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Archive for the ‘Blindness’ Category

Doctors team up to stop preventable blindness – Fox News

Thursday, April 20th, 2017

It takes remarkable drive and ambition for a young boy from the small east Nepalese village of Olangchungola with no running water or electricity to become one of the leading eye surgeons in Asia. Especially considering this village is a long four-day walk away from the nearest school. But after losing his 17-year-old sister to the tuberculosis, Ruit decided to focus on medicine to so other peoples lives arent destroyed by easily preventable and curable diseases.

In the Himalayas, like many other parts of the world, cataracts blindness is considered a natural part aging even though its completely preventable.

Dr. Geoffry Tabin is an ophthalmologist and close friend to Ruit. He told FoxNews.com, cataracts is a clouding of the crystalline lens, which is a small lens that focuses light that sits just behind the pretty colored part of the eye called the iris. In the western world, surgery can easily cure cataracts but those in the third world have to live with it and fall into blindness.

Typically, cataracts surgery involves removing the cloudy lens and replacing it with an artificial one called an intraocular lens. Ruit wanted to bring this procedure to the Himalayas. But, in order to do so the process had to be simplified and made more cost effective. His idea was to remove the expensive technology, make the process manual and somehow lower the cost of the intraocular lenses. To achieve this goal he created the Tilganga Eye Centre - now the Tilganga Institute of Ophthalmology - in 1994, in Kathmandu, Nepal.

The cost of these intraocular lenses at that time was over 200 dollars and that was almost impossible to provide that to people at the community level, Ruit told FoxNews.com. Ruit teamed up with ophthalmologist Dr. Fred Hollows to start making the lenses locally in Nepal. The approach worked. Within three years the costs per lens dropped dramatically to just three dollars.

With costs down and the simplification of the procedure, Ruit was able to provide over 100,000 cataract surgeries for just 25 dollars per procedure.

Using his efforts as groundwork, Ruit teamed up with Tabin to create the Himalayan Cataract Project whose aim is to focus on training and developing the infrastructure and techniques to end preventable blindness.

Weve been able to bring the amount of blindness in Nepal from 1 per hundred down to .28 percent, Tabin said. Their efforts and spreading to other parts of Asia and even Africa.

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India swaps 40-yr-old definition of blindness for WHO criteria: 40 lakh people will no longer be classified ‘legally … – Firstpost

Thursday, April 20th, 2017

New Delhi: India has changed its over four-decade-old definition of blindness, bringing it in line with the WHO criteria, a step that would drastically bring down the number of people considered "blind" in the country.

According to the new definition, a person who is unable to count fingers from a distance of three metres would be considered "blind" as against the earlier stipulation of six metres, which was adopted in 1976.

The aim of revising the definition is also to be able to generate data which can be compared with global estimates and achieve the WHO goal of reducing the blindness prevalence of India to 0.3 per cent of the total population by 2020.The notification in this regard has been issued by the Union Health Ministry.

Going by the new definition, the population of blind people in India will reduce from 1.20 crore (as per National Blindness survey 2007 data) to 80 lakh."Because of the earlier definition, we were projecting a higher figure of blind people from India at any international forum, presenting ourselves in poor light.

Image used for representational purpose only.

"Also, the data that we generated under the programme could not be compared with the global estimates as other countries were following the WHO definition," said Dr Promila Gupta, Deputy Director General of National Programme for Control of Blindness (NPCB).

Further, India has to achieve the goal set by the WHO which recommends reducing the prevalence of blindness to 0.3 percent by 2020 to achieve the elimination of avoidable blindness.

"It would have been extremely difficult to achieve the WHO goal using the earlier NPCB definition since we had been addressing an extra 4 million (40 lakh) individuals blind due to refractive errors. Whereas, by adopting the blindness criteria of WHO, India now can achieve the goal," said Professor Praveen Vashist, in-charge Community Ophthalmology at Dr R P Centre for Ophthalmic Sciences, AIIMS.

Also, the name of the scheme, 'National Programme for Control of Blindness' has been changed to 'The National Programme for Control of Blindness and Visual Impairment'.

"The programme, henceforth, will not only focus on the blind persons but also those with some kind of visual impairment. With the change in nomenclature, the number of beneficiaries will now increase to 40 million," Dr Vashist added.

The previous definition of blindness was adopted at the time of the inception of the NPCB in 1976.

"The probable reason for keeping 6 metres as the cut off distance for defining blindness in India was to include economic blindness cases which referred to a level of blindness which prevents an individual to earn his or her wages.

"In contrast, the WHO definition adopts a criteria for blindness that is which hampers the routine social interaction of a person (social blindness)," Gupta said.

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India swaps 40-yr-old definition of blindness for WHO criteria: 40 lakh people will no longer be classified 'legally ... - Firstpost

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IBM uses deep learning to better detect a leading cause of blindness – ZDNet

Thursday, April 20th, 2017

An eye scan with Diabetic Retinopathy hemorrhages highlighted.

IBM on Thursday announced its latest breakthrough in combating eye disease, with new research methods that could help doctors diagnose and classify diabetic retinopathy (DR).

DR is a complication of diabetes and one of the leading causes of blindness in the US. Using deep learning and visual analytics technology, IBM researchers were able to classify the severity of patients' diabetic retinopathy (DR) with 86 percent accuracy.

The method takes just 20 seconds to identify and classify legions, which could help more doctors screen more patients. Currently, diabetes patients are screened for DR by an expert clinician, in an often manual and time-intensive process.

DR is classified into five severity levels (no DR; mild; moderate; severe; proliferative DR) based on the presence of lesions on the retina and damage to the retina's blood vessels.

IBM's new method for classifying the disease combines two analytics approaches -- convolutional neural networks (CNN) with a dictionary-based learning to incorporate DR specific pathologies.

The research results were presented at the IEEE's International Symposium on Biomedical Imaging this week in Melbourne.

The work builds on IBM Research's use deep learning techniques and image analytics technology to help diagnose a range eye diseases. IBM has invested heavily in using cognitive technology in the health care sector, with 12 research labs around the world focused on using medical imaging analysis for a range of diseases from eye disease to lung cancer and melanoma.

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Understanding Inherited Blindness Through Zebrafish Eyes – Asian Scientist Magazine

Thursday, April 20th, 2017

Discovery of a gene in zebrafish that triggers congenital blindness could lead to new treatments for a similar disease in humans.

Asian Scientist Newsroom | April 20, 2017 | In the Lab

AsianScientist (Apr. 20, 2017) - In a study published in Scientific Reports, researchers report a zebrafish model of Leber congenital amaurosis (LCA), one of the most common causes of childhood blindness that accounts for five percent of all vision impairments.

LCA can be genetically transmitted to a child when both parents possess at least one dysfunctional copy of a gene involved in eye development. Although LCA is relatively common, the molecular mechanism behind the disease remains unclear.

Now, researchers in the Developmental Neurobiology Unit at the Okinawa Institute of Science and Technology Graduate University (OIST) have found a similar syndrome in zebrafish. From this research, they aim to use zebrafish as a model to unravel the causes of LCA and therefore provide new leads for a treatment.

LCA affects the retina, the thin layer of tissue at the back of the eye that detects light as well as differentiates colors and communicates the information to the brain via the optic nerve. A healthy retina usually features light-sensitive cellsphotoreceptorscalled cones and rods. Cones are specialized in bright environment and detect colors while rods are used in dim light but are monochrome, which is why we see in black and white at night.

A person with LCA will display deformed or absent cones and rods. A total of 24 genesincluding a gene called Aipl1have been linked to LCA in humans and mice.

Using a genetically mutated zebrafish embryo that did not react to visual stimuli, the researchers discovered that zebrafish DNA contains two Aipl1 genes, namely Aipl1a and Aipl1b, which are active in rods and cones respectively.

