Royal College of Psychiatrists Statement on #everyonesbusiness campaign

RCPSYCHStatement: From current and past presidents, Royal College of Psychiatrists, on launch of Maternal Mental Health Alliance’s Everyone’s Business campaign

Current and Past Presidents of the Royal College of Psychiatrists come together to highlight Maternal Mental Health Alliance’s Call to A.C.T. - call postcode lottery of services ‘a disgrace’.

everyones business logo

The current and past Presidents of the Royal College of Psychiatrists today jointly welcomed the launch of the Maternal Mental Health Alliance’s Everyone’s Business campaign and their Call to A.C.T. Professor Sir Simon Wessely (President of the Royal College of Psychiatrists) and Professor Dame Sue Bailey (Chair of the Children and Young Peoples Mental Health Coalition (CYPMHC) and Immediate Past President of the Royal College of Psychiatrists) said:

“It is a disgrace that although one in ten mothers will develop a mental illness either during or in the first year after pregnancy, half of the women in the UK do not have access to specialist community perinatal mental health services. The current postcode lottery of provision means women are left to suffer, families risk breakdown, children suffer and society suffers. It is frankly unacceptable that suicide is one of the leading causes of death for women during pregnancy and one year after birth.

“We wholeheartedly welcome the Maternal Mental Health Alliance’s Everyone’s Business campaign which calls for Accountability for perinatal mental health care to be clearly set at a national level and complied with, for Community specialist perinatal mental health services meeting national quality standards to be available for women in every area of the UK and for Training in perinatal mental health to be delivered to all professionals involved in the care of women during pregnancy and the first year after birth.

“We are pleased that the RCPsych Faculty of Perinatal Psychiatry was able to assist the Alliance with its mapping of current services, and we will lend whatever advice or support is needed by those at the helm of health policy in the four nations for them to act to address this iniquitous and unjustifiable variability which penalises women – wives, partners, daughters and friends - at their most vulnerable. By improving the health (and there is no health without mental health) of any woman you improve the lives of their children, generations of children to come, and it leads to more flourishing communities.”


 

Shocking gaps in UK maternal mental health services

#everyonesbusiness Campaign Launched Today

Pregnant women and new mothers across almost half of the UK do not have access to specialist perinatal mental health services, potentially leaving them and their babies at risk, according to data released today (8 July).

Everyone's Business

Maps highlighting the gaps in provision are published today by the Maternal Mental Health Alliance to mark the launch of its everyonesbusiness campaign.

The Alliance of professional bodies, patient organisations and charities, is warning that women who develop a perinatal mental illness are missing out on essential and potentially lifesaving care. (more…)

Volunteering event 2014

 

Highest number of women with lived experience of Postpartum Psychosis come together under one roof!

Volunteer Event 2014On Saturday 26th April 2014, The Barberry in Birmingham was once again home to another fantastic APP event. The Volunteer Event gave thirty women who have experienced   Postpartum Psychosis and their families a chance to join together to talk about the future of the illness and the charity. 
The day combined a more formal agenda with chances for women to chat, meet  each other and share their stories. Several women in the room had never talked openly about their PP episode before and all who attended were deeply moved to be  surrounded  by individuals  who  truly understood  the  illness first hand.
Dr  Jess  Heron,  Vice  Chair,  set  the  tone  for  the  day  with  a warm  and  informative welcome;  she  gave  an  overview  of APP, its history and hopes and dreams for the future. Andrea Lambert, Peer Support Coordinator, then described the amazing work being done to help women and their families via the forum and on an individual level. Lucy Vernall talked about media volunteering, pointing out the pros and cons of choosing to share your story publicly. Nicola Muckelroy spoke about her current project, to launch a Regional Representative network, ensuring APP has every region in the UK covered by at least one active volunteer who will raise awareness and fundraise in their specific area. Heather Heron, Trustee, filled the pre-lunch slot  with  an  enthusiastic   and  passionate   plea  for fundraising and the difference it makes.
After lunch,  Anna  Jones,  Volunteer,  talked  about  her experience   of  PP  and  talks  she has  been  giving  to  the medical profession in her area to help the PP cause. Professor Ian Jones, Chair, bought  the  more  structured  agenda  to  a  close  by sharing his academic research in to PP and answering questions from individuals about the illness, recovery, medication, symptoms and its connection with other mental illnesses.
In the afternoon, the attendees split in two different groups to brainstorm,  collaborate and tackle questions regarding the future work of APP. Topics  covered  included: Regional Rep roles, obtaining and spending future funding, support opportunities for woman and families, providing useful literature, research projects, campaigning at government level, involving high profile individuals and equipping Volunteers with the necessary skills set.
Dr Giles Berrisford, Clinician & Trustee, gave a summary of all these discussions, remarking on the extraordinary progress APP has made to date and how vital its support is to the world of perinatal psychiatry.
Throughout the day, Lucy Vernall, APP’s  Media Coordinator, was ready and armed with a camera in the photo booth to record snippets of women talking about their PP experience with messages to the general public, sufferers and policy makers about the illness. These clips will be made into short films for the APP website to help with campaigns for improved services.
Another remarkable APP event bringing women together to help cement a brighter future for Postpartum Psychosis and improved services for those affected by it.
Onward!

