I came across this article on Justice for mothers: http://justice4mothers.wordpress.com

It’s a fantastic piece of research and well worth a read…..

One of the pieces of research shows that mothers who don’t have their children cope better when it is their choice to hand over the parenting to the father; those who don’t choose their role as the non-custodial parent find it much harder to cope with than those who do. That’s a no-brainer really…..

My ex husband has decided that my son needs orthodontry treatment and so has gone ahead – without my knowledge or consent – to taking him to the orthodontist and getting him braces fitted.

When I heard of this (from my son, not from my ex or from his nanny), I wrote to my ex to ask him why he had done this without my consent and asking him for details of the orthodontist so that I can ask various questions about my son’s treatment.

My ex has not replied to my email and has simply gone ahead and has had the treatment started – braces fixed.

Now I’m really annoyed about this. I agree that my son should have the braces fitted but that’s not the point. The point is that my exhusband had no right to go ahead and give medical treatment to one of our children without my consent. I have parental responsibility, which means:

What is parental responsibility?

While the law does not define in detail what parental responsibility is, the following list sets out the key roles given on the government website: http://www.direct.gov.uk/en/Parents/ParentsRights/DG_4002954

  • providing a home for the child
  • having contact with and living with the child
  • protecting and maintaining the child
  • disciplining the child
  • choosing and providing for the child’s education
  • determining the religion of the child
  • agreeing to the child’s medical treatment
  • naming the child and agreeing to any change of the child’s name
  • accompanying the child outside the UK and agreeing to the child’s emigration, should the issue arise
  • being responsible for the child’s property
  • appointing a guardian for the child, if necessary
  • allowing confidential information about the child to be disclosed
For all you parents out there, you have the right to a say in all the above issues. If you can’t agree, then ultimately it is a matter for a Court to decide.
In the meantime, I’ve asked for my diabetic son to have counseling by the diabetic child psychologist who has previously counseled  our son for his psychological and emotional problems he suffers with whilst coping with his diabetes (he’s only 8, bless him and has had it since he was 2). He is being teased about his diabetes at school and has told me that he hates his illness and just wants “2 days without having diabetes mummy”. He has become very resentful about the fact that he is only 1 of a very small percent of children who get it and is annoyed that he has had the bad luck of getting it.
It is my son’s rights as a human being to have the medical treatment that he wants and needs. He has asked for psychological help, so who has the final say? If it is the parent’s over the voice of their child, is that acceptable? Can the parents simply override his human rights to medical treatment? I will have to look into the United Nations Convention on the rights of children.
My ex has now told the diabetes team that he will not consent to our son receiving this counseling but hasn’t given any reasons why.
I am now going to have to fight yet another little battle in this ongoing tranche of autocratic behaviour on his part…….

I can’t bear this. The emptiness of an empty house; I was goint to call it a “home” but without my children, the place I’m living in doesn’t feel like home. No laughing, no shouting, no arguing, no giggling, no crying, no recorder playing, no arguing over the computer, no one asking for a cuggle, or a snuggle, or a hug or telling me that they love me (”to the moon and stars and back againm,mummy”) that they love me, that they miss me, that they want to sit next to me at the dinner table, that they want to tell me about their day at school, about the fights in the playground, about the lesson they found boring, about the exciting new game they’ve invented, about the picture they’ve just drawn, about the pig they’re making in pottery, about the lunch that they didn’t like, about the cheating in the maths test…………………

No little person creeping into my room in the depths of night scared from a nightmare and wanting to snuggle up to mummy to comfort them and take away their fear.

Nobody running into my room in the morning to tell me that they managed to tie their shoe laces for the first time, that they’ve got themselves dressed without being asked, to ask me for their favourite breakfast, to ask me if they can sit next to me at the table as it’s their turn to sit next to me…..No chasing around trying to find a mislaid tie or a beret or the other plimsoll……No practising spellings or times tables over the breakfast table, answering the hundredth “why” question or explaining why God doesn’t have a mummy, or trying to work out how far we are away from the Sun, or why some people are mean to each other……..or why mummy and daddy can barely talk to each other…….or why they can’t see me more often…..or why the CAFCASS think mummy can’t see them more often…..

Nobody.

Nothing.

Nothing.

Just an empty house. The television adverts show me all the family adverts: adverts for family cars, adverts for washing your children’s dirty clothes, family holidays, family home insurance, children’s medicines to stop them coughing at night, calpol to help your baby sleep………I have been deprived of my “Right to live a family life” which, by the way (or at least in my case its “by the way”) is one of the Rights set out in the Human Rights Act…..

No family for me anymore.

Just an empty house. And silence.

I can’t bear it – it hurts too much…….It really hurts….

 http://www.mind.org.uk/Information/Legal/Legal+briefing+The+Human+Rights+Act+1998.htm 

I’m lying in bed surrounded by my children’s cuddly toys – it’s the nearest I can get to having my children with me. The teddies smell of my children – some even have slightly discoloured bits where one of the children has spilt something on their teddy as they’ve dragged it around with them. Last count, there are around 30 cuddly toys in my room – all belonging to them. They’re crazy about them. There are leopards, lions, sheep, rabbits, bears, glow bears, cats…….all sorts, shapes, sizes, colours. All of them much loved.

