The Phoenix And The Myna

Fawkes

Myna

As I start writing this piece I glance out the window and there is perched a Myna, one of the numerous of that pest of a species that populates my locale. I had already intended to use them as an example in this piece before seeing that little guy.

If you know me you know that I’m a Harry Potter fan, and so it seems natural to me when I need to make a comparison to use a mythical creature – the Phoenix – when I compare my favourite bird with my least favourite. The Phoenix and the Myna. These birds create a strong image when trying to display the impact of mental illness during COVID-19.

I’ve had a rough week, last Friday several hours following an outpatient treatment of ECT I had a panic attack due to thinking I had inadvertently taken a double dose of Lithium and was therefore bound to have another delirium episode. High Lithium levels combined with ECT were the cause of last year’s episode. After a while of trying to calm down and shoo away the flock of Mynas I had to call an ambulance, my heart was 147bpm and I felt a lack of confidence in my ability to maintain proper cognitive function. I knew that there was a Phoenix who wanted to come and rescue me, all he needed was a little belief on my part, but I didn’t have it. Instead of summoning the strong, heroic bird who could carry me to safety. I called the paramedics who went through my medications and concluded that I hadn’t double dosed – this calmed me down significantly, however, I was still anxious for reasons beyond my control and the paramedics were obliged to take me to hospital because my heart remained above 120bmp, the figure at which they have to take you in.

On Saturday my anxiety decreased, but depression took the reigns. Again I allowed the Mynas to overwhelm me, a pest that has overtaken my suburb. I allowed their squawking to drown out the song of the Phoenix, he could have reminded me that there are people who love me, that despite being unable to attend, I have a church family who love each other and even in these hard times are actively serving our Lord and one another. When there are a flock of Mynas and only one Phoenix it is easy to hear the sounds of the many rather than the one, but the one is stronger and not a mere pest.

I didn’t understand why I was so depressed and anxious until seeing my psychologist on Monday; she explained to me that it is completely understandable that I would be experiencing this level of depression having endured hours of believing that I was going to experience another delirium. I did not receive the comfort and validation that I needed in those hours and was left to dread what was coming. The delirium far outweighs anything else as the most terrifying experience of my life.

The rest of this week, despite having two comforting sessions with my psychologist and one with my psychiatrist in which he was validating toward my experience and apologetic for not acknowledging my distress when I messaged him on the night of the panic attack. I have remained deeply depressed; my dose of Rexulti has been increased from an already high 3mg to the maximum of 4mg. My psychiatrist and I are going to see how this increase goes before either increasing my ECT from fortnightly to weekly, or having another admission in the clinic to try one of two new drugs, sadly neither of which are on the PBS (actually Rexulti isn’t either, but I get samples).

COVID-19 is such a small part of my life – yes, I have just purchased five washable and re-useable face masks, but there are bigger things I have to deal with. It is not very abnormal for me to be alone. I enjoy seeing my friends, but I am an introvert and COVID while making things inconvenient, hasn’t changed my life that much. The two annoying things are 1. I’m getting fatter again because the pools are closed and I’m eating too much. 2. I have to get tested every fortnight 4 days prior to ECT and isolate between the test and going to the ECT procedure. COVID is an area where the world feels swamped by Mynas and those of us already living with mental illness feel like everyone is getting a taste of what our lives are like. We feel isolated, burdened, judged – we experience some people being afraid of us like you do now when people are scared you’ll contaminate them.

A Phoenix lives his life – 500 years – as a symbol of strength and renewal, to die in flames and be reborn out of the ashes. Like man he is eternal, but he will see Earth through its phases, a gift, or perhaps burden man does not have. Considering the portrayal of Fawkes, Dumbledore’s pet phoenix in Harry Potter allows us to consider loyalty, strength and hope. In the book Harry Potter And The Half Blood Prince Fawkes flies in circles and sings over Dumbledore’s dead body before departing, never to be seen again in the stories. He is loyal and yet his own master. We are in a phase, COVID-19 will go away.

