Teddy's Weblog
Special Clothes for Special BabiesOn Christmas Day…
On Christmas day, in the United Kingdom, over 250 babies will arrive early; each requiring some form of Special Care. Whilst the festivities will go on all around, for the parents of these tiny babies, little else will exist outside the walls of a neonatal unit, where an agonizing vigil will begin – the impact of which is beyond description.
Were it not for the dedication of staff; and the support of charities across the country, the situation faced by parents would undoubtedly be much worse. So as you tuck into your turkey on Christmas day, spare a thought for these families.
In these difficult times, charities are being hit hard by lack of funds; and the role they play in supporting local units is truly invaluable.
As a member of the management team for premature baby charity ADAPT, I have seen firsthand the important role smaller, regional charities play.
ADAPT is a support network for families with babies on the units at Leicester Royal Infirmary and Leicester General Hospital. This support is available when a baby is in a neonatal/special care baby unit and afterwards when the baby is home with his/her family.
Since Leicester Royal Infirmary is a high dependency unit, this support extends to parents from all over the country, who because of the need to transfer babies to hospitals that are better equipped to help, unexpectedly find themselves miles away from home.
ADAPT provides a service to anyone involved with the care of a baby on the neonatal unit and can put you in touch with other parents and families who have been through a similar experience.
Should you wish to talk to an understanding parent who is an empathic listener, or speak to our Family Support Co-ordinator email info@prembabies.co.uk
How to support ADAPT – You can follow the below link to donate money.. Your support is appreciated
KYM MARSH: Britain’s premature baby problem – and the boy I lost at 21 weeks
This year, like every other, thousands of parents will go through an experience the whole impact of which is almost beyond description. Months of pregnancy, and long hours of nurturing and hope, will end with a still birth, or an agonising vigil amid the dim lights and monitors of a ward for premature babies. For some, like me, there will be a particularly upsetting twist. They will find there is no birth or death certificate, and no funeral. There will be little recognition of any kind, only a note in the medical records to say that the hours of nurturing and hope have ended in the cold facts of a late miscarriage.
To lose a baby is a terrible sadness, as I have found from personal experience. To find your child disregarded, barely a statistic even, is particularly distressing. Hope: Kym Marsh with daughter Daisy Parkin, who was born at 24 weeks. Her twin, Archie, lived for only one week My third child died this way, a cause of pain that I would not wish on anyone. My son was born prematurely at 21 weeks and died. It was all the more traumatic to find that neither the professionals nor the British legal system consider a baby to be a ‘viable’ human being until 24 weeks. He was so tiny, the nurses did not even bother to weigh him, but as far as I am concerned I gave birth to a baby boy and his name was Archie. The hormones kicked in just the same and I was left with the baby blues, but without the child that should go with them. The nurses did their best, but I was offered little professional help to cope with the death beyond a few leaflets about charities that dealt with child bereavement. Although I had the support of my partner Jamie Lomas, and my two older children, I felt incredibly alone. If I wanted counselling or someone other than family to talk to, I had to seek it out myself, at a time when what I actually needed was someone to come to me and offer me support. Thousands of people wrote offering their sympathy, including the Prime Minister’s wife Sarah Brown who, having gone through a similar situation herself, has been hugely supportive. Our loss will never go away nor, similar to so many other parents who have suffered in this way, are we any closer to knowing why things ended as they did. This was one reason I agreed to take part in an investigation for ITV’s Tonight programme about the growing number of premature births and why prematurity is now the greatest cause of infant death in Britain. I knew that if I was to make any sense of Archie’s death then I had to get some answers – not just for me, but for the thousands of others who suffer. The experience of filming brought home some disturbing truths. There are 50,000 premature babies born each year, which is to say babies born before a pregnancy reaches its 37th completed week (full-term is normally 40 weeks). It gives us one of the highest rates of premature birth in Europe. This figure does not even include the sort of ‘late miscarriage’ that took the life of Archie. And there is, of course, a fierce debate about when life is truly viable. As anyone who has seen a 23-and-a-half week foetus crying will testify. Many medical experts believe the high rate of premature births is the result of weaknesses in the way we care for pregnant mothers. For all the improvements seen elsewhere in the health system, maternity services remain badly underfunded, and nowhere is the money so thinly stretched as in the field of caring for premature babies. The NHS Neonatal Task Force, which included doctors, nurses and the charity Bliss, was created in February last year to set a series of guidelines and drastically improve the standard of neonatal care in Britain. Exception: Kym Marsh with mum Kate Branchett and daughter Molly, born at just 1lb 3oz and now making progress at Birmingham Women’s Hospital As a result it recommended an annual investment of £89million – and that a further one-off sum of £102million was required to bring the service up to an acceptable standard.
