Friday, 29 June 2012

Have you bitten 'nicely' by the Olympic bug yet?

Countdown to the Olympics is now 28days and 61days to the Paralympics. And it's now London's turn to host.

So far this year has been quite exciting for a number of people. In particular, some deaf people and sportsmen/women/athletes; one of whom is Matthew Sykes who happens to be an old primary school mate of mine. Matthew was nominated to be one of the Olympic torchbearers. He currently holds the record of being the only deaf canoe slalomist in the world.


Matthew has competed on both national and international levels for Great Britain. After the Sydney Olympics in 2000, he had a 10 year break. Now he's back!

Photo from Matthewsykes.co.uk

Wednesday, 27 June 2012

Congrats!

Today I would like to give a big shout-out to a budding deaf politician, Umar Tukur. At the beginning of June, Tukur was appointed the Senior Special Assistant (SSA) on Disability Matters to the Governor of Adamawa State beating the incumbent, Abubakar Hosere whose tenure has been constantly awash with allegations of fraud and financial impropriety.

Tukur became deaf at the age of 6 following a bout of meningitis when he was in primary class 2. He then enrolled in Special Education Centre in Jada, Adamawa State. Tukur attended Plateau School for the Deaf briefly before returning to Special Education Centre in Jada to complete his O levels studies. He gained admission to study Special Education in which he graduated with a 2.1.  Upon graduation, Umar served at Kaduna. He completed his service successfully late last year and joined politics.



Tukur is very active in the deaf community in NGR and served in different capacities. He wishes to make a great impact in the lives of the PWDs particularly the deaf in his home state. Tukur has always believed that education is the key and strives to enable more deaf indigenes in his state to have good educational opportunities similar to which he has been fortunate to have.

He has the eye on the big political fish down the line...
Here is to wishing Umar Tukur a very successful tenure as the youngest SSA on Disability Matters in NGR and to make great milestones not only in his state but the country.

Friday, 22 June 2012

Then for the good news!

It is no secret that deaf people particularly in Sub-Saharan Africa have low access to (good) education at all levels. Having no/poor educational qualification in this part of the world is like having a one-way ticket to poverty and a miserable life.
Deaf people face numerous and huge challenges in their pursuit of gaining education from lack of good quality special schools with no qualified teachers to lack of accomodation for hearing in 'normal' learning institutions. Very few governments make (good quality) education for Deaf People a priority.

Gallaudet University in the USA is the only university in the world that offers tertiary level education to deaf people. So the good news as shown on the Daily Trust newspaper is (http://dailytrust.com.ng/index.php?option=com_content&view=article&id=165706%3Aal-makura-to-build-varsity-for-the-deaf-in-nasarawa&catid=1%3Anews&Itemid):

'Plans are underway by Governor Umaru Tanko Al-Makura of Nasarawa State to replicate the Gallaudet University in Washington D.C. in the United States in the state, Comrade Abubakar Hussaini, the state’s Commissioner for Education said yesterday. Hussaini, who noted that Gallaudet University specializes in undergraduate liberal arts education, career development and outstanding graduate programmes for the deaf, said Nasarawa is the first state in the country to seek the cooperation of Gallaudet. “The driving philosophy of Gallaudet is that no human being, no matter how physically challenged, is a waste. Gallaudet has provided the platform for the deaf and hard in hearing as well as persons suffering from other physical challenges, to play a role in our modern society, by equipping them with knowledge. That is what we want to replicate back home,” he said. He said the Al-Makura-led delegation met with the management of Gallaudet and extracted a commitment to collaborate with the administration in the establishment of the school. “We were challenged with the development of the students when we visited the university. They are good with modern technology, and we can have exactly that in our state,” he said.'

Now, isn't that cool? I had already mentioned on this blog that I think that this governor means well for deaf people and is working hard to make a real difference.

Monday, 18 June 2012

Sad news...

** Edited as I noticed that the original post was not published as intended- my apologies**

More than 3weeks ago on the 3rd of June, a Dana plane crashed in NGR which claimed the lives of all 153 onboard and an undetermined number on ground. I happen to know 4 people who sadly lost their lives in the disaster. A couple who made a lot of meaningful contributions in the lives of Persons With Disabilities (PWD). Ayodeji and Ngozi Cole were the officiating pastors of the Utako branch of TREM Church in Abuja.

