Tag: pain

Saying a last goodbye to my dear friend

Saying a last goodbye to my dear friend

The dear friend I wrote of in my last post, Father S, passed away last Saturday, a day after I had last visited him. Today was his funeral. It was a very hard but beautiful goodbye.

Father S was a Priest at my friend’s church. He was long retired however continued to serve and minister to his congregation – and to so many more, such as me. I came to know him through another good friend (the same who initially brought me to the faith); I have never lived in his Parish however he took such care of me and I know he prayed for me daily.  I can only imagine how much he is missed by those who knew him longer and more than I did.

Father S was an extremely humble, quiet and private person. He drew no importance or attention to himself. He worked, prayed, cared and gave of himself generously, not seeking recognition, never appearing discouraged, astoundingly giving continually even when there came nothing tangible in return. I think, indeed the Priest who gave the homily at the funeral said, that Father S has no doubt reached and helped far more people than we yet know or than he himself even knew.

I do not think his path was ever smooth. He moved between continents. He converted between churches and subsequently felt the call to become a Priest and dared to answer. I do not think he had many people to care for him in his early life, and he has lost and left behind many family members since. He suffered greatly, physically, mentally and emotionally, throughout I believe, the majority of his life, particularly in his later years. He faced intense physical pain and weakness, major health problems, increasing fatigue, struggles to get around. He suffered not only the mental cost and hurt of those things, but also deep distress, fear and sadness. Through all this, he continued to work and to give so much in friendship.

Only very occasionally did he brush the surface of what he went through, physically and psychologically. I knew and gathered a little from prayer, conversations and letters exchanged with him, and learned more today at the funeral. Though he did not make much of his suffering, he did not sugar coat things either. He did not pretend everything was fine, or not to care, or that he did not struggle, or that he had all the answers, or that we must be strong and healthy, or that all is happiness when we walk in the way of Our Lord. He lived and gave in every moment, acknowledging what exactly it brought, never turning his gaze away from Jesus and never fleeing. He taught me to begin to hold fast to Our Lord of love – seek Him in whatever is happening right now and hold fast (rather than running in fear from an image of a God I have created from all my fears and the torment going on in my head in my illness).

When I visited him the day before he died, all the more than ever, I sensed that he was very close to God. He had become much sicker very quickly at the end. On the way to see him that last day, primarily I was desperately hoping I would be in time. I was not afraid, but I did feel some uncertainty and anxiety as well as the sadness. How would I find him and what would be the right things to do? I have sat with the dying before, having worked in a hospice and having lost other elderly friends at a nursing home I used to volunteer at. Time somehow seems to change; it is not a bad thing, but indescribable; perhaps it is a result of so much that can pose a barrier to communicating, giving and loving, being stripped away. We are left bare and vulnerable faced with the finality of the separation of death. It need not be all sad. Somehow, in precious time like that, what we cannot express as we may wish to in words, can perhaps be communicated between our souls as we are held together by the Love that encompasses all of us. In our defencelessness, the stronger hold the love of God has.

In that visit as I talked with Father S, knelt and prayed with him, I felt I knew heaven was near and Mother Mary’s arms were around us. Kneeling beside him I told him some of the truest things I have been so afraid to admit. I thanked him as I should have thanked him much, much earlier and more often. Father S is one of the people whose encouragement, prayer and friendship has held me up when I have been at the very darkest times and he has played no small part in saving my life when I was at a point that I was going to try to end it. Kneeling beside his bed I prayed as I have not been able to pray for many long months. I felt that already, in the footsteps of Our Lord Jesus, Father S was drawing me after him, just as Jesus draws us after Him. In his prayer and his life that he had offered totally to God, he was drawing me out of fear to learn to know, perhaps for the first time, a God of love.

There was no ceremony, no astounding event in the moment when Father S passed. There were no visions, no glorious rays of light, no voice from heaven, no odour of roses. There was quiet, and love, and friendship, and hearts reaching out in prayer and thanksgiving to God alone. In the same way as he lived, he died, quietly, with those who loved Him, everything offered and united to the God of love He told us so plainly about in his words and his life. He died on the feast of St John Paul II (whom he loved), just before 3.00pm, the same hour at which Our Lord Jesus died. I feel that Our Lady and St John Paul came to carry him to Jesus.

