I know what it’s like to eat salty bacon with tears.

Tags

awareness, bone, cancer, faith, Families, friends, Hodgkins, hope, life, love, partner, Peace, strength, survivor, transplant, weakness

I know what it’s like to eat salty bacon with tears.

I don’t know how many of you have just watched “Growing up with cancer” but I just did. Children that had the cancer i did, children that had to grow up with cancer and face things no child should. Well it took me back once again to that room where I had my stem cell transplant.  Kids are so resilient aren’t they, accepting of their situation and able to rationalise things and adapt. They seem to be able to deal with things quickly and efficiently. 

There was a young lad in the wards that became depressed and lost his appetite. He was unable to eat due to how he felt, he was angry and upset although he was uncertain of why he was so unhappy. Being depressed he was certain of. I know I was low and forced my family away from me, which is actually why I am writing this very post.  The family that wanted to be close to me I pushed away.  I did not allow them on the ward even though they could have really. I was so hung up on the word. Isolation. 

I wanted to give myself the best chance at beating cancer and living longer by not being around any germs what so ever. Well I want to put that right right now. Today should my wife’s dad be alive he would be 74. But cancer took him aged 59. I never knew him. But it’s made me realise I was wrong to be that way, that I should apologise to my family and say Sorry. Sorry for keeping you at arms length, and ask that you all forgive me.

Whilst in that room the chemo they give you, is so horrendous that you get hundreds of ulcers all the way through your body. They tell you that you are unable to eat, and that you would be better to have a nose tube to be fed through, and that exercise would be impossible. 

What I did in there I did for my family, I did what I thought I could to come through. I did press ups on the visiting chair that my wife used sometimes. I walked from the bed to the ensuite which was about 5 steps and back whilst having chemo moving all of the time and eating my breakfast not once but twice everyday. Sounds greedy right? Wrong. I would say eating bacon with ulcers in your mouth throat, intestines, all the way through to your bowl is not easy. You cry whilst eating making the bacon taste saltier. But every bite hurts like hell as it goes through your body making you not want to eat. Without doubt the easiest thing to do is to not eat, to choose nothing off the menu to sleep all day and not excercise. To give up. 

All I did in there I did for my family, and want to say sorry for not doing the things you wanted me to. It was wrong of me. 

To anyone that’s facing cancer or supporting anyone with cancer. What seems normal in life without cancer is most certainly not normal in a life during cancer. 

But I leave you with this, to do something is better than doing nothing, even if at the time it may seem like the wrong thing to do, it’s still better to do.
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. I

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.
You could change a life by sharing this post! Will you?

Copyright ©2017

Family

Tags

age, banned, Bellamy, Christian, Compassion, Families, foundations, gift, Goodness, hope, longevity, Lord'sPrayer, love, Monkey, motivation, Paddington, passion, Presence, strength, unite, unity, weakness, yin

Family

Family does not have to be a place, it’s not something you get. Family is something you give, for many years I have missed the point till right now. No one owes me anything, no family member owes me. People that truly love don’t do it because they are a part of a family. They do it because they want to give NOT receive.. I personally know what it’s like to love someone, loving someone means you never remember what they owe you because they owe you nothing. If you think a friend owes you, then they are no friend. If you scroll through your phone and a person has not called you, that’s when you have to question if the traffic is one way.

I have this saying, that. If someone really wants to see you they will. It’s not your fault someone does not include you it’s their choice. One thing I have learnt of late is this one thing.

I have just bred a litter of pups, and at 16 weeks old our pup has just spent a week with her sister. They both have different personalities and the only time they truly love each other’s company is when they accept each other, warts n all.

 

Having dogs has also helped me to realise what true love is, and it most certainly is not what the dog can get from the other. It’s only when a dog accepts how another dog is and does not count the cost tat the love really starts..

we could learn a lot from dogs, but if nothing else what we should learn is. If someone has their hand out, the person they love is themselves. If the have their hand out yo help you up, their friendship is not just an action it’s a feeling. People love to receive or they give because they wanna give. What you have in your hand is nothing to what is given from your heart. Jesus paid the ultimate price to show us what love meant. Unserstand that, and you will have life.

 

enjoy your life with your hand out to help someone up, rather that a hand out to receive is when you will feel the true freedom of life.

Fonz

 

Transplant 2 years in.

