A Diary Of A Mesowarrior Fighting #Mesothelioma. The Last Keytruda Trial MK3475-28 Has Been Completed At The Royal Marsden

I’m cheating a bit as Ray is doing a blog so I will use that as a guest blog for tonight as I’m so tired and emotionally drained really. So many lovely messages on Facebook, emails, messages and tweets and messages. I have been so overwhelmed at the love and encouragement.


Wow! An emotional day all round. It was Marsden Day. We ran to the car park in  pouring Rain. It didn’t matter much to me I was soaked anyway having walked louis up the lane. It was 10 to 6 we decided to leave early  because of the bad weather. The journey was a stop start one  on the M25.

Oh dear when Mavis booked in they said Your not due  until tomorrow. But  go and wait in waiting room  and we will sort it. Which they did. But it was a disappointment for them because  they had planned a party for Mavis  on Wednesday. They had ordered a cake and buns.  We didn’t know and it was not our  error.

We did the usual bloods and a final with the doctor. Then we set off to the restaurant for a cuppa. Gently sipping my Tea when I had red flashes in my eye that made me jump then instantly  the bleeper  went off and I almost spilt my tea all down me. So we had to dash back up stairs to see whats up. It was only one of the bloods had gelled and a fresh one was needed. WE  chatted to Amanda in reception. After the Doctors chat he re assured us that  all was well with our last scan and that now  for us the Trial had finally  come to an end, not to worry because we will be scanned regularly and any  new growth and we can have a further years drug again. he wished us well. WE  went down  for some lunch  during  maves and my chatting I  lost it. WE had talked to a mesowarrior  who wasnt doing so well. I simply said  to mave we are just plain bloody lucky that you’ve got this far. Wow! I could feel my eyes smarting I tried  looking down to avoid her eyes and she asked me are you alright. Yes  cos I am I spluttered. I was so emotional. WE  made our way back to the waiting room again  that was around 1pm. The drug didn’t  arrive until 3.15.  Eventually we were all done and then it was hugs and kisses all round nurses and us all saying  we will miss each other. We said carry on and have the party tomorrow and we will be with you all in spirit. It was time to leave with mixed  feelings .Glad we didnt have the early riser and M25 journey every  fortnight. But  sad because we wont be seeing  the galls so often. But they have done there job we have cut the cord and are now free to roam. We will  pop in on scan appointments promise.

The journey home was ok and we had to  pick up a bit of shopping before greeting Louis again. He was pleased to see us. A quick walk with louis was in order. Now  for a  while we can try and live a normal life.


Oh well I will put that in a box and shut it away in a corner of my brain !!!

So I went back to enjoying the day. Just a photo record of the day




PHOTO_20160531_134027 PHOTO_20160531_150645 PHOTO_20160531_150716 PHOTO_20160531_150837 PHOTO_20160531_151950

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A Diary Of A Mesowarrior Living With #Mesothelioma Survivor Depression sets in and a Exciting Plan for Amsterdam Conference

I realise I haven’t written an update, but can you believe I have felts so depressed.

I know this time of year as I come up to the anniversary of our darling daughters death, in 1979 I do know I can tell the date by how I feel, but I have been really feeling of down in the dumps.

I have had survivors guilt as I really want more mesowarriors to have the opportunity of drugs. At least to try to see if they could work.

We now have a few going private on this and I know how hard financially that is. I have pushed for the cost of these new drugs to be included in the claims for compensation and that is happening for newly diagnosis, or at least its being talked about.

The winter has seemed so long as the weather has just started to warm up.

I have kept busy and Iv cleaned the Motor Home, after we have neglected it a bit only used it once or twice. But that is going to change as next Tuesday is my last drug day.

But then I read this

Rates of depression and anxiety are very high when treatment ends,” says Dr Michelle Kohn, director of Living Well, a programme that offers emotional and practical support to cancer patients at Leaders in Oncology Care, a private London-based clinic. “Other emotional issues, such as low self-esteem, anger, stress or sleep problems are also widespread.”

On top of this, cancer survivors are often battling with physical and practical challenges, anything from huge financial losses, to the side effects of medication, profound fatigue, a confused-feeling known as “chemo brain”, or lymphoedima (swelling). Their loved ones, meanwhile, might be increasingly baffled as to why they can’t bounce back and make the most of life. “People suffer for years, often in silence, without any real support,” says Kohn. “Life after cancer can actually be very difficult and lonely.”

It does not help, says Devane, that, “the current system is woefully inadequate at supporting the changing nature of cancer survivors”. In the United States, most major cancer units have survivorship programmes where teams of psychologists, nurses, and other specialists offer ongoing information, advice and emotional support to patients when treatment ends. This, of course, is funded by health insurance. In contrast, NHS post-treatment psychological or practical services are limited, to say the least.

The National Cancer Survivorship Initiative (NCSI), a partnership between the Department of Health and Macmillan, was launched in 2008 to help improve the situation but it has a massive job on its hands. According to NCSI research, 60% of cancer survivors have unmet physical or psychological needs; over 33% have problems with close relationships, careers, or have difficulty performing household duties; over 90% have suffered financial losses. Waving these people off with a six-month follow up appointment, is simply not working.

The NCSI is launching a range of programmes that take a more holistic approach to the needs of cancer survivors, for example encouraging physical activity, or helping with issues including work and finance. “It is essential the NHS now implements these solutions,” says Devane. But there is a very long way to go.

The fear that cancer will come back again is huge for me.

My cancer has come back 4 times when being treated with Chemo so I must have a belief that what people say about  Immunotherapy is true and yet that have no proof yet. I’m showing them the way so that puts a lot of strain on me.

I have to believe Im now cancer-free and determined to enjoy life to the full. But still, when I feel unwell the fear sets in and despite so many friends and family I can feel very alone. I sit and think too much. This is how I have felt.

Writing it down it reads like I’m feeling sorry for myself isn’t that selfish.

So actually I’m going through a normal Process so that cheers me up and I’m coming back again. I try to do a job a day like yesterday cleaned the fridge out and today I washed the airing cupboard and a kitchen cupboard out.

We have been out to our fav place at Tankerton and walked Louis along the grass overlooking the beach. The sea was rough and exhilarating. It blew the cobwebs away.

We have been going to the park so this made a change today seeing the wind farm and the sea.

So it’s a case of Pick myself up and start all over again. There are many Warriors fighting the battle and I’m still around to talk to them and be there for them.






