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The Nazi past and troubling legacy of thalidomid­e, 50 years on

- Photograph­s by Laura Pannack

The thalidomid­e scandal, in which 20,000 babies were born with deformitie­s, is one of the worst man-made disasters in peacetime. More than 50 years later, as a new documentar­y is released, the fight for justice is far from over, fnds Martin Fletcher.

No limbs, no limits,’ Lorraine Mercer chuckles, and for 54 years this remarkable woman has lived by that motto.

She was a thalidomid­e baby, born without arms or legs, just tiny hands and feet attached like flippers to her torso. But she enters dressage competitio­ns, controllin­g the horse from a modified buggy, and has trophies to prove it. She has completed three one-mile swims for charity, each taking three hours or more. She writes, paints and makes lace with her mouth. She won an MBE for visiting patients in hospital. She carried the 2012 Olympic torch through Crowboroug­h in Sussex, delighting the crowds by performing pirouettes in what she calls her motorised chariot. ‘That was a fantastic day,’ she says.

But Mercer’s body is beginning to fail her. Five decades of distortion­s and contortion­s are taking their toll. Her back is seizing up. Her jaw is weakening. She needs oxygen to revive her. ‘I feel like I’m 80 years old sometimes,’ she says, and soon she will start losing her cherished independen­ce.

She is planning to move from her tiny fat to a bungalow in Haywards Heath because she needs an extra bedroom for a carer to sleep in, and a bigger bathroom so a helper can be present. The move will cost hundreds of thousands of pounds. The bungalow will need electric doors and windows, a remote-controlled toilet and bath with hoists, and every light switch, surface and cupboard set at precisely the right height. There will have to be room for her four motorised chariots (two for inside, two for outside), and secure parking for her specially adapted Ford Transit van.

Like Mercer, most of Britain’s 468 surviving thalidomid­ers are sufering musculoske­letal deteriorat­ion and chronic pain as they age. Their spines and joints are wearing out after decades of performing mundane tasks with their teeth, toes or stumpy arms. ‘They’re degrading fast… They’re getting the type of damage you would expect to see in people 30 years older,’ says Martin Johnson, a former RAF squadron leader who was until recently director of the Thalidomid­e Trust.

Worse, these proud thalidomid­ers (never call them ‘victims’) face the loss of their independen­ce, and hate the idea of burdening their children as they once burdened their parents.

‘I’m horrifed at the idea,’ says Mikey Argy, a single mother of two children. She has foreshorte­ned arms and suffers both from acute back pain after a lifetime of bending, and from weakening hands that can no longer carry pans or manage zips and buttons.

‘Not to be independen­t will be absolutely devast at ing,’ says Tom Yendell, a profession­al artist though he has no arms. He paints, writes, eats, drives and dresses with his feet, but his knees are now giving way after so much unnatural twisting.

In short, they need much more money to pay for extra help, but they are no longer looking to the British government for that. They are turning their attention to Germany, the source of thalidomid­e. Nor do they just want money. They seek justice too. They want Chemie Grünenthal, the drug’s inventors, fnally to admit responsibi­lity for what they call the world’s most devastatin­g man-made disaster apart from war – worse than 9/11, the Titanic, Bhopal or Chernobyl. They want reparation­s from t he federal government for allegedly shielding Grünenthal from the horrifc consequenc­es of a drug developed by Nazis.

‘What drives them now is a sense of injustice,’ says Sir Harold Evans, the former Sunday Times editor who has spent much of his adult life campaignin­g for the thalidomid­ers. Johnson says, ‘They collective­ly and passionate­ly want justice brought to Grünenthal. They identify the company as the origin of their troubles and believe strongly that it has not been brought to book.’

The campaigner­s have two new weapons in their armoury. They have recently obtained documents that suggest the German government conspired to halt Grünenthal’s trial for criminal negligence in 1970, thereby suppressin­g the evidence with which thousands of thalidomid­ers in ot her count r ies might have secured just settlement­s.

In addition, a documentar­y to be released later this month will tell the stor y of the thalidomid­e scandal to younger generation­s who might otherwise regard it as ancient history, not a continuing source of shame. ‘It will bring this worst of crimes to public attention once more,’ Johnson says.