The mutantcalled gold rush (gosh)presents a genetic mutation in the Aipl1b DNA sequence, and therefore losing Aipl1 activity in cone photoreceptors. Consequently, the cone photoreceptors showed a deformed morphology and sustained degeneration. Rods however were not affected, suggesting that the degeneration is cone-specific.

Probing further, the authors of the study also revealed that Aipl1 is critical for the stability of two enzymescGMP-phosphodiesterase 6 and guanylate cyclasewhich mediate phototransduction, the process of converting light into an electrical signal. Without these enzymes, the zebrafish is unable to react to light stimulus as the information is stopped in photoreceptors and fails to initiate the transmission of visual information into the brain through the optic nerve.

The research indicates that Aipl1b gene is important for visual function and maintenance of cone photoreceptors in the zebrafish. Without it, cones do not detect light stimuli and degenerate during development.

The gosh mutant is a good model for understanding the molecular and cellular mechanism of cone cell death and the pathological process of human LCA. Hopefully, this new knowledge will help to find a future cure for patients who suffer such a devastating disease as LCA, said Dr. Maria Iribarne, first author of the study.

The article can be found at: Iribarne et al. (2017) Aipl1 is Rrequired for Cone Photoreceptor Function and Survival through the Stability of Pde6c and Gc3 in Zebrafish.

Source: Okinawa Institute of Science and Technology Graduate University; Photo: Shutterstock. Disclaimer: This article does not necessarily reflect the views of AsianScientist or its staff.

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India, UK to collaborate for treating corneal blindness – Telangana Today

Thursday, April 20th, 2017

Senior doctors from LVPEI said the focus of Indian eye researchers was on ocular regeneration, which involved developing methods to regenerate eye tissues.

Indian and UK executives speaking at the inaugural function of the four day UK-India Researcher Links Workshop, organised by The University of Sheffield, UK & L V Prasad Eye Institute, Hyderabad, on Thursday at Hotel Taj Vivanta.

Hyderabad: Leading eye researchers from India and United Kingdom have agreed to join hands in an endeavour to eliminate corneal blindness.

Researchers from both the countries participated in a workshop aimed at discussing and developing innovative and scientific solutions to treat damaged corneas, at LV Prasad Eye Institute (LVPEI) on Thursday.

The workshop, titled Application of innovative chemistry and bio-materials to treat corneas damaged by trauma, disease and infection featured close to 200 young researchers who were hand picked by senior eye researchers from UK and India after a thorough scrutiny of applications.

We need young scientists from both the countries who can generate unique ideas to handle corneal ailments. The workshop will establish collaborations between the two countries and nurture a generation of young scientists who can respond to ailments related to corneas, said Deputy Chief Executive, Royal Society of Chemistry, UK, Stephen Hawthorne.

Senior doctors from LVPEI said the focus of Indian eye researchers was on ocular regeneration, which involved developing methods to regenerate eye tissues. A major goal of this collaboration is to eliminate corneal blindness that will involve stem cell therapy for cornea, replacement of cells by using artificial cornea and explore 3D printing of tissues and organs for such eye defects, said Vivek Singh, Scientist, LVPEI.

The Royal Society of Chemistry and British Council through Newton Fund, are investing Rs 2.50 crore to organise Newton Researcher Links workshops for creating a platform for Indian and UK researchers.

Mei-kwei Barker, Director, British Council South India; Professor Sheila MacNeil from University of Sheffield and top researchers from LVPEI were present.

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New treatment for blindness – Cambridge News

Thursday, April 20th, 2017

A new treatment for blindness caused by diabetes is on the way, with Bicycle Therapeutics at Babraham announcing a milestone achievement.

The new treatment, for diabetic macular edema, is being devised in partnership with Belgian company ThromboGenics, which is focused on developing treatments for back of the eye disease.

Bicycles are a new class of small molecule medicines designed to overcome many of the limitations of

existing drugs.

Under the terms of the alliance, ThromboGenics has an exclusive license to undertake pre-clinical and clinical development and subsequent commercialization of a specified drug candidate; in return Bicycle receives development milestone payments and royalties on sales of products resulting from the collaboration.

Were delighted to be realizing our first candidate milestone from a Bicycle alliance and to be

advancing another Bicycle towards the clinic for the treatment of a significant disease, in this case DME, said Dr Kevin Lee, Bicycle chief executive. This achievement confirms the potential for Bicycles to be developed to address a broad range of poorly treated diseases.

We are continuing to expand our pipeline through research collaborations which will extend our reach into new therapeutic areas and allow us to explore new applications for the Bicycle platform.

This is an exciting moment in our partnership with Bicycle Therapeutics, said Dr Patrik De Haes, chief Executive of ThromboGenics NV. We believe that THR-149, a novel plasma kallikrein inhibitor, holds great promise for ophthalmology applications, expanding the range of treatment options available for people with diseases of the eye, particularly DME. We are rapidly moving towards the

clinic, and expect to begin clinical development early in 2018.

Bicycle Therapeutics is developing a new class of medicines to treat cancer and other important

diseases based on its bicyclic peptide product platform.

Bicycles are like antibodies. Their small size enables rapid and deep tissue penetration, allowing tissues and tumours to be targeted from within. Their peptidic nature provides a tuneable pharmacokinetic half-life and a renal route of clearance, thus avoiding the liver and gastrointestinal tract toxicity often seen with other drugs.

The company says it is rapidly advancing towards the clinic with its lead programmes which selectively deliver toxins to tumours. Its unique intellectual property is based on the work initiated at the MRC Laboratory of Molecular Biology in Cambridge by the scientific founders of the company, Sir Gregory Winter and Professor Christian Heinis.

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East Syracuse woman finds strength in her blindness: The – WSYR

Thursday, April 20th, 2017

EAST SYRACUSE, N.Y. (WSYR-TV) - An East Syracuse woman went blind before she turned 30, and she turned what was once one of the worst time of her life into material for motivational speaking.

Diabetes not only took Monica Johnsons sight in 2002 it made her bedridden with nerve damage.

My first words that I had uttered were my life is over and Ill never be able to do anything ever again and that's it my life is over, she said.

She was a manager at a store at Destiny and a horse trainer before she went blind, and she was worried she would not have the same opportunities again.

I had gone from being totally sighted and working all sorts of jobs and opportunities to just to losing my sight. It started getting dark it was almost like a dimmer switch and things just starting a darker little by little by little. Over a six month period of time, on Feb. 9th I woke up and that was that was the last time I had saw daylight, Johnson said.

She said she had to move in with her parents and went into a deep depression.

Johnson said one day, she had a feeling that there is so much more to life than laying in bed and doing nothing.

Today, she lives on her own and travels the country as a motivational speaker.

She says there is no way she should be doing all she does today without the help of Aurora Central New York, an organization that helps both the vision and hearing impaired.

If youd like to get in contact with Monica Johnson, you can reach her at visionwithnosight@gmail.com.

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The simple test that could prevent permanent blindness – Starts at 60

Thursday, April 20th, 2017

Glaucoma is the worlds leading cause of irreversible blindness. And heartbreakingly, so many cases are preventable.

Glaucoma develops slowly over the years, often without any noticeable symptoms. It describes the build-up of pressure inside the eye that pushes against the optic nerve, causing permanent damage over time.

There is no cure, and any vision lost to glaucoma cannot be reversed. But a simple, regular eye examination can make an incredible difference. Early diagnosis can help prevent any additional damage, with eye drops, medication or surgery able to control the pressure.

The risk grows greater with age. At 60, your chances of developing glaucoma will be 4 to 10 times higher than at age 40. If you have a family history of glaucoma, this risk is increased tenfold.

A new campaign called Glaucoma Aware is on a mission to unearth 150,000 Australians who face preventable blindness and dont know it. As per the campaigns recent survey results, around 60% of Australians either havent been tested or dont know if theyve been tested for glaucoma.

Consult your optometrist today, or click here to learn more.