There here with me because the children want me to have something to cuddle when they’re away from me. Each time they come here to me, they bring different ones so that the teddys do a “rota” system: the teddies spend a few weeks here, then a few weeks at their dads…………

My son gave me his favourite rabbit to cuddle whilst he’s gone. When I objected, he said it was the only rabbit that had enough of his love in it to keep me going – he wanted his rabbit to love me whilst he’s gone. He took away another new one and said that I could have the new one once he’d loved it for a bit so that it was filled with his love and then I could cuddle up to the newly love-filled rabbit……Rather like the duracell bunny, I guess….

Only problem is, these teddies don’t cuddle back. They don’t bring tears of laughter to my eyes when we swap a silly joke or make up a story. They don’t have warm, loving hands that hold mine. They don’t tease and argue and fight and joke and laugh and cry  and sneeze and jump and muck about and giggle helplessly. They don’t look at me with love, kindness and care; I can’t even bear to look into their glassy, cold eyes and see………….nothing.

They’re empty in truth.

And that’s what I am without my children.

Well, somehow I knew it was going to happen – the continuing excuses as to why my husband still thinks I shouldn’t be able to see the kids………

In April,I was forced to leave the family home following my husbands Occupation Order to get me out on the basis that my presence in the house was causing the children “significant harm”. I didn’t agree that it was my “continuing presence” that was causing them harm, but the arguing and bickering was distressing for them. My own view though was that it would be even more distressing for them if I left, especially without another home to go to and for them to call their own too. But I was advised by my lawyers that the Judge would force me to go so, rather than spending another £20,000 of wasted legal fees, I was told I should go. So I did, very unhappily. Not surprisingly the children were terribly upset. They told me they kept going into my empty room and couldn’t believe that I was gone………..and so was my bed that they cuddled up to me in.

However, I have Shared Residency Order which states that the children are to live with me for half the holidays and every other weekend during term time, and another afternoon or possibly two each week for the mother as agreed between the parties. So my solicitors wrote to his, suggesting that the kids and I should see each other every Tuesday and Thursday afternoon after school – an arrangement which the Judge had said in the Court Order that she would “welcome” but it would have to be with agreement by both parents.

However, I thought at the time the Order was made that the reality was that my husband wouldn’t agree to it and, sure enough, he is still refusing to agree to an afternoon after school so that the kids and I can see each other. His reasons are still the same as they were 6 months ago: “the children need routine and stability.” Well, surely the same afternoon each week for contact is “routine”. Surely the children will feel more “stable” if they see their mother once a week? “The children have a very important year ahead of them at school.” Oh, and not seeing their mother is going to help them with that??

Where are the children’s rights here? Or their Human Right to have a family life (one of the Rights set out under the Human Rights Act). Or my “mother’s rights”…..Who says there are any such things???

Herein lies one of the biggest problems with a Court Order in Family Law which leaves any kind of extra time with either parent to the agreement between them: it was so obvious to me that my husband wasn’t going to agree to any extra time. When he and his barrister both made oral promises to the Judge that he would definitely encourage and facilitate as much time as possible with me, I could see through his charm, but the Judge was convinced by him. The Judge, however, didn’t go as far as to enshrine any right of the kids to see me mid-week so my requests for more time will continue to be met with refusal.

(To give him his due, he did allow the kids and I to celebrate my birthday together last Thursday which was absolutely brilliant! They got me a Scooby Doo birthday cake with more candles than space on his vast face………yes, I’m ancient……Best birthday I’d had in a very long time. Just me and the kids. Bliss). But that is one rare occasion of “extra” time.

What can I do about it?

I will keep asking, just keep writing, keep writing, keep writing with the same request hoping that he will eventually realise that it isn’t kind to either the kids or me to keep us separated from each other.

The only other option is to go back to the Judge and ask her to adjudicate again on the issue of these after school times. My husband must surely be expecting that I will have to do this; he can’t think that I wouldn’t want to keep asking to see them or that the kids won’t keep asking to see me?  It makes so much more sense though to just be sensible rather than going back to Court again. That would be distressing for all of us, but maybe not as distressing as the continuing absence of my children and I being able to spend time together. 

The thing is, my Bipolar is completely under control and has been ever since before the Court hearing started; I have repeatedly been given the all clear by my psychiatrist who says I am perfectly stable. So it’s not like I’m manic or hypomanic or severely depressed or alcoholic or abusive or anything else – I’m just a really decent, loving mum who wants to see her kids and, most of all, give them loads of love and hugs………..I’ve even told him that he can insist on making me have a psychiatric assessment of my mental health every 6-8 weeks if he needs any reassurance, so why’s he refusing to take me up on it?

His latest reasons are that I have been “turning up at the kids schools and this has distressed them.” What I have, in fact, been doing, is to attend every single school event that I can so that I get to look at the kids even if I can’t hug them or talk with them. So I go to all the school masses, services, sports events, coffee mornings, kids parties etc. I am fully legally entitled to go to these, so I’m not just “turning up”. Also the kids want me there at their sports matches, their masses, concerts etc. The only reason they are distressed is because they’re not seeing enough of me, not because I’m there!

He then cites the fact that on around 3-4 ocasions, I have dropped the children back between 15mins – 1 hour late on a Sunday night after my long drive back up to Kingston through Sunday afternoon, London-bound traffic. This is “proof” that I am unreliable and irresponsible……………..clearly.