A Disappointing Distinction

I went through my Undergraduate Degree with low standards regarding my grades. I hoped for the best in my Drama performance subjects and often got the best. However, it took me six years to complete a three-year degree due to the regular withdrawals and occasional failure of my elective subjects. It’s hard for me to put effort into something that doesn’t interest me, namely something that falls outside of the realm of creativity.

Things have been different in my Masters, I’m only attempting one subject at a time, and being in the field of Creative Writing, I am generally interested. This semester I am attempting a critical subject to prepare me for my 20 000 word thesis. Expecting to scrape a Credit in my first assignment, I was thrilled when my grade came back as a High Distinction. That assignment was worth 35%. With the confidence boost, I handed in my second assignment, only worth 15%, with great confidence. I worked hard on it and thought I had done an excellent job, so yesterday when I received my grade and feedback, I was highly disappointed to see the numbers 7 and 4, 74%. A Distinction, which I would have been over the moon about in my Undergraduate, and which would please most University students. The only relief I feel is from the fact it is only worth 15% of the subject.

I do, however, now face a gripping fear that my major piece for this subject (50%) won’t be good enough for my overall mark to be an HD. This subject isn’t where my strengths lie. I can’t research, analyse and argue perfectly, and I’m working with two ideas I’m still learning about;  How can the Bildungsroman story be viewed through the lens of eco-feminism? I certainly identify as a feminist, but eco-feminism I’ve only just discovered. My story fits snugly as a  Bildungsroman entailing eco-feminist ideals. I need to appreciate that if I do not achieve my HD for this subject, I have at least gained some valuable knowledge to carry with me as I write.

Maybe the PhD is a pipe dream, though.

Electroconvulsive Therapy – A Life Saver

It has been a long time since my last post; I’ve been busy with uni and multiple hospital admissions. Most Friday mornings for the past four or five months I’ve been going into my new hospital for a session of ECT as an outpatient. I’ve been fortunate that lately I’ve been waking early naturally. The 5:45 am wake up I need in order to get to the hospital in time isn’t too much of a challenge. Following the procedure outpatients must be accompanied home, it is not acceptable/allowable to catch a taxi / Uber home. My NDIS support worker has generously blocked out time in her schedule every Friday morning in order to take me home. Without her I couldn’t have the ECT as there is no one else to take me home.

 

Over the last 11 years, through much trial and error, my psychiatrist and I have discovered that antidepressants have little to no impact on me. Although it is a treatment of last resort, ongoing ECT may be our best option. You may be horrified by the thought of this; but ECT is nothing like you see in old films such as One Flew Over The Cuckoo’s Nest. It is not used as punishment and there is a thorough process adhered to prior to beginning treatment, to ensure that all less invasive treatments have been tried on the patient; and that the patient has a good chance of positively responding to the procedure.

 

I remember being horrified when my psychiatrist first recommended ECT. I thought I’d be awake, strapped down and that my whole body would be seizing. I was wrong! During treatment the patient enters the room, removes their shoes and any top layers with long sleeves. Several sensors are stuck onto the chest and head, then a general anaesthetic and muscle relaxant are administered. I must admit, I like the feeling of the anaesthetic kicking in. The muscle relaxant stops the body seizing when the shock is performed, the only physical evidence to the medical professionals in the room is slight curling of the toes. An electric current is passed through the brain causing a seizure; this seizure causes changes in the brain chemistry and can result in improvement in the patient’s condition very quickly.

 

The combination of a doubled Lithium dose and a closely followed session of ECT recently caused a delirious episode in me lasting several days. I am fully recovered now, yet traumatised by it. I have great fear of it occurring again, and truly I say to you that it was the most frightening thing I have been through. Since the episode I have had two sessions of ECT, both of which I was told to completely cease Lithium for three days beforehand. Yesterday was my most recent session. I will resume Lithium tonight. I am back to my original dose, not the doubled dose largely blamed for the delirious episode.

 

Right now, I am at my Mum’s house having our last catch up before I head over to the UK for a month to see the family whom I miss greatly. I look forward to seeing them. I hope that the joy from being around loved ones will outweigh my absence from my psychiatrist, psychologist and my weekly ECT sessions.

