A letter to Rt Hon Hilary Benn MP

Dear Mr Benn,

As a member of your constituency, I am writing to you to ask you to attend an important debate on 8th September 2014 that could literally change lives of patients and families affected by pancreatic cancer.  With just a three per cent survival rate, diagnosis of this disease leaves patients and families with little hope of a happy outcome.

I have wrote this very personal and public email to ask for your help Mr Benn. Personal, because at the age of 38 I was told that I have pancreatic cancer, and public, because it may encourage other MPs like yourself to also help. This is almost 2 years ago I was told I have pancreatic cancer, and during that time, I witness what this cancer can do physically and mentally. If you need any more information please read my blog, or call or email or reply below.

I was one of the lucky ones, I was able to be operated (only 10% can), sadly the cancer came back, but after two lots of six months of chemotherapy and help with private healthcare, I am keeping the cancer away to the best of my means. 

The fifth biggest cancer killer in the UK, pancreatic cancer has been little known, poorly understood and chronically underfunded for decades. 

The debate will take place between 4:30pm and 7.30pm in Westminster Hall, and the backbench committee will be discussing providing more funding and awareness for pancreatic cancer, which is set to become the UK’s fourth biggest cancer killer by 2030.

This follows a successful petition, which passed the 100,000 signature mark in April, started by Maggie Watts.

Maggie from Scunthorpe started the petition following the death of her husband Kevin, who lost his battle with pancreatic cancer in 2009 aged 48, 40 years after his mother died of the same illness.  In the 40 years between Kevin and his mother’s death, the five year survival rate of just 3% has not changed. 

The need for this debate is even more urgent following a question posed by Luciana Berger, Public Health Shadow Minister on 31st March, which highlighted a decrease in overall cancer funding of almost £19 million between 2012 and 2013.  Considering pancreatic cancer already receives a tiny proportion of cancer research funding, less than 1%, the impact of this on future pancreatic cancer research is alarming. 

At just three per cent, pancreatic cancer has the lowest survival rate of all 22 common cancers.  In comparison, 85% of breast cancer patients and 81% of prostate cancer patients will still be alive five years after diagnosis. In fact,pancreatic cancer has one of the highest incident-to-mortality rates of almost ANY disease.

The UK lags behind the rest of Europe in terms of the one-year survival rate for pancreatic cancer.  The UK average is 17 per cent, the European average is 21 per cent and the best in Europe (Belgium) is 28 per cent. 

Please help to change outcomes for pancreatic cancer patients now and the future by attending the debate.  We need as many MPs to come forward and participate in the debate. If you are considering attending, please contact Mr Nic Dakin MP via email: nic.dakin.mp@parliament.uk

Please could you also consider getting involved in the APPG Inquiry on Pancreatic Cancer Research where along with your parliamentary colleagues you can help support the inquiry into pancreatic cancer research? 

I would be happy to talk to you about this further either over the phone or in person. 

I look forward to your response and thank you in advance. 

Kindest regards,

Carl Denning

Street dancing fairy

Well i did it! I booked what i thought was a gig, and in preparation for this, I learnt some new material, and made my way to the talent competion where the prize was two and a half grand.

It was a 'talent competion', now, when i turned up at the hotel where the audition was held, every bone in my body was just turn around and walk away, but for some strange reason i felt I had to do it due to it been booked in.

I knew it was not going to work, as soon as i joined the queue of two. There was a girl in her early 20s dressed as a fairy, when i asked what she was doing, she told me street dancing!  I am not sure what street she was living on, her look was a cross between rainbow bright and someone on smack. 

I was asked what my act was (disappearing went though my head) I told them i was trying to do a bit of comedy.  The lady (who i think was the girls mother) told me that on hospital visits to her friend she had been told she always made the ward laugh, and with that started to do a improvised routine for me, I must admit, it was better than mine, and it did cross my mind to simply steel her act.

The street dancing fairy went in to the large room.  I was asked to fill out some papers. The guy who gave me the documents told me that out of the 40 people in the auction i was the only comedian. I wish i had thought about this for longer than two seconds to realise that there was a very good reason for this. 

He told me that he loved Mrs Browns Boys (yet another sign to run for the hills) he lead me to a old Victorian ballroom, and introduced me to the table of judges all wearing there matching branded talent competion t.shirts.

It was my turn.