So, I just have to keep asking. Most importantly, the kids keep asking me why they can’t see me more often and they ask me to ask him. So I do. And he says no. So I ask again. And he says no. When the children ask me why he says no, I simply have to say “I don’t know why, you’ll need to ask him yourself.” What else can I say?

My eldest daughter (frighteningly mature and perceptive for her age) said: “Mummy, you have to stand up to him. If you don’t, he’ll just keep treating you badly and ignoring you. If you let him get away with it, he’ll carry on doing it. You can’t let him carry on like this.”

Well, that may be the truth and I want to stand up to him for her and my sake. But just how do you stand up to a parent who is determined to put you down and stamp on you? I can only think that I have to be as level headed as possible and appeal to his legal/rational mind. So I keep writing to him.

Unfortunately, due to the incredibly strategic manner in which my husband ran his case (he’s the head of a litigation department, so he knows all the tactics), I have learnt to ensure that there’s a paper trail of correspondence so that he can’t claim that I haven’t requested time with the kids.  I send the emails with the “Read receipt” and “Delivery report” option so that he can’t say that he didn’t receive it (which he has said in the past about emails that he’s denied receiving). When he doesn’t answer, I just keep forwarding the email asking him to reply. If this goes back to Court then I will have all my requests documented that I have continually asked to see the kids and he is persistently refusing. By asking him to reply by email, he has to put his reasons down in writing. Which of course are then also documented so there is no way that he can argue that he didn’t give the reasons that he has, in fact, given. Our whole relationship has always been plagued with the “you said “x”" , “no I didn’t – I said “y”", “no you didn’t” etc. We even discussed this in our 2 and a half years at Relate: how can 2 people sharing a conversation remember totally different things about what was said, in what tone, with what expression etc? Even before we divorced, we agreed that we would write things down in emails to send to each other so that we had a record of what each of us had said in a vain hope of avoiding rows about who said what. Clearly it didn’t work, hence the divorce……..!

Oh, and I forward all the emails and the replies to my lawyer for safe keeping in case there’s any denial that these requests were ever made……………….

However, I am no longer able to afford to instruct a barrister to represent me; therefore I am a “litigant in person”and don’t have to pay any more legal fees. That being the case, any correspondence or further Court applications won’t cost me any more money so I don’t have to worry about the fees. I think my husband will still be paying for his though……

Any other parents out there also having similar problems? Did any of you manage to find a clever way of solving this issue?

Please let me know or just keep hoping for me……………

My children keep asking me this question: “Why won’t the court listen to what we want mummy? When will they have to listen to what we want? When can we decide who we want to live with?”

My son said: “I wish your psychiatrist hadn’t told the Court that you have Bipolar, mummy. Then we would still have you looking after us.”

They don’t understand why the Court has not listened to what they want or, in their eyes, even asked them what they want. They want to know why they can’t write to the Court or stand up in Court and be listened to. I have promised them that I will find out what their rights are………..

As I do my research, I will post up articles that seem to be helpful on various subjects. Here’s what the website “Compact law” says about the Children’s Voice:

The Children’s Voice

    Sometimes a court may decide that the children should be represented themselves, the person who represents the children is the Childrens’ Guardian. This is a person selected from a special panel who will have experience of dealing with and advising children. They may have a social service background or be ex-probation officers. They may speak to the children and find out what the children want.

    Your children are also allowed to have their own solicitor, the Children Act gives children a voice. A Children’s Guardian will usually appoint a solicitor to act for the children, but the children can also instruct their own solicitor.

    It can be very hard for the judge to make a decision when he or she does not know you or your partner and has not met the children. The judge may appoint someone to be the courts eyes and ears, this person is called the “Court Welfare Officer”. They are usually members of the Probation Service and are attached to the Family Court Service.

    They will often visit you and your partner and speak to the children and then write a report for the court, in which they can make suggestions.

    The judge does not have to do what the Court Welfare Officer suggests in his or her report.

    If you are not happy with the report and argue against it, the judge may accept what you say. You should co-operate with the Court Welfare Officer if you can, they are not there to take sides, but that does not mean that you have to agree with everything they say.

    The judge can decide to speak to the children personally. However many judges do not like to do this as the children often get upset, because they do not want to be disloyal to one of their parents.

    Also, part of the job of the Court Welfare Officer is to talk to the children to find out where they want to live and which parent they want to see.

    The judge may feel it is better for the Court Welfare Officer to find out the children’s views.

    If a child is thought to be old enough to understand the court proceedings their views will be taken into account. Children aged 12 or over are usually thought to be old enough to know what they want. The judge can decide to listen to the children or the judge can make the decision for the children.

    The only principal the court has to consider is what would be in the best interests of the children.

http://www.compactlaw.co.uk/free_legal_information/children/childf13.html

 All of the article is very interesting if that is what in fact happens. However, in my particular case, it didn’t happen like that. I was not informed by my lawyers or by CAFCASS that the children could have their own solicitor – in fact, I have only just found that out! Clearly, I will now start to investigate further how a child can appoint their own solicitor.

