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Blog 124 Saturday 15th September 2012

John is Radio Active
The Pet scan itself was no different from any other full body scan I have had, but the preparation was mind boggling!!

In a nutshell, I was injected with a low dose of Radio Active Glucose. Fludeoxyglucose (FDG) The theory is, that your internal organs such as brain, liver, kidneys, muscles etc all use glucose to function. Cancer cells also use glucose in high concentration. The PET scanner uses x-ray technology with the radio active glucose (tracer) to create a 3D picture of the inside of my body. The images will highlight any cancerous cells.

I was not allowed to do any form of strenuous exercise for 24 hours   (hooray!!!)   prior to scanning, this is  in order to keep the uptake of glucose in muscle to a minimum. I also had to fast for six hours prior. On arrival at the unit the obvious previous history questions and consent forms then a cannula in my left arm. This is where the similarities change. A Nuclear Medicine Technologist then attached a metal canister, to the cannula,  that systematically released small doses of the FDG whilst he also injected saline. I then had to totally rest for an hour. No talking, No walking. I am now Radio Active and must not come into close contact with pregnant woman or children in the next 6 hours. Although the first is not a problem I do have a ten year old daughter.

After an hour, I was escorted to a specific toilet with the above, " Radio Active" signs on the door and told to empty my bladder. I was then escorted back to the scanner, via a separate door and led into the machine.............................The scan will reveal the tumour already found, in my left lung the hope is that nothing else will be discovered .............once again we wait for the results. My Oncologist will then decide on what course of action, If its just the lung tumour its back to the Leicester Spire hospital and my surgeon Mr Waller.       

Blog 123 Thursday 13th September 2012

I have an emergency PET Scan tomorrow 14th September at GMT 15.50 I have been told to fast for 6 hours prior and arrive one hour before in order to receive a radio active injection, then lay back for an hour before the scan begins which should last about an hour phew!!!!!  My newly acquired tumour in my lung will soon be history!!!!!!!!!!!

A year ago today via blog 33, I wrote..................

"It has been two years, almost to the day, that a colonoscopy revealed my colon cancer in advanced stages. It has been four months to the day that a CT scan revealed polyp's on my lungs had changed in size and increased in number. Since then Ive been pushed, prodded, injected, anaesthetised, sedated, incised, clamped, stapled stitched and sewn. I have eleven incision scars across my torso, soon to be twelve. Ive attended Nine different medical establishments on two different continents for various procedures. I have seen more of my internal organs via video, photos and on surgeons VDU monitors than I have ever seen of my back, (for instance) ................but in all this time I have never felt ill.............. never felt as if I'm sick .........never felt unwell with the cancer, probably because I was lucky and caught it in time...............................".


I can now add to the above list a further two incisions soon to be five more and having been slowly poisoned with the toxic chemotherapy drugs, and to become "radio active" during my next PET Scan, I have been told I must not come into contact with children or pregnant woman for 6 hours after the PET Scan.

I have never felt unwell except with the chemotherapy.  With the latest Tumour now discovered, growing in my left lung. I am frustrated...................................... if I had left it to the NHS again, I would not have had a CT scan until July 2013, and this current tumour would probably have been my death sentence,  It is only because I have had the benefit of private health care that this latest tumour has been discovered so early, a CT scan ordered by the private health care Oncologist a full 10 months prior to the NHS Scan !

Sorry if I sound a bit tetchy today, but originally I had a mis - diagnosis by an NHS Doctor in Worthing of Irritable Bowel Syndrome all those years ago and it later took an Australian doctor to find my bowel cancer.

After this last episode I feel let down by the NHS thank goodness for private health care, even if it only prolongs my life by another  couple of years, it will be two more years with my family. Thank you to the family and friends for all the prayers the Lord is truly looking after me..................  

Blog 122 Monday 10th September 2012

Today, my Oncologist, gave me the devastating result of my recent CT Scan., a tumour has once again, invaded my left lung,  If you have read my blog previously, you may remember that in July 2011, I had an operation on both lungs to remove a total of 5 tumours. The operation was reported a success. A CT Scan was ordered after the conclusion of Chemotherapy in March of this year, and via blog 97, I reported that I had been given the "all clear".

The euphoria of "beating" cancer has been short lived. Now, I find myself being sent for a  PET Scan  (Positron Emission Tomography) possibly this Friday. A PET scan gives a higher resolution imaging and is used in conjunction with the CT for a much more detailed picture. (please click on the link for explanation) My lung surgeon Mr Waller of the Spire Hospital in Leicester, has been contacted by oncologist Craig MacMillan in preparation for surgery. I telephoned the Medical Insurance company "Simply Health" to keep them updated.....my sons, and my mother ...............and it all starts again.

I was foolish thinking that I could beat bowel cancer in such a short time. I was once told that the first five years are the longest. You are not officially a "Survivor" until after five years. I was confident that I had beaten the disease after the Chemotherapy, instead I took it on holiday to France with me..............................I am still fighting it and keeping upbeat and positive. Wendy is, as always very supportive, but I can see it is hurting her, especially after the news that I will not necessarily be offered Chemotherapy for a second time............as it didn't work, I wonder what else we have in the ...................arse-nal  !!!!!!! There is also lots of help for the loved ones of cancer patients MacMillan Cancer support I have been in contact with MacMillan when I was first diagnosed and they are very informative and helpful.


