I lost my brother to a preventable suicide he fell through the cracks systemic failures by the trust an social care team under and the supported housing team were he lived. It’s the worst way to lose someone you can never prepare for, comprehend an understand why. I lost a baby born still born in 2002 I knew she was to be born stillborn due to severe spina bifida an hydrocephalus I knew as she took her last breath I’d hold her in my arms I’d kiss her on the head and I’d say goodbye, I lost my Grandad back in February 2017 I called in on the Morning of the Day he died to the hospital the Doctor told me that day when my Nanna came in they’d be stopping his medicine, taking his oxygen away he was getting put on an end of life Pathway, I went up to my mums saw my nanna an held her told her prepare for worst, I went to lighthouse academy my friends held me up, prayed with me I was preparing say goodbye. That night I went back to the hospital treatment had been stopped, as many family members as could were contacted, notified mad dashes to the hospital, he was surrounded by family held he was not in pain nor alone I got to say goodbye even though I wasn’t ready. Nothing can prepare you when you lose a loved one to Suicide because you can’t see it coming, you don’t expect if you knew or had a chance you’ld do everything in your power to stop from happening. This week I read in our legal teams argument for Article 2 systemic failings led to the events of my brother’s preventable suicide , I read that my brother had already passed when the paramedics got too him and probably had been a no of hours it breaks my heart to know he was lost, alone an in his final hours an until found had died that way. I wasn’t their to hold him, my mum didn’t get hold him even though an adult was her baby she did didn’t get that chance like I did with my baby somehow prepare an be their and like with grandad we knew we all surrounded wrapped round him he’ll have felt an known was loved I hate the feeling that losing my brother to a preventable suicide has done I hate knowing he may have felt unloved, unworthy, uncared for because he was. Losing a loved one to suicide is not only their lives lost but also part of you, your family dies too it feels strange, unnatural, not right, it’s broken, fractured, damaged your heart, the heart of your family dies too you get swamped into a dark hole, dark skies descend over all you know, life, joy gets zapped from you. I hate that I didn’t know, didn’t get chance stop, didnt get hold my hand out pull him back, I hate that I didn’t get say goodbye I hate that I don’t get angry at him, I hate that I can’t ask him why, I hate that I can’t bring myself to hate those who failed him, I hate I don’t have an axe to grind I hate that I want to give them a chance to learn lessons from his death I hate it’s been me, my family who held out that olive branch and I hate that they’re reluctant too take I hate that I can’t hate them want give them a chance I don’t understand why because they robbed me of my brother, my best friend , I want scream, yell call them murderers because of their systemic failings but I can’t because I know he deserves more, I know I’ve to give those a chance who failed him, I’ve to fight the legal system for article 2 to make his life matter, his memory, his life be remembered, he be remembered as someone who deserved help, be supported, cared for, a life worth saving and him not be just another life sadly lost to suicide, him not be a statitistic because he was worth more than that. Losing a loved one sadly to a preventable suicide flips your world upside down an know all can do is try make sense off and fit the jigsaw puzzle pieces together that led to that day to understand why and then with that completed puzzle find a way grieve, mourn say goodbye an try prevent someone else from sadly taking their live, give those that failed ideas to come up with pathways, measures to build safety nets to try ensure dosent happen again, I don’t have anyone can go to that can talk to about so I share my feelings here in my blog I know people struggle to talk to you about, ask how help, I know because I struggle with too. I hope that people reading who are in same place my brother was would contact me so I can help you so you don’t do what my brother did as you are worth more than that, for those that have lost a loved one to suicide to feel free contact me you are not alone it may feel it but I know the pain you feeling I feel it too, to Services, councils, NHS trusts social care providers that want make a difference to people affected by addiction, mental health and homelessness and put mental health on their patient safety strategies or looking at suicide prevention of people society turns their back on we’re culture around people with combined needs or are seen as unsafeable or attitudes around personality disorders needs challenging or your pathways not inclusive your not getting everyone on one or you need improve your community contact me if you genuinely want learn knock on my door because like I said lives like my brother’s matter let’s work together an make a difference I can’t bring him back but his memory, story can help save life’s.