Tags

camcer, chemo, encouragement, hope, love, marriage, survivor, transplant, wife

Transplant 2 years in.

It’s incredible how things have changed from this day 2 years ago to today. 2 years ago today right now I would be having my first chemo in isolation having had my Hickman line fitted in the morning. I remember who was there for me, my friend Karl who was so amazingly supportive during my stay in hospital doing jobs for me back at our house. My wife is so impeccable at the detail wrote everything down from day to day during my transplant. Whist I don’t like to look back on negative things I just move on normally. But it’s reasonable to say it’s important to look back, so others who face the same can learn from my experience possibly. Your brain is a powerful instrument and I think shuts off from us the trauma we experience at certain times in our lives. That’s why my wife’s write ups are invaluable when looking back at my transplant journey.  For sure I don’t mind telling you I proberbly cried more in the first 24 hours in isolation than possibly any other 24 in the whole of my life before. 

There are two things you never need to chase in life. They are true friendships and true love. Both of which ironically we have no control over.  People that truly love you will be there for you as they were there for me. People that don’t really care about you will not be in touch with you at all. 

My Hickman line was playing up, although I don’t remember much about it. I made friends in that hospital that sadly I am not able to peruse due to hospital protocol. Dr Salem, Heather and Kim. The girls were like my Angels, there for me when ever I needed it. I am not able to get across to you just how amazing the people that work for the NHS are. They are committed and conscientious and vital to the health of us all in the UK. You will never realise how important the NHS is until you need it. There are some that disagree with me, but you have to remember that they do the best with what they have. 

If I have any advice for anyone who has this to face, don’t try and make your friendships happen. They will take care of themselves, the ones that are really important will make it through to the end. Aside of my family my wife Andie, Paul Benson, Johnny Wilson, Karl Boardman, and Simon Naylor were the people that kept me motivated. Phone calls not talking about cancer were a great relief in that small room.  Our cancer stories group which was small back the, had so many faithful people in it that were a great support. To name a few, Rob Fiscbeck, Liz Peters, Eileen Almond, our late friend Eileen Salmon, Judith Taylor, jean Anderson and Deanna Perich, were all good people and many many more that helped along with the whole Cancer stories group. My dad rang me everyday, if your reading this and your supporting someone in cancer. NOT talking about cancer is the best conversation you can have. 

You find out what’s truly important in times like these, aside of friendships. Peace with yourself, God and the planet is vital. What was can not be changed. But the future is in your hands and for sure you can make a differance in this world if you want to.

I guess what I am trying to say is, treasure what you have and enjoy what you have to the fullest. One day medicine won’t be my saviour, but I have and do know true freindship and true love in my life. I leave you today with a song Johnny Wilson gave to me when I went in for my transplant. The 3 weeks that changed me and my outlook forever. I only hope that someone reads this today and listens to this song and it helps you to realise the good you have in your life.

Be good to one another.

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. I

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.
You could change a life by sharing this post! Will you?

Copyright ©2017

Mr Nasty.

Tags

belief, home, hope, hospital, love, lover, marriage, perseverance, together, university, win

MR NASTY.

It’s been a while, whist finishing all my projects someone I met who called round a couple of times. Said “finish one thing before you start another.” As I looked around I realised how much there actually was unfinished at our house. But is that the right way to look at stuff. I mean there is so so much we have done in our home to. Let’s start a list. 

Let’s call it inside out. 

Tiled the whole of downstairs,

Decorated throughout,

Ripped out double doors and made it a through diner,

Built an extension with vaulted roof.

Log fire fitted

Oak floor,

Conservatory built,

Indian stone placed around 360 degrees of the house.

Garage floor fitted,

Drains fitted

Stream fitted with fish and pump and furniture,

Rear garden created with shrubs and plants,

Side garden obtained and planted,

Seating area created,

Orchard started,

Front area planted,

Rear chill out shed next to the stream created,

Log store built in side garden to serve log burner,
Also dream car maintained to a great level.

Oh and all whilst beating cancer, twice. Don’t know if I mentioned that. 

There is a way to fail, but you have to believe that to. Only people that believe they will win, will. You see while we can believe we will fail, we can also believe we will win. People can see what’s not done, or see what’s been done. Yes there are some small piles of bricks, yes I have stuff that’s not moved yet. But there is also a porch that’s not built yet, and a stream that needs finishing (Well building) in the back garden. The roof and rear door needs fitting to the garage and a wall building. But I think it’s best to look at what we have achieved while we could have just let the walls cave in.

