Today my gorgeous girl turns two years old. Sometimes it is hard to believe that she was ever that teeny tiny little prem baby, she has come so far in two years. We are so proud of her, and love her to the moon and back xx
Today my gorgeous girl turns two years old. Sometimes it is hard to believe that she was ever that teeny tiny little prem baby, she has come so far in two years. We are so proud of her, and love her to the moon and back xx
I am linking up with Dorothy from Singular Insanity this week, for “Things I Know”.
I know I have an amazing daughter. She is beautiful and funny and smart. She was born fighting, at 32 weeks, and is about to turn two years old next month. She has always been slightly delayed, particularly in her gross motor and language skills, but I never doubted she would catch up. She is a whirlwind of a child, always on the go. She can switch from happy to sad and back to happy again within minutes. She has little quirky behaviours, some of which make me laugh and some that make me tear my hair out. She charms everyone who meets her, and she knows it. She is perfect, to me.
I know that last month the paediatrician told us that she can see autistic traits in our daughter. That we should get her assessed, sooner rather than later. Last week we took her to the speech pathologist. I was worried, nervous, but I think deep down I really thought we would get told not to worry, that it was just a language delay. Instead we were given a referral to take her to a psychologist, for further assessment.
I know that I am really pissed off. I’m angry at the world, and I want to rage, to scream, DON’T TOUCH MY DAUGHTER, LEAVE HER ALONE. I have fought so damn hard to be a better person, to get my shit together, to give my daughter a normal life. I want her to have every opportunity in the world. I want her to grow up believing in herself, I never want her to feel small, and not worthy, like I did for so much of my life. I want to protect her, to take all of life’s punches in her place. Take my sight, take my ability to have more children, tie that bloody Black Dog to my front gate. I’ll fight it all, but leave her alone.
I know that we have a long road ahead of us. Specialists, assessments, reports. A diagnosis probably wont be made for at least a year. It could be argued that at two years old, she is too young to come to any definitive conclusion. So we just take each day as it comes, put one foot in front of the other, try to ignore the ‘What if’s’ and just focus on the ‘Today’.
I know that whatever the future brings, she will always be my baby girl, my Mooie. She will always be perfect to me. I will love her fiercely, adore her, be in awe of the miracle she is. I know whatever hurdles we are faced with, we will fight them. We are fighters, and fighters never stop fighting.
These are the things I know.
Originally this post was going to about my daughter, her developmental delays, and the fact that our paediatrician wants her to be assessed for autism.
The trouble is, I don’t know what to write. I don’t know how I feel. Some days I’m convinced that nothing is wrong, other days I’m certain the paediatrician is right. We are seeing a speech pathologist next week, maybe that will provide more clarity. Maybe after that, I can succinctly describe my thoughts, my feelings.
For today though, I just want to share what an amazing little girl my daughter is, and how far she has come after her unexpected entrance into the world at 32 weeks. No matter what the future brings, I know she will always remain the strongest, smartest, funniest, cheekiest, cutest girl in the world to me.
There is really very little I can say in this post, that I haven’t already written about in Baby Baby Baby and One Pink Line. Since developing Proliferative diabetic retinopathy during pregnancy, and losing a lot of my sight, it has appeared unlikely that I would be able to have another pregnancy without risking complete blindness.
However, earlier this year, my husband and I made the decision that we would like to try and have another baby. It is something that we both want, and it appeared that perhaps my condition was improving. My left eye that had been operated on last year appeared stable, and although there was still residual blood spots in my right eye, we were hopeful that if the same operation was performed on that eye, there was a chance that the risk of blindness from a susequent pregnancy may be much lower than originally thought.
If we prepared for this pregnancy, knowing all the risks, under strict monitoring, we really believed it could be done. Perhaps even start trying towards the end of the year. We were excited, hopeful.
Just over a week ago, I went back to the eye specialist, all prepared to talk to him about our plans to try and conceive, and the possibility of scheduling an operation on my right eye. We went through the usual process, drops in my eyes, testing the sight, then he looks in them with his fancy medical equipment. He sits back in his chair, and writes his notes. And he tells me that there are further hemorrhages in my left eye, on the outer sides, that’s why I can’t see them yet, and I will need further laser to try and prevent more bleeds. My left, operated on eye. My right eye has grown more abnormal blood vessels, in the centre of my retina, despite the copious amounts of laser therapy I have had. They just keep growing. The Dr explains that there is only so much laser he is willing to do, as every round of laser causes scarring to the retina. It’s a balancing act, between the laser getting rid of the abnormal blood vessels and trying to minimise the damage the laser itself is doing to my eyes. He tells me that if the vessels are not hemorrhaging then it might be safer to leave some of them there, as opposed to risking permanent damage from the laser.