Loneliness

I haven’t written on here for a while, it just never occurred to me. I’ve just finished a semester at Uni where I was given 76% for my short story in the fiction writing subject I was doing. 76% may not sound bad, it is, after all, a distinction. As an aspiring fiction writer, I am disappointed with this mark but there were encouraging comments from the tutor. I’ve decided to continue with my fantasy novel, I can use the feedback to help me write better and seek help from someone more experienced.

 

I’m writing to you from hospital. I came in on Friday 14/06 and will be going home on Saturday 22/06. I’m just here for a couple of sessions of ECT and some respite. My depression has been worse recently and due to foolishly coming off Xanax cold turkey, my anxiety took a plunge. I’m back on a lower dose of Xanax now and will come off it slowly in the coming months. I’ve been severely affected by loneliness, during the day I often have appointments, so I see someone. Or on quiet days I just go out for a coffee and experience the environment of the café. But at night the house is usually dead quiet, and I feel like I’m the only person in the world. I’ve been conquering this by taking my night meds super early and being in bed by 7pm. The sooner the day is over the better. It’s unusual but I’m really missing my Mum, she’s currently part way through a two-month holiday in Europe. I’ve been calling her every two to three days and talking for ten minutes or so. I don’t see her all that often when she’s home as she lives an hour away, so I don’t understand why I’m missing her. I hope I’m not making her feel guilty for going away to have some fun, she deserves the fun after working as hard as she did for so many years and dealing with all the chaos my brother has heaped on her lately.

 

To my friends: I’d like to ask you to contact me more frequently, and if you have the time ask me to do something with you, the company would be greatly valued at the moment.

 

That’s all for the moment.

 

K

Moving

Welcome back to my blog, I’ve had a bit of a break due to having my brain electrocuted every second day for a month. I’ll write about this another time, but I’d just like to tell you that my new hospital is great!

I’ve been home from hospital for 11 days and the first five were brilliant, I actually started planning on getting back to work on my novel. I can’t write well when my mood is rock bottom so it’s been a long time since I’ve done any serious writing. During those few good days, I actually had people commenting on how happy I looked and how good in general I was looking. Now my mood has slipped back down to a 1 – 2 out of 10. I said to my psychiatrist yesterday that if I could employ someone to murder me that would be great. My fear of suicide is not the death part, but rather, getting it wrong and it resulting in a life lasting injury. I’ve shared that on here many times before, so I won’t bore you with all the ideas I’ve had for a successful suicide.

I’m writing today primarily to share the news of my upcoming move. I like the house I’m in, it’s old and needs a facelift, but it does the job; and my bedroom is massive and features a walk-in wardrobe. I decided to move because we only have five months left on our lease and I don’t feel confident about its renewal. We’ve known since we moved in that the house is earmarked for demolition as it’s old and on a very large block of land in an area where real-estate is highly valuable. Last time we had to move three of the five people living in the previous home moved together, so we only had to find one new housemate. This time we’re all going our separate ways and I couldn’t bear the stress of getting a letter from the agent telling me I had one month to get out. I thought I’d rather find a place at my leisure, sure, it meant a premature move but I was willing to do that.

My new home is a 10-minute drive South of where I am now. For some things, it’s more convenient and others, not so. Really though unless I moved next door I was going to have that scenario. I have deliberately neglected to mention my whereabouts on here, but I’ll just say that my current home is near a freeway entrance (without being so close that you can hear the traffic) and I will miss that, it means that I can get into the city very quickly and other places which I can’t mention for fear of giving away my location. My new bedroom is not as large as my current one but should still fit everything. I’ll miss having a walk-in wardrobe. My new room has a large three door wardrobe, so it’s not too much of a step-down. My three new housemates are all Christian females. I’ve only met one of them, she was lovely. Her name is J and she cooked dinner for me last Thursday and we talked for about two hours. She gave me details about the other two girls who I’ll be living with and they sound great. I would have preferred to meet everyone prior to moving in with them, but we can’t have everything.

