Sunday, 9 April 2023

Pain

I've been in bed for close to three hours. I took my pain meds before I went to bed. They've not really done much tonight.

Chronic pain is a weird thing. When I'm busy during the day, knitting, crocheting, playing with the dog, scrolling through social media, pottering around doing what housework I can manage that day, I can pretty much ignore the background pain. Its there all the time, hovering around a 5. I generally don't take my pain meds during the day unless I've had a bad night, or I'm going to be doing more than usual. If I know I'm going to be out and about I take a dose before I go, just to get through whatever it is I'm doing, good or bad,because if I don't, tomorrow will be a write off.

On a bad day it'll start at around a 7 and just get worse during the day. These days I can't ignore it. It nags and grinds me down, saps my energy and my mood. So I have to start the day with the meds. Which then completely naffs my day up. Because then I can't concentrate, focus is out of the window. Walking the dog more than 5 minutes means needing a nap when I get back. Hell, sometimes just taking the meds means an extended nap. Tired if I don't take them, tired if I do. 

On top of this I have my busy, angry, hypercritical brain, swirling thoughts, words and ideas, insults from many years ago and snappy answers I didn't think of at the time 25 years ago. So if it's not my brain, then it's my body, and if I'm really lucky, it's both, shouting to drown each other out and only succeeding in creating a cacophony of misery. 

My sister came for a visit today, we introduced our dogs to each other. Lola, her dog was lovely. Queenie, my girl, was a mardy, grumpy madam who has been sulking since they left. I would have liked to go on a nice walk with my sister and our dogs. Give them chance to get to know each other on neutral ground. Instead we went on the cricket pitch for 10 minutes. I'd had a bad day yesterday so didn't get any house work done. So I had to try and get some done this morning before they got here. But because I was still suffering the after effects of a bad day yesterday and housework this morning, I was in too much pain to push my luck with a longer walk. I live in a beautiful village, with walks and fields and footpaths and scenery and its so wonderful living here. But I can't go on those walks any more. I'm stuck in the house, or on the cricket field. All because of pain.

You see pain doesn't just physically hurt. It's exhausting. Physically and mentally. It is draining putting on a jolly face because you don't want to be moaning about it, you want a normal conversation, to be out of the house around people. But then after 10 minutes you're tired. So then you want to go home. And now you're all on your own with the dual action mental and physical pain, swirling round again.

It's so difficult to explain that physical pain and mental ill health are intertwined, that they aren't two discrete issues, that don't affect each other. And that is something I really wish people could understand. 

Pain is a pain. It's an inconvenience. It's depressing. It's incessant. There is little to no respite from it, because even if the pills do work, they only provide a 4 hour break, at best. 

And that's enough moaning for today.

Thursday, 6 April 2023

PTSD

 I'm not going to talk about me here. I'm going to talk about dogs with PTSD.

Most rescue dogs have some issues with loss, fear, changing circumstances and confusion over new rules in a new home. All of us who have adopted dogs have dealt with the 3/3/3 rule, and have hopefully been successful in getting a dog to settle well and become a full member of the family.

Its more complicated if the dog has been abused or neglected for any length of time, or if they have been street dog. The lack of a full, accurate history of the dog means you have to guess what the triggers are, and that needs patience, calm, and love.

My girl Queenie was imported into the UK from Bosnia. Judging by her reaction on her arrival, it was believed that she had not been in a home at all or in a very long time. She was terrified, wouldn't go over the threshold, and when she finally did, she freaked out, tried to break through windows and was hurting herself to get away from these complete strangers.

Queenie was very lucky. Despite the importing rescue having no rescue backup in the UK, Greyhound Gap were on hand to help. These guys are heroes. Lisa, Sarah and the rest of the team work miracles with dogs every single day.

They worked a miracle with Queenie. She trusted no one. Wouldn't leave her kennel, would not engage with anyone for months. They persisted, because that is what they do. 

They took their time, going at her pace, giving her time to get used to new things, allowing her the chance to learn that they weren't a threat.

She was with Greyhound Gap for 10 months. Then I was entrusted with her. 