CAFCASS, for those of you who don’t know, is the Children and Family Court Advisory and Support Service. They are the Court appointed Guardian for the children. In theory, they should be interviewing the children to find out what the children want and then prepare a report for the court to make recommendations as to what the children want. However, the judge doesn’t have to accept those recommendations, even though he/she hasn’t usually even met the children so can’t know what the children want unless he/she listens to the CAFCASS officer or interviews the children him/herself.

My judge thought the CAFCASS report was “appalling” as he hadn’t met with the children with each parent on our own thereby seeing the interaction. He only saw the children on one occasion and then misinterpreted what they said: I was there when my son said he “wanted to live with Daddy too” but the CAFCASS officer didn’t hear the “too” so reported my son’s statement as “he wanted to live with his father”. This is simply not the case at all; out of all the children he is the one who is expressing his unhappiness most about living away from me. A vital sentiment was misheard but was catastrophic in its consequences. Remarkably, none of these interviews are taped: if they were, then the judge could hear for themselves what the children said, in what tone of voice and with what body language. Given that 93% of our communication is non-verbal, you would think that it would be vital for the judge to hear/see for themselves the details of the interview with the children and not to rely on the CAFCASS officer’s perception of the interview.

In the meantime, here is an extract from a publication produced by CAFCASS advising children what to do when their parent’s go to court over residency:

 Your rights

CAFCASS respects your rights as a child. In particular, we support the UN Convention on the Rights of the Child. This is an agreement made by many different countries about how children should be treated.

Here are some of your rights when there is a case about you at court:

• You have the right to see the Children’s Guardian who will listen to what you want to happen and tell the court about your wishes and feelings.

• You have the right to have your own Solicitor who will see you and listen to what you want. Your Solicitor will speak up for you in court.

• You have the right to ask to attend the court hearings, to see the court or to meet the Judge or Magistrate. Some children want to do this and some children don’t. Talk to the Children’s Guardian or your Solicitor about what you want.

• You have the right to be given written information about your case as long as the information is not damaging to you or to others.

Speak to the Children’s Guardian or your Solicitor about this.

• You have the right to be told what is happening with your case by both the Children’s Guardian and your Solicitor.

• Your have the right to know the decision made about you by the Judge or Magistrate. The Children’s Guardian must make sure you know what happened as soon as possible.

• You have the right to make a complaint if you are not happy about anything we have said or done. See further details on the back of this leaflet.

• If something does not happen that was decided by the court, you have a right to have this looked into by an Independent Reviewing Officer.

 Well, I have had to go on the website to find this: it certainly wasn’t given to my children. I’m off now to print it out and give it to the children next time I see them, together with a print out of the children-friendly version of the Human Rights Act 1998 giving them rights……..

 More on the Human Rights Act in another post……….

I will also do a post about the UN Convention on the Rights of the Child………

DIGG This
A Mum First and Foremost
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The Story:

This is a story of a Bipolar mother who has been in a custody battle over her three children due to her Bipolar. This is the result of my ex-husband’s application to the Court for an Sole Residency Order seeking an Order that he alone should look after the children with me only having supervised “contact” with them. The reason cited for his application is that I am “incapable” of looking after the children due to my Bipolar.His application asked for me to only have supervised contact with them.

A 17 month battle ensued resulting in a 10 day hearing in the High Court in the Royal Courts of Justice. Despite hearing evidence from 3 experts in psychiatry and psychology  all of whom gave evidence to the Judge that I am perfectly capable of looking after the children, the Judge decided that, because of my Bipolar, I should not be allowed to be the main carer of the children. She ordered that the children should be the subject of a Shared Residency Order ie that their care should be shared between me and their father with  them having homes with both of us. Legally, that puts us both on equal footing when it comes to our legal parenting rights. However, the Judge decided that their main carer should be their father on the basis that he doesn’t have the illness and can therefore provide greater stability than I can. He was not put through any psychological or psychiatric assessment to determine whether he was capable, despite the fact that he has been violent to both me and the children. The children’s nanny has had not psychiatric or psychological testing and yet has been allowed to take over their care in preference to me. Their main carer is therefore my husband’s nanny as, the reality is, that he is at work most of the time that he should be there looking after them. He heads up a City law firm litigation department (he’s an ex barrister) and is therefore rarely at home before their bed time.

I was thrown out of our marital home by my Husband who succesfully applied for an Occupation Order, claiming that my presence in the house was causing “significant harm” to the children. The Judge who heard this application was the same judge who heard the Children’s Act custody dispute. She came into court saying that she hadn’t had time to read the papers for the application but that she didn’t need to as it was obvious that my staying at the home would damage the children. She sought to evict me without consideration as to my financial means. I had no capital with which to buy or rent another home until the matrimonial home was sold. My husband was fighting my maintenance claim saying he couldn’t afford to pay me any maintenance out of his £450,000 earnings. My work was not producing enough income to fund a rented property. She gave no consideration for the effect that evicting me from my home was going to have on me and my mental health.

I was given 2 days to pack all my stuff and leave. I had nowhere to go other than to my brother’s house. I have been living there for 18 months in his spare bedroom where me and my three children have to share a bed when they come to stay with me. Yet the Shared Residency Order means that the children are to have HOMES with both me and my husband. I was specifically advised that, under the Matrimonial Homes Act, there would be no inequality between my financial situation for me and the kids when they are with me and those of my husband when the kids are with him.

