Category: The emotional and the physical

Why did the goose cross the road, and other stories

Q – What’s the difference between a Scottish man with a slight cold and an English man with 7 days’ holiday?

A – One has a wee cough, the other has a week off.

I hear you groan 🙂 That was one of the first jokes I learnt to tell as a child. (The other was what do you call a lavatory that keeps coming back to you? – A loomerang. Yep sorry about that. …)

Moving swiftly on! I’ve just had a week off myself and go back to work tomorrow. It was exceptionally bad weather until Sunday afternoon. On the news they said it was colder in my region one day last week than it was on Christmas Day! That same day my bus was delayed because there was a flock of geese that had escaped onto the main road and caused pandemonium. The bus driver said it was a shame it wasn’t really Christmas as we’d have got rid of the problem quite quickly (goose anyone?!)

My friend came to stay for two nights. She was my first overnight guest since I moved to my flat over a year ago. It’s a big step on for me that I was able to have someone stay over. My anxiety has always previously been so high that I could not cope and had to be able to escape from company after a few hours. I did have times I struggled and I was very tired from trying to make sure I stayed “okay” but we had fun together. My friend is in her eighties – she’s my friend L’s nan and I’ve been blessed to come to know her family over the past few years. They really make me feel like an adopted family member. I’m so thankful for all of them. We don’t see each other as often as we’d like as we don’t live very close by anymore but still the friendships have stayed strong and readers of this blog will know that true lasting friendships are rare and precious to me.

Also in my week off I’ve been able to make an effort to get on top of housework and clear my very tiny garden which I had not cared for properly since the winter. I am not a gardener and don’t enjoy it but I’m thankful for my outside space and try to keep it tidy. It really is very small.

Dad came to visit yesterday afternoon.  We had a coffee and walked through the park in the sun back to my flat. We had pasta bolognese for lunch (second in my Ten Dishes challenge) and a good talk in the afternoon. He’d just been on holiday with my step mum which they’d enjoyed. I’m thankful that I feel closer to my dad again now and more able to be curious about his life and express how things really are in mine.

This coming week I need to start a creative project. One of my colleagues is retiring at the end of this month. My other colleagues and I are putting together a scrap / memento book as part of her leaving present. We are going to decorate a page each for her. Some people are sewing, some embroidery, some photo collages – I’m going to put together some decorative text and decoupage based around one of her favourite songs. Updates to follow!

I hope you’ve had a good day. What do you like to do in your holidays?

Ginny xxx

 

 

 

Ten dishes – #1

Cooking has long been something I struggle with.

I struggle to do it because of the pain and lack of strength that comes with my physical health problems. After a day at work it’s too much to cook as well. Plus, I tend to crave junk food when I feel rubbish physically. Also, when I’m feeling low and anxious and the voices are loud or I’m mad with myself, it’s very hard to allow myself to prepare nice food for myself. There’s so much guilt and conflicting emotions associated with eating.

I used to be a fairly competent cook. Actually I used to prepare all my and many of the family’s meals from the age of 9 or so, as my mother stopped attending to that aspect of life for many years,  as her mental health worsened. It used to be something I enjoyed. It made me feel “grown up” and responsible and I enjoyed trying new recipes. But recently I’ve totally lost that confidence, apart from liking to bake for friends sometimes.

So, I have decided to set myself a little challenge of learning to prepare ten different savory dishes, to try to rediscover some of the positive sides of cooking and be a better hostess on the rare occasions someone does come over. Here’s the first attempt – cottage pie. My friend came to stay for a couple of nights so I made it for our dinner. That gave me good motivation to do it. My friend liked it so that was a positive start.

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I’ll be trying to prepare low budget meals as money is still very tight. Perhaps that will make it interesting to share ideas here too for anyone else in a similar situation.

Hope today is a good day for you.

Ginny xxx

 

Not that girl

Alert for stupid self indulgent sad post :/ …

I wrote this post a few days ago. It’s a struggle to admit to these feelings and to how it’s hurting me. It’s one of those times I feel so childish and needy and that I should just get over it. I’m taking a risk and posting this and maybe I’ll see what happens and see what you think. Maybe it’ll help me let it go too.

….

I’m trying to accept that my ex has got married. That though he left me saying the thought of marriage made him want to run, and he never wanted children and had no understanding of the meaning of marriage or the idea of being open to having children, he didn’t want the changes to his life that a relationship would bring, he didn’t want the personal social or financial implications – despite all this he now has a wife and two young step daughters and an extended step family and he’s arranging his wife and daughters’ immigration to the UK.