The documentar­y, Attacking the Devil, has been made by Jacqui and David Morris, a sister-and-brother team whose previous award-winning flm was about the photojourn­alist Don McCullin. This project began as a documentar­y primarily about Evans, McCullin’s editor, but as the Morrises dug deeper their focus switched to his key role in the thalidomid­e scandal. ‘It exemplifie­d Harry’s way of working,’ David says. ‘It’s such an exciting story. It has ups and down, good versus evil, and goes on over decades. If it helps thalidomid­ers all over the world win compensati­on that would be great.’

Grünenthal, a small family frm based in the pretty Rhineland town of Stolberg, put thalidomid­e on the market under the brand name Contergan in 1957, when Germany had few regulation­s governing drugs. The company was run by Hermann Wirtz, a former Nazi. It employed several former Nazi scientists including the infamous Otto Ambros, the so-called ‘devil’s chemist’ who was instrument­al in developing the ner ve gas sarin before the Second World War, ran a work camp at Auschwitz, and was imprisoned for war crimes. Circumstan­tial evidence suggests the drug may have been developed by Hitler’s regime as an antidote to nerve gas and tested on concentrat­ion-camp inmates.

Grünenthal promoted thalidomid­e as a ‘fully harmless’ and ‘completely safe’ cure for morning sickness, though it had never tested the drug on

‘Think of Hillsborou­gh or Bloody Sunday. It’s the same kind of situation where justice has never been done and it burns away’

pregnant animals, let alone women. The ‘wonder drug’ was an instant success. It was prescribed to hundreds of thousands of pregnant women in nearly 50 countries (America’s Food and Drug Administra­tion was one of the few regulatory bodies that rejected it). But over the next four years at least 20,000 babies were born with extreme deformitie­s – which day of her pregnancy a mother took the pill determined the nature of the deformity ‘with the precision of the sniper’s rife’, Johnson says. Many times that number died in the womb or were stillborn. Grünenthal fnally, reluctantl­y, took the drug of the market in November 1961, having ignored mounting evidence of its catastroph­ic efects and having sought to silence or discredit its critics.

In Britain thalidomid­e was approved by the NHS and marketed as Distaval by Distillers, the drinks company that produced brands such as Gordon’s Gin, Johnnie Walker and Pimm’s. Bizarrely, Distillers had ventured into pharmaceut­icals after Aldous Huxley, author of Brave New World, predicted that ‘happiness pills’ would supersede alcohol.

Two thousand thalidomid­e babies were born in this country. Many were so deformed that they were ‘not allowed to live’ – either suffocated by doctors or left in a cold room, Johnson says in the documentar­y, the rights to which have been bought by the flm producers Harvey and Bob Weinstein. One father described his daughter as ‘a torso with little fowers where the arms and legs should be’. Grainy black and white footage shows a mother recalling how she was told to forget her baby, go home and have another. ‘We were all written of,’ says Kevin Donnelly, the son of a northern tugboat worker. He was born with no limbs. Half were dead within a year.

Sixty-two families sued Distillers, which meant the press was gagged by the draconian sub judice rules of that era. Enoch Powell, the health minister, refused to hold a public inquiry, his senior medical adviser having been briefed by Distillers. Parents were left to raise armless or legless children, some severely brain damaged or with defective organs, with minimal support.

Marjorie Wallace, a journalist who spent months with the families, remembers cafes, shops and beaches emptying when they entered. ‘They were being shunned by society. Everyone was afraid of these deformitie­s,’ she says. Readers protested when Evans, as editor of The Northern Echo, published photograph­s of the children. Many parents abandoned their children to institutio­nal care – Wallace remembers visiting a thalidomid­er in a nursing home who listed his solicitor as his next of kin. As many as half the marriages of parents of thalidomid­ers broke up, with husbands walking out saying the deformed children had nothing to do with them. Mothers were consumed with guilt, and at least three committed suicide.

Eventually, in 1968, Distillers gave the 62 families 40 per cent of what they would have received had they won a negligence case in court. Evans, who had by then moved to The Sunday Times, dismissed that as ‘miserably inadequate’, but it alerted other parents to the possibilit­y of compensati­on, and 369 of them launched a new suit.

In 1971 Distillers ofered them a paltry £3.3 million – roughly £8,000 per family – provided they all accepted it. Most were delighted, having survived a decade with nothing. But f ive said no, among them a London art dealer named David Mason who was determined to get £20 million. Other parents denounced him for holding out because they could not be paid.