Her first few days were worrying for her. My greyhound, Sassy was a perfect gentleman and left her to do her own thing. Gradually she started to relax and settle, but didn't want to come for attention or cuddles. I was allowed to stroke her head occasionally. After 3 months, she would come for attention. She was less hypervigilant on our walks and began to enjoy herself. She was making really god progress with a lovely steady boy to give her confidence. 

Then Sassy passed away. 

We were both devastated. Queenie lost so much confidence. Her steady boy was gone. She had to negotiate the world alone. All she had was me. And she wasn't that fond of me.

But she decided that she'd let her guard down, little by little. It was a conscious decision on her part. She was deciding to trust me. And boy has she blossomed. It's not been smooth sailing. 

She gets triggered by dogs barking, gun shots in the distance, vehicle noises, building site noise. She does not want to make friends with new people, one person - me - is enough for her. There are dogs that she will say hello to. Steady girls who don't push at her, her favourites being Betty and Annie. Alice is new to her, but she was calm, so Queenie thought she was acceptable.

What I see when I walk her is a dog thinking about what is happening around her. Considering whether she is too afraid to stay out or whether she's feeling confident enough to carry on despite the triggering noises. 

With encouragement, love and calm handling, she has made the decision to trust me, to try new things, to be naughty (yes I encourage naughty, it shows she is relaxing and feeling confident, feels safe enough to push boundaries). I don't use discipline at all. Always positive encouragement. That's to only way to support a dog who has PTSD. I give her the space to not be triggered by everything, to try new things and not to push any issues she is currently struggling with. 

And because I have given her the space to decide for herself, she has given me her affection. She plays with toys (as long as there are treats in there!), she begs, ever so politely for morning toast and cheese. She snuggles up as I work on my knitting. She sleeps deeply and happily, dreaming, twitching and grunting in her sleep. This, for me is what dog rescue is all about. Not just being a suitable home, but giving your dog the change to recover, no matter how long it takes. And every day she chooses some new thing to do that shows me she trusts me a little more today and that she is happy with me. And that is all I've ever asked of her. What she gives me, every day, is joy. The joy of watching a flower bloom, little by little each day.

I have PTSD, and so does my dog. We are healing each other a little bit everyday. I am grateful for her and I hope that she is for me. 

Saturday, 1 April 2023

Its been a while

 Hello there, if anyone is still following me, I'm back on my blog.

Quite a lot has been happening in that past 6 years. 

I managed to go back to work for a while, survived the pandemic without catching covid, and worked 60 hour weeks during lock-down as everyone else kept getting ill.

Now I've been effectively retired for that past year. Burnt myself out physically and mentally during lock-down and couldn't get over my worsening physical health issues. Despite my best efforts i just couldn't get my body to do what 'i need it to do to continue doing my job.

So here I am, unemployed, unemployable - probably - and skint. But I'm making more, knitting and crochet, occasionally drawing and enjoying the process of making for the sake of it.

Life does get lonely and occasionally boring. But, and its a big but, i'm happier than I have been in a long time, maybe ever. I wake up mostly looking forward to my day, not disappointed I'm not dead. 

I've had some losses along the way. Gaia passed away at the grand old age of 14, still a madam, still a pirate princess. Before losing Gaia, Lexi, Sassy's half sister came along. Beautiful, quiet, shy girl, who was as stubborn as a mule. She lost her leg in freak accident on the field, but that never stopped her being feisty or loving. I lost her last year, arthritis and a tumour in her eye adding to her worsening health, she became fragile after she lost her lag and eventually she couldn't take it anymore and laid down and didn't get up again.

Sassy didn't do well as an only dog, so along came Queenie, a precious little girl imported from Bosnia with no rehab or rescue back up. She was lucky, so lucky to land in Stoke, where Greyhound Gap and the amazing Lisa Cartwright took her in and rehabbed her. To be trusted with this precious girl is my greatest honour and while very timid, still struggling with a lot of trauma and very easily triggered, she is learning to trust me and is proving to be a very loyal and loving girl. Although that side eye is still very much in use with strangers.

Sassy passed on New Years Eve, having never got over the anaesthetic from an emergency dental just before Christmas. A devastating loss, I will never recover from.

