By Julian Gavaghan <\/p>\n
Last updated at 11:00 AM on 13th February 2012 <\/p>\n
Twin brothers have told of their \u2018devastation\u2019 after both dramatically lost their sight to a rare condition that affects just a few hundred people. <\/p>\n
Michael and Dan Smith, 20, are still determined to finish university and get good jobs after being left almost totally blind by Leber's Optic Neuropathy. <\/p>\n
Michael, who is in football training for this year's Paralympic Games, lost his sight in a matter of weeks while in his first year at Bart's and the London School of Medicine. <\/p>\n
Rare condition: Dan (left) and Michael Smith suffer from Leber's optic Neuropathy <\/p>\n
Less than a year later, his brother Dan suffered the same fate while in his second year studying aeronautical engineering at the University of Bristol. <\/p>\n
The identical pair, who can only make out shadowy shapes, have been forced to adapt their lives, learning Braille and re-learning how to cook and choose clothes. <\/p>\n
<\/p>\n
They also plan to embark on a 350-mile tandem bike ride from London to Amsterdam in April. <\/p>\n
Michael first noted changes to his vision in November 2009, forcing him into the \u2018crushing\u2019 realisation he could not continue his degree in medicine. <\/p>\n
WHAT EXACTLY IS LEBER'S OPTIC NEUROPATHY? <\/p>\n
Leber's Optic Neuropathy is a hereditary condition passed on by the mother\u2019s genes. <\/p>\n
The genetic defect, which can lead to optic nerve damage \u2013 or neuropathy, is carried by roughly one in every 9,000 people. <\/p>\n
But genes, which can cause eye cells to die off quickly, can pass though several generations without triggering the condition. <\/p>\n
Around 50 per cent of men and 80 per cent of women with it will suffer no loss of vision. No reason is known for the difference between the sexes. <\/p>\n
In the Smith brothers\u2019 case, they have been unable to find any family history of sudden onset blindness going back four generations. <\/p>\n
The main symptom is the sudden loss of vision, which is caused by a death of cells in the optic nerve responsible for relaying visual information from the eyes to the brain. <\/p>\n
Once cells start dying, affected eyes will begin seeing colours that appear more washed out. Within a period of eight weeks, it can lead to near or total blindness. <\/p>\n
In many cases, only one eye is affected and patients may not be aware of the loss of colour vision until the doctor asks them to cover the healthy eye. <\/p>\n
Most of the time, however, both eyes are affected. Sometimes vision improves, although this is very unusual. <\/p>\n
\u2018My symptoms came on suddenly - one day I was in a lecture and I could not make out the projector in front of me, it was really hazy,\u2019 he said. <\/p>\n
\u2018I lost 70 per cent to 80 per cent of vision in my left eye in a very short space of time. <\/p>\n
'I continued at medical school for a couple of weeks but it was taking me half an hour to read a page of A4 and I was breaking down in tears. <\/p>\n
\u2018I did not know what was happening to me. I could not recognise people's faces and I quickly lost my independence.\u2019 <\/p>\n
A genetic test eventually revealed Michael was suffering from the rare genetic condition, which also caused rapid sight loss in his right eye. <\/p>\n
\u2018It was the end of life as I knew it,\u2019 he said. \u2018I could not carry on at medical school and that was incredibly distressing. In fact, it was crushing. <\/p>\n
\u2018I can never describe how devastating it was to give up on medicine. <\/p>\n
\u2018Not only that but I couldn't go for a run on my own without it being dangerous, I could not prepare food, I did not know what I was wearing.\u2019 <\/p>\n
Dan also \u2018could not comprehend what was happening\u2019 when he heard Michael's news. <\/p>\n
\u2018Michael has been the closest person to me all my life and this struck him in his first week at university,\u2019 he said. \u2018It was incredibly hard to see this happening to my brother. <\/p>\n
\u2018He called me to say he thought something was wrong - he wasn't able to recognise people but didn't know why. That conversation still haunts me. <\/p>\n
\u2018Doctors initially thought he had a brain tumour but tests revealed that he had this rare genetic disorder. <\/p>\n
\u2018The whole family was devastated as we tried to comprehend what had happened. <\/p>\n
\u2018It was the cruellest of timing because it was my brother's first term at medical school and he had his whole life ahead of him.\u2019 <\/p>\n
