
At least 600 CDC employees are getting final termination notices, union says
The notices went out this week and many people have not yet received them, according to the American Federation of Government Employees, which represents more than 2,000 dues-paying members at CDC.
Officials with the U.S. Department of Health and Human Services did not immediately respond to a request for comment.
AFGE officials said they are aware of at least 600 employees being cut.
But 'due to a staggering lack of transparency from HHS," the union hasn't received formal notices of who is being laid off,' the federation said in a statement on Wednesday.
The permanent cuts include about 100 people who worked in violence prevention. Some employees noted those cuts come less than two weeks after a man fired at least 180 bullets into the CDC's campus and killed a police officer.
'The irony is devastating: The very experts trained to understand, interrupt and prevent this kind of violence were among those whose jobs were eliminated,' some of the affected employees wrote in a blog post last week.
On April 1, the HHS officials sent layoff notices to thousands of employees at the CDC and other federal health agencies, part of a sweeping overhaul designed to vastly shrink the agencies responsible for protecting and promoting Americans' health.
Many have been on administrative leave since then — paid but not allowed to work — as lawsuits played out.
A federal judge in Rhode Island last week issued a preliminary ruling that protected employees in several parts of the CDC, including groups dealing with smoking, reproductive health, environmental health, workplace safety, birth defects and sexually transmitted diseases.
But the ruling did not protect other CDC employees, and layoffs are being finalized across other parts of the agency, including in the freedom of information office. The terminations were effective as of Monday, employees were told.
Affected projects included work to prevent rape, child abuse and teen dating violence. The laid-off staff included people who have helped other countries to track violence against children — an effort that helped give rise to an international conference in November at which countries talked about setting violence-reduction goals.
'There are nationally and internationally recognized experts that will be impossible to replace,' said Tom Simon, the retired senior director for scientific programs at the CDC's Division of Violence Prevention.
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The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.
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It is difficult for most parents to imagine their baby going to school. But when little Georgia Hill was born on March 19, 2019, this was more true than for many. Georgia, from Alford, is a SWAN baby – she has a Syndrome Without A Name. Her genetics experts say Georgia is unique and they can't find a diagnosis. What that means in reality is that the six-year-old needed surgery 24 hours after she was born, and has spent more nights in hospital since then than is fair. She is under at least six specialist teams at the Royal Aberdeen Children's Hospital – the number fluctuates depending on procedures. Georgia, whose bowel and stomach weren't properly attached when she was born, is currently just 100cm tall (3ft 3ins) and weighs 15kg (2st 5lbs). That's more like the measurements of a three- or four-year-old. But despite everything that she has gone through in her short life so far, this amazing wee girl is excited about something very important. Because this is the week Georgia Hill, aged six years and five months, starts at Alford Primary School. Georgia is non-verbal, but this hasn't stopped her prepping for her first day. She has learned to sign the word 'school' in Makaton – and she's had at least one practice run in her new uniform. Georgia's mum Ange said: 'Georgia is excited to be going to school. 'She signed school, and even little things like the colour of the seats that they'll sit on for lunch, she'll sign. 'I'm happy and excited for her, but at the same time, I'm just so nervous. 'I'm just so proud of her.' Georgia lives with mum Ange, 47, head of marketing at Aberdeen Sports Village, offshore health and safety consultant dad Dave. 43, and big sister Charlotte-Dee, 12. She was a long-awaited addition to the family, coming after several hard-to-bear baby losses. Ange explained: 'It was quite an emotional journey to get to having Georgia – I'd suffered quite a few miscarriages.' But in July 2018, Dave, Ange and Charlotte-Dee had good news – Ange was pregnant again. With emotions understandably running high and almost expecting tragedy to strike again, Ange had weekly scans at the start. She said: 'Everything seemed to be going great. I was at 24 weeks and the next scan was going to be at 28 weeks. 'So for those four weeks of the whole pregnancy, I actually managed to relax.' Sadly, it wasn't to last – and in January 2019, medics had some difficult news for the couple. Still months away from arriving in the world, Georgia was diagnosed with duodenal atresia – her bowel and stomach weren't properly attached. Surgery was planned for the day she was born, but that wasn't the only worry. Georgia wasn't growing very well in the womb, and the couple were told the condition is often linked to Down's Syndrome. Ange added: 'They didn't think I'd go past 32 weeks, but I got to 35.' Georgia was delivered by Caesarean section and had surgery to repair her bowel and stomach 24 hours later. She was a tiny 3lb 14oz and spent the first five weeks of her life in intensive care. During this time, medics painstakingly 'fed' her bowel and stomach with tiny amounts of Ange's expressed milk. It was tough – Georgia was regularly sick – and Ange said: 'It was a very stressful time.' After another week in hospital in special care, Georgia finally got home to Alford. Family life settled, but it wasn't without its challenges. Ange explained: 'Georgia was tiny when she was born and she's struggled to grow ever since. 'She's never made it onto any chart in the red book. She's never made it onto any of the centiles. 'They just say she's growing at Georgia's pace.' At times in her wee life, Georgia has had phases of being sick 100 times a week. Now, it's 'only' two or three times a week. 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Ange admitted: 'I just think about her going into school and the fact she can't talk and no-one will understand what she's saying.' 'I'm so happy and excited for Georgia, but at the same time, I'm just so nervous. 'I appreciate there are some families in a harder situation, but this is our Georgia and our situation. 'I don't know how life will turn out for her – but I just know I'm so proud of her.' The family have become super fundraisers for the Archie Foundation after the charity's much-needed support when Georgia was in hospital. Charlotte-Dee has her own first day this week in S1 at Alford Academy, so both the girls will be starting something new. Little Georgia will have mainstream with her friends in the morning and then concentrate on her own learning after lunch. Ange said: 'There's a lot of challenges around little Georgia, what I can say is, as much as she's got these challenges, she's amazing. She's really social. 'I just want to give her the best opportunities.'