Following the event we received many messages from attendees expressing how much meeting other PP women face to face meant to them and how much they got from the day on so many levels. Here’s one of them:

"I wanted to drop you all a few quick lines to say simply "Thank You!" for last Saturday at the Barberry. It was the first time I had attended an APP event & most importantly for me, the very first time I had met another living, breathing mother who had also experienced Postpartum Psychosis!! I now truly understand I have not been alone in this long old journey & this was an incredible feeling, very special indeed. I want each of you to realise that what you have achieved so far is worth every single minute & hour of effort that I understand must go into running that kind of Workshop. Thank you so very much." ~ E.G.

On her blog 'Bumps and Grind', Kathryn writes about coming along to the Volunteers Event & also her experience of receiving support via our PPTalk online forum.

Kathryn's blog: 'Bumps and Grind: PP Survivors United'>>

Sarah's story: "Everything scintillated and colours became super-bright".

Simple things fueled my growing ecstasy: deliveries of congratulatory post and bouquets. I felt increasingly important and blessed, buoyed by the nurses’ praise after being induced and giving birth without pain relief. I reveled in quirkiness, telling the midwife I was feeding my mushrooms after suckling W. Before he discharged me, the midhusband put his fist in the cavity where my stomach had divided.  Motherhood shocked me. I believed W had special qualities.

Although I slept well, I stayed up after the 5am feed, preferring to reorder the airing cupboard or under the sink. I fizzed with energy. Hand-painting announcement cards and recording a flood of creative ideas. My list-making became obsessive. Every feed and bodily function was noted.

Uncharacteristically, I started to spend and donated large amounts to charity. Everything scintillated and colours became super-bright. A picture of Clint Eastwood suffused into life. I started hearing voices from the dead, and music. Pleasant auditory and visual hallucinations followed.

I sniggered to myself to keep my psychic abilities quiet or else be thought mad. Sixteen days after the birth I had an epiphany. I was in heaven on earth. I had solved the meaning of life. I screamed at my discovery.

Purple Party in Memory of Rosy

Close friends of tragic young mum Rosy Hinchliffe have launched a ‘life-long’ fund and awareness raising mission in her memory.  Kerstin and her husband Stephen Botham are to put on a host of events for APP and the couple’s first major event will be an all-day ‘purple party’ charity auction and raffle.

Clothiers Arms

They will also compete in the Northwest Triathlon in September as part of their bid to prevent similar incidents occurring among new mothers in the future.

If you are nearby, please do go along and support this event if you can - you'll be sure to receive a warm welcome! Or if you can support  in any way, by donating,  supplying auction items or providing live music etc. please get in touch.

Huddersfield Daily Examiner article: Charity event in memory of Rosy>>

To donate please visit: http://www.justgiving.com/TriActionPP

or text TAPP84 £5, £10, £15 to 70070


 

APP Volunteering Event 2014

World First: Highest number of women with lived experience of Postpartum Psychosis come together under one roof!

Volunteer Event 2014On Saturday 26th April 2014, The Barberry in Birmingham was once again home to another fantastic APP event. The Volunteer Event gave thirty women who have experienced   Postpartum Psychosis and their families a chance to join together to talk about the future of the illness and the charity. 
 