The buzz word in Mental Health Stigma, we must speak out, we must were it label it lovely smiley faces on twitter at the moment I have Mental Health its ok say have , it’s ok you get help. I salute you for being proud, I salute your optimism, I used be loud, be proud open about my experiences was told was inspiring it boosted my confidence, lifted my self esteem a short lived adrenaline buzz but sadly no changes came were made, society gets an understands stigma are open to help they just don’t know we’re go, were access and get doors opened to care, Joe bloggs on the street does care, does understand I usually knows someone or even they themselves affected by. I don’t engage as much now with speaking out campaigns, wear my label on my sleeve now because I lost my brother to a preventable suicide he had both Mental Health and Substance Misuse he didn’t face stigma from his family or friends it was from the services that were meant to support him those that are now behind twitter campaigns like #I have Mental Health, I saw my brother at times at crisis took him to A and E be told he’s to ask for help is not sat in A n E over 8 hours in height of crisis not asking for help, when did ask for got turned away past from pillar to post, Even when stopped taking drugs was always told “it’s the drugs” it’s the drugs. Never asked him why he ever became an addict, Never explored his childhood upbringing, never asked Why if did ask Why they’d have seen then yes it was because of the Mental Health but they never did they stigmatised because of the substance misuse. My brother was stigmatised because of a Dx he was given Anti Social Personality Disorder the condition shut doors to access to recovery, was probably why assessments for suspected learning disability got passed up, passed up not just one professional that suspected was most who came into contact with him, why did you not do when came to you when spoke out said I’m here I need help, his protector Dennis a doll became his tormentor took his identity offer, the doll got into his head told Tim what do we his family asked for help knew he possibly wasn’t mentally ok even asked for support an help but got turned away. I do have Mental Health needs myself an manage I recognised certain things in my brother, Hearing Voices, Dissociative Identity, Depression, Obsessive an Compulsive Behaviour, self harming because he’d felt lost control needed help was not helped he openly said had but didn’t get so is why know I struggle support an engage with #IhaveMentalHealth. I’m only doing this blog because need rant get my upset, anger, frustrations out I’ve to do that to manage mine so don’t obsess about, get worked up about, have it bring me down and me turn on myself internalise and berate myself for not speaking out an challenging the #IhaveMentalHealth. The angry voice inside me wants say it’s patronising, that those that failed in my brother’s care murdered my brother they didn’t carry it out but nor did they step in an prevent it’s too late now for sorry. Campaigns like #I have Mental health are belittling to individuals and families affected an they’re belittled by the association of the unnecessary use of the word stigma, we must talk about yes stigma led to my brother doing what did but it wasn’t because of lack of understanding but care for all those professionals sharing their photos, retweeting posts ask yourselves why are you sharing, retweeting are you actually as a result of that post go out make a direct action, something that does get help, get changes made and actually stand up make a difference it’s time moved on from speaking out an do for those brave enough do, speak out, do for those who ask for help and on my post look at the photo and do for my brother Tim someone who said #IhaveMentalHealth help me the person whose voice not heard and do for my mum, my siblings an our children who have to live with his loss, live with pain knowing asked for help and enough not done because we don’t want people going through what we are.
I was once optimistic Services would improve and improve for the better initiatives an policies around crisis care, no decisions about me made without me were made the NHS an services were to be Liberated the Recovery Bus, Coproduction Bus and Person Centred Care Bus rolled up into town. Did they make a difference, Did they leave people liberated and will the new 5 year forward initiative make a lasting impact I’m sceptical it won’t because I once believed that Services Could Change Improve Lives, Help individuals Regain Control and put the person an those close to them at the centre and provide a whole person approach attitude to care. I was wrong and my optimism that Services Could do that proved to be fatal. In the last few weeks the media has been highlighting cases were deaths are been investigated and a trust is to be investigated in one case. I’ve discovered that my family is not alone as we too are fighting for answers to how our loved one could have lost his life he did not lose his life however in an inpatient setting he lost his in a transitional housing unit a unit that’s supposed to provide care for vulnerable adults who were in crisis, needed mh support, support with homelessness an substance misuse. We put our loved ones care in the trust of services an the local authority that they would ensure an provide the care an support he needed.
