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Monthly Archives: October 2016

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The Gig. (The Stone Roses)

30 Sunday Oct 2016

Posted by fonzandcancer in Cancer

≈ 4 Comments

The Gig. (The Stone Roses)

Now let me just say right from the start, I have never understood the whole Gig world. You have to drive there, park and then go and stand or sit somewhere to watch somone sing songs you already have on a CD, usb, phone, or alike. Why bother spending £82.50 on a ticket. Especially when the band on before is called Public Enema or something like that. For a full 3/4 of an hour we were subjected to absolute garbage. Now I am not one of those people that complains about swearing but there is a line. I was sat there looking at my friends shaking my head, thinking maybe it was all going to be the same. Now whilst I have become somewhat more laid back since living with Cancer, I do still have a like or dislike button. And I can say most enphatically that I do NOT like the man known as. Flavour Flav. 

My wife said to me, “you can’t get an atmosphere like this on a CD” I said “well thank goodness for that. But I was to find out what she did mean. When The Stone Roses came on, the atmosphere did indeed change to one that you could not buy on a CD. The place started to Buzz, and whilst I have been to the Manchester city ground on 5 occasions now. It was never as good an atmosphere while they were on than going to a football match. Going to watch Liverpool at Anfield and again at Wembley are the only times that came close. 


I looked across at my school friend who I had lit buncen burner taps with at high school, and did many other micheivious things with. It’s kinda strange looking across at your friend who was so good at football, the boy who took my place in the rugby team because I broke my leg. Which I never got back by the way. Not that I am sore about that or anything. Now I don’t know much about football but I do know that on some occasions when we are listening to my music collection, stone the roses come on there is a spring in the step of some whilst playing our game of pool. I was later to learn that Manchester United come out to the tune ‘this is the one’ by stone the roses. Or is it The stone roses. I get a bit mixed up sometimes as I am a Liverpool fan or be it a plastic couch supporter. 

I actually started to really enjoy the Gig, I even found myself tapping my thigh and bouncing a little bit. I was rather pleased that we were in seating opposite the band as I don’t believe you get warm beer thrown at you in the seating areas. The standing areas don’t go to the loo because they can’t find who they were with when they get back so it goes is a cup and in the air onto the unfortunates that it lands on. When the last song came on (I guessed it was) as there was 5 mins of no playing before ‘this is the one’ was played. My school friend became very enthused as did I and most around us. It’s a bit political because my wife likes Manchester City so for her to like the Manchester United anthem was a bit, well you know.. 

We all had a great time and I would proberbly go to another one, that s 3 I have been to now. Noel Galligers ‘High flying pigeons” and Oasis at Heaton Park. The heaton park gig I left soaked in other people’s warm beer so have to say it was a whole world apart watching ‘the stone roses’  now when that final song comes on and it’s Manchester United walking out to it, I think of the gig we went to. It’s a memory we made that keeps playing over and over when I think of it. So I think that by now at least I have gotten my monies worth because it’s a memory that I treasure. Even Public Enemy was part of the experience. Which kinda makes me smile that I listened to such garbage for 45 mins. 

My wife is a true Salford girl although she does support Manchester City who as the name suggests are from Manchester. Unlike United that were born in Salford.  My wife’s a bit complicated. So there we are, a great day and evening spent with the man who took my rugby slot in the school team, but also played football for the school team. Just call me John smith. 

So just for the record, or C.D. The atmosphere at a gig is far better than just having it on a device. ITS BETTER.

HAVE A GREAT DAY

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Our support group on our FB

Cancer stories (people helping people through experience) 

It’s a group where people’s experiences are used to encourage others. 

Everything you read are better based on my own experience and my own opinions. I express them here to encourage you. Please share with others, if it meant something tou you it will to someone else. All images are from a Google search. Or my own, taken whilst creating memories every day.

Copyright © 2016

Bless someone, by sharing. You never know who needs to read this.

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From bad to Worse!!!!

13 Thursday Oct 2016

Posted by fonzandcancer in Cancer, Cancer stories, Chemothearopy, Christmas, depression, dogs, Holiday, Hope, Love, Oppertunity, Paris, Pets, Relationships, Uncategorized, Winner

≈ 12 Comments

Tags

chemo, children, faith, family, gift, happiness, hope, IVF, religion, treatment

From bad to Worse!!!!

