I say? I fell over the back door step, I guess I did this to hide the embarassment of RP Ushers.

I was on very large doses of pain killers and liquid morphine and very very tired. I was admitted to the ward and constantly fussed over by everybody. To be honest I hate that, especially as I kept thinking this is your own bloody fault, and that damned Usher Syndrome got me again!

The medical staff were great. They talked in detail about me but I was with the fairies on morphine, only to wake up two days later to find they couldn’t operate on me in Dumfries, but wanted the top man in Scotland to do it: Mr. Hamed at Gartnavel, Glasgow. They offered me a taxi, but I declined. I arranged my mother and father to take me up. Now I faced a further five days in a single room with Ushers, I was more concerned about that than my hand. I was met by the great man himself, a young guy and a good sense of humour. I was gowned up and ready to go, he said “ It says you fell over the back door step. Now tell me what really happened?”. So I did,  I explained about my vision. He promised to try his best, as long as I stayed off roofs and tried hard on my physio.

After a couple of days, he came to see me. He said “You’re a lucky boy, you have 12 titanium pins, but I don’t think you’ll ever get full movement”. Before I left he sent me to physio. They told me five exercises ten times each, three times a day and stay off work for at least six weeks. So off I went back home.

The next day I was at work I had to wind things up, it was very hard. But I did it. I also kept doing my exercises all day. Finally the day came to empty the shop, it was a huge relief and felt right at the time. As if someone was telling me to behave, enough is enough. So I continued my exercises and went back to Mr. Hamed after six weeks he said “how are you doing?” He just laughed. “No more roofs for you. Your wrist is about three inches wide, your neck is half an inch, you’re one lucky boy”. He then laid the backs of his hands on his desk and said “You’ll never ever get this movement back”. I did the same and he was shocked. I told him “You made a promise and I made you one”. I guess I was so mad at the situation, I felt I owed him for wasting his time and being such a fool.

Well I guess the moral of the story is don’t be too proud to let others help, sometimes it is better to just walk away. Life is too precious. 

Pin It
 

Recent Blogs

Helen diagnosis 'I felt my world fel…

Helen diagnosis 'I felt my world fell apart'

My name is Helen Colson. I’m 29 years old & live in Southport, Merseyside. I was diagnosed with Retinitis Pigmentosa and as I am moderate-severely deaf, Ushers Syndrome last year.  It...

Read more...

Olivia's Usher Life - Last few month…

Olivia's Usher Life - Last few months of emotions

Hello Everyone! Would like to wish you all happy deaf blindness week! I’m so sorry that I haven’t posted in it feels like ages! But I’ve got soooo much to...

Read more...

Where did our journey with Usher Syn…

Where did our journey with Usher Syndrome begin?

Where does our story begin..... Alice (now 16) was born profoundly deaf. In Oct 17 at a routine eye test (Alice has always worn glasses) they picked up an issue...

Read more...

The evolution changing Usher Syndrom…

The evolution changing Usher Syndrome

Usher Syndrome is a strange thing, strangely it is evolving even though it hasn’t changed.  It remains a condition without a cure. There are variations in level of deafness, in level of...

Read more...

Whispers in the Dark

Whispers in the Dark

It’s never been easy. Having to scan the floor in front of you when walking down the street. Having to pre-plan the route to the nearest toilet in a restaurant...

Read more...

GAAD - Not if but how!

GAAD - Not if but how!

Indeed back in the 19th Century it was Helen Keller who stated “DEAFNESS SEPERATES US FROM PEOPLE AND BLINDNESS SEPERATES US FROM THINGS”. Back then she was right, she lived...

Read more...

Equal access to sound for all

Equal access to sound for all

Today is ‘Rare Disease Day -2019’ So I decided on a blog about hearing aid technology that can and does enhance lives.  This http://www.nciua.org.uk/latest-new/ was brought to my attention several weeks ago. ...

Read more...

LiNXQuattro 'LiNX to Everything…

LiNXQuattro 'LiNX to Everything"

I have to admit that as time goes by, wearing high tech smart hearing aids has become just a part of me.  I imagine this must be how natural hearing...