Rev. Ayodeji and Ngozi Cole 


 I first met the very pleasant Mrs. Cole when someone directed me to her church  to carry out my project on sexual and reproductive health. It has the largest number of deaf members on their membership roll (over 150people) in Abuja and one of the largest in Nigeria. She was very excited and welcoming when I explained to her what I wanted to do. As she shared her passion for Special People which her church describes PWDs, was impressed with her empathy and vision which enabled  her and her husband oversee an organisation called 'City Shakers' Initiative' where they offer practical help to people. She not only encouraged me but also supported me by offering the use of the building facility to do the interactive sessions.

The last time that I saw Rev. Ayodeji Cole was at the Easter Christian Camp for Deaf People held in late March at Abuja where I volunteerred my medical services. He sponsored the program in which well over a 1000 deaf people attended.

The Coles are just among the handful of people in NGR who impacted the lives of PWDs particularly deaf people positively.

They will surely be missed.

Thursday, 10 May 2012

Another story shared by parents of a deaf child

As part of the Deaf Awareness week in the UK, some parents share their experiences in raising a deaf child. Here Paul and Ruth Neesham tell their story to Sunderland Echo.

http://m.sunderlandecho.com/lifestyle/parents-of-deaf-baby-inspire-others-with-their-story-1-4532643

Being told their beautiful baby is deaf plunged Paul and Ruth Neesham into a frightening world. In Deaf Awareness Week, this Sunderland couple are doing their utmost to inspire others. Women’s editor Linda Colling reports.


IT’S severe to profound deafness. I can remember sitting there and thinking ‘I don’t want to cry’ but then I just sobbed. I couldn’t stop,” says Ruth Neesham, of the moment she and husband Paul were told that devastating diagnosis about their newborn son, Jack, who was just three weeks old.

“It’s so hard to explain. I didn’t understand,” says Ruth, 33, who like Paul was totally unprepared and plunged into a frightening and unknown world.

With no deafness in their family and a son with perfectly normal hearing, Adam, four, Paul, says: “We literally cried for a month, dark days.”

They struggled to take in the crippling news that hit them like a sledgehammer. It was heartbreaking and Ruth recalls how hearing a song or a piece of music and she would break down at the thought that Jack would never hear such beautiful sounds. “It just broke my heart,” she says.

Then there was breaking the news to the family. Paul, 36, a sport’s sub editor at the Echo says: “It just brought it all back. It was such a raw wound.” And Ruth adds, “They wanted to stay strong for us but they needed time to digest it. It was totally out of the blue and you just don’t understand how this happened and how you are meant to deal with it. Ninety per cent of deaf children are born to hearing families like ours. And you have no idea of this world or how to cope with it.

“You grieve for the baby that you thought you were getting. I wouldn’t change him for the world, apart from I would love his ears to work. You are sad and praying for what your family life is going to be like. There’s not a day goes by that I don’t wish it was different.”

At nine months, Jack is a joy. A beautiful blue-eyed boy who radiates happiness. He’s progressing normally and it’s amazing how far Paul and Ruth have come in their determination to give their son the very best chance. From the day they were told that heartbreaking news, they have been supported by the National Deaf Children’s Society (NDCS).

When Jack was just 10 weeks old they went on a family weekend to a hotel in the area where they met others who had travelled the same road and were an inspiration to them.

Ruth says: “We met people who had been in our position and you can see how far you can come. It was very well organised by the NDCS. They shared experiences and what their children had achieved.” And Paul adds: “It was very inspirational to hear their stories, knowing that there is light at what was a very dark tunnel in the early days. And from all the help we have had from NDCS, friends and family, it’s all positive.”

They left heartened that nothing was going to stop Jack.

Playing on the floor at their home in Lutterworth Road, Tunstall, Jack is as bright as a button, watching everything, his facial expressions responding to their smiles and his parent’s total commitment to communicate with him. They talk to him as if he could hear and use baby signs to help him develop his communication skills. Big brother Adam makes him laugh a lot. And Jack is very much a daddy’s boy.

Paul goes to a British Sign Language course at Bede Sixth Form Centre for two hours every week with his sister and mother-in-law and then passes on to Ruth what he has learnt.

She will soon be returning to her job with Sunderland City Council and talks of how she struggled in the early days with stares, nudges and whispers from people as they noticed the baby with hearing aids.

