In our shoes.

Volunteer April Ratajczak blogs for us

I recently shared an article on our Tiny Sparks Facebook page titled β€œ20 Things Not To Say To A Mom Of A Preemie”.  You can read the article here.  This started up quite the conversation on the thread with a lot of people commenting on hurtful things that had been said or done to them during their NICU stay or after once they were home.  Parents know that these things aren’t done or said with a malicious intent; however that doesn’t change the fact that sometimes these things, especially certain comments, can be very painful. 

That inspired me to write this blog.  I could easily write a blog to tell you what to say or what to avoid saying to the parents of a premature baby.   However, I feel like instead of telling you what is helpful (and hurtful), I would just tell you what it’s like to be the mum and dad of a NICU baby.  Unless you’ve been in our shoes, you will have no idea what parents are going through.  Perhaps better understanding what we are going through will help you to be able to provide the support your friend/family/etc needs during their NICU journey.  

(Disclaimer: every nicu journey is different.  What one family experienced may not be the same as someone else.  This list is just a guide based on my experience as a NICU mum to a premature baby.)

1.       We don’t eat well. 
What’s for dinner?  Often whatever leftovers we have in the kitchen from food that was given to us or whatever takeaway sounds edible.  After a while, no takeaway sounds β€œgood”.  After spending the night worrying (and for many mums pumping) and then all day at the hospital, going home to cook a meal (followed by the clean up after said cooked meal) is more than we can bare.   And hospital food?   While it may be decent, after a while it becomes...... old.  A freshly cooked hot meal is pure bliss.
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2.       We are lonely. 
People may comment on Facebook updates, pictures, etc, but the phone isn’t really ringing.  Perhaps it’s because people don’t know what to say, so it’s easier to say nothing.  Perhaps people just got busy.  Perhaps people assumed we knew they were there.  The truth is life gets lonely.  Your day revolves around watching your baby lay in the incubator/cot and watching monitors.  Your social interaction becomes the chats you have with the lovely nurses who become friends (and some become a second family). It’s just the way it goes.  And yes, there are certain people who never let you forget they are there for you and check on you regularly, (and those are the family/friends you are extremely thankful for) but there are a lot of people who just vanish.  

3.       Our baby’s good days are our good days.  Our baby’s bad days are our horrible days. 
It’s just the way it works.  Also sometimes there can be nothing β€œwrong” but after watching your child fight to live day after day, mixed with all the emotions we are experiencing (several discussed throughout this), sometimes we are just exhausted and emotionally drained.  So know that even on good days we may be struggling, but if our baby isn’t doing well, you can assume WE aren’t doing well either. 

4.       We are hearing a LOT of Cliché’s.  And they are painful.
 β€œSleep while you can”  β€œShe will be home when she is ready”  β€œHe is where he needs to be”  β€œOne day this will all be a memory” β€œI know how you feel” (spoiler alert: unless you actually HAVE been in these shoes, that last one will make us angry...very angry...)   I could go on and on and on.  While some of these may have some truth to them, it is basically telling us we aren’t allowed to feel how we feel.  And we have every right to feel upset about the situation.  NO parent wants their child home before they are ready.  We KNOW the hospital is exactly where our baby needs to be.  We know these things.  But we are frustrated, tired, and just need you to listen to how we feel.  Often these clichΓ©s come because people have no clue what to say.  But it’s ok.  We really don’t need you to fix this or say any words of wisdom.  

5.       We know our baby is tiny. 
But please stop saying it.  You may be in shock, but despite all odds, our baby may be 2-3 times their birth size or bigger once you see them.  β€œHe/She is so tiny” seems to hit a sore spot with a lot of NICU parents and takes away from the fact of how much they have overcome to get to the size they are now.  Our baby may be small, but has conquered some amazing hurdles and endured more things than a lot of adults have had to fight. 