Just by looking at the judges I could tell we all didn't have much in common, the only common bond between us all was that at the end of the audition, we all probably could say that we had all experienced a strange experience, but for different reasons.

There was a young child sat at the table. When i get nervous when doing comedy, i swear, and i don't mean to provoke offence but sometimes it does give the joke more drama and makes the punchline more puncher, but I know it was probably not the right thing to do in front of a child. I explained that they maybe some swearing in my act, which i got told that if i get through to the shows, that children will be present so i wont be able to do that.

I can not tell you what happened next, its all a bit of a blur.  Its hard performing comedy to a wall of silence, but its even harder performing to a wall of people looking traumatised.

I knew when the main organiser put her head in her hands, the one legged dwaf joke had not gone down that well. The more horrified they looked, the more nervous I got, the more nervous I got, the more outrageous I became. They thanked me, and said they will call on wednesday to let me know either way, and just before they quickly showed me the door, I had my photo taken, was not sure if it was to use as publicity or use as evidence.

I have wrote some jokes about cancer, and i did think at this point, i should drop them in, if they didn't find them funny I may get the sympathy vote at least, but at the same time I was also thinking that the only one thing that could be worse about the situation i was in, is if they called me this week and said, congratulations you are through! and i would have to re-live it again!

Wednesday as been and gone, and I didn't get a call. Due to them saying that they was going to call me either way, I am slightly concerned there still in the ballroom still frozen in a state of shock.

I walked away wondering if it was me, or if it was the jokes, or if it was them? The only way was to put myself in that situation again, but this time without children and with a audience.

So on Monday I went to Beat the frog, a gong show where the aim is to survive for 5 minutes without getting voted off by the 3 chosen audience members.

The venue was in Preston and was very busy! I went early to see if I could go on first and get the hell out of there, I then found out that the venue choose when you was on, and i was on....

at the very end! 

I did nearly walk out as the acts that where on was very good! and even the ones that was voted off had stronger sets than me.

Sometimes, in social situations my face does not quite work in my favour, but for comedy! it gets me away with murder, and to be fair, I think that is what happened. I survived the 5 min ties and went on to the final, and more importantly, I enjoyed it.

Stumbling to the next step

As I am writing this I am miles in the air! No it's not the chemo that is making me trippy again, we are flying back from Rhodes in Greece. It has been great to just get away and relax, when I say relax, I probably don't mean it in the conventional sense, I mean my type of relaxing where the day to day worries get pushed aside making more room for more exciting problems.  Problems that are man-made and purposely put there to challenge yourself, and make life even more worthwhile.

I had to get special holiday insurance, the girl went through the usual questions, it's the same kind of questions that I used to skim-read, and quickly tick a line of boxes with the word "No" next to them, sadly these days it's usually "Yes". A sigh of relief when I get to the question, are you pregnant? A question I can tick No to and reminisce on the good old days! She then asked me "Is they anything I haven't declared and not been diagnosed with yet" having a brain running on chemo, and that type of question, both don't mix well, and I still don't understand, if I haven't been diagnosed yet, then how would I know to declare it! I paid my £30 as she went through a list of terms that I can not claim for on the insurance, and when she eventually reached the end of the T and C's,  I knew I will be able to sleep at night knowing the fact that I will be covered to use my insurance only if absolutely nothing at all medically happens to me.

I am back to work tomorrow! And looking forward to it. Looking forward to seeing everyone at work and having a bit of normality again. Then the day after I get my results from my CT scan. I don't really want to even think about this right now as it does not matter how many times you sit in front of the doctor and how many times he or she as given you good or bad news, nothing makes it any easer each time you go, nothing can prepare you for the amount of anxiety. (Just got back from hospital, there are testing my bloods, but scanning the ct scans - they forgot to do it! - but the doctor said all looks ok) 

Sadly I missed my Mum dong "race for life" on Sunday, with her friends. It's not too late to sponcer! Half of the money is going to PCUK and the other to the race for life funds. (Thanks Mum x)

http://m.virginmoneygiving.com/mt/uk.virginmoneygiving.com/fundraiser-web/fundraiser/showFundraiserProfilePage.action?userUrl=ShirleyMegson

Since finishing chemo I now don't have a weekly cycle of sickness, this energises me and  I have noticed that there are two types of speed, mine and everyone else. I am nervous I am going to miss out on something so it is like I try living in the  priority queue of life, and I am fast-tracking as much as I can. The things that used to slow me down or stop me, those nagging questions, what happens if I fail, what will people think, will I look stupid, will people judge. Just don't seem substantial reasons to stop me doing what I want to do anymore. What happens if I fail, I fail! What will people think, who cares, will I look stupid, with a face like this how can I look any other way! Will people judge, well that's more about them than me! The only thing that makes me nervous is not having the health to do what I want to do. Insecurities can not stop me, but my health can. 

