Ex-England and Newcastle footballer Peter Beardsley and three-year-old Brooke Armstrong were the guests of honour when the new Tesco Metro store on Clayton Street, Eldon Square celebrated its opening at 12 noon on Tuesday 16th February.

Store manager Dawn Ross presented Peter with a £2500 donation for the Newcastle United Foundation.  Then presented Brooke with a £2500 donation for Tiny Lives.

Brooke was born three weeks premature and weighted just four pounds when she was born by emergency caesarean at the RVI

Brooke’s father Rob said: “Brooke really enjoyed being the guest of honour, and she had a lovely afternoon. We were delighted to be involved in the store opening, and would like to thank Tesco for the donation - the money will be a great help and will go towards some new heat pads for the newborns to use.

“When Brooke was born the dedication and hard work of everyone in the neonatal unit was just wonderful, and this donation will enable the staff there to continue their great work.”
 
Peter Beardsley said: “I am delighted that Tiny Lives will also benefit from the opening - I am a Patron for the charity, and they do brilliant work.”
 
Store Manager Dawn said: “I am delighted to meet Peter and Brooke and her family. Both the Newcastle United Foundation and Tiny Lives are fantastic charities and do such great work locally, I was more than happy to donate to them.”

...for two staff members to go to the UNICEF UK baby Friendly Initiative Conference

Helen Gray (Post Natal Liaison Sister) and Helen Smith (Sister ward 35) attended the UNICEF UK baby Friendly Initiative Conference in November 2009.
The conference was held over 2 days at the Bournemouth International Centre.

Both Helens have a particular interest in breast feeding the preterm/ small babies on ward 35 and post natal and the conference proved to be a very worthwhile overview on current practice.

Strategies for fighting obesity are currently high on the government agenda and the conference was opened by Dr. Peter Bundred who gave a review of current literature on the relationship between breast feeding and the prevention of early life obesity.
Other speakers focused on the health professional’s role in supporting breast feeding and decision making.

A particularly interesting presentation was given by a Social Marketing Agency which implemented programs designed to bring about social change using concepts from commercial marketing. Such projects have been successful in increasing breast feeding rates of targeted populations and this heightened our awareness its power in changing behavior in a health context.

On the second day, we were particularly interested in the presentation by Professor Kerstin Hedberg who works within a neonatal intensive care unit in Uppsala, Sweden. The unit employs a model of care whereby parents are encouraged to stay for 24 hours per day to care for their baby by offering continuous skin-to-skin contact (including those babies who are ventilated). This model proves a stark contrast to those used in UK neonatal units where kangaroo mother care is generally limited to 1-2 hours or less.

The conference was supported by exhibitors such as breast feeding networks and educational (book) suppliers and we were able to meet and talk to other professionals to compare practice.

We were grateful to have been given the opportunity to attend.

Helen Smith

Keith took part in the Great North Run 2009 raising the wonderful amount of  £355.00 for Tiny Lives.  Keith’s employer The Royal Bank of Scotland then donated a further £250.00.  This bought the total to £655.00.  We would like to say thank you to everyone who sponsored Keith, the money raised will go towards helping save these special little lives.

With Lewis following in his dad’s footsteps, he took part in the Junior Great North Run 2009 and looking at Lewis taking part in the race you would never believe he spent his first 2 weeks on the Special Care Baby Unit.  Lewis is now a very healthy eight-year-old boy.

For five years Ramside Hall have supported Tiny Lives, raising a wonderful amount of £4,380.48. 

Julie Carverhill a member of staff at Ramside Hall requested their support, if all money raised over the Christmas period could be donated to Tiny Lives, after experiencing first hand of the Special Care Baby Unit, RVI, as Julie’s youngest son Adam was born ten weeks early.

Helping on the day was Adam himself alongside his big brother Josh, they both done an excellent job going around with a Tiny Lives bucket collecting donations from people.

A BIG thank you to the Carverhill family and also everyone at Ramside Hall for their continuous support.

School of Style

Last month students of Royal Grammar School held their annual charity fashion show in aid of Tiny Lives.  The school’s theatre was full as the sixth form students put on their smiles and stilettos to model a variety of clothing. 

Boys showcased clothes from, Edo, Austin Reed and Jack Jones, with girls modelling Designer and the new Kiara Boutique.  Also on show was sports wear from Canterbury, leather jackets from Second Skin, pyjamas from Marks & Spencer and exquisite pieces from Le Beado. 

Leaf closed the show with a mix of casual and eveningwear.  The audience applauded as the girls and boys strutted their stuff, raising over £2000 for a very worthy cause. 

The show was a great success and thanks go to all those who made it run so smoothly, in particular Mrs Jude Isbister who choreographed the show.

Donation made to Tiny Lives

After their kind donation to Tiny Lives, Ian updates us on baby Justin's progress. 

We hoped they’d have a lovely Christmas with the good news Justin was aloud home.  But unfortunately Justin was rushed to Durham Hospital after turning poorly.  He spent all of Christmas and New Year in hospital, finally he was allowed home on January 2nd weighing an amazing 7lbs, which is great compared to Justin being born 1lb and 15oz.

Rugby Star accepts to become a patron for Tiny Lives

Paul Sculthorpe retired Great Britian Captain and St Helens Rugby star found out about Tiny Lives through David and Joanne Spencer, his close friends and business partners, after they had personal experience of the Special Care Baby Unit. 

Paul wanted to visit the unit to see for himself the phenomenal work the   doctors and nurses do on the unit, Paul asked what he could do to help, when asked if he would like to become a patron to help raise the profile, Paul agreed without any hesitance.  Paul also has connections with Gateshead Thunders Rugby Club who have also agreed to work along side Tiny Lives.

Starting off as he means to go on both Paul and David (whose little boy was on the unit) have both agreed to run the Great North Run 2009 for Tiny Lives, with the dedication that both Paul and David have Tiny Lives can not see the half marathon being a problem for Paul or David……..good luck!

To see photo's of Paul's visit to the unit please click here

Antibody responses in full term and premature babies.

The aim of this study is to look in detail at how vaccinations work in both full term and premature babies. Previous studies have shown that babies born prematurely may respond differently and therefore the aim of this study is to gain further understanding of the level of protection for all babies, including those born prematurely. The study will test the response to immunisations using a number of laboratory techniques which will measure both the amount and the quality of protective antibodies to several of the infant immunisations given routinely to infants in the UK.

At present the main focus of the study is in refining and testing the laboratory techniques that will be used to measure both the quantity and quality of several different types of antibodies. The antibodies we are testing include those that protect against several types of meningitis, pneumonia and serious blood infections.  We hope that these techniques will be up and running in the next few weeks and that sample analysis and data collection will be completed within the next 4-6 months.