European Asbestos Forum's profile photo

We have a new date: 30 SEPTEMBER & 1 OCTOBER 2016, again at the wonderful NH Grand Hotel Krasnapolsky!
Presiding over the day will be Hans van der Wart, who did a marvelous job of it last year.
It is astonishing how many aspects there are to the main topic: Asbestos & Real Estate. Many of them will be highlighted, explored and compared.

I have been invited to talk in Amsterdam which is exciting.

The European Asbestos Forum announced yesterday

Announcing a new speaker: the lovely Mavis Nye and possibly her husband Ray as well! Mavis Nye is a Meso Warrior and long-time survivor of mesothelioma herself. Mavis will share her story and her wonderfully inspiring medical news with the Forum.


The European Asbestos Forum 30 SEPTEMBER & 1 OCTOBER 2016, again at the wonderful NH Grand Hotel Krasnapolsky!
Presiding over the day will be Hans van der Wart, who did a marvelous job of it last year.
It is astonishing how many aspects there are to the main topic: Asbestos & Real Estate. Many of them will be highlighted, explored and compared.

For 2016, the main topic of the EAF conference will be: Asbestos & Buildings. So that is something to plan for and we will be going by Eurostar which is a new for us as we have only ever used the Euro Tunnel Train. Roll on and Roll off so you only use it through the tunnel, this time it will be a 5 hour journey.





A Diary of A Mesowarrior Things Are Moving Very Slowly To Get a Drug For #Mesothelioma

The latest on Keytruda I know its still for Skin Cancer but we now need more trials and Comination trials so we can get it out there as a treatment for mesothelioma Immunatherapy is here and we need more money for research into these drugs So keep backing Mesothelioma UK and Cancer research to fund these trials and encourage the drug companies but our next hurdle is getting NICE to sanction these very costly drugs Or even get the Insurance Companies to count the cost of the drugs into Compensation. We need to push the Lawyers on this one .http://medicalxpress.com/news/2016-05-immune-drug-deadly-skin-cancer.htm

Immune drug for deadly skin cancer shows long-term survival

Immune drug for deadly skin cancer shows long-term survival (Update)

May 18, 2016 by By Lindsey Tanner

A new kind of drug for the deadliest form of skin cancer helped some patients survive for at least three years, a study shows. It’s a remarkable advance for patients who until recently faced dismal chances of living for more than a few months.

About 40 percent of melanoma patients in the study were still alive three years later. The drug, which targets the immune system, was used to treat former President Jimmy Carter, who was diagnosed with melanoma that had spread to his brain.

“This is incredible,” Dr. Caroline Robert, the study’s lead author, said of the results released Wednesday. “I spend my time telling my residents that these patients would be dead if it was five years ago.”

The drug, Keytruda, is among a new class of genetically engineered antibody-based medicines. They block proteins that prevent the body’s disease-fighting immune system from attacking cancer cells. This immunotherapy approach is transforming treatment for several kinds of cancer with drugs that are often less toxic than chemotherapy.

The latest findings for Merck’s Keytruda (kee-TROO’-duh) are among the best long-term data ever for treating melanoma that has spread to other organs, Robert and other cancer experts said.

Keytruda, also known as pembrolizumab (pem-bro-LIZ’-uh-mab,) is one of the treatments Carter received after his diagnosis last year, and he has done well. Carter, 91, was seen beaming last weekend as he helped give an honorary humanities degree to rocker Gregg Allman at Georgia’s Mercer University, where Carter is a trustee.

The new results in 655 patients are a follow-up to research that led to the 2014 approval of Keytruda for advanced melanoma.

In addition to the 40 percent survival rate at three years, Robert said 85 patients remain cancer-free. “Of course it’s not enough,” but it raises hope for an eventual cure for the disease, she said.

Robert, a melanoma researcher at Gustave Roussy cancer center near Paris, has worked as a consultant for Merck and Bristol-Myers Squibb, which makes two other immunotherapy drugs approved for advanced melanoma. The newest drug, Opdivo, targets the same protein as Keytruda, while Yervoy targets a different protein.

Dr. Len Lichtenfeld, the American Cancer Society’s deputy chief medical officer, said the new Keytruda research “is a big deal.”

“Looking to the future, these treatments are going to be used earlier in the course of this disease,” sometimes combined with other immunotherapy drugs, Lichtenfeld said.

The Keytruda study was released at a news briefing organized by the American Society of Clinical Oncology in advance of the group’s annual meeting next month in Chicago.

The American Cancer Society estimates that almost 77,000 people will be diagnosed with melanoma this year and that 10,000 will die from the disease. It’s much less common than other skin cancers and much more aggressive and likely to spread to other organs. The earliest sign is often a large misshapen or unusually colored mole that grows in size.

Yervoy, approved in 2011, has the longest-term data of the three drugs, with an eight-year survival rate of about 20 percent, said Dr. Thomas Gajewski, a University of Chicago immunotherapy expert.

He said success with Keytruda echoes what he’s seen in melanoma patients at his center. They receive IV infusions of the drug for an hour every few weeks for an indefinite time unless they develop severe side effects, which he said are rare. Rashes and internal inflammation are the most common side effects and they are reversible if the drug is stopped. The yearly cost is more than $100,000, a higher price than some conventional cancer drugs.

Some insurers pay for the treatment, which Gajewski called “a game-changer” for melanoma, allowing many patients to return to work and live productive lives.

In other immunotherapy developments, a new drug was approved Wednesday for bladder cancer, and Opdivo was approved Tuesday for another cancer, Hodgkin lymphoma.

A list of the trials for 2016 is at this link and funny enough the list covers Australia.


We havent got a petition running in UK as we are governed by so many ;laws and we just would not get pass NICE  Or best hope is for fast Track and The Promised Saatchi Bill.

Just came up with the very latest report on Keytruda

Final Overall Survival Data from KEYNOTE-006 To Be Presented at ASCO; KEYTRUDA, the First Anti-PD-1 Monotherapy to Demonstrate Overall Survival Compared to Ipilimumab, Shows Continued Benefit with Longer Follow-Up

KEYNOTE-001 Findings Show Continued Benefit in Response Rates, Duration of Response, and Include New Three-Year Overall Survival Data for KEYTRUDA


Lou Williams has a petition for keytruda onto the PSB List although Keytruda hasnt gone through all trials there it has been liscenced and on is on the PSB list for Melonoma.

