Tag Archives: postpartum psychosis

Double your donation this festive season!

‘I don’t know how we would have coped without APP. There was no one else to turn to.’

This festive season, we're on a mission to give the life changing, life saving, gift of peer support to even more families.

Between now and midday on 9th December, we're aiming to raise £10,000 - which could help us reach out to and support nearly 300 women and families affected by postpartum psychosis. We’d love you to help us.

Donate now through our Big Give Christmas Challenge campaign page, and your donation will be doubled, at no additional cost to you, thanks to match funding from the Julia Rausing Trust.

Every donation we receive this week will be worth twice as much – if you donate £5, APP will receive £10, if you donate £25, we'll receive £50, and so on. Double the donation means double the impact.

Will you donate this Christmas and get your donation doubled?

‘­Finding APP and getting support from another grandma who had been through something similar was like a big online hug. I felt heard, understood and supported right from the start.’

Quotes from 2025 APP Peer Support survey
Help us be there for everyone who needs us, for as long as they need us.
Donate today if you can. Thank you.

APP supports expert panel in call for postpartum psychosis to be recognised by diagnostic manuals

An international panel of women's mental health experts has, this month, issued a call for postpartum psychosis (PP) to be formally recognised in diagnosis classification manuals.

Professor Veerle Bergink of the Icahn School of Medicine at Mount Sinai and Erasmus University in Rotterdam, led a panel of prominent PP academics, including APP's Professor Ian Jones and Trustee Dr Clare Dolman, in developing a consensus statement. Professor Bergink said: “We argue that with its specific onset, phenotype, phenomenology, risk profile, and prognosis, postpartum psychosis has distinct prevention and treatment recommendations.”

The team have spent several years pulling together clinical and biological evidence and consulting patient groups, to demonstrate that postpartum psychosis deserves official recognition and a new classification should be created within the bipolar disorder chapters.

Although the term is used widely by clinicians, researchers and people with lived experience, official diagnostic manuals currently force doctors to classify postpartum psychosis under a range of different names in different subsections of the classification manual, leading to confusion for patients, clinicians and researchers alike.

Dr Clare Dolman, King’s College and University of Edinburgh, Trustee of Action on Postpartum Psychosis, said: “The case for postpartum psychosis being recognised as a distinct condition in the diagnostic manuals is clear and is supported by the wealth of evidence provided by the Expert Panel. Both as a researcher in this area for 15 years - and a woman who has suffered a postpartum psychosis - I do not understand the reluctance to make this straightforward but much-needed change.”

Dr Jess Heron, CEO, Action on Postpartum Psychosis, said: “This is a momentous occasion. If these recommendations are accepted by the team who oversee the Diagnostic and Statistical Manual (DSM) in the US, it could lead to significant improvements in patient care and research quality globally.”

The full consensus statement is available here.

The issue of diagnosis is a confusing topic for many people affected by PP and their families (partly caused by its absence from diagnostic manuals). For help and support, please reach out to APP’s peer supporters, or join a discussion on the APP forum.

Hollyoaks work with APP for new issue-based storyline involving Cleo McQueen

Hollyoaks will explore Postpartum Psychosis (PP) when Cleo McQueen, played by Nadine Mulkerrin, struggles with her mental health following a traumatic birth with her first child, Joseph.

APP colleagues and storytellers have advised on the Hollyoaks storyline which will hit the screens this week.

Cleo went into early labour at 28 weeks pregnant and, assisted by Dodger (Danny Mac), was rushed to hospital. After giving birth, Cleo haemorrhaged and required emergency medical attention.

Baby Joseph needs to stay in the Neonatal Intensive Care Unit due to being premature. Cleo, who fell ill after childbirth, is later given the green light by doctors o go home. Red flags start to appear when, at first, she doesn't believe her baby is hers.

This quickly progresses when Cleo starts losing track of time and feels guilty for struggling to produce milk. Cleo’s girlfriend Sienna Blake (Anna Passey) moves into the McQueens house to help support the new mum.