Queenie has settled as an only dog and i am so grateful for her gentle dignity and love.

Ups and downs are part of life. On the upside my sisters have come back into my life and we are rebuilding our relationships with maturity and understanding. I am appreciative or their desire to reconnect and that they are trying to understand why I was such a difficult child. We are all learning a lot about each other and i am grateful for that.

Life has a habit of kicking up surprises and joys as well as sadness and loss. Hardest part is finding the joys when the sadness is all around.

Thursday, 24 August 2017

High Functioning

I've lost count of the number of times people have said to me 'You don't look depressed' or 'You don't seem that anxious' or my all time favourite 'You're the happiest depressed person I've ever seen!'.

What am I supposed to look like?

I recently had my PIP assessment. Apparently I was well groomed, the flat was clean and tidy and I appeared able to answer all the questions without hesitation.

Except the flat hadn't been cleaned for 3 weeks. I hadn't showered or changed my clothes in 5 days and I was on the edge of tears the whole time, and did cry a couple of times as the unqualified, inexperienced assessor made his evaluation based on his prejudice, assumptions and complete lack of real world knowledge. OK, maybe as an experienced paramedic he has seen people in crisis, mid overdose, after a serious self harm episode, drunk, covered in blood and vomit, filthy from weeks of lack of care, malnourished, confused and slap bang in the middle of psychosis. Because that's what a paramedic sees on a daily basis. People who are acutely ill, bleeding, in pain, dying.But mental ill health is not all about crisis. Mostly its about getting through the day as functionally as you can, to keep that veneer of normality and functionality in place.

Why do we do that to ourselves? Why do we pretend to be OK, coping, getting on with it?

I used to think it was shame. I've been made to feel ashamed of my mental health many times. I have recently been struggling with shame and anger. I'm no where near dealing with that but I'm trying. Some days I feel OK, and others I just disgust myself. A personality disorder diagnosis will do that to you. Because, well, attention seeking, needy, unstable, demanding, playing the victim, never take responsibility for their actions, lacking insight, lacking empathy, exhausting, self centred. I don't think I need to go on, you get the gist.

But here's the rub. I'm quite bright. I'm self aware. I have spent the last 30 years or so trying to get better thinking my diagnosis was depression. Plan, simple, depression. I thought I was a failure because I kept falling back into depression. So I'd pic myself up, paint on my 'I'm OK, really' face and off I'd go. Dusting myself off, taking my pills like a dutiful patient. I'd go back to work, exhausted and not feeling anything. Plodding along in this bubble of pretending to be OK. Because we all know the saying 'Fake it til you make it!' And I got very good at pretending to be OK

So for 30 years I have been faking being OK. I've raised a child alone, gone to college and university. Got a 1st class degree, bought a house, learnt to drive. Worked full time. Never quite managed to get on top of my finances, and never managed to save any money. Hardly ever went on holiday. Ever Christmas and Birthday was a magician's trick to get my son a decent present.

I had relationships, friends, mates, coworkers, neighbours.

I was looking OK. Doing about as well as everyone else.

I was drowning in pain and sorrow. I barely coped with the day to day.

I had crushing insomnia, was tired all day, but couldn't sleep at night because my brain never switched off. Weekends when I should have been cleaning, going out, spending time with my son, I was asleep, or sleepwalking.

I was paranoid, I thought people didn't think I was good enough to do my job. I doubted my ability to do everything. I second guessed everything I did.

I suspected everyone's motive for being my friend. At this point I would like to apologise to everyone I ghosted over the years, I never really though that you wanted to be friends with me. I honestly thought you were being polite, or worse, were planning some sort of sick joke where I was the punchline and I was just peripheral in your life, background scenery, not actual friend material.

One or two friends used to joke about my lack of cleaning. I'd make a joke back. In reality it was killing me that I couldn't keep my home clean. I didn't have any idea if I was doing it right, if it would be good enough. It always got on top of me. It weighed me down with shame, anger and fear and added to the depression and anxiety I was feeling. When I did manage to get my house looking nice, it never lasted. I was too exhausted by my daily life to keep it up, so within days it had degenerated again.