Read more...

#GAAD 2018 - Exclusion to Inclusion

#GAAD 2018 - Exclusion to Inclusion

I wanted to write something for GAAD (Global Accessibility Awareness Day) this year to take into account a lot of the work I have been doing over the last 3...

Read more...

Applewatch is lots of useful things …

Applewatch is lots of useful things but also bossy!

When I peer into the mirror I see my right hazel/green eye.  Traveling downwards and towards the left I can see my nose then my mouth.  Following the nose upwards...

Read more...

Happy Haptics

Happy Haptics

How is it that a few simple vibrations can give you SO VERY MUCH?If you had asked me the same question just a few months ago I would have probably...

Read more...

Counselling - My Rollercoaster of Em…

Counselling - My Rollercoaster of Emotion

I haven’t blogged for a while, but feel this heartfelt blog needs to be written. I had never really considered the sadness, even grieving that happens when somebody you have loved...

Read more...

Applewatch Down Under

Applewatch Down Under

Coming to the end of the school year, I have realised how much I rely on my apple watch. The apple watch has given me so much support that has...

Read more...

Charlotte's Applewatch

Charlotte's Applewatch

I was aged 14 when I was told I had Ushers Syndrome Type 2. I was devastated and my dreams for the future were gone in a single moment. Being...

Read more...

Usher Awareness Weekend and Workshop…

Usher Awareness Weekend and Workshop 2017

Well it finally came, a date in the diary both Lyn and I had been looking forward to for some time, Amy Winehouse on the 15th of September and 16th...

Read more...

My "Blind Date with Ushers

My "Blind Date with Ushers

On Saturday 16 September 2017, Usher Syndrome Awareness Day,  I was very humbled to join in on an accessibility workshop hosted by Molly Watt from Molly Watt Trust and Chris...

Read more...

Applewatch, I won't leave home witho…

Applewatch, I won't leave home without it

Hi Molly Watt Trust I want to thank you for funding my applewatch. I had so much catching up to do through the school summer holidays including  training with my new guide...

Read more...

September's Skydive/ Now November Sk…

September's Skydive/ Now November Skydive

Due to mechanical problems with the aircraft on Sunday 3 September 2017 we have had to re-arrange this fundraiser.  New date for this event iis Sunday 26 November 2017 We are...

Read more...

Maidenhead Charity Ball 2017

Maidenhead Charity Ball 2017

I was fortunate to be introduced to local couple Diane and Laurence Armstrong at a Christmas party in 2016. We quickly struck up conversation about both their's and my charity work. Diane...

Read more...

Applewatch, Cochlear Implant for Ush…

Applewatch, Cochlear Implant for Usher Syndrome type 1

When I first got my applewatch from the molly watt trust I was really excited, being profoundly deaf and registered SSI with usher syndrome type 1.  I hoped the watch...

Read more...

Different, Unique, Priceless

Different, Unique, Priceless

Why don't people see the potential in different or in disabled? It is absolutely down to awareness, understanding and attitude in my opinion. As a little girl my parents made sure I...

Read more...

Emotion and Music to my Ears

Emotion and Music to my Ears

I have had some additional personal challenges recently with the reality that my first trusty and gorgeous guide dog Unis is retiring early and that I will continue my journey...

Read more...

ReSound LiNX² to ReSound LiNX3D - E…

ReSound LiNX² to ReSound LiNX3D - End User Review

For the last two years I have raved about ReSound LiNX² smart hearing aids and rightly so, they literally changed my life. I would be lying if I didn't say "REALLY...

Read more...

Applewatch for kids

Applewatch for kids

I recently received an email enquiry from the Mum of a 9 year old son living with Usher syndrome.   I regularly receive email from others living with the condition I’m...

Read more...

Usher Syndrome Children's Event - Se…

Since my young daughter was diagnosed with Usher syndrome 5 years ago I had never met another child or family living with Usher syndrome here in the UK. I'd been lucky enough...