Wendy's Blog

The first time we found out that John had bowel cancer, I treated it the same way I treat life.....let us live it and get on with it. No mental anguish!! The second time it hit me really hard, I think it took me three weeks to once again face it head on, deal with it and get on with life. Today......I don't know? How do I support John, Hope and the boys....how do we cope? I know that this time it will take awhile but we will get over it and get on with life. I love my husband and my "kids" and I will do anything to protect them.........

Blog 121 Thursday 6th September 2012

Sad I know, but one of my favourite daily reads is the Mail On Line. You can check out what you want without being subject to the normal daily newspaper sensationalism.

Anyone who has read my blog before, will know that I sometimes refer to articles taken from the `Mail On Line' and today will be no different. Two articles has hit home with me, `He didn't need to die':  A wife's harrowing story after her husband was diagnosed with IBS and died of Bowel Cancer  and the second article Bowel Cancer soars by 120% among the under Thirties  an older article but goes to show Bowel Cancer is not only an older persons disease, and under thirties can be wrongly diagnosed due to their age.

Both of these articles caught my eye, firstly because I was diagnosed with IBS (Irritable Bowel Syndrome) and later found I had advanced stage Bowel Cancer.The symptoms are very similar and can easily be mistaken. Giles Cowley 41 the unfortunate person in the first article had a stressful job and lifestyle. Although I was 45 my Job was stressful and may not of been eating properly. My GP then diagnosed IBS without any further tests it was in fact the start of Bowel Cancer.

The second article caught my eye because,  as with the first article and IBS if you do not fit the profile of a person that is in the age group of persons likely to be effected by bowel cancer (Over 50) then your GP may diagnose wrongly. Our government still only screens for Bowel Cancer when you reach 60 in England

Who is eligible for screening?
If you are aged:
  • 60-69 in England
  • 60-74 in Wales
  • 60-71 in Northern Ireland
  • 50-74 in Scotland
By taking some simple steps to improve your diet and taking regular exercise can help reduce your risk of bowel cancer. So it is important to:
    Diet & Exercise

Blog 120 Monday 27th August 2012

My experience of the bowel cancer and the treatment given to me, never seem to leave my thoughts, it's always there, somehow in the background, always in my mind.   The follow up treatment is also never very far away. I have received another appointment for a further CT Scan at Northampton general hospital for Monday 3rd September 2012. This scan has been ordered by my oncologist for the Chest, Abdomen and Pelvis. This scan is no different from the others I have had, but is one of a long line of scans and is part of my "early warning system" just in case !! I am thankful for this system as it gives me peace of mind......................for a while.................................... but is nerve racking waiting for the results.    

Blog 119 Wednesday 15th August 2012

Just got back from the North West Brittany Coast of France, having stayed in a beach cottage owned by my good (Old) police chum friend Adrian. Adrian is now a resident of France and lives about an hour away where he tends his Gites. The Breton Gites are also available for summer lets. At the Beach Cottage in Erdeven lots of sun, fishing and snorkelling. Pernod and red wine !! brilliant.

Having followed my plight on this blog, Adrian admitted that he had the opportunity of supplying samples for the French version of the bowel cancer screening test but had declined. In France the government send out the test screening kits at age 50 years the same as Scotland . In England our government only send them out at 60 years. My symptoms started at age 45 years and I would have been dead at  age 55 years had I not caught the bowel cancer in time. I have urged Adrian to complete the test as I would do with anyone receiving the test through the post. If, like me  you are not of the age to receive the kits and believe you have any of the bowel cancer symptoms  do not hesitate to contact your GP or there is a load of information on the Bowel Cancer UK website. 

Quite uncanny, when I got back from France an email was waiting for me from another "Old" police chum Iain, with an article attached from the recent NARPO magazine (National Association of Retired Police Officers) It was exactly what I was talking to Adrian about

Bowel Cancer

"DO THE CHECKS"


"Well I served for 33 years finishing up in Cleveland Constabulary and at 60 years of
age my wife and myself started supplying samples to the bowel cancer screening
program which you do every 2 years.This year I did my samples about the
same time I was reading the article "Bowel Cancer" by Geoff Stuttaford and they
found a trace in my samples and within 6 weeks I had seen all the nurses and
specialists and had the required operation and the area was removed.

I am back to my fit and healthy lifestyle and hope that I get the birthday card from the
Queen in the future. For those who sit thinking I am fit & healthy
please note I had no ill effects or condition to indicate anything was wrong, I was
recently talking to a friend who sent for the sample envelope 5 years ago and stated
it's in the drawer somewhere. Join the screening program it's better to
know and sort it and live a long life".
R M Coverdale MBE
ex PC 154D_ _J
Visit our website at www.narpo.org • Email hq@narpo.org • Telephone 01924 362 166

Blog 118 Monday 30th July 2012

Early diagnosis of bowel cancer saves lives........I am ever thankful to my wife Wendy who kept nagging me to go back to the doctors when my symptoms of diarrhoea didn't go away, I was diagnosed with Bowel Cancer at an advanced stage and ever thankful to the doctors surgeons and nurses who gave me the second chance.........................you can get lots of information from                 www.bowelcanceruk.org.uk 