So I never had many visitors, I didn't want to feel ashamed of the state of my house. If I let you in and you seemed uncomfortable, you never came back. I know its because I didn't invite you again, but in my head, I thought it was because you were appalled at how I lived and didn't want to step foot back in that hell hole.

But if you only saw me at work, never home, you'd have thought I was fine. On nights out I was loud and silly like everyone else. All I wanted to do was get off my face to escape from how I felt. I didn't really want to be out spending money I didn't have, but I didn't want another night at home alone.

I was supposed to go out to a works party. A Christmas do. I was on my way to the shops to get some stuff to do my hair. As a young lad passed me by on the street, he looked at me and said, 'Oh my god, it's Scary Mary!' He walked on laughing at his own inane wit. I went home, cut my leg and stomach several times and didn't go out. I went off sick from work for a couple of months with depression, again.

That remark didn't cause my depression. It didn't trigger an episode. It was there, under the surface all the time, like a crocodile waiting under the water for a deer to take a drink. All of my energy was spent just holding myself together for the ordinary, every day mundanity that everyone else seems to breeze through, but I struggled just to keep on top of. One single remark, was all it took for the crocodile to break the surface and bang, I'm snapped by the jaws of depression yet again.

And back onto my personal merry-go-round of fall down, get meds, take meds, drag myself up by the bootstraps over the next 3-6 months, come off the meds and pretend everything is OK again for the next 12-24 months until I fall down again.

Over and over again.

A never ending cycle of misery and despair.

But that isn't what people saw. Because in between the depressions, I appeared to be functioning, doing my job, keeping up with college, doing my house up, looking after my son. So what they saw was someone else, the public face of me, not the knot of pain, fear and insecurity that I was, and still am.

And because I'm high functioning, professionals dismiss me as not needing help. Employers don't help me when I need a bit of extra time, or support. Services don't get offered, or if they do, its just for 6-12 weeks, 'just til you are back on your feet'. I've not done myself any favours by managing to function. I've made my life incredibly difficult. Eventually, I'll stop being able to function and then those around me are confused, angry, and disappointed that I can no longer project this image of who they want me to be to give them their security and comfort. I never was that person. I'm really not sure who I am, because I've been masking my real self with this 'fake it til you make it' self for the past 30 years.

So now I'm not functioning. Because I can't be this fake person anymore. I need to be me, and in order to be me, I need to find out who I really am without the high functioning facade keeping everything in and out at the same time.

Its going to take some time to peel these layers off, and I'm going to be a complete mess while I do it. I'm not apologising for the mess anymore, and I'm not going to hide it anymore.

Normal service has been suspended, and I doubt it will be resumed.

Thursday, 17 August 2017

A Frame of Reference

I've had a better day today.

I got up early, got out of the house early and spoke to people, mostly about stuff they wanted to talk about.

Yesterday I spent most of the evening at my amazing best mates house. She fed me, didn't expect conversation, and we played around with polymer clay for hours. By the time I got home I was exhausted, but it had been a good day.

A good day. What do I mean by a good day? Almost certainly not what you think I mean.

At the moment, right in the middle of a deeply depressive episode I feel like I am lost in a world of my own. Underwater, but able to breathe, its chilly, but not cold. I'm distant because I'm underwater. I can't feel anything, just like you feel the pressure of water on you when you are in a swimming pool, but you don't really feel anything else. And I feel like this all the time. I can communicate with you in the language that we all understand, but I can't make you understand my experience. I cannot explain to you what my world is like, because unless you have gone through the same thing there is no basis for comparison.

(My apologies now, as I will regularly quote science fiction, cult movies and TV throughout this blog. It is a place I escape to, which I find comforting.)

To quote Mr Spock in the Voyage Home when asked by Dr McCoy what death is like 'It would be impossible to discuss the subject without a common frame-of-reference.' Mental illness is a place you need to visit before you can understand what it is like. 

I am overwhelmed by feelings of sadness, but I am not sad. I am driven by self hatred, but I don't dislike myself. I am tormented by anxiety, but I want to go out and see people. I desperately want to be happy, but I know that will never happen for me. I live in a place where I feel nothing most of the time, but I have the capacity to experience joy unbound at the colour of a sunset.