Going on holiday is supposed to be a way of relaxing and when you come home your supposed to be refreshed. We were for sure just that when w were on the plane holding hands feeling that feeling of feeling refreshed and looking forward to our IVF treatment. We felt excited, we even met people on our holiday that had had the treatment and it worked first time. I mean knowing we have fought so hard for our life together. The room, the treatment, the sickness and suffering. Surely this is our time, surely it’s time to get some good news in our lives and have an opportunity to have our own child. My swimmers are dead, so we are not able to have children naturally so our only chance is to have them through IVF. We were told they were dead on the day before our holiday and our holiday in Greece was time to come to terms with that. I was angry, and upset that cancer had taken that from us. That the consequence of the fight was that we could not have children, that somehow we have been ripped off. 


It was about a week into the holiday that we met a couple that had had their successful IVF. Our anger turned to hope as we heard the story that was theirs. That he had fought for his life after breaking his back, but years later had their gift through IVF of a beautiful baby girl. We began to feel hopeful, we even began to feel excited at the prospect. Our holiday began to be a joyful time as we imagined our new born and what it would be like to be parents. We talked about how we would parent, the methods we would use. We even watched how other parents were with their children, we looked at each other knowing that we would work together to help parent our child and realised that maybe we would make good parents. We spoke how we would ask questions of why they were doing what they were doing as apposed to shouting. (Maybe a far fetched dream right) we spoke how we would parent and how we would love them, places we would go, what we would teach them. 

It really was the beginning of a new life for us, especially as Archibald the guy at the hospital had told us we would qualify for the treatment. We are not people with money, we are people with big hearts and share love with people and help others to overcome what they are going through. It’s what I do with passion, helping others with cancer, dedicating my life to holding out my hand to other people like you. Encouraging people that they to can win their fight, whether it be cancer or something else. I have heard the words, “you will lose your life without treatment” I know how valuable life is, I know how precious it would be to parent. I know how my dog makes me feel, I mean you see people that are parents and apparently some children don’t know what a loving home is. We do, because we live in a loving home and truly hoped to be parents and thought that this was our time.

We arrived home up beat unpacked opened a bottle of red wine and began opening the post, you know the bills ect. Then I heard my wife reading a letter out loud from the hospital. She said the word “unfortunately” followed by “you have not been accepted” it did not hit me really till now. That we are not being accepted for IVF. Right now I feel as though yet again Cancer has taken something else from us. After spending our holiday feeling hopeful that we would become parents. So here we are with yet another disappointment. Another set back, something else to overcome. Yea of course I am upset, we both are but you know me, I won’t just sit back and allow this to ruin me. I will continue to look into the options until they have been exhausted. But I tell you now reading that letter has floored me, for now. 

We will get over this, we will become positive again.

Today is a gift and treasuring what we have, is most certainly important. Life is precious, appreciate what your life gives to you. Also the people you have in it. We are each other’s gift.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Our support group on our FB

Cancer stories (people helping people through experience) 

It’s a group where people’s experiences are used to encourage others. 

Everything you read are based on my own experience and my own opinions. I express them here to encourage you. Please share with others, if it meant something tou you it will to someone else. All images are from a Google search. Or my own, taken whilst creating memories every day.

Copyright © 2016

Bless someone, by sharing. You never know who needs to read this.

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Good is everywhere. 

10 Monday Oct 2016

Posted by fonzandcancer in Cancer, Cancer stories, Chemothearopy, Christmas, depression, dogs, Holiday, Hope, Love, Oppertunity, Paris, Pets, Relationships, Winner

≈ 12 Comments

Tags

believe, care, faith, health, help, hope, Laughter, rich, wealth

GOOD IS EVERYWHERE

So it’s true, that there is good in everything if we look for it. My wife reads to me most nights now as my friend has given me a book to read called “illusions” Although I write believe it or not I am not a great reader, I don’t even read my Blog posts back a lot of the time. I also find that in my dreams sometimes I am spoken to, not by my wife but by someone far bigger than me. Sometimes my dreams are complicated, and others so very very clear. But this came from the book she reads to me.

So picture this, a river not the fastest river you ever saw, but all the same one that never runs dry. A river teaming with life, imagine then that there are some creatures in the river holding on for dear life, they do it everyday. Everyday they have to hold on so they are not swept away by the current. They don’t know why they hold on, but they chat to each other one day and discuss why they are holding on so tightly. One says to the other, we  will be hurt if we let go and will be battered and bruised by the rocks. The other one says “yes but I am bored holding on, I want to let go and trust where the rivers current will take me” 


The ones holding on, do not trust that they will not get hurt. For if they let go they will indeed get hit by the stones and rocks. They have no faith in what they don’t see, they only trust in what they can see. Yet the one who wants to let Ho and trust the stream believes by faith that where the stream is going and must know something he/she does not. Or surly the river would not keep flowing. 