But further terrible news was still to come. Because the pair are identical twins, Dan was told he had a 60 per cent to 70 per cent chance of also going blind. <\/p>\n
Optic neuropathy: Cracks show nerve damage in the eye, caused by cells dying <\/p>\n
\u2018Knowing I could lose my sight was psychologically very, very tough,\u2019 he said. <\/p>\n
\u2018Leber's Optic Neuropathy is known as 'The Sword of Damocles', based on the Greek parable, because your life goes from being great, in a period of heightened happiness, to hitting rock bottom in an instance. <\/p>\n
\u2018I had a pretty tough time knowing that this dark cloud was hanging over me during my first two years at university. <\/p>\n
\u2018It was effectively like sitting on a time bomb that could have gone off at any moment.\u2019 <\/p>\n
In Easter 2010, Dan began to lose sight in his left eye and within three weeks there was also \u2018full scale deterioration\u2019 in his right eye. <\/p>\n
Michael said: \u2018Once I was diagnosed, the one thing I wanted in life was for this not to happen to my brother too.\u2019 <\/p>\n
Although Leber's Optic Neuropathy is a hereditary condition, the brothers have been unable to find any family history going back four generations. <\/p>\n
The twins, from Barnet, north London, can now make out shadows but use white canes to help them move around. <\/p>\n
It is not known if they will lose their remaining sight but their condition is extremely unlikely to improve. <\/p>\n
Nevertheless, they are determined to live life to the full. Michael is now studying geography at King's College London and wants to be a disability lawyer when he graduates. <\/p>\n
Dan is still studying aeronautical engineering and aims to go into investment banking. <\/p>\n
Michael said: \u2018The last two years have been the most difficult but also the most exciting of my life. <\/p>\n
\u2018We have had to learn new skills such as Braille and a new computer language that coverts text to speech. In lectures, we have note-takers. <\/p>\n
\u2018Everything is through touch now, I select clothes through touch and texture and cooking is through touch and smell. <\/p>\n
\u2018I thought I would never smile again, but we wanted our lives back.\u2019 <\/p>\n
Damage: The normally smooth contour of the retina has large black areas where photoreceptors have been lost due to the macular degeneration <\/p>\n
Michael plays for the England blind football team and is hoping to get picked for this year's Paralympic Games. <\/p>\n
\u2018It's incredibly competitive but I'm training all the time,\u2019 he said. <\/p>\n
The Arsenal fans will undertake the London-Amsterdam tandem bike ride on April 6 to raise awareness of their condition. <\/p>\n
They hope to raise over ?3,000 for Blind in Business, a charity which helps blind and partially sighted people into work. <\/p>\n
Dan Mitchell, training and fundraising manager at Blind in Business, said: \u2018Having the Smith brothers embark on such a challenging journey to raise money for this small charity shows they always want to work towards bigger challenges. <\/p>\n
\u2018They have both been challenged academically and have pushed themselves as visually impaired people, working towards careers in engineering and law.\u2019 <\/p>\n
Leber's Optic Neuropathy mostly strikes young men and is caused by complex genetic defects. <\/p>\n
Vision loss results from the death of cells in the optic nerve responsible for relaying visual information from the eyes to the brain. <\/p>\n
Although central vision gradually improves in a small number of cases, for most people vision loss is permanent. <\/p>\n
Michael and Dan can be sponsored via http:\/\/www.justgiving.com\/sevenmenfivebikes<\/a>. <\/p>\n <\/p>\n <\/p>\n<\/p>\n See the original post here: By Julian Gavaghan Last updated at 11:00 AM on 13th February 2012 Twin brothers have told of their \u2018devastation\u2019 after both dramatically lost their sight to a rare condition that affects just a few hundred people. Michael and Dan Smith, 20, are still determined to finish university and get good jobs after being left almost totally blind by Leber's Optic Neuropathy. Michael, who is in football training for this year's Paralympic Games, lost his sight in a matter of weeks while in his first year at Bart's and the London School of Medicine Continue reading
\nTwin brothers' devastation after both rapidly lost their sight due to rare genetic condition<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"