Thread: Labels, etc
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Old 06-07-2008, 08:17 AM
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In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default There is a war on and we are in the middle of it

Power is a funny thing. Fascinating to watch. Intoxicating to experience. Addictive if overly indulged.

At one time medicine was an art and was only too aware of its limitations. Over the last 100 years it has repositioned itself as a "science" and, lulled by the success of antibiotics, become convinced that it is all a matter of chemistry. The unconscious assumption is that combating illness is synonymous with promoting health.

Where once a healer learned humility as a basic tenet of her training (it was usually a woman) now a doctor learns arrogance (and is usually a man). This is particularly true in the specialties and less so at the level of the GP. Many of them are still healers. One of the best things we can do is to find a good GP. At times I am tempted to drop my neuro altogether.

As for the "faith" group (and society itself) the supposition is that the afflicted failed and the fact that we are social creatures is ignored. If they looked at it as a failure of the group itself (or the society) to provide the support the patient needed to maximize her health, then they would be in the uncomfortable position of having to do something themselves.

....Wher's my coffee?...

Quote:
Originally Posted by lindylanka View Post
.... as well as having to deal with what I can only describe as severely unkind group dynamics within her faith group. .... with a letter to her GP, which said no further follow up was needed, and using a term she did not understand describing her diagnosis, and not the name of the condition she has.

I looked this term up - it seems to be a modern euphemism for what in previous times was called hysteria, or illness of psychiatric origin. Her GP has discussed the letter with her, and is outraged by it. ....

I would be interested to know whether anyone here has encountered a sort of institutionalised judgmentalism that seems as potent as racism, or misogyny, especially as with this particular diagnostic slot more than 2/3rds of people who acquire it are women, - one of the 'symptoms' is being knowlegeable about ones own condition, and the medical terms that describe it..........!!!!

I suppose that I am asking about this here for a few reasons:

1. That most of us here DO have this well-informed pro-active attitude to our equally difficult to diagnose neurological condition, and perhaps this medium, the internet, is actually challenging empirical medicine and its methods of discussing illness/disease.
2. That from what I have read here there are quite a few of us who have had doctors try to give a psychological explanation for our symptoms.
3. That neuros, specialists, doctors, etc. in being able to use such labels (and they are NOT psychologists or psychiatrists) and put them on record, sometimes, as in this case, with only a very passing acquaintance of the patients medical history, which can then colour the views of any other medical personnel. and influence any future treatments.
4. That people of a certain age may be viewed as being in some way not competent about their own lives, health, decision making, and may be put into this particular box AT ANY TIME, regardless of whether they are actually showing signs of the mental health issues that may accompany aging, or simply are stressed by events in their lives.
......
6. That neurology seems to have an inordinate amount of male professionals, at least in my neck of the woods! (sorry, all you reasonable males out there)

Just to add to this, my friend IS showing signs of a deterioration in her health, and is quite frightened by it as she is only rarely experiencing any full remission - this is manifesting as high anxiety, with a sort of desperation, and her hospital experience just heightened it. She is on a rather heavy drugs regimen, including some pretty potent pain relief medication, that seem to have side effects such as a very unusual level of forgetfulness, and sometimes some confusion. These go away as medication is reduced and her condition improves.

As an adjunct to this whole situation one of the issues with her faith group was a group belief that illness and disease are not 'real', that in some way you make it for yourself, and she was marginalised in this group for not being able to make herself well again. This does not actually reflect what her faith teaches, and was a very full on and difficult experience.

I am sorry if this has been a bit long-winded, but it has raised so many issues for me, and to be honest I am struggling with my own feelings too, as I know how demoralising it is to go through the daily grind of living with a long term condition and all that it entails, only to have someone who barely knows you imply all that limitation and frustration, pain and genuine disability is some kind of self inflicted subconscious lie.

I would be grateful for any insights, I know not all health professionals are like this, and that there are plenty of good experiences, and good doctor patient relationships too.

Lindy
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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