Australia http://asbestosaustralia.blogspot.co.uk/2016/05/keytruda-fast-track-mesothelioma-pbs.html?spref=fb

Lou says Trevor Grant and myself have on behalf of mesothelioma warriors in Australia sent a letter to the CEO of MSD/Merck who manufacture Keytruda in response to the letter that I received above from Hon Sussan Ley.
Please continue to sign my petition to get Keytruda (and other immunotherapy drugs) fast tracked on to the PBS for Mesothelioma and 30 other rare cancers.  I believe that once are successful in getting Keytruda on to the PBS for all to access as another treatment in Mesothelioma then it will follow for other cancers.  It is getting closer and with a bit more pushing we will succeed.  This cancer is deadly, lethal, aggressive and we simply do not have time to waste!  In unity we can do this!

Lou Williams's profile photo

Rod Smith Of Bernie Banton has a completely different Petition running to get Australia to Trial More Drugs as for some reason they do not get included into to many trials.

We need your support!  The Bernie Banton Foundation is lobbying the Australian Government, via the Health Minister, the Hon. Sussan Ley, to fund trials of drugs with the potential to treat rare diseases, and to reform the Pharmaceutical Benefits Scheme (PBS) application requirements that currently make it impractical for pharmaceutical companies to apply to have valid drugs listed on the PBS.

In Australia, drug trials for treating many rare diseases are almost non-existent, as drug companies find it is not financially viable to conduct trials, due to the relative small number of sufferers compared to more common diseases, such as melanoma.  Not only are trials an important part of helping find cures, and are necessary to obtain data to build a case to justify a drug being listed on the PBS, importantly, they also give sufferers hope – where often none exists!

The Government needs to step up and fund treatment trials for asbestos cancers and other rare and less common diseases! 

Drugs not listed on the PBS for treating asbestos cancer and other rare diseases are prohibitively priced, this often preventsdesperate sufferers with no other treatment options from accessing them!

A good example of the unfairness of the system is where a drug; that has demonstrated benefits, in extending and giving better quality of life, to some sufferers of the rare terminal asbestos cancer, mesothelioma; has been listed on the PBS for treating melanoma – which we think is fabulous!  This means melanoma sufferers pay only up to $38 per treatment, whilstmesothelioma and other rare cancer sufferers are paying between $5,000 and $10,000 per treatmentfor the same drug! 

What’s important to understand is; pharmaceutical companies are often not even attempting to apply to list drugs, with promise to treat rare diseases, onto the PBS, as the application requirements are too demanding and can’t be met in a practical time frame, due to the small number of sufferers involved and the lack of trial data.

The current PBS application requirements disadvantage sufferers of rare diseases – it must be overhauled!

Industry based discussion papers have made a convincing case on how the PBS application requirements could be changed to allow valid drug applications to be fast tracked onto the PBS, without losing the integrity of the system.   All that is needed is for the government to see the need for change and the will to do so!


The whole problem is that its the first drug we have had for Mesothelioma. Its always been palliative care only and we have now got a glimmer of hope at last and we want and need it now.

The USA have had trials for some time and with a 22% response. We need more trials. Verestem have come onto the scene as well  and are working with Merck. So many are working hard to make it happen.

BOSTON–(BUSINESS WIRE)–May 9, 2016– Verastem, Inc. (NASDAQ:VSTM), focused on discovering and developing drugs to treat cancer, today reported financial results for the first quarter ended March 31, 2016, and also provided an overview of certain corporate developments.

“To date in 2016, Verastem has announced two new clinical collaborations with world-class organizations, includingMerck KGaA and Pfizer, and Washington University in St. Louis and Merck & Co., to further elucidate the potential of FAK inhibition to enhance the efficacy of PD-(L)1 inhibitors in patients with pancreatic and ovarian cancer,” said Robert Forrester, President and Chief Executive Officer of Verastem. “The data generated from these trials will continue to inform the ongoing development of our anti-cancer therapeutics which reduce cancer stem cells and modulate the local tumor microenvironment to allow both cancer treatments and the immune system to do their job more efficiently. We’ve had a strong start to 2016 with the announcement of these clinical collaborations in addition to attracting key strategic hires on the development team, including Dr. Greg Berk as Chief Medical Officer and Dr. Toyin Shonukan as Vice President of Clinical Development, to oversee and execute on our ongoing and future studies. We are well financed with approximately $100 million in available capital and we look forward to keeping you updated in the coming quarters on our progress.”

First Quarter 2016 and Recent Highlights:

Focal Adhesion Kinase Inhibition Program

  • Clinical Collaboration with Pfizer and Merck KGaA to Evaluate Combination of VS-6063 and Avelumab in Ovarian Cancer – In March 2016, the companies announced a clinical trial collaboration agreement to evaluate the combination of Verastem’s focal adhesion kinase (FAK) inhibitor VS-6063 and Pfizer and Merck KGaA’s anti-PD-L1 immunotherapy avelumab. Verastem has previously reported initial signs of clinical activity in patients with ovarian cancer when VS-6063 is used in combination with paclitaxel. Under the terms of the agreement, the parties will conduct a planned Phase 1/1b clinical trial evaluating escalating doses of the combination of VS-6063 and avelumab as a potential treatment option for patients with advanced ovarian cancer.
  • Washington University in St. Louis Initiated a Clinical Study of VS-6063 in Combination with Merck & Co.’s Pembrolizumab and Gemcitabine in Pancreatic Cancer – In January 2016, Verastem announced the initiation of a Phase 1 dose-escalation study at Washington University to evaluate its FAK inhibitor VS-6063 in combination with Merck & Co.’s anti-PD-1 immunotherapy pembrolizumab and gemcitabine in patients with pancreatic cancer. The trial builds upon preclinical research conducted by Dr. David Denardo, presented at several conferences in late 2015 and early 2016, demonstrating the ability of FAK inhibition to increase the efficacy of checkpoint inhibition in the reduction of tumor volume and overall survival in models of pancreatic cancer. This Phase 1 clinical trial is currently enrolling and is anticipated to enroll approximately 50 patients with advanced pancreatic cancer.
  • Presented Scientific Data Supporting FAK Inhibition in Combination with Immunotherapy at Key Medical Meetings – During the first quarter of 2016, Verastem presented data in support of its new development programs focused on advancing its FAK inhibitors in combination with immune-oncology agents and other current and emerging standard of care cancer treatments. Data were presented at several medical and scientific meetings, including the 2016 American Academy of Cancer Research (AACR), the Society for Gynecologic Oncology’s 2016 Annual Meeting on Women’s Cancer, the Keystone Symposium on Cancer Pathology, the Keystone Symposium on Stem Cells and Cancer, and Immunotherapy World 2016.
  • Presented Clinical Data from the Window of Opportunity Study at iMig 2016 – In May 2016, the Company announced results from the ongoing open-label, single-center, neoadjuvant Window of Opportunity study evaluating tolerability, along with biomarker and tumor volume response to VS-6063 (400mg BID) following either 12 days (Cohort 1) or 35 days (Cohort 2) of treatment in surgically-eligible patients with malignant pleural mesothelioma. Data analysis from Cohort 1 and Cohort 2 showed that VS-6063 was generally well tolerated with early signs of tumor reduction observed, with six of the twenty patients demonstrating an encouraging tumor reduction after brief treatment with VS-6063.
  • Development of VS-4718 Continues in Solid Tumors – Dosing continues in a Phase 1 dose escalation trial evaluating single-agent VS-4718 and a Phase 1 clinical trial evaluating VS-4718 in combination with gemcitabine and Abraxane® is currently ongoing. Following results from the dose escalation trial, an expansion cohort of VS-4718 + Gemcitabine/Abraxane® vs Gemcitabine/Abraxane® alone in patients with pancreatic cancer is planned.