I pray that now he knows in heaven the fullness of joy with the Lord he has reached out for, for so long; that he also now sees all the good he has done, especially that which remained hidden whilst he was on earth. I know so many hearts here below are full of thanks for him.

May the choirs of angels come to greet you,

May they speed you to paradise;

May the Lord enfold you in His mercy,

May you find eternal life.

(From Song of Farewell, by Ernest Sands)

Image thanks to pixabay.com – https://pixabay.com/en/banner-header-christmas-candles-880323/

I’m sorry – I haven’t forgotten you

I’m sorry I haven’t posted here or visited your blogs in quite a while. I haven’t forgotten you. I know it’s not obligatory but I feel guilty being inconsistent ams not being there for others.

It’s been a few weeks of pretty big changes in my home life, family, friendships, work (or temporary absence of!), finances, therapy – not all the changes are negative however they are all demanding and not necessarily unsettling but all taking energy to work through. Physical pain is still having a big impact on me at the moment and I’ve needed to take things much more slowly than I’d choose. It used to be something I could deal with but now I’m not coping well. I feel as if I’m constantly saying this. It’s not am excuse but it is a big part of my life right now.

There is another event I’ve been struggling with, which has held me back from blogging. I had a really upsetting experience in an internet based support group and blog, in which I had previously trusted, thinking I was finding a reliable source of information, understanding and solidarity with other members as well as being able to offer support to others. I don’t think it is the right time to go into detail here about what happened although I will explain a little more in a future post. Please don’t worry – I’m okay and safe; I was never in any physical danger and I have ceased contact that was proving damaging. Fortunately, I had never divulged personal information like my full name or contact details. Also, just to be clear, this experience was absolutely nothing to do with this blog or any of the lovely people who visit it. It happened somewhere completely different.

The experience has had a big impact on me. I was very distressed. I felt a huge loss although also a huge betrayal. I got very scared of writing anything online, including in my own blog and in messages to anyone, although that is not necessarily rational. My obsessional thoughts were very triggered and the voices got loud. A whole range of feelings and thoughts spiralled out of control about how I trust other people, how I feel about getting support or not and being believed or not; perhaps most scarily, whether I’m harmful to other people without knowing…

On the positive side, the events have brought up lots of issues I need to discuss in therapy. They’ve led me to think about how therapy is changing the way I think. They’ve shown me ways I’ve started to react differently (for example, I did not follow through the compulsion to self-harm).

Most of all, it made me all the more thankful for the genuine and compassionate support everyone who visits this blog has shown me. It’s a rare and precious thing. THANK YOU.

I’m trying to get back into writing, gradually.

Ginny xxx

For the first time in forever

“There’ll be actual real live people, it’ll be totally strange

But, boy am I so ready for this change!”

Anna_costumes_(Frozen_2013_film)

Yesterday was another little but notable step for me. It was my birthday recently and to celebrate, a small number of close friends came over for a bring-and-share lunch. This was the first time in a very long time I have done anything like this. The few close relationships I have are a very precious blessing to me. I never usually mark my birthday in any way and find it too embarrassing and uncomfortable. I am not used to having a home that I can invite other people to. Thankful as I am to be here, it has taken me a long time to get the courage to invite people over and this is the first time I have invited more than one person at a time. Actually, it is the first time for years I have been in a group of people in this kind of social situation, where I’m interacting with everyone for a substantial period of time. Also, it was my first attempt at a gathering where I’d be hosting and caring for everyone.

Building up to the day, I was excited and very touched that my friends cared enough to give the time to come and were spending such an effort to celebrate with me. In particular my dear friend L. was coming from over two hours away with her little girl to be here. I was also very anxious and feeling overwhelmed by worrying that I’d do everything okay, be able to make it nice for everyone, help everyone get along well (not everyone knew each other) and be able to do well enough with everything practically needed since I can’t stand or walk much right now. With everything that has happened in the last couple of weeks with work and my health, I was repeatedly tempted to cancel, but not wanting to let people down or hurt them, stopped me, and so the day came.

