A Bad Week and them some.

 

11953086_10207820531093005_5688721444005854737_n-copyToday is a hard day. This past week has been a hard week. Friday was David’s birthday and unlike him, he seemed very down. We did what we always do, a funny cake, lots of gifts from everyone, animals included and he smiled but not a real smile. We had talked about going out but he had some kitchen ‘stuff’ arriving and so we had a quiet day, together, here on the farm. Went for along walk with the dogs, something I have not been up to for a while. That was good.

We are a small family, smaller now after being sadly betrayed by ‘family.’ It was me they were trying to hurt but as happens, my closer family also bear the brunt of this estrangement. None of it our fault and certainly not my husband’s, as the quarrel that started all of this was between me and my eldest daughter. I am known for my honesty, laughed at in the past for it by the 2 people who accuse me now of being a liar. My eldest daughter and my youngest sister. How easily people change the past to suit themselves in the moment. Keeping my integrity, refusing to lie on an Adoption form was the reason Lisa shut me out of her life. Should I have lied, pretended everything written on this legal document was correct? I don’t think so but I really wished I had been able to,  because the result of not lying has been horrendous.

But back to David and the ‘c’. He is very pragmatic, he says ‘we are where we are’ more often than I can accept. Yes we are where we are, here, accompanied by this uninvited ‘guest’ cancer. I thought all of my anger had gone but I was wrong.

I don’t want to be here! Here in this sadness and fear. Here where I can’t comfort the man I love and tell him everything will be okay. Because I don’t know. No one knows.The other morning he came over and put his head on my shoulder and sighed. ‘Everyone is so down’, he said in a much smaller voice than I had heard before. I could have cried. I held onto him as tightly as I could. As you would a child who was desolate and afraid, although I had never seen either of these traits in my husband. But we have never been here before. Here in the ‘we are where we are’. In the world that has been rocked and shaken so that all the pieces of it have fallen out of place. Nothing is normal now. Nothing is okay now. Nothing is safe now.  

Until this week, I had never thought of the ‘what ifs’ with any feeling. I had brushed them aside, didn’t want to go there. But now we have to. We have made new wills, necessary because he doesn’t want the people who have caused me such pain, to be able to have anything he has worked so hard for. We have written Wills before but the ‘d’ word was way off into the future. Not close or could be. Certainly not imminent and it still isn’t. But the fact that he wants to put his house in order is scary! Heartbreaking and necessary. I know that.

We lost one of our wonderful cats earlier this month and her brother is pining. The dogs are pining, none of them are eating, playing acting normal.

It is a very sad house to live in today. The sun is out, it is very cold but crisp and I pray for snow. When it snows it is as though Mother Nature has sent it to cleanse the world. Here in the beautiful Welsh countryside, it is amazing to see. We need cleansing. Our little world, needs cleansing. We need purifying from the horrendous year we have had, firstly at the hands of ‘family’ and then illnesses and death and now the dreaded ‘c’.

2016 has been the third horrid year we have had. All we ever wanted to do was love those around us, love our family distant and close. Love our animals and give them a good life and as a couple, spend quality time in retirement, here on this beautiful place we call home. Be happy.  This has been stolen from us with the diagnosis David had. But also with lies, deceit, badmouthing and evil people or one evil person  who has made it her life’s work to continue where the woman they ‘called my mother’ left off. 

Perhaps this will teach me.  Teach me not to make plans.  Not to be hopeful for the future. Maybe I was becoming a bit smug about living here, with my wonderful man.  I don’t know. What I do know is that David has not deserved any of this.  Any of the nasty things some people have done to me, therefore affecting him.  Done nothing to be where he is, in an illness that we have no idea of the outcome.  Here ‘where we are where we are’ holding me while I cry at night. Not only for him but over the past 3 years for what my daughter has put me through.

In my Christmas list, which my children would have written by this time when they were small, will be this.

David’s cancer to be cured.

My little cat Luther to be happy again.

My ‘family’ to see the truth and wake up before they are damaged beyond repair and my daughter understands that accepting the truth is the way ahead.

Next week I hope will be a better week.

Maybe 2017 will be kinder to us. I hope so.

Thankyou for reading x

Time-lapse. Victim to Survivor and Barbara Hewson

Hasn’t changed then.