Everything he told me he wanted and believed he now has the opposite. He was so utterly against having children and he now has two. He was against any change or disruption to his routine but he’s maintaining a transcontinental marriage and arranging all the immigration process and naturally bringing his new family to his home, which will completely change every part of his life. And so on.

At the same time as I learnt this I learnt he saw me as a financial drain. He resented the slightest extra expense he saw our relationship (ie me) as causing, even a taxi or bus fare because with my disabilities I couldn’t walk everywhere as he would. He thought I drove his friends away and cost him his friends and lodgers  (at one point I along with two other people rented rooms in the house he owned and we did not always get along and there were arguments and as my and his relationship progressed ams so did that of one of the other lodgers with her boyfriend, she moved out). He resented time I wanted us to spend together. He was more and more angry if I wanted to try to build the emotional side of our relationship or pray together.

I don’t think there was anything good for him in the relationship apart from the physical side. He admitted he was physically drawn to me and had been for some time before our relationship started, and that he continued to be since. That terrified me. And I felt used too. That he resented anything emotional or spiritual and saw me as a drain and source of anger, yet had some physical want for me. I feel revulsion the two are separated and disgust at myself that I was so repulsive to him as a person but there to be taken physically. No we didn’t go “all  the way” or go against our faith’s teaching but there was intimacy and it is enough to terrify me. I don’t understand it properly yet. Perhaps it’s something to do with my childhood abuser’s hate of me but control and use of my body.

Anyway. … it’s also harder to accept because I found out the lady he has married has been a close friend and correspondent of his for over 10 years, that is to say well before my relationship with him began. I knew of her and thought she was an occasional penfriend. I didn’t know the depth of their friendship. I don’t think he was unfaithful but all the bonds that were lacking in my relationship with him were there between him and her all along. Everything he resented and wanted to run from with me, like time spent together or having children, he had and wanted with her. So it felt like it was so clearly me that he wanted to run from, not the things themselves.

It’s ironic that I found all this out at a time I was already thinking that my mental health had greatly affected my relationship with him (my Borderline was not yet diagnosed at the time). I had been planning in any case to tell him about my diagnosis because I did already feel responsible for a lot of why our relationship failed, because of my emotional instability, crying, anger, intense need of his presence and reassurance. So what I found out should have come as no surprise. Yet it is still a shock.

I’m not that girl. I’m not the right person to share his life or bring him joy. She’s got him. She always had him really. I am glad for them. I am happy for them and for the stability they will share. Despite his resentment for me I still feel an ache and painful sadness when I think of us or hear of them. Despite how much he disliked me, basically, and how little it seems we shared from his point of view, in my heart I can’t accept we didn’t share anything genuine in our companionship.  Then again it seems we didn’t from his point of view. There is not going to be an answer to that really.

I told a trusted friend about how I’m feeling and what my ex has now told me about our relationship. She said he sounds like a complete jerk. And the thing is, reading this,listening  to me, perhaps you would think that. But I don’t think he is. A lot of the time I was with him he acted understanding and kind and generous. That was partly why it was such a shock when we broke up. He was committed to his work and the church and gave a lot of help to several people in need. It was only when we broke up, and then now as I’ve found out about the wedding and his wife and daughters and he’s admitted what he actually thought of me, that I feel both used and guilty he resented me so much. It feels like nothing I thought we shared was genuine somehow because all the while he was feeling something totally different from me and totally different from what I thought he was feeling. I don’t want to make out he’s a nasty person. I was so sure he was and is a good person. I’m so confused.

When he brings his new family to the UK, there will be another wedding ceremony over here, and this will be important, as this ceremony will make them married in the Church body as well (at present they have had a civil ceremony in the law of her home country; they have not sealed their vows in the church). I will hear of it, I must be prepared and accept and learn to wish them well. I do wish them well.

I’m not that girl and I must not allow myself any more self indulgent lingering in the pain I’m feeling. There are many questions that won’t be answered. They have found each other as it should be. There is another place for me. I need to give them to the Lord now and keep looking forward to the good relationships that I’m in today and what I can do, not back to the questions and pain I can’t solve.