The reality is stark. I am without my own home at all whilst my husband continues to live in our 7 bedroomed matrimonial home. He has been left with 80% of his salary whilst I have been awarded 20% of his salary as maintenance for me and the children. This maintenance will stop in 5 years time. I have incurred debts of £450,000 which has now bankrupted me given the fall in the housing market. I have no capital left with which to buy a home for the children.

The judge considers all this to be a fair outcome!

My children’s thoughts and feelings:

The children’s thoughts and feelings were simply not taken into account. They did not give direct evidence to the Judge either orally or verbally – a point I discuss further below. They are devastated by the decision and miss me terribly. They do not understand the Judge’s contention that I am not well enough to look after them nor do they agree – they all think that I am a good mother who is perfectly able to parent them and indeed they desperately want me to be parenting them far more regularly. My daughter wants to come and live with me and yet no-one is listening to her; she has resigned herself to the fact that, eventually, she will be able to “vote with her feet” and that eventually her view will count.

They cannot understand why they are not allowed to see their mummy very often and don’t understand why nobody has listened to what they want. They keep telling me that they want to live with me and that they are heartbroken without me. My youngest said “Mummy, there’s no love in my heart when you’re not here with me”. She is regularly having nightmares and is wetting and soiling herself regularly. She is convinced that I no longer love her despite all my assurances that I do. She’s clingy and demands my constant attention when I am with her. Relatives observing her say that she is clearly suffering. My son (8) tells me he is often crying himself to sleep and now talks to me and others through his favourite soft toy. He follows me everywhere, (even into the loo!), not letting me out of his sight. I have nicknamed him “my little shadow”. He cries on the car journey to drop him back to his father, pleading with me not to let him take him away from me. My eldest child, 10 , still asks to sleep in bed with me when she is with me and cuddles me for dear life. She keeps asking when the Court will listen to her views and when she is allowed to “vote with her feet”. She has asked me to get her her own solicitor so that she can be listened to.

They all need their mummy – that much is clear. They love me regardless of my condition and tell me that they don’t believe that I am doing anything wrong to them or harming them in any way. They simply cannot understand it all.

Me and my Bipolar:

I was the children’s main carer for the 9 years leading up to this Judgement, some of this time I was the sole carer at home, some of the time I had nanny help.

I suffer from Bipolar 2 and have therefore never experienced a manic episode. I do not suffer from delusions,nor have I ever been psychotic. I am told that I have the mildest form of Bipolar and it is on the borderline of a diagnosis which is why it went undiagnosed for 16 years!

I have only been in hospital twice, both of which were voluntary admissions – I have never been sectioned. The first admission was for depression, during which time I was diagnosed with depression only. The second time was because the psychiatrist changed his diagnosis to Bipolar and wanted me to be in hospital for the introduction of Lamotrigine and because he was concerned that I might be going hypomanic on the anti-depressants. I was not manic according to me and to the admission notes.

I have never abused the children. I have no substance abuse problems, nor have I ever had any substance abuse problems) and don’t even smoke. I have no criminal record. I have a full, clean driving licence and have never been convicted of any driving offences.

I am fully medication compliant and my condition is fully stable with no relapses since I started on medication 4 years ago. I have been through 2 years of intensive Cognitive Behavioural Therapy (the recommended treatment for Bipolar). During the 6 years leading up to my hospitalisation and diagnosis, I was the children’s main carer and was being their mum without being on any medication or treatment as I hadn’t yet been diagnosed. Yet, I was still managing to look after them. The children were thriving at school with good school reports and the schools reported them to be well-adjusted, highly intelligent, popular, lovely children.

I have experienced 4 depressive episodes (no manic ones) since I was 22 (I’m now in my 40s), each of which followed a major life trauma. I experienced the first during my degree – I still graduated with an honours degree, went through my military training at Sandhurst, became an Army officer and rowed for my university, winning the National Polytechnic rowing regatta, so the depression didn’t hamper my functioning. I experienced my second episode at Law school, but still graduated and became a lawyer. I experienced my 3rd after the birth of my second child, but still carried on parenting my two children (aged 2 and newborn) whilst managing my third pregnancy whilst my son was only 6 months old. During this time, I oversaw the building works in our house and worked part-time.

My fourth episode resulted in my (voluntary) admission to hospital. I had three children in three years, my two year old son developed diabetes, I was working and we had knocked down our house and I was overseeing the rebuilding works. My husband had become physically violent towards me and our marriage was crumbling and high in conflict with a husband who was rarely at home. When he was at home, he was emotionally and psychologically abusive for quite a lot of the time. He was highly critical of my parenting and of my abilities as a wife and housewife – I rarely got anything right in his eyes. I collapsed from the pressure of it all.

I tell you the following about myself only to give you an idea of what I have managed to achieve during my illness when I wasn’t even diagnosed and was on no medication. These achievements did not seem to carry much weight for the Judge and did not convince her that I was able to lead a full, productive life and be competent.

I am a qualified lawyer and still manage to work. I am a regular speaker at conferences, have been a speaker on the Radio, and have had many articles published in both the broadsheets and journals. I am an ex Territorial Army officer, having passed through Sandhurst military academy and was in the TA for over 9 years, both in command roles and in organisational roles. I am a qualified mountain expedition leader, have won sailing races with the Army, ski, run, cycle and have led an expedition team across the Yukon in Canada, leading them through 5 weeks of arduous terrain on a 250 mile trek. I gained my legal qualifications by doing a distance learning course of a law degree whilst working full time.