The task force report identified a shortfall of 2,700 nurses and 300 other staff, such as physiotherapists and dieticians, in the UK’s 162 neonatal units that provide care to babies in the first 28 days of life. But the money to fund it will now have to be found from within local health budgets, which I fear has almost certainly put it right back to the bottom of the political agenda once again. The lack of funding seems particularly perverse when premature births are estimated to cost the UK economy £1billion a year. Neonatal care is hugely expensive, and there are serious implications for many of these babies, who can later suffer a range of chronic problems affecting eyes, lungs, digestive tracts and much else. Last week, Ministers formally endorsed the task force’s recommendations. However, they refused to promise any additional money to bring the care of the sickest babies up to the standard for children and adults in the UK. Children and adults in intensive care units receive one-to-one nursing. Yet only a third of Britain’s units which deal with premature babies offer the same level of support. Birmingham Women’s Hospital, where I began my investigation, is one of these exceptions. It has an impressive, well-staffed £7million neonatal unit and the results are plain to see. I met Gemma Parkin who gave birth to twins Archie and Daisy at just 24 weeks and three days. Archie survived for only one week, but Daisy was allowed home after three months. For Kate and Duncan Branchett it was a similar story. Again, one of their twins died, but doctors kept their daughter Molly. She weighed just 1lb 3oz – such a low weight that many hospitals in the UK would not have considered her worth saving. She remains on the neonatal ward, making good progress. Many mothers have a very different experience, though. Elaine Roberts gave birth to her son Jack at 29 weeks and when he became ill he was shuttled between four hospitals – Dewsbury, Bradford, Leeds St James and Pontefract, a one-hour drive from her home – because there were not enough trained staff available. However, they wanted to ensure he had the best specialised care available and this was the only way. He survived, but the risks to mother and child were obvious. I wanted to find out if anything could be done to identify which mothers are most at risk. Assistance: Kym was supported by boyfriend Jamie Lomas, but she craved some professional help I know that the natural thing was to blame myself for the death of my child, to assume that I did something wrong. I was in no way at fault, of course, nor are thousands of other would-be mothers who suffer in the same way. There was no indication that the pregnancy would end at just 21 weeks and five days. When my first son David arrived in 1994, he was seven weeks early at 33 weeks. He weighed just 4lb 4oz and had to be tube-fed for a week in the special care unit, and was in hospital for a fortnight before we were allowed to go home. He is now 5ft 9in and a strapping, healthy lad. Three years later I had my daughter Emily, who is now 12, and everything was fine. So I had assumed that David’s early birth was a fluke. It did not cross my mind when I got pregnant with Archie that anything might go wrong. Yet, in future, we could all be better prepared – with just a bit more financial investment, of course. Professor Lucilla Poston, director of maternal and foetal research at University College London, believes that the simple saliva test she is developing could help cut the number of premature births, and the dangers associated with them. It identifies which mothers are likely to be vulnerable by detecting levels of progesterone, the hormone that helps stop the womb contracting before the full term of 40 weeks. Low levels of progesterone put women at risk of delivering more than six weeks early. Although tests have so far been successful, she needs funding to extend the study – funding that is not yet available. When I was pregnant with Archie, I seemed to have every test going, from blood samples to checks for sexually transmitted diseases, but none of them was able to detect what was going to happen to me. If I’d had the saliva test and it revealed I had low progesterone levels, I would have been monitored throughout the pregnancy and been better prepared mentally. If doing no more than analysing my saliva could have made a difference, why are we not doing more to finance a breakthrough? Throughout my investigation it became clear that funding in all areas was the main issue. But for charities such as Tommy’s, Bliss and Baby Lifeline, we would be even further behind. Because there is no money ‘ring-fenced’ for maternity services, it remains up to each health authority to decide how much it spends. Health Minister Ann Keen agreed to meet me for the programme. I was grateful for her time. However, although she answered my questions, I felt she could have done more to directly address the issues. She told me the Medical Research Council has been looking into why premature births occur. Yet she preferred to talk about the importance of healthy living before and during pregnancy – through improved diet and avoiding nicotine and alcohol. ‘There is a grant now for mums to get themselves more fresh fruit and vegetables to look after themselves,’ she said. ‘We want to encourage that because some of the evidence we already have is saying that investment in the mum is cost-effective, apart from it being the right thing to do.’ Yet the majority of expectant mothers are well aware of this already. The Minister, a former district nurse, told me that safe care for mother and baby is one of her priorities. Yet the Government’s formal response to last week’s task force report would seem to undermine her assurances. Clearly, the country is under financial strain. We all understand that savings must be made, but this argument is about keeping our children – the future of our country – alive. As a parent who has gone through this, I know you have to be brave to try for a child once again. So, when you do, it is essential that you can put your trust in the care that is available.