Ginny xxX

 

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

 

A closing drawbridge and a silent cry: too much; too big

 

A closing drawbridge and a silent cry

Eating disorders and personality disorder

My body becoming too much

WARNING: this post contains potentially triggering content on the topic of eating disorders, weight, body image and emotions. Please proceed with caution. Please note that in this post I express my distressed thoughts about my body and the relationship between my body, needs, emotions and relationships. I’m aware that a lot of these thoughts are part of my personality disorder and historic eating disorders. I am not advocating or encouraging these perceptions and feelings but describing what the process of trying to live with my body and face emotions is like. I think the stage of therapy I’m going through is bringing a lot of this distress to the surface. 

My body is changing. It’s out of my control (or so it feels, though the angry punishing eating disordered voice in my head says it’s me that’s out of control – disgusting fat b*tch – and my own disgusting failure).

I have gained so much weight in the past 2 years. I have tried hard in the last few weeks to lose and done all the things that used to be my trusted go-to solutions, with the exception of using illicit medications. I have failed and no matter that I succeeded in restriction, my weight has hardly dropped. If anything, now I feel more out of control. Sometimes I wonder if any of it is to do with being in my 30s now (quarter aged spread instead of middle aged spread?!) and my mobility being poorer with so much physical pain just now.  But that does nothing to justify the gain or calm me. Many people taking the medications I take report weight gain as a side effect even when restricting.  I think it increases my appetite but I know so does my need for comfort and my lonely emptiness and my…feeling. Feeling that’s dangerous and unchecked and explosive.

Anorexia meant I was never alone. I was cold and numb and empty and hurting, but needs and unbearable feeling stayed where they belonged and I dissociated, living somewhere whiter, higher, safer, always with the twisted pleasure of bitter success in my spiral to greater protection and greater weakness. Anorexia was my companion, that reassured me all would be well if I did not deviate from this path,  spurring me on with wild energy to control and deprive and make dangerous need and demands unreachable. Soon enough I would detach and dissociate totally then maybe disappear.

Anorexia left me. Abandoned me. I failed yet again. Just like my friends, even my family, my protector and guide left me. Found out I was a vile disgusting greedy failure, undeserving of that whiter place. Anorexia too abandoned me, and sped away to a place I can no longer reach, now that it is proved yet again that really the evil inside consumes and demands and if anyone else thinks differently, it’s only that I’ve tricked them into staying and caring. They’ll leave soon, when they find out.

I could take it if it were only for my protection that I needed my friend anorexia. But the thing is, it was to protect everyone else, first and foremost, from the danger and “too much” “too big”that I am. Without my friend I hurt beyond control and I hurt others beyond control.

I look in the mirror and I’m frightened and recoil from what I see. I wish I could rip myself away from the “too much” in the presence that I see, hating every part of the space I occupy, the weight, the body that absolutely does not seem to fit together right and screams too much, too much. I cannot escape. I cannot get rid of this body and these needs. I cannot stop what it contains, the out of control, the demanding, aching. … alone without my friend to starve and cut and numb and leave this place, I cannot stop the damage I will cause to everyone I so care for and so wish to save, protect and love.

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

Walking this Borderland #11: ice and lemon?

[Warning: the last 2 paragraphs under the *** contain discussion of self harm]

I know I’ve banged on about this technique elsewhere  in this blog but I just realised it may be a useful tip to add to the collection of coping strategies I’m trying to build up  in this Borderland series. Also, last week I learnt another similar very effective tip which I’d like to share. Thank you for bearing with me through the first two paragraphs if you’ve read my previous posts mentioning this topic.

In Borderline, regulation of emotions is difficult. States of emotional arousal shift quickly. Emotions and the intensity with which they are experienced can change rapidly and yet quickly become all consuming. The instability doesn’t make the emotions less real. Emotions may rise more quickly than they do in people without Borderline PD and stay at the higher level for longer. Equally, those of us with Borderline may suddenly enter emotionally numb or cut off states.

Both extremes can be dangerous, in my experience. Both can quickly tip into dangerous impulsivity, recklessbehaviour and decisions, self harm, suicidal intentions, explosive emotions and higher and higher states of distress. In either state we can’t explore our feelings and thoughts or other people’s feelings and intentions. Most coping strategies or systems of value that keep us strong, or protective factors like caring about other people, or religious faith or other beliefs that give us hope, become inaccessible in these states.