Dual PI3K/mTORC1/2 Inhibition Program

  • Confirmatory Recommended Phase 2 Dose and Expansion Cohorts – The maximum tolerated dose of single-agent VS-5584 has been reached in a Phase 1 study, and the recommended Phase 2 dose (RP2D) is being confirmed. Reductions in pharmacodynamic markers of PI3K and mTOR activity and clinical activity has been observed in some tumor types.


We will be looking for the latest reports at


Following our conference in Houston on May 20, the 2016 International Symposium on Malignant Mesothelioma will continue with one-day conferences in San Francisco on September 16 and Chicago on October 7.

Each conference will be a one-day event starting at 8:30am and ending around 6:30pm, including breakfast, lunch, and a cocktail hour, plus coffee breaks throughout the day. Each will feature top mesothelioma experts, professionally-moderated support sessions, and numerous opportunities for socialization.

covered at each location by different speakers
• Mesothelioma Research – What’s on the Horizon
• Clinical Trials for the Newly Diagnosed and Beyond
• Radiation Therapy New Techniques and New Ways to Incorporate into Treatment Modalities
• Surgery: How Do We Improve Outcomes
• Immunotherapy Options
• Introduction to Regional Centers of Excellence
• Do Your Genes Put You at Risk


San Francisco
invited speakers• Thierry Jahan, MD, University of California San Francisco
• Courtney Broaddus, MD, University of California San Francisco
• David Jablons, MD, University of California San Francisco
• Andrew Lowy, MD, University of California San Diego
• Lyudmila Bazhenova, MD, University of California San Diego
• Gleneara Bates, PhD, Meso Foundation
invited speakers• Hedy Kindler, MD, University of Chicago
• Sam Armato, MD, University of Chicago
• Kiran Turaga, MD, University of Chicago
• Dennis Wigle, MD, Mayo Clinic
• Aaron Mansfield, MD, Mayo Clinic
• Tobia Peikert, MD, Mayo Clinic
• Daniel Raymond, MD, Cleveland Clinic
• James Stevenson, MD, Cleveland Clinic
• Wickii Thambiah Vigneswaran, MD, Loyola University
• Arkadiusz Dudek, MD, University of Minnesota Medical Center
• Gleneara Bates, PhD, Meso Foundation

The first conference as part of the 2016 International Symposium on Malignant Mesothelioma will take place in Houston on May 20.


A Diary Of A Mesowarrior Living With #Mesothelioma -No 51 of Keytruda Trial,The Duke of Cambridge was at the London Royal Marsden so we missed him.

The sun was shinning through the blinds as an explosion of sound woke me up. Dam the Alarm


Ray walked Louis and said Hi to his horses in the field

b n w

I was running round the house like a mad woman getting a shower and dressing.

Off up the Motorways to the Marsden and a good run.So we got there early only to be told I will be in a bed as they had so many patients. Oh no it means Im stuck in a small ward of 6 beds and somehow having the drug on a bed makes me feel a patient.

Then in came my Spanish Nurse and she cant find my veins for blood. We found one but she darted right through it and was devastated as she hates seeing bruises.

So it was down to Rex who is the master of finding veins. He cheated though and used my one large vein that we leave for the drug.

Ray presented them with the clock we had bought to say thank you. A box of sweets didn’t seem enough. How can you thank these wonderful people that have saved your life. So they needed a new clock and they were so pleased with the one we bought.

They gave me a card signed by everyone. It eases the fact next time is the last time I will see these lovely people. I have made a promise to pop in every 2 months for a chat and a tea.








Then our lovely Carol came in all bubbly. She had a heart attack in December and had a stent fitted. It didn’t cure the whole problem so she had a heart bypass 7 weeks ago and is now bored at home. I was thrilled to have seen her and to be able to say  bye to her. We had a long chat and then my dinner turned up. Poor Ray had to go to the canteen.He is allowed cups of tea but the dinner is for 1.

When he came back the ward was quiet again and all my visitors were gone. the Doctor came and said that My kidney is playing up right at the end but its better today then two weeks ago. Its over 100 today but had gone right up to 150. ??? Isn’t it funny how we sit there and dont ask all the questions. I dont know what over 100 means. 100 what. do I really need to know and start frightening myself. So I left it as she was passing the drug and that is all that matters to me.

I have lost 2 kg in weight but I explained I have been gardening and all the travel I have done lately I wasn’t worried. Im happy to be lighter.

My drug was made up and came onto the ward so I was soon set up with Number 51 of MK3475.28.


So there it is only 1 more to do and Im free from all this. I dont know the future but neither do the Doctors for one this isn’t in their hands its in the hands of Keytruda and my Immune system.

Here is a wonderful download free from this link if you need information on Mesothelioma

meso book

The new version of the popular JHMRF Mesothelioma Handbook is now available. Written by Dr Helen Clayson, a former GP and hospice Medical Director, who has been involved in the care of people with mesothelioma for over 30 years. Dr Clayson continues to work on research and education concerning asbestos-related diseases – including a training programme in Japan and an asbestosis project in India. She is a co-applicant on a National Institute of Health Research proposal to study the organisation and economics of care for mesothelioma in the UK. The handbook is based on her personal experience and research.

Dr Kate Hill, trustee said, “The JHMRF is pleased to continue to provide useful information to help those affected by mesothelioma. The new handbook has been written by Dr Clayson to provide straightforward information for patients, their families, non-specialist health care professionals and carers. It covers all aspects of the illness including clinical investigations, treatments, psychological and practical issues.”

Hard copies of the handbook can be obtained from The June Hancock Mesothelioma Research Fund by emailing a request tohandbook@junehancockfund.org. Please remember to include your name, address and postcode.