The storyline follows Cleo and her support system - Sienna, Dodger, and her McQueen family – as they convince her to seek help when they start noticing her concerning behaviour.

Cleo will be treated in a general psychiatric ward – she’s not able to go to a Mother and Baby Unit due to Joseph being in the NICU unit.

For this issue-based storyline, Hollyoaks worked with APP colleagues and storytellers, consulting with the cast members involved and advising on the storytelling process.

Nadine Mulkerrin, who plays Cleo McQueen, has said “It’s been a new challenge taking on the role of motherhood and the difficulties that being a new mum can bring, especially the strain it can have on your mental health. We had a consultation with APP [Action on Postpartum Psychosis] whilst filming this storyline, and it was helpful to hear other people’s experiences - my heart breaks for poor Cleo.”

Dr Jess Heron, CEO, Action on Postpartum Psychosis said “Responsible portrayals of PP on popular TV shows such as Hollyoaks are invaluable. With greater public awareness, partners, friends, family members and frontline health professionals will be more able to quickly spot the signs and seek specialist emergency help as soon as possible. We’re grateful to Hollyoaks for playing a part in awareness raising and for their diligent approach to producing a sensitive and accurate storyline.”

Hollyoaks is now available to stream from 7am Monday to Wednesday on Channel 4 or watch live on E4 at 7pm.

Double your donation!

This week we're on a mission to support even more women and families affected by postpartum psychosis, and we'd love you to help us. Between midday on 8th October and midday on 15th October, we're aiming to raise £5,000.

Donate now through our Big Give Women & Girls campaign page, and your donation will be doubled, at no additional cost to you, thanks to match funding from the Big Give.

Every donation we receive will be worth twice as much – if you donate £5, APP will receive £10, if you donate £25, we'll receive £50, and so on.

Double the donation means double the impact.

Our target of £5,000 could help us significantly increase our offer of help and support for families affected by postpartum psychosis (PP) - a treatable medical emergency that affects around 1200 women in the UK each year.

Being diagnosed with a severe mental illness like PP is frightening and shocking for the woman and those around her. With the right treatment, nearly all women make a full recovery, but the journey can be long, have ups and downs and can feel very isolating. APP peer supporters are there for everyone affected by PP, whether the experience was recent or many years ago. By donating today, you can help us be there for everyone who needs us, for as long as they need us.

Will you donate today and get your donation doubled?

'I don’t know where I would be without APP. I was struggling so much and even with perinatal mental health team involvement I felt so isolated and misunderstood. I was losing hope of any recovery and fighting suicidal thoughts even though I had a much wanted child at last. The understanding and encouragement I’ve received has been everything in my ongoing slow recovery. Thank you.'

Quote from a mum who responded to our Peer Support Survey this year.
Help us be there for even more women and families.
Donate now through our Big Give Women & Girls Campaign page and your donation will be doubled, at no additional cost to you.
Thank you for your support.

Shubina’s story: Finding your ‘tribe’ in recovery is so important 

It was 1997 when I got married to a man I didn’t know. I was a very naïve 23 year-old, and wasn’t ready for marriage. So, there was the shock of that and then the shock of marrying someone from a different culture who spoke a different language. Worse still, as the marriage progressed, he became abusive and controlling. 

 I fell pregnant quickly. My pregnancy was difficult – I didn’t put on much weight, I was sick all the way through and my husband’s abuse went up a gear. I turned to my mum and dad for support, and they were just amazing. With them by my side I was able to leave and I finally felt safe. 

 The final part of my pregnancy was more stable, although I did have a long and exhausting labour. My mum stayed with me throughout and, eventually, my beautiful daughter was born. I went home to Mum’s but, two days later, my husband turned up, banging on the door. I was holding my baby and he threatened me while she was in my arms. It was frightening and I think this was the trigger for my postpartum psychosis (PP). 