A further line of study, in addition to measuring specific protective antibodies, is to also look at specific types of bacteria carried by the babies. We know that bacteria can live in the nose and throat of many people including babies without causing disease. However for a small number of individuals there is a risk of developing serious infections. Using nose swabs that were taken when the babies were vaccinated we aim to look at the type and number of bacteria carried at that time and compare this with the level and quality of antibodies in the babies. We are interested to know whether babies with low antibody levels also carry the most bacteria.

We believe these results will provide very valuable information on the response to routine vaccinations in some of our most vulnerable patients, thus enabling us to gain a better understanding of how to achieve the maximum level of protection for all babies.

For the seventh year Tiny Lives Patron, Peter Beardsley hosted the Black & White Party.

The night is Tiny Lives' largest annual fundraising event and our hopes of holding a successful event surpassed all expectations raising over £23,000 through various activities. 
On arrival guest were met with the fabulous Big Fun Club dressed as highwayman. 

After the drinks reception the BarWizards performed a magnificent show before guests moved into the Grandstand Suite, where they were met with the spectacular impact of the masquerade theme, making the room look the best it has ever been.

Once again the Tyne Theatre Stage School Dancers raised the roof with there fabulous performance.

The Auction was conducted by the very funny Big Fun Club whereby guests were given the opportunity to bid on prizes money could not buy such as 'tickets with hospitality for three people for England v Croatia, including watching the England team train Or shadow showbiz editor Gordon Smart at the Sun Newspaper for one day and attend a showbiz party’ plus lots more!!!!

Following the Auction, guests were given the chance to experience the fun casino, and purchase a cocktail made by the fabulous BarWizards. The night concluded with guests being entertained by the ‘Pinstripe Suites’ and the DJ Set.

Thank you to everyone for your generous support, this will enable us to provide specialist training, to continue to make the unit a more homely environment and to fund specialist research projects and equipment seeking to improve care now and in the future.

If you are interested in attending next years Black & White Party please contact Louise on 0191 222 0945 or louise@communityfoundation.org.uk

To see photo's of the night please click here

George Stephenson High School raises
an amazing £10,000 for Tiny Lives

...The first fundraising event was a performance of ‘What’s For Pudding’.  The comedy was performed by the schools A Level Performing Arts class, with all ticket sales going to Tiny Lives.  They raised £95.00

Later in November, the school held George Stephenson High School Game Show Night.  The night was based around students and parents acting out popular game shows.  The shows that took place were Deal or No Deal, Family Fortunes and The Price is Right.  The night raised a further £700.00.

Over Christmas a number of events took place to raise a further £1,200, which included, a raffle that was held at the production of Oliver, three sixth formers created a Christmas CD, which was on sale for £3.  A Tiny Lives rave was held in the dance studio just before Christmas, which was organised by a Year 13 student.  Also some very kind donations from the Senior Citizens party, which got everyone in the Christmas spirit of giving.

After the Christmas break the school continued its campaign with a Year 7 Spellathon.  On the morning of Thursday 22nd January, all of Year 7 sat a spelling test of 25 words.  The event was peer marked and showed some impressive results.  A total of £635.00 was raised and was so successful that a team of students will be competing in a National Spelling Bee.

In February George Stephenson High School held their second charity day, which was centred on the theme Pink.  Students were encouraged to come dressed in Pink or Red and to pay £1, which was put to the total amount, raised on the day.  Activities were carried out throughout break and lunch time along with having a chocolate tombola and a reaction test game which were ran by the sixth form students.  The day was very successful raising £947.50.

On Friday 13th through to Sunday 15th a group of sixth formers gave up their free time to help bag pack at Marks & Spencer at the Silverlink, which raised  £1,800 over the three days.

Other great charity days and events took place to reach the £10,000 target such as setting a justgiving web page up, so the staff and students could have a Champions League Competition and an Ebay war between Year 7 and 8.

Andrea Atkinson Tiny Lives Fundraising Manager said, “Everyone at George Stephenson High School, has been fantastic in helping to hit this target!

I have never seen such high standards of events, the games night was incredible.  Throughout the whole of the school there is such a fantastic friendly atmosphere, staff and pupils worked so well as a team to help raise this money for Tiny Lives, it certainly speaks volumes for the school and everyone involved with it……….you all should be very proud!”

To see photos of staff and students please click here

Following a campaign Jonny did for two companies where for every product sold 1p was to be shared between Jonny’s four personally chosen charities.  This came to a great amount of £4,208.89.

The second cheque was generously donated by a good friend of the Wilkinsons, following a function that Jonny attended.

As one of Jonny chosen charities he visited the Special Care Baby Unit, in 2007 as he wanted to see for himself, the work of Tiny Lives.  Jonny said, “ I have to say I am so proud to be in some small way connected with Tiny Lives, I can see how important the charity is to the existence and continuance of the whole support system.” 

Since 2007 Jonny has donated prizes for our Black and White Party, which is our biggest fundraising event each year.  As well as supporting Tiny Lives in other ways.

Everyone at Tiny Lives would like to thank Jonny and his family for their great support.

Stuart and Helen Anderson recently had a premature baby at the Special Care Baby Unit RVI, Oscar sadly died after a 6 day fight.

It is Stuart and Helen's intention to raise as much money for Tiny Lives as they can and to help them in their quest Medicals Rugby Club are holding a charity comedy night on Saturday 6th March 2010.

The £20 entry fee guarantees a great night with a complimentary buffet and drinks.  As a club they have decided to fund the cost of the comedians, food and booze therefore every penny paid on entry and over the bar during the night will be donated to Tiny Lives.  Members and non-members are welcome and they are hoping to raise £1,000.00.

You can pay on the door between 6pm – 6:30pm.

If you would like more information regarding the night please visit
http://www.facebook.com/event.php?eid=306582254260
or contact
Andy Wilson at andy_j_wilson2@yahoo.com

If you cant attend the charity comedy night and would like to help raised money for the Special Care Baby Unit, RVI, in loving memory of brave Oscar please visit Stuart and Helen Anderson just giving page http://www.justgiving.com/StuartJBAnderson

Tiny Lives Toddler Week, 8th March – 12th March 2010

Would you and your toddlers like to help and support the children of tomorrow, well you can.

We are asking nurseries and toddler groups across the North East of England to help raise money for Tiny Lives, you can do this by organising a sponsored walk in the park or holding a fancy dress day.

So why not gather everyone round and think of a great way to have fun while raising money for Tiny Lives.  By doing this you will be helping save the lives of these special children that have their whole lives ahead of them.