One in two family members of Australians with advanced glaucoma are likely to show early signs of the disease.

Sue, 58, a Melbourne optometrist, knows this sadly all too well, with three out of four generations of her family affected.

Sues grandmother, Nellie, was diagnosed late in life. She was put on topical eye-drop medications, but unfortunately her glaucoma was already well established, she says.

Her glaucoma proved very difficult to control she was virtually blind by the time that she died, aged 95 in a nursing home.

Sues mother, Ellen, also got her eyes examined. Fortunately, she was diagnosed at a very early stage. shes been on topical eyedrops these last 30 odd years, and fortunately shes had good vision.

At 84 she takes no other medications and leads a very active lifestyle, including driving confidently.

Sue, keenly aware of her higher risk, gets an examination every year.

But Sue was taken by surprise when her son Daniel, also studying optometry, called with some startling news.

In the final week of his course, Daniel rang us and said the students had been checking each others intra-ocular pressures in preparation for their final practical examination, and his had been found to be unusually high.

At just 28 (an age where everybody thinks theyre bulletproof), Daniel was diagnosed with pigment dispersion syndrome an aggressive condition that can lead to glaucoma if its not treated at an early age.

Are you at risk from glaucoma? Learn more at Glaucoma Aware

Thankfully, at the time of diagnosis, Daniel showed no visual loss. He now receives regular care, and his pressures are now controlled with eye drops.

The family is optimistic he can continue life with his vision unaffected, and that in time, the pressure will subside.

Nonetheless, it was a startling wake-up call: glaucoma can affect anyone at any age. Even infants can develop the disease.

We routinely tell our patients that it should be checked every two years from the age of 40, or earlier if you have a family history, says Sue. But it certainly brought the message home to us: even at a younger age, this is something that can increase without having any awareness.

Sue believes this is particularly important for Australias over-60s. The incidence of glaucoma increase dramatically through the decades.

A lot of people self-diagnose as they get older. If they have trouble with their eyesight, they assume that its just because theyre getting older.

I think the lesson is that regular check-ups are important for everybody.

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India changes definition of blindness, opts for WHO criteria – Times of India

Wednesday, April 19th, 2017

NEW DELHI: India has changed its over four- decade-old definition of blindness, bringing it in line with the WHO criteria, a step that would drastically bring down the number of people considered "blind" in the country.

According to the new definition, a person who is unable to count fingers from a distance of three metres would be considered "blind" as against the earlier stipulation of six metres, which was adopted in 1976.

The aim of revising the definition is also to be able to generate data which can be compared with global estimates and achieve the WHO goal of reducing the blindness prevalence of India to 0.3 per cent of the total population by 2020.

The notification in this regard has been issued by the Union Health Ministry.

Going by the new definition, the population of blind people in India will reduce from 1.20 crore (as per National Blindness survey 2007 data) to 80 lakh.

"Because of the earlier definition, we were projecting a higher figure of blind people from India at any international forum, presenting ourselves in poor light.

"Also, the data that we generated under the programme could not be compared with the global estimates as other countries were following the WHO definition," said Dr Promila Gupta, Deputy Director General of National Programme for Control of Blindness (NPCB).

Further, India has to achieve the goal set by the WHO which recommends reducing the prevalence of blindness to 0.3 per cent by 2020 to achieve the elimination of avoidable blindness.

"It would have been extremely difficult to achieve the WHO goal using the earlier NPCB definition since we had been addressing an extra 4 million (40 lakh) individuals blind due to refractive errors. Whereas, by adopting the blindness criteria of WHO, India now can achieve the goal," said Professor Praveen Vashist, in-charge Community Ophthalmology at Dr R P Centre for Ophthalmic Sciences, AIIMS.

Also, the name of the scheme, 'National Programme for Control of Blindness' has been changed to 'The National Programme for Control of Blindness and Visual Impairment'.

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Albertan helping combat blindness in the developing world – CTV News

Wednesday, April 19th, 2017

CTV Calgary Published Wednesday, April 19, 2017 11:38AM MDT Last Updated Wednesday, April 19, 2017 11:55AM MDT

Hundreds of thousands of people in the developing world are suffering from blindness or visual impairment due to a lack of one of the worlds most basic resources and a Calgary-based organization, including the efforts of one man, is trying to change that.

Rob Ohlson, the chairman for Operation Eyesight Universal, an organization dedicated to the prevention of avoidable blindness and the restoration of sight, has been going the extra mile to raise funds for his group.

He is credited with bringing in huge donations for the Washing Away Blindness campaign that aims to provide clean water to villages throughout Zambia and protect them from the devastating trachoma, a bacterial eye infection that leads to blindness.

He says he joined to celebrate the life of his father.

It was a way to celebrate his life and his career in India with the Bob Ohlson Centre for Sight Enhancement. I was just immediately struck by the impact that Operation Eyesight had.

In addition to raising money from donors, Ohlson has been matching donations and has come up with $485,000 so far.

Those funds are used to drill water wells for 24 of Zambias most vulnerable communities.

The clean water helps stop the spread of trachoma by allowing people to wash their hands and faces properly.

Brian Foster, the executive director for Operation Eyesight, says he is very happy with Ohlsons involvement.

He brings a lot of energy to the table and hes very involved with us as individuals and he pretty well knows everyone in our office hes pretty familiar with us all.

Ohlson says the work is very rewarding too, especially when it comes to seeing the change that clean, fresh water brings to an African village.

A lot of these areas are fairly dry, specifically in Zambia where were doing a lot of wells. You go back a year or two later and its just lush and green and the population is growing and its phenomenal.

For all he does to combat blindness in developing countries, Rob Ohlson is our Inspired Albertan this week.

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Sports enthusiast doesn’t let blindness slow her down – MSR News Online

Wednesday, April 19th, 2017

Deanna Coach Callender

Deanna Coach Callender is an inspiration. She is a lifelong resident of Minneapolis who lived a great life despite some recent health concerns, just like she did before going blind.

Callender went to grade school in Coon Rapids where, she says, No one looked like me. She then came to Minneapolis and went to Ramsey Junior High and Washburn High School. She graduated from Minneapolis Community College and St. Cloud State. She also formerly wrote for the Minnesota Spokesman-Recorder (MSR).

Teaching was her passion. I retired from school teaching. I was a teacher and a girls and boys basketball coach and a girls volleyball coach at Lake Country Montessori School. Callender told MSR that she misses teaching.

That was the joy of my life, teaching and being around children. She began her career teaching high school physical education, English and health at Holy Angels [High School]. When my son went to school, I taught physical education, health and kindergarten at Kings Christian Academy and Risen Christ [School]. Callender has one son, ShirDon, who is an estimator at M.A. Mortenson Company. He is my pride and joy, of course.

Speaking about some of her firsts, she told MSR, I am the first African American female to graduate from Minnesota Military Academy, class of 1987. I also served in the military, in the national guard from 1982-1984. [I] served in the Army active duty from 1984-1991, reserves from 1994-1998.

I was [the first] African American female Greek, Delta Sigma Theta, on the campus of St. Cloud [State University]. I deactivated when I went down south because they were still segregated. My heart was broken.

Callender began losing her sight nine years ago. She has been blind in one eye for three years and almost completely blind in the other eye for about three months, So it is still kind of new to me. Initially, she was diagnosed with glaucoma. However, by the time they found out, her peripheral vision was already gone. It just progressively got worse. I could not take [eye]drops and there was nothing they could do. A couple months ago, I woke up [to experiencing] a little light coming through. I still get a little light, but I cannot see anything.

After losing her sight, Callendar said, I was probably a little distraught for about a month. Then I thought, Well, this is it. This is what it is, and I [have] to get back up and start moving. She currently is waiting on a call to get a seeing-eye dog.

