When a doctor goes
home at the end of a day, I presume he doesn’t take his work with him, or at
least he shouldn’t for his own sanity and the sake of his family. But for a
doctor to fully understand what it means to live with a chronic disease, he
needs considerably more time than the short allocated slot in a regular
patient/doctor visit.
It’s all very well
comprehending the mechanics of a disease, but can a doctor appreciate the quiet
desperation of a patient who is clutching at straws, ready and willing to try
anything that might eradicate what ails them? A doctor would have to step into
some pretty uncomfortable shoes to get a glimpse of, or understand fully what it’s like from the patient’s perspective.
In the short time
allocated during a visit to a doctor, an awful lot, possibly too much, has to
be accomplished. The seemingly less important factors often get dropped by the
wayside, which are either brushed aside, or dealt with through another channel.
I should imagine for many doctors it’s frustrating not being able to help
adequately and improve quality of life when treating Parkinson’s patients.
Ultimately I'm sure this makes a doctor’s job far from satisfying and is not the reason
why a doctor chose such a vocation.
Although the present
system and medications leave room for much improvement, progress slowly but surely from both doctors
and patients is being made and hopefully participatory medicine is the way of
the future. Take a look at this clip, “From God to Guide” which you may have
seen before, but is well worth watching again.
I've recently added swimming to my weekly routine, but have come up against some strange reactions. To read more take a look at my article in The Huffington Post.
I've recently added swimming to my weekly routine, but have come up against some strange reactions. To read more take a look at my article in The Huffington Post.
No comments:
Post a Comment