New play shines humorous light into the darkest corners of motherhood

 

after birth, written by Zena Forster and directed by Grace Duggan, is a new comedy deeply rooted in the real life testimonies of women who have experienced postpartum psychosis, including many women within the APP network.

The play is being brought to life by Maiden Moor Productions and will open on Monday 10 June at the North Wall Arts Centre in Oxford. Imaginatively staged, with elements of stand-up and a dynamic original sound score, after birth takes us on a journey of recovery.

The story revolves around holiday camp entertainer Ann, who, alongside the Virgin Mary, has been detained without trial on a medieval plague island in the middle of the Venetian Lagoon.  Buffoonish and malevolent by turns, their doctors are intent on curing them of their heinous crime - Being A Bad Mum.   This is the world of Ann’s mind.  after birth’s protagonist is experiencing postpartum psychosis after the birth of her baby.

The lead character’s experiences might be extreme, but they are recognisable and relatable: what mother hasn’t felt judged, or been demoralised by the myth of the perfect mum?

Playwright Zena Forster said; “Just as the women I interviewed didn’t want to be defined by their illness, after birth isn’t a play about psychosis, it’s a play about a tough, witty woman who happens to have psychosis.  The women I interviewed were amazing – courageous, inspirational and often very funny, it was natural that my protagonist was like that too.”

Grace Duggan, Director said, “Zena has created this incredibly detailed and responsive play about the realities of postpartum psychosis.  after birth doesn’t hold its tongue, it doesn’t shield us from the truth, and it doesn’t stop us from awkwardly laughing with a psychotic mother. We want people to start talking about postpartum psychosis and continue the discussion about the pressure of motherhood. Through our characters and with this story we hope to expose it all and have a laugh along the way.”

after birth grew out of collaboration between Zena Forster and researchers at the National Perinatal Epidemiology Unit (NPEU), Oxford University. For 40 years the NPEU has been the ‘go to’ international centre of research into women’s physical and mental health.  Their annual reports have consistently shown that in the UK suicide stubbornly remains the leading direct cause of maternal death between six weeks and one year after birth, with women from ethnically diverse communities disproportionately affected. The NPEU were keen to find new ways of disseminating their findings with a view to effecting change.

Zena interviewed many women with lived experience of postpartum psychosis, travelling miles around the country to do so. Both Zena and director Grace Duggan dramaturged the piece extensively, developing it significantly for performance in 2021. after birth was awarded the Propeller 2020 opportunity by North Wall, Oxford which includes three performance dates 10, 11, 12 June 2021. A film of the staged performance is also being made and the NPEU are undertaking further research of how this filmed performance could be used in both therapeutic settings and in health professional education.

The time has never been riper for a recovery story. after birth is an opposite celebration of resilience in the face of inequality and adversity. There is a growing need and appetite for work that explores the disadvantages that women face in our unequal, patriarchal society.  Between eight and nine out of ten women in the UK will become mothers. The pandemic has exposed and heightened the inequalities they face.  More and more evidence is emerging that maternal mental health has suffered over the last year, with black and brown mums disproportionately affected. after birth creates a timely space for us to talk about these pressing issues.

As an international centre for research into women’s health and as a vibrant creative hub, Oxford was the perfect place for this play to be developed. Oxford’s North Wall has long been committed to nurturing creative talent – Alice Vilanculo (actor), Will Alder (sound design), Grace Duggan (director) all received early career support through the theatre’s various development programmes and are delighted to be back in Oxford as established artists.  Likewise, Oxfordshire Theatre Makers (OTM) and Arts at the Old Fire Station provided backing and opportunities to develop and promote the play.  Oxford’s supportive city council provided important early seed funding.  Oxford colleges have helped with funding too. after birth’s playwright Zena Forster is based in Oxford, as is Bafta award winning film maker Jo Eliot who will be filming the performance.

Commenting on  after birth, Professor  Rachel Rowe, Senior Health Services Researcher, National Perinatal Epidemiology Unit said “through after birth we hope to engage audiences with research evidence about maternal mental health, to raise awareness, reduce stigma, encourage discussion and ultimately improve care and outcomes for women affected by postnatal mental illness. The play promotes some key public health messages about postnatal mental health, but importantly it’s also funny and full of hope – it should be a really good night out.”

To book tickets, click here

Chloe’s story: "I stopped trusting everyone. But now I’m recovered and love being a mum".

I had planned for a calming water birth and, throughout my pregnancy, which was for the most part a happy and healthy pregnancy, I saw no reason why this couldn’t happen. However, things didn’t go to plan, and my labour ended up being incredibly exhausting and traumatic.

My little boy, Alfie, was very much wanted and, like all mums, I was excited to meet my baby. Sadly, however, at week 20 of my pregnancy, we suffered an unexpected family bereavement, my pregnancy became high risk due to a fibroid and my blood pressure began to increase. I went into a natural labour at 41 weeks but had pre-eclampsia and, after two hours of pushing, my baby’s heart rate kept dropping due to the cord around his neck. I was quickly prepped for an emergency c section.

The birth

Thankfully, they managed to deliver my little boy via forceps, but I lost a lot of blood and became anaemic and I was hooked up to monitors throughout. Alfie was eventually delivered, a little bruised but thankfully healthy, at 14.15, and, because I’d gone into labour at 23.00 the night before I was completely exhausted. Alfie was extremely sleepy, not waking to feed in the first 24 hours, but I was assured that this was normal for a forceps birth.

I was concerned that I wasn’t making very much milk and Alfie seemed jittery and a bit yellow, but I was discharged anyway after two nights – only to be readmitted the next day. Alfie had jaundice and had lost 11% body weight in just four days.

