Emergency in the Womb

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Two babies in a womb

Tuesday 19 May 2009

The unborn twins featured in the programme were suffering from a very rare condition, Twin to Twin Transfusion Syndrome - TTTS sometimes called FFTS (Feto-Fetal Transfusion Syndrome) or TOPS (Twin Oligohydramnios-Polyhydramnios Sequence).

This is a complex and rare condition and you can find out all about it, how it is treated and where treatment can be offered in the UK at the Twin to Twin Transfusion Syndrome Association website.

Antenatal Results and Choices or ARC provide non-directive support and information to parents throughout the antenatal testing process and when an abnormality is diagnosed in their unborn baby. They offer continued support to parents whatever decision is made. Call their helpline on 0207 631 0285 (Monday to Friday, 10am to 5pm). You can also email info@arc-uk.org or go to their website.

Bliss support parents of babies born prematurely to help them both practically and emotionally. Contact the family support helpline 0500 618140 (free, confidential Monday to Friday, 10am to 5pm) or email enquiries@bliss.org.uk.

Tamba provide information and mutual support for families of twins, triplets and more. Their support, listening and information service, Twinline 0800 138 0509 (free, confidential every day of the year 10am to 1pm and 7pm to10pm) is staffed by trained volunteers who are parents of multiples, and can answer questions on many topics including sleep, feeding, crying, behaviour, discipline or special needs. Or you can email asktwinline@tamba.org.uk. Tamba Bereavement Support Group has its own website www.tamba-bsg.org.uk for parents who have lost a baby, or babies, during a multiple pregnancy or at any stage after birth.

The Stillbirth and Neonatal Death Society - SANDS provide support for bereaved parents and their families when their baby dies, before, during or soon after birth. Call the helpline 020 7436 5881 (Monday to Friday, 9.30am to 5.30pm) or email support@uk-sands.org.

One of the babies in Emergency in the Womb is born with a congenital heart condition.

The Children's Heart Federation is dedicated to helping children with congenital or acquired heart disease and their families, by providing information, working to gain recognition of their needs, and ensuring adequate resources are available. Call the CHF information line 0808 808 5000 (free, Monday to Friday, 9.30am to 4.30pm). Their website includes the Congenital Heart Disease Portal which provides information about treatment of congenital heart disease so that parents can make informed choices about their child's care and treatment.

When a child, or expected baby, is diagnosed with a disability parents can experience feelings of disbelief, anger, despair and isolation. Whatever medical condition your child may have, Contact a Family can provide support, advice and information and also put families in touch with each other. Contact their helpline 0808 808 3555 or Textphone for people with hearing difficulties on 0808 808 3556 (both free, Monday to Friday, 10am to 4pm, Monday evenings 5.30 to 7.30pm). The Contact a Family website features a directory of specific conditions and rare disorders.

Other support links:

Twins Club - support for parents of twins and multiples
Baby World - for general information as well as congenital heart conditions
Newlife Foundation - offers comfort, support and information to anyone concerned about or affected by child disability
The Child Death Helpline offers support to anyone affected by the death of a child, whatever age

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  1. I managed to watch Emergency in the Womb last night. I couldn't face watching it back in May when it first screened. I was expecting identical twins and last December at 22 weeks had laser surgery at Kings by the Professor to save the lives of my sons who had TTST. Devastatingly we lost our little boy Harry last Christmas, a couple of days after the surgery. Similarly to one of the ladies in the programme, I then begun to leak fluid from the live twins sac. I was expected by my local hospital to go into labour at 22 weeks and lose both twins but by some miracle the baby held on until 28 weeks when I gave birth to a beautiful but tiny baby, Oliver, who is now 9 months old and doing very very well. Harry is our little star in the sky watching over his brother Oliver. I will never get over losing him but I have my miracle son, Oliver thanks to the amazing work by the Professor.
    Posted by Lisa Fairlie on 16/11/2009 13:56:41
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  2. Thank you to Channel 4 for explaining the condition TTTS to the nation. My boys under went the laser ablation at 16 weeks in Bristol and thankfully they survived. Having the surgery so early on, we always had the risk of it returning or further complications. I am a very lucky and very proud twin mummy, my boys arrived without complication at 34 weeks via emergency c section and are now thriving 9 month old babies. Fingers and toes are crossed for all who are undergoing this condition at present and wish them all the very best and hopefully they will too be blessed with such miracles. To all who have lost with TTTS you are truely wonderful parents with special little angels.
    Posted by Kelly Loveless on 22/05/2009 20:06:46
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  3. It brought back a lot of memories for me watching this programme, I was very lucky to be referred to Kings College to have the procedure at 20 weeks. The procedure was a success but we had the worry of not knowing if the smaller twin would have brain damage because of the position she was in, it took 6 weeks to confirm that she was alright. I was advised to have a C-Section at 35 weeks and my twin girls are now 12 years old, one has a slight weakness down her left side but I appreciate how lucky I am to have them as last night showed that not all cases have a truly happy ending.
    Posted by Nicki Powis on 22/05/2009 14:23:17
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  4. We had this very surgery almost 6 years ago when I was 17weeks pregnant. Watching the documentary was both comforting and harrowing - an exact replica of the scenario - the 20 people watching Professor Nikolaides working his magic, the pain and the emotion of not knowing the outcome. Though the larger twin's sac leaked water throughout the rest of the pregnancy and we knew that they could die anytime, somehow, they made it - born at 31weeks and are with us now - 2 perfect specimens of 5year olds! Thank you for doing the documentary - it is rare in that twins are rare, and id twins rarer still, but when you find yourself pregnant with id twins, the risk is high!! Thanks again.
    Posted by Sharon on 22/05/2009 09:32:29
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  5. My friends from Hong Kong are going through this at the moment, they have had to travel to Sydney leaving their first child behind to have lazer surgery and they are very much in our thoughts at the moment.
    Posted by Nicola Hurran on 22/05/2009 00:17:18
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  6. Please correct your statement that TTTS is a 'very rare' condition. In fact it affects 10-20% of monochorionic (identical) twin pregnancies (around 1 in a 1000 total pregnancies). My twin girls died from this condition at just under 20 weeks, the day before we were scheduled to have the laser ablation surgery. Had we been diagnosed and treated earlier the outcome may have been different. Thank you for highlighting the difficulty in dealing with this unpredictable and distressing condition.
    Posted by linds on 21/05/2009 22:23:59
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