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Posts tagged ‘Illness’


It has been a few months since I wrote my last blog about the boys. Tbh I have been really struggling with my mood and keeping my game face on. Took a while to realise it just isn’t possible to do it all, so prioritising the boys and work I took the spare moments I would usually use for writing my blog to just have 5 mins, Practice my Soothing Rhythm Breathing and attempt to be less critical of myself in the process. I have been using the website and I have found it to be a massive tool I have used to help me remain calm and grounded.

The boys have been full of mischief as usual. Out of the 4 places on offer for special education nursery provision in North Lanarkshire my boys were very lucky and were allocated a morning space each. They start Clydeview Nursery in Motherwell in August and will be there for 2 years until they start primary school. I am hoping this will be the game changer in their development progress. Already since May I have seen such a difference in not only Lewis’ speech development but also Logan’s. it is so so cute hearing Lewis shout ‘again’ or ‘my turn’, in the morning waking up to Logan shouting ‘ewis where are you?’

My Baby boys are now 3!!

My ex 25weeker twins boys turned 3 last week. Just a wee look back at the boys birthday week each year.

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Speech and Language

This blog has taken over a week of research to do and I must admit a lot of procrastinating. I think mainly because this area of the boys development scares me. They will be 3 next month and don’t speak. Logan is classed as non-verbal and Lewis has always been making noises and sounds after the SALT (speech and language team) got involved but yesterday he said mummy clear as day whilst looking at me for the very first time. Over the festive break he started saying bye-bye whilst waving. The boys did babble when they were around 9 months then after Both were very unwell with bronchiolitis they just stopped making sounds all together. No babble. Just silence. They spent a year in silence until Kirsty our therapist started coming out to the house every 2 weeks. We had Kirsty for 1 year and I can tell you she made a massive difference in our lives. She taught me that early communication skills do not include speech. There are steps to reach before then.

Most kids start to babble then make sounds then begin to say words. Not needing to give extra thought into the processes that begin to work before actual speech occurs. As you may have guessed it my boys like to be different and we had to start from the complete beginning. From birth to 5 is a critical period for detecting communication difficulties & providing intervention, but studies show as many as 64% of parents are unaware of the early warning signs of speech & language disorders.  Unfortunately, parents are not alone.  Studies show that despite being one of the most common disorders of early childhood, communication disorders are also the least well detected among pediatricians.  More often than not, valuable time is lost between the time a weakness is suspected and a child receives the assessment and intervention services he or she needs.  In this respect though we have been very lucky. By the simple fact that the boys were born so prematurely all eyes have been on them since the moment they were born. They were the neonatal consultants, neurodevelopment consultants as well as physiotherapists and occupational therapists until they reached the age of 2. They were then transferred over to the community paediatric team who have seen them twice since June 2017. As well as the before mentioned SALT intervention due to difficulties with weaning and eating solid foods. All those experts collectively have kept a very close eye on my boys to watch for and treat any delays that occurred. Both boys suffered from brain bleeds when they were born and as much as we know they are delayed due to Prematurity we don’t know how much of this delay is due to the brain bleeds.

So what can parents do to help their children whom they suspect has a speech delay? They should do some research and educate themselves on the signs of common speech and language disorders in children between birth to 4 years of age, an important stage in early detection of communication disorders. No one professional will serve as a better advocate for your child than you, the parent. You know your child better than anyone else in the world. If your gut tells you that something just isn’t right trust your instinct. There is a reason a mothers intuition is so important.

Signs of a Language Disorder:

• Does not smile or interact with others (birth and older)

• Does not babble (4-7 months)

• Makes only a few sounds or gestures, like pointing (7-12 months)

• Does not understand what others say (7 months-2 years)

• Says only a few words (12-18 months)

• Words are not easily understood (18 months-2 years)

• Does not put words together to make sentences (1.5-3 years)

• Has trouble playing and talking with other children (2-3 years)

• Has trouble with early reading and writing skills (2.5-3 years)

If a communication delay is suspected as it was with my boys early intervention is key. Seek advice from your health visitor and/or nursery key worker ASAP. If no one listens to your concerns and continually fobs you off by saying your are too young to be assessed etc just keep raising your concerns. Don’t stop until someone listens. You are not alone.