At this point they acknowledged my poor milk supply may have been due to anaemia, however, to me it felt as though nobody had been listening when I raised my concerns and this led to me not trusting any of the health professionals (despite my husband and I both being health professionals ourselves). Worse still, I didn’t trust my own instincts as a mother.

Three days later I was discharged again and the midwives were coming to check my blood pressure every two days, while the health visitors were coming several times a week. As the home checks mounted up, it felt as though every visit highlighted my incompetence as a mother and my self doubts and anxiety spiralled out of control.

My symptoms of postpartum psychosis

It all began as the worst anxiety I’ve ever experienced and developed into mania. Before long I had lost all concept of time and of what was real and what was not. I stopped sleeping, showering and eating and went to see the GP. By this point I believed that everyone around me was a doll, I was unable to follow storylines on TV, I couldn’t keep up with conversations and I couldn’t retain information. In retrospect the GP was amazing and immediately referred me to the perinatal mental health team. However, at the time, I believed they were trying to put me in prison, I thought everyone at the surgery was a social worker and that nobody trusted me to be around children. I didn’t feel able to tell anyone this as I thought everyone was in on the plot.

When I got home I refused to take the medication I was given as I believed it was poison that they were using to try and knock me out to get me to prison. I was hearing police helicopters outside and thought my house was full of cameras recording my actions. I paced constantly that night as my husband and baby were sleeping in the lounge (to allow me to try and get some sleep), and I kept thinking my husband was planning to leave and take the baby with him.

The perinatal mental health team came the next morning but unfortunately I had a nurse who was new to her role and she wrongly diagnosed me with postnatal depression. Luckily, my husband is a paramedic and he strongly suspected I had been misdiagnosed so he continued to seek more help.

My behaviour spiralled further out of control that day and, while my parents were caring for our baby, I woke my husband up from a nap to tell him that everyone was dead. He called the nurse back and I was sectioned and admitted to a Mother and Baby Unit (MBU) that night.

My admission to an MBU

When I got to the MBU I thought I’d been locked in prison and I refused to eat, drink, sleep, shower and take medications. I spent all my time pacing the unit trying to find a way out. As I was admitted at night no one was around and I believed they’d locked me up on my own because I was such a bad mum and a danger to others. I thought everyone was an actor and my hallucinations made them appear to have really strange eyes. I also started to believe that my husband was an undercover policeman. I spent hours looking at the photos of the staff on the wall thinking they were somehow linked to my normal life and that they’d all been undercover.

The turning point was two days later when they injected me with antipsychotics. At the time I thought this injection had aborted my baby and sterilised me. I’d also lost 10kg by then as I thought all food and drink smelled and tasted weird and was poison, and I had been told I might need to be moved to a different hospital to be tube fed. I’m a Dietitian by profession so I knew what this meant but at the time I couldn’t take it in. I kept asking the same questions over and over. I swapped between thinking Alfie was a doll and they’d taken away the real baby, to thinking that he wasn’t my baby at all or sometimes even believing that he had died. Because I’d had an epidural when I was in labour I hadn’t felt him be born and this was something I became obsessed with and was talking about as if it was evidence that he wasn’t mine. I thought the TV was talking about me and telling me things like I’d lost my career and would never work again and I believed that the songs on the radio were played especially for me. My husband bought me a magazine and it felt like everyone in it was pregnant and they were taunting me as I could never have a baby (thinking I had been sterilised). I wouldn’t use my phone as I thought it had been intercepted by the police and at first I thought I couldn’t even phone my husband as I wrongly believed he had asked for no contact, despite him visiting and spending most of the day with me every day.

The road to recovery

I eventually started taking medication willingly and began to recover. The first time I was allowed for a walk on the beach with a member of staff and my husband I was so excited but I still had some paranoid thoughts, thinking that everyone was an actor and that if I went into the public toilet they would run away with my son while I was there. But these delusions began to subside.

I was on the MBU for two weeks and think I should have probably been there longer but I was able to convince everyone I was fully recovered -  Coronavirus had made an appearance and I was very aware that lockdown was coming and I wanted to get home before it did. Lockdown in fact happened just a week after I was discharged.

The mental health team reviewed me over the phone and I never disclosed how down I was feeling as I feared they would re-admit me and I wouldn’t be able to have visitors. I really struggled and did not want to get out of bed, leaving my husband doing a lot of the caring for our son. I didn’t feel a connection with Alfie at this point and felt awful that this magical bond hadn’t appeared. I knew I loved him but I was scared that he would never be able to love me.

Another major turning point came six months later when the GP treated me for an under active thyroid and I finally started to feel like me again. It was the final piece in my treatment jigsaw and really made a big difference.

I now have the best bond with my son and he is a complete mummy’s boy! I still feel sad and guilty about the time I feel I missed out on as I felt like I was living in a fog, but I’m so glad what we went through hasn’t seemed to affect him and he is a happy, healthy boy.

My recovery story: "I thought I was in a computer simulation - now I’m back to being the old me".

One mum shares her story of recovery to inspire hope...

If you were to ask my best friend a word to describe me, she will for sure say ‘anxious’. It’s a part of me that I’ve always carried and of course it showed up during my pregnancy too. I kept thinking ‘is the baby ok?’ ‘is the baby moving?’ But overall, everything was going fine…that is until the end of February 2020 when COVID-19 starting spreading across Europe. For me, being pregnant and away from home meant only one thing; there was no way my family would be able to be with me for this amazing moment in my life.

At 41 weeks of pregnancy, on 27th May, my little boy decided to make an appearance. I read a lot about people giving birth after pushing for ten minutes or an hour, but that was not the case for me. I don’t want to go into all the details of my birth, but to summarise we had a fair few complications and I felt completely traumatised by the end of the labour.