She says: “It was really difficult taking him out. I wanted to protect him from it. You can see people looking. It’s alright for an older person to have a hearing aid but when it’s on a baby some people don’t know how to react. It’s ignorance and people don’t know how to deal with a baby with hearing aids. But recently, when I took Adam to nursery one of the mothers spotted me and said ‘Oh, your little boy has hearing aids. My little girl has them too!’” In nine months Jack has had a staggering 79 hospital appointments. He’s there every two weeks having impressions taken for new moulds for his hearing aids as he’s growing fast and also having hearing tests.

Ruth says: “Everyone at Jack’s hospital appointments have been wonderful, especially the Audiology Department at Sunderland. Ed Brown and his team are doing an amazing job.”

They don’t know what has caused his deafness – it could be a gene called Connexin 26 – which means that as a couple they have a one in four chance of having a deaf child. But nothing has been confirmed yet.

Ruth has just helped launch a playgroup for parents of toddlers and pre-school tots with a hearing loss. They meet in the Fingerpaint Nursery, Ryhope every fortnight on a Monday 1pm-3pm. The next meeting is on May 14.

Ruth can’t believe how far they have come since that bleak diagnosis and says: “It’s one of those things that will never change. However much technology can help Jack, whatever kind of hearing aids or if he gets cochlear implants, he is still going to be deaf. It’s not like anything can fix it at all.

“But there is hope and it gives us strength hearing how well other people’s children have done which just shows anything is possible for Jack. In the future he can do whatever he wants to do. We will make sure that he gets all the right support.”

In gratitude of all the support they have had and which is still on-going from NDCS, Paul is doing the Great North Run in September and the Great North Bike Ride on August 26 cycling 60 miles from Seahouses to Tynemouth to raise money for the charity.

Ruth says without NDCS they would have been completely lost. She says: “I wouldn’t know where to start. I wouldn’t have met any other families and wouldn’t understand what appointments we have to go to or what his future prospects are and what support is available to us. They do wonderful work.”

And in this touching appeal for sponsorship, Paul has written: “On the 24th August 2011, I was told the devastating news that my baby boy Jack was born profoundly deaf. He was only 23 days old. My world completely fell apart. He can’t hear my voice, he can’t hear music, he can’t hear the birds sing. Every little thing that we take for granted. It breaks my heart.

“However, if it wasn’t for the help and support of the National Deaf Children’s Society I don’t know how I would have begun to cope. They have helped me and my family deal with Jack’s deafness, providing advice and support.

“This charity is very dear to my heart and I can’t begin to imagine what I would do without it. Please give all you can to help this invaluable support continue for deaf children and their families.”

•To sponsor Paul go to justgiving.com/littleears or text Jack97 £5 to 70070

•For more information on the Hearing Impaired Playgroup contact lynndryden@dsl.pipex.com

EVERY year five or six babies are born in Sunderland with a significant hearing loss in both ears.

And this is being picked up at between four and eight weeks of age through the Local Newborn Hearing Screen Programme (NHSP) provided by City Hospitals Sunderland NHS Foundation Trust. This covers about 7,000 babies born across Sunderland, South Tyneside and Gateshead.

Ed Brown is a Consultant Clinical Scientist (Audiology) and Local Director of NHSP. And he is in the front line of breaking the news to parents, like the Neeshams, that their child has a significant hearing loss.

Before the introduction of NHSP in 2006, significant hearing loss was typically not identified until about 12 months of age. The earlier the detection means that there are much better outcomes for the child and family.

High quality Digital Sound Processing hearing aids are designed specifically for young children. The Royal also has the benefit of its own earmould laboratory which means that specialised earmoulds can be made quickly for babies and young children.

About three children a year might be referred for assessment for a cochlear implant usually to the North East Cochlear Implant Programme based in Middlesbrough. A cochlear implant is not appropriate for everyone and is for severe-profound hearing loss, where assessment has shown that there is limited benefit from conventional hearing aids.

Most children who are accepted for cochlear implantation will usually receive an implant in both ears. The cost of one cochlear implant, including surgery and followup is about £30,000.