Callender is a member of St. Peter A.M.E Church, a chaplain for the Minnesota Blind Veterans Association, the ambassador for the Challenged Athlete Foundation for Minnesota, and a member of the Youth Association of Blind Athletes.

I do a lot of traveling, she said. I am very much a sports enthusiast, even though I have lost my sight. I still do everything. My favorite things to do are whitewater kayaking I love doing that and skiing, tandem biking, scuba diving and goal ball [blind soccer] at the Winter Sports Clinic for disabled veterans. I have been going there for five years. Callender also likes fishing, baseball, rock climbing and bowling. I just do everything, she said. I have been on two whitewater kayaking [trips] that lasted a week at a time, one in Yellowstone River in Montana and one in the Sandwater River in Utah.

She is employed part-time at the Hennepin County Medical Center. I work as a moulage patient for the fire fighters, EMTs and first responders, as they do their training and certifying. [A moulage applies mock injuries for Emergency Response Teams and other medical personnel.] It is not every day but an on-call kind of thing. Sometimes I will work every day from nine to noon, and sometimes I will only work once a month.

The greatest thing in her life right now, she said, are the sports. The Challenged Athlete Foundation allows me to do a lot of things. They pay for a lot of my trips. They send me on a lot of trips as the ambassador. Its really is a wonderful life. Despite all the life changes she is going through, Callender plans to keep living on her own and doing various activities forever, she said adamantly. Being blind is not a big deal. [It] only makes you want to do more things.

Brandi D. Phillips welcomes readers responses to bphillips@spokesman-recorder.com.

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Look again: How to fight data blindness – Campaign US

Tuesday, April 18th, 2017

In the book "Blind Spot: Illuminating the Hidden Value in Business," authors Nathan Shedroff and Stephen Diller tell a story that perfectly dramatizes the problem with todays over-reliance on quantitative data.

Years ago, a team at Levis was researching customer segments and became puzzled over something: While the brand is upscale, many of its customers are not. To find out what was going on, the team took a road trip in Texas and visited people in their homes. One of them was a single mother with two kids, Francine, who was clearly struggling. Yet every year, she bought Levis for her family.

The obvious assumption would be that she was vain and irresponsible. But when they met her, they learned she worked two jobs and was obsessed with her childrens future. Asked why she chose to spend precious dollars on Levis, she replied that she didnt want her children to think they were poor and couldnt achieve more in life.

This story serves as a wake-up call to anyone who thinks that data alone is a sufficient tool to understand human behavior. Not every person fits into a neat category.

Qualitative methodologies can tell you the what (that lower income people buy Levis), but they often fail to tell you why (because theyre aspirational). They cant tell you what motivates the large part of Pradas customer base, which is not affluent. Or why many high-income people shop at big-box discount stores. Is it convenience, or because they dont like overpaying? Only qualitative research will tell.

For decades, however, qualitative research has had a bad rap. It has largely meant focus groups, which can be a costly hassle. You have to recruit respondents, conduct interviews, and travel to different citiesall of which seem time-consuming and antiquated compared to statistical analysis of a rich data set. Product strategists and executives crave insight, but they dont extend that desire to home visits, shop-alongs, and other person-on-the-street work. As a result, in the last 10 years qualitative research facilities have been closing, and quick-turn panels and mobile phone surveys have taken the place of traditional, on-the-ground methods.

But if we want to reach customers in an authentic way, we have to understand the true psychological motivation behind their behaviors. And luckily, we have some new and sophisticated ways to do just that:

Watch what people do, not just what they say. Behavioral economics has opened a new field for understanding human motivation. For example, many behavioral economists stress that quick and effortless, "System 1" thinking dominates the choices we make. The majority of people,most of the time, operate on autopilot. As a result, observing how they actually shop for things can provide deep inspiration for new services that improve store performance. For example, Newsworks award-winning "How People Buy" study literally looked through the eyeglasses of people shopping. It revealed, oddly enough, that many customers do research, not to find the best product, but to ensure that they wont regret buying their preferred brand!

Co-create, dont just evaluate. Research projects typically seek to evaluate concepts and pick a winner. A better idea is to bring people in early, and use their responses to influence design thinking. For example, innovative research firm System 1 Group seeks to improve ideas by putting emotional responses at the heart of their testing methods. This allows their customers (or potential customers) to help build on product concepts, not just evaluate them.

Get outside to understand your category. Person-on-the-street interviews have come a long way in sophistication. Today, production companies such as Snippies offer networks of professional videographers who can generate fast global feedback. Such surveys can give you insight into how people feel about products and brands, helping you move beyond the limitations of traditional tracking surveys and social listening data.

Of course, we know that data big and small isnt going anywhere. With more sources of it and better analytic methodologies, business leaders are finding it easier and easier to extract value from data. But that is only part of the storyand not always the most important part.

Compelling insights and competitive advantage still come from getting out into the world to observe, converse and create with people. While positive results may not be as assured, the insights we can learn are essentialif we want to find out what really matters to our customers.

Brandon Geary is global chief strategy officer of Possible.

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No more PC blindness and appeasement: Trump is the wartime president we needed – Conservative Review

Tuesday, April 18th, 2017

Under Barack Obama, not only did the world become a more dangerous place, but his lack of will to defeat ISIS, the baloney fed to us by his failed secretaries of state, and his willingness to accept an apparently yet unreached number of American deaths due to the activity of those barbarians actually caused the demise of his partys effectiveness nationwide. Obama was on the wrong side of history.

Many Americans, like my husband and I, finally decided to vote for Donald Trump when the shooting in Orlando happened. Our preferred candidate, Ted Cruz, R-Texas, had pulled out of the race. Seeing a very nasty side of Trump, we were unconvinced he would have a level head and be able to lead the nation. So for about a month, I was sure I could not vote for Trump, nor could I vote for Clinton.

But Orlando did happen, and we agreed with Ted Cruz who believed our nation was already at war with the sickness of ISIS. My husband and I could only see more terror happening in our own country with Clinton. For all of his flaws in the understanding of basic constitutionalism, separation of powers, the proper role of government in the economy, and his tendency to relish in big government, we could see the difference between Trump and Clinton in that respect. He was gonna bomb the shit out of ISIS.

And so he has started. Thank you, President Trump.

Did Obama know that cave formation in Afghanistan Trump recently bombed was being used by ISIS as a hideout? I dont know the answer, but I think rational people could see that it is more than likely that he did. How long was ISIS using that area? What kind of attacks were carried out while that area was used by ISIS? Did the people in the tunnels cheer when Americans were killed in the numerous attacks by their soldiers of ISIS here in America? Why didnt Obama take them out?

When President Trump bombed the Syrian airfield, so many were skeptical. From where I sit, the Russian propaganda machine here in America has been gaining steam for years, as Putin used imbecilic mouthpieces here to fill the void of American leadership. Many pro-Putin Americans continuously praised him as a Western reformer, a real Christian, and just the type of strongman our nation needed. Many of them saw the strength of Trump and figured Putin and Trump would be able to team up to kill ISIS together. But the bombing in Syria and the ridiculous propaganda from Assad and Putin since should crystallize whose side Putin is really on. For those who refuse to admit they have been duped by a superior propaganda campaign from the former KGB agent, well, I guess youre on your own.

Now that the bombings have started, and we are answering a war that was declared on us, regular folks are concerned that President Trump has started WWIII. But it is not possible for President Trump to start a war we are already in. The jihadis received appeasement and Americas other cheek, arm, leg, and throat year after year under Obama. Those attacks on America mentioned in the beginning of this article could have been prevented, had we had a leader who took ISIS seriously, who followed through on ridding Syria of chemical weapons, who didnt blame the Syrian war on the silliness of global warming, and who didnt take every chance he could get to downplay the dangers of radical Islam. Who, instead of acknowledging the violence brought on by fundamentalist radical Islamists, took time rather, to repeat that America cant be at war with a religion, insinuating that it was Americans who didnt understand the threats, when it was him all along.

