Gastroschisis

(gas.tros.chi.sis) Support and Resources

May-8-08

my poor lil girl

Posted by gemma

hi, i have a little girl called Ebony leigh, she was born with gastroschisis. after she was born they put a silo on around her bowels for a week then she had her operation which was a succsess. My daughter is now seven weeks old and still in SCBU.

She just wont tolerate her milk and is only on 1ml every 2 hours and her TPN to keep her nutrients up. It just seems every one who i have read about or spoke to with babies that have the same condition have only been in a few weeks. Its really fustrating i just feel like im missing out on her. I was just wondering if anyone else felt the same way it would be really good to hear a reply
X

May-1-08

my daughter had gastroschisis

Posted by slade2sleney

I have a daughter who is going to be 12 in june 2008. she was born with gastroschisis. i found out she had the condition at my 16 week scan. i was nearly 17 years old and single. she was born in Lewisham hospital and had surgery to fix the problem straight after birth.

i saw her for the first time aged 8 hours old. she was fed orally for the first time aged 2 weeks and she came home aged 4 weeks. she is a happy and healthy girl who i still look at in amazement every day.

She doesn`t have a normal belly button but is aware of her birth and why she has a different tummy button. i want you all to know…those of you who are expecting a baby with gastroschisis or have recently given birth…that its not always a dark tunnel. it will be a long and difficult journey but keep positive and enjoy your special, brave child who you are blessed to have.

i am happy to email anyone personally. email me at sleney@hotmail.co.uk

sherry sleney

Apr-18-08

Gastroschisis daughter born 4th Nov 2007

Posted by Dean

My daughter was born with gastroschisis on 4th Nov 2007 by emergency c section at 37+1 weeks due to reduced foetal movements and a possible twist in the bowel. Luckily Ella was born with uncomplicated gastroschisis and there was no twist in the bowel.

Ella had surgery 9 hours after birth and after only around 35 hours on a ventilator, 5 days in SCBU and 9 days on the ward, Ella came home.

She spent a total of 15 days in hospital and since coming home has had no problems since! She is a very good baby and has been sleeping through since 9 weeks!

I know we were very lucky with our experience and I wish everyone the best. Feel free to contact me at emersonbrown@tiscali.co.uk for any advice or to chat.

Apr-18-08

Just a word of encourgement

Posted by Dean

My husband and I had a beautiful baby girl born on November 9, 2007 with gastroschisis. It was a long hard journey, but she is now home with us after 52 days in Chidlren’s hospital. This was a very difficult time and we had good days and bad days. One thing that was really hard for me was that someone else was constantly taking care of my baby and making important descisions in her life. It was very hard to leave her and go home at night.

She came home on December 31st and is doing great! She’s eating well and going to the bathroom regualrly. She does have a lot of gas and grunts very often, but otherwise she’s a very happy healthy baby! A miracle child! And we love her lots!

I have read the stories about people in their 20’s that have survived this condition and since I have a daughter that has this condition I would like to know if there have been any women who have had gastroschisis and then grown up and had a baby of their own. If so please let me know how that went for you. I know my daughter is still very young, but of course I want her to be able to have children of her own someday.

I also want to encourgae all those moms out there who are wondering “what did I do to cause this”….no one really knows…so stop blaming yourself.  I know in our situation I was 26 years old (not that young) and I have never used drugs and I did not take any over the counter medications when I was pregnant or before I knew I was pregnant, and I don’t smoke nor am I around smokers while they are smoking on a regualr basis. No one really knows what causes this condition. Sometimes bad things just happen, so please don’t waste time blaming yourself.

Apr-18-08

Daughter now 20 months old

Posted by Dean

My daughter Sophie was born in April 2006. She was diagnosed with gastroschisis at my 12 week scan and the roller coaster began. I find it hard to believe now but we discussed terminating the pregnancy, such was the fear of this condition we had never even heard of.

Sophie was born 7 weeks early. I started having contractions and they tried to delay them for 4 days, finally deciding to go ahead with a C section.

Like any mother, I cannot really convey the emotion of overwhelming love I felt at that moment. But the hard part was just starting.

Sophie was operated on the following day but had complications and proceeded  to have 3 more operations over a 4 month stay in hospital. She contracted infection after infection and 3 months after she was born she developed such a serious one that she nearly died. Those 4 days in intesive care were horrific. We saw other babies pass away as we prayed for ours to live. We even had her baptised incase she never made it. She did. Thankyou God. Maybe those daily visits to the hospital chapel and tearful pleadings helped sway him. Whatever the case, I am now in his debt and will always be.

A month after that time in intesive care, Sophie came home from hospital. July 21st 2006. I cried my eyes out with happiness on the journey home and I will always swear that she looked at me with the most loving gaze I have ever seen, I took that as “We made it Mum”.

Sophie is now 20 months old and a bright, happy, mischevious little soul who is our world. She had some diet issues for the first year but these have all been ironed out and she is now a normal toddler with a normal appetite! Her scar is not nice, but this is a very small price to pay for her life.