Going outside and meeting people is exhausting. Not because I have to make the effort to get up, dressed and go out, but because I have to present this happy, coping, ok, normal face to the world. I have to perform for everyone else. There are very few people who have truly seen me when I have been in the deepest places of my pain. I hide it because I am ashamed. Because I am ugly in my desperation to find something, anything to hang on to, so that I can stay alive, just one more day, because despite how often i have felt like killing myself, I really do not want to die. I don't want the world to see that, because I don't want pity. I don't want people avoiding me because it makes them sad, uncomfortable, angry. 

So I staple my 'OK face' on and I greet the world. I perform the normality dance and everyone is happy. Except me. I am knackered. Its bloody hard work hiding how sick I really am. Its not even something I do consciously. Its something I've done my whole life, because to tell someone what is really going on in your life, well then they just judge you, dismiss you as a liar, an attention seeker, a problem, a criminal, a waste of space, lazy, stupid, pointless. 

I recently went to a friend's party. I wasn't in the mood, but I'd said I would go. I pasted on my smiling face and walked around pretending to be OK, while wanting to tell people to fuck off for suggesting the most idiotic and pointless 'cures' or 'self help DVD's', or 'have a drink, you'll feel better'. Then one of my friends who is wonderful, but this night was a bit drunk, announces 'I'm so glad you are happy again, you look so lovely when you are happy!' And bang, just like that, I had nothing left to say, nothing left to do but go home and feel utterly shit about myself. 

Why? Because I wanted to enjoy myself, but I was too tired. I didn't want to be there, but I had promised to go. I wanted to really relax and chill, but everyone has an opinion on my mental health and how I can cure it. Big news there, ITS NOT CURABLE! I'm never going to get better. the best I can hope for is lots of long term coping mechanisms, pacing myself, and getting stable. But getting better? Nope, never going to happen. My wonky brain is not going to suddenly reorder itself and repair the actual structural damage my childhood did to it. The disorganised brain chemistry s not gong to miraculously correct itself and start working right. It simply doesn't work like that.

Now sympathy is OK. Understanding is a little more problematic, because unless you have really been there, you cannot possibly understand. 

No, sorry, feeling a bit sad cos you didn't get the house/job/car/dress you wanted is not a basis for comparison. Having your good mood dampened a bit by next door's dog shitting on your front lawn does not equate to massive, irrational mood swings and anxiety attacks slapping you upside your head when you least expect it.

Being a bit distracted because you had an argument with your boy/girl friend is not the same as getting no sleep because your head has been racing around all night going over every single conversation you have had since you were six and then telling you that it all proves how stupid and irrelevant you really are.

And, honestly, I know you mean well, but self help books/mindfulness DVD's/exercise videos/special diets/just choosing to be happy instead type advice isn't helpful. In fact its incredibly insulting and upsetting. You wouldn't suggest to a diabetic that their foot will grow back of they just watch this DVD. Or that mindfulness will cure someones blindness. These suggestions are not about easing my pain, or helping find ways to support me in my journey to better health. They are about making you feel better by feeling like you are doing something. 

Honestly, I don't need you to do anything. Just be my friend without making any judgements about my health or making any suggestions for cures. Be supportive, be sympathetic, be sensitive. But really, don't try to understand, because you just have no basis for comparison.

Wednesday, 16 August 2017

Why Not?

I'm in a state of mourning. Not for someone that I love. Not for someone I know. Not even for a real person. 

I'm in mourning for the person that I thought I could become, if I could just get myself together for long enough to get a decent job, stay stable, save some money and have holidays, new car, resources, someone to love forever who would love me unconditionally.

That person will never come to be. My opportunity to be that person was taken away from me by my illness, by my complex mental ill health. It was also taken away from me by the people who were supposed to be caring for my health who decided that I didn't need to know about my diagnosis. The ones who followed on who failed to offer me real long term treatment for my diagnosis, but instead threw proverbial sticking plasters at me and were disappointed when I showed up again six months later, a year later, even 2 years later, still ill, still struggling.