I have many long-standing friends, all of whom say that I have never exhibited any form of mania, nor any substantial depressive symptoms. None of them could believe that I have been given this diagnosis.

Discrimination, prejudice, ignorance and Human Rights and the Law

I will write separately in detail about the law on the Children’s Act,the Disability Discrimination Act, the Human Rights Act, the United Nations Convention on the Rights of the Child and the other pieces of legislation. Being a lawyer I can strive to effect a change in the legislation. This will take a great deal of time and energy but I feel strongly that the law is not serving the interests of the children where a parent suffering from an illness is deemed incapable. The law I discuss here is my understanding and interpretation of it; I may be challenged on this but it is my view currently.

I believe that this whole situation and judgement is as a result of ignorance and a misunderstanding of the complexities of the condition; in particular the fact that there is an entire spectrum of manifestations of the condition from the extremely mild (as in my case) to the extremely severe. There is also an ignorance of the fact that there are two types of Bipolar: Bipolar 1 which is a mix of mania and mild depression compared to Bipolar 2 which is only hypomania but more severe depression. Clearly, the manifestations of these two types of the illness are very different and result in very different sets of behaviours of the individual sufferer and therefore the effect that this has on the family and especially the children.

Discrimination:

I also think that this case falls within the realm of mental health discrimination, prejudice and stigma by the Judge, my exhusband and his witnesses. There is still a high level of prejudice surrounding mental health conditions which is pervasive throughout our society and I aim, through this blog and my legal background and skills (I am a qualified lawyer), to fight it and challenge it through both the court system and the media.

I am fighting this issue as I now know that I am, unfortunately, one of many parents with this condition who is suffering from this kind of prejudice and losing custody of their children as a result. There are now many stories both on this blog and sent to me through my private email, which are heart-rending stories of parents having their children taken away from them as a result of their mental illness. Clearly, some parents are not well and struggle to find the right medication to stabilise their condition, some have substance abuse problems and some have such a severe form of the illness that they would find it very difficult to be a full time parent. However, there are many, many others who have managed to stabilise their condition such that it no longer impacts their day to day life in a debilitating way and these parents should not have their children taken away from them simply because they have a diagnosis of a condition which is not of their making, is not “their attitude, fault or fundamental flaw of personality” but is simply a disease which they are extremely unfortunate to have got.

There are parents with epilepsy, diabetes, cancer, alzheimers, paralysis, Down’s syndrome, Autism or any other illness which can be debilitating either physically hampering the way that they can parent their children or emotionally/psychologically debilitating, yet do these parents have their children taken away from them because they are ill? There are parents who have alcohol and drug problems yet these parents don’t usually have their children taken away from them. Why should people with mental health problems be deemed to be automatically more incapable of parenting their children than these other sufferers?

My son has Type 1 diabetes (a form which is NOT the result of a poor diet), and I witness his extreme fluctuations in mood and functioning. When his blood sugar levels fluctuate, his mood fluctuates: he can become aggressive, irritable, bad-tempered, very fatigued, have headaches, feels nauseus, can’t concentrate, and at times can’t function at all. All this happens on a daily basis and yet how many diabetics have their children taken away from them on the basis that they are “incapable” of looking after their children?

They don’t, because every one would argue that that would be discriminatory and unnecessary. And yet it is allowed to happen to the mentally ill.

The United Nations Convention for the Rights of A Child.

This states clearly that all children have the right to be have their voice heard. Yet the Judge did not hear my children’s opinions at all. They did not give evidence either orally or in writing. They were deemed to be “too young” and yet there is no age stipulation in the legislation. It simply gives guidance that evidence of children will be taken into account if they are deemed to be sufficiently mature enough to understand the issues involved. What does that mean? Who makes that assessment? Who funds the children’s separate legal representation? A CAFCASS officer was the only person who heard what the children had to say.

CAFCASS: The Children and Family Court Advisory and Support Service

Apparently, the Court case was all about what was in the best interests of the children. Yet my children were interviewed by CAFCASS on only 1 occasion for approximately 50 minutes. They gave evidence to the CAFCASS officer that they want their mummy. My youngest daughter told CAFCASS that she wanted to live with me, my son said he wanted to live with both of us and my eldest daughter said she wanted to live with me but see a lot of her father. CAFCASS did not report this properly and there is no transcript taken of the interview so I cannot prove what I heard the children say when I was in the room with them when they said it. It is my word against the CAFCASS officer’s report.

The CAFCASS report was, in the judge’s own words “appalling” and highly deficient in its thoroughness and findings yet the proceedings continued, despite the fact that the Report was the only truly objective evidence on what the children wanted. The judge told the CAFCASS officer that it was the most depressing example of how badly a CAFCASS investigation could go, yet it was still admitted as evidence. He didn’t even interview the schools or my new partner or come to the home to see if the allegations of my disgusting housewifery were true.