Download a PDF of the JHMRF Mesothelioma Handbook (11.6MB)

Alternatively a flipbook edition of the handbook can be read via ourMesothelioma Handbook page.


We didnt see  William as it was in the other half of the Royal Marsden in Fulham so here is the story that is in the Telegraph


Ralph Lauren opens £4 million new breast cancer centre, inspired by his friendship with Princess Diana

 The Duke of Cambridge and Ralph Lauren unveil a plaque during a visit to the Royal Marsden NHS Foundation Trust in Chelsea
The Duke of Cambridge and Ralph Lauren unveil a plaque during a visit to the Royal Marsden NHS Foundation Trust in Chelsea 

The American designer first met the Princess in 1995 when she was already the president of The Royal Marsden Hospital – said to be one of her favourite charities.

Ralph Lauren with Princess Diana in Washington in 1996 
Ralph Lauren with Princess Diana in Washington in 1996  

And today he spoke of the “honour” he felt at continuing the life-saving work of the hospital with her son, the Duke of Cambridge.

After formally opening the new Ralph Lauren Centre for Breast Cancer Research at The Royal Marsden in Chelsea, the two men were given a guided tour of the new facilities.

William joins Ralph Lauren to open new cancer centrePlay!01:30

The centre has been named after the American businessman and philanthropist who has made an undisclosed donation to the £3.9million facility.

Ralph Lauren told The Telegraph: “Having known Princess Diana and how much she cared about the important research pioneered by The Royal Marsden, I am uniquely honoured to partner with her son HRH The Duke of Cambridge and see that work carried on and supported with his great dedication and the opening of our Ralph Lauren Centre for Breast Cancer Research.

View image on Twitter

Speaking about his support of breast cancer institutions, Mr Lauren said: “A good friend of mine in America had breast cancer, and she said ‘Ralph, you deal with so many women, it would be a wonderful thing if you helped’. She said, ‘I haven’t gotten any support from anyone’ and I said ‘I’m going to help you’.

Ralph Lauren and the Duke of Cambridge meet breast cancer patient Kathryn England
Ralph Lauren and the Duke of Cambridge meet breast cancer patient Kathryn EnglandCREDIT: DOMINIC LIPINSKI/PA 

“She didn’t make it, but I got hooked into feeling really strongly about breast cancer.

“I have a daughter and a wife and it’s a family situation. The mother might have it, the sister might have it, but…the family goes through it, it involves everybody.”

View image on Twitter

He told one patient he met that friends of his had suffered with cancer.

And in a lighter moment, he told another woman receiving treatment about how he was starting to look at schools for his children.

He said: “They’re both doing very well at the moment – noisy but lovely – just trying to sort out schools now, it’s going very well.”

The Duke of Cambridge meet Professor Stephen Johston with Ralph Lauren and his wife Ricky
The Duke of Cambridge meet Professor Stephen Johston with Ralph Lauren and his wife Ricky CREDIT: DOMINIC LIPINSKI/PA 

Speaking after the unveiling of a plaque to signal the opening of the centre, William said: “Seeing the courage and spirit of the patients I met today, it would be hard not to feel positive about the work being done here, and the real difference it makes.

“A difference which I know extends beyond the four walls of this hospital, to cancer patients across the UK and internationally.”

Globally it is the most common cancer in women, with an estimated 1.4 million women diagnosed every year and 460,000 deaths.

The new research centre will begin a pilot study at the end of the year which could – if it proves successful – lead to a blood test being used to detect if any cancer remains in a woman’s body once she has been given the all clear.

Another project is trialling the use of a new drug, which puts the tumour into “suspended animation”, in combination with a standard drug which lowers oestrogen levels – a hormone known to benefit tumours – in post-menopausal women.

The Royal Family has had a long connection with the hospital, beginning in 1910 when the hospital was granted its Royal Charter of Incorporation by King George V.

A Diary Of A Mesowarrior Living With #Mesothelioma International Day Of Families


Today we say thank you to the family’s that go through so much when their loved ones get that diagnosis of Mesothelioma. Their lives go on hold as they become a carer to a very sick person who is in so much pain and discomfort.

They watch as they go through the talc op and the radiation and then Chemo and all the horror that brings. Their loved one laying in bed sick for days at a time.

The other side of the coin.

This story began in May 2009 when Mavis was rushed into Hospital.
A Month Later In June at Kent and Canterbury Mavis original prognosis for this disease was 3 Months. Just get on with your life we were told.
All 3 months of it.
I can now leap forward a few years because you are all aware what the standard regime for meso is.

UP to May of last year . 2014 We had been fighting mesothelioma for 5 years
Fighting through 4 different Chemo regimes
And 2 phase 1 trials
All unsuccessfully trying to beat Mesothelioma
Now Kent and Canterbury told us there is no more treatment available.
So once again we were back to that old :—
OK go home and get on with your lives.
But By this time Mavis was not in a good place, .And in no fit state to enjoy many things.
She was Unable to walk more than a few paces without breathing problems she was constantly falling over. And was reduced to the use of a walking frame.
She was on her last legs.
It broke my heart to see her reduced to this.
But mentally she was sound and she just refused to give up. She was running her Global mesowariors suport groups on Facebook. A daily blog with over 350.000 views Her web page onestop mesothelioama. She was a NHS patient rep attends many NHS meetings. Is on the end of the phone for anyone looking for help and support. Speaks in the House of Commons On speaking terms with Lords and Politicians. All of which respect her.

During one of her many conferences she was talking to Professor Dean Fennel. Who had become a great friend.
This was a major turning point in this long nightmare. He advised her to go to the Royal Marsden.
There were just 3 places on a trial for mesothelioma on the Keytruda Trial. She was lucky to be offered the last place.
We gratefully accepted this as more or less our last chance
The Trial at Royal Marsden has been a fortnightly visit for 50 infusions.
Getting up at 4.30 am I then have to quickly walk the dog up the lane in the dark cold mornings before setting off for the 2 hour fight on the M25. Spending all day there and the fight back home in rush hour It’s usually been a 12-hour day. It has been hard for both of us.
But if this means I can keep hold of Mavis for another day then it is worth every second of those cold dark journeys. And I am certain our dog feels the same bless him.
The Marsden has worked wonders for Mavis but sadly not for the others on her trial. We have Complete Response  . I cannot put into words just what this means to me. And I am so happy to have most of my wife back.