If you have any helpful hints or tips on how to help your child with early communication difficulties please feel free to comment. Let me know your personal experiences and how you managed to secure the help your child needs and deserves. Please feel free to ask any questions you may have.

As always. Stay cool.

Scottish Twin Mamma

Winter bugs

As you will be aware from the recent media attention, winter bugs are at an all time high at the minute. Norovirus, shingela and influenza namely Aussie flu seem to be doing the rounds currently. For the life of a preemie parent this fills us with dread and despair. A simple cold could have fatal consequences for our vulnerable babies never mind the host of bugs that can cause even the fittest of people to become unwell.

As expected, our household didn’t manage to avoid them this year. By Christmas I had been lulled into a false sense of security thinking this was the first year since the boys have been born that we hadn’t been struck down with some sort of major illness. We had skated by with Just running noses and the sniffles. I hadn’t even needed to give the boys their inhaler via the asthma protocol the doctor had put in place. Oh how wrong could I have been? This twin mammas household was struck by the dreaded Norovirus.

First came Lewis, then Logan then hubby and I. It was absolute hell and we are now only beginning to come out the other end of it. Keep in mind we are on 7th January!! 13 long days of at least one of us being ill. As per usual, poor Logan seemed to take up the lions share of this time. For the past 2 winters he has been admitted to the children’s ward at Wishaw General Hospital due to dehydration for a fluid challenge. I know you are all thinking – Well why didn’t you just fluid challenge him at home? For those of you who don’t know a fluid challenge for a child of his age is 5ml of water every 5-10 minutes. We do this each and every single time he is ill with a vomiting or diarrhoea bug such as Norovirus, but this poor wee lamb normally can’t even tolerate a few mls of water in his stomach. Luckily this time we managed to avoid an admission by the skin of our teeth. I am so grateful we weren’t admitted for a few reasons. The obvious being it’s best to keep him home and also our local NHS along with many other trusts are in a state of crisis at the minute. They are experiencing even further staff shortages due to this and many other bugs hitting their staffing levels hard. Visitors were turned away through the week as wards went on lockdown to prevent visitors passing bugs onto staff and of course vulnerable patients.

The above picture does make me giggle though. I am a nurse and never in my days have I ever seen 3 people cleaning a bed! Even on a deep clean protocol.

So what can we do to prevent bugs from being passed to each other?

• Wash your hands thoroughly after going to the toilet. Ideally, use liquid soap in warm running water but any soap is better than none. Dry properly after washing

• If a potty has to be used, wear gloves when you handle it, dispose of the contents into a toilet, then wash the potty with hot water and detergent and leave it to dry

• Don’t share towels and flannels

• Don’t prepare or serve food for others

• Regularly clean with disinfectant the toilets that you use.

• With hot water and detergent, wipe the flush handle, toilet seat, bathroom taps, surfaces and door handles at least once a day. Keep a cloth just for cleaning the toilet (or use a disposable one each time)

• Stay off work, school, college, etc, until at least 48 hours after the last episode of diarrhoea or vomiting

• Avoid contact with other people as far as possible during this time

Excuse the pun but sending your children to nursery when they are ill is a real bug bear of mine and other preemie parents. My boys return to nursery next week and I am terrified that they catch something with their immune system already being compromised. 48 hours after the last episode of vomiting or diarrhoea is essential to stop the virus from spreading to other children and staff. I know people worry about their sick time at work and we don’t live in an ideal world but it seriously upsets me when I see staff at the boys nursery unwell with the cold etc. To the point I have actually said to the nursery manager and her reply is normally that staff shouldn’t come in when unwell but if they do they are kept away from the children. Again, I know this to be untrue as the staff numbers incorporate everyone and breaks need to be covered etc. I just hope and pray that their hand hygiene is top notch as I don’t want my boys ill. Last March Logan was blue lighted to hospital as he was so wheezy and exhausted he had a blue pale complexion and was floppy. A common cold for him had progressed into the dreaded RSV. So please, please, please keep your children away from nursery if they are unwell. Even if you use nursery as your childcare provider. It is time to be less selfish and think of others.