 I couldn’t sleep, I was too afraid to eat and I became extremely paranoid. After about five days of no food or sleep the hallucinations started. My younger brother tried to encourage me to eat, but the paranoia I was experiencing was too strong. 

By this point I was in the midst of a psychotic episode and I didn’t trust any healthcare professionals, convinced that they were going to hurt my baby.  

 My family didn’t know what to do so my mum went to the doctors and asked for help. A couple of doctors came out to the house but they didn’t know what was wrong with me either. This was a time when there wasn’t much awareness of PP.  

A family friend at the time was a nurse who suggested it might have something to do with giving birth so my dad took me to the mental health unit where I was voluntarily admitted. There was no Mother and Baby Unit at the time so I had to leave my baby at home in the care of my amazing sister who took time off work to look after her for me. 

A headshot of Shubina smiling to camera with long dark brown hair and a black top

I was in the mental health unit for a total of three weeks. I remember when I first got there, still in the psychosis, I was confused as to where I was, and my superhero - my dad - would visit me every day, even though he wasn’t allowed in to see me, but he would just sit in the grounds to be close to me. 

After I was discharged, my dad took all the family on holiday. He said we’d all been through so much we needed to get away. Tragically, whilst away, he suddenly died after being in a car accident. It was horrific. I had fully recovered by now, but feared I might relapse. I didn’t though. In fact, I haven’t experienced an episode of psychosis since.

I gained so much strength from my dad and in life he really helped me to recover. 

Since then, I had another baby, a son, and after he was born I became a single mum again and have been ever since. When I was pregnant the second time I had a lot of healthcare support in the run up to the birth and I didn’t get unwell again. In fact, I’ve never had to have any mental health support since first having PP. 

Driven by my own experience, I went back to college and retrained as a psychotherapist so I can help others who have experienced mental illness. I’ve also started volunteering for APP’s Muslim Women’s Support Group. There was so little awareness when I experienced PP that it took me 25 years to find peer support through APP – which I discovered after a Facebook ad popped up on my feed.  

The Muslim Mum’s Cafe Group is so important on many levels, but what is particularly important for me is that, as human beings, and this goes back to the beginning of time, we’ve always lived in tribes.

And for a Muslim woman, because our experiences can be unique to our culture, finding other women who look like us, who sound like us and who have been through some of the things we have is invaluable.

There’s a huge cultural aspect to PP in my community and stigma is very much alive and well, so being visible and sharing my story is so important because many Muslim women still don’t seek help.  

I know that having PP is a really scary time, but I want others to know that there is help out there, you’re not alone and the APP community is here for you. And, like me, you can recover. 

Our 2025 Great North Run Team

We're very proud to have five runners representing APP in the iconic Great North Run this year.  They've been training hard throughout the hot summer months, ready to take on the world's biggest half marathon on Sunday 7th September. 

Meet our 2025 Great North Run Team:

Gemma and James

Siblings Gemma and James are no strangers to the Great North Run, having taken part in 2016. Now they're back, with the aim of beating their younger selves (and maybe even each other!)

Hoping to have a great time on the day, they're really looking forward to running together through their local area for a cause that means a lot to them.

Gemma says: 'I'm so proud to be running for APP and we're really excited about the day! It's nice to be running with my brother, we don't get to spend as much time together as I'd like so this is a good excuse!  Everyone has been really generous with their donations - thank you!'

You can support the siblings here.

Debbie and Jo

Debbie smiling wearing her purple APP running vest, standing in front of a fieldDebbie and Jo are experienced runners who have taken part in numerous events before, but this will be their first experience of the Great North Run.

Debbie encouraged her friend Jo to run with her for this event - knowing just how important the work is that APP does.

Debbie is Ward Manager at the Margaret Oates Mother and Baby Unit in Nottingham.

Debbie says: 'We would appreciate your support if you can to help raise funds for this amazing charity.  As many of you know I work with women suffering a severe mental illness following childbirth and it is vital that our families are supported. Suicide remains the leading cause of maternal deaths in the first year post partum, but these illnesses are treatable and women recover.  Supporting APP will help raise awareness of this illness.'