The days in the maternity ward proved to be more difficult than I had anticipated. I was in a foreign country with no knowledge of the standard hospital procedures, and this unfortunately created lots of unnecessary confusion and uncertainty. Nonetheless, the biggest challenge was taking care of the little one as I had never held in my hands such a tiny and precious human being.

My little baby decided to show his character from the beginning: he didn’t want to be forced in doing something he didn’t want to do (like his mum), which sadly included breastfeeding. We tried for a week to get him to latch, but he was crying so much that the whole process made me really really upset. Breastfeeding was not going to work and that left me feeling really guilty - I felt that I was not able to do the one thing I was supposed to do as a mum. I felt like a failure. It was only after months that I realised that a fed baby is a happy baby regardless of how they feed, and that a mum simply needs to be loving. The rest didn’t matter – I was doing my best.

After five days in hospital, it was time to go home. Unfortunately, after five days of very little sleep in hospital, I realised that the situation wasn’t going to improve at home either and I was exhausted.

I had a terrible feeling of doom, and I thought I was dying

On the first day back, the midwife came to check on the little one and, despite assuring me that we were doing everything correctly, my anxiety didn’t leave me. I ended up having a major panic attack and I feel that, looking back, this is when the psychosis also began.

During the panic attack, I had a terrible feeling of doom, and I thought I was dying. It felt as though my entire body was shaking despite my legs remaining completely still as stone when I looked at them. An ambulance came and I was taken to A&E. I spent a few hours there and everything seemed fine; they discharged me and suggested I get in contact with a perinatal mental health team. Little did they know that they would see me again in less than 24 hours…

Once I arrived back home after the first trip to A&E, things started quickly deteriorating. I really wanted to sleep but I wasn’t able to close my eyes. I began feeling that everything around me was unreal. My husband took me on a walk to show me that everything was just as it always had been, nothing outside had changed, but it didn’t convince me. My mind wouldn’t stop racing and at one point I convinced myself that I was in a coma – perhaps from the panic attack or from the birth – I wasn’t sure I just felt as though I was in another state and that the doctors were trying to communicate with me through computer simulation.

My head was spinning and I kept thinking I needed to pass levels – as though I was in a computer simulation - in order to stop certain situations playing over and over in my mind. It was only when a friend came to visit that she realised something was very wrong and a second ambulance was called resulting in another trip to A&E.

We spent 24 hours in A&E but the situation kept worsening. I was highly paranoid and kept repeating: Is the baby fine? Am I fine? Are we going to be ok? Why me? I was also really worried that I could have harmed my baby as I was not able to take care of him properly.

During this time, I truly convinced myself that I was indeed in a computer simulation. It also became clear that I was having hallucinations. It was as though I was projecting my feelings onto other people’s faces and I thought I could see my husband and the doctor crying, but when I asked them about it the tears suddenly vanished and their faces returned to normal.

It was at this point that another doctor came into the room and diagnosed me with postpartum psychosis.

I wasn’t scared of the diagnosis – I hadn’t heard of it so the name of the illness didn’t mean anything to me. But I was terrified by what I was experiencing and I just wanted it to stop. As things continued to deteriorate fast they made the decision to section me in a Mother and Baby Unit (MBU) which ultimately saved my life.

I had never heard of an MBU and I am not sure they actually exist in my home country.

MBU’s are psychiatric hospitals for mothers like me experiencing severe mental illness. They are a place you can recover keeping the baby with you the entire time. These are amazing places and the doctors that work in there are fantastic people; I cannot praise them enough.

The first day in the MBU was hard as I was still convinced I needed to reach my next level in the computer simulation, and that to do so would save me from being trapped in a coma. A doctor came to explain to me that I was experiencing psychosis and that I would need to begin taking special medications that same evening.

Both the medicine and the ability to sleep for an entire night helped enormously in my recovery. Indeed, the day after, I had a short psychotic episode but it lasted only 10 minutes…and I’ve never had once since then!

Time flew by in the MBU: I gained confidence with my baby and I also met some lovely mum friends, all of who were clearly experiencing their own battles (I wish them all the luck for the future).

My recovery went so well that I was discharged within three weeks, followed by home support from the perinatal mental health team. Coming home was scary and daunting but my husband and my family where there to support me (luckily my family managed to find a flight to reach me). I had ups and down at the beginning. I felt ashamed, sad about my illness and devastated about not being able to breastfeed. Nonetheless, I had my baby there with me and we had a beautiful bond. Everyday I was showing myself that I was in fact able to take care of that little human being and that really boosted my confidence. He was smiling and happy and that was all mattered to me.

After a few months had passed since my discharge from the MBU, the medication was stopped and I am happy to say that I am back to being the old me (and actually less anxious, which is better than before!) This month is going to be my baby’s 1st birthday and life couldn’t be better!

I wanted to share my story to show that postpartum psychosis is indeed a severe mental illness but you can recover very quickly with the right help. Reach out for help and, although you might think you’ll never be your old self again, that really isn’t the case. You will recover. There is help. Stay strong.

 

 

 

 

Stephen's Virtual Marathon

 

 

 

 

 

A huge thank you to Stephen Vinter who took part in a virtual marathon on Sunday 30th May 2021 to raise awareness and money to support APP’s work. Stephen’s friends Alex, Colin, James and Mike also ran with him for parts of the marathon. Stephen is the husband of APP Volunteer Gemma, who organised pamper packs to be delivered at Mother and Baby Units (MBUs) last Christmas, and to the new MBU that has recently opened in Wales. You can read a news article about this on our website here.

Stephen had originally planned to run the Edinburgh Marathon in 2020, but after it was cancelled for the third time due to the Covid-19 pandemic, he decided to run the marathon virtually instead.