If you would like to get involved in toddler week please contact Louise Carroll for an event registration form on 0191 2220945.

The Christmas Reunion Party gives parents a chance to meet other parents who have had a similar experience and also reunite with parents who they had become friendly whilst on the unit.  It is also an opportunity to meet some of the nurses and doctors who took care of their special ones.

But most importantly with over 200 children attending they had fun meeting Skippy the Tiny Lives Kangaroo, visiting Santa Claus while receiving a Christmas goody bag.  We had a special appearance from Tyne Theatre Stage School of Dance who performed Grease in which they were phenomenal.  Mr Twister was there showing the children his magic tricks, the children also had great fun on the bouncy castle and soft play area and after dinner the children took part in a Christmas quiz.

A raffle was held for the parents with lots of great prizes including a box at The Journal Tyne Theatre to see Aladdin, a ground tour of St James Park, a signed framed print of The Stadium of Light with a Certificate of Authenticity and many other great prizes. 

We would like to say a BIG thank you all the volunteers who helped out with out them the day would not have not been such a great success.  Also a BIG thank you to all the companies that donated a raffle prize and the other great gifts that were handed out on the day.

 
To see great photos of the Christmas Reunion Party please click here

If you have had a child on the Special Care Baby Unit at the R.V.I and would like to attend next year’s Christmas Reunion Party please contact Louise Carroll on 0191 222 0945 or E-mail: - louise@communityfoundation.org.uk.

The Biggest Boy on the Ward

Our beautiful son Brodie was born as a full term baby at Wansbeck hospital on February 20th 2009. He weighed a healthy 7 lb 2 oz and although he had been born by emergency section and had a bit of a squashed nose and a bruised head he appeared to be a perfectly healthy baby.
 
However a few hours later that the Special Care Team at Wansbeck wanted to review him as his breathing was not as good as it should have been and he was placed in SCBU for 4 days so he could be more closely monitored and then hopefully we would be allowed to take him home.
 
On the fifth day however we happened by the grace of God to meet the RVI's Dr Alan Fenton who requested we keep Brodie in for a while longer, he had a feeling he shouldn't go home as early as we had hoped for. Dr Fenton's professional judgement and instinct proved correct when that night Brodie got into severe breathing difficulties and a one point stopped breathing altogether. The registrar from the RVI was called out to Wansbeck and at 4am Brodie was ambulanced out to the RVI. The registrar had discovered a shadow on Brodie's lung and the only place he could be completely looked after was at the RVI with their specialist equipment and a wealth of consultant’s knowledge on what was wrong with Brodie.
 
I was utterly devastated and in complete shock, my husband and I left hospital without our baby, not how I had imagined our home coming at all. We were told to visit Brodie the next morning at the RVI after the consultants had all reviewed him and he was stabilised. We rushed to see him the next morning and found him in the Red Zone of Intensive Care. He was on various equipment and had all manner of tubes and drips in him, he was clearly a very poorly boy.
 
The consultants told us Brodie has an eventration of his diaphragm, one side of it is higher than the other making one lung slightly smaller and therefore he had more difficulty in breathing. This was a diagnosis we had never anticipated, but the work of Dr Fenton and his team was incredible. Brodie's care was world class, the consultants and teams of nurses taking care of him worked tiredlessly round the clock. After 2 weeks on the Green Bay we were finally allowed to take Brodie home, he had been the biggest boy on the ward in a long time. He still has regular check ups with consultants but his condition seems to be strengthening with time. 
 
My husband and I and both our families are indebted to the amazing work of Ward 35, and for Brodie's recent Christening we requested that donations were made to Tiny Lives so that more babies both premature and full term poorly babies have the chance to go home with their parents too.
 
Francesca and Jonathan Craik

To see more of the biggest boy on the ward please click here

The Miracle Work of the Special Care Baby Unit

In May 1995 my husband Bruce and I were delighted to discover that we were expecting our first baby due on or around 6 January 1996. More surprises were in store when in August 1995 at my first scan it was revealed that I was expecting twins!!! My pregnancy continued with no complications until at a routine appointment at the RVI in October 1995 I was found to have early signs of pre-eclampsia. I was admitted to hospital immediately and a few days later the doctors decided to induce me. On 29 October 1995, Beth Charlotte Nichol (2lbs 15 oz) and Rachael Catherine Nichol (3lbs 3oz) were born 10 weeks early by caesarean section. They were immediately whisked away to Special Care Baby Unit (SCBU) where they stayed for the next 7 and half weeks.

Initially the girls were admitted to the “Red” area (high dependency part). They were in incubators attached to various wires and tubes to monitor and feed them. Rachael needed to be ventilated so was on a ventilator for the first few days of her life and both girls needed help with jaundice. The staff on SCBU were very supportive and demonstrated to us how we could do the girls “daily cares” etc through the side doors on the incubators. They explained what all the equipment was for and how the various machines worked. Unfortunately it was found that  the girls were suffering from septicaemia and needed a blood transfusion. We were allowed to watch as this was set up and the transformation in the girl’s appearance as this took place was amazing they gained so much colour!

After a couple of weeks they were moved to the “Green” area which was much less daunting. They were allowed out of the incubators and put into cots with apnoea alarms attached to their bodies which I really relied on and didn’t want to remove even when they were no longer needed!

Everything was more relaxed here not as much equipment or alarms sounding and we felt more in control of our own babies here. As a leaving date approached we were allowed to stay in a room available to parents near the SCBU where we could take the girls along to at night with the back up security that the nurses etc were just along the corridor should we need them (which occasionally we did!). This experience was invaluable and prepared us for when they would leave. Just before Christmas 1995 we were allowed to take the girls home. Whilst delighted at this we knew we were going to miss all the staff who had become friends to us.

Beth and Rachael continued to put weight on etc. and often people couldn’t believe that they had been premature. Rachael needed a nebuliser for the first 2 years to help her breathing but by the age of two this was no longer required. When they were born I’d asked a doctor what would be the implications of them being born prematurely. He said that they may be prone to chest infections etc and may not be able to run very fast. Luckily other than the usual childhood ailments the girls have never ailed a thing. They are now healthy 13 year olds doing very well at High School and are extremely fit having competed in regional events such as Northumberland Schools Cross Country Championships, North East England Schools Trampoline competition and being Runners up in the North Tyneside Schools Tennis Doubles Event. They are both on the Gifted and Talented list for Physical Education!