Thank you Debbie for all you do to support families, and to both you and Jo for taking on this challenge for APP.

Support Debbie and Jo here.

Fiona

Two smiling women taking a selfieFiona is taking on her first ever Great North Run, inspired to take part and raise funds for APP by her good friend Laura (pictured together with Fiona on the left of the photo here).

Fiona says: 'I am running for my friend Laura who has had postpartum psychosis after both her children were born'.

Good luck Fiona!

Add your support for Fiona here.

As always, the Great North Run will be covered live on BBC TV so keep an eye out for our runners in their purple APP tops.  And if you can be there in the North East in person, do give TeamAPP an extra big cheer as they run past!

Good luck to all our runners and thank you for taking on this amazing challenge for APP.

The Great North Run is a fantastic event to be part of, so if you're feeling inspired by our 2025 team, we will have places again next year - contact our fundraiser Fliss if you're interested in running for APP in 2026.

 

Aimee’s story: I wish I could have spoken to someone else like me when I was in hospital

In the years  since I gave birth I felt completely overwhelmed by shame and guilt – until I met someone else who had experienced postpartum psychosis (PP). Getting that peer support from APP helped me come to terms with what I had been through - and marked the first time I felt any degree of normality since giving birth.

I had been in hospital for almost a year after becoming unwell with PP. There were times when I honestly didn’t think I would get better. In fact, I think if I could have spoken to someone else who had been through it when I was in hospital I might have found hope and recovery sooner. But today, me and my son George have the absolute best bond, I’m back at work and I’m even managing George’s junior rugby team. There was a time when I never could have imagined this life.

Aimee standing at the back with black vest top, red hair and sunglasses, next to a man in a grey t-shirt on a rugby field. In front are six children in green rugby shirts.

My pregnancy was generally fine – up until the point that I was induced, got sepsis and had to have an emergency C-section. I was in hospital for about five days and I didn’t get much sleep. As a single mum, I lived with my mum at the time and, when I first brought George home, she noticed something was really wrong with how I was behaving. It was as though I went completely round the twist – believing that the girl from The Exorcist was living in my wardrobe and thinking that I was going to die or George was going to die. I also stopped my mum from touching George because I believed she was poisonous and that the poison would seep out of her blood and get into him. I wasn’t sleeping and I was excessively cleaning and panic buying things. I was also talking manically and was very hyperactive.

It was a strange situation because I didn’t think there was anything wrong with me, it was everyone around me, all my family members, who noticed that there was something very wrong.

I agreed to go back to the maternity unit for a check up and was assessed in hospital by psychiatrists. I was incredibly manic at the time and becoming really out of control. They gave me a lot of sedatives and put a section on me, which they then lifted. That was when I was admitted to a Mother and Baby Unit (MBU).

A couple of hours later the sedatives wore off and I completely flipped out. I was restrained and injected and, from that point on, I barely remember a thing. It was like I woke up in hospital and it was next year.

A close up of a baby being held by his mum, Aimee. She has her hair tied back, glasses and a white vest top on.

During that period I was moved between the MBU, a psychiatric intensive care unit and two other psychiatric hospitals. I wasn’t responding to medication, so it took a few months to find the right one and come round from the psychosis. But for some time I was basically like a zombie in a chair - dribbling, non-verbal, unkempt and putting on a lot of weight. During this time my mum looked after George but she also looked after me – advocating on my behalf at the hospital and asking for more support.

Being in hospital was traumatic. At one point I was on a mixed ward and I was punched in the face and sexually assaulted by a couple of the male patients there. In December of last year I started having really distressing nightmares about my experience there.

Luckily, the all-women hospital I was moved to was where things started to improve. The clozapine was working and the environment was much better – the staff were lovely and being among all women patients and having more homely areas and activities to take part in really helped. I started to get snapshots of memory back. They let me have more visitors as well, and at one point I was able to go home for a night at a time. They also used to help me shower and help me do my hair and make-up, bringing a degree of normality back into my life.