I’m really struggling with being in the real world after just coming out from a month in hospital and having only a week at home prior to that. Most of the last few years have been spent in hospital. If you can spare some time to spend with me I’d greatly appreciate it. Most adults have full-time jobs which means Monday – Friday is a tough time for me. Actually, weekends can be tough too because then the people who work during the week want to rest or see family. I’d like to give a thank you to DF, BH, AW, JJ and KN all for spending time with me or for being about to spend some time with me.

That’s all I’ve got to say without giving you a paragraph just complaining about how much depression sucks.

Have a nice day.

You’re Dumped!

I’ve had a challenging week. Tuesday, in particular, was intense. I had been in hospital for a few weeks having ECT. I was supposed to reach 12 treatments including the few I had in my previous admission. My last treatment was on Friday 7th September. I missed Monday’s because I was in the Alfred with a cold which was affecting my breathing and causing dizziness severe enough for them to keep me in there for 21 hours and have three neurologists assess me. My next ECT should have been on Wednesday, but on Tuesday morning while I was queuing for my medication, the Nurse Unit Manager approached me and informed me that I was being moved to a shared room. The whole hospital knows that I don’t do well in shared rooms, it triggers my anxiety and hinders my recovery. I reminded her of this and said if I am forced to move I will instead discharge. She said “Fine, go home.” I called my psychiatrist and asked him to speak to management on my behalf and explain that I needed to stay to continue my treatment and that I couldn’t share, he did so, but it made no difference. I packed my things and left. I couldn’t go straight home as I had a massive day ahead of me. Last week someone in Germany tried to take $500 out of my bank account, so my bank cancelled my card, thankfully before any money was withdrawn. Under the impression that I’d be in hospital for quite some time I had arranged for my new card to be delivered to the branch near the hospital. Straight after discharging I went to the bank hoping the card had arrived. I was very fortunate it had just arrived. Then I killed some time in a café and had the best kombucha I’ve tasted in all of Melbourne. I have it so frequently there all the staff know my order except for the odd occasion I have a latte instead. Following my kombucha, I had to drive across the city to my psychologist appointment. My new psychologist is excellent, she’s highly capable and really gives the impression that she knows her shit. She’s young but I trust her, and my psychiatrist recommended her personally, he wouldn’t send me to anyone subpar. So more action in the day. I went back from my psychologist to the hospital to see my psychiatrist in the consulting suites, he wasn’t there in the morning, and he wanted to see me before I went home; also the hospital wouldn’t give me my medication until I’d seen him. It was a bit of a nothing appointment, we both admitted that we were disappointed in the hospital management and we questioned how we would go about completing my course of ECT. He suggested coming back in about 10 days, but I was reluctant because even if they gave me a single room, there’s nothing stopping them from repeating this situation.

I was extremely depressed (I still am) and on Wednesday I had a bit of a brainwave… “Fuck that hospital, I’m moving!” I had to check with my psychiatrist that he’s willing to keep me as his patient, see me as an outpatient but have me cared for as an inpatient by someone else. I called him, and he was okay with that, he even suggested a good doctor (Dr C) at the hospital I intend to move to. I then called my friend, L, who has had a few admissions to this hospital and I got the low down about it. They only have single rooms, they have ECT on premises, they have a gym, the smokers’ courtyard is huge (I’m not a smoker) which means I can hang out outside without inhaling second-hand smoke, it’s closer to home than the hospital I’m leaving, it’s a short stroll to several cafes and shops. Sadly they have no art program, and the nurses aren’t as good, I’m not happy about that, but after being treated with so little respect I never want to go back to the previous hospital.
Yesterday I saw my GP and got a referral to this hospital, specifically to Dr C, the psychiatrist mine recommended. I called them a couple of hours afterwards to check the referral had come through, it had, but Dr C isn’t in until Monday, so I have to wait. My mood is very low right now, and I’m worried that Dr C won’t be taking new patients or that the hospital will be full. Realistically it’s unlikely they won’t take me at all, it just might not be right away. I haven’t written a formal complaint to my old hospital yet, I want to make sure the new one will take me and have my first admission to make sure I’m going to be well looked after there. When all’s taken care of I’ll be writing a complaint to the general manager emphasising how disrespected I felt and how everyone at that hospital knows I don’t do well in shared rooms. I will also speak to my insurer and ask them if there’s a process of complaining though them, as they are the ones providing the hospital with money they may have a bit more leverage.