 Information & Support freephone:                      0800 8403540

East Midlands Cancer Network has asked Bowel Cancer UK for help in contacting local colon or rectal cancer survivors. The Cancer Network is a useful resource for local information for cancer patients, their friends and relatives and Health Professionals from the East Midlands area. East Midland Cancer Network understands that many patients following treatment for a colon or rectal cancer face many and varied challenges which may not be met by their local hospital team.
To this end they are planning to make a DVD which will be handed to patients and carers six weeks after their treatment is completed. The Cancer Network would like to interview 5 patients about their experiences.
In addition, they are also looking to film 5 patients to share these experiences. .In my attempts to spread the word Bowel Cancer UK has asked if I would be a willing participant to be interviewed for a DVD and filmed whilst sharing experiences. WELL I recently jumped at the chance of being interviewed "ON AIR" for Northampton Radio and being photographed for the local paper which highlighted this blog.....................so if I can help persons embarking on the rehabilitation period after treatment then bring it on.

 

Blog 117 Monday 16th July 2012

OK, I need to make some sense of my recent ramblings, so a short synopsis . I developed a severe case of Tinnitus  on my fourth chemotherapy session back in 2011.  I was immediately taken off the chemo drug Oxaliplatin as this was believed to be the cause. My Oncologist Craig Macmillan left notes for my GP that if the Tinnitus does not get better two months after my chemo, I should be referred to an Otolaryngology or ENT Specialist for further investigation.
(Synopsis John synopsis !!!!)

Ok, I had an MRI Scan which was clear of any focal abnormality ie metastases or acoustic neuroma so that's good !!!!! but I have been told that the MRI scan picked up that I have generalised cerebral atrophy (shrinking of the brain) with periventricular ischemic change.

Although this is not uncommon in the older person and is associated with dementia, but in my case described as "possibly slightly more than might be expected in a patient of my age". (55 years) Today my GP gave me a copy of the Radiology report and suggested that I again contact my Oncologist. Just in case  I have also informed the medical insurance people................."Simply Health" they have been very good.......and continue to be sympathetic and supportive.

This is just too weird ! I have received an appointment from the NHS to attend a CT Scan on Wednesday 25th July 2012. It specifically mentions abdominal scan. I telephoned my bowel cancer specialist nurse and spoke with Mark Kingston as this scan is out of sync with what I have recently been told at El-Rabaa surgery. Mark made enquiries and reassured me that in fact this letter is a mistake by the radiology department and should in fact be 25th July 2013 I am a great believer in "everything happens for a reason" or am I just pessimistic. Mark told me to tear the letter up and not go......................

Blog 116 Wednesday 11th July 2012

I was given an appointment with my bowel cancer consultant yesterday which is a normal 6 monthly check and I took the opportunity to ask for the results of my recent MRI Scan ordered by the ear nose and throat specialist. Thankfully I was told the scan results came back clear and the consultant said they were unable to determine the cause of the tinnitus. I was very happy. However the CEA count, which is the cancer marker in my blood, was slightly higher than it has been, so I was sent for further blood tests. I'm not worried by this as when undergoing Chemo my CEA marker was often climbing then dropping but always in the "normal" zone. My consultant asked me to make an appointment with my GP so the results of the scan can be discussed further........... which has been set for next week Monday. The reason why the consultant asked me to make this appointment with the GP is, that apparently she was not qualified to discuss MRI (????????) so be it,  a trip to the GP it is then...............      

Blog 115 Friday 30th June 2012

My MRI scan was quite eventful, whilst waiting and dressed only in the open backed, blue hospital, gown, an unfortunate sedated soul was wheeled through from the hospital A&E on a hospital bed,  and immediately wheeled into the MRI suite, an entourage of doctors followed, this unfortunate soul took my place which I gladly gave up, there is always others worst off than yourself..................

I was therefore quite late going in for my MRI scan compared to my original appointment time.  I always get quite claustraphobic whilst being drawn into the machine and always try and think of other things .........this time a song by Pink Floyd, popped into my head, "Welcome to the Machine" 

The MRI was a lot louder than I remembered,  headphones on and with my panic button in hand it was soon over. My MRI took approximately 30 minutes, and the wait for the results begins...  

Blog 114 Monday 25th June 2012

I have my MRI Scan appointment today at 13.30 GMT. This MRI scan is for my Head and has been ordered by my GP due to my suffering from Tinnitus since the Chemotherapy drug, " Oxaliplatin" was administered back in September last year. I was eventually taken off the drug in December 2011 due to this condition . My hearing has been tested as "Normal" and the MRI is a further test to see if there is anything present that may be causing this condition.

 The NHS has come through with a priority appointment as expected. Suddenly all the fears of "What if" come flooding back. My previous MRI scan revealed my bowel cancer had travelled to my lungs, so forgive me for being a bit pessimistic on my appointment today. I joined a very good web site some while ago, where you can discuss any form of fear or pessimism as a sufferer or carer  http://www.journeythroughcancer.com/ please check it out its full of good advice or somewhere to connect with others going through the same or similar journeys. An extract from this weeks message. on the journey through cancer web site

"We must build dikes of courage to hold back the flood of fear"
                                Martin Luther King Jr,
Rick, the author of this site and a Colorectal Cancer Surgeon, tells of a case this week "of a woman diagnosed with cancer 3 years ago but never came to see the oncologist due to fear. Truth of the matter is, she was curable then, but now is not. Trouble is, this isn’t the first time I’ve seen this and probably won’t be the last.  I’ve heard that just hearing the “c” word can create such paralytic fear."
                       