I got angry with myself for not getting better. For just not trying hard enough to get better. And in those angry states I blamed myself for failing, I blamed myself for being ill. I blamed myself for just not trying hard enough.

During that time my physical health was also declining. But whenever I sought help for that I was treated as if I was a hypochondriac, I was making symptoms up. There wasn't a lump there, there wasn't pain from that, you are just drug seeking, attention seeking, you don't get pain there, its all in your head.

I'm not stupid. In fact I'm really quite bright. And that somehow, makes it all worse, because the curse of being very bright is self awareness. 

I can see and hear myself when I'm having a meltdown. I look and sound ridiculous. I look and sound like a child having a tantrum. I berate myself for getting anxious, crying, being angry at the wrong person, being for all intents and purposes a total fucking basket case. 

I hate living like this. But no matter how much I try to be like other people I just can't do it. My brain doesn't work that way. I'm fighting childhood abuse, school bullying, PTSD, chemical and structural changes and differences in my brain that cannot be corrected no matter what medication you throw at me. Yes, there are very real structural changes in the brains of people with mental illness. Look them up on Google. There's pictures too. They are pretty, and horrifying all at the same time. 

I'm difficult. I'm fragile. I have a sense of humour, even on my most lost days. I'm surprisingly resilient, because I really, really want my bloody life back. I'm cynical, because I know even if I get offered the help I need I'm still at the mercy of it being whipped away because 'someone else has a greater need'. Because mental health services are rationed, and portioned out just enough to have you appear OK, dressed, washed, house clean, and 'Oh fantastic, you have a job!' Out the door you go.

Because mentally ill people are still treated as if they have caused this to happen to themselves with drugs, alcohol, sexual promiscuity, being female, living with domestic violence, running away from home, suicide attempts, self harm, disclosing sexual abuse, not believing in God, believing in God and asking for help and then rejecting that help when it doesn't help. When in fact these are symptoms and not causes.

As an example, a man goes to the doctor with a persistent cough. Turns out this life long smoker has lung cancer. He's put on a list for treatment. Gets seen within 2 weeks. Has all the most appropriate treatment, until his cancer is cured, or until he dies, but all with lots of care, lots of patience, and loads of support. 

No one suggests that his smoking is the reason he is ill and therefore he did it to himself and the treatment will only be offered to those who never smoked or who quit more than 10 years ago.

No one says, 'Sorry, there are people much worse off than you, who will get the treatment instead'.

No one would even consider saying, 'well even though you still have cancer, we think you look well now, so off you pop, your treatment is done. See how you get on.'

So why is it acceptable to say this to someone who is bipolar, schizophrenic, has a personality disorder, PTSD, OCD, or chronic clinical depression and anxiety? These are life long conditions. They are also, if left untreated, life limiting conditions. In many ways they are terminal illnesses, as the incidence of suicide is so high amongst people diagnosed with these illnesses that it is seen as an inevitable outcome.

So why cannot people with mental illness be treated in exactly the same way, with the same expectations, and the same dignity as people with physical illnesses?

Why are you embarrassed about my mental ill health? I'm the one who lives with it day in and day out. No you. You get to walk away when it gets hard, messy, inconvenient, painful and upsetting. I don't. 

So suck it up buttercup, I'm not going to be quiet about it anymore. I am who I am, I'm bloody angry that my life has been blighted and I have been blamed for what was done to me to cause my ill health, and I am damned sure I'm not having poor quality treatment because you are a judgemental ignorant idiot who insists on remaining ignorant, because everything else is effort. You have no idea what effort is until you have had to spend half a day fighting your own brain just to get out of bed for a piss.

Tuesday, 15 August 2017

Good Day, Bad day, What a Waste of a Day

I fully intended having a good day today. Went to bed shattered last night and slept until 7.15, when I woke up feeling energetic and motivated. So much so I was out of bed by 8.30, put washing out, washed the pots, walked the dogs and had another load in the washer all by 12.

I was due a visit by the (un)friendly, neighbourhood Housing (Gruppenfurer) Officer about my 'overgrown' garden. A less sympathetic, understanding and tolerant pair I've not met since the last time I got queer bashed outside The Cossack back in the 80's.