Distillers upped the pressure. It threatened to withdraw the ofer. It encouraged a successful applicatio­n to have Mason’s daughter, Louise, made a ward of court because he was neglecting her interests. ‘ Bleak House is not in it,’ Evans remarks in the flm. Mason regained guardiansh­ip of Louise on appeal only because an American lawyer contacted him to say a client had won $2.7 million in a thalidomid­e case. Mason few to the US, got the papers and presented them to the judge, Lord Denning, the next day as proof that thalidomid­e cases could succeed.

The Sunday Times had meanwhile obtained thousands of documents showing how Grünenthal and Distillers had failed to test the drug adequately and ignored warnings about its dangers, but because of the ongoing legal battle it could not publish them without being in contempt of court. Finally, in 1972, Evans found a way to circumvent what he called ‘the most restrictiv­e press laws in Western democracy’. His paper would focus on the moral, not legal, issues. It launched its campaign with a front page headlined ‘Our thalidomid­e children: a cause for national shame’, and followed up with Wallace’s heartbreak­ing reports of their plight.

It worked. That November Jack Ashley, the Labour MP who chaired the all-party disability group, forced a parliament­ary debate on what he called a great national tragedy. ‘What kind of an adolescenc­e will a 10-year-old boy look forward to when he has no arms, no legs and is only two foot tall? That is the height of two whisky bottles placed on top of each other,’ he said. ‘How can an 11-year-old girl look forward to laughing and loving when she has no hand to be held and no legs to dance on?’

Other media outlets began to report on the longneglec­ted thalidomid­e children, and the public was appalled. Evans received thousands of letters of support. Distillers’ shareholde­rs started to protest. Posters denouncing Dist illers appeared on t he walls of British cities. Mason helped organise an internatio­nal boycott of its products. Flying to New York, he followed the drinks trolley down the aisle and urged passengers not to consume any Distillers’ product – none did. Distillers’ share prices plunged, and in 1973 the company was fnally compelled to ofer the £20 million that Mason had demanded.

It was a great victory, but the attorney general still banned the The Sunday Times from revealing

Many parents abandoned their children… Wallace remembers visiting a thalidomid­er who listed his solicitor as his next of kin

the facts on which the campaign was based – how Grünenthal and Distillers had managed to put such a lethal drug on the market. The newspaper successful­ly appealed against that ban. The House of Lords over turned that verdict. The newspaper went to the European Cour t of Human Rights (ECHR) in Strasbourg and won by two votes in 1979. After a decade of campaignin­g, its exposé of the two companies’ negligence and unscrupulo­us marketing was fnally published under the headline ‘The story they suppressed: thalidomid­e’.

The ECHR’s landmark ruling unshackled what Evans called Britain’s ‘half free press’ and bolstered the public’s right to know. By exposing the pharmaceut­ical industry’s failures Evans also ushered in a new era of tighter regulation and greater corporate accountabi­lity.

In the decades since then, conditions for Britain’s thalidomid­ers have improved markedly. That £20 million settlement has been repeatedly topped up by the government and Diageo, which took over what remained of Distillers in 1997, though the fnancial support the thalidomid­ers receive still falls well short of their exceptiona­l needs. In 2010 they extracted a formal apology from the government for their sufering. They have survived much longer than anyone expected, and – the brain-damaged apart – have mostly led remarkably fulfilled lives.

Though good jobs were scarce, many have married (mostly non-thalidomid­ers) and had healthy children. They have variously skied, glided, scuba-dived, skydived, climbed Kilimanjar­o, and travelled to the furthest reaches of the Earth. One, born armless, learnt to saddle a horse with her foot and took up showjumpin­g. Another became an astrophysi­cist at Oxford.

‘They have fared extraordin­arily well. They have broken every rule in the book as to what should have happened to them,’ says Wallace. Jacqui Morris says, ‘They are humbling, such inspiring people.’ The thalidomid­ers have also become skilled campaigner­s who are determined that both Grünenthal and the German government should fnally be called to account for what happened half a century ago.

In 2012 Harald Stock, Grünenthal’s chief executive, unveiled a bronze statue of a limbless girl at the company’s headquarte­rs and apologised for the frst time to the survivors and their families. But he refused to accept any legal liability for what happened, repeating his company’s long-standing contention that thalidomid­e was tested according to the standards of the time and that nobody realised a drug could cross the placental barrier.

‘That’s a lie,’ said Evans, whose journalist­s long ago demonstrat­ed that all the leading pharmaceut­ical companies were subjecting their products to reproducti­ve testing during the 1950s, and that Grünenthal was receiving complaints about thalidomid­e as early as 1959.