Saying that, my recovery has been quite slow. I was on clozapine for two and a half years after being discharged and my follow-up care wasn’t great – possibly because it was during the pandemic. I was never offered any therapy and I had put on ten stone while in hospital, so I was physically unfit as well.

I eventually came off the clozapine in 2022 and was put on antidepressants but I wasn’t sleeping and kept waking up with night terrors. Eventually, I found a private therapist who was fantastic and helped me talk through my trauma and work on my self esteem.

She helped me come to terms with what had happened and helped me to understand that it was an illness – it was nothing that I had done wrong.

George, s young boy with short hair and a purple/blue t-shirt stood with his mum, Aimee, with her hair tied back and wearing sunglasses

It was around that time I found APP, too. I got in touch with Ellie from the peer support team and took part in my first zoom café group. I was then matched with Krystal as my one-to-one peer supporter who was also really great. It was the first time I had met anyone else who had experienced PP and who had been through a similar trauma. Talking to others who have been there really gives you hope and helps you feel less ashamed and alone.

I have since been diagnosed with bipolar but it hasn’t stopped me living my life. Speaking with others who can relate was a big turning point. And my mum has been a wonderful support and the therapy really helped me too. I think it’s important to reach out for that help because locking it away is the worst thing you can do. You need to process it and you need to find hope to help you recover more quickly.

I feel so lucky that me and George have such a great bond now – he’s such a mummy’s boy.

I was worried it might never happen because we were separated for such a long time and it took a little while but we got there.

I just want others to know that you can be in the absolute worst place ever, but it does get better. It’s hard work and it takes time but you can do it. You just need to learn to reach out and ask for help. If you feel like your meds aren’t right - say so. If you feel any warning signs creeping back in - go and get help. Plodding along and saying that everything’s OK when it isn’t is the worst thing to do. I never had that hope which is why I struggled so much and for so long. I genuinely believe that if I spoke to someone like me when I was at my worst it would have made a huge difference. Everyone needs to be able to see the light at the end of the tunnel.

Rory’s story: It was supposed to be the best year of our lives but we ended up living apart for five months

2023 was supposed to be the best year of our lives, having our first child in Spring and getting married at Christmas time.

Within 12 weeks we went from the feeling of reassurance that the 20 week scan gave us, to living apart for nearly five months when Megan was admitted to a Mother and Baby Unit (MBU) following a mental health crisis.

I'd heard of the baby blues and postnatal depression but I'd never heard of postpartum psychosis (PP), which happens in around 1-2 in 1000 pregnancies. I also didn't know the most common cause of death of women within a year of having a child was suicide, a risk I didn't think we would be managing after becoming parents for the first time.

While PP most often occurs following birth, our case was slightly different and things started to go wrong while Megan was still pregnant. She became more and more anxious about the pregnancy, worrying that something awful was happening and that she couldn't feel any movement. We were visiting A&E regularly, being sent for yet another scan, waiting for hours to be told everything was fine and being asked if this was our first child. People suggesting we were worrying for no reason became our  norm.

However, we were told she didn’t meet the threshold for perinatal mental health support when we finally got an assessment. This cycle went on for weeks with Megan's anxiety becoming worse by the day, and her severe sleep issues led to stronger delusional beliefs. It was only when Megan became suicidal that I feel like we were finally listened to.

At 32 weeks pregnant she was sectioned. It was awful for her and I will never forget the sadness in her eyes as I had to say goodbye. As difficult as that was I knew that her safety, and our unborn child were the priority. A few weeks later, our beautiful son was born prematurely and he spent some time in a Neonatal Intensive Care Unit, while I spent my days visiting him in one part of the hospital and Megan in the other. Three weeks later was the first sign of hope I had, as Oscar was discharged and able to move to the MBU to be with his mummy, and supported by the most wonderful nursery team who looked after my family outside of visiting hours and when I returned to work.