And I know. I ask anyway- “So, if I was to get pregnant again, the vessels would hemorrhage?” Without a doubt. And I know. The time has come that I need to be realistic. My body, my eyes, will not handle another pregnancy. My condition has deteriorated even without the stress of pregnancy. The specialist is not sure how much more laser my eyes will take. Hopefully, enough that I will regain enough sight back to be able to drive. Enough sight to be able to lead a normal life, to be able to see my daughter grow up.
As much as I want to wallow, and cry, and lament about how unfair it is, (and trust me, I have already, a little!) I need to count my blessings. I have a beautiful, healthy daughter. I am a mother. I am more blessed than many women, who are desperate for a child and are unable to conceive, or who have carried a child, but not been able to bring them home.
I am not blind, despite it having been a real possibility when I was pregnant. In fact one specialist said that I probably would have lost my sight if my daughter hadn’t have been born two months early. Now there was a real blessing in disguise!
I am sad, desperately sad, that I will never carry another child, that I will never have another baby. However the only way I can move forward, is to not let the sadness blind me (pardon the pun!) from the fact that I am truly blessed. Not let the sadness be stronger than the gratefulness I feel for all that I have in my life. I will count my blessings every day, every time I look at my daughter. xx
“Mummy Fail”. I had never heard or used this term, before I had my daughter. I had always believed there were either ‘good mothers’ or ‘bad mothers’. I know, how could I have been so naive, so black and white? I had no idea. I have no idea.
19 months since becoming a mother to my daughter, and most days I can’t even tell you if I am a ‘good’ mother or a ‘bad’ mother.
I can tell you that some days, by the time I put my daughter to bed, I am so exhausted, so stressed, so strung out from the tantrums, or the crying, or the battles over food, or a combination of all of the above that i just sit and cry. I wonder what the hell I’m doing wrong that makes this so freakin hard.
I can tell you that by the second or third time that she has woken overnight, I sit next to her cot, crying, as I try and pat her back off to sleep. And when that doesn’t work, sometimes I shout at her ‘JUST GO TO SLEEP!’. Then I hate myself, a little , for shouting at her. I go and wake my husband, because I know I’m losing it. I tell him I hate my life, and I crawl under the doona and cry, whilst he takes his turn to try and get her back to sleep.
I can tell you that some days I am so tired, so mentally and physically exhausted, that I put one TV show after another on for her, just so I can breath, and think, and not lose my mind. Then I hate myself a little, as I remember all the articles I’ve read about how bad television is for children, as they shouldn’t even watch any television before they are 2 years old, let alone two episodes of Hi5 in a row.
I can tell you that sometimes I honestly feel like I hate being a mother. That I am no good at it, that I am failure, that I am messing everything up. The term ‘Mummy Fail’ should hang around my neck, like a scarlet letter.
I can tell you that I wish someone had told me being a mother could feel like this. That there is no such thing as a ‘text book baby’. How can there be, when every damn book is different?? That being a mother is wonderful, and amazing, and joyful, however it is also the hardest thing you will ever do. That you will doubt every decision you make, that you will be so tired some days that from the moment you wake up, you will be focused on just getting through the day, and getting back in bed again. That your worst enemy, at times, will be other mothers. That some women will cut you down, tell you what you are doing is wrong, attack your choices, and, the biggie, judge you. It will happen, at least once.
I can tell you, that no matter how many other mothers judge you, it will be nothing, NOTHING compared to how harshly you will judge yourself. As a mother, you are your own worst critic. At the risk of making assumptions, I think I can tell you why that is too.
A good mother is never going to be able to meet her own expectations. A good mother, loves their child so much, that they want to be the perfect mother. A good mother is always going to declare a ‘mummy fail’, as there is no such thing as a perfect mother. They are a myth, along with the ‘text book baby’. A good mother is going to make mistakes, and is going to feel guilty about every single one . A good mother knows there is no such thing as black and white when raising a child, just all shades of grey, mixed with a kaleidoscope of crayon colours.
So, maybe today, I can tell you that I’m a good mother. That I love my daughter more than I ever imagined possible, and I tell her that several times a day, even on our worst days. Maybe today, I can believe that I am not doing such a bad job.