The day combined a more formal agenda with chances for women to chat, meet  each other and share their stories. Several women in the room had never talked openly about their PP episode before and all who attended were deeply moved to be  surrounded  by individuals  who  truly understood  the  illness first hand.  
 
Dr  Jess  Heron,  Vice  Chair,  set  the  tone  for  the  day  with  a warm  and  informative welcome;  she  gave  an  overview  of APP, its history and hopes and dreams for the future. Andrea Lambert, Peer Support Coordinator, then described the amazing work being done to help women and their families via the forum and on an individual level. Lucy Vernall talked about media volunteering, pointing out the pros and cons of choosing to share your story publicly. Nicola Muckelroy spoke about her current project, to launch a Regional Representative network, ensuring APP has every region in the UK covered by at least one active volunteer who will raise awareness and fundraise in their specific area. Heather Heron, Trustee, filled the pre-lunch slot  with  an  enthusiastic   and  passionate   plea  for fundraising and the difference it makes.  
 
After lunch,  Anna  Jones,  Volunteer,  talked  about  her experience   of  PP  and  talks  she has  been  giving  to  the medical profession in her area to help the PP cause. Professor Ian Jones, Chair, bought  the  more  structured  agenda  to  a  close  by sharing his academic research in to PP and answering questions from individuals about the illness, recovery, medication, symptoms and its connection with other mental illnesses.
 
In the afternoon, the attendees split in two different groups to brainstorm,  collaborate and tackle questions regarding the future work of APP. Topics  covered  included: Regional Rep roles, obtaining and spending future funding, support opportunities for woman and families, providing useful literature, research projects, campaigning at government level, involving high profile individuals and equipping Volunteers with the necessary skills set.
 
Dr Giles Berrisford, Clinician & Trustee, gave a summary of all these discussions, remarking on the extraordinary progress APP has made to date and how vital its support is to the world of perinatal psychiatry.
 
Throughout the day, Lucy Vernall, APP’s  Media Coordinator, was ready and armed with a camera in the photo booth to record snippets of women talking about their PP experience with messages to the general public, sufferers and policy makers about the illness. These clips will be made into short films for the APP website to help with campaigns for improved services.
 
Another remarkable APP event bringing women together to help cement a brighter future for Postpartum Psychosis and improved services for those affected by it.
 
Onward!
 

Following the event we received many messages from attendees expressing how much meeting other PP women face to face meant to them and how much they got from the day on so many levels. Here’s one of them: 

"I wanted to drop you all a few quick lines to say simply "Thank You!" for last Saturday at the Barberry. It was the first time I had attended an APP event & most importantly for me, the very first time I had met another living, breathing mother who had also experienced Postpartum Psychosis!! I now truly understand I have not been alone in this long old journey & this was an incredible feeling, very special indeed. I want each of you to realise that what you have achieved so far is worth every single minute & hour of effort that I understand must go into running that kind of Workshop. Thank you so very much." ~ E.G.

On her blog 'Bumps and Grind', Kathryn writes about coming along to the Volunteers Event & also her experience of receiving support via our PPTalk online forum.

Kathryn's blog: 'Bumps and Grind: PP Survivors United'>>


 

Women on antidepressants more successful at breastfeeding if they keep taking medication

University of Adelaide researchers have found that women on antidepressants are more successful at breastfeeding their babies if they keep taking the medication, compared with women who quit antidepressants because of concerns about their babies' health.

These results have just been presented this week at the 18th Perinatal Society of Australia and New Zealand (PSANZ) Annual Conference in Perth. Using data from the Danish National Birth Cohort in Denmark, researchers in the University of Adelaide's Robinson Research Institute studied the outcomes of 368 women who were on antidepressants prior to becoming pregnant.

"We found that two thirds of the women (67%) stopped taking their antidepressant medication either after becoming pregnant or during breastfeeding," says Dr Luke Grzeskowiak from the Robinson Research Institute.

"A third of the women (33%) continued to take antidepressant medication throughout their pregnancy and while breastfeeding, and these women were much more successful at maintaining breastfeeding up to and beyond the recommended six months.

"In contrast, those women who had stopped taking antidepressants were also more likely to stop breastfeeding within the recommended six months."

Dr Grzeskowiak says the health benefits of continued breastfeeding greatly outweigh any perceived risk to the baby from antidepressant medication.