Right now my mood is about 2-3 out of 10. I’ve hardly eaten in days, the idea of putting food in my mouth and chewing is like running a marathon. I’ve committed to cooking for my housemate tonight, it’s just a simple meal, but at least it’s some food in my belly, and it’s fresh, which is better than the little bits I have managed to eat lately.

Well, I’ve got nothing else to say. Life sucks!

Deep Brain Stimulation: A Treatment of Last Resort

I’ve been home from my five-week hospital admission for nine days. During that admission, I had nine sessions of ECT. This Wednesday my psychiatrist decided I need more, so tomorrow I’m going back in and on Monday I’ll resume treatment.

My mood has been at rock bottom, I can’t cook, I can barely even work up the energy to make a cup of tea. I’ve eaten a lot of McDonald’s. In order to prevent a heart attack, I purchased some meals from IGA which are relatively fresh and only need to be microwaved, they aren’t as healthy as a home cooked meal, but they are better than frozen ready-meals or fast food. Tonight I’m having pumpkin gnocchi and all I have to do is boil it and throw in a jar of sauce.

This morning I read a Humans of New York post regarding a Parkinson’s patient who had undergone Deep Brain Stimulation, and it triggered the memories in me around the discussions my psychiatrist and I have had regarding it as a treatment for depression. Feeling completely hopeless at the moment and just wanting to die I thought, “well, I’m scared of having my head cut open, but I’m also scared of living a life feeling this low.” I mentioned it to my psychiatrist during my appointment this morning and confessed the thought was triggered by social media, but he agreed that I most likely meet the very strict criteria and that it may be life changing for me. In my presence, he sent a message to the professor heading up the program in Melbourne and informed me that usually, this professor is a prompt replier. I will see my psychiatrist tomorrow when I am admitted, so hopefully, he will have an answer for me then.

Here’s a bit of information for you about Deep Brain Stimulation:

“Deep Brain Stimulation involves the precise implantation of very small electrodes into specific areas of the brain, in an attempt to change activity in those and related areas and improve the symptoms of very severe, treatment-resistant depression.

As DBS is considered a treatment of last resort, only individuals who have trialled all less invasive antidepressant treatments and remained severely depressed can be considered for the procedure; this means having trialled multiple medications from all antidepressant drug classes, combinations of antidepressant medications, cognitive behavioural therapy, transcranial magnetic stimulation and extensive electroconvulsive therapy (ECT).” http://www.maprc.org.au/depression-trials

I’m encouraged by a friend who has cancer and maintains a strong faith in God’s ability to deal with something so small in comparison to creating the world. I wish I had that. I absolutely believe that God could get rid of all my mental illnesses in a heartbeat, but I don’t believe it’s his will. Some of us were meant to suffer. I went to Bible study on Tuesday and left after 30 minutes while we were still having tea and coffee, my mood was so low that I couldn’t bear to be around all these people who (externally at least) seemed to be doing so well.

I’ll keep you updated about the Deep Brain Stimulation progress. For now when you think of me just assume I’m bloody miserable.

DBS Image

The Lovan Incident

A few things have changed since my last post.
I’m now in hospital and on day three of Memantine. On Sunday my dose will be upped from 10mg to 20mg, the seven-day titration is what they were doing in the trial, and my psychiatrist is replicating that with me in here, except of course I know I’m getting the real drug and not a placebo. On Sunday I had headaches all day and was drowsy since then I’ve picked up a bit, I’ve just got a slight headache, and I’m worn out. On the whole, I suppose I’m satisfied with where I’m at. I was looking forward to the trial and being cared for by the experts in the field, but I’ll be cared for here, and at least by doing the introduction of the drug as an inpatient I’ll be safe should one of my wild reactions occur.

