Hi @trenteliason i hope someone has already let you know about the Voices from the Shadows project here in the UK and all interviews they did a few years ago but I thought I’d post a link for you just in case
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What Doesn't Kill You [Forthcoming Documentary]
- Thread starter forestglip
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The rise and rise of the psychosomatic cult is the greatest and cruelest catastrophe in modern medicine.
If you can only get one message across in your film it is that patients are not the problem here. It is the medical profession, and broader governance, that have so grotesquely failed us, and are continuing to do so, with their pathological obsession with forcing psychosomatic/behavioural non-answers on us.
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Ravn
Senior Member (Voting Rights)
Welcome @trenteliason, great to see you here and engage. You come across as someone who wants to get this right and is sensitive to the issues
Speaking of sensitive, I’ve listened to a couple of the TikTok accounts and they highlight an extremely sensitive and tricky issue to navigate: the balance between letting people tell their own stories in their own words while not perpetuating misinformation
Many pwME - and some prominent ME doctors and researchers - have very definite and deeply held ideas about what ME is, in their mind: it is autoimmune, it is viral persistence, it is neurological, it is metabolic, it is this, it is that. Trouble is the science isn’t there yet, nobody knows what ME is (the real scandal here is that we haven’t had enough rigorous research to figure it out)
Similar for all the things people believe helped them. Some of these may be accurate observations albeit not necessarily generalisable from that individual, others may be cases of desperate people deluding themselves. In many other illnesses this wouldn’t matter too much but in the context of ME things are more delicate
In the ME context phrases like ‘it helped me’ or ‘important for the healing journey’ are not innocuous and neither are many of the recommendations by some of the prominent ME doctors. Often anything any pwME reports ‘helping’ is seized upon - by other pwME or the people around them - as something other pwME must try because maybe, just maybe it could improve the illness itself (rather than just help cope with it). The actual 'remedy' may be harmless enough - though some are not - but the endless pressure to chase yet another false hope can be noxious. It also places all the responsibility for finding solutions on the individual rather than where it belongs, i.e. the research and medical systems
The best solution here may be to avoid those two areas as much as possible and instead focus on the way people experience their illness, or caring for a pwME, including the impact of being left to fend for themselves, largely abandoned by the systems that are supposed to help. As a bonus that would also make the movie more emotionally impactful. Going by your posts that seems to be broadly the line you’re trying to take. I look forward to the result
Speaking of sensitive, I’ve listened to a couple of the TikTok accounts and they highlight an extremely sensitive and tricky issue to navigate: the balance between letting people tell their own stories in their own words while not perpetuating misinformation
Many pwME - and some prominent ME doctors and researchers - have very definite and deeply held ideas about what ME is, in their mind: it is autoimmune, it is viral persistence, it is neurological, it is metabolic, it is this, it is that. Trouble is the science isn’t there yet, nobody knows what ME is (the real scandal here is that we haven’t had enough rigorous research to figure it out)
Similar for all the things people believe helped them. Some of these may be accurate observations albeit not necessarily generalisable from that individual, others may be cases of desperate people deluding themselves. In many other illnesses this wouldn’t matter too much but in the context of ME things are more delicate
In the ME context phrases like ‘it helped me’ or ‘important for the healing journey’ are not innocuous and neither are many of the recommendations by some of the prominent ME doctors. Often anything any pwME reports ‘helping’ is seized upon - by other pwME or the people around them - as something other pwME must try because maybe, just maybe it could improve the illness itself (rather than just help cope with it). The actual 'remedy' may be harmless enough - though some are not - but the endless pressure to chase yet another false hope can be noxious. It also places all the responsibility for finding solutions on the individual rather than where it belongs, i.e. the research and medical systems
The best solution here may be to avoid those two areas as much as possible and instead focus on the way people experience their illness, or caring for a pwME, including the impact of being left to fend for themselves, largely abandoned by the systems that are supposed to help. As a bonus that would also make the movie more emotionally impactful. Going by your posts that seems to be broadly the line you’re trying to take. I look forward to the result
You have expressed that really well @Ravn. If a filmmaker is wanting to add some credibility to patients' claims of pain and hardship, the obvious people to go to are clinicians. There are ME/CFS specialists who will certainly talk to that subject, often very convincingly, but unfortunately almost all of them are offering diagnoses and treatments that are far from evidence based. Even if the film doesn't use footage of them talking about treatments, their presence in the film is effectively an endorsement of the treatments they offer to their patients.
Many of the acronym co-morbidities that you will hear people saying they have been diagnosed with are disputed - MCAS, POTS, hEDS... It's not that the symptoms that people have should be disputed, definitely not, rather, it's the labels that imply knowledge of the causal mechanism. We just don't know yet what is causing the illness.
Incidentally, that's one of the reasons why the Netherlands film project showing doctors who are now ill themselves worked well - they brought medical authority but also illustrated the shock of realising that lots of people have a horrible illness that no one knows much about.
Even then, doctors who come down with ME/CFS are not immune from grasping at the hope that causal diagnoses and treatments seem to offer. Pretty much all of us have done it at one time or another, believing that a particular treatment is helping, only to realise sometime later that it probably isn't.
Many of the acronym co-morbidities that you will hear people saying they have been diagnosed with are disputed - MCAS, POTS, hEDS... It's not that the symptoms that people have should be disputed, definitely not, rather, it's the labels that imply knowledge of the causal mechanism. We just don't know yet what is causing the illness.
Incidentally, that's one of the reasons why the Netherlands film project showing doctors who are now ill themselves worked well - they brought medical authority but also illustrated the shock of realising that lots of people have a horrible illness that no one knows much about.
Even then, doctors who come down with ME/CFS are not immune from grasping at the hope that causal diagnoses and treatments seem to offer. Pretty much all of us have done it at one time or another, believing that a particular treatment is helping, only to realise sometime later that it probably isn't.