Stephen said ’In 2017, after the birth of our wonderful son, my wife suffered from an illness called postpartum psychosis (PP), hospitalising her for three months in an MBU. She was absolutely amazing and inspiring in the way she handled her recovery while continuing to be a fantastic mum. She suffered severe anxiety and depression for the following 12 months. She is now doing volunteer work for APP, helping other mums in their recovery as well as visiting MBUs.

It is definitely my turn to do my bit for a charity that is now very close to our hearts. Just under a year ago I could hardly run around the block but I decided I would set myself the challenge of getting fit with the secret objective of taking on a big challenge of completing at least one race a month for 12 months to keep me motivated. I have now completed eight 10 kilometre runs, a 10 mile race, a half marathon and a family Santa run with a further 10k and a half marathon to go before I attempt to run the big event.’

 

 

 

 

 

 

After running the virtual marathon, Stephen said ‘I am really pleased to complete the marathon and more importantly raise money to support APP. Thank you all so much for your unbelievably kind donations and support throughout. Myself and Gemma have been blown away by your kindness’.

Stephen’s fundraiser has raised more than £3,000 for APP. We would like to thank Stephen, Gemma and their friends for supporting APP and everyone who has donated.

You can still visit and donate to Stephen’s fundraising page here.

If you have been inspired by Stephen, we would love to support any fundraising ideas you have. Get in touch here.

 

 

 

 

 

 

 

 

Nikki's poem: My journey to recovery.

Looking back now I realise just how far I have come
since that awful illness after becoming a new mum
1 in 1000 mothers can be affected, yet none of us knew
a mixture of scary symptoms, not just feeling blue

I needed support and had to stay away from my home
thrown into the deep end, feeling afraid and alone
my new baby girl was thankfully there with me
but I didn't have a clue what to do or how to be

After a while symptoms passed and back home I went
to a house that felt massive in every extent
from having people all around me all of the time
I realised I felt alone and was far from fine

depression setting in, I was too scared to be left alone
no nurses anymore, I was thrust into the unknown
husband going back to work having to carry on with life
but I was now a new mum aswell as a wife

I was very lucky having loving family to support
but I was too scared to go out, I needed an escort
always on edge and fearful of so much
not able to focus or wanting physical touch

unable to smile yet I carried on with it all
I dare not stop, so fearfully that I would fall
functioning as best I could I carried on going
trying to hide my numbness from ever showing

dreamy and vacant as though I wasn't really there
but forcing a smile to try and prove I did care
eventually time went on and support fading to low
so I could start doing more, to get better and grow

taking tiny steps I went out more on my own
just my baby and I in the big scary unknown
it was hard to do I am not going to lie
but I needed to do it for my baby girl and I

although hard to see, time is a healer indeed
it allowed me to move on, to grow and succeed
the fear seeming to settle not controlling me anymore
although the ride isn't over I am doing much more than before

facing demons along the way to help me self heal
these last 8 years of my life having been so surreal
although I am now healed from PP I have times where I am low
this experience has taught me more than I know

finding my smile again, becoming more like the old me
it has been a bumpy ride, and a long journey
I am what I am now I will never be quite the same
but I must always remember, the challenges I overcame

Miles for Mums and Babies Fundraisers

APP would like to say a huge thank you to everyone who is supporting our #MilesForMumsAndBabies challenge. We’re aiming to raise more than £10,000 to support our work by asking people to walk, run or cycle 10 miles, 20 miles, 500 miles or even 1,000 miles! Each mile reflects the journey mums, babies, partners and families travel to be together, whilst mums receive care in Mother and Baby Units (MBUs). We’ve had a fantastic response to the challenge so far. Our fundraisers include:

Katherine Paul and her son Harris walked 3 miles in one day on 6th May (during Maternal Mental Health Awareness Week). Katherine was hospitalised in 2019 and 2020 and each mile represented the journey she and Harris made in and out of Florence House MBU. Katherine and Harris raised £76.82 for APP. You can still visit and donate to their JustGiving page  here.

 

Dorota Donigiewicz walked more than 100 miles during May to support MilesForMumsAndBabies. Dorota experienced postpartum psychosis (PP) in 2015 after the birth of her first child and says during her recovery she found APP’s forum and other resources very valuable. Dorota has raised £420.75 for APP.

 

Consultant Psychiatrist, Neha Rawat, and her family covered 534 miles in May through a combination of walking, running, jumping and crawling! The Rawat-Sharmas chose their target to represent the distance between the NHS Lothian Livingston MBU in Scotland and Jasmine Lodge MBU in Devon. Neha said they wanted to highlight the fact many families travel hundreds of miles to be together whilst a mum is being treated in hospital for severe mental illness. Neha and her family have raised more than £300 for APP. You can still donate to their JustGiving fundraising page here.

 

The team from the MBU at Glasgow’s Leverndale Hospital and colleagues from the Community Perinatal Mental Health Team challenged themselves to walk 10,000 steps a day throughout May. APP has supported the MBU and the Glasgow team wanted to take part in #MilesForMumsAndBabies to raise awareness of postpartum psychosis and to support APP. The team went for walks before, during and after work (with and without patients), and have raised more than £5,800 for APP. You can still donate to their JustGiving page here.

 

Hannah Bose walked and cycled 95.19 miles during May – that’s the distance from her house to the nearest MBU in Exeter, Devon. Hannah was joined on her walks by her cockapoo, Tessie. Hannah works for the DadPad (a guide for new dads developed with the NHS), and APP's Partner Peer Support Facilitator Simon O'Mara recently wrote a blog about PP for their website which you can read here. Hannah has raised over £290 for APP. You can still donate to Hannah – and Tessie’s –  fundraising page here.

