On Saturday we adopted this adorable little fluff ball, who craves attention and loves from us all and have chosen to call her Water Lilly. She is 8 months old and a tabby, joining Ocean who was 1 year whilst we were away.

On Saturday we adopted this adorable little fluff ball, who craves attention and loves from us all and have chosen to call her Water Lilly. She is 8 months old and a tabby, joining Ocean who was 1 year whilst we were away.

It was beautiful, we were awake at 430am, left Leeds at 5am for Great Yarmouth to meet up with Chris (my partner) 2 girls from his previous relationship, his parents, his sister, her husband and their 2 girls. So all 11 of us had a wonderful time on the beach and in the arcades, laughing and joking enjoying ourselves living life as it should be making memories as a family.

No idea how to phrase this blog, what to say or if it will even make any sense? so going to type and just hope for the best.
About 4-5 weeks ago Chris (my partner) became concerned for me, if honest I was worried for me, walls were moving and my head was loud and noisy, congested, nothing made sense, a sentence was unable to be followed without me forgetting simple words, fibro fog it wasn’t and dissociation it wasn’t this was new it was scary in fact it was terrifying.
My movements were random, Id be transfixed anywhere but making eye contact, I couldn’t cos then my world would be exposed, but what would happen if it was? Sleep was my friend and place of solace but was hard to achieve,
Somehow and I don’t know how Chris got me to A&E to see the duty psych team who confirmed it was a Psychotic Break/Psychosis. this was a new label for already failing mind that had previously given multiple diagnoses.
They wanted to admit me, but no beds, so care in the community in the form of the home treatment team or ICS, I was paralysed with fear and paranoid at best. Everything moving, nothing staying still.
I started on some new medication, that I hadn’t any prior experience of other than friends taking it, so Haldol it was. After 3 days of taking them I was asked if they helped, and I was honest and said not yet so they got stopped, that was not a good move as ended up with further symptoms louder voices and more moving walls and other visual hallucinations it was not a nice place and resulted in self injury two weeks in succession and ambulances called on me both times because I was literally away with the fairies unable to consent to treatment and with reflection I am glad those who called them called them.
Today as I blog I am 16 days clean of self injury it is not the 13 years and 1 month and couple of days I had achieved before I had a breakdown last year but it is a start.
We are fortunate as a family to have some incredible friends whom had Mima last week on school days and different friends who had her for Shabbos, so we had her home Saturday night before she went back to a friends where she stayed till Tuesday. Not easy to admit I was in no state to parent my own daughter as the fortnight or so prior to that she had been staying with my parents but they were on holiday for mums birthday, just wasn’t in the headspace and I was too volatile to be in control and scared myself rigid with paranoia so was far safer to have the small taken care of.
I have always said I am fortunate to have my village of humans, whom when needed mobilise and support, that is a blessing, I know I am fortunate and not all whom are mentally unwell and have physical health needs like myself do not have that village, but my village thank you all for being you and helping me raise an incredible human, who is a blessing not only to me but the world at large.
I am still under the care of ICS, the psychosis is slowly calming and voices not as loud n walls have stopped for now at least from whirling and other things from being in my already limited vision.
Thank you Chris for remaining by my side and not running when the tough got well tough, you are my rock and give me reason to keep fighting to reclaim my mental wealth, it is not a easy ride but with you by my side it is a hell of a lot easier than itd be if I was facing it alone.

We had no plans for New Years so opted to go away for New Years. We went to The Dalmeany in Lytham St Annes, for a well deserved and much needed break and rest.
Chris and I both had a massage which was utter bliss and Jemima had a wonderful time in the kids club. So a relaxing time for us all. We failed at a walk on the promenade as it was rather cold and windy, so Chris and I had a impromptru date morning to Costa one of the mornings whilst Jemima enjoyed watching a film with other small humans.
I had a lovely swim whilst Chris had a sneaky nap and Jemima had more time with new friends playing with Hamma Beads for the first time, she made a beautiful butterfly which was in rainbow colours and is now probably buried in a suitcase that I am yet to unpack and wash the clothing within.
Jemima made us very proud on the 1st evening in the disco by preforming the dance she had learnt at school to Circle of Life, and was trying her hardest to teach the moves to a couple of other small humans.
It was beautiful to have a few days of family time, just to relax and do as we wanted with no pressure to be anywhere for a set time or do anything by a certain time.
It was a little frustrating that the New Years Eve Buffet was what appeared to be left overs from the previous night so wasn’t really anything special but we were put on a table with a little girl who Jemima had become friends with so the kids liked that they were allowed to sit together and talk as they ate.
Chris and I even managed to hit Happy Hour and have a couple of sneaky drinkies whilst Jemima had fun without us decorating cakes in the kids club.