I do not envy anyone at the start of their journey with gastro and I hope my story does not scare. I just had to be honest about the emotional journey that we had to travel to get where we are. But I tell you today - It was worth every minute to have our daughter in our lives.

Lots of love and best wishes.

Kx

Apr-18-08

Healthy and Happy at 5 Years Old

Posted by Dean

My daughter Erin was born with gastroschisis in 2002.  Her father and I were completely shocked, as we were both healthy and not at all high risk.  My doctor had no idea how to handle this defect and referred us to Perinatal clinic.  That week before the appointment with the specialist was the worst of my life.

The internet was full of horrific stories, and one pro-choice website described this condition as a reason mothers should be granted late-term abortions, that the child was sentenced to a short, painful life.  The misinformation I found was incredible.  I was barely able to function, wondering if my baby was in pain, and what I could have done differently prevent this.

Lucky for us, the specialist put or fears to rest, and assured us that with careful monitoring, and timing the birth properly (after the lungs were developed, before the intestines became too damaged) our daughter had a great chance at a normal life, was not in any pain, and there was no way to determine why this occurred.

My daughter arrived 4 weeks early.  Her intestines had begun to dilate (a sign they are becoming damaged by amniotic fluid) and I entered the hospital to have my labor induced, only to find I was already in labor!  The surgery went very well, although basically all of her intestines were outside of her abdomen, they were able to get them all back in again.

It was intimidating and hard to bond with her, she was my first child, and I was afraid of hurting her.  The nurses seemed so competent and knowledgeable, and I felt so uncertain that I would just sit by her side, often afraid to touch her for dislogding her tubes or bumping the respirator.  I think it may have been a mild case of post partum depression, because I remember feeling awful because while my daughter was beautiful, I didn’t feel that instant bond so many women describe, and it was intensified by my fear of touching and holding her.

After just 23 days, Erin came home, and then everything changed.  Without the nurses and doctors looking over my shoulders, I relaxed, and learned how to care for my baby.  She built up much scar tissue in her abdomen (she also had kidney surgery at 5 months, unfortunately she had kidney defects as well) and was prone to constipation and vomiting, and a bit slow to hit developmental markers, due to all the time in the hospital and being a bit early.  As we bonded, I realized how blessed I was, to be a mother to this spirited, beautiful girl.

Today my daughter is 5, and in kindergarten.  She is completely normal aside from still being prone to constipation.  She is so smart, loves to “help” with household chores, cut out pictures from magazines to make collages, and read whatever children’s stories she can get her hands on.  To anyone facing this issue now, with a pregnancy or a newborn still in the hospital….I know how lucky I am, and my daughter is….I pray you willl be just as lucky, so 5 years from now you feel the same joy that I do every day.

Apr-18-08

helping others

Posted by Dean

Hi my daughter Courtney was born in 1996 in UCH London with Gastroschisis. She is now ten and a half and is like any other child. she was discharged from hospital at 4 months old. She is a fit and healthy child, i hope that anyone who has to go through this takes comfort to know that you can get through it and it does get easier.

Apr-18-08

Tanisha`s Story

Posted by Dean

Our daughter Tanisha was born on the 11th of December 2001 weighing 4lbs 12oz`s.

She was diagnosed with the Gastroschisis condition at my partners 12 week scan at the natal ward within Sunderland General hospital. Before the diagnosis came it was just another scan which you tend to look forward too especially as a new parent, as I was going to be.

My partner already has two other daughters who underwent normal pregnancies and deliveries without complication, so when we were called back to the hospital and Gastroschisis was diagnosed it came as a huge shock.
Immediately we both started asking questions,

  • How has this happened?
  • Is it genetic?
  • What have I done to cause this?

You come away from the hospital wondering if you, your partner and ultimately your baby are going to get through this, all of these concerns we know now are perfectly natural, they are a natural human response when you have just received the worst possible news as a parent to be.

Every parent all over this planet only ever wishes for a healthy baby so dealing with the shock of Gastroschisis without even knowing the full implications of what it all means is only the beginning of the road for parents of unborn babies with the condition.

After the initial diagnoses we returned to the hospital every week for the next 16 weeks to monitor Tanisha`s heart rate.

From the early stages of my partners pregnancy her heart rate was a bit irregular, but you come to realise later on and just before delivery that this needs to be monitored in readiness of the delivery.

After leaving hospital for the first time we headed for the nearest library to research the condition for ourselves, unfortunately we only came across medical books that only described the condition in a way that only a doctor would understand.

We then used the internet as a tool to research the condition, but back in 2001 the result was more or less the same, so we seemed to have been left with more questions than answers.

It was not until we made our first appointment at Newcastle RVI to meet Professor Ravencroft who was to be the consultant that would deliver our baby did we get the answers we were looking for.

Dr Ravencroft explained the delivery procedure to us and how our baby would need an immediate operation to limit the extent of the Gastroschisis, this advice came 2 days before my partner was due to be admitted where she would undergo inducement at 38 weeks.

The evening before the planned delivery date we travelled by train the short distance from Sunderland to Newcastle Central Station where we took a slow walk while we discussed between us everything that was going to happen.