The Judge, accountability and Appeals

Astonishingly, a Judge is exempt from the provisions of the Disability Discrimination Act when acting in their judicial capacity! I simply do not understand why a Judge should be exempt from being held to be potentially discriminatory and held accountable for that bias. I am told also that I cannot appeal this decision as there are only 2 grounds for appeal:

1. That the Judge misapplied the law: well, she didn’t because the Children’s Act is entirely silent on the point of how a Judge should assess a parent’s capability or indeed a parent suffering with mental health issues.

2. That the Judge exercised her “judicial discretion” in such a way that no other judge would have exercised it in that way!. Clearly, an individual’s subjective discretion is such a nebulous concept that it is extremely difficult to criticise it. I was also advised that judges very rarely criticise another judge’s exercise of this judicial discretion. I find this an extraordinary protection to afford judges.

You also have to have leave to appeal and this leave has to be sought from the Judge herself. In other words, the judge who made the decision that you wish to appeal, has to agree that you can appeal it! She has reserved the case to herself too, which means that if I wish to bring a fresh application under the Children’s Act for the residency issue to be re-evaluated, I will get the same Judge!

I simply fail to see how this is justice or how it prevents miscarriages of justice from happening as there seems to be little room for challenging the decisions of the judges.

Human Rights

There are also Human Rights issues in all of this. There has, in my view, been a breach of various articles in the Human Rights Act including a breach of privacy, a breach of my right to a family life and a unfair trial.

Breach of privacy:

I was ordered to make a full disclosure of ALL my medical notes, both in patient and out patient and regardless of whether they pertained to my condition. They were also allowed to see ALL my psychology session notes. My computer was gone through by my husband as were all my mobile phone calls and texts and he was permitted to give evidence on the findings of his investigations. He had me followed by a private investigator.

Right to a fair trail

Whilst all of my medical history was obtained and given in evidence, none of his medical notes had to be disclosed, nor his notes from his psychology sessions that he had been having. No medical reports were conducted on him. This meant that the Judge heard all about my medical history and nothing about his.

I spent a week listening to my medical notes being taken to pieces by his barrister: excerpts from my psychology sessions, from my psychiatric assessments, from my previous medical history.I was absolutely destroyed as a person and as a mother by my husband, his witnesses and his barrister. I spent an entire week not being allowed to speak at all but having to  listen to my exhusband’s barrister ask his witnesses to explain certain behaviours and thoughts and emotions that I had as though I was completely invisible and as though they were able to understand what was going on in my head. It was deeply humiliating and degrading and very largely untrue and exaggerated. I then endured 3 days of cross-examination by a barrister who bullied and humiliated and taunted me in the most disgraceful manner about my illness, my behaviour and my emotional and psychological state. His entire aim was to make me seem like a complete danger to myself, to my children, to claim that I had a fundamental personality disorder despite having been told by the experts that I did not suffer from any personality disorder. My whole inside of my mind was taken to pieces by people who knew nothing about my illness and yet claimed that they “knew” me well enough to give evidence about my condition.

My husband’s legal team knew that the only way to ‘convince the Judge that I was the incapable, “mad” wife and mother that he said I was, was to try to focus on the period running up to and following on from my hospital admission and to assert that this was the norm. This he did with devastating success. He was able to focus the Judges attention away from all the years of my parenting prior to admission (ie 6 years) and only focus on the 4 months leading up to my admission and the 12 months following it.

I asked my legal team to include all his own bad behaviour but I was advised that we shouldn’t “sink to his level”.His violence towards me resulted in the police being called out to our home, yet no police records were brought into the trial. His drug taking in the past was not brought up, nor was his visits to places he shouldn’t have been visiting. None of this was considered important in terms of assessing his own personality and fitness to parent.

The witnesses were allowed to give evidence which was outside their realm of expertise ie they were not psychiatrists or psychologists and yet they were allowed to give evidence on my state of mind, on my personality and behaviour and were allowed to contend that I was mentally ill and that I had a personality disorder.

Law on expert evidence

The law on evidence is usually that no witness is allowed to give “expert evidence” ie evidence which should only be given by an expert in their field. So, for example, in a hearing on negligence of a construction of a building, a lay person cannot give evidence on whether or not the building had been constructed properly or not as they are not experts in construction. Yet, in a case involving Bipolar, the witnesses were allowed to give evidence on my state of mind, on my emotional background and on my thoughts. The Judge stated in her Judgement that the evidence of my neighbour was “particularly persuasive” yet my neighbour knows nothing about my condition.

This was therefore not a fair trial in my view. There was a huge disadvantage to me and none to him as he did not undergo any of the same scrutiny into his personality, his thoughts, behaviours etc yet mine were gone through in minute detail.

The Children’s Act – guidance on mentally ill parents

The Children’s Act is totally silent on the issue of parent’s with mental health conditions. It gives no guidance whatsoever to either the Judge or to CAFCASS on how to assess a parent’s capabilities when they are suffering from a mental health problem.

The Judge is given the sole responsibility for assessing any evidence. This is despite the fact that the Judge has no psychiatric or psychology training. They are given the jurisdiction to decide on issues which are beyond their training and experience.  Neither are they qualified in child psychology yet they are allowed to adjudicate on the effects of a particular parent’s illness on a child.

There is no panel of judges and experts; simply one judge.

How is this a “fair trial” and how is it justice?

