Transplant 2 years in.

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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

From bad to Worse!!!!

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

Do it anyway.

Tags

belief, cancer, challenge, chemo, down, hope, perseverance, reality

Well there it is, we went to a place today that had a suspended staircase. Quite high up, many that know me know I am scared of heights, or just not keen. It’s a feeling I have when I am not seemingly in control, wires suspending me in mid air just don’t rock my boat in fact I would much prefer a world without any heights what so ever. But hey we don’t live in a world where anything is perfect do we. But what really is it that stops us doing anything, why do we let fear or any other feeling stop us from doing anything at all. After all what we choose to do or not do, won’t we still feel the feeling we feel anyway. 

As I approached those stairs, I was told the risks. That if I suffered from vertigo don’t do it, if you don’t like heights don’t do it. Well my friends wife Said to me. “Just do it anyway” Her words compelled me to do just that, to turn what a thought was impossible into a memory. My thoughts again went to my transplant and how impossible that was, yet I was able through faith, self belief, prayer and doing it anyway. I managed it. So surely a few steps would not stand in my way. Would they?

My thought pattern was if I can do my BMT I can walk up those steps. I put one step in front of the other anyway, I walked up them anyway. It did not change what I felt, I still felt the fear. I still had the same feelings but I did it anyway. It was a victory and although I did not hang around to see the view but I did do it anyway.

It’s a challenge I would like to make to you, that no matter how something makes you feel that you yourself, find it in you to do the same. To look outside of what you think is possible and do it anyway. I think you will suprise yourself. A couple of days later I walked over a rope bridge that I never considered doing in the past due to my fear of heights. Doing something that you think is impossible makes you more of a person, it hones you and moods you into a person that becomes a beacon. Smoothing the rough edges of you making the diamond that you are. Shine brighter. I guess it’s down to that choice again as to what you want out of life. To do it anyway or to change nothing.

What will you 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. 

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.

Copyright © 2016

Have courage and be kind.

Tags

business, cancer, chemo, courage, dentistry, faith, hope, kindness, love

It’s, a precious gift kindness. I don’t know why  it makes us feel vulnerable. I guess that’s because we expect something in return, hope that the person we are being kind to will be as kind to us. It was a long time ago when I gave someone a gift, I was so wrong to even expect a thank you. Because real kindness does not give to receive. Real kindness just gives and your gift in teturn is the pleasure of giving. It takes years that we live to learn the value of the courage of kindness. These days I give with a non expectant heart, I find it gives me freedom in my soul and my spirit. 


I guess without getting the dictionary out that courage means facing something you have to face, and bravery is facing something or someone that you have a choice to face. Courage is to keep doing anyway, I see courage in parents everyday. Of course I have only a glimpse of what being a parent actually is. My only true exsperience that comes close is picking up my nephew from school in the little TVR, I waited outside and watched all the dolled up well kept parents arriving to collect what I now understand to an exstent. To be their most special gift on the earth, their children. I was given an insight into the courage of kindness. 

You see I now realise that as a parent everyday you need to have the courage of kindness, a relentless giving heart to your child expecting nothing in return. Everyday you have courage in your constant journey of dedication to the little people you bring into the world. I know if I was a parent and my son was my nephew, I would not feel anything but pride and thanks for the gift I would have in him. Picking him up, made me realise how truly precious children are, it made me understand a snippet of the courage of kindness. 

Giving without expectation does indeed need courage, though some kindness is instinctive. The reward you get for it is what you feel inside. How giving makes us feel with in that no other gift can give. How wrong I was to give that gift exspecting something in return. It robbed me of the feeling I should have had. The gift giving gives to our inner self, but maybe I would not have learnt the differance in giving to receive, compared to the courage of kindness. The courage of kindness does without doubt give to our spirit a revival. A renewing of our inner self because of what we gave. Giving does not need to be an item or exsperience. It can be words of encouragement to another that Spurs them on, when you see a difference being made in someone’s life because you did. That’s priceless and something that money can not buy. 

Here is my question to you this week. Will YOU have the courage of kindness this week. Will you give and expect nothing in return? Well if your a parent I think you already do that everyday, you do it instinctively. You have a responsibility that transforms this world. Imagine what the world would be like if we all adopted the courage of kindness for someone everyday. Have a great week.

Fonz  

Love yourself.

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Throughout my life there have been many stages, but one lesson I would say is perhaps the hardest, or maybe took the longest. Was to learn to love myself, you see most people blame situations people, ( I was dealt a bad hand)  my friend says it like. The people in the pub that have a woulda coulda story – if only it was not for such and such. Well it’s all a load of rubbish. Absolute BS. Our future is in our hands but unfortunately, if we don’t live ourselves we will find life is so much harder than it would otherwise be should we be happy with who we are. We have to become that person that when the person who is looking back, your content with. I am not saying the full article because no human is ever the ful article in my opinion. We learn until the day we die if always want to improve ourselves. 