The time came that they let go, and sure enough the stream sent it smashing into the rocks below, hurt battered and bruised by the Flow of the water. It was not the water that hurt, it was what was in the river. The stream continued to flow and carried him up to the surface where there was sunlight and a new way of living. He had never seen the sunlight before, but because he had let go and had faith in what he could not see. He/She was able to see how beautiful they were, the colour of how he was made and learned that he had wings and was able to fly. He was given a gift because he used faith in what was unseen to become the beautiful person he became.


Life has been like this for us all I suspect at certain times, but not knowing what will be is the same for us all. Having faith in what will be is the same for us all to, only we can let go of what is so we can know what could be. Only we can allow what our true destiny is, to be discovered by having a few hits but still moving forwards. I just wonder if you will hold on tight to what you know, or if you will allow yourself to trust what is going to be by letting go.


Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Our support group on our FB

Cancer stories (people helping people through experience) 

It’s a group where people’s experiences are used to encourage others. 

Everything you read are based on my own experience and my own opinions. I express them here to encourage you. Please share with others, if it meant something to you it will to someone else. All images are from a Google search. Or my own, taken whilst creating memories every day.

Copyright © 2016

Bless someone, by sharing. You never know who needs to read this.

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It just is.

04 Tuesday Oct 2016

Posted by fonzandcancer in Cancer stories, Chemothearopy, Christmas, depression, dogs, Holiday, Hope, Love, Oppertunity, Paris, Pets, Relationships, Super Bowl 50, Uncategorized, Winner

≈ 10 Comments

Tags

cancer, depression, freedom, health, prepare, selling, sicology

Living on this planet, I find every day is a school day. I am always learning about life and my opinions, are not just changing but becoming more accepting of the world. You see I was brought up to believe so many things are wrong and so many things are right. This is not how I live today, because what ever it is I believe people may not agree with. What right do I have as a person to disagree with the way someone lives a life. Who says it’s wrong really? The snow falls at certain times of year, is that wrong? The sun shines and the planet thrives on the gift of life the sun brings, the water feeds plants and the world Carrys on. The world just is, this planet is amazing and as my dear friend says. The world works in harmony, if we like it or not it just is. 

The question people ask is “is there a God”? Well what ever your opinion on the subject, you are what you are. Your life is for a reason and all that you do has some effect on the planet we belong to. What we do makes ripples and we will never know just how much effect what we do, does or does not for other people. It’s a very peaceful place to find yourself in, to realise that the world just is. Your perceptions to things change, they become more meaningful. Yet they also become effective by just letting people be who they are. People I have been around all of my life have judged others and had opinions on how those people should be. Well here are my thoughts.



The more we as people worry about what others do, the more unhappy our lives will be. I wrote a blog called the garbage truck. I talked about how people that are concerned with what others do or do not do keep loading the rubbish of others into the truck that is ourselves. Loading ourselves up with other people’s issues that are no concern of ours at all. I had a friend once that used to come to my house and constantly tell me how otherpeoples actions offended him. Yet he could have just accepted who they were and had a peaceful way of life.

Nearly losing my life has taught me that I have a lot to offer this planet, but if others don’t think that’s not the case why should I worry about that. It is after all an opinion of another. It’s ok isn’t it, or is your opinion of mine differ from that which I think. That’s ok, the trees grow, the birds sing, people get ill, people get better, people don’t. It’s all ‘just is’ we can get annoyed, upset anything we like but that’s our ‘just is’ I have had much time to contemplate losing the ability to be able to give my wife children naturally. It’s been a very upsetting process for me to come to this point in my understanding of life. That it just is and no amount of upset can change my world in this. 

For me it’s amazing to be able to live, maybe IVF will work and we will have a miracle but together me and Andie will just relax in our ‘just is’ it’s far better to accept the lot we have been given and to focus on what we can do, not what we can’t. To accept the world as it is, rather than to wish it was different. As I have written this blog, I have found things that were bothering me disappearing. Because it’s about our perception of what is and is not that makes all the difference. The world is your playground, it’s not a place with continued problems it’s only our perception of what is that makes your world a better place to be. So from now on I will be learning to accept what is, not wish to change what I think is not. As my friend says.

Peace.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Our support group on our FB

Cancer stories (people helping people through experience) 

It’s a group where people’s experiences are used to encourage others. 

Everything you read are based on my own experience and my own opinions. I express them here to encourage you. Please share with others, if it meant something to you it will to someone else. All images are from a Google search. Or my own, taken whilst creating memories every day.

Copyright © 2016

Bless someone, by sharing. You never know who needs to read this.

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