6.       We are exhausted by the monitors.
Watching monitors all day sounds boring.  Until those monitors are hooked up to your baby, and every alarm that goes off causes you to worry.  You sit and worry that this time your baby won’t bounce back.  This time their heart won’t go back to beating at a normal rate.  This time their oxygen levels won’t recover.  You also don’t hear just your baby’s monitors, but also all the babies around you.  During your NICU stay you will likely experience your baby or another baby in an emergency situation, require resuscitation, and sometimes become critically ill and/or pass away.  The reality around you is impossible to escape.  You worry about babies around you, as you have become attached to them and likely have become friends with their family.  You also worry the β€œwhat if” in terms of your child.  β€œWhat if we are next”.

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7.       We are scared.  Really scared.
We are watching our child fight to live.  It’s scary.  Really scary.  Many NICU families have no experience in a NICU until their child is in one.  It’s a whole new world full of tiny humans, unfamiliar faces, and noisy monitors.  When you welcome a child into your family, you think that it’s natural to be scared, but this is a whole new WORLD of scared.  We have no clue if we will even be taking our babies home with us. The first time we get to hold them, while it’s a moment of pure bliss, is also nerve wracking.  They are so small, fragile, and still hooked up to all the monitors and breathing aids.  This isn’t what we envisioned when we thought about holding our baby for the first time.  It’s absolutely terrifying and the list of terrifying things is long enough to be its own blog entry.

8.       We are TIRED.
We spend all day at the hospital.  Many mums are also pumping every three hours (that’s three hours from start of pump to start of next pump, so around 2 hrs of sleep between if you are lucky).  While you are up, you also call the NICU for an update.  Sometimes the phone isn’t answered straight away so you enter a panic β€œsomething is wrong” mode.  A few minutes later the phone is answered, you get an update, and go back to bed.  As soon as you lay down you wonder if your baby is still ok.  Afterall, a lot can happen in five minutes.  As your mind races, you realise you have about an hour until the alarm goes off for your next pumping session.   Even without the pumping, your mind doesn’t stop.  Again, β€œsleep while you can” is a statement that is an absolute joke for a NICU parent.  Don’t forget for a lot of families, one or both parents are also working.  So add full time work life into that mix.  Yeah.  We are tired.

9.       We feel guilty.
It’s a very normal and often talked about emotion for NICU parents, especially mums.  While we may KNOW this was not our fault, good luck with us fully believing that.  Many of us followed the β€œbook”.  We didn’t eat foods on the β€œno” list for pregnancy.  No drinking.  No smoking.  Never forgot a prenatal vitamin.  However we tell ourselves that we should have started maternity leave earlier.  We should have pressed harder when we  felt something was wrong and the medical team blew us off.  What if we had pushed and they detected this earlier?  Maybe a second opinion and this would have been caught?   What about some of our cravings?  Did we eat the wrong foods?  We had no signs, did we miss something?   The guilt will eat us alive.   Actually, the guilt DOES eat us alive.  Remember that when you ask us questions about our baby and our pregnancy ending early.

10.   We don’t know.  We simply do NOT know.
We have no clue when our baby is coming home.  We have no clue if he/she is coming home on oxygen or any other equipment (but really, does it matter?).  We have no clue if our baby will have any long term effects or problems.   We are stressed out about it and we simply don’t have the answers to these questions.  Trust me, when we have the answers, we will tell you.

11.   We grieve for the things we lost; it’s normal.
This is one that a lot of us don’t expect, but when it happens the grief is quite overwhelming.  The list of things we lose when we have a premature baby is quite long.  And while we are so happy that our baby is doing as well as he/she is, we are going to be upset about the things we missed out on.   

12.   We will never ever ever ever consider ourselves LUCKY we missed out on the aches and pains of the last month of pregnancy.     
This could fall in the clichΓ© category or the grief category, but it deserves its own mention.  I think the comment speaks for itself.

13.   We cannot afford to get sick.  Neither can our baby (or any baby in the NICU for that matter)
If you are sick, please avoid contact with us.  We know that people get sick, but we can limit our contacts with people we KNOW are sick.  For parents, missing on time in the NICU because we are unwell is pure torture.  For the babies in the NICU, a common cold or stomach bug lose in the NICU could be deadly.  That is no exaggeration. 