We sadly got it wrong we like many other families now are fighting for answers we’ve had reach out too advocacy support, lodge formal NHS complaints, left outside the serious incident review process yet had our hearts ripped wide opened when had the people running come visit us at my mums family home but yet still no answers no been asked did we want input nor told what they will learn or put in place been sent a document though however that supposedly has in can we sign off on it. How can we if you’ve not sat gone through it with us or had us been involved in any of the process no one can make a decision on something not involved in but shouldn’t we have been after all we’re searching for answers to why, why our loved ones death was not prevented. We had to reach out to a charity Inquest because we didn’t know anything about what to expect, how to be involved the types of inquests and if not for them we wouldn’t have been put in touch with a solicitor an barrister but we’ve had to meet criteria for Legal Aid an that only covered representation to help prepare the case for inquest we then had to apply for separate funding for a grant to have barrister representation at the inquest but yet the Services who failed automatically have the money behind them to represent them but for families they have to search an find that help an that’s sad it’s also sad we don’t get automatically represented as do the services as it’s a live been lost here a life that mattered and a death that should be held accountable for and answers need to be answered how could it have happened and why and was enough done theirs also issue you had a duty of care an families put that trust in you and that is why then you become accountable because that trust was put in you. As a family member I witnessed my loved one passed from pillar to post, told to ask for help an when did told couldn’t help so why tell him ask for, I saw pleas from my family ignored, I saw my loved one slowly become even more invisible, dehumanised, made feel unworthy an in end not listened too, not cared for or supported that’s hard to face an accept especiallly when don’t expect from services that were supposed to be their an provide that. Sadly my loved ones passing won’t be the last an that too is hard to accept because you then wonder what will they learn from the incident report carried out an what will they learn from the impending inquest because sadly my brother won’t be last. I also suspect under the area he came under he was sadly not the only individual failed and probably other families going through what we are too. Whilst awaiting I see initiatives around patient safety, suicide prevention an the new buzz one 5 year forward. Will they make a difference I suspect not it’s just a recycled blue print that for last few years keep rewording add a few more charts an statistics an wow a new policy or charter to follow sadly not worth paper printed out on because sadly lives are continuously been failed, no one been held accountable, no lessons been learned from, their lives not mattering. Services are still been under funded, cuts still been made, workforces at breaking point, charity sector organisations stepping up and lifting the burden from you holding you up their the ones trying the best but are not given the credit for nor do you liase with them and assist in supporting someone you just quickly like pass someone on so not on your case load yet you need to work with them they can’t do it all alone but yet as with families you isolate them too. Crisis Care is shocking too the crisis care concordat act did that make a difference if did my brother would not have been turned away twice an also got in housing were living, but sadly their isn’t enough beds in or out of are, not enough home intervention teams and respite places available an thing we’re my brother lived is only 8 crisis beds available. Wasn’t the crisis care concordat act supposed to address that. Vulnerable individuals languish in police cell’s awaiting mh assessment some end up in the prison system locked up unfairly because at crisis committed offences but because not enough beds professionals say can see unwell but doesn’t warrant admission an so under public nuisance an anti social activity get imprisoned as well as many other offences during my brother’s care that too happened just impeded him further. It makes you wonder why as a society are we allowing that to happen why is the police and judiciary system allowing that are they powerless to act against the services can’t they enforce services to act especially when they clearly know difference between a vulnerable an mentally unwell person an hardened criminal. Why is it that over the years what’s published, guidelines not implemented you’ll tweet about, talk about have development meetings about but not implement, no changes be made and very little service improvement. Yet you market yourselves, give fancy awards, and too have buzz weeks fab change week the latest so what will you do what change an implement will you make what will you do to prevent lives been lost, Will you make your services inclusive to all, stop cutting services that matter, work with organisations lifting you up, will you stop labelling an stigmatising people under your care, will you stop turning people away because don’t fit your Dx an recovery models more importantly support loved ones who’ve lost someone under your care. Families shouldn’t have to fight for answers, set up justice groups an campaigns and have to search an fight for the answers because they need compassion an care an time to grieve they don’t just deserve empathy but also deserve be treated with dignity, respect and upmost of all they need the answers so can grief, hate say have closure an make pretending moving on with life’s easier. It’s also now time ask why in this day an age why are services still continuing to fail an sadly lives been lost.