Interview by Nikki Murfitt • Tonight – Kym Marsh: Born Too Soon is being shown tomorrow on ITV1 at 8pm. www.bliss.org.uk
We’re expanding!
We will be expanding our product range over the coming months and to accommodate this we have created a new website. Teddy & Me – Early Baby (www.earlybaby.co.uk) which will focus on, as the name suggests, tiny babies providing premature baby clothes, essential accessories, gifts plus information and support. Providing a one stop shop for parents of early babies.
Our original site www.teddyandme.co.uk will focus on our clothing collection as a whole, which will initially expand to fit babies up to six months in age; gradually increasing in size to accommodate a clothing collection for babies and toddlers up to 2yrs.
Our new range, which will become available next month, introduces three new themes
. Rosie – Incorporating pastel pinks and bright whites with a delicate rose embroidery
. Cars – One for the boy’s! Our cheeky red bubble car design is really cute
. Stripes – A mix of traditional styling with a modern feel.
As ever you can be confident that our clothes are comfortable, practical and correctly sized; made from the usual high quality fabrics you have come to expect.
We are showcasing some of the new garments at The Baby Show, Earls Court, London 16th – 18th October Stand A52. Come along we’d love to see you!
St Tropez Founder Backs Mumpreneur Finalist

Sharon made it to the finals of Mumpreneur in October last year, after beating thousands of entries to the competition. She said: “Investments of this type are only usually seen on programmes like Dragon’s Den so as you can imagine we are very excited.”
“Following my appearance on This Morning we were inundated with requests for details about our clothes, from as far away as Dubai. Judy’s investment will allow us to take advantage of the many opportunities that have come our way.”
Judy commented: “I was overwhelmed by the style and quality of the Teddy & Me clothing range, the likes of which I would normally associate with clothing from high end baby boutiques.”
Developed with help and advice from neonatal specialists and mums of special care babies, Teddy & Me clothes differ from the norm because they actually fit. They are also designed to accommodate any drips, leads or monitors babies may have, making them practical and comfortable.
Whilst continuing to design and manufacture premature baby clothes, in response to requests from customers, Teddy & Me are expanding their range to offer clothing to all babies, up to six months in age from September.
Teddy & Me clothes are available to purchase online at www.teddyandme.co.uk and will soon be available in most high street baby boutiques.

Congratulations to Eastenders, Jo Joyner
Congratulations to Eastenders actress Jo Joyner and husband Neil Madden, who have recently announced their expecting twins.
Jo, who plays Tanya Branning, the long-suffering wife of philandering Max, is due to give birth towards the end of the year.
Writers are said to be working on a plotline for the departure of Tanya, one of EastEnders’ most popular characters.
I had the pleasure of meeting Jo, along with Abi Clancy at the This Morning studios, when we filmed the regional heats of Mumpreneur, last October.