Read more...

Is the NHS listening? Usher Syndrom…

Is the NHS listening?  Usher Syndrome, when you no longer hear with your eyes!

We met a lovely lady from Northern Ireland at a Molly Watt Trust ‘In it Together’ event in Edinburgh in October 2015, she has been a hearing aid user since...

Read more...

The love of Unis

The love of Unis

Unis came into my life when I was 16 years old.  Looking back I know I did not thoroughly embrace her, I also acknowledge the constant bullying and questioning of...

Read more...

A Visit to ATOS London Offices

A Visit to ATOS London Offices

I recently visited the ATOS London Offices, for an appointment set up by my Mum, Jane. We were there to meet with Dr McKillop to discuss varying issues and negative experiences...

Read more...

Mario's day to day life with Usher S…

Mario's day to day life with Usher Syndrome

My day to day life with Usher Syndrome (Retinitis Pigmentosa) is a constant fluctuation between moments where I can ‘get by’ and moments in which my disability presents real challenges...

Read more...

Disjointed Care or Digital Data?

Disjointed Care or Digital Data?

I was delighted to be invited to meet with Digital.Health London to discuss a variety of things relating to my journey with the NHS and the various services. It certainly got...

Read more...

Bali - Sound Sensations

Bali - Sound Sensations

At the end of my work and networking trip to the other side of the world, Mum and I decided on a a trip to the beautiful island of Bali...

Read more...

Usher Syndrome / Christmas Challenge…

Usher Syndrome / Christmas Challenges

Hello, my name is Josh Parker and I have Usher Syndrome type 3. Most of you reading this probably already have an idea what Usher Syndrome is, so I’ll keep...

Read more...

A toolkit to enable deafblind to acc…

A toolkit to enable deafblind to access the world

San Francisco in November was an amazing experience, not just because I got to speak in Silicon Valley to some of the very top people in digital at Qcon I...

Read more...

Singapore Airlines - Never again

Singapore Airlines - Never again

I blogged about my not just poor but disgraceful treatment by Singapore Airline cabin staff on 13 November during my flight, Heathrow to Singapore.  I very unpleasant start to travel...

Read more...

Singapore Airlines a Very Unpleasant…

Singapore Airlines a Very Unpleasant Experience!

13th November, the start of my adventure to the other side of the world.  It had been just two days since Mum and I had come off a plane from San...

Read more...

Deafness makes you more blind

My name is Colin Hetherington and I suffer with Usher Syndrome which is retinitis pigmentosa (blindness) which gives me all sorts of daily troubles from glare tonight blindness, headaches flashing...

Read more...

Facebook - Anti Social Media!

Facebook - Anti Social Media!

Dear Facebook I am a 22 year old who struggles with accessibility. I am registered deafblind, however, I was not born deafblind but deaf.  What that means, to you, is that I...

Read more...

iOS10 Accessibility

iOS10 Accessibility

Dynamic text galore! As we all know Apple products, get fairly regular software updates.  I had read and heard a few things about iOS 10, but was intending on waiting to experience...

Read more...

My Trip to Parliament

My partner Lyn decided that we should head for the big smoke to celebrate my 50th Birthday.  We are both have guide dog owners and both love London. I used to...

Read more...

University: To Listen, to Learn, to …

University: To Listen, to Learn, to Understand!

I have been asked over and over why I didn't complete my initial dream to be a primary school teacher and for some time it was a sore subject, however...

Read more...

I was hopeful but disappointed

I was hopeful but disappointed

My hopeful journey into the Wireless Bluetooth hearing aid world.   With Danalogic ifit cs71w hearing aids, Resound phone clip+ and a mini mic. I started off by asking my local NHS ...

Read more...

Being an Usher Mum

Being an Usher Mum

Being an Ushers Mum.  In 2011 I went for routine eye appointment and after a small discussion, the optician wanted to refer me for some tests.  I immediately had an in house...

Read more...