 

Crisse Buttery works within the community perinatal team as a mental health nurse and has close links to the MBU at Wythenshawe. Crisse walked 22 miles in a day - which represents the 22 MBUs in the UK - on 21st June, International Fathers Mental Health Day. Her aim was to raise awareness of the impact that PP has not only on mum and baby but on fathers too. Crisse has raised £490. As this illness impacts the whole family unit, the money will be split between APP and the MBU at Wythenshawe. You can still visit her JustGiving Crowdfunding page here.

 

Ailania Fraser walked 22 miles in June to support MilesForMumsAndBabies- that’s the distance between Edinburgh Royal Infirmary and the Livingston MBU. This represents the journey she travelled when diagnosed with PP in April 2019, during which time she spent around seven weeks under the amazing care of the Livingston MBU. Ailania’s husband Stephen and their two year old son joined her on a lot of the walks.  Ailania and her family have raised £100 for APP.

 

Lucy Nichol, APP’s Media Coordinator, and her friends Caroline, Bex, and Johanna, challenged themselves to walk, jog, cross train or run as many miles as they could throughout the month of June to raise money for APP. Lucy wanted to raise awareness of PP amongst a wider community, and spread the word as far as possible. She wanted to get outside and build her fitness back up as exercise is good for mental health. She and her friends completed 381 miles and have raised £290 for APP. You can still donate to their JustGiving page here.

 

Anna Grisedale had PP in 2015 and 2018, and challenged herself to walk 119 miles, which represents the journey she made from Leeds to the MBU in Morpeth with her first born. Anna was initially admitted to Morpeth as no bed was available in Leeds MBU. After a few weeks, she was transferred back to Leeds, which enabled Anna’s family to visit her regularly. She says this was a lifeline to her and her family. During her illness she experienced the therapeutic benefits of walking.

Watch this Leeds and York Partnership NHS Foundation Trust film to find out more about Anna's challenge;

Anna has raised over £1500 for her challenge via JustGiving and said 'Thank you so much for all the amazingly generous donations which will help support so many women, babies and their families. I have loved every step of my walks and have been overwhelmed by the wonderful messages of support. I have huge appreciation to all the staff at Leeds MBU who enabled me to be with my babies throughout my illness, which allowed our bond to remain strong throughout and  is paramount for families like ours'.  You can still donate to her JustGiving page here.

 

Danielle Thomas APP’s Assistant South Wales Coordinator, and her husky dog Lyra, walked 106 miles during June and July, which represents the distance from their house to the Melbury Lodge MBU in Winchester. Danielle experienced PP after the birth of her daughter in 2017, at which time there was no MBU in Wales. This meant she was a 2.5 hour journey away from family and friends during her stay at Winchester MBU. This April the new Uned Gobaith (Unit of Hope) MBU opened in Wales and Danielle was able to collaborate with its planners and artists through APP. Danielle and Lyra have raised £660 for APP. You can still donate to their JustGiving page here.

 

Emma Charlton works at Beadnell MBU in Morpeth. Along with her colleague Katie, Emma walked 161 miles over a 12 week period to raise money for APP. Emma chose the distance to represent the 161 women admitted to the ward since she started working in Perinatal Services. Emma and Katie were accompanied by other colleagues on some of their longer walks and have raised £1150 for APP. You can still donate to Emma’s challenge here.

 

Naomi Gilbert, APP’s Assistant Peer Support Coordinator, took part in her first ever triathlon on 26th September. She chose a triathlon to highlight that during her recovery from PP she had to go to three separate psychiatric hospitals without her daughters, as there was no local Mother and Baby Unit (MBU) at the time. Naomi completed three challenges - swimming, cycling and running - in 1 hour 53 minutes and her younger daughter Ella helped her to run to the finish line. Naomi has raised more than £1,100 for APP via her Facebook fundraising page which you can still donate to here.

 

Rachel Kerr walked 100 miles for her MilesForMumsAndBabies challenge. Rachel was hospitalised for three weeks in 2016 having developed PP after the birth of her daughter. Last year, she gave birth to her son and received support from APP. Rachel has raised more than £45 for APP.

 

The team from the new Perinatal Mental Health Service in Ayrshire and Arran challenged themselves to walk 1,400 miles throughout October. They work with mums who are affected by severe mental illness in the perinatal period, and wanted to take part in #MilesForMumsAndBabies to raise awareness of PP, support APP, and come together as a team. They chose the distance as it represents the 1,400 mums who experience PP in the UK each year. The team have raised more than £1250 for APP. You can still donate to their challenge here.

 

Emily Saunders, a peer support volunteer with APP, walked and cycled more than 500 miles between 1st July and 14th November 2021. These dates are important to her as they are the dates she went into and then finally came out of Nottingham MBU in 2017 (having had two stays) when she had PP, severe PND and anxiety after the birth of her daughter. Emily chose the distance as it represents the almost 500 miles from the most northerly to the most southerly MBU. Emily has raised more than £506 for APP. You can still donate to her challenge here.

 

Shirley Holmes, a health visitor, has walked the six different paths up Snowdon, a total of 48.5 miles. with her husband and sister joining her for some of the walks. Shirley decided to fundraise for APP after recently learning more about postpartum psychosis. She’s also keen to support our campaign for an MBU in North Wales. Shirley’s first part of her challenge started in May and she finished the six routes in October. Shirley, her husband and sister have raised more than £472 for APP. You can still donate to their challenge here.