On Wednesday I’m going to Westminster with National Mind an the MP’s to their bring to the table event to discuss Mental Health Going Forward and what needs be done, theirs lots been highlighted about austerity, of postcode lottery, even the diagnosis lottery an conveyor belt. These issues are complex, challenging and have crippling impact to individuals affected by Mental Health. I’ve been asked to represent Yorkshire an Humber I will to an extent highlight my brother’s death and failings in his care. I have also spoke with my friends at Lighthouse Academy in Leeds an to my friends at Healthy Minds in Calderdale and I was alarmed at some of concerns raised and highlighted and that as much as we shout out for better mental health care we are so far from it.
Services are been closed without proper consultation to the service users that access and they’re unable be referred into alternative therapies as they don’t fit the recovery timescales, diagnosis to complex been told all has been to try help them and worst of all they’re now struggling find private alternatives because that one thing that made a difference has been took away.
For some accessing treatment and support and getting the foot in the door is hard specifically for rehab for overcoming addiction and I see regularly individuals, friends, little communities forming trying to support each other overcoming addiction and it breaks my heart to see them stumble because you know they are desperately trying following things like routine, keep busy, avoid temptation but the underlying issues not addressed, no support to detox, withdraw and overcome addiction and the space an Time and safe place to do and rehab is what would make all that difference but for some they are sadly overlooked, the waiting lists are too long that people are told waits of up to 2 years no point referring you in. Why then are their no alternatives why are we not demanding more specialised services why are we overlooking this vulnerable client group. Is it because they don’t deserve help, is it because society says they don’t fit just as services say we can’t help because we can’t fit you into a box. Austerity is penalising these individuals setting them up to fail be persecuted, isolated, attacked and further dehumanised and sadly why so many life’s are lost and in today’s society we should be holding up those most vulnerable.
People’s mental wellbeing is been impacted by austerity people know it’s good to volunteer, want to volunteer are told by professionals do it will aid your recovery and then they do volunteer and do little bits building themselves up, getting skills may not necessarily have an then bam DWP is taking them of benefits that awarded because of their conditions an impact has an been told well you can volunteer you can go on Job seekers or some universal credit been set up to fail not supported sanctioned if don’t apply for x amount of Jobs, write cvs do job searches and get x amount of interviews and many get passed up, employers won’t take on an so they get hit with sanction after sanction money stopped go without food, heating, hot water, basic provisions, spiral further into debt trying keep a roof over heads and the pressure of and lacking basic needs is detrimental to their health and we are turning our backs on them what are we doing to challenge the hardest hit be supported we’re are we fighting for their right to health equality not inequality.
One guy mentioned to me he wanted work volunteer be phased an supported in he’s not worked in a long time just finding his feet got placed on Job Seekers could I ask for more supported employment programmes I wished I could but sadly those services are few an far between an waiting lists get on are high so for him I pray he doesn’t stumble because of the dwp system setting people up to fail. DWP shouldn’t be allowed treat people in the inhumane way they are they are having a detrimental impact on health.