  
I personally want to better today than I was yesterday, I think they call it growing. Always learning and always becoming a better you. Let me put it this way, a house needs solid foundations to last. Without solid foundations there will be cracks in the plaster in time, bricks will move and the house will become unstable. Loving yourself is the foundation for everything we build on top of it, a relationship, the ability to live with your whole heart, holding down a good job, respect from others. No one will respect you if you don’t respect yourself.  

  
I found the right person to marry because I had found myself in travelling Australia, yup that’s what it took for me. It was not till I was 36 and a broken marriage behind me that I became truly happy with the reflection in my mirror. Very late in life I would say, but at least I got there in the end. Cancer has honed me, made me a better more rounded person enabling me to see life through the eyes of a disability. The disability being the disabling treatments that my cancer demanded. In your life you will have your own challenges, but what ever happens in your life love the person who you are before you build a life.

Have a great weekend

Fonz

http://www.fonzandcancer.com
Follow me on Twitter
@fonzmark
Our support group on our FB
https://m.facebook.com/groups/1595998743956536

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. 

Chemo Brain.

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achieve, affair, age, animal, attitude, avec, awareness, baby, banned, be live, because, believer, Bellamy, best, birthday, black, blood, bone, BONE MARROW TRANSPLANT, brain, can, cancer, chemo, chemotheropy, Christian, Christmas, Christmaseve, Cole, Compassion, courage, cricket, cruise, CS, dad, David, dead, death, define, Depressed, depression, desire, destiny, diagnosis, did, died, Do, does, Edmonds, empathy, encouragement, energy, England, Eve, expect, Experience, facebook, faith, falling, Families, family, floating, foundations, friends, gallery, gift, gifts, given, goals, GOD, Good, Goodness, great, greatness, guilt, Hannah, hansolo, happiness, happy, hard, healing, health, help, Hodgkins, hope, hospital, Jewish, jobs, Johnny, know, last day, Learn, Leicester, life, lire, Listen, live, lived, Liverpool, London, longevity, Lord'sPrayer, love, loved, Low, machine, marks, marrow, MDU, meal, meaning, memories, memory, Monkey, morph, Morris, motivation, mum, muscle, Muslim, Natalie Cole, Natking, neurology, neutrapeenic, new year, Noel, not, of, oncology, one, one day, onedirection, Paddington, Paris, partner, passion, Peace, people, persevere, precious, Presence, R2D2, raise, real, reality, recover, regret, Rejected, Rejection, relentless, Remember, resolution, rises, Samaritan, SENSATION, Sharing, shortbread, silverback, somebody, southport, Spirituality, square, stage, star, stats, Stemcell, Steve, StevenHawkins, StMichael, stories, strength, struggle, survived, survivor, swopshop, taught, teach, tennis, Thames, thankyou, there, time, today, together, Tohetehr, Tony hart, transplant, Transplanted, travel, tree, true, tvr, twitter, unite, unity, wars, WE, weakness, wealth, wealthy, what, white, who you are, will, win, Wordpress, working, Writing, yang, year, yes, yin, you, yourself

I read an article today on a site called Had cancer, talking about different ways that we feel sometimes years after having had chemotheropy. Some doctors say it does not exsist, (apparently) I have never had this exsperience with doctors myself but then I am quite a large person both physically and in personality. After reading the article I realised that maybe I could write about the very thing that frustrates me so much. So let me explain how it is for me as a cancer patient that like the person who wrote the article. I had cancer!

So for me when I was having chemo, even my first chemo (mine was very strong) it had to be I was at 4 a and in a bad way. Close to losing my life and riddled with cancer. Remember in previous blogs I have talked about chemo feeling like snakes in your head, it did. Sometimes your head even hurts as you remember stuff, but then your brain is a muscle. It has lots of connections in the brain that need to work in a certain way. Now I am not a doctor, but it makes sense to me that maybe the brain has been affected in a small way by the drugs pumped into my body. I do forget things where I didn’t before. So I have to write things down to remember them. Where as before I really never did I just remembered.

Trust me no cancer patient uses it as an excuse, after all who wants to forget? I look like a Pratt sometimes because I repeat myself, repeat myself. Seriously though it’s embarrassing.