This blog may end up being deleted as it sure as hell is going to be a hard one to write, that is if I hit the “publish” button after I have out poured onto the screen.
My dad and I have always had a challenging relationship to say the least, he is short tempered and lacks patience, doesn’t express emotion towards me unless it is negative and has a guard up the vast majority of the time.
As a teen I can recall being sat in front of my then Psychiatrist, who was a wonderful kind woman but she would regularly despair as had no idea what to suggest to try reach me, to help me, to fix me. But anyways back to that meeting, I was about 13 sat colouring mindlessly as dad was having a rant about he saw no benefit of the family therapy sessions as I was “ignoring” and “daydreaming” “oblivious” to all being said n he was “loosing money” by not being at work, so why were we there in that room when it was surviving no positive purpose?
It is now with reflection a realisation dawned on me today, my dads mum whom whilst was present in my life for 21 years I know very little about, undoubtedly she lived with Holocaust survivors guilt and that resulted in what as a now 36 year old I can see how she saw and viewed and dealt with her world and no doubt reflected on her parenting of you and in turn some of that may have influenced you and how you choose to react to situations and or behaviours and parenting me as a whole. I do not blame you if it did, but a part of me longs for n wishes she had that daddy child relationship many friends had and do have, I crave it, I mourn for it, I need it even now as a adult, I am jealous of those whom have it as it something I have never had just seen others have and haliched for but never had despite my yearning for. And that is a hard and bitter pill to swallow
Fairly recently my brain is fog to when exactly you offered me a lift to the hospital following an episode of self injury, this was incredible, you had never not since my mid teens offered a lift, you sat there with me in the waiting room, you remained calm (I was confused as so unfamiliar with you calm) you just sat n read your kindle passing the odd comment to me, but that time was precious and I am cherishing, yes it was not the most ideal of settings, but it was quality time spent with you that was not confrontational and didn’t result in a argument or raised voices, by sitting their n waiting with me those few hours, you showed me love, you soothed part of me that craves your love, your affection and your care, but rarely had it as a child. Even now a a couple of months on from that it remains with me that you gave a shit to be there and wait with me and didn’t judge me based on my behaviour you just saw your child was injured and required medical assistance and you were able to give the comfort that I needed. Thank you. (yes I am crying and no I am not ashamed of that as I write this paragraph as in my teens when self injury was such a dominant force in my life, my dad would yell, hed scream, hed refuse to acknowledge the pain I was experiencing and the emotions that led to my behaviour instead just regard me as “attention seeking” or “if your gonna try kill yourself try harder” so to have unconditional support now as a adult meant then n even now means far more than I can put into words)
Yes we have our battles, but from now on I will pick them with more care as most are just not worth it..
A simple on the surface family activity, go to the Pantomime, it is that time of year, have fun, laugh, join in with the jest and be fortunate to go back stage afterwards and meet the stars of the show.
The reality for someone who is me, who lives with Fibromyalgia, ME, and other things today I have been exhausted, I am in radiating excruciating physical pain, I am lethargic, to the extent of I had a 3 hour sleep which is very rare for me this morning as I couldn’t keep my eyes open any longer.
It sucks, no two ways about it, being a parent is exhausting even those whom are mentally, emotionally and physically well tell me it is, but when you add in to the blend Chronic Illness and being an empath and in tune that my partner is also struggling the pain feels all consuming and crushing, yet somehow I find a way to voice it, to describe it and to keep on living it. Every single part of my body is heavy and hurts, simple actions taking far longer than they should, yes medication has been taken, and CBD has been vaped, but the fatigue and physical exhaustion remain.
Just irks me that a simple family activity leaves me like this once more and causes me to question so much. We will continue to make family memories, to have good times and enjoy ourselves, just frustrates me that it all comes at cost to my body and tries to over shadow the positives of what we experience.
But hey a distraction is good and here is a photo from yesterday of my world, Jemima and Chris and I.

Parenting is far from easy, this much is fact. But then you add in complications. That said I guess I will start at the beginning so you have a rough idea whom I am, my family is, n why this blog has come to me.
May 2012, yes that long ago I did a pregnancy test, I remember it vividly sat in the bathroom of a high street department store, peeing on a stick, and then waiting, the wait that appeared to take an eternity, whilst not the most glamorous of settings it served its intended purpose BUT their was a issue, I am legally blind, have been since March 2010. I couldn’t see a line let alone two on said test, so ended up Whatsapping a photo of said test to a friend who knows whom she is and asking her what she could see! The outcome being those 2 lines are now a human called Jemima who will be 6 years young in January.
That is the crux: now to the more complex aspects of why I have opted to set up a blog.
I am many things yet nothing, I am someone yet something, I live with and deal with a lot, far more than many actually could or try to comprehend and that impacts on every element of my being.
I am a solo parent, all be it dating an incredible human called Chris.
I am a human of lived experience, which includes but doesn’t just include as to list all would bore you to tears n pain my hands to type:
Bipolar Disorder
Complex Post Traumatic Stress Disorder
Fibromialgia
ME
and have I mentioned I am blind.
Alongside all this I also happen to be Gender Fluid, Pansexual and Jewish.
Whilst this blog will cover a lot including my day to day life, it may also let you the reader into darker aspects of my being, as earlier this year I was raped twice in 6 days by someone whom was at the time a friend, his actions resulted in me loosing my Mental Wealth and ending up in a dark hole of Mental Illness once more. I am now left failed by the system as have had the police tell me due too lack of witnesses and or CCTV they can’t take the case Luther, no support from the Community Mental Health Trust ie NHS I am having to self fund private Trauma Therapy – if you can spare anything itd mean a lot
https://www.gofundme.com/continuing-mental-wealth
So settle down, take a seat, and come on a journey as I attempt to process my head via the medium of blogging