14.   Our future is uncertain and scary.
We have no clue what the future holds.  Will there be long term medical issues?   Developmental delays?  Will our baby be on medical equipment when they come home and if so for how long?  What medications will the baby be on?  Most premature babies have multiple follow ups over the first few years and beyond, so we may wonder what our care plan will entail.  However, the big question we ask is, β€œwill our baby come home”.  These are not the questions new parents should ever have to be worried about or think about.  Yet, for parents of premature babies, it is.  And further past that, many think about the future.  What happens if we chose to have another baby one day?  Will we have to endure this again? 

15.   Our life will not instantly become normal just because we get discharged.
Once we get to take our baby home, we don’t just instantly become a β€œnormal” family who just brought their full term, freshly born baby home from the hospital.  We have specialist appointments, weight checks, Neonatologist appointments, GP appointments... the list is quite intense and exhausting.   Our life revolves around our baby’s appointments.  We also may have medical equipment at home that we are still using.  We have a very fragile infant whose immune system is not the same as a full term baby and whose organs are still fragile, especially their lungs.   A simple cold for some babies will easily land our baby in the hospital back, possibly back on oxygen and respiratory support.  All this while also coping with an infant’s needs, sleep deprivation, and normal life such as eating, cooking, cleaning, etc. 

16.   We celebrate every milestone so much more.
All parents celebrate milestones.  However when you have a child born prematurely you have no clue what the future holds, especially with developmental delays.  So when our babies roll over, talk, crawl, or any other milestone for the first time, expect a celebration that you may find over the top.  But when you have no clue what effects on development your child’s prematurity will have, when they do hit these milestones, and on time (corrected age) not only are we excited and proud, but we have a sense of relief as well.

17.   We will keep hand sanitizer for visits and continue to avoid us you when you are sick, even once we go home.
Do not be surprised when you come visit at home when we have a bottle of hand sanitizer and remind you to use it every visit.  Do not be surprised when we avoid functions because someone who will be attending is sick.  Our baby is fragile and all of our specialists have guided us on staying healthy.  Hospitalisation is extremely common for prems once discharged, especially in winter when winter colds and viruses, including the Flu and RSV.  We may not avoid an illness or needing to be hospitalised, but we will certainly do everything in our power to avoid it.  Who wouldn't do the same?  Our child does NOT need to build his/her immune system by being exposed to people who are sick.  We are NOT being over protective.  We WILL take our medical team's advice every time over anyone’s β€œtheory” on our child’s health.  Every.  Single.  Time.  

18.   We left the NICU, but the NICU did not leave us.
It’s not a chapter of our life we will just forget.  We may wish we could, but it’s there.  There will be random occasions that bring emotions back.  Perhaps the sound of monitors on a TV show.  Perhaps it’s seeing a pregnant woman who is very far along.  We have no clue what the triggers will be.   We would not wish the NICU experience on a single person, yet for the most part, we wouldn’t change much.  We came out stronger than we went in.  We came out more knowledgeable than when we went in.  We came out more appreciative than when we went in.  And for many of us, we were lucky enough to walk out with a true, living, breathing miracle in our arms.  Often that little miracle has taught us more about life in their short time on this earth than we have learned our entire lives.



Izzy and Pea - The NICU journey revisited

Guest Blogger Allison F writes of her journey to have two gorgeous girls, both born at 28 weeks. You can follow her blog izzyandpea here.

For as long as I can remember I have always wanted a big family, I have always felt that it would be my greatest achievement in life.  Greg was at me for years to start a family, though I wanted to finish my degree before we started trying.  So when we got married we went through the whole β€˜honeymoon stage’ and fell pregnant straight away.  I felt in my heart that this was going to be the year of our lives, getting married and starting a family straight away.  We had been together 7 years by now so we weren’t technically rushing into anything.