She was lovely, very genuine and sincere; and best of all she loved Teddy & Me! Describing my business as ‘A fantastic idea that fills a much-needed gap in the market’

I went on to win the regional heat and appeared in the finals the next day, I was thrilled to discover that Jo had tuned in to see the results!
Very best wishes to you both, what wonderful news!
Have you Heard, We’re Expecting…

Have you Heard We're Expecting...
At Teddy & Me our aim is to design and create beautiful, premium quality baby clothes, for all babies; however small they might be. We’re known for our specialist premature baby wear, however from September we’ll be offering much more…
Acting upon requests from customers, we are expanding our range to offer clothing to all babies, up to six months in age. We’ll be exhibiting garments from our new range, along with our premature and tiny baby clothes for the first time at The Baby Show.
Come along to stand A52, where you’ll receive a warm welcome from the team and you’ll be able to see for yourself just how lovely our clothes are.
If you’re expecting the pitter patter of tiny feet, visit our stand.
Earls Court, London – 16th – 18th October 2009
STAND A52
Visit Share your Story’s on the Teddy & Me website
Visit our website and read the remarkable premature birth stories of Tommy, Evie and Alex http://www.teddyandme.co.uk/company.asp?ID=98
Premature babies’ posture points to IQ by Rachel Nowak, New Scientist
POSTURES adopted by young babies who were born prematurely are a powerful indicator of their intelligence later in life. Observing these postures could identify individuals who should be monitored for signs of learning difficulties.
POSTURES adopted by young babies who were born prematurely are a powerful indicator of their intelligence later in life. Observing these postures could identify individuals who should be monitored for signs of learning difficulties.
The early movements of babies are already used to predict which ones may go on to develop cerebral palsy, a physical disability caused by disruption of the nervous system. Phillipa Butcher of the Australian National University in Canberra and colleagues wondered if they could also predict intellectual impairments early on. “If you can identify those at risk of a lower intelligence you can intervene earlier by providing a richer learning environment,” says Butcher.
They turned to babies born very preterm – at less than 33 weeks – as these children are more likely to have low IQs than typically developing children. The team filmed 65 such babies 11 to 16 weeks after they were expected to be born, and counted how many normal postures they held in the space of 5 minutes. Such postures included the fingers of one hand being made to point in different directions at once, a sign that they can move their fingers independently, or lying on their back with their head held straight rather than lolling to one side, which is difficult for babies due to their relatively heavy heads.
Years later, they tested the intelligence of the children, at ages 7 to 11, and found that all 16 of those babies who adopted just one or zero normal postures had IQs below the average of 100, while 60 per cent of those who held two or more normal postures had IQs above 100 (The Journal of Child Psychology and Psychiatry, DOI: 10.1111/j.1469-7610.2009.02066.x).
Butcher reckons the adoption of certain postures may be a marker of healthy brain development or the cause: it could be that infants need adequate motor skills to explore their world in order for high intelligence to develop.
“It raises the possibility of being better able to identify children that are at high risk of later learning problems and in need of intervention,” says Peter Anderson of the Victorian Infant Brain Studies team at Murdoch Children’s Research Institute in Melbourne, Australia.
I was a premature baby who very nearly missed my chance of life, but now I’m a.. rocket scientist by Beth Neil
She’s the girl who gives frantic parents of premature babies more hope and reassurance than any doctor.
Vinita Marwaha was born at 28 weeks weighing a pitiful 1lb 10oz and was so tiny she was nicknamed Minnie by nurses who did not expect her to survive but two decades later, the 22-year-old is brimming with health and blessed with an abundance of brains – and is now a rocket scientist who has just started working for Nasa in California.
And she visits the special care unit where staff battled to save her as often as she can to help ease the fears of parents keeping vigils at desperately sick children’s incubators.
Still affectionately known as Minnie by her adoring family, she says: “I’ve always known I was close to death when I was born, and have always been incredibly grateful to the doctors and nurses who cared so well for me. I was the smallest baby they’d ever treated.
“Throughout my life that’s made me work harder, knowing I almost missed my one chance of life and knowing so many people were rooting for me.
“A few weeks back we had a reunion at the hospital, where I met all the team who looked after me and it was overwhelming.