I was so grateful L. was there. Her presence gave me confidence and her beautiful little girl, overflowing with interest and happiness, made me feel better. L. helped me finish setting things out and without her being there I don’t think there’s any way I’d have had the confidence to go through with it.

It was a beautiful day of blessings. The food seemed to be well received and appreciated and everyone brought something to add to the meal (actually, leading to plenty more inspiration for my future Ten Dishes posts!). A lot of the simple practical things I had worried about, like whether everyone would be comfortable in my small flat where decoration and furnishing are still something of a work in progress, were actually okay. I’m very fortunate to have friends who are understanding of the time it takes to bring a home together. Everyone chatted easily together and it was possible to find common ground and interests surprisingly quickly given that not everyone had met each other before. The two beautiful children (one 9 months, the other nearly 3 years old) were adored and delighted in.

I was full to overflowing with thankfulness and the lovely illustration that people wanted to be there and cared enough to come and join in generously. The shame, worry and embarrassment I had felt beforehand was steadily taken away during the afternoon. I was struggling physically after a time and the pain was bad but I was helped and nobody was angry or expressed that they thought I should be doing more or was a bad hostess. I hope they really were happy not just saying nothing out of kindness. Mentally I felt drained and was aware that I could not concentrate as well as I wanted to, because I was “missing” things, not able to take in what people were saying or dissociating very briefly but repeatedly. However, nobody reacted as though they noticed or thought I was being weird. I wonder if they did notice or not. Were they actually being considerate and accepting of what was happening or could they not tell? I wish they could not tell but I don’t know… I’m sure they must have…perhaps I can check this with someone I trust most, like L. Nevertheless, things still seemed to be okay. I hope.

Afterwards, in the evening after everyone had gone, the pain and exhaustion were severe but I my heart was still brimming with the surprised joy of the gathering and the kindness everyone had shown. The gifts of God in friendship mean so much to me right now and help me believe things will be okay.

For now, I have several thank-you cards to write, as well as this very happy memory to think on!

“Because for the first time in forever

There’ll be music, there’ll be light…”

Frozen_Anna_Wallpaper_2

Ginny xxx

Lyrics from “For the first time in forever”  from Disney’s “Frozen” as sung by Kristen Bell. (How much my little goddaughters would approve!) Images with thanks to wikipedia.org and disney.wikia.com respectively.

 

The pain is no longer numbing

I’m finding this physical crash really hard. I feel useless. I’m scared by the pain though I don’t know exactly why. I can’t face going outside. I don’t feel safe. At home feels slightly safer. Outside is too much and I’m tired so quickly. I’m not frustrated, I don’t think, but I do feel sad and the pain is scaring me. I don’t know why. Nothing bad is going to happen just because of the pain. What am I scared of exactly? I don’t know.

I’m sure when things were this bad last time, a few years ago, I dealt with it “better”. I got on with things better. I stayed on more of an even keel outwardly and kept going. It didn’t affect me so much emotionally. Last time it actually shut my emotions down more. The pain felt safe. It was a bit like my self-harming. It was as if, though the pain from my physical illness wasn’t self inflicted or chosen, it absorbed some of my emotions and deadened them and the voices in my head said that was safe because it stopped me being a danger to other people. I wasn’t afraid. I didn’t feel so shaky and tired and vulnerable and exposed.

Now the pain and physical disability doesn’t seem to be swallowing up my emotional being and numbing me anymore. This must be something to do with changes the therapy is working in my mind and the fact that I have stopped self harming.

It’s quite scary to admit that this change and separation is occurring. Physical pain no longer equals safe and numb inside my head and not a danger to other people.