If you are unwell:

  • Stay at home – gp surgeries and hospitals cannot offer any treatment to deal with these common bugs. Unless complications arise.
  • Drink plenty of fluids and stay hydrated. Use rehydration sachets if need be.
  • Take paracetamol to combat any fever you may have or the general aches and pains you feel when unwell.
  • Rest as much as life and your circumstance allow.

As always: Stay Cool.

Scottish Twin Mamma

Merry Christmas

I hope everyone had a lovely day celebrating Christmas with their loved ones. A special thought to our nearest and dearest who had a party in heaven to celebrate the birth of Jesus with us.

For our current NICU mums I hope you managed to enjoy ur special day with your little miracles. Celebrating in hospital isn’t ideal but just think of what next Christmas will bring if health willing everyone is at home together. Father Christmas still stops by to check in on the babies in hospital. As we know a preemies fight does not stop when they are discharged home. A special prayer goes out to one of my cyber mum friends who has twin boys the same age as mine. Both boys spent Christmas in hospital seriously unwell. At one point they were in different hospitals. I can not imagine the pain and heartaches those mummies have felt this year and I’m guessing it wasn’t the most festive. Massive hugs prayers and good thoughts going out into the universe for those two fighters.

Due to their developmental delays my boys still didn’t really know what was going on except they seem to have new toys to play with. Unsure if this is controversial or not but I did buy my boys twin dolls and a buggy. My family weren’t too keen but I think my Lewis is destined to be a twin dad someday as at the young age of 2 he is smashing it!

Logan even seems to love the dolls and has been cuddling them – something he has never done with teddies. He has also been feeding them himself and me with the baby bottle that came with them. Again this is brand new imaginative play for him so I feel I did the right thing getting them. In this day and age we shouldn’t be worrying about gender stereotypes anyway. We should just love our children and try and get them what they need to develop and grow. Of course also what they want as a wee extra special treat!

Merry Christmas everyone. Hold your babies tight and thank all that is good you have your babies to snuggle In tight too.

Scottish Twin Mamma



Having a look at my Facebook and the memories pop up. Sitting here in tears yet again. Last winter was a particularly brutal winter for my preemie friends. At the time Logan’s chest had also been very bad and all my anxieties were heightened. This winter – touch wood, has been better for our family in regards to chest infections, although I would say Logan has had his fair share of illness earlier on this year with him having RSV, turning blue going limp needing to be 999 rushed to hospital in an ambulance and having nebuliser and oxygen therapy in March. The post I wrote is written below:

I honestly thought wow today was tough with my boys. But I have just learned that a preemie warrior just like them has passed away and grew their angel wings. I would take today’s sickness tantrums and random scream hysterical crying times a million just to make sure my boys stayed here with me. Puts life and our supposed struggles into perspective. There are too many families not spending Christmas with their babies. Some I know personally some have become cyber type friends via preemie support groups. I cried today and felt like I wasn’t coping as well as I should but there are families crying for more serious problems than mine.

“Tonight I came to bed to find my boys snuggled up like this and I cried again. Not because I was sad or stressed but because I realised how extremely lucky I am to have these 2 amazing fighters to kiss and cuddle good night.

I love my boys more than words can ever describe.

Also I should add before any bashing begins that I did move Logan’s leg away from his brothers neck.”

The last few months have been hard for us in other ways. Extreme tantrums due to the boys lack of understanding and social communication skills. The paediatrician putting it in black and white that Logan more than likely is on the autistic spectrum and for tests to begin next year. Yet again however, seeing this post pop up on my memory feed has brought me back down to earth with a bump. At least I still have my boys with me happy, mostly healthy and more importantly alive! Mums of angel babies would give anything to have their gorgeous babies back here on earth and in their arms dealing with whatever life throws at them.

I can’t reiterate enough how lucky I am to have these 2 amazing warriors clinging to my side fighting over who is getting cuddles from me everyday. No matter what life throws at us and how bad we feel we have it, it is important to remember there are people out there who are going through worse. We all have our own journeys to face but remembering those angel babies for me is a priority.