Life has many good things to offer.
Happiness and Health And Love.
But above all for me it has to be the Love for that Special Person that inspires Hope and trust I am lucky to have this in Mavis.
That old saying Seek and ye shall find is proof that you must fight on, there is always hope..
. . ..
My heartfelt thanks and gratitude goes out to ALL Those Doctors and Nurses who have been there for us.
Without them my life would be so different.
It’s now left only to say
Mavis please keep it up Long may you continue this fight.
I need you And So many warriors need you.————-

I have always kept my children and family out of the publicity as they have suffered enough. We often forget the family and what their thoughts are as they travel the roller coaster with us. I see the tears in the eyes when I say, I have cancer, then the smiles when I say ” ITS SHRUNK. !!! Then the tears again when I say “Oh dear I have something to tell you its growing again” 5 times I did this to them. How cruel was that? so now I want them to all settle down and live their lives but I know that every time I go back for a scan every 2 months they will share my Scanexity with me. They will be at work worrying until I can phone and say all clear.

This is the same story through all the Mesowarrior world so many families have gone through hell and back so many going through it now and more in the future. When will all this madness, pain stop.

So a huge hug for all the families on this  International Day for families.

flowers 8

Thank you.





A Diary of a #Mesowarrior Living With Mesothelioma 7 Year Survival

Well the summer has gone and the rain has taken over again. We had a huge spider sheltering by a box. The warmth at the weekend must have bought it out. They are growing very large a round here Image result for big uk house spiders

We had to go to Kent and Canterbury to deliver the Mesothelioma UK Handbook

New mesothelioma handbook now available

Dr-Helen-ClaysonThe new version of the popular JHMRF Mesothelioma Handbook is now available. Written by Dr Helen Clayson, a former GP and hospice Medical Director, who has been involved in the care of people with mesothelioma for over 30 years. Dr Clayson continues to work on research and education concerning asbestos-related diseases – including a training programme in Japan and an asbestosis project in India. She is a co-applicant on a National Institute of Health Research proposal to study the organisation and economics of care for mesothelioma in the UK. The handbook is based on her personal experience and research.

Dr Kate Hill, trustee said, “The JHMRF is pleased to continue to provide useful information to help those affected by mesothelioma. The new handbook has been written by Dr Clayson to provide straightforward information for patients, their families, non-specialist health care professionals and carers. It covers all aspects of the illness including clinical investigations, treatments, psychological and practical issues.”

Hard copies of the handbook can be obtained from The June Hancock Mesothelioma Research Fund by emailing a request tohandbook@junehancockfund.org. Please remember to include your name, address and postcode.

Download a PDF of the JHMRF Mesothelioma Handbook (11.6MB)

Alternatively a flipbook edition of the handbook can be read via ourMesothelioma Handbook page.

I had promised to deliver a box to my CNS and I wanted to see here as she has been on  maternity leave.


We went to New Dover Road P&R and didn’t know they had stopped the hospital bus so had to drive and park in the hospital car park. Luckily we found a space.

The box was heavy but I carried it into the hospital and Toni came round to meet us. As we got to the canteen My Oncologist was there getting a coffee. Lots of smiles and hugs that now completes meeting all my medical team as there was so many at iMIG.

I was busy telling her how I was and she said she has been receiving all the letters from the Marsden. I forgot that.

My Oncologist had to go to Clinic so we had to say bye and we went and sat down. We talked about so much it was great to catch up.

One thing we did talk about When is the right time to talk about the coroner  She wants me to ask a question. When is the right time to tell us about the need of a coroner. It turns out that a GP doesn’t always know and there have been some cases where it was being missed. We as patient or carers have to be told to be prepared. it is in the Macmillan pack but people gloss over that. So I asked the Mesowarriors and they have really been good and told us what they thought and message me. The majority have felt like I did that we need telling when diagnosed. Young people have answered to at least wait until they have come to terms with the disease. So the answer is the CNS should still make her mind up and be guided by the age of the patient and how bad they have the disease.

Involvement of the coroner

Mesothelioma is classed as an industrial disease. This means that, in England and Wales, all deaths from mesothelioma must be referred to the local coroner’s office. The coroner will then decide if a post-mortem examination is required and will hold an inquest. A death certificate can only be issued after the inquest.

This can be a very difficult time for family and loved ones and it really helps to be clear about the process surrounding the inquest. The government has a short guide to coroner services and coroner investigations.

In Northern Ireland, while deaths relating to mesothelioma must be reported to the coroner, an inquest is not mandatory. Usually, after consultation with the GP and family of the person who has died, no further action will be taken.

In Scotland, mesothelioma deaths must be referred to the procurator fiscal. The doctor who reports the death will use a simple form, known as a pro forma, to record details about the health and circumstances of the person who has died. The procurator fiscal will then decide whether a post-mortem is required.

If compensation has already been obtained, a post-mortem will not be required. It is unlikely that your family will need to be interviewed for further information. Clydeside Action on Asbestos has more information.

Once it has all been discussed its like writing you will once done we can relax and carry on living and enjoying life.

Ray took photos on his camera but it didn’t work which made us laugh. We walked around to the Chemotherapy room but I didn’t know any of the staff as they were all new. Things change and I was nervous back in that room as all the memories came flooding back.

So we said good bye and hugged Toni and will see her at meetings as I’m a Patent Rep. We walked past Invicta Ward where I was in 7 years ago exactly I had had my 7 litres of fluid drained and was awaiting for the cells to grow in a culture. My whole journey started from there.

The start of this blog had begun.




A Diary of a Mesowarrior Living With #Mesothelioma iMIG 2016 photos


Prof David Waller            Prof Dean Fennel


It is a great pleasure and an honour to extend you a warm invitation to attend the 13th International Conference of the International Mesothelioma Interest Group (iMig 2016), to be held May 1 – 4, 2016 at the International Conference Centre in Birmingham, UK.

Building on the success of preceding meetings in Boston in 2012 and Cape Town in 2014, the Conference will feature a highly interactive, stimulating and multidisciplinary program including workshops, plenary sessions as well as oral abstract and poster sessions. Under the theme of ‘Towards Personalized Care’ the meeting will address the entire patient pathway and look beyond the scientific topics alone.

The Conference will provide the ideal forum to stimulate ideas and establish collaborations as well as to initiate intense discussions. Extended networking opportunities will foster communications between delegates.

It is an exciting time for mesothelioma research and we hope to see you in Birmingham in 2016 for the iMig 2016 Conference.

So we travelled to Birmingham for this wonderful Conference and had a great time.