At the same time, it seems pretty clear Americans dont want to be seriously involved in nation-building. We dont have a reason nor ability to try to make countries that dont understand how civil societies operate into countries that do.

Let the history books show that it was the continued blindness of and appeasement toward radical Islam that caused so many innocent deaths around the world of late. Let history record that America didnt fall asleep after 9/11, but that she was hobbled for eight long years while her enemies grew stronger.

We needed a wartime president, and we got one. Now we need resolve.

Jen Kuznicki is a contributor to Conservative Review, blue collar, wife, mom, political writer, humorist, conservative activist, a seamstress by trade, and compelled to write. Follow her on Twitter @JenKuznicki.

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No more PC blindness and appeasement: Trump is the wartime president we needed - Conservative Review

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Overlooking blindness – K24 TV

Tuesday, April 18th, 2017

Photo: Ochieng during his graduation.

Samuel Ochieng, 37, lost his sight as an infant. However, he has lived his life to the fullest, winning an award while at it

Samuel Ochieng Odawo is the perfect embodiment of the maxim that lack of sight is not lack of vision. He swam against the tide at a time his parents could hardly educate him and his siblings. Now, he is the only child from in home to set foot in a university lecture hall. His mission, to empower persons with disabilities.

He has been vocal in the formulation of disability streaming policies and advocated for the rights of refugees at Daadab. It is what keeps him going; the hope that one day, the blind will lead more useful lives. Things like crossing roads, reading and using technology will be friendlier.

Well, six months after Samuel was born, he developed measles. My late mother told me when I was nine months, my eyes became completely swollen and the doctors said I had lost my sight completely, he narrates. Samuel, the ninenth in a family of 10 says by the time his dad came back from Nakuru, where he worked, it was too late to save his sight.

Challenges

I was bred in Siaya County, Alego and I grew up blind. I didnt know I was blind, I thought that was how life is, until I overheard my mother chatting with her friends about taking me to a special school. However, it did not bother me as much since I was used to my life and didnt know how it is to see, recalls the 37-year-old. He then went on to St Order Primary School for the blind at the age of seven, performed well and later joined Thika School for The Blind. My condition helped me a great deal. My siblings education was cut short whenever they got to class seven, but I had to be kept in school and I excelled, he says.

Also read: My married baby daddy accuses me of trapping him

Despite the lack of fees, hustle to get fare, upkeep and attending school a month to closing day, he passed. After high school in 2000, he was admitted to Kenyatta University in 2002 to pursue a bachelors degree in Special Education and French. I had to find a way to pay my fee. My parents could not raise it at all and so, I looked for well-wishers and donors and that is how I sailed the four years. Being blind in campus was tough, an emotional Samuel says.

He had to sweet talk people into reading for him so that he could catch up with school work. Never in the four years did I present my fee structure to my parents, their position could not even help raise the amount he says.

Breakthrough

With a huge fee arrears after the four years, he failed to graduate and moved to Nakuru. While there, I taught French at a primary and a secondary school. It was tough because most people who see blind people assume they are out to beg. I outgrew Nakuru and decided to relocate to Mombasa in 2007, he says.

Also read: Dennis Mukundi is only at the beginning of his career

While at Nakuru, he was robbed of all of his belongings. The fact that the school needed him to teach more subjects only fanned his desire to relocate. I remember arriving in Mombasa and as I waited for my friend to come and pick me, people were giving me money. They thought I was begging and that just went to show how much people think of the blind in Kenya, says the father of one.

In 2014, he was given the Care Humanitarian Award from Care Canada for his works. The most memorable part of his work was when he was teaching at the Daadab Refugee Camp and his learners with visual impairments got their first classroom.

In 2015, he was helping a friend register for a scholarship and he too applied. I submitted my application on the last day. I was accepted and I attended Birmingham University in the United Kingdom to study a Masters in Management of Special Education in Developing Countries, he beams.

Samuel works as a consultant for special needs education and disability issues at his private firm. I am passionate about empowering persons with disability. Theres a lot of discrimination against peoples with disability in Kenya. A lot needs to be done, Samuel says.

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Overlooking blindness - K24 TV

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Answer for why cave animals go blind? – ScienceBlog.com (blog)

Tuesday, April 18th, 2017

Why do animals that live in caves become blind?This question has long intrigued scientists and been the subject of hot debate.

Clearly, across the animal kingdom, blindness has evolved repeatedly. There are thousands of underground and cave-dwelling species, from naked mole rats to bats, and many have lost their

sense of sight. A well-studied blind cavefish (bottom), the Mexican tetra (Astyanax mexicanus), is a small, docile, pink-hued fish just a few centimeters long that could easily make its home in an aquarium. ASU evolutionary biologist Reed Cartwright chose this Mexican tetra because there is also a surface-dwelling form (top) that has retained its sight. Download Full Image

Charles Darwin originally suggested that eyes could be lost by disuse over time. ButReed Cartwright, an ASU evolutionary biologist in the School of Life Sciences and researcher at the Biodesign Institute,may be proving Darwin wrongin a recent publication in the journal BMC Evolutionary Biology.

We think that blindness in cavefish is indeed Darwinian, but ultimately this disproves Darwins original hypothesis of disuse, Cartwright said. In new research, he explains that eyes are not lost by disuse, but rather a demonstration of Darwins fundamental theory of natural selection at work with blindness selected as favorable and the fittest for living in a cave.

For their work, his research team choose to model a well-studied blind cavefish, the Mexican tetra (Astyanax mexicanus), a small, docile, pink-hued fish just a few centimeters long that could easily make its home in an aquarium.

Its inhabited caves for 2 million to 3 million years, giving it 5 million generations worth of time to evolve blindness. Cartwrights group chose this Mexican tetra because there is also a surface-dwelling form that has retained its sight. And for scientists, this built-in comparative power makes it a good choice for further exploration. They have two populations to study that can interbreed and are polar opposites for physical traits.

So Cartwrights group decided to use computational power to investigate how multiple evolutionary mechanisms interact to shape the fish that live in caves.

The problem we have in these caves is that they are connected to the surface, and fish that can see immigrate into the cave and bring genes for sight with them, Cartwright said. Under these conditions, we dont typically expect to find such a difference in traits between surface and cave populations. Unless selection was really, really strong.

How strong? In their model, the selection for blindness would need to be about 48 times strongerthan the immigration rate for Mexican tetras to evolve blindness in caves. Cartwrights groupestimates that a measure of fitness for blindness, called the selection coefficient, in the tetra is between 0.5 percent and 50 percent.

These coefficients are high enough that laboratory experiments should have detected a difference between surface and cave forms of the fish; however, none have to date.

Cartwrights team turned to a hypothesis going all the way back to a letter to the editor of Nature in 1925 by E. Ray Lankester, that essentially stated that the reason you have blindness in caves is because the fish that can see simply leave.

If sighted fish swim towards the light, the only fish that stay in the cave are blind fish. They arent trying to get to the light anymore because they cant see it. Which actually is a form of selection, and thus, Darwinian evolution in action, Cartwright said.

According to Cartwright, explaining a fitness difference as big as 10 percent between sighted and blind fish may be difficult, Iosing eyes might not give you 10 percent more offspring. However, if 10 percent of your seeing-eye fish leave the cave, the migration rate is reasonably low, and that could be enough.

If over time, enough of the seeing-eye fish are systematically being removed, they will also be removed from the gene pool, and that could be enough to drive the evolutionary process.

It could be this sort of habitat preference that maintains the local blind fish population, and the fish that can see are preferentially moving out of the cave. We found that even a low level of preferential emigration, e.g. 2 percent, would provide a significant boost to local adaptation and the evolution of blindness in caves.

Cartwrights team hopes that field biologists begin to consider Lankesters 90-year old hypothesis when studying cavefish. It would be great if someone could develop a study to test Lankesters hypothesis and whether it is driving the evolution of blindness in caves. That would really help answer one of the questions that have intrigued biologists for over a century.