I had to stop Lovan about a month ago because I had a bad reaction to it; from history my psychiatrist and I know that starting a new drug, particularly an SSRI can be dangerous to me. I dissociate and then get into an impulsive suicidal state where I have little control over the impulses. I started Lovan during my last admission here but after a week I was deemed safe, and home I went! Exactly a week later I was feeling flat and went to rest in my room; a switch flicked, and I decided it was a great idea to cut my femoral artery and bleed to death in my bedroom. It is not the suicidal ideation that is peculiar here, but that I was going to do it at home. In the past when suicidal I’ve left the house to ensure my housemates don’t find my body, this time it was so quick and the idea had hold of me, there was no time to do something as frivolous as go for a drive to somewhere deserted. I had an idea of where the femoral artery is but couldn’t find it. I looked up some diagrams, but still no success. (I think to get to the femoral you have to cut really deep.) Giving up on that I settled for the radial artery – more accessible, but a slower death. Here my self-preservation kicked in, and I first called my psychiatrist, who wasn’t available but I then called my support worker and explained the situation; she encouraged me to go to a friend’s house and that she would call back in a few minutes to see if I had made arrangements to do that. Fuck that I wanted to die not bother a friend with my problems!

While I waited for the phone call, I picked up a razor blade and made a few little cuts to work myself up to the big one. If I had a higher pain tolerance I would have been dead years ago. I got the phone call and continued to cut while talking to her. It’s a strange state to be in, totally dissociated and suicidal but acknowledging that you need help that you don’t really want. My support worker was left with no option but to call an ambulance, and I tried to talk her out of it but to no avail. The next patch of time is a blur. I know I got a phone call telling me that the police were coming because I was “armed”, but I have no idea who called to tell me that.

The police arrived while I was in the toilet, I still hadn’t dressed my wound, so there was a bit of blood trickling down my arm. My fantastic housemate, S greeted them and was good to have around during the whole ordeal. There were three police, which was a bit intimidating, but they were very friendly. The paramedics arrived and had a peek at my arm and then left. The police remained until another two policemen (note there are now five police in my house, all of them men) came with whom I call the psych assessor dude – I never got his title. He did a psych evaluation and decided I needed the night in a psych ward. The paramedics returned and away I went. Thankfully my local one was full, so I got sent to one a few suburbs away. Here’s where I finally grasped the fact that God was looking after me that night. … Not only was the bad hospital full, but I got a single room with ensuite at the one I got sent to. A private room in a public hospital is like gold, and I would have been up all night and terrified had I been sharing. Instead, I got to wind down take a shower and go to bed. In the morning after breakfast, I moved my armchair over to my bed so I could sit on the chair and put my feet up on the bed and read in comfort. I was discharged at 3 pm, approximately 20 hours after admission, having been seen by several psychiatrists, had my wounds tended to and just come back to earth.

Two days later I saw my psychiatrist for one of our twice weekly appointments, and he immediately took me off Lovan. The ordeal I’d been through is what he was expecting if something were to go wrong, he had made the mistake of discharging me after only one week on the drug, but he wasn’t to know it would take two.

I sit here at the desk in my comfortable room in the private hospital, using their recently installed wifi; and I feel grateful that my mother is kind (and able) enough to pay my private health insurance, without which I believe I would be dead. Public mental health facilities just aren’t up to the task, they don’t have enough money, and I wouldn’t cope in such a terrifying environment, the sickest of the sick are there. Yes, we are all sick here, but it’s depression and anxiety type symptoms, not psychosis, everything doesn’t have to be nailed down.

So, to wrap up:
Memantine = Some possible hope
Police = Need more women
Lovan = From the Devil
Public Psychiatry = Please give them more money
Mum = Lifesaver

 

Lost Cause

Anyone who knows me would tell you that I’m not one to easily look on the bright side. My number one fear in life is becoming homeless, and as each month passes and we draw closer to the end of our lease that fear tightens like a noose around my neck. Unlike last time we probably won’t all move together as housemates, and no one wants to take on an unemployed housemate with a mental illness. It’s four months away, and we may get a new lease, but every day I wonder whether I should be saving for a tent and a really warm sleeping bag (and a crowbar for self-defence). That lingering issue, however, is not the point of this post; it was merely to showcase my inability to see past possible disaster.