Now in my current physical struggle I feel the fear and vulnerability and even heightened emotions. Now I just wish someone were here to hold me. But at the same time I know I have to find out how to do this when I am on my own. Because that’s the day to day. Because I can’t ultimately depend totally on another person – in the end that puts an unfair weight on to someone else and puts me at risk if I can only go on depending on someone else every moment needing them always to protect me, allow me to to feel, allow me safety…. I don’t mean that I want to be isolated or want to reject other people. I really don’t; I long for the opposite. Just I meanthat I have to learn how to exist and experience physically and mentally for myself. This probably doesn’t make much sense yet. I’ll try to explain in better in another post.

In trying to learn some kind of ability to exist alone, exist without total dependence on others, I can trust totally in the unchanging love of Our God. The God who says fear not, for I am with you; the God who loves us first so that we can learn to love Him; the God we can count on as our hope just as surely as daybreak follows the night; the God who comes into our darkest, poorest times when we are lost and delights in us as His children.  In times of pain and alone-ness His presence is often now all the clearer to me and gives me hope that even when I fail totally at simple things and fear I disappoint everyone by being able to do so little, my life is not too little for Him. He loved each one of us before He even brought us into being. That has to mean HOPE.

Ginny xxx

Is this pain real?

WARNING: this post contains brief mentions of eating disorders and self-harm.

Which is harder to deal with: physical pain and physical disability / ill health, or mental pain and distress and poor mental health? Is there a difference for you? Does one seem more real than the other?

At the moment my physical health is poor and my physical pain and limitations have been worsening fast, in particular in the last couple of weeks. Any standing or walking is painful and shaky. I need to use my walking stick again, having had 5 years or so not needing it (apart from one time for a few weeks).

Physical health problems can be tangible and visible in a way that mental health isn’t. People can see that I’m using a stick or that I need to rest often. They can’t see in the same direct way when I’m having obsessional thoughts or hearing the voices. I’ve posted before on how many people I’ve met who have Borderline or other mental health problems, feel a shame about their mental health condition and support needs and a guilt for needing help or “not being normal” or not being able to cope. Many of these people, again myself included, have physical health issues too, and the common feeling seems to be that these are more allowed and acceptable (in others’ eyes and also our own thoughts) than the mental health needs. Often that does ring true with me and I’m sad so many people find that. I’ll post on that topic more separately.

Just now I’m struggling to trust that my physical pain is real and allowed too rather than being something I’ve invented, is my fault, not real…

Physical pain is still subjective. Nobody can objectively see how much, say, my back hurts or there are weird numb sensations then burning pain in my feet. Anatomic problems can be seen and measured on scans and tests but what our experience of pain and weakness is, can’t be.

I have been desperate for more visible and concrete proofs of what I experience physically. I have some, for example, a scan has showed some degeneration in my lower spine, the GP performed various tests which diagnosed they inflammatory condition in my knees, and so on. However much of my physical struggles aren’t documented in the same way. You can’t see nerve pain or nervous system inflammation, painful joints, muscle spasms, poor regulation in the autonomic nervous system (well not directly anyway, although some tests can show disrupted adrenal or thyroid function or high white blood cell counts)…

The lack of physical, external evidence of what I’m experiencing is a real problem for me. If i let myself think on it the voices get loud. I think I must be going mad. It must be my fault. It must be my invention or my imagination. I should just get on with it and push through. I’m weak. The worst thing is the thought I must be a fake. I hate using my stick because of it even when I’m in more pain and more unstable without it. I’m deceiving everyone, the voice tells me. Look. Everyone knows. Everyone’s looking at me. Everyone’s talking about what a fake I am. They all know nothing’s wrong with me really. I’m terrified it’s all made up and I’ve faked it all without realising. I’ll never stop it but my whole life I’ll be a fake and at the end I’ll be judged and punished for it. Other voices tell me I’m doing it for attention to make people worry about me. Don’t you know how much upset you’re causing, they ask…

In the past I’ve felt I’ve deserved physical pain. That it’s safe if I have pain or cause myself pain. It means I’m being punished and suffering and that’s safe. It means I won’t be so bad. I won’t be so dangerous. I’ll be weak and that’ll be safe. That was how I thought during my anorexia. That was how getting thinner and thinner and more ill kept me safe. It is/was part of how self harming was safe too because it punished only me, just only me, stopped the evil emotions as I saw them getting out. I say “was” because I’ve managed not to self harm for a month and I’m grappling with the feelings that come to be now I’m not doing it.