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I am in the process of writing two books. One on my Dysfunctional Family, not telling their stories but the part they have played in mine as an adult. Never had any thoughts of writing this but the happenings of the past few months, Anne’s evil and treachery, the effect she has had on my eldest daughter, has made me think the book needs writing, even if only cathartic for me. It may not ever be published but kept within my family here. They both knew of my contract and need to remain anonymous, the reason I write under a pseudonym. In the beginning I didn’t understand this as I wanted to name and shame as my abusers sons had asked me to. What I didn’t take into account was the effect on others in my story so I agreed. Everything I have written about is true, to have taken…

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One Year On and How Different My World.

11412198_1749790735247976_8993691269577626663_nThis past week has made me realize how fragile this thing we call life is. How delicate relationships and family ties can be. As a child the week before 12th November, my birthday was always fraught. No-one mentioned my birthday at any time of the year and so when my Dad William arrived home, without a gift, he was in for a blasting from my ‘mother’. Until I was 11 and I had realized, that throughout the year, as my siblings big day was getting close, their birthdays would be discussed and so Dad knew when they were. He was a Royal Marine and had fought in the war and had been away a great deal. He had been away for 2 plus years when I was conceived and born. I wasn’t fathered by this wonderful man and he had no reason to remember my birthday. As my 11th approached, I bought a colouring book and some crayons and wrapped them up. The night before my birthday, I gave them to him out in his shed. I will never forget the sadness in his eyes as he understood I was trying to prevent another row. It failed, the row was different but still happened. So my birthday as a child was no fun to say the least. As an adult, having daughters I was fussed over and spoilt on the day and this has continued by my wonderful husband and youngest daughter for the past 31 years.

However, for regular readers of my social media, you would have seen the nasty cruel comments on here last year around my special day, and since, that have been written to try to put me back in the place I had been as a child. Alienated by ‘family’ and made to feel different and alone. Well, I am different and glad to be different. Last year I had most of my family on Facebook or Twitter but because of evil lies spread, I took everyone off for my sanity and safety. Of course I wish my ‘family’ were by my side at this difficult time but it ‘aint gonna’ happen. Not my doing but. I have accepted that now. But I have made contact with 3 relatives who are happy to be back in touch and that’s good.  This year I was spoilt and had a lovely day except for one thing. Sunday last, after writing my blog, my little 14 year old cat Boukie Rose was taken ill and sadly later that night she died. I was devastated as my husband was. She hadn’t been ill and that was something to be thankful for but a huge shock to us here ‘on the farm’. Her brother Luther is lost without her and it is heartbreaking to see. So the 12th November was blighted in a different way from last year with her death.

Other differences from 2015, my youngest daughter married in April so that is another  huge change. We lost another pony and our little herd is just that, little now. But the biggest blow is my beloved husband’s cancer diagnosis. We had no idea, nothing had made us suspicious, no symptoms, no pain. Nothing. Just a routine blood test and our world turned upside down. I have talked about this, my anger, my fear, my helplessness and fears for the future in earlier blogs. Today I was thinking how odd that he has cancer, with a little ‘c’ and is fit and well and I have been so ill! I would do anything to take the uncertainty from him, the worry but it seems his worry is for me. As I have said before, I have always been the strong one, in the family and at home. The one who others come to, but not currently. I am coming back, I know that, but it just seems strange that he is still looking after me. Everyday he reminds me of the things I have endured, both as a child and as a young adult. Recently in the unforgivable treatment from ‘family’. Hence the verse at the top of the blog.

Today I was sent a video of a man singing in a square. The song he sang went like this:

‘You raise me up to stand upon the mountain

You raise me up to walk on stormy seas.

I am strong when I am on your shoulders

You raise me up to more than I can be’.

Of course I have heard the song as you will have,many times but today I say these words to David. He is my rock and I am beginning to be his, I can see a way forward now as I couldn’t before. This year has been momentous. Many losses, huge changes and scary health issues. But together, with me on the shoulders of the man I love, we will make it. Family may not need me, not want me in their lives but we have each other and that’s what counts, in our truth, with the truth on our side, we will make it.

One of the reasons I believe I was successful in my work as Counsellor and Psychotherapist, is because of my own experiences. I have always believed that the best people to turn to, to help you through the storms of life are the ones who have endured their own storms. Having suffered most things in life that can hurt us, not said for sympathy, just a fact, I am able to understand where people are coming from. I never insult them by saying ‘I know how you feel’ because we are all different. But I can understand the depth of their feelings and their fears. I have facilitated groups and group work is very successful. Since David’s diagnosis I have joined a couple of groups on social media,Prostate Cancer Support group being one of them and the help, advice, support and love has been amazing. Can’t do it without that input so thanks guys.