My point is, your words can have a devastating effect on people’s lives. But it can be devastatingly positive, or negative. The word devastating can also be positive but then you knew that right? Have you ever seen someone who’s devastatingly beautiful. I don’t mind telly you I have. That lady stole my heart so many years ago and she is the reason I live today, she is the reason all of what I have spoken about has been created.  Her devastating beauty stole me from me. But hey I needed stealing and if I were to start over it would be with you Andie. 

Thank you for all you have done, and all you will do. I ask also that you would forgive my failing as I am not perfect. But one thing is for sure you are perfect for me.  Every brick I move I move for you.

Forever yours

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. I

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.
You could change a life by sharing this post! Will you?

Copyright ©2017

Who you are.

Tags

facebook, faith, family, happy, hope, instagram, Puppies, religion, tmbrir, twitter

Who you are. 

Isn’t this what matters, who we are. In my life I have heard people tell what I am not rather than hearing the good that I am. It’s been tiring to change from what I have been taught, to what I believe now. But it’s true of society as a whole that people seem to focus on what we should be and not what we have chosen to be. Society wants to put us in boxes and have us stay there and be quiet. While acceptance for who someone is, most certainly something I have had to learn. Although I must have just accepted people for who they were as a child. We are taught not to accept certain people arnt we. We are taught that some ways are not the right ways and others are. 

Who are we anyway, that gives us the right to judge another. Should we not just be happy to accept another’s point of view and not change it. Should we not lead by example. Jesus said ” suffer the little children that come into me ” as children we are not consumed by any of the world. Time is all children crave, they only want things because of adverts they may see. 

A man should be strong and not cry says society. Yet I find the tender touch of a man is so much more appealing than a man that is arrogant and boistrois. Maybe that’s because I am boistrois myself. We have puppies here at the moment, and those puppies are showing me who I am rather than what I am not. They trust me, because the do not know anything other than love and tenderness that’s been shown to them. Their lives and what I show them in it will have an effect on them forever. These little guys just trust and love completely. How special that is, to love someone and not expect anything in return. That’s who I am, a man that gives not expecting to receive. I accept people, and dislike people that can’t accept who I am. 

Acceptance is something we have to relearn, after a TV and society has untaught  our innocence. 

There is nothing weak about showing others love and compassion. In fact I would say it’s a quality, how others respond is up to them. For me life is about paying it forwards no matter how it’s received. How someone chooses to be we should I suppose just accept even if it’s not the way we would be ourselves. 

Me I am sensitive, I cry. I can tenderly touch a new born puppy and look in the mirror and like who I am. I can be who I am, and be happy with that. 

Can you?

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. I

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.
You could change a life by sharing this post! Will you?

Copyright ©2017

Relativity

Tags

belief, depression, faith, hope, manchester, relavant, relavency, survival, united

Relativity

So is it possible, to change how we feel inside. Is not how we feel relative to our souroundings, is not how we respond relative to what we think and say things will be. Today I want to help you. Someone said to me the other day, that our family has mental health issues. I laughed inside, because I realised at that moment that the persons point of view was indeed right. That her family did have mental health issues, but then as I thought on the sentence and considered it. I realised that the sentence was relative to that persons experience and it was up to me to accept it as relavance in my life or to change what is relavant to us in our lives.

How many times have you said “oh no not such and such again” or “we have to go again” things we do and say in our lives are relative to our surroundings. So whose responsible for these surroundings, the people that suggest the relevancy in our lives. The throw away sentence of “there is mental health in our family” was a statement believed by that person. See my relavancy is this. We have strong people in our family. The two refer to the same thing, but we are taking from it what we deem to be relavant in our own lives. WE (Me and my wife) do our best to turn seemingly negative situations around. That’s why I write. One song we listen to a lot is 

We listened to it a lot when I was having treatment, and we still desire to have the relavance of faith in our lives. I tell my wife often how much I appreciate her, and that there is power in we. I personally believe that forgiveness is one of the most poswerful tools in the world and without it people can’t move on. It’s not possible to find a relavancy that’s stronger than the negativity that surrounds other sentences feeling s and actions. People have said to me “I am depressed” “there is depression in our family” well your right. Because that’s the relavancy you have chosen to adopt in your life. I prefer “We are surounded by fighters” 


Who you are in life depends on your own personal relavancy to situations, you choose to include in your life what ever you believe to be relative to you. One thing I do know and that is I prefer things and people that smile and speak positively. I find people like that relative to how I want to live my life. Now that’s not to say that your not supposed to feel grief, that your not supposed to get sad. Of course you are, again that’s relative to your own situation. If you have just watched someone fight cancer and die, your relavancy would be different to someone that had gotten a disease and chosen to give up to it and die. Trust me the two are the same in that they both involve the person dying. But the relavancy in the two situations are very different. 