I’ve shared with you my disappointment about being booted from the Memantine trial. The consolation and the only thing preventing a full meltdown was that they had scheduled an appointment for me to see the Professor again and get some alternative help. She has decided there’s nothing more she can do for me and so cancelled the appointment. In her letter to my psychiatrist following our initial appointment, she suggested a hormonal drug called Prometrium, but they’re still studying it for CTD (BPD) patients, and my psychiatrist isn’t going to have a clue about it. Today my GP said it can actually cause depression, so she was a bit baffled by the suggestion. I hate hope, it’s so rarely fulfilled, and when it’s taken away from you it hurts so much.

I feel like such a lost cause. My psychologist admitted on Tuesday that she feels out of her depth with me, and she’s a clinical psychologist with a lot of experience, not just some person with a diploma in counselling. I’m sure Tuesday’s session was worsened by me telling her that her home smelled like cat piss right as I walked through the door – it always smells, but it was particularly bad this week. I thought I had an ally in her, but she’s frustrated that I’m not responding to treatment and I’m frustrated that she’s always trying to figure out which emotions are going on in me but I can’t access them. In Schema Therapy terms what I’m experiencing is the Detached Protector. I think the name describes the condition well so I won’t go into that. The thing is you can’t just tell the Detached Protector to fuck off, it’s there for a reason, to protect you from overwhelming feelings which would otherwise have you curled in a ball and vomiting. The trouble is that you can’t go through life feeling nothing except the anxiety and indescribable and unexplainable depression which manage to slip through the cracks. My psychologist is trying to analyse a brick wall, and you can’t do that.

Thankfully I have eight years of rapport with my psychiatrist, and I trust him not to dump me. He’s always willing to try something new (or old) and has yet to throw his hands in the air in defeat. My GP is also excellent, and while she may not be an expert in the field she helps where she can and offers moral support, not to mention keeping the physical side of things in check.

In conclusion: I can’t live to be an old woman feeling like this constantly. Maybe I should give up on the gym and diet so I’m more likely to die young from heart disease. Right now I don’t feel suicidal, but that’s actually a bit weird considering the few weeks I’ve had.

I still have the story to tell about The Incident. I’ll try tomorrow; I wanted to talk about all this today.

No Alison Project For Me

Last Monday I had a three-hour appointment with two of the researchers involved in The Alison Project, a trial to see how the Alzheimer’s drug, Memantine affects people with Complex Trauma Disorder – also known as Borderline Personality Disorder, but it’s a much less stigmatised name that I will be using from now on.

As I’ve written in a previous post, I was looking forward to the trial and getting help from people who specialise in this disorder. I have been greatly disappointed. Apart from being worried about my high ongoing suicide risk, everything seemed fine at the meeting; two days later I received a phone call telling me they’d been in touch with my GP and she’d given them my liver enzyme results dating back to 2014. In short, they didn’t think it wise to put extra stress on my liver. I have fatty liver from the combination of being on shit loads of medication and being obese, do remember that Seroquel caused the obesity and I’m making significant efforts to drop the kilos.

The news of being off the trial sent my mood plummeting; it was almost as bad as last year when I had some hope of recovery thanks to TMS being amazing but then my body stopped responding, and that hope was ripped out from under me. At least this time I hadn’t started the drug, but I did have some hope. Even if I were on the placebo I’d still be getting expert care, and at the end I could be prescribed the drug by the people who thoroughly understand it. Having hope is a beautiful feeling, but I would have preferred to never have it than experience having it ripped away.

My GP tells me that I may still be able to get the drug, just separate from the trial. My liver isn’t in a terrible state, and it’s possible they just didn’t want someone with an anomaly affecting the data of the study. On the 7th of June I have an appointment with the Professor who is heading up the study, she is world renowned in women’s mental health and was the one who initially put my name forward for the trial. Hopefully she has something else up her sleeve for me.

Right now I feel bitter and resigned to a life of dissociation punctuated by strong negative emotions and impulses.

Unless there’s something more interesting my next post will be about my run-in with the authorities following a terrible reaction to Lovan.

K