“This is a really important message ... on the balance of it, we believe that continuing to take antidepressant medication and maintaining regular breastfeeding will be the best outcome for both the baby and the mother”

"This is a really important message because we know that breastfeeding has immense benefits for the child and the mum herself, including a degree of protection against post-natal depression," he says.

"The amount of antidepressant medication that finds its way into a mother's breast milk is very low. On the balance of it, we believe that continuing to take antidepressant medication and maintaining regular breastfeeding will be the best outcome for both the baby and the mother."

Dr Grzeskowiak says many women struggle with decisions about what to do with medications both during pregnancy and lactation.

"If they're taking antidepressants, they should be supported and encouraged by family members, friends and healthcare professionals to continue with their medication, knowing that good breastfeeding outcomes are all-important for them and their child," he says.

This research was funded by the National Health and Medical Research Council, and the Women's and Children's Hospital Foundation.


 

Anna's Story: "I hadn’t slept for three nights. A whirl of excited competence".

Where have you gone?

It started with a mighty fry-up.

Bacon, eggs, mushrooms, sausages, baked beans, toast. Hearty platefuls,  one for me, one for my husband. My newborn in one arm, frying pan in the other.  This having a baby lark is a piece of cake, invincible me, I can do it all.

“We need to eat a big breakfast, big breakfasts are important, especially  now I am breast feeding!”

Talking again, fast, unstoppable. I hadn’t slept for three nights since coming home from the  birth unit. A whirl of excited competence. We just thought it was the famous love hormone Oxytocin, which serenades all new mums. Endless phone-calls, emails, texts to friends and family.  Euphoric. “It’s amazing, I love it, I’ve never been so happy, oh you should see my baby, she is gorgeous, such a good baby. I even love breast feeding, it’s going so well.” Loud, fast, nonstop.

As we tucked in, a hot, overwhelming rush hit me, sinking, dizzy.  I needed to lie down.  I abandoned the fry up, handed our baby to my husband and headed upstairs, black dots in front of my eyes and  lay down on my bed. Thump, thump, thump, heart racing, within seconds, gasping for breath, clutching at my chest, choking. I yelled to my husband, up the stairs two at a time.

“I can’t breathe, I think I’m dying, quick call an ambulance.”  My chest was tightening, heart crashing, convinced this was the end. “Take good care of our baby, tell her I loved her, you’re going to be just fine on your own, you’ll be such a good Dad, I’m so sorry we can’t do it together.”

The ambulance took half an hour; that’s a long time when you think you are dying. They checked me, reassured us, a textbook panic attack. They said my husband should take me back to see a doctor and that birth could be very traumatic for the body.

It was February 2005, a few days after the birth of our beautiful girl, our first baby.

The next 24 hours were dark. Enveloped in paranoid thoughts, plagued by the panic attack consuming me again. The mania had gone, replaced by extreme anxiety, the tight chest persisted.  I felt scared to try anything, go anywhere. Irrational thoughts, fearful of the knives in the kitchen; maybe they were a danger to me. Delusional imaginings. I was convinced I would become a famous author that lived in Hampstead, that I had great wisdom to share with the world. Words leapt out, symbolic; crossword clues, newspaper headlines with hidden meanings. Insomnia. Rushes of anxiety coming in waves, rising up, overwhelming me, fading away. I called out, befriending them “Here you are again, I know you, you can’t harm me.”

I knew I was deeply unwell. I was losing my mind.

My husband took me back to the birth unit and they called a psychiatrist. Questions. Then, “Anna, you have a rare postnatal illness known as Postpartum Psychosis, we need to take you in to a psychiatric hospital and medicate you, watch you for a few weeks, in case you try to harm yourself or your baby.”

The words smashed, shattered, suffocated me in fear. Disbelief. Me? No previous mental illness. No familial history of mental illness. How? Why? It made no sense.

The pregnancy had been a breeze. The birth itself was reasonably normal, overdue at 41 weeks; they decided I should be induced. I had an epidural and our baby girl arrived after a normal delivery.

Thirty years old. One of the happiest, most positive people I knew. Good job, strong marriage, sporty, fun, sociable, balanced, loving family.

Bang.

Postpartum what? Psychosis? How on earth has this happened to me?