  Picture by Fine acupuncture.com
People that have not had cancer will never understand how it affects a human being. How can they, we must excuse their ignorance in not trying to even understand. I have been insulted, even misjudged by people close to me. I have to realise it’s not something they will understand unless they try to. Walking around pointing the finger at someone suffering does not help anyone.

Chemo brain can last for years so if it’s you, know it’s a possible normal for you. It’s frustrating because people may get annoyed at you, no one will understand unless they have researched what you maybe feeling. It does not mean we have lost our intelligence. It means we have been affected by chemothearopy, our memories may not be up to scratch but it does not mean we are inadequate. Far from it, chemo brain is real. But the fact is that chemo brain is much more frustrating for the person with it than it is for the person communicating with that person. Have a great day and know that your not alone, there are I suspect many that will read this and realise that it’s normal and even feel a bit better about it. Because others feel what they do.

Have a good weekend

Fonz

http://www.fonzandcancer.com
Follow me on Twitter
@fonzmark
Our support group on our FB
https://m.facebook.com/groups/1595998743956536

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. 

Why I share my storey.

Tags

battle, cancer, chemo, chemotheropy, giving, hope, lost, love, war, winning., won

Morning, how are you today? It’s a funny old place to find yourself, having a storey to tell. My mind is full of gratitude for the NHS. My heart is full of gratefulness to have beaten cancer again, I feel a love towards others fighting. My heart is to help other people get checked out and hope they get into remission as well. Everyone that has faced cancer, are some of the bravest people on earth. Pioneers emerge like “Steve Prescott” Although Steve lost his life after the pioneering surgery, his name will live on because he was willing to put himself under the knife, in turn paving the way for others lives to be saved.  I love hearing about people like that, people that have a giving heart. I was getting a take away yesterday, and the LEP was there on the counter. With our storey in it, the man said to me “that’s you isn’t it” “how much you get for doing that” he said.

  
It was like someone had stuck a pin in me, I did not even think of making money out of the article. Only that I hoped a life would be saved. That’s all I want, for others to exceed the life expectancy by stepping forwards, fighting and winning. No one but the cancer sufferer knows how hard cancer is, and like my dear friend at the Indian said ” I didn’t know what chemo was until my dad had it” it’s time for unity. Time for us all to pull together no matter what our religious beliefs. It’s time to stand together, to work together to help more people choose to beat cancer. 

  
It is a choice after all, after diagnosis the person chooses to take what life is left for them or to have the gruling treatment. Obviously I chose to be treated and WON, I am not in persute of financial gain. Just the look on a persons face that says “I won” you see when you have won many battles to eventually win the WAR. It consumes you, it energises you to want that for others. I want to encourage you today, what ever your facing. That you have what you have, so use it to benefit someone else. Give without wanting anything in return. You will be blessed but maybe not with a new Ferrari. Maybe it’s life with out cancer will be your gift, you won’t find out unless you stretch out your arm to help someone else.

  
Of course there will always be that person that thinks about how much. But remember that’s how that persons brain works, we learn to be compassionate. Then we choose to be compassionate or not, allot of people are driven by money. I was guilty of it to before I realised that no matter what life is the most precious gift of all. What will you do with yours? 

  
Giving is such a selfless thing to do.

Have a great day

Mark  

There IS life after cancer.

Tags

cancer, Cancerstory, chemo, energy, feeling, finished, freedom, grace, grateful, healing, heamatology, hope, last, love, respect, special, survived, treatment

As someone that has had cancer and beaten it TWICE! I am one of the few people on the planet that knows what it takes to beat it. My NO 1  thought has always been. “How much of me will cancer take from me” how much of me will be left after all the chemo and procedures are finished. Well the last procedure was done on Friday by having my pentamidine. I just have to have a lung function test done on Monday, then my dear friends reading this, then I will be walking free from cancer. I will leave southport hospital free from this dreaded disease, from all the things that’s needed to fight. I have slowly weened myself off of the medication and am out the  otherside. 

  
All the drugs leave you with kidney pain, chest pain, leg pain and nerve pain. But you know what non of that seems to matter. What matters is that the battle is now won. During the whole journey I have concentrated on going away with the lads as my end goal. To jump up and down together celebrating that this huge battle has been won. To see the smiles on the faces of the people that really care outside of my immediate family. To feel the freedom of being cancer free, and to share it with those that have been spurring me on. 

  
This will happen 1 week after my last test, the feeling I have within me is amazing. The prayers that have gone up by the many thousands of people around the world, the miracle granted to me that’s called life. I am so thankful, grateful, and blessed to have this life. I only hope that the people that have read my journey have been able to relate it to thier own situation, struggles, and challenges that you have had to face whilst we have been fighting to beat cancer. My wife is shattered, totally spent emotionally. She has faced everything with me, even holding my hand when I have been on the brink of losing my life. She has helped me find the strength to carry on. As have so many people along the way, people I was not to exspect to help have been there.