“I have a highly developed sense of denial”
                                      Gwinneth Paltrow
 At a recent survivorship celebration a gentleman shared that after 6 year of survivorship, a counseling session brought out the revelation that his radiation treatment markings (tattoos) were an all too constant reminder of his cancer and its treatment. Conventional wisdom would tell us that this is a classic coping mechanism, denial, getting in the way of somebody actually addressing the issue. Others may offer that you’ll deal with your issue when you are ready to deal with it, so denial gives you the space and time needed until you are ready to cope.

 Have you noticed a time, even many years after the event when denial actually protected you until you were ready to deal with a painful memory?  
My message is always the same, Bowel Cancer is curable if caught early enough. Bowel Cancer claims thousands of lives needlessly every year. Visit the Bowel Cancer UK website  for some great information.

Blog 113 Wednesday 13th June 2012

I had an appointment at The Corby Diagnostic Centre yesterday. I was seeing the Ear Nose and Throat consultant  regarding the Tinnitus I have previously blogged. I became involved with Tinnitus after the fourth chemotherapy session when Tinnitus suddenly effected me,  I reported this to my Oncologist and he took me  off the Chemo drug Oxaliplatin straight away. It is apparently a very rare side effect of the drug (I've had a few very rare side effects during chemo) I had to go through all the audio tests first before seeing the consultant. After the tests my hearing was reported as "Normal" so why do I continuously tell Wendy to "Turn the TV up"?....................pardon

Having had a thorough examination of my ears, the next stage is to see if anything is causing the problem internally. I was previously warned by the GP that referred me, that I would have an MRI Scan on my head, given the problems I have had with bowel cancer.

The ENT Consultant concluded that I need an MRI scan and this should be through in the next few weeks. Apparently I was treated as a priority case by the consultant that reviewed my referral letter, so hopefully this will continue and I will not have to wait too long for the MRI scan.   

Blog 112 Monday 4th June 2012

 Bowel Cancer UK volunteer week 1 - 7 June It was a very nice surprise this week, to get a "Thank you" card, and volunteer certificate, not to mention a decadent bar of chocolate, through the post.

It reminded me of the reason that I originally became a volunteer for Bowel Cancer UK. I wanted to tell everyone of my journey through Bowel Cancer then realised that having reached over 40 countries through my blog, my exposure via the Corby Evening Telegraph and Northampton Radio that I could possibly make a difference.

Now I am hoping that I may be able to raise awareness and make people think about the symptoms they may be experiencing in order to prevent to them, what happened to me. I am very lucky, that after all those years, a misdiagnosis, on-going  symptoms  and two major operations that I have been given the all clear. I caught Bowel Cancer early enough to make the difference. I now understand Bowel Cancer and so should you
 
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Blog 111 Wednesday 30th May2012

Been quite busy lately trying to push my new outlook on life not only have we lost some loved ones early in the year and cancer revisiting my friend Michael our next door neighbour was diagnosed with lung cancer recently and having been taken into hospital due to a collapse was buried two weeks ago. My heart goes out to a very brave lady that I have recently read about.  Melanie Swan-Horton a mother of two from Norfolk, took on a high protein diet and had a dramatic weight loss, size 16 to dress size 10 enduring hours in the gym and unfortunately putting her side effects down to her diet regime and gym. Mel has been diagnosed with Bowel Cancer the actual reason for her weight loss. Mel has had chemotherapy and bowel cancer operation but nothing more can be done the cancer has spread to liver and lungs...........................this very brave lady is terminal.  

Mel's Quote " Before I die I want every man and woman in Britain to know the signs of bowel cancer. I thought I was getting really slim and fit but it was the cancer killing me and other slimmers need to be aware.’"

Read more: http://www.dailymail.co.uk/health/article-2152134/Woman-dropped-dress-sizes-thought-getting-fit-actually-terminal-cancer.html#ixzz1wNhbBQHt


Bowel Cancer UK has been spreading this message

BOWEL CANCER: THE FACTS AND THE SYMPTOMS TO LOOK OUT FOR


Bowel cancer affects more than 36,500 people in the UK every year.
It is the second most common cancer in women - around 18,400 new cases were diagnosed in the UK in 2009.
The biggest single risk factor is age as the chances of having bowel cancer go up after 50.
1 in 10 people are under 50 when they get bowel cancer - Melanie Swan-Horton (featured) is 46.
Early bowel cancer may have no symptoms. Initial symptoms can also occur in people with less serious problems such as haemorrhoid's.