Sending prayers and hugs into the universe for those babies we never got to meet or were taken away from us far too soon. Also, praying for the families here on earth they left behind.

Scottish Twin Mamma.


Extreme Prematurity and risk of Autism Spectrum Disorder (ASD)

Every parent worries about the risks of ill health to their unborn or newly born child. In fact, at 35 years old I’m pretty convinced that my parents still worry about my health and now of the health of their grandchildren. My GP informs me new mothers make up the bulk of their emergency appointments due to their child just not being quite right or being off some how. Rightly so, the new mothers seek medical advice to put their worried minds at ease.

Since the boys were born at 25 weeks gestation I have had my own and very personal set of worries on my mind. It started with the immediate health worries. First and foremost with Lewis and/or Logan survive the next hour,day or night. This happened on so many different occasions whilst in the NICU it almost seemed to become the norm. When we got home from the NICU the boys were still oxygen dependant and remained that way through out the winter months fighting off the usual winter bugs such as chest infections and the Noro virus, however, with possible deadly consequences for my boys.

As the boys have went from physical strength to strength there has always been this niggling worry that their neurodevelopment May be delayed or indeed impaired. As science has progressed, the survival rates for premature babies has dramatically increased especially among the smallest and sickest babies. Studies show that when survivors of Prematurity reach school age they are 50% more likely to exhibit signs of significant higher order neurodevelopmental impairment. This includes difficulties in learning, behaviour and executive functioning often requiring additional needs and special education support. Recent reports go on to suggest that this increase in atypical socio-behavioural functioning in the premature survivors population is strongly suggestive of Autism Spectrum Disorders (ASD).

According to the NHS website Autism spectrum disorder (ASD) is the name for a range of similar conditions, including Asperger syndrome, that affect a person’s social interaction, communication, interests and behaviour. In children with ASD, the symptoms are present before three years of age, although a diagnosis can sometimes be made after the age of three. It’s estimated that about 1 in every 100 people in the UK has ASD. More boys are diagnosed with the condition than girls.

There’s no “cure” for ASD, but speech and language therapy, occupational therapy, educational support, plus a number of other interventions are available to help children and parents.

Some children with ASD need to stick with routine as even the tiniest of changes can trigger tantrums, some children may engage in repetitive activity such as turning light switches on and off or neatly lining up their toys. A massive worry I have personally is even though the professionals are concentrating on Logan as they believe he has ASD Lewis also exhibits these symptoms as well. Many children with ASD also can go on to be diagnosed with ADHD or Sensory Perception Disorders.

The reason, I have found in articles that links ASD and Prematurity so strongly is that the brain develops best in the womb. When the child is born extremely early such as before 28 weeks the brain development is altered and almost wired differently to that of a full term child. This is due to the child being exposed to so many stressors during a critical stage of development. Researchers go on to explain that although ASD is not a curable condition early intervention with speech therapy, OT and behavioural/education support we can help our children move more into the mainstream of society.

Early signs of autism to look out for in babies and toddlers are:

If your baby or toddler doesn’t:

• Make eye contact, such as looking at you when being fed or smiling when being smiled at

• Respond to his or her name, or to the sound of a familiar voice

• Follow objects visually or follow your gesture when you point things out

• Point or wave goodbye, or use other gestures to communicate

• Make noises to get your attention

• Initiate or respond to cuddling or reach out to be picked up

• Imitate your movements and facial expressions

• Play with other people or share interest and enjoyment

• Notice or care if you hurt yourself or experience discomfort

I’m sure this is a topic I will go to familiarise myself with and write more about. However, if anything I have written has struck a chord with you in regards to your own child then I would advise contacting your GP or health visitor. Whilst it is important to remember all of our children develop at different rates so some children may take longer to sit up unaided walk, talk or meet their developmental milestones I have found parental instinct can also be key. You know your own child and if you feel that there is a possibility that the delays your child are experiencing aren’t normal then it is best to seek medical help and take it from there.