We are forever grateful to the Special Care Baby Unit and to all the staff and equipment which enabled Beth and Rachael to recover from their very early arrival. Of course we have had our worries but without SCBU things could have been so different. We are very keen supporters of Tiny Lives and will continue to be. We are also delighted that the girl’s school have chosen Tiny Lives as their nominated charity this year and aim to raise £10,000 through various events such as TV Quiz nights, Oliver Production etc.

To anyone going through similar circumstances my advice would be to always have hope, be involved at the hospital as much as you can and listen to the advice the SCBU staff will no doubt give you. It is not an easy time but hopefully everything will work out so be as strong as you can be.

Best wishes
Pam Nichol.

To see how Beth and Rachael have grown click here

Tilly May Adamson

Tilly May Adamson started her little journey way back in December 2007. Aimey and Peter had been longing for a baby for some time and they were overjoyed to find out that Aimey was expecting. It was a lovely time, Aimey and Peter enjoyed every kick and hiccup. She was loved and protected in every way from day one.
 
At 24 weeks Aimey became very ill with pre-eclampsia. The doctors at Wansbeck thought that they would have to deliver Tilly at 24 weeks but Aimey was transferred to ward 34 of the RVI maternity unit. With the love and care of Peter and their friends and families and the fabulous care of the midwives and doctors, Aimey managed to keep Tilly in her belly for three long weeks.
 
Aimey and Peter had the pleasure of seeing Tilly every day on the scans where she wriggled and kicked and played with her feet inside Aimey. She looked so happy and content. It was lovely for Aimey to feel and see her kicking her all at the same time. On Saturday the 14th of June 2008 Aimey became much more unwell and on the scan Tilly didn’t move as much as she normally did.
 
The doctors in fetal medicine had been using the scans each day to decide when Tilly had to be delivered. They decided that with Aimey’s declining health and the signs from Tilly that it was time to deliver her by emergency caesarean section. Professor Robson and Doctor Cameron skilfully and safely delivered Tilly May at 18.46 to the sounds of Dr. Dre the next episode, one of Aimeys favourite tunes. Peter was there the whole time, holding Aimey’s hand and cracking jokes to lighten the mood. They were shown Tilly briefly before the neonatal team rushed her off to the Special Care Baby Unit.
 
She was tiny, 1lb 9oz, a lovely pink colour with a little wrinkled forehead and a little button nose just like her Aunty Lucy’s. Tilly managed to breathe on her own at first but the paediatricians found a pocket of air in her lungs so they had to give her a chest drain and ventilate her. She met her wonderful daddy first; he was so brave looking after both his baby daughter and his wife in separate intensive care units. Then Tilly met her Nunu and Pops who were so proud of their first grandchild, especially Nunu who she was named after.
Aimey was wheeled in on her bed the next day to see her and she got to touch her perfect little hand. Aunty Lucy met her later on that day and then her Mamar and Grandad who loved seeing her for the first time.
Everyone was amazed by her long legs and how she kicked them and pointed her toes, a definite ballerina in the making… Daddy’s girl.
 
On Monday Tilly had the pleasure of meeting her Great Grandma and Granda; they were so very pleased to meet her. Aimey and Peter spent a lovely night with her where she was opening her eyes and looking around. She started to fight her ventilator and take her mammy’s milk. Tilly had lots of visitors on Tuesday, her Aunty Lesley and Uncle Kevin and her Uncle Mark and Aunty Gilly who were all astounded at her size and how beautiful she was. She had lots more visits from her Nunu and Pops and Aunty Lucy who thought she got more beautiful every day. She had lots of sneaky midnight visits from her mammy but mostly she loved it when her mammy and daddy sat with her. There were lots of tears, tears of happiness and pure wonderment at beautiful Tilly.
 
On Wednesday Tilly’s ventilator was reduced as she was trying to breathe on her own and she kept on wrapping her tiny fingers round her ventilator tube and trying to pull it out. Daddy got to clean out her mouth today and mammy changed her little nappy.
 
On Thursday Tilly got to see both her Nunu and Mamar together which must have been nice for her. She saw her pops and Aunty Lucy too and then mammy and daddy bathed her and had the pleasure of changing her nappy. It’s a simple thing but it was amazing and it’s what mammys and daddys do.
 
On Friday Tilly was taken off all of her medication and her ventilator, and she could show her Great Grandma Irene how clever she was. Her Great Grandma was so pleased to see her, her little treasure. Tilly did her first poo today, again simple pleasures.
 
On Saturday Tilly and her mammy had a girly morning with just the two of them. She was wrapped up all cosy in her incubator but she was quiet and lethargic, not the kicking, dancing little lady we knew and loved.
That afternoon she had an episode where her heart stopped beating and she stopped breathing, she had to have cardiac massage. The doctors thought she had an infection so she was treated for that and put back on the ventilator. Nunu and Aunty Lucy were there but they left so Aimey and Peter could spend some time with Tilly. It was wonderful, their little family, just the three of them. Nunu and Pops came back to celebrate Tilly’s one week birthday with Peter and Aimey at 18.46 where they sang happy birthday to her through streaming tears.
 
Aimey and Peter were told later by the doctors that the next 12 hours were critical but never thought that that night the infection would take over her little body. She was resuscitated by the doctors and nurses for 45 minutes, her mammy held her hand and told her all of the things she wanted her to know, about her and Peter and how much they loved her and each other, and their fantastic families. Tilly’s family was there and they all got to hold her and say goodbye.
 
Then her mammy and daddy held her close to them and sang her a lullaby as she went to sleep.
 
For 7 days that little lady touched many hearts, as she did for the 27 weeks before she was born and we celebrate her beautiful life, however tiny. Her mammy and daddy are very proud of their brave little princess.

When you have a baby in special care, however early they are, you need some hope. We believe Tilly May’s story is full of hope. We had 7 amazing days with Tilly, she gave us unbridled joy. The doctors and nurses in the red area of the special care baby unit did everything medically and humanly possible to try and save her. She felt no pain and was treated with respect and dignity.
  
Since Tilly’s passing, we have tried to say thank you in some small way to the doctors and nurses on ward 35. So far we have raised over £4500 with a charity night at Blakelaw and District Social Club, and Tilly’s daddy has raised £2500 by doing a bungee jump off the Middlesbrough Transporter Bridge. We have events planned over the Christmas and hope to hit £10,000 by the year is out. We are being supported by Marks and Spencer at Silverlink, who are matching each pound raised.

We miss Tilly May every second of every day.