However, the NHS recommends seeing your doctor if you notice the following:

  • Blood in your stools or bleeding from the rectum
  • A change to normal bowel habits for a number of weeks – such as diarrhoea or constipation, abdominal pain or a lump in the stomach, unexplained weight loss.
  • As the disease progresses it can also cause anaemia leading to fatigue and breathlessness.
If you are worried about any symptoms you can also call the Bowel Cancer UK Support line on 0800 8403540


 

Blog 110 Tuesday 15th May 2012

Previously back in July last year during my Lung operation I blogged about a very nice chap called "Michael" (read here July 2011 Blog) Michael was having the same operation as me, albeit in one lung only but had severe complications. Today I contacted Michael for a chat and was told by Jean his wife that he has developed cancer in his bladder and has recently been fitted with a catheter. When I met Michael, in hospital at that time,  he made my experience in hospital that much better. Michael made me laugh and gave me an opportunity to discuss cancer and chemotherapy for the first time, with someone that had actually gone through it. Michael had been through three bouts of chemo after suffering Bowel Cancer which had also later effected his liver and lung over a twenty year period. Having met Michael briefly during our stay in hospital and later at a consultation again in hospital, I know he will fight this new intrusion and also find time to smile and joke. Our thoughts are with you Michael and Jean.   

Blog 109 Sunday 13th May 2012

It is my birthday today and I've been thoroughly spoilt. I have seen or spoken to the majority of my family who have all wished me well.......................................... I can't help thinking; it could have been a lot different. A year ago, I was considering the worst scenario. For it was on the 13th May 2011, a year ago today, I had my CT scan that identified the bowel cancer had now travelled to my lungs. It was just before the scan that the radiologist joked, "Why was I having a scan on my birthday and that I should find better things to do" ..........after the results  I  could not foresee a future much beyond the immediate. Have faith, Keep faith and Make plans ! that is the best way, I found, to get myself out of the doldrums at that time .

As ever, I keep finding stories to read concerning bowel cancer.

Statins 'cut risk of bowel cancer': Danger 'halved' by cholesterol-busting pills
Read more: http://www.dailymail.co.uk/health/article-2143264/Statins-cut-risk-bowel-cancer-Danger-halved-cholesterol-busting-pills.html#ixzz1umUGjVV5.

!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

BE SURE TO READ THE COMMENTS SECTION ............Comments Section  by persons on Statins

!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

Blog 108 Wednesday 9th May 2012

Following my 4th Chemotherapy session back in November 2011, I reported to my Oncologist that I had developed a severe case of Tinnitus . I was immediately taken off the chemotherapy drug Oxaliplatin, as this was believed to be the cause. I was told that the Tinnitus, is a rare and unusual side effect of the Toxic drug Oxaliplatin, but may get better after my chemotherapy treatment ends. If you click on the link to Tinnitus above you will see that Tinnitus can be caused by many things. Cold Plays Chris Martin was in the local paper recently with the same condition He said: Quote "There's no doubt it's been caused by years of being on stage and subjected to very loud decibels of music.".         I was told by my Oncologist that I should visit my GP after two months if the symptoms do not get better.

Yesterday I visited my GP, as its been two months, and the ringing in my ears seems worse.  The GP didn't hold out much hope of my condition, but said she would refer me to an  Ear Nose and Throat specialist,(ENT) but first I would be sent for a head scan....... scans now always worry me.

I read a good article in the Mail on-line this week, and although its not directly about Bowel Cancer it is very interesting and Bowel Cancer UK also advocate a healthy eating regime  .The Anti Cancer Diet (Eat Your Way to a Healthier Life) and for all you curry lovers out there please see the next article also from the Mail on-line Curry Favour with your doctor unfortunately with my love of curry over the years it obviously didn't help me, but I'm sure there are some truths in it. Maybe with my love of spices that's why I,m heading towards being a survivor..........





Blog 107 Thursday 3rd May 2012

Today at 2pm I had the pleasure of meeting BBC's John Griff  of Northampton Radio and the great experience of being "On Air" in the studio, to discuss my blog and of my journey through Bowel Cancer. As always with the intention of raising awareness of this dreadful disease. You can listen to the interview again.........

HERE with John Griff (its available for the next seven days). Just click on the link!! My interview is straight after Paul Youngs "Come back and stay this time"





  

Blog 106 Monday 30th April 2012

Spreading the word about Bowel Cancer and  as a volunteer for Bowel Cancer UK,  I have recently been interviewed by Hannah at "Northants News" my article, "Cancer Survivor Blogs Experiences" can be read Here . I am also going to be interviewed "On Air" by BBC's John Griff  this week, John does a great show about local stories and local people.

You can listen to my interview with John Griff "Live" HERE at 2pm GMT on Thursday 3rd May.

The more I hear about people dying from Bowel Cancer, the more I think........ `Surely they experienced some symptoms.......blood in their poo, or a change in bowel habits for a few weeks....... Diarrhoea maybe ...........a pain or a lump in the abdomen extreme tiredness for no reason. It is important to have yourself checked out quickly, or get more info from a trained person at Bowel Cancer UK , 0800 8 40 35 40.

I originally went to my Doctor with some of these symptoms. I was 45 years old at the time. My Doctor sent me away with a diagnosis of Irritable Bowel Syndrome. Mydiagnosis was wrong, Bowel Cancer took hold and started to grow eventually spreading to my lungs.

The UK Government only send out Bowel Cancer screening kits for people between 60 and 69 years old. Fifteen years after my symptoms started would would have been too late for me......... thankfully I am one of the lucky ones,  my Bowel Cancer was caught in time......................  

Blog 105 Thursday 26th April 2012

Having blogged my Journey through cancer and my experiences, I said very little of the emotional Physical or Psychological effects on me. On diagnosis I experienced a terrific sense of  Sorrow and Sadness, not unlike loosing a loved one, a sudden reality that my future may not be as I had lived to expect. Anger & Resentment, were also emotions I felt at first,...............Depression..... It helped me to stay positive at this time, that doesn't mean you have to feel happy and cheerful it just meant for me, that I acknowledged with the situation and found ways to cope, and even made new plans for the future taking account of my treatments.

