Living With Mesothelioma -My Diary- Peterborough Motor Home Show, The Royal Marsden Hospital Make Contact FRiday is me Appointment- and The Saatchi Bill is on its way.


We are back home from a great weekend. Wonderful to be with friends and have a great time.

I managed to walk around with my new walking frame and shopping was stored in the bag so that made carrying even easier.

I found people were great and let me pass through but it was hard trying not to trip people up with wheels.

There were many Motorhomes on show but nothing that really took my eye so happy to come home with my Clubman. she has been so easy to keep clean. I enjoyed have a good clean around and cooking in her.

We had a nice morning in the Marquee on Saturday.

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Many cakes were made and laid out to go with coffee.

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We then went around the show and spent some money.

In the late afternoon everyone piled they tables high with food to last all evening.

That was a really nice evening chatting away with friends until we went home to bed for a great sleep

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Sunday morning is breakfast where the cooks love cooking the 840 rashes of bacon 420 rolls. Bless them You can see my friend Jock with his blue gloves on really getting stuck into it. xx

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Sonja Linda and me waiting for the cooking our breakfast.

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Sunday people were going home and that left a few of us to meet up and go to a show.

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Beach Boys Uk were very good

 

Saturday Bee Gees were also very entertaining so a good night was had by all.

Back to the M/Home for the last sleep.

Leslie’s Photos for those people that know me and my friends https://picasaweb.google.com/101332044306934202354/Peterborough2014?authkey=Gv1sRgCKLrnem8ifrUxwE

So we came home today and the journey was very good.

When I arrived home I had two letters from the Marsden. I sat there with them in my hand and burst into tears. I dont do that very often but then I have had official treatment upto now. This is all new Phase 1 trials that I asked for. I was so pleased to be a  guinea pig but when it comes to it, my courage takes a plunge. How silly. Every thing will be explained to me. I think its because it has hit me it could be my last chance.

So Friday  2nd May Im off early to the Royal Marsden.

I have a large form to fill -Patient Pre-Registration Form.–Then a Pre-Attendance Form.  They will be filled up.

I will keep reporting back what goes on.

The Saatchi Bill  closed with more than 18,000 people signing -A great job done by all and Lord Saatchi must be so pleased with that.

The Department of Health’s consultation into the Medical Innovation Bill has closed and we now know that the evidence demonstrating a need for the Bill is compelling.

So far, more than 18,000 people ¬– including patients, doctors, researchers, scientists and charities – have responded to the consultation supporting the Bill, many confirming that they have experienced the deterrent effect that an increasingly risk-averse culture is having on responsible medical innovation.  Lord Woolf, former Lord Chief Justice – highest legal position in England – states why is necessary:  http://www.telegraph.co.uk/news/features/10785352/Saatchi-Bill-your-last-chance-to-help.html

The Saatchi Bill team is grateful for all the comments and input we have received throughout the consultation period. Thank you for your help and support.

All the concerns expressed about the Bill have been heard and a new draft Bill is already in play – it remains true to the core principles of nurturing the innovator and protecting the patient, but is clearer on the process that doctors must go through if they are to innovate safely.

The Bill team will publish a guide showing how the new draft Bill meets concerns expressed by legal and medical professionals. (For those lawyers reading this, it will make it clear that Bolam-Bolitho still stands and that the Bill will not support reckless experimentation).

At the same time, the new Bill will hold fast to our guiding principles. Doctors must be given the freedom to innovate responsibly, with the confidence that the law will protect them if their decision is made with the support of a responsible body of medical opinion and consultation.

They must not be forced to wait until their decision is tested in expensive and traumatic litigation or disciplinary proceedings. Nobody wants that, except perhaps a small group of lawyers who make their living from the existing litigation-focused system.

The Bill will be an opportunity for all those who are concerned that the legal system is not properly serving patients with rare diseases, whose hope rests entirely on innovation.

Patients want to know that every responsible avenue is being explored in order to help them, and that doing nothing is no longer the easy and safe answer.

And patients will still be protected from negligent treatment. A doctor who harms a patient through bad practice or negligent treatment or who makes a mistake can still be sued. Bad doctoring is still bad doctoring and a mistake that causes damage, remains a mistake.

Good doctors must be given the protection and encouragement of the law to innovate safely and responsibly.

And bad doctors must be deterred from innovating without support of their colleagues.

The Bill achieves both aims.

So, what happens next?

Jeremy Hunt promised to pass the Bill into law if the public wanted it. You have spoken and you have said, clearly and in numbers, that you support the Bill.

Civil servants in the Department of Health will analyse the results and then make a recommendation to Jeremy Hunt whether to support the Bill or not.

We are confident that he will.

It will then be up to the Government to find time to bring the Bill before Parliament for debate and to be passed in to law. This should happen before the next election.

The new Bill and the guide will be published shortly.

Rays blog http://mesoandme.wordpress.com/2014/04/28/monday-82/

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