So another year gone and I will be glad when 2016 says goodnight. 2017 can’t be worse, in any way so I will look forward and see the light, standing tall at my husband’s side whatever life throws at us.

Thankyou for reading x

 

 

My Letter To cancer with a little ‘c’.

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14915575_10211175969096858_2023287538040280785_nYou don’t know me but I know you. We have met many times before. You crash into people’s lives uninvited, destroy dreams, take away the future they planned and their dreams along with that. You steal their peace of mind and replace it with anguish, fear, sadness and grief.

You are a sneak thief, creeping in without being seen or felt, spreading your damage with nobody aware of your presence. We don’t want you c. Nobody wants you but here you are! Not satisfied with taking those already taken, those we loved and knew, you continue to inflict your poison not only on your prey, but on everyone in the lives of your victims.

You put grief for those we love, in place of surety of a future. We talk of people dying from cancer but what about those living with it? David is fit, active and healthy but because…

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My Letter To cancer with a little ‘c’.

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You don’t know me but I know you. We have met many times before. You crash into people’s lives uninvited, destroy dreams, take away the future they planned and their dreams along with that. You steal their peace of mind and replace it with anguish, fear, sadness and grief.

You are a sneak thief, creeping in without being seen or felt, spreading your damage with nobody aware of your presence. We don’t want you c. Nobody wants you but here you are! Not satisfied with taking those already taken, those we loved and knew, you continue to inflict your poison not only on your prey, but on everyone in the lives of your victims.

You put grief for those we love, in place of surety of a future. We talk of people dying from cancer but what about those living with it? David is fit, active and healthy but because of you, a stowaway on our journey that is called life, he has to undergo treatment that could make him poorly. Give him problems, make him unwell. Yes that may be temporary but this will happen and he does not deserve any of it! You have put fear into us, both your victim and  the people who love that victim. You were not invited, we didn’t want you , we didn’t even know you were there! How cowardly and cruel is that! You gave us no warning, we didn’t go looking for you. A simple routine test and suddenly, there you were with all you nasties, all your fear, pain and heartache.

You make us angry, not with our loved ones but with you! I hope I am speaking for all of us who are on this unwanted journey alongside those you have tainted with your evil disease.

You have crept in and caused the reason for our sadness and fear, cunningly, quietly giving us no chance to shut you out because we didn’t even know you were coming. An unwanted and unexpected ‘guest’ at our table.

But most of all you give us helplessness, something I for one, find hard to cope with. So Damn you cancer. Damn  Damn  Damn you!!

Yes I am angry but mostly I am afraid. For my husband and what is ahead for him but more afraid of the unknown for us both. Afraid that feeling as sick as I do now, with my own health problems, that I will not be strong enough to cope. To care for this man I love. I would do anything to take his place. Anything.

Friends say ‘You are the strong one Carol Ann, look what you have been through so far and survived. You will cope’. But I have my doubts, especially on days like today. I have scary irrational and intrusive thoughts, that bombard my aching mind without respite. I ask myself, ‘I feel so weak, I am in such pain how will I cope feeling this way?’ At first I don’t have an answer.

I wrote in an earlier blog, not to you cancer, but to readers, that as a child I was never allowed to say ‘It’s not fair’ or ‘I hate..’. Well do you know what? I grew up in a dysfunctional family without the love of a mother, without love that was showered on my siblings and without feeling safe. I was often the scapegoat. I never ever said it wasn’t fair. I suffered a lifetime of CSA, lived in fear and pain. I never once said it wasn’t fair. I never hated. I was helpless. But as I said, I grew up. I eventually found lasting love in David, found happiness and love . I wrote my story, recovered enough to deal with the legacies of my childhood and even then never hated.

Today, this morning, I was that child again. Living in fear, in pain and terror and helpless to a fault. How dare you creep back in, as ‘family’ did a few years ago, through the back door, silently with no one knowing what was happening and try to steal the reason for my happy life where fear didn’t exist! How dare you take people from those who love them, in such a cowardly horrible way?!

You stole many in my life with your cancerous illness, loved ones who didn’t survive your onslaught. Relatives, siblings and best friends, now you think you can steal my man, my rock, my life! Well not on my watch! I need to be kinder to me in all of this, give myself some leeway.