There is to much to write about so I will say it with photos.





mavis imig1


Dr Jeremy Steele who I first met at Barts Love the sign behind us xx


I have to say that it was the best Conference I have been to. It was so friendly and so Informative and so many people Well over 500 booked without those that came for a day.I met new and old friends and had so many hugs and returned so many hugs that I felt the whole experience was a celebration of my survival of 7 years with Mesothelioma.

The staff in the Conference hall couldnt have been more welcoming and help Ray and I to find lifts etc etc

International Convention Centre, Birmingham - geograph.org.uk - 1034916.jpg

The whole experience was wonderful and Ray and I will never forget one minute of it

A Dairy Of A Mesowarrior Living With #Mesothelioma Keytruda drug Day and The 10th Birthday Party Of The Royal Marsden DDU

It was drug day yesterday so we travelled up the M25 and it wasn’t a bad journey as I was dreading a Friday.

I sat in the waiting room and then went and gave my bloods and chatted with the Doctor who went through everything and had already ordered my drug for me.

She said as it was number 50 and I only had 2 more to go. It was explained that I wont be left on my own, that I will have a scan every 2 months and IF the Mesothelioma came back then I could have the drug for 1 year. So I have this as a back up plan.

I asked all my questions and had answers so Im very relaxed about the ending of the trial.

Off we went for breakfast and Ray and I walked to find where they were holding their 10th Anniversary Party that evening. So we just sat in the waiting room back at the Drugs Development Unit and Oak ward.. I was called in early and my wonder drug was soon running through my veins.

We waited around and then walked to the 10th Birthday Party to meet everyone for the evenings fun.

I was able to chat to so many of the staff that have been involved with me through my journey in the last two years and everyone was so Excited about iMIG and all I had achieved there. No one was cross that Dean and I had announced to the world my wonderful news.

They were all so thrilled and loved the video of my speech on the stage. Im so sorry that the quality was not good but it was just all we could do and I hope that someone has recorded it better and will send it to me.

So I had a great time

The Agenda for the DDU Open Evening is as follows:

4:30 pm Arrival

5:00 pm Welcome and introduction by Dr Shelley Dolan, Chief Nurse who told us how the Unit started with just one trial.


5:05 pm Opening speech by Prof Johann de Bono, Director Drug Development Unit My hero told us all about trials and patients and how Gary Lineker had opened the Unit 10 years ago.


5:15 pm Experiences from patients and staff



I have met these lovely Patients they spoke so well tonight

5:45 pm DDU exhibits and meet the team

6:50 pm Closing speech by Dr Udai Banerji, Deputy Director

We had to go home as they were running late at this point but I had a lovely long chat to Dr Udai Banerji


The photo of the night was my Nurse Rex and his lovely family


The Oak Foundation Drug Development Unit is one of the largest facilities in the world dedicated to testing new cancer therapies. Over the past year, almost 300 patients entered early clinical trials to test a whole range of new drugs and treatments. The unit is based at The Royal Marsden’s Sutton hospital, where it conducts trials that will lead to the development of new cancer medications and stretch the possibilities for future cancer treatments. It has been ranked ‘double outstanding’ by Cancer Research UK.

Innovation in cancer research

Recent breakthroughs include abiraterone, a groundbreaking drug that targets aggressive prostate cancer, and the first ever trial with a new agent that could offer more targeted treatment for ovarian cancer. The unit also conducted an important study comparing the effectiveness of CT and MRI scans in detecting cancer in blood vessels.

In recognition of their life-changing work, a multidisciplinary team from The Royal Marsden and The Institute of Cancer Research, led by Professor Paul Workman, received the prestigious Team Science Award from the American Association for Cancer Research (AACR) in April 2012. This was the first time it had ever been won by a team from outside the USA. The AACR said its decision was based on “the tremendous impact this team has had in preclinical and clinical studies of cancer therapeutics”.

The post of one of the members of this team, Dr Udai Banerji, is funded by The Royal Marsden Cancer Charity.

Phase 1 clinical trials

Professor Johann de Bono, Professor in Experimental Cancer Medicine, had this to say: “The unit enhances our ‘bench to bedside’ approach to treating patients. It is specifically designed for Phase I clinical trials. There are ten inpatient beds, five treatment chairs and two outpatient suites, as well as laboratory facilities and a seminar room. We are benefiting patients by offering them access to more than 30 trials.”

Your support

The Royal Marsden Cancer Charity raised £2.8 million for the Oak Foundation Drug Development Unit which opened in February 2005.

Support The Royal Marsden and you’re investing in a future beyond cancer for you and everyone you know.


– See more at: http://www.royalmarsden.org/drug-development-unit#sthash.suL1s4Ya.dpuf


Our Speeches We gave at iMIG Mesothelioma Uk Patients and Carers Day

Rays Speech

After Mavis had twisted my arm into talking to you today
I put together these notes.
So This is my brief account of how mesothelioma has impacted on me.
It started 7 years ago in 2009. After returning from a 3 month stay in spain
Mavis began having breathing problems.
An urgent appointment with our GP and An emergency admission was quickly arranged
This was to be the beginning of 7 years of heart ache.
A diagnosis of Mesothelioma was made.
We were told its Terminal there is no Cure.
Prognosis was around 3 months.

That’s 12 weeks. 12 short weeks. Can you imagine how that news exploded in my brain.
We had been together 52 years . since Mavis was 15 years old we have grown up together.

Now something that I unwittingly brought home on my clothes over 50 years previously was going to be my thank you for all those years
Her death sentence..

So now I became Mavis`s carer

I don’t have to tell you what this insidious disease can do.
We were never told that it was dangerous never given protective clothing.
In shipbuilding It was just an every day substance that we worked with , worked around. And worked amongst.
I am sure that if we were told Wow watch that stuff it could kill you. Most of us would have run a mile.

This mental pain has been with me through 4 different chemo regimes . and 3 trials and a pleurodesis.
I was Powerless to stop it or make her pain go away. Can you imagine how useless that made me feel Watching the person you love the most slowly dying.

Some time later an avenue of hope was offered
a trial in Maidstone
But this was cut short After a few sessions It did not work
It was such disappointment
Next a last chance offer of a trial in London.
Several more weeks of consultation and tests and biopsies only to be told sorry you do not fit the criteria.
Devastated we were referred back to our Local Hospital for one more go at chemo.

You know the score A 12hour day connected to a bag of chemo every 21 days for 10 months.
Each infusion gave us about 10 days of sickness with her head down the loo.
Then 10 days recovering only to start over again.
At the end of those 10 months a scan .We get the news
sorry its just not working Your tumors are growing again.
We have nothing else we can give you.