I hope and pray that my children grow up to be healthy and happy individuals. We will deal with whatever the universe throws at us. The only one thing I know for sure is that I love my children more than anything in the world and no diagnoses of ASD or similar conditions will ever change that. The research does show that there is a massively increased risk of ASD among pre-term children. But that is all it is. It is not a definite diagnosis, it is a risk. At the end of the day our preemies are warriors and they will continue to beat all odds and surprise us at every step of the way. Nothing will change that. Just as nothing will stop us as parents fighting for our children and loving them unconditionally.

Stay cool.

Scottish Twin Mamma


Fur Babies and premature babies. Do they go together?

I appear to be known in my friendship circle as the crazy cat 🐈 lady. I hold this title proud and Love all animals big and small. I did have 4 gorgeous Cats however, this weekend saw the unexpected death of one of my fur babies. I rescued him and his litter brother when they were 6 weeks old and loved them very much. All my kitty cats are rescues. Sadly, Paddy passed away from a suspected stroke and joined max his litter brother at the rainbow bridge. I was devastated and even tried mouth to mouth but to no avail. Now, some people may wonder why the death of ‘Just a cat’ could cause so much upset and heartbreak when there are so many different bad things happening in the world at this very moment. Or even when I have been there beside Lewis and Logan when they have been very near death, why would the death of an animal upset me so much. Well I shall tell you.


Paddy & Max

Even as a child I loved our furry friends. My mother always told me to never trust anyone who didn’t like animals as it spoke a lot to their character. As I grew up I adjusted this slightly as there are many people who do not like animals but would never wish them harm. So as long as you couldn’t hurt an innocent animal then I could trust you.

My fur babies have always been seen as and treated as members of our family. We tried for 10 years to have children and through every failed attempt of IUI, IVF or every month when that pregnancy test said negative I had my fur babies to comfort me. They could always tell if I was sad. Paddy would come and give me a head bop settle on my lap and purr away even if his fur was damp with my tears he would never leave my side. When we were lucky enough to become pregnant, Paddy seemed to instinctively know and would cuddle in on my tum. The first Time I felt the boys kick it was were Paddy was lying on top of me and he obviously felt something too as he looked at me like ‘what the hell was that? ‘


The amount of people who expected me to re-home my cats when I was pregnant astonished me and I soon discovered many people have a fear of pets especially cats with young infants. When the boys arrived 15 weeks early then even more people approached me and said ‘so who will take the Cats for you when the boys come home?’ The look of disgust I would get is unexplainable.

Preemies are at higher risk of having respiratory issues such as chronic lung disease or asthma. Both of which my boys have. The negative comments I received after explaining I has no intention of re-homing any of my pets included, you will give the boys a higher chance of allergies, do you want your children to have asthma? I had already done some research into this area and found that by having a pet in the home I was likely to reduce the boys risk of developing a pet allergy as they will have been exposed to the proteins that are found in the pets dander and saliva at an early age and will build an immunity to it. Figures show that out of the 60% of families with premature children that have pets only 6% of the children become allergic to their pets.

Paddy chilling with his ‘baldy’ brothers

Asthma has caused more debate however, recent figures also show that pet ownership does not increase the risk of adults or children becoming asthmatic. Also, asthmatics can have pets. They just follow some simple rules in order to ensure pets are not the cause of any asthmatic flare ups. This we already knew as my husband developed asthma as a child. There are plenty of things to try before re-homing a beloved pet because of asthma such as hoovering often, cleaning hardwood floors, keep pets out of bedrooms, change bed linen frequently, keep pet Well groomed and not allowing the children to change the litter trays. To me this is all common sense and should be done anyway even if you do not have a pet.

It is well documented that Cats can also bring a health benefit to the adults in the home.

• Cats are low maintenance and petting a cat can have a calming effect of adults. This helps ease stress, lessen anxieties and reduce blood pressure.

• Studies show that cat guardians are less likely to suffer from a stroke compared to guardians of other pets.

• The therapeutic benefits extend to both adults and children. In adults, the calming experience of petting a cat releases a hormone called oxytocin which is known for inducing feelings of love and trust. A cat does not judge so allows for a person to speak freely or grieve. Almost like a free therapy session. In children, studies have shown that Cats can help children with autism be less anxious, and calmer.

