You started by saying the NHS has poor outcomes for cancer (I agree) and that the reason was because the NHS does not use modern meds.
I counter - pointing out that the problems are at the diagnosis end.
You respond with a comment about the five year survival rate of innovative med.
I tell you that those meds are used within the NHS, and ask for an example med that is not used within the NHS. I give an example of how there are inefficiencies in the diagnosis end.
You post a link that doesn't mention meds; does mention delays in diagnosis and treatment. You still haven't posted an example of a cancer medication that provides good outcomes that is not used in the NHS.
Your little dig about referal times is weird. What do you think the referal times are? There is a legally enforced maximum 2 week time from GP referral to see a cancer specialist.
> Patients with urgent conditions such as cancer and heart disease will be able to see a specialist more quickly. For example, you have the right to be seen by a specialist within a maximum of two weeks from GP referral for urgent referrals where cancer is suspected.
You appear to have a political ax to grind. That would be okay if you weren't spreading lies and misinformation.
EDIT: you made an antiNUS documentary? You don't think that's the kind of thing you should mention? I'd be interested in fact checking it because, looking at this thread, you probably made a right fucking mess of it.
PS I don't know what documentary you are talking about? I have never created a documentary on the NHS. Certainly not any documentary that was "Anti-NHS" That is a patently falsehood.
I did work a documentary on Rheumatoid Arthritis patients across Europe, not just the UK and not focused on health systems. The patients experiences with their respective health service were out of scope and not on screen. I did however speak with them at length on the subject. Before you go casting about accusations please have some rudimentary idea of what you are talking about.
The NHS patients we met with each mentioned that in order to see a specialist on a timely basis they had to get private insurance after which their months longs waits dissolved to days. A close friend who was a staunch defender of the NHS after being diagnosed with MS has soured on the program and has also secured private insurance for specialist access. In another instance a young woman with a bowel perforation secondary to Crohn Disease has been waiting for at least two months to have surgery scheduled. Yes, yes I know anecdotal experience and all that but I guess it's just a poisson distribution that everyone I've ever known met or heard of that has needed specialty care from the NHS has gone the route of private insurance for access to specialists.
Take a close look at the quote from the article I posted with the prefix "Note:" and then sound it out. Use your vowels and note that it VERY CLEARLY states that one of the problems is "poorer access to treatment".
If you want to go on a formulary hunt to see which drugs are not paid for by the NHS that are recommended under NCCN guidelines or spend your night frothing over pubmed searches be my guest.
PS I have no axe to grind. I'm not the one bringing profanity and personal accusations into this. You don't know me. You clearly have no clue about my politics but are clearly incensed that someone deigns to take issue with the NHS. The bottom line is that patients are dying sooner in the UK than elsewhere. If that is okay with you then great, I'm just saying as a personal opinion informed by my reading and personal experiences that it is not a system I would choose to live under or advocate the adoption of in my country.
If you are happy with the health care system in your country that's great.
> You have the legal right to start your non-emergency NHS consultant-led treatment within a maximum of 18 weeks from referral, unless you choose to wait longer or it is clinically appropriate that you wait longer.
> If you want to go on a formulary hunt to see which drugs are not paid for by the NHS that are recommended under NCCN guidelines or spend your night frothing over pubmed searches be my guest.
You made the claim, you should back it up. You said that poor cancer outcomes on the NHS was caused by lack of access to new cancer meds. Your inability - over four posts - to name any drugs that are not available on the NHS is telling. Your choice to support your claim with an undetailed BBC report is odd. It certainly doesn't say what you think it says: poorer access to treatment is exactly what I describe in edit2 above.
> Yes, yes I know anecdotal experience and all that but I guess it's just a poisson distribution that everyone I've ever known met or heard of that has needed specialty care from the NHS has gone the route of private insurance for access to specialists.
What's your sample size? How do you counter the fact that there is legally enforced maximum waiting times in the NHS?
> but are clearly incensed that someone deigns to take issue with the NHS.
I criticise the NHS, in this thread. I am angry that someone continues to lie about the NHS, even after their lies have been debunked.
Check the Anger. This is an academic exchange of ideas. If you are angry go to the gym it's better for you.
A. You have debunked nothing.
B. There are no lies here.
C. Just because some random guy on the internet tells me to do something, I am no obligation to do that.
D. "Access to treatment", could mean the moon is made of green cheese but it is unlikely.
E. Since you are angry about it, cite specifically the the formulary content of the NHS and compare it to available treatments at Sloan Kettering. Since your so convinced it's true, prove it. (two can play at that)
F. Support you assertion that novel treatments only extend life by "a few months" with multiple citations from peer reviewed journals, oh and make sure their recent.
G. As far as the legal mandates. I am sure that everything in the UK is done exactly to the letter of the law in all cases and that deadlines are never missed.
H. You're assertion that closing the two week gap between when the GP starts testing and the specialist would start testing would close the mortality gap between the UK and Europe strains credulity and common sense.
"A cancer drug hailed as one of the biggest breakthroughs since chemotherapy will not be made available on the NHS, despite research showing it doubles survival"
I counter - pointing out that the problems are at the diagnosis end.
You respond with a comment about the five year survival rate of innovative med.
I tell you that those meds are used within the NHS, and ask for an example med that is not used within the NHS. I give an example of how there are inefficiencies in the diagnosis end.
You post a link that doesn't mention meds; does mention delays in diagnosis and treatment. You still haven't posted an example of a cancer medication that provides good outcomes that is not used in the NHS.
Your little dig about referal times is weird. What do you think the referal times are? There is a legally enforced maximum 2 week time from GP referral to see a cancer specialist.
http://www.nhs.uk/choiceintheNHS/Rightsandpledges/Waitingtim...
> Patients with urgent conditions such as cancer and heart disease will be able to see a specialist more quickly. For example, you have the right to be seen by a specialist within a maximum of two weeks from GP referral for urgent referrals where cancer is suspected.
You appear to have a political ax to grind. That would be okay if you weren't spreading lies and misinformation.
EDIT: you made an antiNUS documentary? You don't think that's the kind of thing you should mention? I'd be interested in fact checking it because, looking at this thread, you probably made a right fucking mess of it.