Coming back to an empty flat for the best part of five months broke my heart but mums and their babies need each other and that's one of the reasons MBUs exist. Sadly,  there still isn't enough of them across the UK and none at all in Northern Ireland where we planned to have our children. I spent a lot of time researching postpartum psychosis and finding the stories on APP’s website and forum gave me hope - as did the MBU staff reassuring me that "she will get better".

A photo of a young boy with blonde hair and beige short-sleeved shirt
Rory and Megan's son, Oscar

When Megan and Oscar came home I told myself if I could get through those months, everything else would be a breeze. And whilst things slowly got better, my personal resilience was shot, just as I was finally feeling like a proper dad for the first time and not relying on hospital staff. In truth the last year and a half has not been easy as Megan continued to recover at home, and we have both had our mental health challenges.

Megan continued to engage in the professional services even when she didn’t want to. Her  hard work, support from our family who visited regularly, our patience for each other and the love of the most amazing little human have got us to where we are now. Now we are looking forward and building memories as a family and have a lot be thankful for. Sadly not everyone makes it this far, but those who access the support we have are able to have a much better chance.

Seeing how far Megan has come in the last 6 months makes me proud. She kept a lot of her feelings and experiences inside as there is a lot of stigma associated with mental illness, but she has come through that and no longer feels shame. She has now shared her experiences openly with friends and family, many of whom had no idea what she went through, as well as social media, and that's what's inspired me to write this.

The work of APP is critical in raising awareness including their campaign to open Northern  Ireland’s first MBU, and educating medical professionals in maternal mental health. For anyone reading this who is going through something similar, don’t lose hope as things really can get better.


Rory is running the London Marathon for APP in April 2026. Find out more and add your support for his run here.

Frankie’s story: I was lucky to get a bed on an MBU – every woman with PP should have access to one

By Frankie Roe

My friend said I’m the world’s worst patient and she is absolutely right. My brain doesn’t cope well with being told what to do or being stuck indoors, so I keep it happy by being active and spending lots of time outside. So, if I’m being honest, I absolutely loathed being stuck in an MBU. But I don’t know where I’d be today without the high standard of care that I received in there.

It was after giving birth to my firstborn that I became unwell, although, when I look back on it, I was struggling with anxiety for a long time before I even got pregnant. I found the pandemic really tough - not the fear of being ill, but the fear of being confined. I was also struggling with anxiety around the pregnancy, as I miscarried the first time which was really traumatic. Due to covid restrictions my partner waited in the corridor while I sat on my own waiting for our scan to confirm the pregnancy had ended. He was briefly allowed in before being sent back outside.  We weren’t offered any counselling or support.

I got pregnant a few months after the miscarriage and hated every second of the pregnancy. Even after the 12-week scan when they told me my baby was well and wriggling around, I couldn’t relax. I became convinced the baby had stopped moving and was going to die.

I told myself that when the baby arrived I’d be able to relax, but my daughter wasn’t gaining weight and seemed so vulnerable. And so after the birth my fears about dead babies intensified.

I wasn’t sleeping, I was having to drive to the other side of the city for health appointments because of the pandemic and I was exhausted. But I kept powering through. When I couldn’t sleep at night I was cooking or painting furniture at 4am, and I was putting my daughter in her baby sling and going for four-mile walks across the moors. Because I’m such an active person these things didn’t stand out too much, but in retrospect they were definitely extreme - even for me.

I saw my GP and was diagnosed with postnatal depression and given antidepressants – and things rapidly deteriorated.

After starting antidepressants, I was cycling through rapid mood swings – being absolutely manic one minute and telling my partner I felt like jumping off a bridge the next. Plus, my sleep at this point was pretty non-existent and I became convinced that it was because of the colour of my bed sheets. I was terrified that I might never sleep again and the lack of sleep would kill me. I became increasingly possessive over my baby and refused to let my partner take on his share. I was hearing babies crying when I did manage to step away from her for a shower or to rest but would come downstairs in a panic to find her sleeping peacefully.