 

As a team of 11, Rachel Lucas and her family and friends walked 1,400 miles for APP during November. Rachel experienced PP two years ago and spent six weeks in Leeds MBU. Rachel is a big supporter of APP and is also one of our trained Peer Support Volunteers. She held a fundraiser with her family and friends called ‘Four million steps for APP’ during November last year. She has also developed the ‘Blooming Mum to Be’ and ‘Brand New Mum’ boxes which she is selling via her website www.pourlamaman.co.uk, donating some of the profits to both APP and PANDAS Foundation. Rachel and her team have raised more than £360 for APP and the donations will be match funded by Rachel’s employer. You can still donate to their challenge here.

 

Stephanie was hospitalised in an adult psychiatric ward in the USA in 2020 after giving birth to her daughter. Covid-19 restrictions meant she wasn’t allowed to see her baby for five days. Stephanie has walked 100 miles during 2021 – the round-trip distance it would have taken for her to visit her daughter once a day during her hospital stay. She was joined by others on her fundraising walks to share postpartum and perinatal stories and to offer support. Stephanie has raised more than £1070 for APP. You can still donate to her challenge here.

 

Debbie Sells is the Ward Manager on the MBU at Nottingham and has covered more than 1,000 miles during 2021 through a combination of walking and running. She has worked on the ward for 24 years, and the 1,000 miles represents the long distance many families travel to receive specialist inpatient care. Debbie says that APP provides vital support for women and families who experience maternal mental illness. Debbie has raised more than £967 for APP. You can still donate to her challenge here.

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Inspired to join in the #MilesForMumsAndBabies challenge? Find out more and sign up here >

APP urges HSC Northern Ireland to invest in ‘critical’ Mother and Baby Unit to save lives

Representatives from Action on Postpartum Psychosis (APP) are speaking at the Northern Ireland Maternal Mental Health Conference this week to raise awareness of postpartum psychosis and the need for specialist life-saving facilities.

Postpartum psychosis is always a medical emergency and yet, while many parts of the UK now have specialist Mother and Baby Units (MBUs) to treat women experiencing this severe mental illness, Northern Ireland, North Wales, Northern Scotland and the Republic of Ireland currently have no such facilities.

MBUs accommodate multidisciplinary teams of experts able to care for both the physical and emotional needs of new mothers. They have specialist knowledge of the issues surrounding medication management in pregnancy and the postnatal period. Presently, because women in Northern Ireland do not have access to an MBU, they would be admitted to a general psychiatric unit – resulting in separation from their baby during this critical time, with potential lifelong consequences for both mother and baby.

Dr Sally Wilson, National Research and Training Co-ordinator, APP, who is speaking at the conference on Thursday (6 May) said: “Postpartum Psychosis is a devastating mental illness that can occur completely out of the blue and it always requires emergency specialist care. However, if affected families are able to quickly access the right treatment, the prognosis is good and women recover. MBUs are a vital service for mothers experiencing severe forms of postnatal mental illness, and we believe that every woman experiencing postpartum psychosis should have access to this critical specialist support.”

Postpartum psychosis is a severe postnatal mental illness that affects 1,400 women and their families every year in the UK – from all backgrounds. Half of cases are ‘out of the blue’ with women having no history of mental illness. Symptoms include hallucinations, delusions, mania, depression, restlessness, anxiety, confusion, and erratic behaviour  - which can manifest within days of childbirth. With the right treatment, women can fully recover.

Dr Jess Heron, CEO, APP said: “We’ve been campaigning for more Mother and Baby Units for many years. We hear so often from women and families about how traumatising and inappropriate general unit admission was. Our research shows that women who receive care for postpartum psychosis within an MBU feel more satisfied with the care they receive, they feel safer, more confident in staff, more confident with their baby, and are able to recover more quickly. These are essential services, not nice-to-haves, and they play a critical role in keeping families together and saving lives.”

The Northern Ireland Maternal Mental Health Conference takes place on Thursday 6 May during Maternal Mental Health Awareness Week. It aims to bring together parents, health services and the third sector to ensure that nobody is left alone to struggle with postnatal mental illness.

Both Dr Sally Wilson, National Research and Training Co-ordinator, APP and Ellie Ware, National Peer Support Co-ordinator, APP have experienced PP personally and will be presenting on behalf of the charity. Delegates can expect to hear more on what postpartum psychosis is, why it’s always a medical emergency, what care pathways for PP should look like, and why MBUs are essential. They will also discuss the importance of peer support and the myriad ways APP can support women and families, including some of the organisation’s future plans in Northern Ireland.

To book your place, and to find out more, click here

For further information on postpartum psychosis, or to access peer support, visit www.www.app-network.org

APP volunteer, Oorlagh Quinn, launched a petition calling for an MBU in Northern Ireland. To find out more about Oorlagh’s campaign and to sign, click here

Raising awareness of postpartum psychosis this Maternal Mental Health Awareness Week

This week (3 – 9 May) marks Maternal Mental Health Awareness Week, a campaign organised by The Perinatal Mental Health Partnership to raise awareness of the fact that 1 in 10 women experience a mental health problem during pregnancy or in the first year after birth.

At APP, we know that postpartum psychosis plays a key role within this and it can have a devastating impact on many women and their families. In fact, postpartum psychosis can affect 1-2 in every 1,000 new mothers in the UK each year, and a lack of awareness makes it harder for families to reach out for help and more challenging for health professional to spot the signs.

As such, we are going to be using the week to further raise awareness of this illness and campaign for better services – including more Mother and Baby Units to help keep families together and to recover more quickly.

 

How you can help

We’d love for as many people as possible to help us spread our message and signpost people to support and there are many ways you can do this:

  • Share our social media graphics. Hop on over to Twitter (@ActionOnPP) or Instagram (@actiononpp) and share our ‘What is Postpartum Psychosis’ content – not forgetting to tag us and use the relevant hashtags too (#postpartumpsychosis and #MaternalMentalHealthAwarenessWeek)


  • On your own social media, share why you think Mother and Baby Units are important, tagging @ActionOnPP

 

  • If you’ve experienced postpartum psychosis and would like to join our peer support or storyteller network, please sign up using this form.