We need something that changes or emotional state so that we are able to reach again for these strengths and beliefs and strategies. One thing that can do this is giving the body a (non harmful) shock or surprise. We can only experience a certain number of sensations at once. A sudden strong physical sensation can serve enough to slightly bring our emotions away from the extreme. Once our emotions are coming away from the extreme, and only then, can we access other thought processes and coping strategies such as self soothing or the rescue box.

My top two ways to create this shift are as follows:

  • Lemon juice: lemon juice is a sharp sour taste. Take a couple of mouthfuls of neat lemon juice. You can even keep a small container of lemon juice in your bag when you’re out (easily available in supermarkets, eg the plastic “Jif” lemons).
  • Instant ice packs: I just discovered these! A really helpful nurse have me one when I was getting panicky in hospital last week after my op. I find this more effective and more practical than holding ice cubes, which is another alternative. Instant ice packs are really small and light, containing little crystals which activate to become cold when you squeeze and shake the packet. The tactile aspect is another helpful distraction too. I’m going to try to get some more. They appear to be available online from about 50p each, though I haven’t tried and tested any sources yet.

It sounds crazy, but the sudden ice and lemon shock does work. (Note to self, don’t follow the ice and lemon with the gin every time 😉 ! Remember to stick to Cola. Joke. No offence intended.)

Other potential ways of achieving the same effect include chewing small pieces of chilli (not too much and make sure you aren’t allergic first!), putting mustard on your tongue, or putting your head under a cold shower. The lemon and the ice are just the ones that work best for me and that I find most practical. I can use them even when I’m out or away from home.

This isn’t intended to be a long term solution but a short term way to keep safe and regain some stability. After you’ve used one of these techniques, you may then find you’re in a position to use other coping strategies once your level of distress is reduced (self soothing or mentalisation, for instance).

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Incidentally, I wonder if there’s ever a link between why these techniques work and the drive to self harm. I say this with caution because it’s a sensitive and painful thing and what drives someone to self harm will be different for each person. For me, sometimes there’s pain, loss, need, anger, or self hate, or needing to hurt myself so I don’t hurt anyone else, or needing the physical pain to numb and quiet the noise in my head and voices, or to know what the physical pain will almost faithfully be as it stills some of the much more unbearable mental pain for just a little while. For the next person it’ll be different.

One CPN I talked to describes the ice pack and lemon type techniques as safe self-harm. It’s a shock, a not pleasant, over powering physical sensation. Personally I don’t see it as similar to self harm or at all a way of self harming safely. Nor do I think it has in itself directly reduced my self harming. I don’t think it’s yet something I could do to avoid self harming once I’m at the point I’m about to self harm, although perhaps it does stop me reaching that point in the first place. However I think perhaps I see some of the point the nurse was making, in that the ice or lemon shock serves to still and control the emotion a little bit. Maybe part of why I started to self harm was needing to control unbearable emotion.

Anyhow.  When life gives you lemons, as the saying goes. …

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

 

 

Post op confused.com

Post op confused.com

I’m sorry for such a long silence. On Thursday last week, I had my small operation. It has taken me a few days to get back to the point of being able to write again. Anaesthetic and I are not the best of friends so the first couple of days after the op were not very nice. Now it’s good to be back! I’ve missed you all and I’m looking forward to getting caught up, both here and with your lovely blogs. I still have pain but it’s manageable.

The operation did not go in the way expected and it isn’t medically bad, but it is confusing.

The plan of the operation was to do a laparoscopy and laparotomy – look inside the womb, look outside the womb and at the surrounding organs, remove the endometriosis and insert the coil, all under general anaesthetic. (I don’t want to bore people going into too much detail as I’ve posted on this several times before, however you can read more about it here , here and here.)

I had been told for around the last 2 years that I have endometriosis and that this is what has caused the last 10 + years of heavy, really long and painful periods, bladder problems, constant pelvic pain, back pain, amongst other things. So I was expecting a big benefit of the operation to be removing the endometriosis and that therefore my symptoms would reduce or go away afterwards.

When I saw the consultant right after the operation, he said that they found no endometriosis at all. I don’t have it. It was the wrong diagnosis. They cleaned out my womb (eeek!) but found nothing wrong with my womb or the fallopian tubes. There were no cysts and no growth of cells outside the womb or onto other organs like the bladder, which they had previously been sure there would be. They did insert the coil.