• Adults also get a boost of their immune system.

• Cat guardians have a 30-40% less chance of having heart disease or a heart attack compared to their non cat guardian companions.

Paddy purring and cuddling into his mummy after I had broken my humerus. I was crying and in a lot of pain and he never left my side.

l of this in mind, yes I will grieve for the loss of a big part of my family. Paddy taught my boys what the words nice and gentle meant. They would clap him – with supervision of course, and I would repeat the words over and over whilst moving their hands. Now when they come across any furry creature and wish to pet them all I say are those 2 words. Nice and gentle and the boys will make an awww sound and pet gently. My boys can’t speak and don’t understand simple language such as yes, no or stay, yet they know and understand how to be kind to an animal. It was Paddy who taught them that.


Jess my Aunts German Shepherd looking over the boys whilst they have a bath. She and the boys have a wonderful relationship stemming from what Paddy has taught them.

So in reply to my original question. Do fur babies and premature babies go together? Yes of course they do. Just use common sense, never leave any pet alone with your children and keep your home as clean as you can. All things people already do. Before you rush out and adopt a pet make sure that you have the commitment there that if you become pregnant you will find a way to make it work and keep everyone safe. It is a very doable task. With so many pets in shelters awaiting their furrever home I would always recommend adopting and not shopping. My cats have not only taught my boys social skills but have helped boost their immunity as well as encourage them developmentally. I loved growing up with my furry family and I hope my boys will grow up with the same love and kindness in their hearts.


I hope you are running free over the rainbow bridge playing and cuddling with your brother Max.

I love you Paddy cat. Thank you for being such a kind and wonderful fur baby. I will miss you always. Big kisses and cuddles. Mum. Xx

What not to say to a parent whilst their baby is in the NICU

I am by nature a very romantic person. I always dreamed of my big white wedding and having 3 kids. 2 girls 1 boy. I dreamed of everything just short of a white picket fence. Now being a grown up I knew that life isn’t like a romantic movie and we don’t always get everything that we dreamed of, somehow though I always thought that certain aspects of each dream would come true.

I always wanted to spend time getting the nursery ready for my child and having all of my family together for my baby shower. I had visions of leaving the hospital loaded with my gorgeous wee baby, multiple balloons and gift bags that eager and generous family and family had brought with them to visit my cherub. Coming home to a full house decorated with balloons and bunting to celebrate this new tiny life we had brought into the world. As with any mother to be, I also had my birth plan already in my head waiting to discuss it with the midwives. Turns out the universe had other plans for this girl who lived in a romantic bubble. After 10 years of various fertility treatments we finally conceived who would turn out to be our 2 wee miracle babies. After a very complicated pregnancy. The boys were thrown into the world at Just 25 weeks gestation. I always joked that I had to wait 10 years for them but the wee to-rags couldn’t wait 9 months on me. I had to leave the hospital 3 days after their birth with no babies, no car seats, no flowers, no balloons, no gift bags, no full house, no decorations and certainly no celebrating. My heart was broken, I didn’t want to leave my boys behind in the hospital. I wanted them to be with me, I was their mother and they should be with me and my husband. After the boys fight in the NICU they finally came home. Yet still no balloons etc. They didn’t even come home on the same day. It was as if the world had made it its mission to turn everything upside down.

Throughout these months there were many comments made to me and I can guarantee you each and every single comment came from a good place. A place of love and compassion. It’s just as humans our words tend to fail us at times of worry and grief. So either the wrong thing is said or worse. Nothing is said at all.

So I have compiled a list of things that you should never say to a parent who’s child is in the NICU. This list is not exhaustive by any means, if there is anything you feel that should be added then please feel to leave a comment and tell me what else should be there.