So I have given myself permission to say it’s not fair. Permission to feel scared, angry and sad. I need to try to look after ‘little Carol Ann’, to make her well enough to fight her fears and gain strength from remembering how far I have come. I thought I had survived the worst that could happen in my life but was not ready for you. I need to try to find the fight that I used to have.

Tomorrow is a new week, I am hoping this sickness I have will turn a corner and I will be on my way to recovering and fit to face whatever life throws at us next. You won’t keep me down for long, believe me.

So cancer; my enemy and every one elses’ enemy, sorry, but medicine has improved, people are working all over the world to toss you out with the garbage. When all of this is over, when I have regained my strength, helped my man through this, hopefully comfort him if he feels scared, carry him if he is weak and love him all through, I will, with every ounce of my being, fight you all the way to your own death. Your extinction.

Yes I will shed more tears, some out of fear for where we find ourselves, some of anger and frustration but mark my words, I won’t go down without a fight. I will win.We will win and we will one-day have a world without you.

Carol Ann the strong is a formidable character, and I hope she will be back here very soon, so watch out!

Get ready.

Your enemy

Carol Ann

 

 

 

The Importance of ‘me’ in this journey.

For Jane

carolannwright's avatarcarolannwright

12108955_861888687240178_9023040360935467352_nI tell the person in front of me, everyday, that they have to keep going. Sometimes  I don’t think she is listening or rather she doesn’t hear but I will tell her everyday anyhow. Who is she? The person in my mirror.

This blog is my story, not David’s not any one’s but mine. Indulgent? Maybe. Selfish? I hope not. Necessary? Yes.

Writing things down is a tool I give my clients so I am taking my own advice.

I said, the first week of this blog at the end of August, early September, that this is the story of how I am dealing with my beloved husband’s diagnosis and ultimate treatment for Prostate cancer.Not how he is dealing with it, not from his perspective because that is his journey but how I deal with or don’t deal with the many shocks and fears since he was diagnosed, out of the blue…

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The Importance of ‘me’ in this journey.

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I tell the person in front of me, everyday, that they have to keep going. Sometimes  I don’t think she is listening or rather she doesn’t hear but I will tell her everyday anyhow. Who is she? The person in my mirror.

This blog is my story, not David’s not any one’s but mine. Indulgent? Maybe. Selfish? I hope not. Necessary? Yes.

Writing things down is a tool I give my clients so I am taking my own advice.

I said, the first week of this blog at the end of August, early September, that this is the story of how I am dealing with my beloved husband’s diagnosis and ultimate treatment for Prostate cancer.Not how he is dealing with it, not from his perspective because that is his journey but how I deal with or don’t deal with the many shocks and fears since he was diagnosed, out of the blue on the 24th August this year.It will cover the things we do together but mostly this is my chance to offload my anger, fear,sadness and shock at finding myself in this helpless situation that life has thrown at us.

Of course we are not the first couple facing this horrible disease and we won’t be the last. We are not special or needing sympathy because how would that help? We are an ordinary couple, still very much in love after 31 years together, who thought the next part of our lives, the time we hoped was for us, would be different from how it is panning out. This was ‘our’ time. Not having to worry about children, who have all gone their own way, not worrying about money because we have all we need . Not concerned about anything but the two of us. Well, perhaps we became complacent, a bit smug living here in this beautiful home looking out over the wonderful Welsh hills. I don’t know. All I do know is that we weren’t ready! Did not expect this. Never even thought of cancer entering our lives and turning our peace and quiet on it’s head. Wrenching at the pit of our happiness and replacing it with fear, pain, uncertainty and helplessness.No. We were not ready.

Today I am writing my blog from my sofa after being attacked by another nasty, Shingles. I have been and still am quite poorly and in excruciating pain, so although I will check this before it goes live, forgive me if I have made mistakes.My GP says it is because over the past few years I have been under a great deal of emotional strain and suffered bullying by family that has rendered me very low. That is when this virus attacks people, when they are vulnerable . So here I am, under attack from something else outside of my control. Not a good feeling and just when I need to be strong to plan ahead for David’s treatment. This illness has been coming on for a while and in a way, knowing what it is explains a great deal for me re my moods. Perhaps it wasn’t the shock of the cancer alone, maybe some of how I have been feeling or how I handled it,is a result of the Shingles. I don’t know.