Grünenthal has also been protected by a secret deal that it appears to have struck with the federal government and that of North Rhine-Westphalia in 1970. Wirtz and eight other Grünenthal employees had been put on trial and charged with involuntar­y manslaught­er. Documents recently unearthed in official German archives show that a year later Grünenthal’s lawyers and federal health ministry ofcials met secretly to discuss an ‘overall solution’. The trial was shut down by Josef Neuberger, the state’s minister of justice, who happened to have been a par t ner in t he law f ir m represent ing Grünenthal. The judges freed the defendants and granted Grünenthal immunity from further prosecutio­n. The company cont ributed 100 million Deutschmar­k to a fund for German thalidomid­ers.

What Evans calls a ‘judicial scandal’ not only spared Grünenthal; it suppressed copious evidence of the company’s misconduct, making it much harder for thalidomid­e families to win proper compensati­on in Britain and elsewhere. In the words of the London law frm Ince and Co, ‘The early discontinu­ation of the trial caused the vast majority of the contempora­ry evidence that the prosecutio­n had gathered in support of their case against Grünenthal to remain unheard and unseen.’ That rankles. ‘Think of Hillsborou­gh or Bloody Sunday,’ says Johnson. ‘It’s the same kind of situation where justice has never been done and it burns away. There’s something in the British make-up that doesn’t let injustice rest.’

Led by Nick Dobrik, the Mill Hill and Cambridgee­ducated head of the Thalidomid­e Trust’s national advisory council and a thalidomid­er himself, the campaigner­s have engaged lawyers and are now gathering support in the British and European parliament­s for their assault on Berlin. The Morrises are planning a special screening of Attacking the Devil in Stolberg. Specifcall­y, the campaigner­s want a statement of regret from the federal government, restitutio­n for all of Europe’s thalidomid­ers so the likes of Lorraine Mercer can live the rest of their days with dignity, and a judicial inquiry to determine the true extent of Grünenthal’s culpabilit­y.

The German government shows little sig n of accept ing t hose demands. A spokesman at its embassy in London denied any secret deal was struck in 1970 and said British thalidomid­ers should seek restitutio­n from ‘the British side’ unless they took Contergan, t he bra nd t hat was made in Germany. Grünenthal, now a big multinatio­nal company, said in a statement t hat it ‘sincerely regrets the thalidomid­e tragedy’, had given more than €100 million to the German compensati­on fund, and establishe­d its own foundation for those in urgent need – including British thalidomid­ers. However it again insisted that thalidomid­e’s danger to foetuses was ‘not foreseeabl­e’ in the 1950s.

The campaigner­s are unimpresse­d. Dobrik calls Grünenthal’s payouts derisor y compared to its modern-day profts, and says of the German government, ‘It can deny, obfuscate and bury its head in the sand, but it can’t run for ever. It has to face up to the past.’ Evans insists, ‘The German government has a moral responsibi­lity fnally to get to the bottom of this.’

The indomitabl­e Lorraine Mercer says bluntly, ‘They didn’t test it. It’s time they came clean. I suppose they’re waiting for ever yone to pop their clogs, but I’ve no intention of doing so.’

Attacking the Devil: Harry Evans and the Last Nazi War Crime is released on January 22

One thalidomid­er, born armless, learnt to saddle a horse with her foot and took up showjumpin­g. Another became an astrophysi­cist

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 ??  ?? Above the artist Tom Yendell, who paints with his feet. Left Yendell’s second birthday party
Above the artist Tom Yendell, who paints with his feet. Left Yendell’s second birthday party
 ??  ?? Above Mikey Argy is a mother of two. Left Argy aged six. Below Sir Harold Evans, the former Sunday Times editor who has campaigned for thalidomid­ers for decades
Above Mikey Argy is a mother of two. Left Argy aged six. Below Sir Harold Evans, the former Sunday Times editor who has campaigned for thalidomid­ers for decades
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 ??  ?? Above Kevin Donnelly. Left Donnelly as a young Cub. Below Louise Medus-Mansell (née Mason)
Above Kevin Donnelly. Left Donnelly as a young Cub. Below Louise Medus-Mansell (née Mason)
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 ??  ?? Above Lorraine Mercer carrying the Olympic torch through Crowboroug­h, Sussex, in 2012
Above Lorraine Mercer carrying the Olympic torch through Crowboroug­h, Sussex, in 2012

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