The power of autosuggestion is extraordinary; when someone tells you “you are psychotic” the fine line between sanity and insanity is washed away, leaving behind a pool of doubt for every thought to flounder around in. I didn’t trust my own mind anymore.

I was terrified.

Unlike Postnatal Depression, Postpartum Psychosis is deemed a psychiatric emergency requiring urgent treatment. I was taken in to a private psychiatric hospital in central London. My home, my prison for the next two months. A Mother and Baby Unit would have been preferable but we didn’t know they existed. My baby could only be with me during the day but had to return home with my husband at night.

The lavender scented  bath was a nightly ritual, ‘good to calm the nerves’ they told me. I was an obedient patient. I was going through the motions of yet another doped up, numb night with a broken heart and head. My husband and Mum had just left with my smiley, sleepy, peaceful angel, now a few weeks old. That was the hardest time, the hour after they left the hospital, alone again, in my soulless, white room, every pulse of maternal love aching to hold my baby, be with her, feed her, love her, be normal again.

I was mad. A mental patient. Really? This wasn’t meant to happen.

I pulled my hair back in to a ponytail and stepped towards the bath. I caught my reflection in the small, square, institutional mirror above the sink. I came closer and looked harder. Skin sallow, eyes distant, afraid and empty. I heard myself whisper,

“Where have you gone?”

I whispered again “Will you ever come back?” No answer.

Quiet, frightened tears welled and brimmed and fell in to the sink below.

How about our little baby? Women who’ve suffered Postpartum Psychosis will often talk of a broken bond.

I wonder to this day if she knew something was wrong. She slept and slept and smiled and slept. Undemanding, content, asking nothing of me other than the cuddles and feeds and the nappy changes I could muster. Of course there was no more breast-­feeding,  I was so disappointed, it had been going so well. A big chunk of my heartbreak came from being on medication and not being able to feed my baby in the way I’d imagined.

The emotional pain aside, my most often repeated line about my experience with Postpartum Psychosis is that I was one of the lucky ones. I was diagnosed and treated quickly and I had a phenomenal husband, wonderful parents and close friends beside me. My amazing Mum moved to London and alongside my husband (who had to return to work in time) looked after our baby with me. My mum and baby came to see me every single day in hospital, we would go for long walks and I would do all I could manage for her.  My husband came every evening. Thankfully, with this daily connection, she and I never once lost our bond. Had I been in a mother and baby unit, with perinatal expertise, the heartbreaking separation at night, could have been avoided.

The stint in the psychiatric hospital under a generalist psychiatrist lasted a couple of months and my drug treatment seemed to have limited success. My medication took a long time to get right. I was allergic to the first combination and didn’t seem to respond to the second. After about two months the psychiatrist recommended a course of intensive ECT (Electro Convulsive Therapy).

This felt very dramatic and was an incredibly hard choice for my husband and my parents to have to make on my behalf. Having spoken to another psychiatrist, a friend of the family, they took the decision to give it a go. I had no capacity to object or even fathom what would help me. Zombie-like, semi-mute,  I had an intensive course of treatments over a two-week period. Each treatment meant a general anesthetic. This was an awful time, etching a deep mental scar.

I stood outside myself looking in, detached but present.  I watched myself being wheeled in. The room and everything in it dauntingly white, overly cheerful faces of the clinical team greeting me, trying to reassure me as I lay powerless, helpless, tense, terrified, exhausted. Here I go again and then the anaesthetic and then nothing, until I woke, then tears. I’ve never known vulnerability like it, before or since.

It’s not always helpful to second-guess what you cannot change. Looking back I’m not convinced a perinatal psychiatrist would have made the same choice with the ECT. We had no way of knowing there was a better way and everyone did what they thought was best.

The long days dragged on, numb days, family and friends visited. My only reason for keeping hope was my angel baby, sleeping and smiling and sleeping.

Was this how it was going to be? Was I ever going to be my old self again?

I was allowed out for a small trip to Kent in late April and that changed everything.

I was to spend a few days at my parent’s cottage, fresh air, homemade food, restful and wrapped in love. Everyone was hopeful, an expectation that maybe this was it, maybe I was on the mend.

On the first morning away from the hospital, I awoke feeling anxious and vulnerable. Suffocating agoraphobia, deep fear of another panic attack. I came downstairs, shaking, tearful. Why won’t this leave me alone?