So, From tomorrow I am back to work as a web developer again Monday to Wednesday and the rest of the week concentration on my street food business. I should be getting the keys for the new kitchen this week, and I am trying to get our pulled pork wraps into shops.

A bit of a shameless plea but if you know anyone with a shop please let them know about our pulled pork wraps! 

Also, I have mentioned in my blogs before about performing stand up comedy. I used to perform amateur comedy. In all fairness I was never going to make my millions in this area, and it was leaning more on the word "amateur" than "comedy". I used to forget my jokes, I then went off subject and forget what I was talking about, and sometimes I went on stage, let nerves get so in the way, I would almost explode!  At the best of times people looked at me thinking that my act was more of an art form, and at the worse of times,  just shit! But.... Still, as I dodged the looks of the puzzled and confused audience, I still enjoyed it, so I have a gig booked in July, there is a reason for all this, but will write about this on my next blog.

http://youtu.be/n09BIX0Zk-s

The above video may offend by stuttering, bad jokes, and swearing and panicking. 

After everything, why am I putting this pressure on myself? There are moments in all of our life's that we all do things that contradict against what we categorise as "common sense". I know, right now,  that choosing to push the business and expanding and doing just more in general is one of them times especially when the future for me is so uncertain and all the doctors are telling me to rest, take it easy, there is still chemo in your body. But, sometimes there is an underline feeling, a feeling that goes against the grain of rational thinking, and in that feeling, I trust, I am not sure where those actions will lead, but I guess that underline feeling is one of wonder, which is better than dread.

End of chemo

Well, i have finished my chemo, and my line is out! It feels strange. I don't miss a plastic line dangling from my arm, but I keep acting like it is still there, (careful when I pull my sleeves up, etc). My hair has grown back and I had my first haircut in the past 6 months.

It is a good job that the line has come out, I had pulled it out by getting it caught of a number of items that I could of almost used it as a skipping rope. When the nurse puled it out, you prepare for the pain, in my head it had been tangled around my heart. It does not hurt and I didn't feel a thing.

When I talk to the nurses some make it sound like my chemo as not finished, and this is just a break. For my own sanity I'm going to see it as finished. 

In my last blog post I wrote about how I was in hospital with an infection in my line. Well they kicked me out after about 4 days. I did feel like I was just there for the meals as I felt fine. The chemo is making my feet and hands feel really numb this is getting worse and sometimes can be very painful. The side effects is also frying my brain. I forget what I'm talking about,  but when that happens I don't just go to the next subject, I try and remember. You can see it in peoples faces that after five minutes they really wish they had listen to the conversation as they may be able to help and remind me what I had been talking about.  After ten minutes when I remember, I realise why they didn't bother listening in the first place.  

I have had backache that has driven me slightly crazy. Pain is not just a sharp ache, but now a constant reminder that things are not, and never will be the same again, and it's impossible to ignore. 

I have another CT Scan this week, I am not sure when I am getting my results as they haven't told me yet. It doesn't matter how many scans you have, or what the results are, on each one It fill your head with anxiety. I don't want to do it! I have always been one of them people that stick my head in the sand for most situations that I don't want to do.

My last blog I wrote about living in the now. I know what I am about to say is hypocritical, but since my chemo as finished and I'm about to venture back in to normal life, I'm a bit scared. I feel like each step I have to tap with a stick to make sure the ground doesn't fall. Anxiety as become a normal part of my life. I catered for a party and the majority of people there where around 40. Due to my situation sometimes I feel so old. Then I see a group of people, laughing and dancing and enjoying themselves and most of them were about my age. I then realise I am not that old.  I know this type of thoughts are not my usual ones I write about on my blog, I also prefer the more upbeat, positive thinking self. But it would be also wrong to deny myself of these thoughts.