“Personality v symptoms”

Because many of the symptoms of the illness can be mistaken for inherent personality traits, this is the main barrier to people being able to see the person for who they are rather than as a cluster of mistaken personality traits. The fatigue associated with depression is perceived as “laziness”, the lack of communication as “being anti-social”, the anxiety as being “over-sensitive” etc.

The mainstay of therapy for Bipolar consists of helping the sufferer develop “coping strategies” to stave off depression and minimise stress. Each sufferer has their own “triggers” ie stimuli, which will bring on either an episode of depression or an episode of mania/hypomania. During my therapy, I recognised that stress was a major trigger for me so I learnt to avoid taking on too much eg too much work, too much housework, too much organising social activities etc. I also learnt that a coping mechanism for stress was to go running, listen to music and do other pleasurable activities to bring balance back into my life.

During my recovery from my admission to hospital with depression, I was advised to “put my recovery first” for a while. This was interpretated by my husband and others as me being “selfish”, “self-absorbed” and not interested in being a wife and mother. I was “lazy”. On the one hand I was being advised by my medical team to put my recovery as the highest priority, on the other hand I was being criticised roundly by my husband and others for being “selfish” and “lazy”.  This contradiction was causing even further stress and was making my recovery harder. To have a husband who says, on the one hand that he understood and supported me and yet was highly critical when I implemented my coping strategies, was very difficult to cope with.

Noise is another trigger for me and London is extremely noisy and crowded. I therefore sought to regularly escape from the noise and crowds and travelled down to the seaside to get away. This was considered “unnecessary”, “self indulgent” “putting my own needs before my children’s”, “irresponsible”. The Judge decided that my reasons for doing this were “disingenous – as it was really for my socialising”. Yet this need to escape the noise and stress of my town was highlighted as a positive coping strategy by my psychologist.

All these symptoms and coping strategies were misinterpreted and I was condemned as a result.

My Bipolar Partner


My new partner has Bipolar 2 – a mild form like mine with no mania, delusions or psychosis but depressive episodes and anxiety. We met in hospital and formed a close bond as a result of our mutual understanding and empathy of our respective suffering and struggles to come to terms with our condition. He was diagnosed at the same time as me and he and I were the only people we each knew with the condition. We relied on each other during the first year of diagnosis to support, inform and listen to each other. He was discharged after the first week of my admission yet he came back to visit me, take me for walks and to the cinema, send me encouraging texts and so on. My husband visited me twice during my 5 weeks of hospitalisation, saying that he was “too busy” looking after the children and working to find the time to come and visit me. Not surprisingly, I came to rely increasingly on my new found fellow sufferer for support rather than my husband. After a year, I decided I wanted to leave my husband and be with someone who understood me and my condition and be fully accepting of the limitations it might impose on me.

My husband immediately issued proceedings against my new partner for a Prohibited Steps Order ie an application to the Court to prohibit my partner from seeing the children claiming that he was a danger to himself and a potential danger to the children. No supporting evidence was submitted with this application – it was based purely on my husband’s contention. This application was in place for 17 months before Judgement was handed down by the Judge.

My partner was prevented from seeing the children for this entire time simply based on  my exhusband’s  assertion that my partner had Bipolar and therefore shouldn’t be exposed to the children. He has no criminal record, no alcohol or drug abuse and has never hurt or threatened the children in any way. But he was still not allowed to see them until the Judge ruled that he could.  Unlike criminal law “innocent until proved guilty”, in these proceedings my partner was “ill and dangerous, until proved otherwise”.  This is despite the fact that the children adore him and kept asking why they couldn’t see him.

He went through hell in those 17 months; having been made a party to the proceedings he was required to be a witness and therefore be interviewed by my lawyer and prepare witness statements. He had to be examined by a psychiatrist to prepare an expert witness report, he was in the witness box for 2 days and his medical notes were trawled through in court. Unsurprisingly, he found this deeply humiliating, insulting and degrading. My husband’s barrister did everything he possibly could to depict him as unstable and incapable of being a parent.

When the Judge did hear the application, she threw it out on the basis that it was unfounded. Yet, during this 18 month period awaiting judgement, my partner was forbidden to see the children. This also meant that he was brought to trial where full disclosure of his own medical notes were ordered and he was cross examined for 2 days. He was again bullied and humiliated by the barrister cross examining him, and being told repeatedly that he was “unstable” and clearly not capable of parenting.

This was also used as a reason for my children not coming to live with me: the two of us together are clearly unable to care for children, according to the judge. But why?

  • Neither of us has a criminal record.
  • Neither of us has a drug or alcohol problem and never have had.
  • Neither of us have abused the children in any way, nor threatened them.

Yet we are considered to not be capable of looking after the children, based on our mental health condition.

Kids need mums:

The vast majority of people believe that children need their mothers and not just on an ad hoc basis, but on a regular one with a great deal of love, nurturing and understanding of their needs on the mother’s part. The mother-child bond is fundamental, deep and irreplaceable. All the psychological studies into the importance of the role of the mother bears testament to my contentions. My children desperately want me; they are unutterably sad that I am forced to see them so rarely and are emotionally and psychologically suffering as a result.

This blog is my attempt to highlight that all parents, regardless of their illness, are needed by their children and that discrimination, ignorance, stigma and a lack of empathy is are all in the way of blocking those children from their parents.

Any comments, or offers of support would be greatly appreciated.

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