I allowed myself at first, not to bother to change out of my PJ's in the morning..... I was being nursed at home, "Why should I"?  A sudden bout of reality later kicked in...............I can give up or I can fight..............I chose to fight....... Psychologically, I felt very vulnerable, I was on toxic drugs that were killing my immune defence system. I was told that any sort of virus would see me immediately admitted to hospital. This also gave me feelings of panic and lack of control. My network of family and friends were made aware of this and stayed away for the duration of their colds and flu viruses!!  I became extremely tired and submitted to enforced sleeps during the day, resorting to sleeping tablets at night. Again reality later kicked in and I decided to get busy around the house, walk the dog, start painting again, do voluntary work..... It sure helped.

It is all to easy, like me at first to allow the diagnosis of cancer to stop you in your tracks and almost submit to 'Due Process'. Studies on the subject of keeping "Positive" or "Positive Thinking" are not understood and have had mixed results......... In my experience, having endured major bowel surgery for cancer and major lung surgery plus 6 months of chemotherapy, I believe that by staying Positive, Active and discussing openly, my thoughts,  and having a sense of "I want this disease out of my system" worked for me .......................There is lots of help and support out there that got me through, like Bowel cancer UK or Macmillan cancer support these sites are full of good information.

Early diagnosis of bowel cancer is the key see "Signs and Symptoms" for early diagnosis.

Blog 104 Tuesday 17th April 2012

Today, I have included  a copy of Bowel Cancer UK's 25th Anniversary press release and parts of the Executive Summary................... Tomorrow; as part of the Bowel Cancer UK awareness campaign, I am being interviewed by a journalist from "Northants News"  who will be reporting on my personal experience with Bowel Cancer.
Embargoed press release: 00:01 Wednesday 18th April 2012
GOVERNMENT COULD CUT BOWEL CANCER DEATHS BY 60% BY 2025 SAYS BOWEL CANCER UK
The Government could cut deaths from bowel cancer by 60% by 2025 if it followed the recommendations in a new report launched today by Bowel Cancer UK. Bowel Cancer UK's ambition is also for an additional 2,500 people with bowel cancer per year living for at least five years after diagnosis by 2025. The report also reveals that more than one in five patients weren’t treated with respect and dignity by doctors and nurses

 Bowel cancer is the UK’s second biggest cancer killer, and the overall five-year survival rate of those diagnosed is just over 50% 2. In its report, 2025 Challenge: Saving and Improving Lives, Bowel Cancer UK calls on the Government to examine its targets in reducing mortality, improving patient experience and increasing survival to dramatically improve outcomes in all three areas by 2025.
 The report reveals that:
  • Deaths from bowel cancer could be cut by 60% by 2025 – from 18 in 100,000 to 7 in 100,000 – if realistic goals were followed.
  • Almost one in four patients do not understand doctors’ explanations about their disease, and one in five say that they are not treated with dignity and respect 3.
  • 20% of patients say they have received conflicting information about their condition 4.
  • Currently, the survival rate of patients with bowel cancer is just over 50%.
Bowel Cancer UK’s ambition is to increase the proportion of people with bowel cancer diagnosed at an early stage, and improve the survival rate of people diagnosed with advanced disease. Achieving these goals would save an additional 2,500 more lives per year by 2025.
Bowel Cancer UK is calling on the Government to improve all three aspects of cancer care by:
  • Encouraging greater uptake of screening to ensure earlier diagnosis. Uptake is only just over 50% at the moment
  • Improving diagnostic capacity and reducing waiting times to cope with growing demand.
  • Detecting and diagnosing bowel cancer at an earlier stage. Currently only 9% of patients in the UK are detected at the very earliest stage of the disease 6.
  • Ensuring access to and support in decision making about the best treatments for advanced cancer regardless of where they live.
  • Making sure patients receive the best care by ensuring that hospital, community and social care services are joined up.
  • Improving the quality and consistency of written information given to patients with bowel cancer – currently one in three patients receive no written information.
Deborah Alsina, CEO, Bowel Cancer UK said: “We want to dramatically improve outcomes for people affected by bowel cancer, minimising the disease’s impact and helping people lead longer, healthier and happier lives.”
“We have a duty to save more lives and the proposals outlined in this report should be the Government’s absolute minimum goal.
“We look forward to working with the government, NHS and other charities to help save more lives from the UK’s second biggest cancer killer.”
 About the Bowel Cancer UK ‘2025 Challenge: Saving and Improving Lives’ report:
This report explores the progress over the past 25 years in relation to mortality, survival and patient experience. It celebrates the progress over the last 25 years and identifies the areas where more work is required and establishes realistic goals for improvement by 2025.
Mortality
The past 25 years:
Nearly half a million people in the UK died from bowel cancer in the past 25 years.
Our goal:
An age-standardised mortality rate of 7, meaning 7 people out of a standard population of 100,000 dying from bowel cancer by 2025.
Survival
The past 25 years:
Until recently, the majority of people with bowel cancer had not survived five years after their diagnosis.
Our goal:
An additional 2,500 people with bowel cancer per year living for at least five years after diagnosis by 2025.
Patient experience
The past 25 years:
Overall, cancer patients’ experience of care has improved since 1999, but not in all areas.
Our goal:
All trusts achieving 98% on all key patient experiences measures by 2025.
       