Mr Brown and his team work very closely with colleagues based in local Education Service (Sensory Support) and many of the early appointments with the family are held jointly. He says: “We also have excellent links with medical colleagues in the Ear Nose and Throat Department, children’s doctors, speech and language and other health care professionals. We try to make sure that we communicate effectively with families and other professionals. All our reports are written to parents, carers with other professionals copied in as appropriate.

“We are committed to improving services and have engaged with national quality initiatives in audiology such as the Quality Enhancement Tool (QET) and Improving Quality In Physiological Diagnostic Services (IQIPS). However, we know that we may not get things right all of the time and we hope that by having an open an honest approach families feel able to contact us and discuss any issues with us.

“The local NHSP is subject to a national quality assurance process every 18 months. The last assessment was in March 2011 and we were highly rated (our overall score was 4.24 out of 5).

“The challenge is to ensure that the through high quality services, support and good communication between professionals that a child with hearing loss has the very best chance of developing communication along the same pathway as their normally hearing peers.

Mr Brown has 23 years experience in clinical audiology. He is a lead examiner for the British Academy of Audiology and has also contributed to the development of national protocols for children’s audiology and various quality assurance activities for both adult and children’s audiology services.

Article from Sunderland Echo.

Tuesday, 8 May 2012

Deaf Awareness Week in the UK

...started yesterday (7th May) and ends on 13th May.

I wrote briefly on hearing dogs and I still have a lot to learn about them! Here is another brief article about them and the role they play in the Deaf community.

http://www.itv.com/news/central/2012-05-08/deaf-awareness-week/

"James Cheung from Derbyshire is part of a pioneering project placing hearing dogs with deaf children. His is one of only 12 placements of its kind in the country.

Now James and his hearing dog Kurt have become the poster couple promoting the Hearing Dogs for Deaf People charity, which is celebrating its 30th anniversary.

It takes around £45,000 to train and place a hearing dog. Kurt helps James in all aspects of his life, including getting ready and walking to school.

James and Kurt have already been on show at Crufts in Birmingham, and have also met the Prime Minister who helped celebrate the charity's anniversary."

Sunday, 6 May 2012

The latest on the Disability Bill in NGR

I wasn't sure what to make of the passing of the Disability Bill by the lower chambers of the country's law-making assembly-the House of Representatives. It was sponsored by Abike Dabiri-Erewa, a vibrant female member of House of Representatives (a truly nice compliment- not because she's female but because she is really making impact both within and without her constituency unlike the vast majority of her counterparts.)

Courtesy of Africanexaminer website
Apparently there was some really stiff resistance from the other members. About two years ago, the current president passed the Bill which went through lots of hassles in his predesessor's time-more than 7years!The President refused to sign it into law before he was sworn in.


Which now means the process has to start all over again. Who knows how long it will take this time?

*sigh sigh*

Thursday, 3 May 2012

Ted Evans- Deaf filmmaker

Recently I posted about a Deaf filmmaker who was embarking on a project on role models for deaf people in London. Good news! He has finished that project which is called 'From us to you'.

And with his expressed permission, I'd like you to have a look at it through this link:

https://vimeo.com/41284380

And also pass it on to others.

Well done Ted!

Saturday, 28 April 2012

'Deaf and dumb' 'Deaf and dumb'

If I was to be paid a tenner for hearing that phrase (along with 'deaf and mute') since the beginning of the year, I tell you that I'll become a thousandairesS.. o joke!

Seeing that many people are not able or fail to connect the necessary dots between hearing and speaking ab nitio, I have had to ask them to imagine what it means to speak the way they do. Did they imagine it into existence?  How do they know the 'I' in words should be pronounced as an 'ee' or an 'ai' without looking at a dictionary or hearing someone say it.

Using the word 'dumb' is a no-no. Dumb in today's speak means 'stupid' and deaf people are certainly not that!  I have come across the usage of 'speech-impaired' as a politically correct term but I do not think that it is accurate. Simply because many deaf people CHOOSE not to speak or prefer to use sign language. Another word 'unvoiced' brings up some varying reactions as is the word 'silent'.

The word 'deaf' is enough and acceptable by for many deaf. There is no need to waste ink or carbon dioxide to add '...and dumb'. Really.

Thursday, 26 April 2012

Deaf discrimination

Yet again, I received another complaint about deaf people being discriminated against. I just cannot help but wonder if it is deliberate. I will recount and you can make up your mind on that.