What I do know is that I have to start taking care of me. As I tell clients, how can you take care of others if you don’t take care of yourself. That it is actually okay not to be there for everyone who ‘needs’ you. It’s okay to step back, to opt out, to rest. It’s okay to let others take the strain now and again, especially now. I need to get strong again to be there for David. I need to look after me to be able to look after him. I think this to be good advice for other wives, partners and families of men going through this horrid disease. The waiting, the not knowing, the researching and calculating and the endless tests and visits to hospitals that seem to have no immediate answers. We, the partners of our men, need to firstly be selfish and look after ourselves, or like me you may find yourself ill and not even capable of looking after you.

Nothing has changed since last week. We are still waiting for the appointment with the ‘team’ to discuss the way forward, so that in itself, is a strain.

We are all on this journey. You, reading this maybe, your husband or your partner, your family and in some way your friends. All battling this fight together and so we must start with looking after ourselves. It is okay to feel every emotion under the sun, goodness knows, those who read earlier blogs know to what extent I have felt them. Yes, I am still angry. Still scared. Still confused and bewildered by how a man as good as my beloved man has this nasty disease and this horrible fight on his hands. But I am here and will be here, standing alongside him and hopefully giving him strength when he needs it. But to do this I must look after me. David has been my rock, especially during the onslaught I have suffered over the past 3 years. He has always been here, held me in his arms and comforted me, no question. I need to be here for him.

Many years ago, a young mum of two daughters, I lost a baby boy at 25 weeks. I had been offered a termination because I was unwell but chose to continue with the pregnancy. My life wasn’t in danger and I wanted this baby. But it wasn’t to be. My son didn’t form properly in the womb and he was born sleeping. That evening my dad William, came to see me and I cried to him asking him why did It happen. Why did he die. My lovely dad said it was a test from ‘God’ and that I had passed. I didn’t feel I had passed anything, I felt such sadness that I can’t explain. My Dad told me that the easiest thing for me to have done, as the baby would have been disabled severely, was to have chosen to have the termination. I refused and he told me that was the test. Because I chose the hardest way forward, the decision had been taken away from me and I had passed God’s test. I never understood then, as I don’t understand all the very many other tests I have been given since. If this latest blow is a test then I have to pass with many gold stars.

Prostate cancer has been in the news lately, talking of not doing routine PSA tests. Yes, I wish I could un know what we now know. Yes, I sometimes wish David hadn’t had the test as a routine check because then we wouldn’t be going through all of this. But the alternative doesn’t bear thinking about. Had he not had the test, then years ahead the cancer may have spread, unknowingly to us and killed him! So whilst all of this scare, this shock and this worry is painful, losing the man I love would have been indescribable. So NO. We can’t allow the PSA testing to stop.

So. Today I feel like ‘s..t. I feel scared still. I feel down and depressed but I also feel determined to get myself back to being me. So, I will keep looking in that mirror and keep telling the woman looking back at me, that although she feels tired and poorly, she must never give up. I will bounce back, I always do. I just wish it wasn’t taking so long.

So remember, always look after you first, then you will be able to look after those you love.

Thank you for reading .x

 

 

 

Taking My Own ‘Advice’

Keep missing it, sorry here it is again. x

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Well perhaps I should start by apologizing for last weeks blog. It was down beat, self indulgent, angry and full of sadness. Maybe apologizing isn’t good enough, I don’t now. So I won’t say sorry but will say that I am today, understanding how my clients feel whilst in therapy. This is the first time since I began Counselling, that I fully understand how each person who has been brave enough to come into therapy, can feel. Using CBT (Cognitive Behavioural Therapy) I work with my clients to enable them to make changes. If they are not functioning properly, changing may enable their lives to improve. If they are depressed, working with their thinking, being more positive and this can be hard for those feeling down or anxious.Looking at their thoughts, the way they think, because it is this that controls the emotions and that results in their behavior. You can’t…

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Taking My Own ‘Advice’

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Well perhaps I should start by apologizing for last weeks blog. It was down beat, self indulgent, angry and full of sadness. Maybe apologizing isn’t good enough, I don’t now. So I won’t say sorry but will say that I am today, understanding how my clients feel whilst in therapy. This is the first time since I began Counselling, that I fully understand how each person who has been brave enough to come into therapy, can feel. Using CBT (Cognitive Behavioural Therapy) I work with my clients to enable them to make changes. If they are not functioning properly, changing may enable their lives to improve. If they are depressed, working with their thinking, being more positive and this can be hard for those feeling down or anxious.Looking at their thoughts, the way they think, because it is this that controls the emotions and that results in their behavior. You can’t go straight in and change the emotion or behavior without first looking at to how your thoughts are at the time. Some will say, ‘I can’t change, I have always been like this’ or ‘this always happens’. And that is often the issue.’ If you always do what you have always done, you will always get what you always got’, is something I was told during training. If you don’t like what is happening, only you can change it. This can be harder for clients than I think I had acknowledged in full.