I can tell you, beyond a doubt, that good mothers are not perfect, they just wish they were. xx
On the 24th of November 2010, we finally walked out of hospital with our daughter, after a month in the NICU and Special Care Nursery. As far as I was concerned, I never wanted to see another hospital ever again. Ironically I had planned on writing a post about our NICU experience this week. Instead, I am writing about Milla’s latest experience in hospital, just last week.
She hadn’t been well for a few days. Her temperature kept spiking, it would come down with medication, then as soon as it wore off, straight back up again. She would wake in the middle of the night, burning up, and vomitting from fever. She had been to the Dr already, and he said it was a virus, keep her fluids up, etc etc. We just couldn’t keep this damn temperature down, as her medication wore off, she would become flushed, lethargic and miserable.
When I took her temperature on Tuesday, and it read 40 degrees, I felt my heart jump into my throat. I took it twice more, just in case it was wrong, 39.9 , 40.0. CRAP.
We soon found ourselves in the emergency department of our local hospital. Where we waited for over 2 hours, with our toddler who was burning up, and screaming. Actually, the screaming was probably a good thing, as eventually I think we were ‘rushed’ through, just so the waiting room could get some peace and quiet again.
Something to know about Milla, she’s not really a fan of other adults. She is a very sensitive little girl, and rarely tolerates being held or sometimes even spoken to by anyone other than myself or her daddy. A health nurse told us once that it could be due to her time in NICU, every time someone came near her, it generally brought pain. Blood tests, drips, feeding tubes, breathing apparatus. She did not have a gentle introduction to the world, and it seems to have affected her social/emotional development. With this in mind, being examined by drs and nurses does not go down well.
She screamed hysterically when they just tried to listen to her heart. When they said that they were going to have to put a drip in, I felt a clench in my stomach. They said we could wait outside. No. I would be there for my daughter. They wrapped her tightly in a blanket, with just her arm out, whilst they attempted, several times, to put an IV into her little tiny arm. I wondered if she remembered this pain from when she was born? Did she have flashbacks to her time in NICU? I know I did. I stroked her forehead, and whispered shhh, over and over again. I think this was to calm me, as much as it was to calm her. By this stage though, she was almost beyond burning up, and was so lethargic, she was slipping in and out of sleep, even as the Dr was still working on the IV. I didn’t know whether to be relieved that she was not screaming, or panicked that she seemed so out of it.
They finally gave her something to bring her temperature down, which had been hovering around 40 degrees. She slept for a while, somehow in that noisy emergency department.Then we had to take her for a chest xray. I held her down whilst she screamed. At least I knew it wasn’t hurting her, she was just scared. (just scared? That’s bad enough really)
Back came the Dr. Her blood results showed an infection. Despite managing to get a urine sample, which also showed infection, the Dr decided she wanted a more accurate sample, which involved inserting a catheter to get it straight from the bladder. I felt that clench in my stomach again. By this time we were on the ward. As I carried my little girl to the procedure room, already with an IV in her arm, I tried not to think about what was going to happen. Where I was taking her. I had the option not to be in the room, but again, I said no. Of course it would be easier for me to just wait in another room, not see what they did to her, not hear her crying. But why should I have the easier way out? She was the one going through the pain, I would be strong for her. As I held her down, whilst another Dr held her legs, and yet another Dr inserted the catheter, she screamed and screamed and screamed. She fought against me, she fought against the Drs. Again I kept whispering ‘shhhh’ ‘it’s ok’ ‘it’s nearly over’ and ‘I’m sorry’. And I was, so so sorry, that my baby girl had to go through this. I tried to be strong for her, but the tears escaped, spilling from my eyes. I imagined her wondering why her mummy was letting people do this to her, why was her mummy helping them do this to her? Finally it was over, I held her so tight, and just kept whispering over and over again, ‘I’m sorry’.
She screamed most of the night, on and off. She screamed when they came back in to hook up antibiotics, and discovered her IV was loose and had to reinsert it. She screamed as her temp crept back up, and she started shivering and shuddering. She screamed when she threw up all over herself, the cot and me. She screamed and cried and screamed all night.
At about 5.30am, she finally fell asleep out of sheer exhaustion. At 6.30am, her temp spiked again, and she woke up vomiting. I was exhausted, I had vomit on me, my body ached from leaning over the cot all night, from holding her down for one procedure to the next. But the worst pain was in my heart. Watching my baby girl go through so much, hearing those screams, wondering what she was thinking, did she feel betrayed by me? Imagining how scared and confused she was. Relishing the few moments that she managed to sleep, grateful that she had at least a little peace.