Mental Health is impacted by physical, housing, social, financial influences, influences that government need address especially if mental health support has a chance to change improve an save lives as part of the 5 year forward strategy on Wednesday when I take people’s voices to the table I’ll try ensure heard because I can’t sit back an watch the most vulnerable be forgot about anymore.
On social Media I’ve seen people debating Patient Safety in relation to my brother I’ve realised that more could have been done for him and that Patient Safety did not come into his care. To help me come to terms with his passing I’ve to understand an process why and find the solutions to could have what made a difference it is what manages my self care an also putting pen to paper gets my thoughts an ideas out an mapped out. So today while I’ve had an empty house an cleared up house listening to the song that played at the start of my brother’s funeral I listened to the song ” How to Save A Life by the Fray and asked myself that question. I asked myself how Services from a Patient Safety point of View could have saved a Life and been all Tim needed and here’s what I came up with.
1.See me as a Person
2.See my Circumstances
3.Include my family and Friends in my Care
4.All Services needed to work together an not in Isolation
5. Choice an Opportunities
6. The important one Listen When I ask 4 Help
7.Judgement Free Care
8.Check my Records be it Safeguarding,Crisis,Suicide Prevention,Care Plans and Recovery Plans are all up to date, working an implemented an everyone including Me an My Family were made aware off.
9.Take Responsibility Don’t keep passing me to service to service from Pillar to Post.
10. Carry out All assessments
11. Don’t exclude me from Services Because of Labels Attached to Me
12. Support through Major transitions
13 Finally Compassion an Understanding as Human Beings we are all entitled to having that met.
These things don’t seem like much but to my brother they’d have made a big difference and he’d still be here for all those looking at Patient Safety please look at this and ask yourselves could you have been All Tim Needed.
Theirs been lots in the media debating the pro’s an cons of taking Medication for Depression, BBC Panorama highlighted the dangerous of an how individuals became mass murderer’s an that’s in extremities.
I suffer from a Dysthmic Disorder in layman terms a neurotic mood disorder, Depression,Anxiety, Obsessive and Compulsive Behaviours, I have complex PTSD hear voices and Dissociate.
I don’t take medication for my conditions I used to they were harmful for my physical health I ballooned to just under 19 stone was a walking zombie did not interact, engage the world passed in a blur and still I was seen as disengaging by services it wasn’t that I was disengaging but the needs completely shut of all my receptors so I couldn’t engage.
The conditions I have are the result of Childhood Abuse, Losing a Child Born Still Born and the result of been a revolving door patient on an off throughout my teens to my early thirties. The medications I were on varied from Anti-Deppresant’s, Mood Stabilizer’s, Anti-Psychotics, Relaxant’s and Sleeping Pills. The medications just sedated my so called behaviours to me their now just my traits be it survival, be it instinct, be it my defensive mechanisms. Dissociation at times though can be a pain when things in my locked box want to surface as that hits when am at my most vulnerable an most risk and I’ve just to ride it out.
It’s been hard not been on medication and not easy but I try face each day as I can medication will only plaster over the scars of my past, therapy can help me address but the unstable emotions and how I handle things they’re what I’ve to learn to address, I recently nearly ended up back on medication I struggled with coping with my brother’s passing thought long an hard and in my heart knew wrong as it may take the pain away numb it but eventually have to face it and so may as well fight may way through it now but also the anger side of my cptsd has come in handy as I’m using that part of my grieve to fight for him wished did more when he was alive, also if agreed go back on the slow cocktail of men’s would build up again I’d be talked into needing more for different things and different behaviours an probably extra Dx and my son he needs me, he needs me to be strong for him be brave for him most importantly be alert and functioning and be all he needs so as hard as the days are I throw myself into It theirs days I feel mentally drained, exhausted, on edge, thoughts scrambling but for my son I attack each day, I also do for my family, I do for my brother too as he so wanted overcome his past.