Go home and do what you need to do.
Stunned silence. Followed.

But Mavis was not prepared to sit back and just die. She said I will not accept this.
She set out in search for something else.
She is heavily involved as a mesowarrior and in helping fellow sufferers By doing this she has many contacts
Now due to a chat with Prof Dean Fennel with whom she had become friends ,he advised her to talk to the Royal Marsden As there was a trial geared to mesothelioma.
It took a few more agonising weeks But We travelled to Sutton to speak with prof De Bono. MORE Agonising weeks passing in which I could only sit and watch her condition deteriorating fast.

She was by now in a bad place. Unable to walk ,supported by a walking frame and sticks. Constantly falling over. On one occasion she fell flat on her face on the pavement. Her glasses smashed narrowly missed her eye as the stem dug deep into her face.
Our Dog just sat down beside her watching. I am sure he was thinking this is not the place to sleep mum.
We ended up in the accident centre for treatment. She then had to explain to friends where she got the. Black eyes and scars.

. . Eventually the Marsden letter arrived YES she had been offered a place on the mk 3475 trial now known as the keytruda.
We can start in May 2014
Without going into detail it was an infusion every 2 weeks and would last for 2 years.
We are now only weeks away from the end of that 2 years. You can see for yourself how well Mavis looks. Yes she still has issues
Lots of Meso and chemo damage she has suffered is not visible or repairable.

During this trial each scan result had good results with various degrees of shrinkage or stability. Up to August 2015 we were so happy with 80% shrinkage.
We were un prepared for The scan results we had in November 2015 they were stunning.

Quote” Some of your tumors are no longer visible and those that remain have shrunk to 1mm or less. And those tumors show NO evidence of mesothelioma.

OMG that’s the best news we have had in over 7 years .

Continuing with fortnightly treatment and a further scan in January of this year. The results which we were dreading because Mavis said This good news cant continue. But the results were NO evidence of meso and no additional tumors visible.
Fantastic News
Once more we continued with treatment
Now today I can bring this ,journey up to date
The latest scan results taken on 19 April only a few days ago show
It was described as THE PERFECT RESULT.

That’s a nice way of saying Remission.

Now we hope to live the rest of our lives in happy cancer free days.
And now to end this journey on a lighter Note:
During this period of becoming a Carer.
I have become quite domesticated.
Those bits of crockery sitting in the bowl . I can now wash them up.
Not only did I find a hoover in the cupboard I can work that too.
I have mastered the washing m/c and the tumble drier.
Top of my domestic degree is using the microwave.
But saving the best till last. I began learning to cook
now for me that was worth a cap and gown.
My general housework skills now are second to none.
My diploma must be imminent.
I now just want to conclude by adding my eternal gratitude to ALL the Doctors and nurses that we have met along this journey . my heart felt thanks is un measurable.

They will never fully know how grateful we are for our treatment. Without your dedication Mavis would not be standing here today.
Bless you. All.
Finally I have a special thank you to Peter Rawlings from MSD .
The company that made the Drug Keytruda.
Thank you Peter to you and your team, for without the intervention of this wonder juice The Doctors and Nurses could not perform this miracle . And Mavis wouldn’t be here.with me today.
Thank you Peter

So! This is How Mesothelioma has Impacted on Me.

Now I thank you all for listening to my journey today



Mavis IMIG Speech
Well You have just heard rays account of how mesothelioma has impacted on him as a carer.
Obviously it impacted on me also But in a different way as the victim.
So I wont repeat the details he gave you.

To date I have had 49 infusions with just 3 more left to complete this 2 year trial On keytruda.
My body feels a mess as the drugs have taken their Toll. The drug is not designed to repair the damage done by years of chemo and the previous 5 years of Mesothelioma.
I am left now after 7 years with a 3rd of my lung gone . I have neuropathy and edema.
But Hey I am here I am alive after 7 years fighting .
A bit better than the original 3 months I was given.

Its been a long fight dealing with the meso and also trying to find trials. But I have done it and I have also shared this information with other meso warriors through my help groups
In a strange way it has filled my days with work I would never have dreamed of before this disease struck. I run several groups on facebook .I run a blog that has reached over 3 hundred thousand hits. I have a website onestopmesothelioma . I am a NHS patient rep. I am The Patron of Hazmat Pro. I have been invited to speak on several occasions in the House of commons. I have been invited to speak at many forums to highlight and raise awareness of the dangers of Asbestos and the plight of mesothelioma sufferers..

I also have published 2 books taking you on my journey with this disease. I am a mesowarrior was my first one followed by 5 years a mesowarrior. Book number 3 is a work in progress.The list goes on. I don’t know where I find the time to be ill.

I have made so many friends that I would never have had .
I have just come back from a mesowarriors gathering weekend.
Where we all met in a Holiday caravan Park.
By using my help groups I have helped and guided many sufferers to fill trial places at St Barts on the Trap Trial
and also The Royal Marsden for a small MK3475-158 Trial

At a recent meeting with MSD I have pleaded with them to expand this Trial. Explaining that there are many more patients desperate to fill the limited number of places.

These new imunotheraphy Drugs are ground breaking and are the way forward .But it must be remembered Chemo stills plays a big part , it sets the ground and hits back the meso to give you time to find Trials.
You will hear me time and time again Saying this ,as you will need time. Chemo gives you that time,.
Also Chemo in a combination with a drug The drugs do need a little help. So much hype has been caused by Keytruda but we must give the drug companies time.
That’is easy for me to say I know ,but trials are the only safe way to monitor our new drugs ,but when there is a glimmer of success lets use fast track and The Satchi Bills vehicle to get them out to us ASAP.

We sufferers of mesothelioma are like no other cancers. We have been done a huge wrong.by generations of governments. Who knowingly put greed before lives. Now lets get it right for the mesowarriors that are being diagnosed now and tomorrow. Let the government stand up and fight with us to end this misery.To give us back some of what they have stolen of our lives.
It will be decades before we see a decline in victims . Its not to late to put all their efforts into 100% help for us and future victims.
Don’t believe them when they say it has now peaked.It has not peaked it is still rising.
It is often stated that mesothelioma is rare. Well Its not rare as often quoted. Its an Epidemic of huge proportions around the world.
IF All mesothelioma patients around the world who are on or have been on Keytruda trials were to talk openly about it . And Share their story. This action alone will help to feed the statistics. All of which can assist drug companies to improve and innovate.
Events like this one today certainly help to spread the word.
I am greatfull for the opportunity to speak here today.

If anyone has questions about keytruda please see me and I will try to answer them.