Cartwrights research was supported by National Science Foundation Advances in Bioinformatics program and Arizona State Universitys School of Life Sciences and Barrett, The Honors College.

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Genentech’s Lucentis Approved for Blindness-Causing Diabetic Retinopathy – Pharmaceutical Processing

Tuesday, April 18th, 2017

FDA approves Genentechs Lucentis (ranibizumab injection) for diabetic retinopathy, the leading cause of blindness among working age adults in the United States.

Genentech, a member of the Roche Group, announced that the U.S. Food and Drug Administration (FDA) approved Lucentis(ranibizumab injection) 0.3 mg for the monthly treatment of all forms of diabetic retinopathy. The most common cause of vision loss in people with diabetes, diabetic retinopathy is the leading cause of blindness among adults aged 20 to 741and affects nearly 7.7 million people in the U.S.2

With this approval, Lucentis becomes the first and only FDA-approved medicine to treat diabetic retinopathy in people who have been diagnosed either with or without diabetic macular edema (DME), a complication of diabetic retinopathy that causes swelling in the back of the eye. In February 2015, Lucentis received FDA approval for the treatment of diabetic retinopathy in people with DME based on data from the pivotal RIDE and RISE Phase III clinical trials.

The FDA granted Lucentis Priority Review for the treatment of diabetic retinopathy without DME based on an analysis of the Diabetic Retinopathy Clinical Research Networks (DRCR.net) Protocol S study. This NIH-funded study compared Lucentis treatment to panretinal laser treatment in diabetic retinopathy patients both with and without DME.

In the analysis that supported this approval, patients with and without DME in the Lucentis group experienced improvements in the severity of their retinopathy. Adverse events were consistent with those seen in previous studies.

Diabetic retinopathy is the leading cause of vision loss among working-aged adults in the U.S. between the ages of 20 and 74. We are very pleased that Lucentis is now FDA-approved to treat retinopathy in people with and without DME, said Sandra Horning, M.D., chief medical officer and head of Global Product Development. In multiple clinical studies, Lucentis demonstrated a significant improvement of patients diabetic retinopathy, and it is the first and only anti-VEGF therapy approved to treat all forms of diabetic retinopathy.

Priority Review Designation is granted to medicines that the FDA has determined to have the potential to provide significant improvements in the safety and effectiveness of the treatment of a serious disease.

The FDA previously granted Lucentis Breakthrough Therapy Designation for diabetic retinopathy in 2014 based on the pivotal RIDE and RISE phase III clinical trials. Breakthrough designation is intended to expedite the development and review of medicines with early evidence of potential clinical benefit in serious diseases and to help ensure that patients receive access to medicines as soon as possible.

Diabetes affects more than 29 million people in the U.S.3The longer a person has diabetes, especially if it is poorly controlled, the higher the risk of developing diabetic retinopathy and vision loss. Diabetic retinopathy occurs when blood vessels in the retina become damaged. This can cause vision loss or distortion when the abnormal vessels leak blood or fluid into the eye.1 ___________________________________________________

References:

1U.S. Centers for Disease Control and Prevention. Common Eye Disorders: Diabetic Retinopathy. Available athttps://www.cdc.gov/visionhealth/basics/ced/index.html. Accessed March 7, 2017.

2Prevent Blindness America. Diabetic Retinopathy. Available athttp://www.visionproblemsus.org/diabetic-retinopathy/diabetic-retinopathy-definition.html. Accessed March 7, 2017.

3American Diabetes Association. Statistics About Diabetes. Available athttp://www.diabetes.org/diabetes-basics/statistics/. Accessed March 7, 2017.

(Source: Business Wire)

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Book Review: Notes On Blindness: A Journey Through The Dark by John Hull – Press and Journal

Monday, April 17th, 2017

If you are a sighted person and wonder what it might be like to lose the visual world, the gripping Notes On Blindness will challenge your preconceptions about the condition and leave you reeling at the complexities of a life deprived of sight.

Writing movingly of how he finally came to identify as a blind person and relinquish those things every sighted person takes for granted, the academic Hull who died in 2015 has a flair for evoking the sensations, ironies and even moral quandaries of the blind (how to escape tedious conversations at parties when you cant see a friend to head for?).

First published in 1990 under the title Touching The Rock, this edition ties in with its BAFTA-nominated cinematic namesake, and contains an introduction by Cathy Rentzenbrink.

As an account of dealing with disability, it remains as visceral and lucid as it did when first published.

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Restoring eyesight with a simple, inexpensive surgery – CBS News

Sunday, April 16th, 2017

60 Minutes followed the Himalayan Cataract Project in their fight against preventable blindness to Burma.

Eric Kerchner

Blindness and partial blindness are not epidemic here in the U.S. but they are in certain parts of the world. Our story is about two doctors who decided to do something about it. And incredibly, to date, theyve restored sight to more than 150,000 people. Doctors theyve trained have restored sight to four million more. Their partnership seems improbable. One is a hard-charging, Ivy-League, American, adrenaline-junkie; the other a serene, Buddhist surgeon from the remote mountains of Nepal. We joined them on one of their most challenging missions -- in the isolated country of Burma. Their goal: to lead Burma out of darkness one patient at a time.

One by one the patches are peeled away and the world comes back into focus youre witnessing the moment when the people in this room realize they can see for the first time in years.

Bill Whitaker: Can you see my fingers?

60 Minutes correspondent Bill Whitaker watches Dr. Geoff Tabin perform eye surgery.

Eric Kerchner

Their eyes and their faces begin to light up with a quiet sort of joy and wonder at the gift of sight. As they look around, they see who changed their world, with an operation the day before that took just minutes. Doctors Geoff Tabin and Sanduk Ruit are eye surgeons. And now, they are life savers. To hear Doctors Ruit and Tabin speak, they are the beneficiaries.

Bill Whitaker: Whats it like when that bandage is taken off and that person sees for the first time, sees you?

Sanduk Ruit: I may have seen it thousands of times, but every time, theres a new tickle there. And I feel like my batterys been recharged.

Geoffrey Tabin: I still get such a thrill when people dont expect or realize theyre gonna have their sight restored. And then a transformation when they see, and the sort of moment of hesitation, what are they seeing, and then the smile.

Burma, also known as Myanmar, is one of the poorest countries in Asia.

CBS News

U Myint Oo hadnt seen for two years, until this moment. Others here had been blind for decades. They all had cataracts a milky, white build-up of protein that clouds the lens of the eye. In the U.S. they mainly afflict the elderly; removing them a routine operation. But here in Burma, also known as Myanmar, cataracts go untreated and blindness is a way of life.

Geoffrey Tabin: Its a Buddhist population, theyre very fatalistic. Theyre very accepting. And theres almost an acceptance that you get old, your hair turns white, your eye turns white and then you die. And the idea that you can actually have your sight restored has not really permeated all levels of Myanmar society.

Bill Whitaker: What does that tell you about the state of eye care here?

Geoffrey Tabin: Well, its a place we can make a difference.

Burma is one of the poorest countries in Asia, slowly emerging from the darkness of decades of dictatorship. After years of trying, Tabin and Ruit finally were permitted to bring their treatment here. We met them in Taunggyi in central Burma, where the lack of care has led to some of the highest rates of cataracts in the world. Through radio and pamphlets and conversation, word of the doctors visit spread.

After hearing of the doctors visit, hundreds of Burmese came to Taunggyis hospital in central Burma.

Eric Kerchner

Hundreds of Burmese whod lost their sight found their way to Taunggyis hospital with the help of care givers many trekking for days. Here, cataracts are not just a malady of old age; they take the sight of the very young too, caused by infections and malnutrition.

By the time the doctors scrubbed in, the corridors were choked with people hoping to have their sight restored.