When the Dr came and told me that she wanted to put a feeding tube through her nose and down her throat, my instant reaction was NO. Please, no more procedures, please don’t hurt her anymore. I desperately tried to get her to drink. ‘C’mon baby, you have to drink, please drink’ I begged her. The Drs were adamant. I tried to be strong, but I couldn’t stop the tears, as I tried to convince them to give her fluid through the drip that she was already connected to. No.
Once again, I carried her to that damn procedure room. They bandaged her hands so she couldn’t pull the tube out. Once again, I held my baby down, whilst she screamed and thrashed around. Once again, I whispered meaningless words, that she wouldn’t even be able to hear over her screams. My tears flowed freely now. “I’m sorry baby”.
Can you believe, a couple of hours after this photo was taken, we were allowed to take Milla home?! She was so upset, so distraught, that’s the real reason i think she wasn’t drinking or sleeping. She needed to be at home, where she felt safe and comfortable. The Dr agreed. We could give her antibiotics at home, they had already pumped so many through her IV over the past 24 hours or so. As long as we could get her to drink, otherwise she would need to come back. Thank God we were right, and once she was home, she drank nearly her whole bottle of milk.
Later that night, when I finally went to bed, after being awake for around 40 hours, I lay in bed and cried, silent tears. My body felt like I had run a marathon. My muscles were so sore, so sore from holding my daughter down, whilst people hurt her. Her screams still echoed in my head. I’m not silly, I know the reality of the situation was that she wasn’t actually that ill, that the Drs were helping her, that so many children go through far, far worse than she did. But she is my daughter, I am her mother. It is my role to protect her. It goes against nature to pin your child down, whilst they scream in pain and terror.
Being a parent can be hard work, every day. It can be tiring and exhausting and frustrating. Being a parent, when your child is sick, is not just hard work, it is heartbreaking. The reward is, when they get better. They smile and laugh, and seem to forget all about the ordeal they went through. And as a parent, it’s our job to dust ourselves off, harden up and move on. How does the saying go, “
In 2007, my whole world changed forever when my first pregnancy ended in miscarriage, made even more traumatic with the discovery that I was carrying twins.
For 12 months, I suffered in silence, not understanding my grief, thinking I should be ‘over it’. Crying every day, in secret, trying to ignore the ache in me that just wouldn’t go away. Then one day, I stumbled across a facebook page called ‘Bears of Hope’. I visited the website, joined the online forum, and finally began to heal. I can honestly say that if it wasn’t for the Bears of Hope, I think I would have eventually had some kind of breakdown. I was carrying so much grief, and guilt, and felt so alone, until I met these beautiful, amazing Angel Mummies, who have become lifelong friends. I was sent two beautiful bears from another mother, who had also lost twins, Jacinta and Madelin. I treasure these bears, and like to think Jacinta and Madelin are playing with my girls, up in the clouds, and looking after them.
Bears of Hope do so much fantastic work for bereaved parents. The website has a wealth of information and support, not just for parents, but also for friends and family. There are also links to forums for parents to connect online, as well as a number of ‘in person’ support groups in NSW.
Bears of Hope work tirelessly to raise funds, so they can continue to donate bears to families who have experienced loss. (From their website): “Through the donation of a bear of hope, parents are provided with the comfort of knowing they are not alone from the very beginning, and offered significant ongoing support to heal their broken hearts. This includes support for all parents who experience miscarriage, genetic interruption, multiple loss, stillbirth, neo-natal & infant death throughout Australia.”
How can you help this amazing organisation continue with their fabulous work?
Firstly, please help raise awareness by ‘liking’ their facebook page, and sharing it amongst your friends. You just never know who is out there, suffering in silence like I was.
You can donate a bear or a care package, with the option of doing so in honor of your own or a loved ones angel baby.
For all my Sydney followers, Bears of Hope are holding their annual Benefit Ball on the 28th of July. This is a fabulous night, where not only are you contributing to an incredible cause, but you will also have a blast! Ticket includes canapes and drinks on arrival, beer, red, white & sparkling wine, and soft drink, 3 course alternate serve meal, dancing, candle lighting, prizes & auctions. As an extra incentive, Bears of Hope are offering an amazing prize, drawn at random, from all persons purchasing tickets by the 31st of March ~
One Lucky attendee will win the Cinderella Treatment for the night. Prize includes:
Tickets are selling fast, so book your tickets here to go into the draw for the Cinderella Treatment.