  
I went to see 1 of those people the other day, I went and had a Brazilian coffee with him. His children really loved interacting with Faith, and the feeling of freedom and being cared about were prevalent in that visit. i felt as though it had all been worth it, that there was a reason for a fight to have been won.

  
Happy family day, that’s what Sunday is to me. A day when me and Andie try to be together enjoying each other, giving our time to each other. wow how amazing that we can even have a family day. In my journey beating cancer, I have learned what good people are, what selfishness there is in some people. I have learnt that people can surprise you. I have learnt that not everyone is prepared to send you a message to wish you well, even IF people have had bad motives I always have tried to wish them well. I am also finding some diamonds on my journey. I am finding there are a few people that we can lean on, people that are reigniting my positivity for folk. People that want the best for you, accepting your situation but looking at the person not the disease. People that I want in my future, and are welcomed with open arms, because there is no hidden agenda.

  
It’s now time for me to remove all the cotton wool and bubble wrap, to start to live a life whilst I continue to blog and encourage those still fighting what it’s like on the otherside of Cancer. You may be able to pick up my excitement and expectancy of the things we will enjoy. Also the places we will visit whilst enjoying being cancer free. I can’t say those words often enough. 

  
Have a great week

mark

http://www.fonzandcancer.com
Follow me on Twitter
@fonzmark
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.

Making things happen.

Tags

ABVD, beam, Bloodcancer, bone, Bonecancer.transplant, cancer, change, chemo, chemotherapy, haematology, health, hematolohy, Hodgkins, hogkins!Lymphoma, Ice, live, myloma, PET CT scanner, positive, remission, results, scan, survive

Morning, some films are a complete and utter inspiration. We as humans can get inspiration from anywhere if we choose to look for it. Me and Andie watched one of my favourite films today. “The worlds fastest Indian” a film I love to watch. It’s one of those against the odds movies. A movie that makes you want the outcome to be a positive one. The man called Bert, played by Anthony Hopkins, sees the man embark on a seemingly ridiculous journey. He has built a bike that was supposed to do 54mph when first made, and hopes to achieve 200mph on it. The trouble is that there is 8000 miles between him and the place on earth he would try to make this record happen. 

  
The man was completely and utterly determined to make it happen, against all the odds and suffering many setbacks he day after day pursued his passion, believing that he would achieve his goal. Many people tried to stop him, discourage him. Make him feel inadequate. But nothing had an effect, he pressed on regardless. This true storey is an inspiration to many, giving me anyway a reason to fight. It encouraged me when I was down and out to carry on. It encouraged me to not quit, to peruse a cancer free life.

  
The movie can be related to any persons quest to triumph in adversity, anyone can achieve what they set out to do if the do not quit. If they stand when it seems impossible to stand, to fight when there seems to be no strength left within you. It’s a tale of courage, of human achievement. You don’t have to be interested in a piece of machinery to get something out of it. All you have to do is be willing to say the words “I WILL” what ever effort you make, whatever the outcome. It’s amazing what can be achieved by saying I WILL.  WE ARE MASTERS OF OUR OWN DESTINY. 

  
Listen to this track today and believe that “you can” believe it and reach for the sky and make it happen. Put a step forwards and pursue what ever your dream is. Don’t let anyone hold you back, just keep moving forwards no matter what. Finding solutions along the way. When your tired rest, when your hungry eat. But never give up! Ever!

  
I hope you have a good week.

Mark

http://www.fonzandcancer.com
Follow me on Twitter
@fonzmark
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.

Picc line Removed.

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chemotheropy with a picc line is a great way to have it administered. It’s a small tube placed in your arm into a vien going to a main archery near your heart. Mine was 35 cm long. I had mine fitted in January to have my ICE chemo. It’s a real pain having it as it protrudes from your body and it’s uncomfortable sometimes. That line became my friend, because with it in there are no more injections to take your blood. 

Well today was the day I had to say goodbye to that friend, but it also signified that I would not be having treatment at southport anymore. It was a little emotional saying Thankyou to all my day care nurses at southport oncology. But somehow a relief that we had completed the journey with no hick ups. This will take me to a small space in royal Liverpool hospital for 4 weeks where I will have to have my transplant. I can see light at the end of the tunnel now. That day I dream of is coming nearer.

You can find details of my journey on 

https://www.facebook.com/groups/1595998743956536/
A 7 year fight all because of a lump. Still I stand, time to dig in once again next week and see off this Cancer once and for all.. 

 

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.

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