Isabelle's 1st birthday and pregnant

Isabelle's 1st birthday and pregnant

After my first miscarriage it didn’t take me long to want to try again, but after my second miscarriage it just wasn’t the same.  That feeling of being so happy to be pregnant had gone.  It almost felt like a chore, a chore of having to wait to see if my pregnancy was viable, we needed find that passion again for a family.  When we found out we were pregnant with Isabelle, I was so relieved that I call fall easily, though petrified at the same time.   I remember the day my Aunty phoned me to say my cousin had had her twins, I was 21 weeks pregnant at the time, and my cousin was only 25 weeks pregnant.  Something inside of me made me keep in contact to see how she was getting on.  When I lost my plug at 25 weeks, I knew, I knew I too was going to have a premmie and we did.  Isabelle was born at 28+4.  She is now 16months and perfectly healthy.

With having a big family we wanted our kids close together, which was one thing we had always agreed on. Even though Isabelle’s corrected age is only 3 months, we aren’t going to be using her corrected age forever.  So when Isabelle was 6 months actual we started trying.  I have to be honest, I wasn’t sure I could go through it again.  I was more worried about Isabelle and the thought of having to leave her if we went early again.  I was so torn when we found out, we were both so happy and I was also petrified, we had a scare at 7 weeks and I honestly didn’t think I could take it anymore.  My heart was breaking and the thought of losing a baby this early again was so overwhelming.  I want that big family though the heartache of it all was starting to take over.  At 20 weeks everything was perfect, by 24 weeks my cervix was still closed and perfect, by 26 weeks my cervix had halved.  My checkup at 28+4 I had no cervix and fully effaced, I was sent straight to hospital.  I was calm when I went into labour 30minutes later, I remember the nurses telling me that I can be upset if I want to be.  I was alone, my husband was at work and I was laying on the table in theater and all I could think about was Isabelle and how the hell am I going to do this again. 

Penelope at birth and due date 

Penelope at birth and due date 

Isabelle meeting Penelope outside of NICU/SCN2

On a visit to see Penelope I overheard the LC ask a mum, β€˜how much do you think he has had?  Do you think he will need a top up?’  I broke down; it all came back, all the little things that I had blocked out of my head, all the little things that I had forgotten.  We were back, we were in NICU/SCN and we were going to be here for weeks.  I cried myself to sleep for the first 3 weeks, I felt like I had failed at being a mum and I couldn’t deal with the fact that I had to have a c-section.  It broke me, it truly did.  Then one day something just clicked and I turned a corner, I was on a mission to get Penelope out of there as soon as I could, and we did.  She was 8+4 when we brought her home.  That was 3 weeks ago.  I still want more children and I know in my heart I am not finished.    

Β© 2015 Allison Filinski | www.izzyandpea.com


tiny bites for tiny sparks - World Prematurity Day 2015

We would be delighted if you would like to support us by hosting a morning tea or high tea for World Prematurity Day 2015! Bring out the finger sandwiches, delicate patisseries, the pearls and stylish outfits to create a memorable event for you and your guests. You can choose your own location, whether it be hosting at your home, workplace, local park or cafe. The official date for World Prematurity Day is the 17th November 2015, but you are welcome to host your morning tea or high tea anytime during November.

Your contribution helps us to continue to raise awareness, educate and support Western Australian families experiencing the trauma of a high-risk pregnancy, their neonatal journey and growing up.

Once registered we will supply you with your own Event Hosting Kit. This will include:

  • downloadable posters
  • downloadable invitations

On conclusion of your event please contact our office and we can advise you the best way to forward the funds raised.  If you would like any further support or have any queries, please don't hesitate to email us at admin@tinysparkswa.org.au.

On World Prematurity Day, the 17th November, we would love you to post photos to our Facebook page, instagram, twitter or pinterest and hashtag #tinysparkswa and #worldprematurityday2015.

Fundraising Ideas

  • Ask your guests for a gold coin donation
  • Hold a raffle of goods or services donated by a local business.
  • Ask a local patisserie or bakery to donate delicacies or provide at a discounted rate.
  • If held at your workplace, ask your company to match donations.
  • Have a cover charge for your event.
  • If guests want a tax deductible receipt for their donations, please forward their details to us and we will send out a tax receipt. Otherwise, they can donate directly here.