Aimey and Peter Adamson
Cramlington, Northumberland

Click here to see more of Tilly

Ella’s Story

Ella Marie Smith
Born 18th January 2007 at 25 weeks, weighing 1lb 12oz

My waters broke in the middle of the night, without warning, when I was 24 weeks pregnant (I initially thought I needed to do more pelvic floor exercises!). I was kept in our local hospital, University Hospital of North Durham, then a week later was transferred via ambulance to the RVI when it was realised I was 3cm dilated, and Ella’s foot was in my cervix!
After a rather traumatic delivery – we were warned Ella may not make it and that she may have lots of broken bones (luckily, she didn’t) – we finally got to see our daughter on the special care baby unit a couple of hours later. She was covered in bruises from the delivery, one leg was really swollen, she was ventilated, and had lots of lines in... but she was perfect. Tiny, but perfect.
Looking back, those first few weeks were so surreal, almost like a dream – we relied on our family, friends and staff on the unit to keep things in perspective, and took one day at a time.
We got our first cuddle with Ella when she was 5 days old, and thereafter we started kangaroo care, which was just magical for us – and certainly helped with my milk production (I was expressing so much, some had to be thrown away, and it was a standard joke that I could’ve fed the whole unit!)
Ella’s initial problems apart from her breathing was her heart duct was open (this closed with a course of indometacin, so no surgery needed), she needed a couple of blood transfusions, and her temperature kept fluctuating – a lot of stress, but Ella sailed through it.
Despite all these worries, every week, Ella got bigger and stronger, making more effort with her breathing, and after 15 days, started on CPAP, steadily progressing to low flow oxygen. One magical day came when Ella was 7 weeks old and we tried her on my breast – she knew just what to do, it was beautiful.
Day 49 saw us move to the ‘blue area’, only for two days, as we were transferred back to Durham – this was very emotional for us, as although we knew it was a step closer to taking Ella home, it felt strange and unsettling leaving the RVI, not just because we trusted the staff and their expertise, but we were leaving parents and their babies whom we’d got to know so well during this time.
Our time at Durham became positive, focussing on establishing Ella’s feeding, and getting oxygen stabilised for discharge home.
On 11th April 2007, after 83 days in hospital, and 3 weeks before Ella’s due date, we took Ella home, weighing a ‘huge’ 5lb 12oz! She came home on low flow oxygen, demand breast feeding, but came off oxygen by July.
Ella is now 22 months old, runs everywhere, and is a mischevious, gorgeous girl who giggles a lot!
Ella’s nana, my mum, sadly died on 1st September this year, after a very short illness. One of her wishes was to donate £5000 to the special care baby unit, as my mum and dad were so grateful for all the care Ella and we received.
We’d like to dedicate this story to the best mum and nana in the world, and we’d like to thank all the staff on Ward 35 for all their wonderful care, support and knowledge. We will be eternally grateful.

Told by Vicky and Mark Smith, Ella’s proud parents x

To see more of Ella please click here

Our son Callum was born at 29 weeks weighing just 3lb 10oz on 6th September 2005 at Newcastle RVI while we were on holiday from Scotland in Kielder Forest.  On arrival at Newcastle RVI an emergency caesarean section was carried out as we were advised if Callum was not delivered within about 10 minutes he might not survive. We were told by the consultants that a placental abruption had occurred but we do not know if it was the rapid onset of preterm labour which forced the placenta away or if the placenta came away first bringing labour on.
 
Callum was then rushed straight to Intensive care where he spent about 24 hours being ventilated before being moved onto CPAP.  His arm was badly bruised due to the difficult delivery and his arm was X-rayed, as there was a chance that it was broken. However this proved to be negative. Callum was stabilised over a period of 8 days in Newcastle RVI and we were lucky enough to have our first cuddles with him during this time.  Callum also received his first blood transfusion at Newcastle RVI, before being transferred to Glasgow Princess Royal Maternity.
 
During his time at Glasgow Princess Royal Maternity Callum received a second blood transfusion and received 2 doses of antibiotics due to suspected infections but luckily for him these infections proved to be negative.  He was also weaned off CPAP but spent a long time linked to an apnoea monitor and would also suffer from bradicardias right up until about 5 days before going home.
 
Callum spent a total of 60 days in hospita.l However once he was home we had to pay a visit to Yorkhill Sick Children’s hospital for an MRI scan as there was a suspected bleed close to one of Callums ventricles and his ventricles were also on the larger side of normal and may have been squashing part of his brain.  We were given the good news of this scan on Christmas Eve 2005 showing that there had been a minor bleed but there was nothing to worry about and that his ventricles were not causing a problem.  We could not have asked for a better Christmas present.
 
The staff at Newcastle RVI saved our son’s life and we owe them so much.  This has encouraged us to raise funds for Tiny Lives over the last 2 years and we have recently completed the BUPA Great North Run.  This felt an appropriate way to raise funds for Tiny Lives as the run starts just a short distance from the RVI and we will continue to raise funds in the future.
 
Paul and Yvonne Hendry

To see how much Callum has grown please click here

My name is Nicola and my partner is Daran. I had a fairly normal pregnancy apart from extreme morning sickness and everything seemed to be going quite well. On 19th Oct 2007 my waters broke at 4am. To be honest I thought the baby was lying on my bladder and had made me wee but after jumping in the shower I realised that my bump had deflated and Daran had already rung the hospital who told us to go straight in.

Even when we arrived at the hospital I thought we would be told that all was OK and I would be going back to work, as I was only 26 weeks and 5 days pregnant. The baby was measured and checked and I was kept in for 2 days and told that I wouldn't be going back to work and the baby was likely to come sooner rather than later. I think I was still in denial because I was only 6 months pregnant and thought this couldn't really be happening.
I got home had a bath and then started feeling uncomfortable, like I needed the loo.
My mum and Daran grabbed a bag and off we went to the hospital. By the time we got there I knew I was in labour but thought that they would give me something to stop it. I was lucky that they had managed to get 2 steroid injections into me while in hospital to help the baby's lungs and was told by the nurses when we arrived that I was going to the delivery suite. I still thought I wasn't having this baby yet.
 
I was monitored and given diamorphine and then quite suddenly a lot of doctors appeared in the room and told me the heart was dipping so they needed to get the baby out.
After 5 mins of pushing our beautiful baby girl was born at 27 weeks and 1 day and weighed 2lb 4 1/2 ozs. She was held up quickly in front of us and then was checked by the doctors.
Georgia breathed initially but then had a blockage and the doctors were working hard to get her breathing again and after 4 mins they cleared the blockage and she was taken and put on a ventilator.

We were so happy but also terrified and desperate to know if she was going to make it.
The midwife and the doctors who delivered Georgia were fantastic and looked after us really well. Georgia was put in an incubator in the Special Care Baby Unit (SCBU) and I stayed on a ward for the first week.