About ten weeks post-birth I mentally hit a cliff edge, the crisis team was called, and I was admitted to a Mother and Baby Unit (MBU).

I already knew what an MBU was because they came up in my Google searches when I was trying to find out what was wrong with me. I knew something wasn’t right - I just didn’t know what - so I agreed to go in voluntarily. My partner later told me that had I not agreed, I would likely have been sectioned the following day.

It was a weird experience because it was during the pandemic, and I had to stay in 24-hour isolation upon arrival, but it was good for me because I was given lorazepam and finally slept.

They immediately took me off my antidepressants and started me on antipsychotics and the psychosis improved really quickly. Still, I didn’t enjoy being in there. I know people need MBUs and hospital care, but I resented being inside and feeing like my life was controlled – and all the pandemic restrictions on top of that were tough, too. But I knew it was the best place for me.

Although the psychosis subsided quite quickly, I had really bad anxiety and my sleep patterns were all over the place. Even after discharge, I had recurrent periods of insomnia and I lost a lot of confidence. I found myself deferring to my partner when I’m naturally independent and stubborn.

I was back at work 10 months after giving birth and, although in hindsight I probably wasn’t fully ready for it, my manager was great and I felt really supported.

After having PP, I didn’t think I’d have another baby. But after a few years I felt ready to try.

I became pregnant really quickly and have been lucky that the second time around I didn’t become mentally unwell – but I also knew I had lots of NHS professionals on the case if I did.

I feel so grateful that, when I needed it, that specialist care on an MBU was there for me – because the idea of being separated from your baby on a general psychiatric ward is inhumane. I was told there were only eight beds for Yorkshire and the Humber so I was incredibly lucky to get a place when I needed it – and that’s why we need more MBU beds available for anyone who needs them. You hope you won’t need one but if you do become seriously ill, it’s definitely the best place for you. It will probably be hard but what would be a damn sight harder is sitting at home and letting it get worse and worse.

That’s why I think, if you get the choice to go voluntarily, you should absolutely take it. You might feel as though you’re losing your freedom at first, but you’ll get your freedom back so much sooner if you accept all the specialist help on offer. And when you look back on it, you’ll feel good about making that choice and accepting that help. I know that being on a mental health unit doesn’t make me a crap parent – and that accepting the help was the best thing to do for me and my baby.

Mental Health Team take on Great North Swim for APP

On June 14th, a team of healthcare professionals from the South West Yorkshire Community Perinatal Mental Health Team will heading to the Lake District to take part in the Great North Swim to help raise funds and awareness for APP.
Attempting the one mile swim in the UK's biggest open water swimming event will be Claire, Louise, Mary, Roban and Laura - all of whom work together in the perinatal mental health team.
Claire explains more about how they got started and why they chose to take on this amazing challenge for APP.

'We started going out swimming once a month and now meet two - three times a week. It really has had a fantastic impact on our lives. It is so freeing being out in the water. We chat, put the world to rights, laugh and off load with each other, or swim bits on our own to just get some real time for ourselves in our busy lives.

It’s been really nice recently swimming (literally) alongside baby ducklings, swans and geese. It’s feels really special and the warm weather is definitely making it a pleasure to be out in the water. 

Although we are not distance swimmers, we have all now swum a mile in the open water so this has given us a real confidence boost for the actual swim. 

We are blown away by the generosity of people who have donated to your charity. We work with families affected by this illness and they often tell us no one had ever told them this was an illness that could affect them after having a baby, so we wanted to help raise awareness so women and birthing people and families know what the illness is and how to access support if they feel they are at risk or are experiencing symptoms.
We hope the number of donations reflects we have managed to spread the message and raise funds so you can continue all the work APP does.'
A huge thank you to all the team from all of us at APP - we can't wait to hear how you get on, fingers crossed for nice weather on the day!