It’s such an honor for me to be able to share my experience and how Bears of Hope have helped me, and to hopefully raise awareness about all the work they do. I encourage all my fellow bloggers to please share this on your blog/facebook page. You really never know what pain people may be harboring around the loss of a pregnancy, and like in my experience, not know where to turn for help. Thank you xx
I want to preface this post, with the fact that I love my daughter and husband more than anything in the world. Would die for them, either of them, in a second. I know how blessed I am to have them, not for one day do I forget that. But still. Tonight, this Friday night, I miss ‘Me’.
There is a reason why I named my blog ‘The Hesitant Housewife’. Because I want to be that person, so badly. I want to be the housewife, the stay at home mother. I want to completely rock it, to be honest. I want this life, to be me. But, just quietly, I wonder if I will always be hesitant. I wonder if it will ever come naturally to me, whether I can 100% commit to the person I want to be. Because tonight, I miss “Me”. I miss the person that wasn’t my daughters mother, my husbands wife.
I miss the ‘Me’ that could be ridiculously irresponsible, and the only person who would pay would be me.
I miss the ‘Me’ that didn’t wake up every morning, and have to be responsible for a whole other life.
I miss the ‘Me’ that was fun, and crazy, and spontaneous.
I miss the ‘Me’ that put make up on, straightened her hair, wore clothes other than singlets and shorts/tracksuit pants.
I miss the ‘Me’ that left the house, and went to work. Chatted and joked with people, adult people.
I miss the ‘Me’ that was a coordinator, that demanded respect from people. People who didn’t giggle, and laugh, and run across the room. People that listened, because they had to. People who, though I didn’t realise it at the time, validated me, and what I had to say.
I miss the ‘Me’ that cares. Cares that I hadn’t shaved my legs, cares that I am wearing the same maternity shorts that I’ve worn for the last 3 days. Cares that I really don’t care anymore.
As much that I have wanted this, to be a mum, to be a wife, for my whole life, surely, I must be more? Surely I have not been dissolved by all that I have attained to be?
I love my daughter. I love my husband. I want to be everything to them. But, I want to be ‘Me’ too.
If only I knew who ‘Me’ was.
Am I the only one that feels this? Or are other “Mummies’ fumbling their way back to “Me” too? xx
I have an issue. It started just over 4 years ago. After I lost my twins. I became addicted to home pregnancy tests. From that day on, I became obsessed with carrying life. I’m ashamed to say, it didn’t matter what circumstance I was in, I just wanted to see two pink lines. I did use birth control, but nothing is 100%, and as it approached ‘that time of the month’, there was alway a part of me that wondered, (hoped?) if I was pregnant. So I would pee on a stick. And see one pink line. And would feel disappointed, despite knowing that I was nowhere near a situation that bringing a child into would enhance. But damn. I wanted to feel that life again.
So, three years later, with my boyfriend of three months (who turned out to be my soulmate, thankfully!) imagine my shock, when I finally saw those two pink lines! (I think this was the 3rd test into our relationship. I told you, I have a problem!) 32 weeks later (!) I gave birth to our darling premature daughter. She is now a healthy 16 month old, and I am married to her fabulous father. I am also nearly blind. The combination of my pregnancy and my diabetes have caused a condition in my eyes, which, according to my specialist, if I hadn’t have given birth 8 weeks early, I would have gone blind. I am still undergoing treatment, in the hope that I will regain enough sight to be able to drive again.
Here’s the thing. I have started peeing on sticks again. Despite being blessed with my beautiful daughter, I want to have another baby. I have always wanted a big family. My husband is one of seven. I want to feel life in me again.
I had an ‘anterior’ placenta last pregnancy, which meant I didn’t feel movement until late in my pregnancy (about 28 weeks) My waters broke at 31.5 weeks. A week before my baby shower. My daughter was born at 32 weeks, by emergency cesarean, after her heart rate dropped, and didn’t come back up. I wish I could say it was the best day of my life, but in reality, it was the most terrifying. I thought my baby was going to die. My daughter is now 16 months old, and is doing fabulously. And I am peeing on sticks.
I want another baby. But it’s not that easy. I can’t just say ‘I want another baby’ and start trying. I am high risk. I have type one diabetes. High risk. I have a history of miscarriage. High risk. I have a history of twins. High risk. I have a history of prematurity. High risk. I could go blind, if I fall pregnant again. HIGH RISK.