I was stunned. Of course, it is really good that I don’t have endometriosis. From the reading up I have done over the last couple of years (for example, here), I know what a terrible condition it is. On the other hand, this outcome has left me really confused. It has left me without any specific explanation for my symptoms. It means I do not know whether or not I am going to get the improvement in my symptoms, especially the debilitating pain, which I had so much hoped for after the operation.

Also, I felt really stupid, fake and that I must be imagining it all. I shouldn’t have had the operation – yet again I’m a fake – my mind was screaming at me. The doctors were kind and they said it wasn’t my fault and wasn’t wrong that they did the operaiton. It was their decision to do it and my symptoms had worsened to the point that they needed to do it, if only for the exploratory purposes of finding out exactly what is going on. Endometriosis growth typically does not show up on any kind of scans – the only way to find out 100% for sure if / where it is present is to operate.

It’s a good thing they have checked out the situation. If it was essential to look inside, I almost kind of wish they’d have done it years ago rather than giving me all different kinds of medications potentially to treat the wrong thing. However, I do understand some women find that whatever the exact problem is, medications like the Pill and tranexamic acid can manage the symptoms and that’s how it’s treated, even if you can’t remove the root cause (kind of weird to try to get my head round).

Everything feels very confusing. My head is getting noisy at times with all the thoughts of being fake, having imagined it, having deceived people, specifically having deceived people into helping me and treating me. Fraud, fraud, fake, you made it all up, liar…. the voices say. When you have that struggle in your head already, having a load of “unexplained” physical symptoms that are horrible in themselves but are hidden and not able to be proved (you can’t see them on a scan, for example) is horrible and really triggering.

The doctor said that there could be a problem with my ovaries. I’m not sure exactly what problem he is thinking of. I was still reeling from the “no endometriosis” news and was still confused and foggy from the anaesthetic. I will have to check that out with my GP. The doctor also said that some women do have really heavy painful periods simply because of hormonal problems.

The coil I’ve had fitted should help with that. It’s definitely a plus that they have been able to insert the coil. All being well, I can have it for 5 years before it needs to be changed. It is good that it was done under the anaesthetic because for various reasons, some to do with the effects of the sexual abuse when I was a child, it is too difficult for the doctor and painful for me to fit it without anaesthetic. The doctor explained that the coil can take 3 – 6 months to settle in. (Seriously? 3 months? What’s it up to for goodness sake – is it popping out to buy a new 3 piece suite at Ikea? 😉 Still…) Then, it’s hoped that I will have no monthly periods, or that they will be much lighter.

This means the next step is to wait to see what happens in the coming months with the coil, and to find out what may be the issue with my ovaries. In addition, I will potentially need some more investigations. They may need to look further into what is causing my bladder issues, since it wasn’t endometriosis growths. This could be part of my fibromyalgia, or the neuropathic symptoms.

I’m also at the start of being investigated for a potential connective tissue disorder. I’ll leave that one for another post as it’s rather a long story, but I have just found out that it can contribute to a lot of gynaecological problems, as well as joint problems and pain.

Thank you so much everyone for your support in all your lovely kind comments leading up to the op. I do feel guilty now after you gave me all that support and it then turns out to be not at all the diagnosis that it was thought to be! I’m sorry. I feel really bad for posting before having been so sure it was something it wasn’t. It was what the doctors had told me it was, but I still feel bad. Your encouragement and friendship still really means a lot whatever the ultimate diagnosis and treatment is. I’m thankful.

Ginny xxx

[Image sourced from memecenter.com – with thanks]

Op tomorrow – and a short silence

Here we are. It’s my op tomorrow.

Surprisingly for me, until I left work today I was not feeling nervous. Then my colleagues who knew about it were all so supportive wishing me well. ..and ah yes up popped the anxiety again. Hallo there 😉

Tonight I have several things to do – check my transport for tomorrow, to see if there’s an early enough bus or if I need to get a taxi, get some groceries as I may not be able to get out for a few days after the op, text my friend who is very kindly bringing me home on Friday, call Dad, tidy up at home, pack, get myself ready….eek. But plenty to think about which is probably a good thing!

Thank you so much for your support, messages, wishes, prayers and caring. It really means a lot at the moment. I never expected to find so much friendship through blogging and I’m hugely thankful.

I imagine I won’t be able to post for a few days whilst I’m recovering. I’m sorry in advance for the silence. You are in my grateful prayers and I’ll be back in touch as soon as I can.

Ginny xxx