Georgia came off the ventilator after the first day and I was in a daze. I just used to go and sit and look at this tiny baby through the incubator willing her to be OK. The staff in SCBU were amazing and really gentle. They showed us how to help Georgia and do her cares, change her nappy, clean her face and how to handle her.

Georgia was doing well, but wasn't gaining weight as quickly as they would have liked and had a huge swollen tummy. she was given x-rays and they showed nothing sinister so we just carried on watching her grow. After 4 weeks we were moved from the red area to the blue. She still had a huge tummy and had to have two courses of antibiotics for infections but she was doing fairly well. She also had to have two blood transfusions, and had to have quite a lot of blood taken for tests etc.
 
After 2 weeks in the blue area, we were thrilled to be told that we were ready for the green. Georgia still wasn't gaining masses of weight but she was strong and breathing well with CPAP. She'd only needed oxygen occasionally and was breathing alone for longer and longer periods. They had discovered that she had an ectopic heart beat which was monitored but the heart specialist said it was nothing to be too worried about.
 
Just before Christmas after 8 weeks in hospital we were allowed home as we were eligible for the home tube feeding programme but once home Georgia wouldn't sleep and was vomiting all night and seemed to have cramps. We were admitted into ward 6 in early January where we stayed for another 8 weeks while they carried out tests. Consultants and some of the nurses from SCBU came to see us and continued to look after us.
It was found that Georgia's pancreas wasn't working as it should be and her white blood count was always down and her kidneys were leaking. She was diagnosed with Swachman Diamond Syndrome (SDS), a life threatening condition. We were distraught and the doctors and nurses spent hours comforting us as we tried to come to terms with it.

Georgia was given medication and one of the doctors decided to try her on a dairy free milk instead of breast milk and overnight she changed. She started sleeping and her tummy went back to normal and we were allowed to go home. Two months later we were given the amazing news that Georgia was OK. We had been waiting for the results of the genetic test to confirm SDS but it had come back negative. Georgia had simply outgrown her symptoms and they retested her and everything was working OK.

Georgia is now almost one and she is a joy. She has an allergy to milk that she will grow out of but apart from that she is a beautiful healthy baby who is developing well. We will never be able to thank the staff at the RVI enough for the love and care they showed to us as well as our daughter, they helped us through a truly awful time.
 
I hope any other parents who are reading this and remember we are now doing OK and enjoy their special babies too.

 
Lots of love

Nicola, Daran & Georgia
 
xxx

To see more of Georgia click here

Josh Ryan Leader Born April 10th 2008 at 26 weeks and 3 days.

Our story begins when I was 23 weeks pregnant and was told I had pre-eclampsia. At the time I didn’t realise what it was all about and the dangers that I faced - I was actually on holiday down in Cornwall. I spent the next couple of weeks in and out of hospital at Durham before being transferred to the RVI in Newcastle. I was told my baby would come sooner rather than later as I had too many complications. I managed to get to 26 weeks and 3 days before our baby boy was born by an emergency c-section on April the 10th 2008 at 14.31pm weighing 1lb 6oz. I only saw our son briefly as he was whisked away to special care (S.C.B.U) ward 35 in an incubator. 

I was told not to build my hopes up as our son was born so prematurely. When Josh made an appearance into the world we endured many ups and downs. Along the way we were also told that Josh’s duct near his heart wasn’t closing and medical treatment didn’t agree with him. The only option was to send him to the Freeman Hospital for an operation (PDA ligation) on Bank Holiday Monday 26th May 2008. This came as a complete shock but we were both prepared for this.  At first I didn’t realise that this was a common operation but the staff explained it to us and I was quite happy to send him. He needed it doing as he couldn’t come off the ventilator. Josh had quite a few infections which delayed him from going for the operation.

It took Josh a week to recover and be transferred to CPAP and then weaned to low flow oxygen. Along the way Josh had 5 blood and 1 platelet transfusions but finally after 100 days he was transferred to our local hospital where he spent another 18 days. On August the 6th 2008 (age 118 days) Josh finally came home. He is currently on oxygen and is doing well. As I’m writing this story Josh is nearly 6 months old and weighs 12lb 5oz. Without the doctors and nurses both at the RVI and Freeman our son wouldn’t have survived.

Many Thanks Emma

To see more of Josh click here

Sam's Story

Sam was born 16 weeks early weighing 1lb 3oz.

When I was 23 weeks and 6 days into the pregnancy my waters ruptured with no warning. We rushed straight to the RVI where we were warned that if the baby came now he would most likely not make it.

Sam only managed to hang on a few more hours and was born in the early hours of October 18th 2005.

After being stabilised he got to meet his dad quickly before being rushed to Ward 35, Special Care baby Unit. This was to be his home for the next 7 months.

It seemed that almost every other day presented a new problem for Sam.
At 10 days old a Blessing was organised. This was a way of welcoming Sam into the family and of us all saying goodbye. He was very poorly.
Sam had suffered a grade 4 IVH, he was suffering from seven different infections, he was in renal failure (his kidneys weren't working) and there were problems getting his blood pressure under control. His veins would break every time the doctors tried to get a line in to give him medicine. Then there were no more veins to try.

We asked if we could take him home to die.

The next day we came to the ward expecting it to be Sam's last. We were greeted with the news that Sam was a little better! Sam somehow managed to hang on for 3 days until his veins had recovered enough for the doctors to get a line back in and give him the medicine he needed.  He had won his first major battle but there were many to come.  Sam had an operation at the Freeman to close a duct in his heart. A few days later we became a proper family when his dad and I were married.  But then a few days later it was discovered Sam had a defect in with one of the valves in his heart.

By Christmas things were going well, Sam was weaned from CPAP onto low flow and it looked as if he was all set to move round to the blue area.  Then out of the blue he starts to struggle and had to go back on the ventilator.  He went back onto CPAP and started to have time off again at the beginning of January. He was then diagnosed with stage 3 retinopathy of prematurity (ROP) which meant he had to go for laser eye surgery to prevent him going blind.

In theatre they tried to intubate Sam and discovered that his airway was completely swollen shut, it was a miracle he was even breathing.  Being intubated had caused scarring and swelling to occur (subglottic stenosis). They were left with no option other than to perform a tracheostomy.

In February the cardiologist found that Sam's aortic valve was not growing with him and he now has moderate aortic stenosis.

In March, a broncoscopy showed that Sam has floppy airways so would be dependant on CPAP till he grew out of it, all going well we were told 2 years.  The hope was to wean him onto oxygen during the day so he will only need the CPAP at night.