On admittance to the hospital we were given a private ward within the delivery suite and this is where the lack of sleep began.

At 5.30am the following morning my partner was given a pill to help induce the delivery, little were we to know that it would be a further 18 and a half hours later that Tanisha would arrive.

Those anxious hours were spent watching the t.v, reading papers and wandering aimlessly around the hospital grounds with the unknown in the back of our minds.

The contractions were still too far apart and dilation was not at the right level for delivery so a further pill to help was given.

Our consultant, his nurses and other delivery staff were waiting on standby ready for the moment which did not arrive until 11.55pm at which point what seemed like an army came rushing into the delivery ward pushing an incubater whereupon Tanisha was immediately put on oxygen and after all of her signs were checked she was passed back to her mother for not more than a few minutes before she was rushed to the Special Baby Care Unit to undergo her treatment.

For the next hour or so I spent a small fortune using the public payphones telling family and friends that our daughter had arrived and trying to reasure them that everything was ok, while not knowing exactly what was going on myself.

We had already been awake for more than 36 hours so it was hardly suprising that we dropped off for what turned out to be not more than an hour at which point our midwife woke us to tell us tat we could go and see Tanisha now in the baby ICU.

We had already visited the unit on our initial consultation with Professor Ravencroft who introduced us to the staff as we warily looked around at the incubaters and machinery and listened to the beeps of monitors and other equipment.

When we arrived in the baby ICU to meet our daughter confronted with what seemed like far too many tubes and wires I was again full of questions for the nurses there, I am more than sure thay would have answered the same questions a hundred times before, but for me I had to understand how each and every monitor and tube performed.

One of the hardest things to control is your babies body heat and Tanisha was having difficulty with hers but thanks to the constant nursing care given to our daughter during her thankfully brief stay in the ICU she got better quicker than most babies with Gastroschisis can expect.

When the time came to leave the ICU to move to a less dependant ward we could only thank ourselves very lucky, especially with everything that was going on around us. We did unfortunately experience the loss of other babies and children around us at the time and we can only thank the grace of God for our fate.

16 more days were to pass before Tanisha was allowed to be discharged but those early days within that ward were not as easy as they might first sound.

The PN line was the most harrowing experience during our stay. Initially we had to sign a release form because of the risks that go with such a delicate procedure, this was no easy task.

There were not too many options open to us, the form was signed and again Tanisha underwent her next procedure. The long line was to be inserted into one of her arms but after my phone calls to the operating theatre i was told that the first attempt had failed, then they tried her other arm without success, then one leg, then the other every time her veins would collapse.

Eventually the Long Line was inserted into her head leading up to a short distance from her heart, now she could start receiving the essential vitamins and minerals to keep her going until she could receive her first feed.

Tanishas first milk was going to be from her mother, who for the first time had to express her milk using a pump, this was not to her liking despite the advice given by the nurses that this would help. Tanisha then went on to 5ml of formula milk every 4hrs, this was the beginning of the process of persuading the bowels to work.

Waiting for that very first bowel movement at the same time as waiting for the colour of the contents from the naso-gastric tube to change was not the fastest process.

Sooner or later it would happen though and that day did come, you knew from all the questions you were asking doctors and nurses at the time that the poo was the milestone you were aiming towards before the next milestone of taking your baby home was to arrive.

We had completely disregarded sleep while we attempted to rest on the Z bed within the same room as Tanisha, but to this day we were very thankful we never left her side save the od meal of our own, even then we would sit in the hospital cafeteria filled with guilt that we could actually eat while she was not managing more than 15ml of formula every 2 hours or so.

Christmas day came and went, this was no time for celebrations, we were still struggling with the fact that we could not carry our baby more than 3 feet away from her cot with the amount of wires still appearing from what seemed like a million angles.

We had our visitors of family and friends with plenty of get well cards, we were thankful for the visits it stopped us from going insane.

The big day arrived when my partner was told that Tanisha could go home, I was returning from one of my brief outings to the news, which I immediately disbelieved because of my naturally pesimistic view that we were going to be there for months.

It was actually true, all we had to wait for was a doctor to remove the Long Line and we could go, I immediately made arrangements for a lift home and waited in anticipation for the line to be removed so that we could put the new dress we had bought on her and take her out of the hospital like so many other parents had done while I was grabbing a bit of fresh air, at the same time wishing that was us taking our baby home.

That time had arrived Tanisha was coming home.

Lilypie 6th to 18th Ticker

Apr-18-08

My Expected Grandaughter

Posted by Dean

We have recently found out that our son and daughter in law are expecting a girl, that has Gastroschisis…..

…..quite a shock to say the least. However, we are all positive, but somewhat nervous of the delivery, and the surgery.

Can anyone alay our fears

Thanks Red

Apr-18-08

My Baby

Posted by Dean

Hi, i went for my 12 week scan on the 17/9/07 but i found out that my son/daughter will have to have an operation when he/she is born as my baby has gastroschisis. Me and my boyfriend are really upset as i really want this baby, i wouldn’t know what to do if i lost him/her and my boyfriends other son died five months ago and now i am pregnant i dont want the same to happen.