  1. At least he will be smaller for longer and you get to have a cute newborn for longer than other parents.’ I genuinely didn’t know how to respond to this one. But I could tell you one thing. I’d have given anything to have my boys born at a regular newborn size. That would have meant my boys were born at term and most probably healthy.
  2. ‘Oh, they just couldn’t wait to meet their mummy and daddy’ now as I said earlier, I have joked about the 10 years 9 months ratio before but really until you have watched your baby turn blue because they don’t know how to breathe by themselves yet then you will never know how hard it is to hear. They are basically saying your baby chose to fight for his life so he could just nip out and say hello.
  3. “You can’t keep wrapping them up in cotton wool’ Boy I heard this Time and Time again. Especially in the early months when the boys were on oxygen, now it seems to be rearing it’s ugly head again now they are nearly 3. As with any parent I will always put my children first. Yet people seem so shocked when you change plans at the last minute due to the wee ones being sick or refusing to go to a party where there are sick people just in case my boys get ill. If I hear one more Time ‘it’s just a cold’ I swear I will scream. “Just a cold’ could lead to breathing issues such as RSV, which could lead to my boys being incubated with a machine breathing for them, which could lead to death. So no, to a preemie mum, there is no such bloody thing as ‘Just a cold’
  4. “Don’t worry, everything will be ok’ As with most comments on this list, this is said from a good hopeful place. That being said they can also brush aside the very real fears that parents face. Nothing can prepare you for the first time you see your precious little bundle with more tubes coming out of their body than you thought could ever be possible.
  5. ‘I take it you are breastfeeding?’ This one was a very sore topic for me. I felt like a big enough failure that I couldn’t get pregnant without help, then I could make it full term, but to then be told I was not allowed to breastfeed after the nurses made such a big deal to tell me how important it was for my sons that they be given breast milk just made me feel so so low and like the biggest failure ever. I thought maybe I wasn’t supposed to be a mother after all. I still feel tremendous guilt over this to this day. I know deep down that a fed baby is best. I also opted for donor breast milk to give my boys the start I felt they deserved. I didn’t want them to be punished for my failures. It will take a very long time, if ever for me to completely forgive myself. So please, don’t ever just assume. Unless you know the circumstances, don’t ever just assume.
  6. “Wow, 1lb 7 and 1lb 11? You must have just sneezed and they popped out? You are so lucky you didn’t have to give to birth to 2 full size babies!’ I still find it difficult to see this comment as anything other than insensitive. Actually, this comment makes me want to scream. WTAF?????
  7. “At least you got to miss that really big uncomfortable stage’ I would have given my right eye to be big sore and uncomfortable to stop my boys from know the pain of needles and tests before they knew the touch and cuddle of their mum.
  8. “At least you get to go home and get a good night sleep.’ You never want to leave your baby in the hospital but sleep? Hell, when or if I ever get a good nights sleep again I will let you know.
  9. “When will the boys be normal and catch up with other kids their age?’ What is normal anyway? How dare you say my boys aren’t normal. Like any child they will do things in their own time. I will love them unconditionally no matter what their developmental age is. There are no crystal ball, NICU babies progress over the years at their own rate. The fact that they are alive and breathing is miracle enough. They will reach their own milestones in their own time.

10.Thank god that is over and done with.’ We are nearly 3 years down the line now and our journey still isn’t over. Many people assume that once baby is home that the NICU is a distant memory. However, many preemie babies are often left with long term health difficulties. Some of these will resolve over time, but many can be life long complications. The boys are at this stage just now. Many people feel they should be just like their peers and I have even been told to my face that the boys aren’t anything special. They are children and all children are special. I agree all children are special but not all children have had to face the uphill battles like my boys so yeah my boys are god damn special. We will be dealing with health issues due to their Prematurity for many more years to come if not forever. Our lives have been changed so much by having the boys and the likelihood is we will need to adapt and change our lives to suit our boys forever. Do you know what? I wouldn’t change the boys for all the tea in China.

Instead maybe say congratulations, celebrate the birth of a new life. Don’t be scared to do this because you fear the wee baby might not make it. As true as it is that not every baby makes it home from the NICU it is important to remember that every baby deserves to be celebrated. If you don’t know what to say, just say that. Don’t stay silent or worse say something that could be deemed as insensitive. Tell your friends you will be there for them whenever they want to talk. Make them a dinner for coming home from the hospital or offer to help with housework. Let them know that they are the most important people in their babies lives.