About Bowel Cancer:
Bowel Cancer is the second most common cause of cancer death in the UK, affecting both men and women. Every year just over 40,000 people are diagnosed with bowel cancer and more than 16,000 people die of the disease.
About Bowel Cancer UK:
Bowel Cancer UK is celebrating its 25th Anniversary. We are a charity aiming to save lives by raising awareness of bowel cancer, campaigning for best treatment and care, and providing practical support and advice.

2. Executive Summary
This report explores progress over the past 25 years on mortality, survival and patient experience. It celebrates the progress that has been made, identifies the areas where more work is required and establishes realistic goals for improvement by 2025.
The projections are made on the basis of what we know about bowel cancer, as well as the progress that has been made in the past. The goals should therefore be seen as a minimum objective for improving bowel cancer outcomes.
Achieving these goals will inform Bowel Cancer UK’s work over the next few years, helping us focus on what matters most to patients. We have developed several calls for action which, when implemented, will help even more people affected by bowel cancer and help us further improve the experience of people with bowel cancer.
Mortality
The past 25 years:
Nearly half a million people in the UK died from bowel cancer in the past 25 years
Our goal:
An age-standardised mortality rate of 7, meaning 7 people out of a standard population of 100,000 dying from bowel cancer by 2025. This would mean that there would have been a 75% reduction in the age standardised mortality rate from 1987.
Our calls to action
Reducing the number of people who die as a result of bowel cancer will require improvements in prevention, early diagnosis and treatment. We need to:
· Focus on preventing bowel cancer through simple changes to diet and lifestyle as these can reduce someone’s risk of developing bowel cancer.
· Improve diagnostic capacity with short waiting times. Endoscopy capacity should more than double over the next five years to cope with the growing demand created in part by a rise in incidence due to an ageing population.
· Encourage greater uptake of screening as it can prevent cancer for some people and ensure that others are diagnosed at an early stage.
· Implement new screening technologies and develop the next generation of screening tests so that we can maximise the number of cancers prevented and lives saved.
· Investigate the symptoms of bowel cancer. This must involve empowering and supporting GPs to refer people with possible symptoms properly.
· Raise public awareness of bowel cancer so people understand their risk and are motivated to act promptly.
· Ensure consistent best treatment for every patient irrespective of postcode.
Survival
The past 25 years:
Until recently, the majority of people with bowel cancer had not survived five years after their diagnosis.
Our goal:
An additional 2,500 people with bowel cancer per year living for at least five years after diagnosis by 2025.
Our calls to action
Helping people who are diagnosed with bowel cancer to live longer will require improvements across the patient pathway, ensuring that patients are able to benefit from the best of what we already know, as well as the results of continuing efforts to develop more effective interventions. We need to:
· Detect, diagnose, prevent and manage bowel cancer at the earliest possible stage when interventions are most effective.
· Improve treatment rates and offer the most appropriate treatment for all groups in society. There are currently wide variations in the numbers of patients who are offered a choice of treatment, both across the UK and according to demographic group.
· Ensure access to and support in decision making about the best treatments for advanced cancer. This should be regardless of geographical area as it is now possible to significantly extend and improve quality of life.
· Improve bowel cancer patient safety by using good practice guidance on infection control.
· Help and support people to recover from treatment by developing appropriate services and interventions. This is including for the late effects of treatment.
· Provide high quality palliative care as a vital component to improving the quality of life of cancer patients.
· Improve data collection to understand more about what improves survival as well as why variations in survival occur.
· Continue and prioritise research into bowel cancer as this will have a significant impact on survival by 2025.
Patient Experience
The past 25 years:
Overall, cancer patients’ experience of care has improved since 1999, but not in all areas.
Our goal:
All trusts achieving 98% on all key patient experience measures by 2025.
Our calls to action
A positive experience of treatment and care should be a minimum standard for every bowel cancer patient. More can and should be done. We need to:
· Expand access to bowel cancer clinical nurse specialists as they have a significant positive impact on the experience of cancer patients.
· Ensure strong multi-disciplinary working to ensure the best interests of the patient which in turn is the key to good patient experience.
· Ensure healthcare professionals communicate effectively and compassionately with patients about their condition and treatment.
· Improve the quality and consistency of written information given to patients with bowel cancer so they feel supported throughout the different stages of their pathway.
· Promote access to specialist supportive services, including diet and nutrition advice and stoma care as this can help with a patient’s experience of treatment and care.
· Ensure that joined up services are shaped around the needs of patients rather than the other way around.
Conclusion
Over the past quarter of a century, the way in which bowel cancer is perceived has been transformed. Public attitudes are changing, awareness is higher, screening offers the opportunity of earlier diagnosis and new treatments have transformed patients’ prospects. Although this is a cause for celebration, we must also remember the half a million people who have lost their lives to bowel cancer in the UK during this period and the many thousands more who have had their quality of life limited by the disease.
Now is not the time for complacency. It is the time to raise our ambitions. This document sets out some challenging but achievable goals for improving every dimension of bowel cancer outcomes, as well as the practical steps that need to be taken to meet them.