LIFE in most situations is up to us, but the relavancy we choose is for sure 100% up to us. What we choose to be relavant to is in a situation is for sure our choice. What others say is their choice. 

My challenge to you is this, can you find relavancy in your situation that helps you today?

I hope you do.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Ps, I have committed to doing this for 365 days every morning, what I ask of you is that you share these blogs I make on email, facebook twitter, you can affect people by pressing a button. Please do that. I asked ppl to share yesterday 18/05/2015 at 8pm they did and 100 people saw my blogs in 2 hours. It only takes a click or two.

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. I

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 ©2017



Are you afraid to die?

Tags

britishgas, cancer, chronic, efl, energy, hacksaw, pain, survived

Are you afraid to die?

Well asking myself that question, I was but not now. You see my first post in this blog was “I am Mark a cancer fighter, and I WILL win” many have forgotten that was said. One thing I know is that we ALL WILL die. Now for me personally, having been hit with that 500lb yellow fin Tuna right in the face. Yea I have heard it, and then fought it and won. Now whilst that was the toughest time of our lives together. I can tell you now, that people that remind me of the bad parts of me. Well, they just don’t get my time now, those people that don’t like me for me. God loves me just the way I am, but to much to let me stay that way.

You can be if you say you are. It’s been said by me. “You want to know the substance of man, look at his friends”  I am a fortunate man, that I have friends that are the family I choose. People that care about me and us, people that love us. People that focus on what they can do with us, rather than find fault in us. For is it not true that “All have fallen short of the Glory of God.” Without exception. 

This is one of my favourite tunes, and while we don’t know where our world or steps will take us. One thing is certain. That is that from having our first breath means that we will breath our last. As I sat with my wife tonight watching the film ‘miracle’ we were holding hands and I looked around and thanked God for the miracle of life. For sustaining my life and for what he has given me, not what we are left without. Yesterday I spoke how we turned an IVF decision into a positive, and whilst we may never have children because of someone’s power. We will always have today, each other and all we have achieved together. 

It is for sure better to do something than to do nothing. Yes of course it’s also true that if someone says ‘no pain no gain’ then they do not know chronic pain. We have and have not. There are reactions and reactions. All the ones you choose are yours, and are so powerful the choices and actions and no actions we choose in our lives will have a consequence or an impact in this world we live in. That’s why your reading this, because if you did not you would not know what’s written here. You did read this, which will cause your next reaction. Your more amazing than you will ever know, and you will have an impact on the world if you allow it.

That’s up to you isn’t it.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Ps, I have committed to doing this for 365 days every morning, what I ask of you is that you share these blogs I make on email, facebook twitter, you can affect people by pressing a button. Please do that. I asked ppl to share yesterday 18/05/2015 at 8pm they did and 100 people saw my blogs in 2 hours. It only takes a click or two.

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. I

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 ©2017

Friends are the family we choose.

Tags

belief, faith, family, friends, GOD, hope, strength, together

Friends are the family we choose.

As I sit here on the settee minding my Dam ‘Faith’ I am watching the movie ‘CREED’ it’s brought a lot of memories back to my mind. Rekindled my cancer journey and even why I embarked on treatment in the first place. The first reason of course was my wife. My friend turned LIFE long partner, then my wife. Which she will be till my last breath. Loads of things are spinning around in my head, in not very long faith will give birth to her puppies. Life will be because of the fights I have had to have and won. Strange for me to think, that without cancer there would be no Faith. Without cancer I may not have realised who my fake friends were, but also who my real, true friends were and indeed are the family I have chosen.