Now I have a big issue with anxiety. Also I have a big issue with threatening letters from anyone. I don't give a flying fig-tree who you are, what your powers are, or even if it is a 'standard letter'. If you threaten me by post, what you get when you make an appointment to actually meet me is someone who is angry, frustrated, anxious, afraid and, to be honest, down right bloody rude. Be prepared for all of that to double up if you admit on the phone that the threats you have made in the 'standard letter' are actually empty ones, because you don't in fact have the power to do what you threatened in the letter.

So there they are on my doorstep. Oh they were NOT coming in my house. They were there to look at the garden. To actually come in my house I would need a weeks notice, a support worker, a mental health advocate and a fucking solicitor matey. So there you stay, on the doorstep. No hospitality for you. You can't be courteous to me by not sending threatening letters, then no way can I be courteous to you by inviting you in. I know better, I've watched every episode of Buffy and Angel. I know you don't invite the monsters in.

Apparently they are very happy that I have 'made a start' on the garden and that the weeds have now been cleared. What's the timetable for completing the garden?

I was gobsmacked. I have arthritis just about everywhere and a glass back alongside a Personality Disorder (which I'm still adjusting to the diagnosis of) depression, anxiety, PTSD, Bipolar Disorder, self esteem issues, being a survivor of childhood abuse and neglect, self harm issues, a history of drug and alcohol misuse, suicidal actuation and para-suicidal behaviour and general trust issues (though I really have NO CLUE where they come from). Really? You want someone who often can't get out of bed and feed herself to give you a timeline of when her garden is going to be acceptable to you? Incidentally, I have almost no income as I am shocking with money and most of my benefits are swallowed up by deductions for bills I've struggled to pay on time or at all, so I'm trying to sort the garden on ZERO budget, negative emotional energy and the physical capability of a mayfly with fibro and you want a timeline.

Cue blank disbelieving stare.

I went into the house and produced a copy of my GP report for my upcoming employment tribunal (more of that later). This explains in great detail what my mental health issues are.

I explained as patiently as I was able (so not very patiently at all) that they should never, ever send me threatening letters. Because these make me very anxious. That all communication should be by email, as I seem to never get the 'three previous letters'. That all emails will be acknowledged by me and if they aren't, should be resent. That I need help, not threats. That they asked me when they signed me up for the tenancy if I had any health issues, which I reported as they were known to me at the time. The housing Officer who signed me up was actually embarrassed and um'd and ah'd shuffling around on the spot when I spoke openly about my mental health. At no point did they offer me help or support with my tenancy, benefits advice, or available support for vulnerable tenants.

Why ask the damned question if there is nothing they are going to do with the answer, or is it simply a tick box exercise to prove they are caring landlords? Don't ask if you aren't also offering help, because I'm not going to improve your stats for nothing. You get extra money for hitting targets. I'll have some of that please, it is technically my money after all, as I do in fact pay council tax, and quite a high proportion of my rent.

So after they had gone, which was immediately after I terminated the meeting because I was about to get shouty out of sheer fury and frustration that they just didn't understand the stress they were putting me under, I sent them an email, asking what their expectations were with regard to the garden, as originally I was told simply to cut the grass on the front and clear the weeds at the back. Oh no, they said, its only if it gets overgrown again then i will have to contact them and give a timescale for when it will be done.

Erm, can I just explain again that if it gets overgrown again, its because my mental and physical health will have declined again, and there is no chance of me being in any state whatsoever to communicate with Herr Housing Officer, let alone advise when I will be able to get on top of the garden. How is this difficult to understand? Its not a won't communicate, its a can't communicate. I'm not uncooperative because I'm awkward (although to be honest for you two I would make an exception), I'm uncooperative because I am unwell, and I'm not ever going to get better. Would you be this unfeeling with someone who had become a wheelchair user? Had terminal cancer? Alzheimer's? Was just plain old? So why is it acceptable when someone is mentally ill?

So off you go the pair of you, educate yourselves on what you can do to support vulnerable, mentally ill people in their tenancies. Its not my job to tell you how to do this. you have policies, procedures and access to the internet. Go and Google it like normal people do.