The physical pain from my illnesses that I can’t control is different. It is overwhelming. It isn’t safe. It might show my badness (because I’m fake). It’s overwhelming and can feel inescapable but I feel I don’t have the right to think it’s real.

It interacts with my mental control too. When the pain is bad part of my mind freezes. I cannot be warm or present for other people. Trying to interact at all is a fight. Sometimes I want to hide and sleep. Being around anyone can be too much. I panic and want to be safe at home in my secure place. I mix up words and sounds and can’t get a simple sentence out straight. The all encompassing nature of emotions and especially anxieties and fears and psychotic thoughts increases. I feel shut tighter into the world of my Borderline.

I doubt the reality and truth of my physical and emotional experiences. The only pain I knew was real and undoubted was the pain of self harming or starving. The rest of my experience I doubt, as though the real me that’s bad really, angry, fake, deceitful, will be found out in the end, but I can’t escape from it/her. I only just realised that in writing this post. Trying to stop self harming is going to change a lot, I think.

Ginny xxxx

Not my day off

Today has been demanding. It’s one of those days that seems too much to have been only one day. I got big stuff done but also I’m losing time in unsettling ways and I know I was dissociating a lot between the different tasks and meetings I had to do, slipping out of being engaged with what’s going on and what I’m feeling and struggling to come back. Nevertheless I got through quite a few challenges.

Last night I knew I needed to tidy and clean my flat. My support worker was coming today. Also I hadn’t been on top of the housework since my operation and it was bothering me more and more. Recently I’ve started to find a greater sense of order and calmness if I don’t have too many things disorganised around me. This is interesting because til now, I’ve tended towards accumulating things I don’t need and not being able to keep my house ordered, not exactly hoarding but not being able to face items and paperwork and household tasks without going into panic.

Yesterday I was very anxious about today but put some of the physical drive from the anxiety into cleaning and then went on to clearing out some of my cupboards. By late evening I’d cleared 7 big bags (between rubbish and charity shop) and set 3 more big bags of things to try to sell at a car boot sale. The fact I don’t have a car for the boot element of that plan is potentially problematic 🙂 but there are the odd few table-top, largely indoor, sales in community centres / church halls here in the summer and I’m hoping I can find one to join in.

Today was a struggle to get up. Everything hurt. Still, I got together the papers I needed to show my new support worker (more on this tomorrow), then it was off to my care coordination appointment with my CPN. This wasn’t easy to go to because, although my last appointment was okay, in the two previous appointments I’d been really distressed and felt I didn’t get heard when I was desperate and at risk. Today’s appointment was actually really good. We looked at some DBT skills and we did a review which was overdue (every 6 months or so is a review appointment). I’ve not yet felt able to discuss with my care coordinator exactly what went wrong in the difficult appointments earlier this year when everything was going to pieces. I’m scared I’d lose control and the feelings of anger and not being believed would return and I’d do bad things and be back where I was. However my care coordinator and I have managed to move forwards having 2 positive appointments. I was scared after what I’d done – how upset and angry I’d got – he wouldn’t believe me or want me anymore and they’d know how bad I am and that I didn’t deserve help. That hasn’t happened. That’s something that I don’t usually get to experience.

Straight after my care coordination I met my support worker, H., who is from a housing support charity I was referred to recently. He is going to help me sort out my benefits like Housing & Council Tax Benefit, Tax Credits and disability benefits,  as well as liaising with my landlord about the rent arrears that I got into when I lost my job last year. It was a long appointment. We went through the background to how I’d got here, financially and in terms of my health, and we looked at lots of documentation, my income and my benefit and Council Tax notices. This took a lot out of me and I came so close inside to panic and losing it and emotions shooting too high. H. was very calm and non judgemental, which helped a lot. (More on this in the next couple of days.)