 

 

 

For further information on postpartum psychosis please use this link

If you are in urgent need of help, please follow this link for useful information

 

Jocelyn’s story: "I don’t know where I’d be today if it wasn’t for peer support".

I was living abroad when I became unwell with postpartum psychosis. I had left friends and family behind in the UK and moved to Brazil to get married to a Brazilian I met while teaching there a few years previously. When I became pregnant, however, I did toy with the idea of having the baby in England, but it just wasn’t practical to come back at the time.

Of course, I knew that giving birth and looking after a baby would be hard work, but I had no idea of the scale and intensity of what was to follow...

84% of women in Brazil have C-sections and I was determined to have a natural birth. However, my baby’s heart rate dropped when I was being monitored in hospital and I ended up being rushed for an emergency caesarean.

At that point, everything was fine and I was sent home. However, after about three weeks I developed a fever and had a pain in my stomach. I had it checked out and, through CT scans, they found that they’d left a swab inside me. The language barrier made all of these conversations quite challenging, but one thing I was told by the doctor from the first c-section was that I nearly died due to loss of blood. This added to the confusion and paranoia of who to trust.

This is when things became really confusing for me. I was convinced that, because I’d had two operations, I must have had two babies. In Portuguese, they don’t pronounce Seth, my baby’s name, in the same we that we do in England. Instead they say ‘Sete’ (pronounced ‘Seche’) and it reinforced the idea that I’d given birth twice, that there were two different babies.

I became really anxious and paranoid, and I had a really heightened sense of smell, believing that I could tell which nurse was coming to see me just from the smell in the air.

After leaving hospital for the second time, I kept believing things were happening that weren’t real. We got on the bus in the middle of summer and I was absolutely convinced that I was bleeding everywhere – but I wasn’t bleeding at all. And when one of the drivers came to look at Seth in the pram I was convinced they were staring because I was pushing a pram around with no baby in – I truly believed at that point that Seth had died.

Other delusions included my mistrust of my husband, who I was convinced had installed cameras everywhere, and I stopped eating because I thought that lots of different foods were causing colic. I remember my husband trying to put me in a sleeveless summer dress too and I became really agitated, convinced that he was strapping me into a straitjacket.

I tried to find places or activities that might help to calm me. For example, there’s a saying in Portuguese – banho de sal grosso – which means cleansing yourself in saltwater. So I decided that if I went to the sea it would cleanse me and make me feel better and stop all of the fear and anxiety. So we kept going to the beach one time when I went in the water with my husband I thought I was dying.

I continued to be really concerned about Seth’s wellbeing too. At one point, I thought he was the devil and that he needed to be exorcised to save him – even though I wasn’t actually religious in any way.

As things became worse, we went to see a psychiatrist but, due to the difference in language and my complete confusion, I struggled to get across how I was feeling. They tried to sedate me but then just sent me on my way with six months’ antidepressants in my pocket.

I felt confused, frightened and as though I had no real medical support. To add to that, I was back at work when Seth was just four months old because you only get four months’ maternity leave in Brazil. By that point the psychotic symptoms were petering out (they lasted around two weeks in total), but I had really bad anxiety and depression – in fact, the anxiety stayed with me for over a year after giving birth. Because Seth was so young when I returned to work, I had to have him with me in the classroom where I was teaching English and try to use my hour a day for breastfeeding as effectively as I could.

It was such a challenging time and, feeling alone, I decided to do some of my own research. I started googling postnatal depression but it just didn’t sound at all like my experience. However, luckily, I stumbled across a website about postpartum psychosis and realised that I had all the symptoms. Upon further research, I found the Action on Postpartum Psychosis (APP) peer support forum which felt as though it was the only knowledgeable support that was out there – after all, my doctors hadn’t mentioned psychosis.

 

Reaching out to people on the forum was a lifeline – it was here that I found other women who had been through what I had. The first woman who responded to me really helped me and we are still in touch to this day. There was no judgment on the forum, no language barriers and I felt free to speak openly about what had happened to me and what I was going through.

We came back to England when Seth was nine months old and I saw some doctors over here who confirmed my diagnosis. As I started to make sense of my experiences, I decided to train to become a peer support worker with APP because I couldn’t bear the idea of another woman going through what I went through with no knowledgeable support.

I honestly don’t think I would be where I am today if it wasn’t for the voluntary peer support that I received. There’s a lot of stigma around psychosis, particularly around PP where people have these ideas that mothers want to harm their babies, but it really wasn’t like that. If anything, I was terrified of something happening to my baby. I was over-protective.

Everybody’s experience of PP and subsequent recovery is unique to them, but there are shared similarities between us and that means the world. It stops you feeling so lonely and ashamed.

Through APP I feel that I have found my tribe – these amazing women who have been through such intense struggles, but who are united in joining forces to help others. And while NHS support often has time restrictions placed on it, peer support is there forever. I’m so grateful to benefit from and, today, play a part in that much-needed service.

Catherine’s story: "One day I did remember him, and I felt like a mother again".

There’s a Korean tradition that when a baby is born, mother and baby stay home for the first 21 days. The first 100 days are considered a vulnerable time, and so we are meant to be cautious. It’s a belief rooted in keeping mothers and babies safe from harm, but in modern life, it’s a difficult tradition to follow. For me, it felt impractical and unreasonable, and I spent the first days out of the hospital inviting friends to our home and going out to restaurants and parks. We even decided to travel to the US when my son was two months old on an extended trip to visit family and friends. However, in the back of my mind, I would remember this tradition of confinement, and it was a decision I would question when I was eventually diagnosed with stress-induced postpartum psychosis.