Yesterday, I was told that in Adamawa State 105 Persons With Disabilities got employed by the state government (laudable effort in itself). But can you guess how many out of the 'fortunate' 105 were deaf? Guess? Guess again... Just TWO! Believe me, Adamawa State has a high proportion of deaf people and a number of them are educated. To make matters worse, none of the educated deaf was hired/appointed. Now don't get me wrong...it would be nice for an uneducated deaf to work in their state Civil Service. What would they be working as a result of their illiteracy? I won't answer that questi
on but I am sure that you'll have a fairly good idea. My take on this is the 2deaf people who were hired should go back to school to improve their literacy so they stand a better cchance in life than being consigned to a miserable life down at the lowest rung of the Civil Service.
It is totally unfair that the Special Assistant to the Adamawa State Governor on Disability Matters not to have consulted first with each disability group. And extremely unfair of him to do the pickings himself and not pick the deaf graduates.

So you can see why I earlier asked if the deaf discrimination is deliberate.

Saturday, 21 April 2012

Sad passing of UK's first deaf MP

Yesterday, the first deaf MP Lord Jack Ashley passed away at the age of 89 years old..

http://www.huffingtonpost.co.uk/mobileweb/2012/04/21/lord-ashley-of-stoke-dead-disabled-rights-campaigner_n_1442469.html?1335006271

courtesy of the huffington post website
Disabled rights campaigner Lord Ashley of Stoke, the first deaf MP, has died aged 89, it was announced on Saturday.
The Labour peer passed away last night after a short illness, according to his family.
BBC presenter Andrew Marr, who is married to the peer's columnist daughter Jackie Ashley, said: "Lord Ashley of Stoke, the former Labour MP Jack Ashley, died last night, April 20, after a short illness at the age of 89."
Jack Ashley won the seat of Stoke-on-Trent South in 1966, but lost his hearing less than two years later after an unsuccessful ear operation.
He recalled in his autobiography that the last voice he heard was that of the late rugby commentator Eddie Waring.
After initially fearing he would be forced to give up politics, Ashley learned to lip-read.
Other MPs, including political foes such as Prime Minister Edward Heath, turned towards him during Commons debates so he could get a clear view of their mouths.
Lord Ashley also worked hard to modulate his speaking voice, which he could no longer hear.
However, his deafness never affected his combative attitude.
"Early on when I first lost my hearing, I think people were a little fearful about attacking me. But as I re-established my confidence, that soon fell away," he said.
As his fame as an advocate for disabled rights grew, Lord Ashley became president of the Royal National Institute for the Deaf.
He also played a major role in the campaign for better compensation for children disabled by the drug Thalidomide, which was given to mothers to treat morning sickness during the 1950s and 1960s.
In 1993, a year after he was made a life peer, Ashley's hearing was partially restored by a cochlea implant, an electronic device which stimulates the nerves in the inner ear.
Lord Ashley worked in a factory after leaving school at 14, becoming a shop steward and a local councillor.
He studied at Oxford and Cambridge on scholarships, and worked as a producer for the BBC before entering parliament.
Andrew Marr added: "The campaigner for the rights of the disabled, who had been the first ever deaf MP, won major victories for the victims of the drug Thalidomide, for victims of army bullying, and for victims of domestic violence.
"He is survived by his three daughters, Jackie Ashley, Jane Ashley, and Caroline Ashley."
Jackie Ashley paid tribute to her father on Twitter:
Ed Miliband led the tributes from politicians and peers:

Friday, 20 April 2012

Disability and media

Yesterday morning (19th April), I attended a seminar on 'Disability and media' which was organised by the Disability Rights Coordinator of CBM, Dr. Duro Onota who is partially-sighted.

Quite a handful of the media/ press women and men came. I think that they were mostly from tv. And of course, some members from the disability community were present.

We all know the very influential role that media (be it tv, radio, newspapers,social media) play in shaping the perception of the public. When I say 'very influential', I mean exactly that. It does seem that some presswomen/men are making efforts to present Persons With Disabilities with a positive image rather than as objects of pity.

It was encouraging to see that they paid attention and participated in the group discussions. During the group discussions, we covered unacceptable terms or phrases used to describe PWD like ' deaf and dumb/mute, cripple/lame, invalid, handicapped, spastic, mentally retarded, deformed, polio victim, afflicted (by), suffering (from), mongol'. The list is inexhaustive.