Quilters Needed - Christmas Quilts

We are looking to provide 200 Christmas quilts to neonatal nurseries right across Western Australia and need your help!

Jill of Patchwork Place in Albany has kindly designed a pattern for us to share with our sewers and hope that they might join them in creating some beautiful memories. You can download the instructions here, or find them below.

You can post or deliver items to Tiny Sparks WA, PO Box 1114, West Leederville WA 6901.

We would appreciate if they could be sent in by the 4th December to allow us time to put together and send off to the metro and regional hospitals.

Update: Thankyou to all of the generous quilters across Western Australia and even the rest of Australia who have contributed to this program and answered our request for assistance! We have been overwhelmed with the response and surpassed the 200 quilts requested. Make sure you subscribe to our blog and 'like' our Facebook page to keep up to date with all things Tiny Sparks WA and for news of next years project! Original blog and request below FYI)

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Christmas Quilts for Tiny Sparks WA

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Size 16" x 24"
 Or
41 cm x 61 cm

Requirements

Piece backing approx. 18" x 26"  (45cm x 65 cm) - white or cream
Piece 100% cotton light weight batting/wadding same size as backing piece.
Small amounts of Christmas coloured fabrics.

Suggestions

Any basic 4"  or  8" block pattern

No borders.
Keep blocks simple.
Avoid using yellow or gold.
Use conventional quilt binding or a commercial satin or pre-made binding or finish by β€œbagging” then turning through to right side. Top stitch around edge if using last method.
100% cotton fabrics (though not essential) are easier to work with.

A - Basic 4" Block - Total of 24 squares cut 4 Β½" x 4 Β½ "  in Christmas colours

  1. Arrange design into 6 rows of 4
  2. Join together into rows with ΒΌ " seam.
  3. Press seams in row 1 to the right, in row 2 to the left, row 3 to the right etc
  4. Join the rows together.
 
Basic 4" Block - 2 alternative designs

Basic 4" Block - 2 alternative designs

 

B - Basic 8" Block - Cut 6 squares 8 Β½" x 8 Β½ "in at least 2 Christmas colours.

  1. Sew into 3 rows of 2.
  2. Press seams in alternating directions then join rows together.
 
Basic 8" Block

Basic 8" Block

 

Finishing Quilts

  1. Lay the backing right sides down, place the wadding on top and finally the pieced top right sides up. Pin together and quilt.
  2. Prepare binding by joining the 2 bits end to end with a mitred (angled) seam.
  3. Press in half lengthways. Sew onto the right side of the quilt having ALL raw edges level. Mitre the corners as you sew.
  4. Trim off the excess from the edges.
  5. Handstitch the folded edge of binding over onto the back of the quilt.

Finished Quilt created by Jill of Patchwork Place, Albany

Workshop - SENSE-ational Mealtimes

Parents/carers of premature and sick babies often face battles with feeding. Do you want:

  • To introduce solids sense-itively?
  • Your child to enjoy mealtimes; try new foods; and to eat enough to maintain/improve their health?
  • The mealtime experience to be calmer?

Come along and hear from the co-author of SENSE-ational Mealtimes, Dr Denise Stapleton. Denise uses understandings about sensory preferences to explore these and many more concerns.

Dr Denise Stapleton is an Accredited Practising Dietitian and Nutritionist with 27 years experience in nutrition and research. Denise passionately supports families with varying mealtime difficulties and therapeutic dietary needs throughout Australia as a private practitioner, senior community dietitian, researcher, author and mentor. Denise has training in Picky Eaters vs Problem Feeders: The Sequential Oral Sensory (SOS) Approach to Feeding and Making SENSE of the Senses. Denise collaborates nationally and internationally with professionals from a wide range of backgrounds who are supporting families with mealtime difficulties.

The free workshop will be held in Subiaco on Tuesday 13th October 2015 at 7pm. are conducted in a relaxed environment and are open to all families and carers affected by high-risk pregnancy, premature birth or having a sick newborn. T

Update: Registrations are now closed.

SENSE-ational Mealtimes will be available to purchase on the night.