Bill Whitaker: Is it ever daunting? I mean, you look out there and you see that line of people, all who need this surgery.

Geoffrey Tabin: Its daunting on a worldwide basis. It may be a long line but this individual person Im gonna give the very best care I can.

Dr. Ruit set a rapid pace. He repaired an eye; the patient got up; the next patient was ready on an adjoining table. Just minutes an eye, then onto the next. Dr. Tabin performed the delicate surgery just feet away.

Geoffrey Tabin: Want to take a look. See how nice and clear that is. I dont know what that was - maybe 4-5 minutes. And its going from total blindness to great vision.

They kept up this pace until 7:00 in the evening.

Bill Whitaker: Its almost like an assembly line. But assembly line sounds too mechanical. I mean, this is peoples eyes.

Geoffrey Tabin: Its peoples lives. You know, once someone goes blind in a developing world, their life expectancy is about one-third that of age and health matched peers. And for a blind child, the life expectancy is five years. And also in the developing world, it takes, often, a person out of the work force, or a child out of school, to care for the blind person. So when we restore sight to a blind person, were freeing up their family and restoring their life.

Among the throng waiting to have their lives restored we found Kancchi. Her son, a farmer, had been her eyes and devoted caretaker since cataracts took her sight. 15-year old Yawnu had been blind since age seven. He was overwhelmed, but grateful.

In four days in Taunggyi, Dr. Ruit and Dr. Tabin -- with the help of local doctors -- performed 503 cataract surgeries.

Eric Kerchner

Thank you, he said. Doctors Ruit and Tabin heard that a lot. In four days in Taunggyi, with the help of local doctors they were training, they performed 503 cataract surgeries. Her eyes now bandaged, Kancchi waited with her son.

Bill Whitaker: You are going to be performing as many cataract surgeries as the hospital does normally in a year.

Sanduk Ruit: we are basically here to ignite fire. Ignite fire of the possibility of doing high quality, high volume cataract surgery. It is still possible.

Bill Whitaker: You want to ignite a fire here.

Sanduk Ruit: Ignite a fire here.

As long as he can remember, Sanduk Ruit has been burning to change the world around him. He grew up desperately poor, in this village with no electricity or running water, high in the Himalayas of Nepal.

The nearest school was a 15-day walk away. Ruits illiterate parents saw education as the way out for their children, but the grip of poverty and poor health was too strong to escape. His younger sister, with whom he was very close, died of tuberculosis.

Sanduk Ruit: I saw her pass away in front of me. And then it was a very strong determination from inside that maybe this is the profession that I should take and make healthcare available for my countrymen.

Eye surgeons Sanduk Ruit, left, and Geoff Tabin have restored eyesight to more than 150,000 patients in 24 countries.

CBS News

That determination took him to medical school in India. He came back to Nepal an eye doctor, committed to bringing modern care to remote mountain villages. The documentary Out of the Darkness showed them carrying equipment on their backs. His team hiked for days. His goal as revolutionary as it was simple: to cure blindness in the Third World with a quick, cheap technique to remove cataracts. Soon the medical world took notice and so did a young Geoff Tabin.

Geoffrey Tabin: I imposed myself on Sanduk and came to work in Nepal.

Bill Whitaker: What did you think of him when he first showed up?

Sanduk Ruit: You know, I was a bit scared in the beginning, you know. He had tremendous energy. He would never get tired. Energy in working, energy in eating, energy in drinking. Energy in talking, you know?

It was like being hit by a human avalanche fitting since Geoff Tabins passion was mountaineering more than medicine. Hed raced through Yale, Oxford and Harvard medical school. But he had made his name as one of the first people to climb the highest peak on every continent. He met Dr. Ruit and thought hed found his next challenge. Ruit was skeptical this frenetic young man had the same dedication to ophthalmology he had to adventure.

Sanduk Ruit: I sent him to an-- to a hospital in eastern part of Nepal in the middle of summer. And I said, Hes not gonna survive there.

Geoffrey Tabin: During the summer, in the monsoon, its quite oppressive. Its sort of 100, 105, with a 99 percent humidity, and lots of mosquitoes.

Bill Whitaker: Wait a minute. You sent him to-- a difficult place on purpose--

Sanduk Ruit: Difficult place. Difficult-- definitely. Yeah.

Bill Whitaker: Did you know thathe was testing you?

Geoffrey Tabin: No. I thought he sent me there because there was so much need. I scratched my mosquito bites and was excited to go to work that there were all of these blind people that, you know, I could make a difference in their life.

Bill Whitaker: He won you over?

Sanduk Ruit: Yes, yes, definitely.

Their relationship has grown from teacher student to collaborators and friends. Like yin and yang, these opposites complement each other. They created the Himalayan Cataract Project, started here at Tilganga, Ruits hospital in Kathmandu. They perfected the procedure called small incision cataract surgery: just one small splice the cataract comes out, a new man-made lens goes in, no stitches required. Its quick and costs about $20.

Bill Whitaker: How does the quality of care youre providing here, compare to the quality of care youd be able to provide in the U.S.?

Geoffrey Tabin: For these advanced cataracts, Im performing the same quality of surgery that I would be doing in America.

A Burmese woman celebrates her restored eyesight.

Eric Kerchner

Dr. Tabin spends most of his year at the University of Utah where cataract surgery costs a couple thousand dollars an eye. He might do four or five a day. Here, he does that many in a half hour, removing cataracts hed never see in the U.S., because theyd never go untreated so long.

Their project is funded by donations and grants. Theyre able to keep costs down because they dont use expensive equipment and they make their own lenses at their factory in Nepal. The lenses are crucial to the process theyre a permanent implant. Each costs about four dollars. In the U.S., because of strict, safety requirements, they can cost 50-times more.

Bill Whitaker: Comparable quality?

Sanduk Ruit: Very comparable. Id put that in my mothers eyes.

So far theyve operated in two dozen countries, including North Korea, Ethiopia and now Burma. Theyve brought hundreds of doctors, including the Burmese doctors working with them, to Tilganga for training. And everywhere they go, they train other doctors to carry on their work once theyve moved on.

Sanduk Ruit: How many fingers?

We saw the immediate benefit the morning after surgery.

The patients gathered in a Buddhist monastery. As the bandages came off, first wonder; then smiles and celebration. Remember U Myint Oo, blind for two years? His family sent us this picture. He can read again, his favorite pastime.

Fifteen-year-old Yawnu, blind half his life, seemed somewhat bewildered by this new world of sight.

For Kancchi the wait was over. Her son was overcome when she saw his face for the first time in years.

Then there was this woman.

Bill Whitaker: Is this the first time shes been able to see in months?

Man: Yes.

She called Doctors Ruit And Tabin gods. They assured her they are not. But in this room it certainly seemed they had performed miracles.

Hallelujah!

The doctors recently got more good news. The Himalayan Cataract Project is one of eight semifinalists for a $100 million grant from the MacArthur Foundation.

For more information on The Himalyan Cataract Project, visit their website or call888-287-8530.

Produced by Henry Schuster and Rachael Morehouse.

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More Resources About Blindness and Visual Impairment

Sunday, April 16th, 2017

American Action Fund (AAF) for Blind Children and Adults

Baltimore, MD 410-659-9315 actionfund@actionfund.org

A service agency that specializes in providing to blind people help that is not readily available to them. The Tarzana office houses a postage-free national lending library of braille and Twin Vision(R) books for blind children. They also publish and distribute a braille weekly newspaper and calendars.

American Council of the Blind (ACB)

Arlington, VA 800-424-8666 info@acb.org

National consumer organization with local, state, and special interest affiliates; providing support, information, referral, and advocacy.

American Foundation for the Blind (AFB)

New York, NY 800-232-5463 afbinfo@afb.net

Provides comprehensive information on every aspect of blindness and visual impairment and a searchable database of nationwide services.