Sam has suffered from intermittent bouts of tummy distension since he was quite small. His tummy was so big it was impacting on his breathing.  So in April he had a laporoscopy to see if a cause could be found and hopefully remedied. They could find nothing but air so performed an ileostomy to help relieve the pressure. They also repaired his hernia and gave him an appendicectomy into the bargain!!

In May Sam finally started to realise he wanted more than the four walls he was stuck in. He started to tolerate longer times off CPAP till eventually he started to tolerate being off throughout the day.  He started on demand feeds and finally got rid of the NG tube!! After 7 months he finally moved out of Special Care and onto a children's ward.

He had has his own room complete with TV and even a telephone!! He still needed the CPAP at night and still got a swollen tummy. He started to get to go out and about for short spells and even made it to Grandma's for Sunday lunch.

Eventually, after 9 long months, Sam was strong enough to come home.  Just days before coming home he finally managed to be weaned off CPAP completely and onto just oxygen.

Once home Sam really started to thrive. After 18 months he grew out of the need for oxygen. He no longer has a tracheostomy nor an ileostomy.  He is a happy, cheeky two year old. His development has been slightly delayed by his early arrival and all the medical problems but given time he will catch up with the other children his age. He is a very bright little boy.

His Dad and I would like to express our heart felt gratitude to the staff of Ward 35. Without their care and dedication Sam would not be here. We owe them everything.

I made a montage of Sam's Story –
http://www.onetruemedia.com/otm_site/view_shared?p=12f5ba73890a76a12a0da4&source=category&category_id=12

On Thursday 17 May 2007 I went to a routine antenatal check up, where my blood pressure was found to be dangerously high. I was admitted to my local hospital in Whitehaven, Cumbria where my blood pressure kept going up and down like a yo-yo. It was decided that I needed to have an injection of steroids to help my baby (I was 26 weeks + 3 days), but because my blood pressure was so unstable so early in my pregnancy they transferred me to the RVI.

I arrived at the RVI at 3am on Friday 18 May, where I received another steroid injection. The following day I felt fine but my blood pressure was still too high. By Sunday I felt a little unwell after I had my breakfast. I put it down to the fresh orange juice but then the headache, stomach pains and sickness started. By teatime I felt OK again, so I told my husband to go home and get some clean clothes etc. He didn't leave until after 11 pm so the roads would be quiet. Within an hour of my husband Kevin leaving things started to go very wrong. I started with pre-eclampsia which then developed into HELLP syndrome (this is a condition that attacks your vital organs and your body goes into shut down mode).
Just as Kevin was about to turn down our road he received a phone call to say that they where taking me for an emergency caesarean section. At 2.18am on Monday 21 May our beautiful little miracle Jack Francis arrived weighting 1lb 8 oz at 27 weeks.

He was placed in a rosti bag and whisked to Ward 35 Neonatal Unit. Jack was unable to breathe for himself and needed to be put on a ventilator. On his first day a lovely lady called Joan Loveday looked after our beautiful boy.
After a few days Jack began to show his grit and determination; he began fighting the ventilator so they tried Jack on CPAP and he managed for about 12 hours before becoming very tired and needed to be placed back on the ventilator. On Friday 25 May I finally got to see our little boy!!!
This is when Jack’s rollercoaster journey began.

On a daily basis Jack had a team of dedicated consultants, doctors, nurses, family and friends to care for him and us. The teams give Jack the best support and care you can imagine and took time to explain and discuss things with us.
Jack had a lot of ups and downs! He developed infections and became very unwell, but with the correct care and attention Jack started to improve bit by bit. He came off the ventilator onto BiPAP and eventually got onto CPAP at the beginning of July. After a few more ups and downs he started on Vapotherm and did really well.
By the 2 August we were in the Blue area and Jack was on low flow oxygen.

For the first time we could finally see the road home.
On the 9 August Jack was transferred back to our local hospital in Whitehaven and on the 14 August we got the best news yet.................... we could take our little miracle home and be a real family!

Jack has just celebrated his first birthday on 21 May 2008. He is a happy little man, full of smiles and a very cheeky character. We are so lucky! Every night myself and Kevin look at our little miracle asleep in his cot and thank the staff at the RVI for our perfect little family. We know that without them and Tiny Lives our story wouldn’t have had a happy ending.

Thank you love Kevin, Antonia and our little miracle Jack x

To see more of Jack - - click here

STORY TOLD BY MUM WENDY JOHNSON (April 9th 2008)
 At the age of 42 in January 2007, I decided to try for a baby (my 1st one).  I was lucky enough to fall pregnant within 8 weeks, and baby Ella was due Christmas Day.
My pregnancy was going as well as expected.
 I was at 29 weeks, when on October 17th I woke up feeling unwell with stomach pain.  The only way I can describe the pain is the feeling you get when you need to empty your bowels, but you can’t.
For nearly 2 hours I wriggled about with the pain and made several visits to the toilet trying to empty my bowels. 
In the end my worried partner Paul (who would not have normally have been at home at this time - and just as well he was) said he was going to ring the hospital to get some advise.  The staff told him to bring me in straight away.  I told Paul I didn’t want to go because I would just end up poohing in his car, and I pleaded with him to give me another 10 minutes because I was convinced that I would empty my bowels and all would be well.  But he wasn’t having it and insisted I got ready and got in the car.  I reluctantly did as I was told.
Within 10 minutes of arriving at the hospital I was examined then rushed to theatre for an emergency section.  I was told that the baby had to come out immediately.  It all happened so quickly that I didn’t get the chance to ask why, and the staff didn’t have time to explain.
When I came around after the operation the consultant who performed my section explained to me why he had to do it.  He told me that my placenta had ruptured and my stomach had filled up with 1 & 1/2 litres of blood which was putting myself and my baby's lives in danger.  He said that if my partner had got me to the hospital 10 minutes later, it could have been fatal for the two of us.  Wow, what a scary thought.
Baby Ella was 2lbs 11ozs and was rushed to the Special Care Baby Unit. She was given oxygen for a couple of days until she was able to breathe for herself.  After that she went from strength to strength and gaining weight steadily without any worries or concern.
When she was 8 weeks old we were delighted after being told that we could take Ella home. But as preparations were being made, Ella turned poorly.  She had contracted RSV which is a viral bronchial infection.  We were told that she might have to go back to intensive care to get help with her breathing.  As this was a virus, she had to fight it off herself and nobody could say how long this would last.  This was a worrying time for myself and Paul and it was heartbreaking to see her like that. 
But being the little fighter she is, she made a full recovery within 10 days and we were able to take her home on the 19th December, the best Christmas present ever.
We are still in awe of our gorgeous smiley happy girl, and we feel so lucky and blessed.
We can’t thank the staff on Ward 35 enough, we feel forever in their debt.  They do a fantastic job and the dedication is second to none.  Not only did they care for Ella, but also they were there for mum and dad too for over 10 weeks.  Without their care, help and support we couldn’t have got through that very stressful time.
I have already made plans to raise money for Tiny Lives because they so so need and deserve it. 
Thank you again to all concerned.