There is really nothing in my favor. And I know, I KNOW, I should just be grateful for what I have. I am so blessed to have my daughter, to have a child. I know so many people who haven’t even had that opportunity. I know I am blessed.
But still. Still I pee on a stick, every freaking month, and I cry when I see that one pink line. At the same time, I am terrified that I will fall pregnant again, terrified of the threat that I could lose a baby. Terrified that I may go blind, and not be able to look after the baby that I have. Yet still, I want to see those two pink lines so badly. I suddenly feel myself back where I was before, tears welling at every new pregnancy announcement, every ultrasound picture, every new life, that I am not carrying. I have carried three lives, yet only can see one. I am selfish. I know of people that have carried more than I, and still have no children on earth.
Yet still. I am selfish. I want another child. I want it more than anything. I would have to risk everything, really, to have it. Could I risk that? Should I risk that? xx
I have always wanted to be a mother. My whole life, I’ve truly believed that is what I was meant to do. I think I have even possibly uttered the phrase- “I was born to be a mother”. I have worked for many years in childcare, looking after other peoples children, and thinking I knew exactly what I was doing.
The reality is, now that I finally have my own child, the one thing I have desperately wanted, I have absolutely no clue. None whatsoever. I have never felt so incompetent in my life. I’m not an idiot, I didn’t think it would be easy, as such. But I had no idea how hard it would be. I thought I knew what I was doing. I don’t. I do a really good job of pretending though. I think even my partner believes my charade. She cries, and he looks at me, ‘what’s wrong with her?’ I am, after all, the expert. I’m great with kids, have years of experience, was a good childcare worker. Unfortunately, the only answer that comes to mind, is that I have no bloody idea. Maybe ask the postman, because I don’t have a clue. I thought I was so clever, I wont fall into all those traps that other parents do. I never rocked my baby to sleep, never put her to sleep in the pram. I didn’t want her to rely on ‘props’ you see, to go to sleep. Of course, now she is nearly 12 months old, and will not sleep anywhere except for her cot. That kind of rules out leaving the house for long periods of time. And I still have to pat her off to sleep at least one sleep a day. That is if she will go to sleep at all. Never pictured myself sitting next to the cot, in tears, begging her to Just. Go. To. Sleep. Just F#@%ing Go To Sleep. Because, I’ve dealt with hundreds of babies that wouldn’t settle. I’ve never cried or lost patience at those babies. Because I knew what I was doing.
My baby wont eat. Clamps her mouth shut, turns her face to the wall, and if all else fails, screams bloody murder. I don’t know why. I feel like I should know why, I should have the answer, but I don’t. I do what all those ‘clueless’ parents of children I used to look after do, and offer her everything under the sun to try and get her to eat. And when that doesn’t work, I cry. Again. She fights all her bottles. She fights getting dressed. She fights getting undressed. She fights her nappies. She wont go to other people. She screams in anger if I don’t come to her attention fast enough. She wakes at 5am almost every morning, despite me trying every technique in every book I can get my hands on. She has somehow managed to possess every bad habit, of every child I have looked after. And I don’t know why. By the end of the day, I feel like I have spent the whole day bashing my head against a brick wall. My partner works two jobs. I have a medical condition that prevents me from driving. So it’s just me and her. Every day, all day.
Don’t get me wrong, I adore my daughter. She is gorgeous, and in between all this drama, she is delightful, full of smiles and giggles and sloppy kisses. I love her to pieces. And that makes it worse. Because I want to do the right thing by her. I am the adult, I am the mother. so I should know what I’m doing. I should be in control of the situation. I should not be in tears, wondering what the hell I should do. I should be better.
I asked for help today. Because I’m not coping. I’m struggling, and I want to be a better mother to my daughter. She deserves better. So I rang the health nurse, and have organised for some ‘Enhanced’ care, where they come out and talk to me in my home, and give me some strategies. I know it was the right thing to do. But still, I feel like such a failure. I really thought I would be better than this. I really thought I would know.
Part of me is a bit ashamed of this post. Kind of ruins the image that I have been trying to keep up, that I am, of course, the ‘perfect’ mother. But the other part of me is wondering, maybe I’m not alone? Maybe there are a lot of us out there who just don’t know. And maybe another mother will read this and realise that she is not alone. One thing I actually do know, motherhood can feel like the loneliest job of all. xx