American Printing House for the Blind, Inc. (APH)

Louisville, KY 800-223-1839 info@aph.org Shopping site

Worlds largest company devoted solely to researching, developing, and manufacturing products for people who are blind and visually impaired. Founded in 1858, it is the oldest organization of its kind in the United States.

Babies Count

Alamogordo, NM

Babies Count is a national registry of young children aged birth to 36 months of age with visual impairments that works in conjunction with public and private agencies to collect standardized epidemiological and demographic data regarding children, their visual conditions, and the systems created to support them and their families.

Blinded Veterans Association (BVA)

Alexandria, VA 800-669-7079 bva@bva.org

An organization of blinded veterans helping blinded veterans. All legally blinded veterans are eligible for BVAs assistance whether they become blind during or after active duty military service.

Bookshare

Palo Alto, CA 650-352-0198 info@bookshare.org

An initiative of Benetech, a nonprofit organization, a person with print disabilities can read a newspaper the same day it hits the newsstand or a best-selling book online as soon as it is released.

Books Aloud

San Jose, CA 408-808-2613 info@booksaloud.net

The Books Aloud "Reading by Listening" Program provides a wide variety of recorded reading literature to eligible individuals of all ages. This is a FREE service.

Canadian National Institute for the Blind

Toronto, ON 1-800-563-2642

CNIB is a registered charity, passionately providing community-based support, knowledge and a national voice to ensure blind and partially sighted Canadians have the confidence, skills and opportunities to fully participate in life.

Dialogue Magazine

Salem, OR 800-860-4224 info@blindskills.com

Each quarterly issue of DIALOGUE Magazine, from the non-profit Blinds Skills, Inc., contains a wide range of subject matter and comes in four formats: cassette, 18-point print, braille and on computer e-mail.

Family Connect

familyconnect@afb.net

FamilyConnect is an online, multimedia community created by the American Foundation for the Blind (AFB) and the National Association for Parents of Children with Visual Impairments (NAPVI). This site gives parents of visually impaired children a place to support each other, share stories and concerns, and link to local resources.

Hadley School for the Blind

Winnetka, IL 800-323-4238 info@hadley.edu

Provides academic, personal enrichment, and compensatory, or rehabilitation education through free home study courses for parents, family members, professionals, and paraprofessionals.

Helen Keller National Center for Deaf-Blind Youths and Adults (HKNC)

Sands Point, NY 516-944-8900 hkncinfo@hknc.org

The Center is a national vocational and rehabilitation program exclusively serving youths and adults who are deaf-blind. Their mission is to enable each person who is deaf-blind to live and work in the community of their choice.

Learning Ally (formerly Recording for the Blind and Dyslexic)

Princeton, NJ 800-221-4792 custserv@LearningAlly.org

Founded in 1948 as Recording for the Blind, Learning Ally creates and maintains over 80,000 audio recordings of textbooks, reference, and professional materials that are not available on tape or disc from other sources. There is a registration fee for this service.

Lighthouse Guild

New York, NY 800-829-0500 info@lighthouseguild.org

A worldwide organization dedicated to preserving vision and to helping people of all ages overcome the challenges of vision loss. Provides vision rehabilitation services, and partners with organizations to ensure that all individuals suffering vision loss have access to the services they require.

Lions Club International

Oak Brook, IL 630-571-5466

By conducting vision screenings, equipping hospitals and clinics, distributing medicine and raising awareness of eye disease, Lions work toward their mission of providing vision for all. They have extended their commitment to sight conservation through countless local efforts and through their international SightFirst Program, which works to eradicate blindness.

Matilda Ziegler Magazine for the Blind

New York, NY 212-242-0263 editor@matildaziegler.com

Editors at the Ziegler magazine scan four national newspapers a day and over 30 magazines a month selecting a broad selection of articles to be reprinted in the Ziegler. The magazine is free-of-charge to legally blind subscribers and is published in a variety of formats including: contracted braille, four track cassette, on-line and by e-mail.

National Braille Association

Rochester, NY 585-427-8260

National Braille Association (NBA) is the only national organization solely dedicated to the professional development of individuals who prepare and produce braille materials.

National Braille Press (NBP)

Boston, MA 888-965-8965 contact@nbp.org

The National Braille Press focuses on practical information to enable persons who are blind and visually impaired to be responsible and productive individuals. Categories include childrens braille literacy, computer access, and self-help books.

National Camps for Blind ChildrenChristian Record Services

Lincoln, NE 402-488-0981 info@christianrecord.org

An international organization serving blind and visually impaired individuals in approximately 80 countries worldwide that operates summer camps throughout North America for children and adults who are blind and visually impaired.

National Federation of the Blind (NFB)

Baltimore, MD 410-659-9314 pmaurer@nfb.org

National consumer organization, with local and state chapters and special-interest divisions that provide information, advocacy, and employment programs.

National Organization of Parents of Blind Children (NOPBC)

Baltimore, MD 410-659-9314 parentoutreach@nfb.org

(part of National Federation of the Blind/click on Info about Vision Loss for Parents and Teachers)

Focuses on the needs of parents and families. Find resources to help children thrive at home, school, and in the community.

National Prison Braille Network

Supports and promotes braille production facilities in prisons across the U.S. and helps ensure that inmate transcribers are well prepared for successful careers as braille transcribers upon release.

Newsreel Magazine

Columbus, OH 888-723-8737

Newsreel Magazine by and for the Blind is a unique monthly interactive audio magazine produced in the voices of its blind or visually impaired subscribers.

Perkins School for the Blind

Watertown, MA 617-924-3434 info@perkins.org

Conducts training activities for programs and staff serving children who are multiply disabled with blindness or deafblind and provides support services for parents.

Seedlings Braille Books for Children

Livonia, MI 800-777-8552 info@seedlings.org

Seedlings Braille Books for Children provides high quality, low cost braille books for children at every level of development, from toddler board books to classic literature for older children.

U.S. Association of Blind Athletes

Colorado Springs, CO 719-866-3224

This Association enhances the lives of blind and visually impaired people by providing the opportunity for participation in sports and physical activity. Offers training camps and competitions in swimming, track and field, wrestling, gymnastics, goal ball, skiing, skating, power lifting, judo, and tandem cycling.

WonderBaby.org

Watertown, MA email hidden; JavaScript is required

WonderBaby.org, a project funded by Perkins School for the Blind, is dedicated to helping parents of young children with visual impairments as well as children with multiple disabilities. Here youll find a database of articles written by parents who want to share with others what theyve learned about playing with and teaching a blind child, as well as links to meaningful resources and ways to connect with other families.

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More Resources About Blindness and Visual Impairment

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60 Minutes Eye Doctors Curing Blindness Giving Away Books – 2paragraphs.com

Sunday, April 16th, 2017

Drs. Sanduk Ruit and Geoff Tabin on 60 Minutes (CBS video)

The 60 Minutes segment Out of Darkness features two eye surgeons, Dr. Sanduk Ruit and Dr. Geoff Tabin, who are giving sight to people who have been blind for years due to cataracts. CBS correspondent Bill Whitaker travels to Burma (also known as Myanmar) to see the doctors in action in the operating room. With the doctors theyve trained in Nepal to perform the simple operation, Ruit and Tabin claim to have reversed blindness in more than 4 million people.

[Left: Buy thebookSecond Suns: Two Trailblazing Doctors and Their Quest to Cure Blindness on Amazon and the publisher will donate to the Himalayan CataractProject]

Ruit and Tabin have formed the non-profit organization CureBlindness to provide more surgeries to more people in the developing world. If you donate $100 or more directly to the project, you will receive a free copy of the inspirational book Second Suns:Two Trailblazing Doctors and Their Quest to Cure Blindness, One Pair of Eyes at a Time.60 Minutes airs Sundays at 7pm on CBS.

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60 Minutes Eye Doctors Curing Blindness Giving Away Books - 2paragraphs.com

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