I wouldn’t wish our NICU journey on our worst enemy. If someone you know is currently going through their own NICU journey have a thought about what I have written above.

Stay Cool.

Scottish Twin Mamma

World Prematurity Day 17th November 2017 — Triggering PTSD

Today is a very significant day for parents of premature babies world wide. As with many health issues you can find support groups on social media platforms such as Facebook etc personally I am a member of a few groups aimed towards anxiety, premature birth and multiple birth. It is a well known fact that multiple births are high risk pregnancies and a high percentage end with the babies being born early. Usually the more babies are there, the earlier the babies are born. What isn’t discussed as often is Singleton babies born too soon. According to The World Health Organisation (WHO) there are sub-categories of pre-term birth, based on gestational age.

  • Moderate – late preterm (32 to <37 weeks)
  • Very preterm (28-<32 weeks)
  • Extremely preterm Aka micro preemie (<28 weeks)

My boys were born at 25 weeks gestation. Lewis was 1lb 7ozs. (652grams) Logan was 1lb 11ozs (765grams)

Of the 1 million preterm babies who die every year it has been reported the 3/4 of these babies could have been saved if they had access to proven and usually inexpensive care, such as warmth, breastfeeding support and basic medical care for breathing difficulties and infections. Just let that sink in. 3/4 million babies could be saved every year. That one statistic is enough to prove raising awareness of preterm birth is essential. By raising awareness we are able to raise funding that can go towards research to prevent as many preterm births as possible. Although, as a preemie mum it can be so so difficult to see all the pictures of tiny babies with breathing tubes fighting for their life in incubators I understand the importance of getting those images and stories out there. If you read blogs or articles that take you through someone’s NICU journey you will find most of the mums state that they had very little knowledge of preterm birth and it’s causes.

My case was a bit different however, I grew up knowing that the miracles of science could save a baby born so early. My older brother was born at 26 weeks gestation in 1977. The doctors didn’t give him a real chance of survival. He weighed less than a bag of sugar. He is now 40 years old with his own family. My poor mum then went into labour with me around the same gestation, however, this time they knew that there was a chance of this happening so she had been monitored very closely throughout her pregnancy. So with some medical interventions I lasted until mum was 30 weeks pregnant. It was always thought that spontaneous preterm labour was not heredity, yet recently WHO have stared there could be a family link.

I have tried to speak about my experiences of preterm birth with my boys in this blog but I have successfully managed to avoid my personal feelings and speak more about the facts. This has been one of my biggest personal demons. I’m like an emu. When life is stressful I put the biggest smile on my face, pretend to the world that everything is A-ok and bury my head along with my problems in the sand. I recently discovered this only works for a certain length of time then all those fears, feelings and anxieties rush to the surface and there is no way to hold it all back. The last few months have been like a living hell and I’m sure my family who are my biggest support network will agree it wasn’t pleasant for them either. I went from being a happy bubbly person to someone who took every tiny thing to heart and would explode in a rage to defend herself when in actual fact I wasn’t being threatened in the slightest. Some studies suggest that up to 71% of NICU mums go on to develop PTSD. Is it any wonder though? The body and mind go through such a massive invasion at childbirth and that is when mum and baby are in good health. Now add in additional stressors such as traumatic birth, premature birth, complications to mum and baby.

So today is National Prematurity Awareness Day. Please take some time to pray for and/or send Well wishes for those babies who are still currently riding that NICU rollercoaster.

Think of the babies born too soon who didn’t get to go home from the neonatal unit.

Think of the babies who fight life threatening illness every winter due to their lungs being damaged from Prematurity.

Think of the babies who due to being born early and fighting for life daily in the early stages are now left with physical, cognitive or learning disabilities.

Think of the parents who fight along side their little warriors praying to take their place and not see their little miracle suffer everyday.

Think. Just think. The fight doesn’t end for many parents and babies when they leave the NICU and often this is a time where the parents need more emotional support than before. The fight can continue for years and even be lifelong.

To all the babies born too soon, I salute you.

Stay Cool.

Scottish Twin Mamma.

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