I cannot link my postpartum psychosis to tradition or culture, I’ve learned from this experience that postpartum psychosis can happen to anyone, and I can trace the roots of my psychosis to something that started well before my decision to make this trip.

My psychosis started while I was in the United States, I’d wanted to introduce Cato to family on the West and East Coasts, and to celebrate his 100 days with family and friends.

It was towards the end of our trip, while I was staying with my in-laws that the symptoms of psychosis started. I hadn’t been sleeping for weeks, and the stress of travel and concerns from our families had taken its toll. I did not realise that what I was experiencing were symptoms of postpartum psychosis. I’d become paranoid, believing that my mother-in-law was signalling to me in a language separate from the others in the family. The house had Nest cameras installed for security, but I thought I could hear the cameras in the walls, I thought I was being watched. The warnings and concerns expressed kindly by my in-laws took on a darker meaning, I felt increasingly worried, and I could not sleep. It culminated in a moment when I looked at my son’s face, and his face was not his own, but the face of a devil.

I did not know what was happening. The moment felt too surreal to believe, but it felt so real to me. I did not understand. I knew that I needed to leave the family home, I had a sense that something very bad was about to happen, I just didn’t know what. I begged James, my husband to take us to a hotel, and he immediately packed our bags, and we left.

At the hotel, things descended quickly. I thought we were being tracked, and so I deleted all the apps on my phone. I started to see figures in the halls, people with strange faces staring at me, brushing past me. And my son’s eyes were still like the eyes of a devil. In the hotel, my husband tried to get me to sleep, but I couldn’t. I started losing sense of time, each moment was replicated a multitude of times. I thought I heard the voice of God, telling me that I was in hell, that my life had been a simulation, and that my son was going to die.

In some ways, it felt like a relief to hear this, it seemed to make sense, everything I’d been experiencing, all the stories of my past, of my family’s histories, I could see the patterns in them. I didn’t tell my husband what I ‘knew’, because I didn’t want to frighten him. He could tell that I wasn’t well, and so he asked his parents to come take our son, and then he drove me to the emergency room.

At the hospital, I lost all sense of what was real and not real. I started tearing off my clothes in the waiting room, I was attacking the nurses, they looked like demons. I remember hearing my husband shouting for help and being forced onto a gurney.

The next days are fragmented. I was given different medications, but nothing was working, and I still couldn’t sleep. I didn’t sleep for four days. I lost all sense of who I was, I thought I was my husband, my son, sometimes I was my mother. I remembered different versions of my life, versions that couldn’t be true. My husband would call my parents to come and help take care of me, but I didn’t recognise them. I thought that one of the nurses was the angel Gabriel, and I couldn’t eat because I thought the food I was being given was human flesh. There were times I remembered I had a son, that I knew who I was, but most of the time, I was terrified.

I would experience what I thought was the end of days

After four days, the decision was made that I would be sectioned to a general psychiatric ward. I was transferred via ambulance, and I remember thinking that the medics taking me were taking me to be euthanized. I am still grateful to the medic who held my hand the entire way, while I talked nonsensically and screamed at the animals surrounding us.

At the psychiatric ward, I would experience what I thought was the end of days – it was partly in reaction to the roughness of the staff who were trying to calm me, but it ended with me stripping off my clothes and urinating on the floor. I was sedated, and for the first time, I slept. I do not know how long I slept, I think it was for two days, but I woke up in a blank room with my hair tied in a strange way, with fragmented memories of who I was and what had happened. I spent eight days in the psychiatric ward, following instructions, attending the classes and waiting desperately to be released.

I was released to the care of my husband. I felt like myself, but I know now that I still wasn’t well. My time away from my son had taken its toll – I felt completely separated from him, and I had no memory of my bond with him. It felt physically painful to touch him. When I thought about it later, I would believe that this was my mind’s way of protecting him, of protecting him from a mother who could not be trusted.

We would return to London, where I was referred to the perinatal mental health team. A few weeks after psychosis, I would fall into a deep, clinical depression. It happened suddenly, where one morning I woke up, but I couldn’t move or get out of bed. Those months were some of the most difficult times of the experience. It felt unending, and I felt despair, because I couldn’t imagine being well again.

My husband made the decision to keep me at home instead of admitting me to a mother baby unit. One day when I was feeling too much pain to lift a spoon, my husband called my psychiatrist, and she referred me to the mental health crisis team. The crisis team would visit our flat every morning. Each visit forced me to get out of bed, and they would give me a task for the day. I started keeping lists of simple tasks – making a cup of tea, brushing my hair. They would smile at me, even as I sat unmoving and silent, unable to speak. They promised me that I would feel better, that one day this would be a memory. I tried desperately to believe them.

They asked me to spend time with Cato each day, to help rebuild our bond. I would do this as a practice, and I didn’t understand how I couldn’t feel a connection to my own son.

I would remain on an antipsychotic and antidepressant for a year. It was several months before I could start noticing moments of light. I would be sitting and realise I wasn’t feeling pain, that I was noticing the colours around me, and I would know that I was getting better. Those moments would be temporary, and then the darkness would come again, but eventually the darkness would come less frequently, and I would feel I’d reclaimed myself.

The bond with my son took longer to build. I approached it with intention. I went through the steps, and I hoped he would understand that I was working to come back to him, that I was trying to remember.

And one day I did remember him. I was holding him and feeling his weight against my body, and it felt familiar. And I felt like a mother again.

For more of Catherine’s story, you can read her memoir, Inferno, which is out now in hardback and paperback from Bloomsbury. You can also watch this moving film that Catherine recorded in March for the Maternal Mental Health Alliance.