Medication can help mask things and give me a rest from but in the end they’ll stop me from seeing the beauty in the world even though theirs too sadness in it, the voice i thought so hard to re-find would too agin be lost and one thing I’ll always tell my son fight for what you want well if I’m not living it he can’t practice it.
Don’t get me wrong it’s not easy theirs days when I can just drag myself up ready, Myles though he’s always immaculate, theirs days I’ve snapped my anger lids burst an that’s not been good for person who got brunt off, theirs days I have just crumbled just broke look liked a car wreck and all around gets to much and times to preserve myself I’ve to shut out the world keep my bubble to myself .
I’m not telling people to stop taking mess nor if they help you to stop believing that they don’t an to stop.
I’m asking that as I respect medications for you please respect though it’s not for me an in fact has been life altering an harmful an I don’t want that for me, I also need you to respect that just because I say no also does not mean I don’t have my conditions an my experiences an opinions like well you can’t be that bad if you don’t take because I can be.
The brave face people see is just a mask as if accepted people a) don’t get or understand me so I give up trying explain, b) if I don’t try I give up an where does that leave my son an family and c) if I go on meds the world will be shut out again.
If their was better monitoring of my help, safeguards an provisions that stopped me going on more an more mess then maybe, but I know for me I have to address my pain be it therapy, be it pretending life’s ok or be it writing my blog like now, I’m exploring having faith in my life that’s been a challenge an battle of perseverance, I throw myself into soft play just as much as Myles an that s my anger energy, we do crafts, go for walks we play the child in me likes that as that’s reminded sometimes life is good, being an activist for awhile was hard but then I missed it so am slowly going to re-dip my toes in the water and look to do again as my heart an a part within me missed that an so listening to myself keeps me going.
I suppose because I didn’t feel listened too an knowing my brother wasn’t listened to is why I’ll always shy away from medication in time that may change I’ve to meet that one person who will listen and give me the perfect care package so till then I’ve just got to listen to myself.
Whilst I do that though please don’t shame me an belittle my depression, my pain just as I don’t pill-shame you an vocalise the drugs are bad. It is these debates that create divides in the mh community an we need to be supporting each other and each getting the support that works it’s time focus on getting it right for everyone as at present services aren’t working and we need to work together to get that so let’s #endthepillsdebate.
How do you help someone have hope an believe in themselves when they have been wrote of with a Dx of Anti-Social Personality Disorder.
Anti- Social Personality Disorder is defined as sometimes been called Sociopathy, a mental condition in which a person consistently shows no regard for right or wrong, ignores the feelings of others, People with antisocial personality disorder tend to antagonise, manipulate, treat others harshly or with callous indifference. They show no remorse for their Behaviour.
(Taken from NHS Choices)
Doesn’t make nice reading,, Does not look like a. Dx that someone would get support an help for, Dose not inspire hope for a shot at recovery nor Does it ask the important why an individual may be this way, what factors have contributed to, what’s happened in certain situations, Does not take into consideration an individual may have an Alternative Personality or Part and what if it’s the part that’s the anti-social and not the individuals themselves is it then helpful to give that person a Dx of Anti-Social Personality Disorder. I’d go with a big fat no because you then exclude that person from the right help an support because the Dx gets people wrote off.,
My brother Timothy in his notes had this listed he did not have Anti-Social Personality Disorder he himself wasn’t the things highlighted above. Timothy until became Mentally unwell was hard-working, would help anybody out, do anything for anyone this was what sometimes got him then into trouble he’d accept responsibility for other people’s behaviour and actions that to me showed he understood right an wrong if he could do that, My brother Tim nor was manipulative or treat others harshly, Tim was a protector, a supporter, a friend and amazing big brother, when my son was first born he waited in Leeds city centre after finishing work 6 hours to see his nephew and god son for visiting hours to start because he so desperately wanted see him, my sister who has MS her 2nd child was born on the toilet he was their with my mum on hand to help my mum help look after both my sister an baby and get sorted the ambulance to have them rushed to be checked out doesn’t sound like a sociopath does it, In 2002 I lost a child the day after my little girls passing he was their by my side supporting me through my pain doesn’t sound like someone does he that doesn’t care for others or have no feelings for does it you could probably safely say Timothy did not have Anti-Social Personality Disorder.