Mum called a local clinic, she knew they offered psychiatric help; they said they could see me right away. I was disappointed, terrified and so upset. Here we go again. Why can’t I get better?

We were greeted by a relaxed and peaceful man in his fifties, if he owned a word it would be reassuring.  I took a tentative seat and began to recount my story to this new psychiatrist. He nodded knowingly and within minutes, I heard the magic words, “Anna, you do know you will recover from this don’t you?”

No one had been able to say that until now. It changed everything. I broke down and sobbed.

This new psychiatrist was a perinatal specialist and had seen and treated countless cases of Postpartum Psychosis. He gently recommended I should be admitted for just a few days whilst he changed my medication. He insisted my baby was with me at all times unless I was sleeping. Within just one week, I had made a remarkable leap towards recovery. Already I could look in the mirror and see Anna again, me. There I was with a hopeful smile. The whisper again, “There you are, I know you.” I knew then I was coming back.

By May, with my four-month old girl in arms, I was enjoying my baby, surrounded by friends and family, functioning as myself again. Laughing, socialising, long walks, day trips, good food, and living life once more.

I saw this wonderful new perinatal psychiatrist weekly at first, then monthly, slowly, gradually, gently reducing my medication with each visit. He talked to me like an adult rather than a patient and reassured me with every doubt I had. I went from better to one hundred percent by the end of the year and made a full and complete recovery.

I was finally discharged a year later, almost to the day of the mighty fry up and catastrophic panic attack. As we said our final goodbye, “Anna, there will be a high risk of recurrence if you do decide to go on and have a second baby, but you know where to find me.”

Our son, was born on the 13th May 2008, three years later.

As with our daughter, my due date came and went and this time we let nature take it’s course, no drugs, no intervention, a calm, relaxed, natural birth at 42 weeks. Great debate came before the decision to have a second child and we were all worried. I spent a long time preparing, especially mentally. Acceptance, I decided, was the only way to approach it. I’d learnt vulnerability the hard way. I accepted that it may happen again and that, whilst terrifying, it would be all right because I knew. I knew what Postpartum Psychosis was, where to go for help, how to deal with it and that it was all right, in time I would recover.

I was one of the lucky ones. Thankfully, there was no hint of psychosis second time around, no anxiety, no mania, no delusions, no insomnia. Nothing.

I was myself; I was there, free to enjoy a happy, peaceful and special time as a Mum.

To my girl, thank you my angel baby.

To my husband, thank you my rock.

To my Mum, thank you my hero.

Andrea's story: "I held my phone but couldn’t work out how to call for help".

The fourth day after the birth of my first baby was the start of my meltdown. I had no history or mental health issues. Confusion, extreme anxiousness and terror mounted and I hadn’t slept for four days. It happened suddenly and severely, within hours. I was manic and couldn’t walk, talk or think. I held my phone but couldn’t work out how to call for help.
Over two weeks, I had delusions and scribbled notes frantically. My mind was spiraling yet I had moments of clarity. My thoughts raced so fast, I developed a stutter. I felt like a baby re-learning how to eat, walk and talk. It was exhausting. I couldn't read or watch TV and was terrified by people moving or speaking too fast. I couldn't process thoughts quickly enough to understand. I was learning how to care for my baby at the same time as trying to survive myself. I was scared I’d be separated from my baby. I wanted information but nothing was explained to me. They thought I was crazy. I was so very scared.
Severe depression developed. I was numb and rarely left the house. It took a year to bond with my baby. I was suicidal for three months. After two years I made a full recovery but chose not to have more children.

Daniel's story: "It was the best of times, it was the worst of times".

So, why am I involved with APP? Well, my family has been through it and come out the other side, let me explain….

2004 our first child was born and everything seemed perfect, it was “the best of times”. The baby (a boy) was beautiful, healthy and happy. My wife also was beautiful, healthy and happy. For a week I was the happiest I had ever been, I was a dad, I had a beautiful family, I finally felt like a grown-up.

My wife was amazing, she had so much life and energy, and we were really enjoying parenthood and showing off our new son to friends and family……but….after about a week I began to notice that my wife’s behaviour was getting a bit…. unusual…she was still happy and energised but now it was as if she was too energised…the volume had been turned up to 11. She started coming up with bizarre schemes to make our fortune becoming obsessed with one particular idea. I discovered she had donated large sums of money to charity and was starting to arrange all our possessions by colour. She spoke about how colours appeared particularly vibrant, sounds were amplified and smells were overwhelming. Finally she began to have conversations with her dead father…obviously something was going very, very wrong.