We also talked about issues for media campaign like inclusive education, inclusive development, passing the Disability Bill into law and for the Nigerian film Industry aka Nollywood (to cast PWDs and for criptwriters to include PWDs in their scripts)s

Disability and media

Yesterday morning (19th April), I attended a seminar on 'Disability and media' which was organised by the Disability Rights Coordinator of CBM, Dr. Duro Onota who is partially-sighted.

Quite a handful of the media/ press women and men came. I think that they were mostly from tv. And of course, some members from the disability community were present.

We all know the very influential role that media (be it tv, radio, newspapers,social media) play in shaping the perception of the public. When I say 'very influential', I mean exactly that. It does seem that some presswomen/men are making efforts to present Persons With Disabilities with a positive image rather than as objects of pity.

It was encouraging to see that they paid attention and participated in the group discussions. During the group discussions, we covered unacceptable terms or phrases used to describe PWD like ' deaf and dumb/mute, cripple/lame, invalid, handicapped, spastic, mentally retarded, deformed, polio victim, afflicted (by), suffering (from), mongol'. The list is inexhaustive.

We also talked about issues for media campaign like inclusive education, inclusive development, passing the Disability Bill into law and for the Nigerian film Industry aka Nollywood (to cast PWDs and for criptwriters to include PWDs in their scripts)s

Wednesday, 11 April 2012

Deaf people are left out......again!!!!

I have just sent an email to one of the researchers from my alma-mater (London School of Hygiene and Tropical Medicine) who is involved in a BIG project in Burkina Faso. It is a radio campaign to reduce child mortality. Why do researchers, media companies keep forgetting that deaf people cannot readily access radio campaigns for obvious reasons??!

It is a very good initiative as it is life-saving.....for those who can hear the messages because the project involve targeted 60second message on the radio and radio phone-in programmes. The project was launched in early March and will run over a period of two and a half years. You can see the issue here?

In the email, I politely requested that the deaf population be involved in THIS campaign in one way or the other. They just have to find a way of doing that. Not doing that means that the deaf community gets marginalised for 2.5years and unfortunately bear the sad burden of child loss if they don't or can't access these messages.

Here is the link: http://www.lshtm.ac.uk/newsevents/news/2012/radio_campaign_launches_burkina_faso.html

And the article:

The London School of Hygiene & Tropical Medicine (LSHTM) and Development Media International (DMI) have launched a cluster randomised controlled trial of an innovative child survival intervention.
The project is funded by the The Wellcome Trust and the Planet Wheeler Foundation, set up by the founders of the Lonely Planet travel series.
The campaign – launched on March 7 - involves the broadcast of targeted 60-second health messages on the radio and radio phone-in programmes that will run for the next two and a half years. 
The messages, developed by the School in collaboration with DMI and other partners, are designed to change the behaviour of pregnant women and mothers through increased awareness and information, and reduce the number of children dying before their fifth birthday in Burkina Faso.
The study represents the first time that the impact of mass media on lives saved has been either modelled or measured.
Lead investigator Simon Cousens, Professor of Epidemiology and Medical Statistics at  the London School of Hygiene & Tropical Medicine, said: “We’ll be measuring the impact using a robust scientific methodology: a cluster randomised controlled trial. It will be the largest, most rigorous evaluation ever conducted of a mass media intervention and it will be exciting to find out how many lives can be saved using this approach.”
The first radio spots will promote exclusive breastfeeding – a behaviour which reduces the risk of a child dying from diarrhoea or respiratory infections. The spots will be broadcast on seven community radio stations in the West African country of Burkina Faso which have partnered with DMI to deliver the campaign.
“The project is innovative in three ways”, said  Roy Head, Managing Director of DMI. “Firstly, we’re broadcasting messages on all causes of death, not just individual issues. Secondly, we’re broadcasting very intensively: ten spots per day, and two hours of phone-in programming every night on every station. Thirdly, we’ll be measuring the impact more rigorously than has ever been done before. We’re hoping to prove that we can change behaviours on a scale large enough to save a lot of lives.”


Here is the equation that many people do not get:

  
From tumblr website
AND
                  
                                                       









IS EQUAL TO:

 
From photosofcutebabies.com







OR.................

From glamquotes.com





Yes really!!