Blog 103 Thursday 12th April 2012

All went well yesterday with the removal of the Porta Cath albeit quite painful. As I was in as a day case surgery, the intention is to get the patient out as soon as possible. In less than two minutes my right side chest was shaved, spray frozen, daubed with iodine, and injected with anaesthetic, I was covered almost like a tent and the incision began. within fifteen minutes it was finished and sewn up. With the surgeon's wishes of not wanting to see me again (Meant in the best possible way) I was on my way home. When the anaesthetic wore off , Wow................... trying to sleep was a pain !!!!

Today I was so pleased to read the following article in our local paper for those that have suffered this particular cancer .......................................

NEW WAY TO PREDICT CANCER RETURNING           

Researchers have developed a new breast cancer test “that predicts whether or not their breast cancer will return after surgery”, The Daily Telegraph has today reported. The newspaper says the test may mean that thousands of women with a low risk of recurrence could be spared unnecessary chemotherapy.
The story is based on new research that compared an existing method for predicting cancer recurrence, the Oncotype DX recurrence score (RS), and an adapted version that also took other clinical data into account. To test this new method, called the “recurrence score-pathology-clinical assessment” (RSPC), researchers examined long-term study data on 1,444 women with early-stage, hormone-sensitive cancer that had not spread beyond the breast.
The researchers found that under the RSPC model, more patients were classified as being at low risk for disease recurrence compared to the original test. It did not, however, improve the ability to predict which patients would benefit from receiving chemotherapy. As such, the test should be considered “still in development” and not yet ready for use in practice. Its accuracy and ability to guide treatment choices will now need testing prospectively by applying the model to women with breast cancer before treatment and waiting to see if its results later prove to be accurate.

Read the full article HERE 

Blog 102 Tuesday 10th April 2012

Finally ......................I will be attending The Three Shires Hospital in Cliftonville Northampton tomorrow at 13.50 to remove the Porta Cath in my chest. The Porta Cath is a wonderful device is inserted completely under the skin via surgery and takes the Chemotherapy drugs without fear of infection. It can take approximately 1000 injections before it needs replacing.  I have been very fortunate having my Chemo at home via the above it made it all so easy. Having said that I haven't really got on with it, Its become quite sore and irritating especially when trying to sleep.The last remnants reminding me of the cancer and a journey that has lasted almost three years. My consultant for tomorrow is David A Ratliff MD FRCP FRCS Vascular, Laparoscopic and Endocrine Surgeon. My son Matthew & his galfriend Timone are safely back from Australia and will be driving me to/from hospital. I'm warned no driving for 48hours after the surgery............Brilliant !!!!!!Wendy will have to drive when we visit our friends Iain & Myra next weekend.

Blog 101 Wednesday 4th April 2012

Anyone who has previously read this blog will know, I have volunteered for Bowel Cancer UK. Unfortunately I missed the 2nd training session due to the recent loss of my father. Bowel Cancer UK volunteers attend events and give talks to raise awareness of Bowel Cancer, using statistics, symptoms, risk factors, and prevention. The volunteer is armed with leaflets with loads of information for good bowel health and also on the UK's screening programme. Bowel Cancer UK give you the facts about bowel cancer Telephone      0800 8 40 34 40         If, like me you are diagnosed early, bowel cancer is very treatable. What you must look out for is :-)

(1) Bleeding from your bottom and or blood in your poo. (2) A change in your bowel habits, lasting three weeks or more. (3) Unexplained weight loss. (4) Extreme tiredness for no reason. (5) A pain or lump in your tummy.

In my experience, I only had one of the above symptoms being, a change in my bowel habits. I had diarrhoea, which my doctor wrongly diagnosed as Irritable bowel syndrome. It still makes me angry, because, apparently I didn't fit the "profile" of someone that could have the early signs of cancer. (I was too young at 46) , my doctor at the time didn't bother with further tests. It took a doctor in Australia when we emigrated, to take things further and finally diagnose the disease.

Bowel Cancer UK warns of eating too much processed foods, ie bacon, ham,salami, sausages and burgers, and suggests that we should eat them as a treat only, as these foods could lead to bowel cancer. Studies from Sweden, also show that  just 50grams of processed meat a day raises the risk of pancreatic cancer by a fifth.  SO!!!!!!! I was amazed to read in
the Mail on Sunday "Review" paper that "Bacon can be good for you" by Zoe Dare HALL.

Be sure to read the bit that says  buy "Good-Quality Sausages"  "Made from Outdoor-Reared",  "Toxin-Free Pork" and which contain "90 per cent pork meat".  I'm sorry, but like the majority of British people, I do not shop at Harrods for my sausages !!! and reading the fine print on sausage packaging from supermarkets is becoming evermore problematic for me with age!!!!!

Zoe Dare HALL also quotes Rachel Green, of BBC3’s Kill It, Cook It, Eat It, who suggests that we buy from Farm Shops. Rachel says ..."I like to use more mature, flavoursome rare-breed porks such as Gloucestershire Old Spot or Tamworth."  We do not have the luxury of a farm shop selling such high end sausages in our area, but Zoe, I will try in Tesco and Morrisons for a laugh!!!!!!! I believe its headlines like that above that causes confusion amongst the majority and aimed at the minority who are demographically privileged.