Julia
In Memoriam
- Joined
- 10 May 2005
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herzy, thank you for your comments and your own experience which seems like a pretty objective personal insight.
This, inter alia, says
All very vague and I'd be very surprised if it were to be peer reviewed or printed in any substantial journal.
I might, of course, be completely wrong.
(I also had glandular fever at age 16, with the resulting post-viral symptoms you describe, off school for more than a year and intermittent recurrences of the acute phase for more than two years afterwards. Since then any significant viral infection will result in the same syndrome, biologically demonstrated by significantly elevated liver enzymes which lead to the conclusion that it is in fact a biological disorder, rather than one which is purely psychological.)
Of course, psychological repercussions would seem to be a pretty normal response to months of feeling sick, loss of appetite, fevers and chills, and minimal energy.
One I consulted about the repetitive nightmares emanating from PTSD had the profound suggestion "just think happy thoughts when you turn out the light!"
Right. Could have got that from "New Idea" or the "Women's Weekly" for a couple of dollars.
I like the AA philosophy of worrying about only the things about which you can effect a change, but it's easier said than done.
Thanks again for such an interesting post, herzy.
I should probably also qualify my comments with the effects of having worked for many years in the multinational pharmaceutical industry, including very short stays with two major companies because of ethical differences. There are absolutely companies which have sound ethical frameworks, but rather more which will manipulate data and interpret results to their own ends.
One of the very real problems (unless it has very recently been established) is that there is no such thing as a central register of drug trials. No requirement for any researcher to - when engaging on any sort of study - register details of that study so that it can later be followed up in terms of results.
As a consequence, drug companies can and do simply junk trials that do not elicit the results they seek.
They might do ten trials which all show unacceptable side effects of their potential new drug, just obliterate them as though they had never happened, and then widely publicise any trial which shows their product in a favourable light.
A simple register of all trials with full results of each one would give a much more clear and authentic framework for the prescribing community.
This may be of interest - but it's very far from being hard science. http://www.iol.co.za/lifestyle/blood-test-may-help-diagnose-depression-1.1754474#.VCZPt51--70
This, inter alia, says
As you say, it's not any sort of hard science. 32 patients are not statistically significant and neither do we know anything about the methodology. Further they say they have 'identified nine chemicals in the blood which are raised during depression' but do not list these chemicals. Then they claim to have devised a blood test which measures just three of these nine chemicals.scientists from North Western University in Chicago say they have identified nine chemicals in the blood which are raised during depression.
They have devised a blood test which measures three of these chemicals to diagnose depression.
The researchers measured chemical levels in the blood of 32 patients with severe depression and compared them to 32 non-depressed individuals.
All very vague and I'd be very surprised if it were to be peer reviewed or printed in any substantial journal.
I might, of course, be completely wrong.
Which is possibly going to predispose you to think about inheriting the genetic disposition toward depression?I have a family history of depression and come from a fairly neglected childhood.
Very common, and used to be called 'post viral syndrome' often subsequently interchanged with 'chronic fatigue syndrome' for no particularly good reason that I've ever seen documented.When I was 17 I got glandular fever, which knocked me out (left me depressed, demotivated and exhausted) for about 6 months.
(I also had glandular fever at age 16, with the resulting post-viral symptoms you describe, off school for more than a year and intermittent recurrences of the acute phase for more than two years afterwards. Since then any significant viral infection will result in the same syndrome, biologically demonstrated by significantly elevated liver enzymes which lead to the conclusion that it is in fact a biological disorder, rather than one which is purely psychological.)
Of course, psychological repercussions would seem to be a pretty normal response to months of feeling sick, loss of appetite, fevers and chills, and minimal energy.
Good for you. A long time ago before many of the current terms were adopted, there used to be in the literature a clear differentiation between 'reactive depression' and 'endogenous depression'. ie perfectly rational to feel depressed when unwell and not seeing a resolution to that, and a sense of misery for no discernible reason.I found it impossible to get out of this negative sphere, and was quite depressed (but able to recognise that it was - hopefully - a temporary state, and was therefore not suicidal).
Some are a waste of time and money. Others are thoughtful and very helpful.I started seeing a psychologist but found that entirely useless.
One I consulted about the repetitive nightmares emanating from PTSD had the profound suggestion "just think happy thoughts when you turn out the light!"
Right. Could have got that from "New Idea" or the "Women's Weekly" for a couple of dollars.
Glad to know it worked for you.I started antidepressants (and went on exchange) and stopped taking them a few months later. I thought they were great, and have a personal theory that post-glandular I had a chemical imbalance / consistently lowered serotonin (this can also happen during traumatic events) which became the new 'baseline'/normal level. As such, the SSRIs were great for re-establishing a 'normal' level, and cognitive behavioural therapy relatively useless.
Sounds like a very thoughtful conclusion and not too dissimilar to my earlier expressed notion of minimal expectations of "happiness".I do think my case is rarer though, and psychologists are generally a MUCH better solution than SSRIs. I still feel like my default state is 'unhappy', and that it actively takes effort for me to be neutral or happy (although I am most of the time). I wouldn't classify myself as depressed any more (by any means) but rather as having a tendency towards depression.
+1, yes very much so.I think things like social support, being outside as much as possible (and as physically active as possible) are essential. These things have consistently been proven to be immensely good for health.
Again, a thoughtful and realistic comment. I think you're right. If we are involved in pubs, pokies and partying we will perhaps be less disposed to be concerned about global and national worries.I do also feel like more intelligent people tend to 'think' more about the world, and that given how many bad things there are in this world (climate change, humanitarian crises, etc - pick your poison), it's impossible not to take this to heart to some extent. That said, that might just be because of my depressive prism - I'm not sure.
I like the AA philosophy of worrying about only the things about which you can effect a change, but it's easier said than done.
Thanks again for such an interesting post, herzy.
I should probably also qualify my comments with the effects of having worked for many years in the multinational pharmaceutical industry, including very short stays with two major companies because of ethical differences. There are absolutely companies which have sound ethical frameworks, but rather more which will manipulate data and interpret results to their own ends.
One of the very real problems (unless it has very recently been established) is that there is no such thing as a central register of drug trials. No requirement for any researcher to - when engaging on any sort of study - register details of that study so that it can later be followed up in terms of results.
As a consequence, drug companies can and do simply junk trials that do not elicit the results they seek.
They might do ten trials which all show unacceptable side effects of their potential new drug, just obliterate them as though they had never happened, and then widely publicise any trial which shows their product in a favourable light.
A simple register of all trials with full results of each one would give a much more clear and authentic framework for the prescribing community.