BA listened please listen more

BA listened please listen more

After my recent report regarding very unacceptable treatment whilst flying British Airways Premium Economy to Las Vegas in May I’m very pleased to announce that they have at least changed...

Read more...

Centre Stage Applewatch

Centre Stage Applewatch

AppleWatch and smart technology are brilliant for people with Usher Syndrome!  I have Usher Syndrome, which means I was born deaf and in the last ten years I have lost most...

Read more...

Unacceptable Audiology

Unacceptable Audiology

I have Usher Syndrome, I am deafblind and my condition is degenerative. The fact that it gets worse and my abilities change all the time means that I have to make...

Read more...

Life is a Rollercoaster

Life is a Rollercoaster

As part of my ‘rollercoaster ride’ I have experienced huge ups and downs over the years. A husband and four children comes with challenges but nothing out of the ordinary accept...

Read more...

Molly Addressing Accessibility with …

Molly Addressing Accessibility with British Airways

My outward journey to Las Vegas was nowhere near the way it should have been. The necessary call to ‘special assistance’ had been made by my mum prior to the trip...

Read more...

Usher to Usher

Usher to Usher

I hope you don't mind but after researching usher's syndrome and RP I came across your blog and I wanted to introduce myself. My name is Bethanie (or Beth), I'm...

Read more...

Applewatch for Award Winning Paracli…

Applewatch for Award Winning Paraclimber John Churcher

Hi I am John Churcher and I have Usher syndrome type 2. I have always had a hearing loss and was diagnosed with retinitis pigmentosa at the age of 14...

Read more...

Safe and Secure with Accessible Ring…

Safe and Secure with Accessible Ring Video Doorbell

About a month ago The Ring Video Doorbell was brought to my attention and I was asked if I'd like to try it. I love technology, particularly assistive and enabling technology. What...

Read more...

Global Accessibility Awareness Day 2…

Global Accessibility Awareness Day 2016

Usher Syndrome for me means my whole world is accessed via accessible assistive technology. A year ago to the day I was fitted with Resound Linx2 hearing aids.  It has been...

Read more...

Learning from each other - 'In it To…

Learning from each other - 'In it Together @ W Midlands'

Walsall 2016 'Hear no. See no, Techno' Jo Milne, Colin Hetherington and Me. Once again we were blessed with a room full of people all on similar journeys.  With Usher Syndrome or RP...

Read more...

Ready to meet others with Usher Synd…

Ready to meet others with Usher Syndrome

I decided I would like to meet some fellow ushers as never met anyone and my sight has been steadily getting worse . I had support worker for blind visit...

Read more...

Why Access to Social Media Matters

Why Access to Social Media Matters

I have been asked many times what my favourite social media is and why and my answer is always Twitter. The reasons I like Twitter are firstly from an accessibility view...

Read more...

What is in a logo

What is in a logo

We are often complimented on our logo. Molly designed the logo for our charity. Below she describes how and why she designed it. The first thing you will notice is the Molly Watt...

Read more...

Applewatch - Thank you Molly

Applewatch - Thank you Molly

My son read Molly's applewatch blog to me last year.  She made everything sound so easy and to be honest I didn't believe it. My son kept on and and and...

Read more...

San Francisco Adventure

San Francisco Adventure

San Francisco had been on my long list of places to visit and I was lucky enough to go on a girls only adventure with Mum and my younger sister...

Read more...

Effortless Applewatch One Month In

Effortless Applewatch One Month In

So I've now had my Watch a month and the best way I can describe it is 'Effortless.' When I first got it all in its beautiful packaging it felt like...

Read more...

When a Picture is more than a Pictur…

When a Picture is more than a Picture

Taking a photo to me is not just a picture, its capturing a moment, capturing sight I no longer have.   I take a picture and then take it apart to...

Read more...

Applewatch Awesome but Hearing Aids …

Applewatch Awesome but Hearing Aids Disappoint

I recently received an applewatch from The Molly Watt Trust, via their GlobalGiving project. I love gadgets. I have ushers syndrome type 3 which is gradually robbing me of both my...

Read more...