Then I had to rush to my GP appointment, which was the first since I’d been very distressed and angry at the surgery a couple of weeks ago;  also the first since my operation and finding out endometriosis isn’t actually the explanation for my pain and gynae issues. I’m still working through what happened in today’s appointment. I was dreading going into the surgery because I’m still terrified of what I did and how much I lost it. I was ashamed and embarrased and knew that they probably didn’t want me around again. I knew I’d really upset and inconvenienced and disturbed people. I’d scared people. That’s the worst thing,  the harm I caused, the bad I’ve always feared getting out of me. Talking to the GP  and discussing what happened and then also talking about my physical health was really emotionally charged.  It’s hard trying to deal with a lot of uncertainties about my physical symptoms. I know not having endometriosis is a really good thing but not having any explanation for all the things I thought it explained, and the fact the doctor isn’t really interested any more in investigating what may be wrong – well, that’s hard and triggers all my fears that it’s all in my head, I’ve made it up or I’m mad, it’s my fault. …

After the GP it was off to the pharmacy with my prescription, then finally home.

It’s been quite a day. I had a soothing bath tonight. Today was the first day I could have a bath since the operation (don’t worry I promise I did still wash 😉 !). The doctor sealed the wound with dissolvable stitches so it was important not to soak them in water too soon or they could have come undone. Also it was not safe to try to get in and out of the bath whilst my mobility was further reduced with post op effects. Falling is a risk for me anyway because of the problems the fibromyalgia and arthritis cause in my legs. So, tonight was a good little relaxation and refreshment. The little things do help!

How has your day been?

Ginny xxx

 

Carers who really care

The doctors and nurses who looked after me when I was in hospital for my operation last week were fantastic. I owe them huge thanks. It was really busy on the ward the two days I was there, probably all the more so because a lot of surgeries had had to be rescheduled from the previous day. From my arrival, they were sensitive and compassionate. I was there because of my physical health but they knew about my mental health as well and we discussed it during my assessment when I arrived. The nurse taking care of me took time to be really aware of how both my physical and my mental health issues were affecting me and to enquire about whether I was getting the help I felt I needed and would be supported once I returned home after the operation.

It was a minor op but still daunting to me. The nurses and doctors’ compassion, communication, availability to answer questions, even simply their general presence, genuinely doing all they could to help, made such a huge difference. One nurse even taught me the instant ice trick!

I wasn’t an emergency, an urgent or complicated case, thanks be to God. They treated so many people in those two days, most of whom I’m sure needed much more care than I did. Yet they still had time for me.

I am so thankful for these people who give so much.

Ginny xxx

That should have been me

Do you ever feel that someone else’s place or circumstances should have been yours? That you really wish you could swap, or take for them what they are going through? I am not talking about good things, more about difficult things. So many times, when someone I care about is suffering, I’ve wished that I could take for them what they are going through. I guess that much is natural, when we care for someone, particularly with parents and children – I’m not a parent but I imagine loving parents would probably willingly take suffering themselves to spare their children’s suffering. Weirdly, I get these feelings with people I don’t really know. I can get really strong feelings that I should have been in their place, that it should have been me, not them.

When I was in the hospital for my operation last week, there were several of us on the ward having similar procedures. Lovely NHS blue curtains round the beds are fine for privacy in visual terms but do nothing to stop you overhearing what is going on, much as you really try not to! So, I ended up gathering that the lady in the next bed, about the same age as me, was having the same operation as me for suspected endometriosis. We both went into theatre and both came out and the doctors came round to see us to tell us the outcome. I’d gone in expecting to be told I had extensive endometriosis and that it had grown across my bladder and potentially other organs. I’m single and I do not want to have my own children. The lady next door to me had a (from what I saw) caring, loving husband or partner and I gathered that they were at the stage to consider starting a family. She didn’t know what to expect in the op. We both came out. I got told that there was no endometriosis. She got told that she has severe endometriosis, it has grown through her other organs, it was so severe they could not remove it in that operation and will need to do another more complicated operation, and if she wants any chance of having children it’s very unlikely and she would have to go through freezing eggs and having IVF. She was so astoundingly brave, talking to the doctors and talking to her husband / partner, I was stunned, but she has this shock and loss to face of likely not being able to have children.