But distraction is for me the best medicine, and like I said my chemo as finished so it's now time to find more distraction and time to move on to the next thing. We have started getting more bookings for private events, and I keep pushing for more.

 

I am going back to work in a few weeks. I have also started to put some plans to work for my business.

But to say that the title of this blog involves the words "street food", I haven't really spoke much about it in these blogs. 

A few years ago I started my street food business.  I wanted to do something that involved the 3 loves in my life, cooking, eating, talking! And after a brainstorm session, I started Market Wraps. A market stall selling food that I had made, not knowing what street food was. I just wanted to do something I enjoyed.

At the start I never had a queue, I never really had a customer! The occasional pigeon seemed teasingly interested, but that's about it. This went on for months, I spent 40 pound on food, and never took anything. My business plan was not going to win me Business person of the year.

Leeds market decided to move one of it's twice monthly farmers market, and put it on one of the busiest streets in Leeds. This was one of the best moves for us. From there on we had customers! 

I see Market Wraps not as working. Rob and me knock ideas together and then put into practice, some work, some fall on miserably on there backside. I see it more as playing. Our menu changed, and we once put pulled pork on the menu, during an holiday we decided to risk losing our queues by taking everything off the menu and just do pulled pork, but make sure we do it to the best of our abilities, it worked and we got busier.  

A few weeks ago when I said to my doctor I want to work again, she told me I could occasionally work between sickness from my bed. Not capable to do much physical work I started to work on a business plan.

The bank, due to my situation have said NO! to a loan, so I have turned to a enterprise scheme. It was probably not one of the best ideas writing a business plan while I was off my head on chemo. I got to a certain point, realised that the idea would not work, went back and re-wrote it. This happened about 4 times, and when I got to the end and I had got the idea to work on paper I read at the bottom of the pre-formatted word document that I should only have wrote two a4 pages. I had written a book! One that involved drama, blood, tears, highs and lows!  And about 4 trees worth of paper. It took too much time to make it condense, so I sent it off. I think when they received it they thought it would not make any sense to read it, as it would cost more money in man hours to go through the business plan, than it would to just give the loan.... It worked!  I must admit I was surprised when I got the loan, and it has now put me in the situation where I now have to do something about it.

I have so many ideas what I want to do with Market Wraps, but it is impossible to do as I need a bigger kitchen to pull it off, so that's my first plan, and I should get the keys in a week or two for the new premises.

 

I am also had meetings with a marketing company to see how I can push Market Wraps out to a wider audience, I will write about is in the next few weeks.

My man made distractions battle with my anxiety, some days anxiety wins, but most days it doesn't. 

Yes the future makes me nervous, but with a switch of direction of thought, it also excites me.

     

What's next

It is 3am, I am not sleeping, and I am laid in an hospital bed. I have forgot how hospitals have a special way to see how you deal with sleep deprivation. I have had a infection in my picc line. A picc line is a tube that has been dangling from my arm that feeds chemo near my heart, and for the past 3 months this line as made it possible for me to have chemo without injections once every 2 weeks. Then just before my last chemo this has happened. 

I'm feeling ok now, but yesterday my temperature was up to 39, 39 is fever. Yesterday I laid in the hospital bed with my eyes at the back of my head acting like I should be in A&E on a Saturday night. When your temperature goes up and blood pressure goes down, you basically act pissed. Which when your temp falls back down and your blood pressure goes up to normal and you're back in the room, it can be slightly embarrassing when your not sure if you have been swinging on an  cancer patient next to you while trying to organise a singalong in the oncology department.  "Come on everybody! Always look on the bright side of...".  I apologised to the nurse, which, luckily I was told I had nothing to apologies for. Later on Rob told my that the only thing I was organising was the structure of a sentence, which I failed. 

As for the side effects, my hands and my feet feels a sensation like pins and needles, and also numb. I was told that after the chemo, feelings may come back, but also they may be permanent damage, not great if your playing Twister, but great if your trying to get away with the washing up.

So, my last chemo is coming, the tumour I had has been cooked and destroyed using the new treatment in London.  My doctor as told me I am his first patient that as had it, and let's see where we stand in 3 to 6 months, so what next, scared about the future? Well, I guess a little, but then I think about what I want to do.

And then I'm buzzing with ideas! 

Those ideas, I have already started to plant, and I'm sure that's another blog post.