The crisis came after I returned to work. My wife was due to attend a “Birth reflections” session at the hospital (where new mothers share their experiences of pregnancy and birth). The poor organisers didn’t know what had hit them! So concerned were they at my wife’s behaviour that they told her to go and see a Dr. this was precisely the right advice, given to precisely the wrong person. She took it very badly (seeing their advice as a direct challenge to her perceived view of the world). But, knowing we had private health insurance she presented herself at the local private hospital demanding to see a psychiatrist. That’s when I got the phone call and my life began to fall apart….

When I got to the hospital it was clear that my wife was in the middle of a severe psychotic episode. We saw the duty psychiatrist (who had no experience of post-natal mania) the experience was best described as “difficult”…well…my wife started throwing things at him. After 20 minutes we were packed off with some tablets (I never did discover what they were) and the telephone number of a crisis team should the need arise. We were to return to the hospital the following morning for a more detailed assessment…..we never made it.

At home that evening things went from bad to worse. I was desperately trying to get my wife to eat and to sleep (having been told that rest was “critical”). But, that was the worst thing I could have done. Trying to get someone to sleep whose brain is busily frying was impossible. What made it worse was that she saw me as an obstacle to her achieving what she wanted, in her eyes I was the one with the problem and I must be removed from the equation. I don’t what to go into exactly what happened; even now 9 years on the memories are very raw…

I tried phoning the crisis team….the number I’d been given was wrong. I tried and tried again, changing the last digit until finally I got through. Two women turned up 30 minutes later (by now it was 11:30 at night). My wife instantly went on the offensive, smashing jars and bottles to create a glass barrier between us and her so they couldn’t get to her. The decision was made that my wife needed immediate hospitalisation. Now we were faced with another problem. To get my wife to hospital required the authorisation of a psychiatrist, the duty psychiatrist that night was unavailable for several hours. We couldn’t wait that long. I was told the only other option would be the police; they had the power to detain under section 35 of the Mental Health Act. 20 minutes later a police van turned up with two burly coppers. I was then told that their power to detain only extended to public areas, they could not enter my house to detain my wife, even with my permission. My only option was to “persuade” my wife to leave the house. There was no way that was going to work so I had to physically pick her up and carry her outside where she was detained.

The police stuck her in the back of the van and then they and the crisis team drove off into the night leaving me, quite literally, holding the baby…he was 16 days old.

In the space of 48 hours I had gone from being the happiest, proudest dad in the world, to seeing the woman I’d spent 15 years with, the mother of my first-born destroyed by an illness I had no idea even existed….it really was “the worst of times”

Swirl5

What to do now….there I was, in the middle of the night, suffering from shock, holding a baby who would need feeding within the next 2 hours. Then I found out who my friends really are. At 1am I phoned my best mate who lived 30mins away, his wife was at my front door 45 minutes later. She was wonderful. She phoned the hospital and got a duty midwife to call with supplies of formula. She swept up the broken glass and shattered crockery and, most importantly made me a cup of tea.

The following morning I made my way to hospital…the secure psychiatric unit…a truly dreadful place, somewhere I never, in a million years, thought I would be seeing. My wife was sedated. I was told it was likely she would only be there for a day or two before transferring to a specialist Mother& Baby unit (MBU). 10 days later she was still there. I would visit twice a day with our baby (all visits were strictly supervised), this enabled my wife to feed the baby and attempt some sort of bonding.

Eventually after 10 days a bed became available at a specialist unit 35 miles away. We transferred on the 11th morning, my wife in a secure van and me following in the car with the baby. Little did I realise how familiar I was to become with the MBU over the coming months. Once she and the baby were settled the duty nurse sat me down and tried to explain what had happened to my wife. Finally there was someone with experience of this illness, which I was told was called Puerperal Psychosis. It was explained that after birth a hormone is released that gives a sense of euphoria. In the vast majority of cases this euphoria is very mild and the supply is quickly “shut-off”. In puerperal psychosis the opposite happens. Production goes into overdrive until eventually the brain “blows a fuse”. But, the most important 3 things the nurse said to me that day was:

1. Don’t worry
2. Your wife and your baby are safe
3. She will get better

It’s only subsequently when reading up about PP that I realised how important no.2 was. There are cases where, tragically, help did not come in time and the mother harmed herself and/or the baby.