To see how much Ella has grown click here

The first 5 months of my pregnancy went with no complications or concerns. Then a routine appointment with my midwife changed everything. She noticed that my blood pressure was unusually high for my stage of pregnancy and sent me straight to the Pregnancy Assessment Unit at the Wansbeck Hospital. My blood pressure was monitored every 20 minutes with no change, it was still high. That’s when we got the news that I was suffering pre-eclampsia a potentially life threatening condition for both myself and my unborn baby. During the next month I had frequent visits to the unit for blood and urine test’s, scans and medication. During this time I had one admission into hospital as my blood pressure became extremely high. During one of my scan at 25+6 weeks I could tell something was wrong the room went very quiet and they wanted a second opinion. The scan had revealed Jessica had stopped growing at 23-24 weeks and my placenta had stopped working effectively. Once again I was back up to the assessment unit where I was told that my baby would be coming much sooner than expected. After this news I rang my partner as he was at work and told him the situation and to come to the hospital. While I was waiting for him I had my mum at my side and my mind was racing, all I keep saying was its too early. While the midwife was on the phone to the RVI, I had my steroid injections to help develop my baby’s lungs.

The next thing I know I was on my way to the RVI thinking that my baby was coming today. Once I arrived I was checked onto the assessment ward and monitored and settled down for the night. The next morning I was sent for another scan and the situation hadn’t changed my placenta still wasn’t working effectively. This carried on for a week. We managed to get Jessica to 27 weeks, which gave her a better chance of survival. Jessica’s birth wasn’t how I had planned it and ended up being an emergency c-section, when I went into liver and kidney failure due to my pre-eclampsia.

Jessica’s was born at 27+1 week gestation (3 months premature) weighing only 675g, which is 1lb 7oz. She came out kicking and screaming, which is always a good sign. She was rushed off to the SCBU where she was put onto a ventilator as she was unable to breathe on her own. She was diagnosed with Chronic Lung Disease. Within 2 days she had dropped her weight to 1lb 5oz. We were terrified and shocked and just so worried about are little girl.  We didn’t know whether she would be able to survive, she was so small and fragile.

However the wonderful staff on the unit gave Jessica all the help and support she needed 24 hours a day. When Jessica was 26 days old and weighing less than a kilo we were told that she needed a heart operation to close a duct. If it hadn’t of been for the staff I’m not sure we would have got through this difficult time. Jessica had many more ups and downs whilst on the unit. It took 8 weeks to get her off her ventilator and a further 4 weeks on CPAP before she could breathe with just low flow oxygen. In total Jessica spent 100 days on the unit and came home on oxygen, weighing 5lb 7oz in March 2007.

Jessica is now a happy and playful 14 month old little girl who wants to be into everything. Jessica still has a few problems but is getting bigger and better all the time. No matter what is thrown at her she fights with all her might. She is our little fighter and we are eternally greatful to all the dedicated staff on ward 35 for all the care and attention they gave our little girl.

It has been a pleasure to help Ting Lives and share our story and show our appreciation for all the dedicated staff for saving Jessica and looking after her mummy and daddy as well.

Daryl’s Story, told by her proud mum Diane Davison

On the 19th September 2007, whilst 26 weeks pregnant I visited the nurse due to changing my GP. During a routine check my blood pressure was found to be very high, after further examination I was sent straight to the R.V.I. for further tests. I had a severe case of pre-eclompsia and was admitted straight to hospital.

I found this very hard to understand, as I felt completely fine within myself.  Daily antenatal soon revealed that although I was 27 weeks pregnant by this time, Daryl was only the size of a 23 week fetus and the blood flow was sometimes absent from the umbilical cord to her.

While I was on the ward I received two doses of steroids to help Daryl’s lungs and organs to develop. 

On the 28th September 2007 my daily scan revealed Daryl had stopped breathing and my health was deteriorating.  Daryl had to be delivered by emergency caesarean within the hour. 

Daryl was born at 8:28pm a mere 540 grams. I was relieved to hear her let out a little cry as she was brought into the world.  The paediatricians were fantastic and got to work immediately. Daryl was intubated within two minutes and put on ventilation.  She was taken straight to the red area, special care baby unit.  Daryl was only ventilated for around six hours before she was transformed to CPAP, which meant she was strong enough to receive less help for her breathing.  Daryl’s weigh dropped at first and at one point only weighed 480g.

By day four Daryl was feeding through a tube and was going from strength to strength.  We fell back a few times and she had good days and bad days, as did her mam and dad.  It felt like it was two steps forward and one step back, but she was strong and for every bad day there was a good day. 

As Daryl progressed to the blue area we began to see a real change in her appearance as she grew bigger every day.  We stayed in the blue area for a few weeks until she began to breathe on her own without the help of the CPAP, but still required low flow oxygen.

Next stop was the green area where Daryl blossomed and we knew our little girl was going to make it.  Daryl required 4 blood transfusions, as she wasn’t producing her own red cells. She also had a complication with her thyroid, which needs daily medicine.

On News Years Eve (31.12.07) Daryl was able to come home weighing 6lb3oz. She still needed her oxygen at home, but she was home.

Daryl’s dad and I can’t thank all the doctors and nurses at the R.V.I. enough for helping our baby survive.  They are all fantastic and their care is nothing less than first class.

Daryl continues to thrive and should be free of her oxygen by the summer. 

To see more photo's of Daryl click here

Joseph was born three months premature, seconds after he was born weighing just 2lbs, Joseph was rushed to the Special Care Baby Unit where he was put on a ventilator, diagnosed with lung disease and bleeding in the brain.  We were terrified and shocked and just so worried about are little boy.  We didn’t know whether he would be able to survive, arriving so soon.

The staff on the unit gave Joseph all the help he needed and also supported us through those first few harrowing weeks and even at three weeks when Joseph went through an operation to close a duct in his heart the staff was there for all of us.

Joseph is approaching his 4th birthday, which was a age we did not think we would reach, had it not been for the help and dedication of the Staff on ward 35

It has been a pleasure to help the Tiny Lives fund as it goes to show our appreciation of the hardworking and dedicated staff for saving Joseph and that you never know when you may find yourself in the same situation.