Most times with collaboration, we can achieve the goal the client has been seeking and so they improve. Given strategies for survival and maintenance, they are often less likely to have the same problems in the future.

We go through, ‘nothing can change this’ ‘I can’t do this’, To ‘I feel more capable of doing it now’ Things get better. Their lives improve.

But sometimes you can’t make it better, you can’t make the nasty go away so you have to work on acceptance. Like in loss. The bereft can’t have the person they grieve back and so by working on their feelings, we can gently change the thought process and allow them to grieve properly. Grief will take as along as it takes but sometimes needs a little push, to enable the person left behind to accept the situation and ‘move on’. Always at their pace.

Here endeth the first lesson!

Well, none of this has been working for me. Physician heal thyself, as I have said before isn’t working. I know it will, but I am impatient and need it now. I don’t like the Carol Ann I have become. I don’t like feeling as I did as a child. Alone in my thoughts and pain and helpless .

So why am I feeling this way? The alone is because David is strong, pragmatic. He says whatever happens we can’t influence it. We can’t change the fact that he has Prostate cancer. We can’t un know what we know. And he his of course, right. So,  I need to find away to stop thinking about it all of the time. Stop researching, reading everything sent to me and some I find myself.

The helpless is back to childhood. No love from my ‘mother’, a dysfunctional family and sexual abuse that I suffered all of my life until I was 22. No one helped me because no -one knew and I was helpless to stop the horrors. One of the reasons I support spreading facts about the devastating long term impact CSA can have on victims and work to help some of them become survivors, like me.

Today.

Things are moving forward,we now know David’s ‘case’ has been discussed with the ‘team’ and we are now waiting for the appointment to go and see the Oncologist/Surgeon to discuss options. Does that feel better that something is happening? You would think so but it only makes it more real. But it is real and that’s the problem.

So today I have been reading a journal that I kept while I was working and am reminded of clients who struggled as I am struggling. Sometimes, after weeks of work I would think nothing was actually helping them. Nothing was changing.But then one day, a client would come to session and say they suddenly had ‘ a light on’ moment. Something would suddenly look different, life would look different and become clearer. It didn’t mean their pain had stopped. It wouldn’t mean they were suddenly ‘cured’ of the bad thoughts or behavior or had stopped having the nightmares etc. But something had happened and they could see their way forward. A different approach to a situation, a way out of the grief and pain. And then there it would be; a smile. Every therapist’s ‘worth it’ time.

I am waiting for that light. I know I can’t counsel myself but I can listen to others who have been where I am. Other wives and partners of beloved husband s who are fighting this fight. I can gain strength from those who write about recovery and the future. I can stop feeling sorry for myself and find my inner strength that has been alluding me of late. Don’t know how but I will.

 

The future is where my thoughts need to be so I am house hunting. I know we can’t consider this yet but there is no harm in my looking. It may be back in Hampshire where I have family and friends. It may be in Pembrokeshire or Somerset where again I know people. We have no idea but looking forward is something I have always encouraged in clients and so that is what we will do.

When it is all over, I aim to try and raise awareness in younger men of this awful disease, promote testing and helping with fund raising. Not yet but after.

I think and hope that Carol Ann is coming back, so cancer, you had better watch your step!

Thank you for reading x

The Falling of Tears and the rolling of Emotions

For Peter who missed it.I must be posting it in the wrong place. Sorry. x

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11059960_10153596562234714_2907489225298921393_n-2In my work, I teach clients how to let go, how to be ‘in the moment’, how to allow themselves to cry. Tears are healing I will say. Just let them come and you will feel better, I will say. Well, do you know what. I lied. You don’t feel better, I don’t feel better and I have cried buckets of tears these past weeks. Do I feel better? Does letting go make you feel better? No it doesn’t and I apologise to everyone I have told that they do.

I thought that once we had made the choice, as to what treatment David will undergo, we, or rather I as I can only speak for myself, would feel better. I don’t. We don’t as yet know whether the surgeon will operate as my hubsnad is over 70. This in itself causes us obvious worry. It is all in the hands…

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