Now – apart from acknowledging the fact that I have distinctly too big ears and need to stop being such a nosy moo (bring ear plugs next time!?) – I instantly felt that my place and hers should have been swapped. I should have been the one to have the endometriosis. I’m single. I don’t plan to have children, for so many reasons. I knew that already. I expected endometriosis. I’d not really have lost anything if I had it. She has a partner and they love each other and probably wanted a family and she’d have been a lovely lovely mum.

I didn’t know her and I’m sure I’ll never cross paths with her again but I cried and prayed to God, that should have been me. It should have been me, not her. It hurt.

Frequently, I get this strong feeling that it should have been me. It happens with friends, where I really wish I could, and feel I should, be able to take on pain that they are going through and go through it in their place. It also happens with people I barely know. Possibly it’s connected to times I dissociate, or my feelings that I “shouldn’t have been me”, shouldn’t have been who I am, I’m not real, everyone knows my thoughts and intentions are something other than what I think they are (something bad) – but this is different. Feeling I should have been in the other person’s place when they are suffering… that I wish I could take it on for them… that I want to take it away from them (but it’s more than that)….

Is that a typical Borderline Personality Disorder feeling? Or typical of Personality Disorders in general? Do you ever experience these feelings?

I’m sorry this is a badly written post.

Ginny xxx

 

 

It just doesn’t stretch, whatever I do

I’m scared I’m so close to everything falling apart. Financially. But it feels like everything.

I got an automated voicemail message from my landlord telling me I’m to call them urgently to discuss “ways we can help you to pay your rent”. They had closed by the time I finished work so I have to wait til tomorrow to call them and find out exactly what it’s about but I know it will be about my rent arrears. I doubt they will be “helping” me pay, somehow! I know the fact of having to call them doesn’t instantly change anything but I’m really panicking.

I was struggling already today, feeling very sad after a difficult 1:1 therapy session on Monday, a friendship having broken down and a few other things. After getting this message I just wanted to crawl under my duvet, cry, shut off, everything and nothing…and the urge to cut is very strong but I’m trying to resist.

Nothing is working out. I got into arrears last year when I lost my job, wasn’t paid notice and holiday pay as expected, and my housing benefit didn’t come through for 10 weeks. Working part time I’ve been entitled to some housing benefit but my claim has been messed up, suspended, altered back and forth from start to finish and I’ve had more periods of weeks with no money coming in. I’ve been paying my rent, with great difficulty, but not able to clear the arrears.

Now they have stopped my housing benefit because my salary has increased by a few pence per hour. This leaves me unable to meet even the tightest budget. I do not have enough money to cover the bare minimun of rent, council tax, bills like electricity, telephone, prescriptions, travel to the hospital, some access to the internet and food (let alone any other expenses like buying clothes when needed, any longer distance travel, or socialising). I’ve cut back as much as I can, especially on food. I don’t make proper meals, just toast, cereal and cheap snacks. It makes me feel awful (plenty of guilt for bad fattening food) but I can’t afford anything else.

I know the arrears are my responsibility and I have to pay. I feel panic and guilt every day over them. I know that in the past when very unwell I made poor financial decisions and was irresponsible with money, which has contributed to why I don’t have savings. So has the fact that I’ve been too ill physically to work full time at several points in the last 10 years.

Part of what is so upsetting is that I am now doing all I can but I still can’t stretch to cover the tightest budget or see any way to change things. I am pushing myself as hard as I can to keep going to work. It’s very difficult mentally – and I’m sad that it is so hard to do it but that is the situation I have to accept right now. It’s very difficult physically too. The pain I’m in from the fibromyalgia, arthritis and so on has been increasing since I started and each day it gets harder to do certain things (going up and down stairs, staying on my feet for lengths of time, etc) and if it carries on it’ll get to a point the pain is too much or I can’t stand long enough or something like that. I hoped if I kept pushing I’d get better at dealing with it but that isn’t happening and instead everything is flaring up.

