Originally posted by d000hg
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Reply to: 23andme
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Previously on "23andme"
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I read your post without looking at the authors name and guessed it was you.Originally posted by SueEllen View PostAnd which diseases have massive charity campaigns behind them?
There are more diseases that certain sectors of the population and certain individuals should have checks for but aren't included.
There are also some issues with the current national screening regimes as they are finding a lot of false positives. Also the screening regimes mean there are GPs who are ignoring symptoms in younger individuals due to them not fitting into an age category.
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And which diseases have massive charity campaigns behind them?Originally posted by d000hg View PostWell, women have regular cervical and breast exams, and men have regular bum exams, past certain ages, IIRC? So the frequency of such things could be modulated based on your genes.
There are more diseases that certain sectors of the population and certain individuals should have checks for but aren't included.
There are also some issues with the current national screening regimes as they are finding a lot of false positives. Also the screening regimes mean there are GPs who are ignoring symptoms in younger individuals due to them not fitting into an age category.
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Well, women have regular cervical and breast exams, and men have regular bum exams, past certain ages, IIRC? So the frequency of such things could be modulated based on your genes.
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The NHS isn't generally about preventative medicine unless you fall into one of the groups where there is a massive charity behind you.Originally posted by d000hg View PostI wonder if the NHS or other groups will start doing this as standard one day, to optimise sending at-risk people for more regular scans, etc. You'd think it could save money long-term and improve outcomes.
Apart from the individuals I know whose GPs have refused to do simple blood tests to monitor conditions, there are whole populations they are refusing to screen for certain things due to fears about costs.
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I wonder if the NHS or other groups will start doing this as standard one day, to optimise sending at-risk people for more regular scans, etc. You'd think it could save money long-term and improve outcomes.
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Before you decide to have a gene test : Cancer Research UK : CancerHelp UK
Cover your arse - quick!
Financial considerations
Many people are concerned about getting health and life insurance after having a genetic test. Currently the Association of British Insurers (ABI) and the Government have agreed to a temporary ban on asking people for the results of genetic tests for cancer. This agreement is called a Concordat and Moratorium. The agreement lasts until 2014 when they will review it.
Insurance companies can still ask about family history and may charge more for families with a strong family history of cancer. If you have had a genetic test and it shows you don’t have a gene, you may choose to tell the insurance company.
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I was thinking more about sickness cover and that kind of thing.Originally posted by DieScum View PostYeah, it's really useful.
I'll start having regular checks when I turn 40, as is recommended for those with a family history of it, rather than 50 for gen pop. Previously I had no idea I was a higher risk but it's good to know.
For insurance, I'd probably use the NHS but my private insurance just asks for pre-existing conditions not genetics. If it's ever an issue I imagine other countries would copy the GINA law from the US which forbids insurers from discriminating on grounds of genetics.
When you have a terrible bum condition like me that's heartening.
I suppose a good plan would be to take out a policy, have the test, then cancel the policy if you're not likely to need it!
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Yeah, it's really useful.Originally posted by mudskipper View PostSo do you feel better for knowing that? And what about insurance - can you now get cover for botty cancer?
I'd rather not know!
I'll start having regular checks when I turn 40, as is recommended for those with a family history of it, rather than 50 for gen pop. Previously I had no idea I was a higher risk but it's good to know.
For insurance, I'd probably use the NHS but my private insurance just asks for pre-existing conditions not genetics. If it's ever an issue I imagine other countries would copy the GINA law from the US which forbids insurers from discriminating on grounds of genetics.
When you have a terrible bum condition like me that's heartening.Last edited by DieScum; 24 October 2013, 09:16.
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So do you feel better for knowing that? And what about insurance - can you now get cover for botty cancer?Originally posted by DieScum View PostIt's international human specimen shipping.
For me the cost, including shipping, is incredibly low. It's like living in the future. A future in which I am more likely than most to get bum cancer it says.
I'd rather not know!
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Get yourself off for a colonoscopy.Originally posted by DieScum View PostIt's international human specimen shipping.
For me the cost, including shipping, is incredibly low. It's like living in the future. A future in which I am more likely than most to get bum cancer it says.
SUCH fun.
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It's international human specimen shipping.Originally posted by SueEllen View PostThe fact that if you lived in the US it would be under $110 shows this is rip off Britain.
For me the cost, including shipping, is incredibly low. It's like living in the future. A future in which I am more likely than most to get bum cancer it says.
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