Timothy wasn’t perfect nor was he bad he was at times easily manipulated himself and yes easily influenced and yes unfortunately did take drugs but Timothy did not grow up in a perfect background, perfect home, it was far from growing up his childhood was more survival based but that’s for another Time. Also growing up with a father as an Alcoholic probably played a factor in why turned to drugs but that too is a separate debate but also a factor consider, I hate saying too both my brother an I were susceptible to MH as was on our Fathers side of the family and traumas in our lives an how we dealt with led to us both be affected by.
In June/July 2013 my brother Tim went missing an in that time something happened we don’t know what an the Timothy that was found was not Timothy, Timothy had become Dennis, Dennis was not just a doll that he started carrying about, Dennis could be described as the above person the person with the Anti-Social Personality Disorder, Dennis made Tim a danger to himself, Dennis was never an issues Services addressed, took into consideration, Dennis was a part, the voice inside tims head, Dennis had took hold of the individual the person, Timothy. We tried to get services to get help regarding the Dennis part acknowledge it address the voices, address that Tim was Tim no more get him therapy but it was never addressed or acknowledge yet recorded in his notes. We as a family always told Services an his key worker did too when Tim mentions Dennis he’s a risk to himself not other’s not addressing Dennis enabled it to take over Tim so why he never stood a fighting chance.
Tim did try recover, regain control attended Hollybush, Lighthouse, George’s Crypt they describe Tim as Tim was but with a Doll in his man bag, they described him as friendly, helpful, loved getting involved in his art, doing jobs and too was quite liked at times just blend into the group or sit in the corner read his paper. Following his Facebook posts, seeing him at mums he was alive Tim again always tried getting us go down £1 dinner, Robynn would love the gardens were he’d been helping at the kids would enjoy too, This does not sound like someone who was manipulative, dangerous, did not know right from wrong, his worry though about moving from were he was to somewhere new he worried he’d fall through cracks an yes sadly it came true,
A diagnosis of Anti-Social Personality Disorder shut doors to Assessments for Psychological Therapy, Referal to see if he had a Dissociative Identity i.e Dennis, recommendations for Hearing Voices groups, recovery focused groups, shut the door to referral to a rehab and recovery unit to address all his needs, and why so many other assessments never got done, why plans became out dated and why became dependent on the few people who tried.
If you go back an look at how NHS Choices Defines Anti-Social Personality Disorder reflect on how it’s defined what stands out for me Sociopath, Manipulative, not knowing right from wrong sounds like they’re dangerous a risk to others and individuals do get made to feel that imagine if the Dx was wrong and the implications it then will have on a person surely then that has a detrimental impact an potential human right breach when impacts on their lives an sadly that does happen since losing Tim I’ve met people he met on his journey an seen how impacted them an too those people I would say did not have because they’ve carried me through my storm an been a support, a friend and I’m streetwise and an abuse survivour too and have a 6th sense who’s ok an who’s not.
Ask yourself if you saw Anti-Social Personality Disorder on someone’s notes how would you see them, treat them, what help you would give them, if they were at crisis would you realise that help them if they’re not ok, would you even help them but more importantly how you view the Dx and would that influence you.
Antisocial personality disorder potentially labels people off Antisocial personality Disorder should really only be used in extreme cases and as a last resort when gone through every other assessment an diagnosis an no interventions have an impact.
I’m only someone who’s lived experience, I’m someone who was someone’s sister an know am friends with people who have the Dx an if I can see is a harmful Dx one that does not in anyway inspire hope, recovery, regain an control then sureley you should too and turn your back on Dx Anti-Social Personality Disorder an try look for an Alternative too.
More lives will be saved as a result, More individuals will be better supported, No one will fall through the cracks an be turned away for help.