So then began the slow process of treatment and “normalising”. I was expecting my wife to be in hospital for a week or so…how naive…..I was told she would most likely be an in-patient for 3-4 months….and full recovery would like take 12-18 months.

I started to struggle, physically and emotionally. At this time my work involved a 40 mile commute. Unfortunately it was 40 miles in the opposite direction to the hospital. I got into a routine of driving to work, doing a full day at the office and then driving the 70 miles to the hospital to get about 45 minutes with my wife and son and then drive the 35 miles home. After 10 days of this I was exhausted and needed a break. I wasn’t eating very well (lots of take-away’s and ready meals) and I must admit I had a drink or 3.

The worst thing I felt during the drive from work to the MBU was not knowing what I would find when I got there. Would my wife be lucid, “normal” or sedated? Even worse was arriving at the unit and going into the nursery and not recognising my son…I honestly didn’t know what he looked like…I had to recognise him by the teddy he had. This was the straw-that-broke-the-camels-back. I couldn’t take any more, I was in a very bad place….

After a couple of days, and thanks to my mate for providing a shoulder to cry on, I got myself together and was able to cope a little better. But, what this highlighted was the lack of support for partners of women suffering post-natal mental illness. My wife was safe; she was being cared for and treated. I was on my own, having to hold down a job, dealing with questions from friends asking about the baby and my wife…trying to be normal.

After 3 months we were told that my wife and child could come home and the next stage of our lives as a new family could begin. This turned out to be more challenging than anything that had happened in the previous months. There was the misconception that, as she is being discharged she must be better, surely. Nothing could be further from the truth. I was completely unprepared for her return. I was told that she needed rest and peace and quiet. I had to minimise all stimulus. All the “New Baby” cards were taken down, all the presents put away. My wife was totally unable to make a decision, a simple question like “would you like rice or potatoes for tea” would send her into a spiral of confusion and doubt that could take hours to recover from. I quickly learnt not to ask her again.

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A few weeks ago I read “Touching Distance” by James Cracknell and Beverley Turner, they talk about James’ recovery from a traumatic brain injury (TBI) after he was knocked off his bike in the USA. So much of what Beverley said about the change in personality cause by the TBI resonated with how I felt about my wife in the months that followed her discharge from hospital. The incredibly bright, vivacious, funny & decisive woman I had fallen in love with at university was nowhere to be seen.

But, and it’s a very big but, there was light at the end of the tunnel. We had a truly brilliant Community Psychiatric Nurse. She visited every day and gradually over the next 6 months I could see the life returning to my wife’s eyes, her personality was coming back. We also were put in contact with a brilliant organisation called “Home Start”. They put us together with someone who would visit to offer practical help looking after the baby to give us a break. She was brilliant and has, in the years that followed, become a close personal friend and “honorary granny”.

So, after about 10 months we had reached a stage where my wife was probably 75% back to “normal”. The turning point was realising that she could laugh out loud without those around her worrying she was becoming manic. She was making decisions and generally feeling “in control”.

In 2007 we decided to have another baby. This was a pretty momentous decision as we were told there was a 50/50 chance of another episode. But we decided that, with the proper care plan in place, we would risk it. Our reasoning was that we knew the warning signs and could get help before things escalated. Our 2nd son was born in February 2008. The care plan swung into place immediately. We packed our eldest off to his grandparents for the week, my wife was given a private room at hospital where she would have complete rest. We had been told that if we reached 14 days without any symptoms then we would be OK. Needless to say, they were a pretty intense 2 weeks. We were also told to avoid all stimuli, so we had the bizarre situation of having a new baby, but not being able to celebrate. No cards, no presents, no visitors.

Day 14 was wonderful; we had made it and at last could begin the (muted) celebrations of a new baby. Now, 5 years later, we are good. My wife is the woman I met and fell in love with and is coping as well as any mother with two boys can.

I still find it difficult to talk about those months in 2004, writing this has not been easy, but it has been cathartic and is long overdue.