I have always wanted to write about things I have learnt during this process as I know what is happening is, I guess is rare. But due to my brain been fried with chemo I know I haven't got my faculties to be eloquent, to be fair who am I kidding I have never been eloquent! Also I am conscious it may come across as been slightly pretentious. I have had THIS 'rare' experience so I know better!  I don't think I now know better, but I do think I now think  differently. But to say I now think differently, does that mean?   I now know better? No, due to me being still alive, I am also still learning.

So, the future? Well, I really don't know! I can use percentages and live scared, but two years on, I don't use percentages or probability anymore, so with that, I have only one thing, and that is the present tense, and personally that's not only magical, it's powerful. To totally fully appreciate the now. 

To live life in the now, and not fear the future anything is possible, I don't mean live life recklessly, but I do mean live life. Should I worry about something happening to stop my plans? No! What's the point, The only thing I should worry about is not acting on those plans now, as now is the only thing we have all got.

Of course there is always that voice, I think we all have it, unless it's just me! that voice that edits our actions, that stops us from doing things, that puts worry on our shoulders, and also that has the power to blind us of the now. But for me that voice doesn't place much worry about the future anymore.

I can see the irony, all those years of being healthy and well and at times worrying about the future, then suddenly you  have something to worry about and I then decided to stop worrying about it!   And with that, when I say I'm buzzing with ideas, those ideas have the space to grow, and be far more creative.

Now is the truth, now is really appreciating the conversation with our love ones, now is just stopping and looking, now is not only making that decision, but acting on it,  now is just enjoying the moment, now is saying, sod it! I will give it ago and try my best.  

I guess what I'm trying to say is, we all might as well make now the very best we can, because now is the only thing we have got.

Regarding that voice,  it may not worry much about the future, but it is still there and it still try's to edit. My voice right now even though It shouldn't is letting me worry how I am coming across in this blog, Its saying, most people loss there hair after chemo, you turns into Oprah! This suppose to be a blog about my experience, not "A road less traveled", but then turn that voice off and appreciate the now, and just think sod it, push the publish button. 

The new normality

 I have not written a blog item for quite a bit of time now. I am currently about to have chemo (Thurs), after that I have another 2 to go.

My hair as started to grow back, I am not sure why, as i have not finished chemo yet, it is more fuzzy felt more than hair.

It does seem that last time the chemotherapy made me sick less that usual, but this sickness has been replaced by a bit more pain.  The other day I had abdominal pain, and I went dizzy and thought I was going to pass out, i am not sure if this is side effects from the chemo.

So, my future plans are:

3 more rounds of chemo, then after that a CT scan, then I am hoping to put a bit more normality back into my life.

I will be going back to work at this point, now I am not sure what good I will be, due to this amount of chemo. My brain feels like it has been taken out, and replaced by a brick.  My official title may change from web developer to flower pot, as they sit me next to the window holding some flowers.

But whatever happens, I am looking forward (and a bit nervous) about going back to some form of normality. 

When I say, some form, I guess I know the situation probably will not allow me to go back to the normality I used to have, I guess the key is to get it as close to it as I can. 

Cancer has changed me. It has changed me physically and what I am able or unable to do, my body will not allow me to just get up and go anymore, but my brain does, which adds to the frustration. I get really tired and there is sometimes pain, and my thought process can be very clouded.  I am now classed as disabled, by looking at me, no one would know there is anything wrong. I have applied for a disabled car parking badge, this seems to be a controversial subject. The government does regard this as a disability and have been helpful with advice, but when I have told some that I have applied, I have felt a bit of hostility, I guess people judge on the better days, sadly it's only my close family that see me on my worse days, a parking badge will help not just me, but Rob and my family at the hospital when I am leaving after chemo, there is never any parking spaces, and 4 flights of stairs while been sick is never very nice. I now know and accept that it is a disability, no I am not severely disabled, and it is not one that people see, a missing pancreas is not like a missing arm, but a pancreas as got it uses, and with half of it left, I do miss the other half! It has also changed how I look, from scars to experience, it as changed me physically and it has also changed me mentally, and I don't mean just chemo frying my brain, I mean the whole experience as made me see life in a different way.