It’s bringing back to my mind not just why I beat cancer but how. In the film Rocky gets the cancer I had, which opens the flood gates for me every time. I can’t help remembering the day, the day your told what’s making you so tired and weak. You see when you fight cancer, it’s every scan, every blood test every chemo. It’s Avery person that sends you a text that helps you to go that one more round when you think you can’t. That’s what beating cancer is about, ‘one round at a time’ Faiths about to give birth and whilst she will never understand the words I write, our friendship is without a doubt real. 

What ever you face on your journey, I want you to know that you can. That no matter how many obstacles there are in the way. If you keep getting up and moving forwards that you can.  You have to have the heart to stand and move forwards though. I don’t know about you but the friends I call family have given me the strength to get up when I thought I couldn’t. The visits from people when I didn’t want them, because I wanted to give in to cancer and die. I want to right here right now, thank those people for helping me get to today, for my actual family for the love and support they showed me to. That through his people God gave me the strength to choose life.. in choosing life, there will be new life in the form of faiths puppies. 

So thank you cancer, and thank you for helping me choose life.

Together we are stronger.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Ps, I have committed to doing this to encourage people, what I ask of you is that you  share these blogs I make on email, facebook twitter, you can affect people by pressing a button. It only takes a click or two.

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. I

Everything you read are better based on my own experience and my own opinions. I express them hereby 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 ©2017

My TVR and me.

Tags

brain, classic, health, nerve, neuropathic, nootropics, pain, tvr, wealth

MY TVR AND ME.

When I bought my TVR, was when someone said I may have cancer and that my life would be compromised because of if. I laugh because I felt fine, no pain what so ever. Just this growing lump in my neck that had gone misdiagnosed for so long. When I first drove my new car and went over the first bump. I realised it was going to need some work, rear shocks were desperately needed and many other jobs were required also. Little did I realise that me and Trev. I call him that because Trevor was the guy that invented TVR. Every car is different, not one curve is the same. There are even some funny stories about how the Chimaea shape, mine became the shape it was. It’s reported that whilst in clay, being shaped by the designer who had his dog with him one day took a chunk out of the bumper next to the indicator. That’s why all Chimareas have two curves next to the indicators. Which are themselves from a Sherman tank. 

I didn’t realise just how similar our journeys were going to be, mine and Trevor’s. Whilst in hospital having my transplant, my friend took the interior out for me and another friend took the interior and sprayed it. Bringing it back to new. This happened whilst I was undergoing my transplant. 

I looked like this.

And Trevor looked like this.

At the same time we were both getting a new beginning, becoming renewed. The only difference between me and the people working on my car. Was that I had a chance of not making it, I know I did and am also getting stronger even though pain is so hard to deal with. I am here to write these blogs. I was encouraged today by another TVR owner that my posts to my blog were inspiring. It gave me a sense of achievement that because of cancer I owned a TVR and because of that connection she got to read my blog. It’s kinda time to thank cancer again isn’t it.  Cancer maybe cruel and things may perish and need repair. But we are far more fragile than any piece of machinery. Whilst we are living longer and medicine is helping to sustain life. Machines are able to be fixed forever should the owner wish for that to happen. 

Everything I put on my car is the best, Bilstien shocks. Updated engine, powder coated struts. It’s all been done right, of course at a cost. But no cost is greater than to put your life on the line is it. Unless you have a passion for something, even if that’s your faith. You will not understand what I am saying. Your are delicate, controlled by a few degrees in temperature higher or lower than should be, your life will cease. It’s the same with my car, except my car is nuts and bolts to most. To me my car is so much more.

You see, a brain is only able to do so much at the same time. Whilst a person is being distracted, a person does not feel the pain. Oh it’s there alright, but your brain is distracted from it. Yesterday I managed to make it to pain clinic, someone had brought in his Samsung VR. You have seen the advert that the Dad records the concert so his daughter can see what he saw.  People that used the VR whilst using it were distracted from their pain. It was still there but the brain was not sending the signal, because to many other things were going on that the brain was otherwise engage. That’s what my TVR does for me, it distracts me from the real world. The world and its treatments have damaged me forever. But driving my car helps me to be distracted from what I am feeling inside. If I try to remember how much pain I was in when driving and I can never remember any at all. Of course I am not saying everyone needs to go out and buy a TVR, or VR system to enable a pain free period. But what I am saying is that, a distraction can help . Only you know what you love, only you know what’s great for you. But what ever you do, make sure you do something that distracts you from the real world. Here are some pics of what my car looks like now and how I look today.