“So I’d love to think I’ve helped other parents of premature babies at the hospital by giving them some positivity, because I just want to try to repay the huge debt I owe.”
Minnie, from Surbiton, Surrey, overcame fears of brain damage and other health problems often linked to premature birth.
She will teach physical sciences at Nasa for the International Space University and is on course to become an astronaut in around seven years’ time.
She has a masters degree in astronautics and space engineering from Cranfield University in Bedfordshire and has spent the past few months doing her thesis at the International Space University in France.
Her work sounds like science fiction. She says: “I spend most of my time designing rockets, my latest project is studying the effects of moon dust on space suits.
“It’s funny when I meet new people, because as soon as I tell them what I do their jaws drop. They rarely believe me.
“But I want to learn to fly and it’s my life’s ambition to become an astronaut and fly to the moon. I’ll work as hard as I possibly can to get there. I feel I owe it to everyone who’s cared for me.”
Minnie’s parents Kim and Bob, both bank workers, are fiercely and understandably proud of their daughter, who was born at Kingston Hospital. Kim, 55, says: “Seeing Minnie now, so healthy, happy and successful, makes me want to burst with pride. I can barely believe she is the same tiny little mouse we could barely see in the incubator, clinging to life.
“When Minnie was born I couldn’t see her for three days. I was sure she’d die and couldn’t face getting attached. Two years previously Bob and I lost a baby girl, who was born at 30 weeks weighing 3lbs.
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“My husband had to turn off her life support machine when she was only a few days old and we were broken hearted.
“So since Minnie was born even earlier and lighter, I was terrified every time a nurse came to see me at hospital because I thought it was bad news. “But they said, ‘Minnie’s a fighter. She’s doing well and you must come to see her.’ “And of course I fell instantly in love. “We worried she was brain-damaged because she was so tiny. Who knew she’d grow up so brainy. She could read and write aged three.”
“She was so small nurses used to pop her in their pockets to keep her warm. She was so weak they banged on the incubator to startle her and remind her to breathe because she’d drift off. She didn’t even have the strength to cry.
“But she had a strong head and was well enough to come home three months later.”
Minnie, whose sister Nikita, 18, was born at 30 weeks weighing 3lbs, showed early interest in space, science and engineering.
Bob, 64, says: “Minnie’s cot was by the window and we’d always find her standing up, looking up into the sky at the moon.
“As a toddler she was obsessed with the children’s TV programme Button Moon, watching it for hours and hours. Aged five she taught herself to pre-set the video recorder, which I still can’t do now.
“When she was six she could name all the stars. Three years ago we flew in a helicopter over the Grand Canyon on holiday but she was more interested in asking the pilot about his controls than staring at the incredible sight below.
“But Minnie has never forgotten the people who helped her come into the world and gave her the chance to enjoy life. She is always raising money for charity Born Too Soon, which helps premature babies and their families. It is that, not just her achievements, that make her mum and I so proud.”
Anne Boatman was a sister at Kingston Hospital and part of the team that helped care for Minnie. Now a liaison health visitor, she met her again for the first time last month.
Anne says: “Seeing Minnie and comparing her to how she was, moved many of us to tears. “Minnie doesn’t remember all the medics who helped look after her, but we have never forgotten her. So although her family are proud of her, we are too.”
To donate to Born Too Soon visit justgiving.com/borntoosoon or contact Pauline Woods, co-ordinator, Neonatal Unit, Kingston Hospital NHS Trust, Galsworthy Road, Kingston, Surrey KT2 7QB, 020 8974 9157. For more information visit www.borntoosoon.org.uk
BUT MINNIE WAS NOT QUITE THE MINNIEST
The world’s most premature baby is Miami’s Amillia Taylor, who was born at 22 weeks in October 2006, weighing just 10oz. She measured 9.5in.
Britain’s tiniest baby Aaliyah Hart was given a one per cent chance of survival after she was born weighing 12oz at Birmingham City Hospital in May 2003. She arrived 12 weeks early measuring nine inches long and could fit in the palm of her mother Lorraine’s hand.
Around one in eight babies requires some form of special care. This equates to more than 80,000 babies every year. Around 22,000 of these need intensive care, often for many weeks or even months