I am really looking forward to get back to my street food business too, I have really missed it. I was talking about this to one of my doctors and how much I miss the work, she told me to do it from my sick bed, I am not sure if she understood what street food is, I know it involves a bit of theatre, but I am not sure if making pulled pork wraps from a bed while not being that well, in the middle of Briggate would work.

But I took her advice, and started making plans of some changes of "market wraps" from my bed. A change in menu, a change in the look of the stall, and a change in doing what we do now, but just doing it more. I decided to call the bank during one of my better days to see if they were the new helpful bank they now claim to be on there advert. All was going well on advice of how to ask for a bank loan, until we got to the point of pancreatic cancer been mentioned, I felt the draft from the virtual closed sign been shut down on the phone. This is what I mean by accepting that things won't be the same again.

I was able to work on the stall this weekend, and with that I brought in my new idea of the new menu, gourmet wraps and sandwiches, made in front of the customer in the morning.

They went down well, and we sold out, but more than that, it felt great doing something different, working at the stall, and seeing everyone at the market. Just a small sense of normality again.

On talk radio was a discussion about what it is like to live with cancer. I found it interesting, not as many would think. I was not comparing notes, it was more seeing how others do it and try and follow suit. If someone asked, how do I live with cancer, I am not sure what I would answer. 

To go through this experience, it is bound to give you some lesions in life, and it as! I think... And it would be great to reveal and share those big life's lesions in an almost revelation way! Sadly due to chemo brain, I think I have forgot most of them! Shame really as it would make a great blog item! 

I was thinking about how we treat getting older. Last December I hit 40, I did not really experience the hitting 40 in a normal way, so I am unable to write about it from that view point. I am guessing that you get to 38 and then suddenly you start to prepare mentally for the big four zero. For me it was different as I found out I had pancreatic cancer at 38, so the last thing on my mind was, I am 40 in two years time. 

I hit forty, and was asked the usual questions, "how do I feel about hitting forty" "it's downhill from here" etc.....

My blank face probably gave the game away that I had not put any thought process into this subject.

I guess I asked myself those questions after I got to 40. When someone hits a rounded age, questions like that I guess are standard, it's what we all do, we send joke cards about getting old, showing images of a couple of old dears with various body parts hanging low, or someone loosing their mind etc.  We all seem to treat getting old as a negative thing, and that is something that has changed for me.

How do I feel about hitting forty? I'm extremely thankful for it. A birthday does represent getting older, it represents another year of surviving, and a year of the experience of life. A year of sharing moments with love ones. It's a shame we all treat getting old as a negative experience, imagine how it would be if we all saw it as a positive, that would truly be a celebration.

Ct Scan

GIt is now just gone past midnight, I am in bed and I don't want to sleep as I know when I fall asleep I have to awake to my next chemo session.

I have not written in my blog for quite a bit of time, and I have had a couple of tweets asking if I was ok. All is good, thank you.

In the past week I went for my CT scan, which I was nervous about, this was the first CT scan after the treatment in London. This was the important one. 

I had my scan before the Easter holiday and I got my results after. The doctor told me that, on the scan the tumour looked like it had grown on first sight, but because of it's density it was not living. The tumour looked bigger due to the ablation I had in London, the Prof  burnt the  tumour  and the cells around it, which made it then look bigger on the scan. My ca-19 (tumour counter in the blood) had gone down to normal levels and they were no other tumours and due to this I could come off chemo if I wanted to, but they have recommend another 4.

This is big news, for now, I am cancer free, and It is big news as doctors have said that to be cancer free would  probably never be the case. 

Now, I understand that I am long way from a safe zone, and some people have asked does that mean an all clear, this is pancreatic, and sadly it doesn't work like that. 

But it (in theory) does take me back to where I was in December, so the next plan is to keep as healthy as I can, carry on and do as many of the 4 chemo sessions I can take. 

I spoke with the charity Pancreatic Cancer UK today, they are a great charity and I have never felt alone due to them. 

They were equality happy about the results and said do I understand how "groundbreaking" this is. it was not really until that was said to me, I realised how important this procedure is.

The procedure I have had is not on the NHS, now, if this works, and I stay healthy and fit, this could be proof that it is worthy of the NHS, it is available for other cancers, but not for secondary pancreatic cancer.

So it's back on with the healthy eating as I have slipped recently and looking forward to booking an holiday very soon. Chemo  finishes on the 5th June and then I would have another CT scan.