And me.



I guess it’s up to us to do again, or do nothing. For sure when we do nothing it will be more painful, because our brains are not stimulated. So there you go my blog inspired by a TVR called Kate, one called Trevor. Not forgetting Julie.

Let me know if you got something out of this blog.

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 hereby 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 ©2017

My story

Tags

cancer, death, demetia, faith, fumeral, grace, help, hope, life, matters, trump

My names Mark, Fonz to my friends. My story isn’t a A heart wrenching one or anything, it’s just my life. A life I never expected to live. I always had plans to be a dad some day, but with the right girl. The girl that made me quiver, the girl that loved me for me. I was not especially good looking normal I guess, mr average although not in all departments. I always thought I would be a high achiever. Live in an above average house, not that the house was big, just that it would be full of love. One song I can’t forget was ‘feel’ by Robbie Williams. 

I always dreamt of feeling the feeling of love in the home that we live in.  My first marriage was born out of hate, a bomb in Ireland my girlfriend bk than was stood 10 feet from the bomb when it blew. We married and love was born out of a tragic bomb that affects people’s lives today and will forever. Married life failed. Back then I wanted to end the hopes and dreams, I felt as though I should die . Leave you all behind as it were. I decided to travel instead to look for my Mrs right. To have some fun whilst doing it, I drank to forget. When I drank I was numb,numbed by the alcohol. I lived and did things I loved. Went to Sydney on New Year’s Eve, Brisbane at Christmas. Travelled New Zealand. Along the way I turned down life long dreams. Swimming with dolphins, seeing a glacier, many things that I wanted to do with a true love. I did go to an F1 grad prix in Melbourne though and came home soon after. Tears rolled as I flew back to GB.

I moved to Manchester. Where I met some amazing people, but one I met in the most unlikely of places on the most unlikely night. A night out with a friend, a different pub and there she was. Blonde hair, the most amazing smile and sourounded by men. I whispered in her ear ( I will be back when your boy friend is gone) I then flicked her hair into her face.  That was the start of our lives together, the girl I had gone around the world looking for was there. You know, the one that makes your heart melt. The one that’s for you. 

We worked hard, moving into a really little semi detached house after 4 years renting a big terrace. Then losing her mum to cancer so suddenly it shook us both. 4 years later we moved to Preston where we now live. Little did we know what was ahead. 1/4/2011 we moved in June 2011 I was told I would die with out treatment diagnosed with cancer. July I started treatment. They told me I would become infertile so I had to store some boys. Swimmers or sperm to the medical among you. I did, and hoped one day I would be able to use them after the fight to beat cancer. 6 months of treatment, chemo every 2 weeks. We had Christmas together 2011, friends disowned us. Family did not understand. Our fight carried on, until I started to get better, work again, the extension I started when diagnosed was finished. I started to do bits in the garden, help a friend, my energy came back a little and we bought our dog faith. 
Faith was my shadow, a wonderful dog. She still comes with me where ever I go,  and loves her dad like no other. For me she would do anything.

Ah but then I have to say, she licked me on my neck, again and again and barked at me often. She was telling me it’s back, my cancer had come again. A Bone marrow transplant, a tiny room. All the time believing my deposit would be used one day. 18 months ago I had that transplant weak though I still am and not able to work full days, we hoped that IVF would be given to us. My wife was 39 but got to 40 when we had our appointment, we were told we would be able to go ahead to now eventually have a child. A gift from God, although stored by me and saved in the nitrogen bank. 

Then that day, the letter came. No it said, your wife’s to old and you should have tried earlier. You are not able to have children. But not giving up we made an appeal, supported by phycologist doctors and reports. Yet still the answer is no. Is it? 

That’s when we decided to let our beloved faith have pups.

So here we are, that’s where our journey has led us.

Meet our puppies that will get a new home. But also our blonde girl Lilly Hope. Our new blessing.

Rejoice with us.

Fonz

http://www.fonzandcancer.com

Follow me on Twitter

@fonzmark

Email – fonzicloud@icloud.com

Ps, I have committed to doing this for 365 days every morning, what I ask of you is that you share these i make on email, facebook twitter, you can affect people by pressing a button. Please do that. I asked ppl to share yesterday 18/05/2015 at 8pm they did and 100 people saw my blogs in 2 hours. It only takes a click or two.

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