I really want to keep working. I’m blessed with kind and happy colleagues, a caring employer, a creative environment, varied days, lots to learn and so many good things. Psychologically this job is so much less stressful than the legal secretarial work I couldn’t cope with. There’s so much that should be positive that I don’t want to waste.

However I’m in a situation that I just can’t cover day to day living going forward let alone clear the arrears I owe. It shouldn’t be a reason to give up but when things seem to be falling apart anyway, it’s harder to keep pushing through the physical pain and mental struggle to keep working.

I feel really trapped because with the rent situation alone I think I’m going to end up losing my flat. I know the landlord, being a housing association, has given me more time with the arrears than many other landlords would. A private landlord would have thrown me out ages ago. I know that’s another way I’m fortunate. It’s my responsibility but I don’t know how I can or will be able to pay.

Even if I could clear the arrears  I don’t know how I’d pay the rent going forward. If I can’t,  I don’t know where I’d live because I have no money for a deposit to rent privately. If I went back to renting a room as a lodger my mental health would crash downhill but at this point I would have to be grateful for anything. If I lose this place and end up homeless I’d lose my job. I might anyway if my physical health keeps going down.

It’s horrible thinking even if I get evicted and lose my flat, I don’t know how I’ll change my situation. It’s horrible that trying as hard as I can to do the work I can, I’m not able to live on what I earn and I’m assessed not to be entitled to any benefits despite this. I want to work as much as I can but I’m actually in a worse situation, it appears, than if I were not working at all signed off sick. My rent and council tax would then be covered by benefits. Not that that would help with the arrears but it would at least cover rent going forward. The system says it shouldn’t happen that you are worse off working than not, but it does. I’m actually put into a situation where doing the most work I can means I’m left with not enough to live.

I was referred well over two weeks ago to an organisation that would help me sort all this out and talk to my landlord. I was supposed to have been seen by them within two weeks. I chased up as I hadn’t heard, only to find out they said they had not received my referral from the support worker. It had got lost in the secure email system somewhere,  ironically. It has been sent to them again but now they are not likely to see me til after my operation.

I have no idea what to do. There are so many “if”s and a spiraling whirl of consequences that make it feel that everything’s already falling apart.

I don’t want to make out I have it harder than the next person. I know so many people are in this situation. I know I have to deal with it. It’s a time I wish someone could catch me when I’m falling like this but I know that’s nobody’s responsibility. I’m scared and everything’s already unravelling inside.i suppose I have to try not to listen to the spirals in my head until at least after I’ve spoken to my landlord tomorrow.

Ginny xxx

5 Things – update

I’m sorry for the late update. Yesterday took a rather unexpected turn. If I tell you one thing to be thankful for was the nice A&E doctor, you’ll start to get the picture! :-0 🙂

I fainted at work and had so much pain I went to A&E. I wasn’t sure whether to go or not especially as this is now chronic, but work pushed for me to go.  It was the worst pain yet. It was probably the right choice to go as if things had got even worse later at home I’d only have been even more stuck and maybe ended up going anyway. As it was, they were able to give me a stronger dose of analgesics which have started to control the pain so that is really good. It took about 4 hours before I could walk slowly without feeling so dizzy I thought I’d faint again. I got discharged home in the late afternoon.

Roll on the surgery…

Still, I promised to update with the 5 things I’m thankful for, so here goes:

1 – That I have a caring manager and colleagues who really did seem to care more about my health than the trouble my absence would cause on a busy Saturday. How different this was from all my previous experience.

2 – The particularly caring doctor at A&E. It matters so much to feel listened to and that a plan is put in place to manage and cope better with symptoms when they can’t necessarily be cured immediately.

3 – The friend who most unexpectedly was in the area and came to bring me some grocery essentials and stayed to talk a while.  Someone caring enough to go out of their way to give practical help and give me company made a huge difference.

4 – A sea of beautiful daffodils spotted on the way to work. Pretty things are close at hand if you force yourself to look.

5 – My hot water bottle and my blanket!

Ginny xx