crps247 Complex Regional Pain Syndrome
  • HOME
  • My Story
    • My Story - A Short Version
  • Art About Pain
  • Grief & Identity
  • About CRPS
    • Positive & Negative Words
  • Blog
  • Help & Links
  • FAQ
    • Coping >
      • How is it Treated?
      • List of my Treatments
      • Family & Friends
  • PRIVACY POLICY & DISCLAIMER
    • Spoon Theory & Breathing
  • Thanks to Those Who Help Me

Working Towards Better Doctors: What is Being Done?

11/9/2017

 
Picture
I am a fairly private person or rather I used to be, but it all seems to have changed since publishing this site over 4 years ago. A few opportunities have come my way that probably would not have otherwise happened.

One of these opportunities occurred last year in February. I did not write about it at time as I did not want to be seen as blowing my own trumpet but due to the increasing number of CRPS patients I read about having bad experiences with doctors who are not educated in CRPS and often lacking in empathy I have decide to write about last year’s experience as a patient pain ambassador at the Faculty of Pain Medicine at ANZCA (Australian and New Zealand College of Anaesthetists) in Melbourne.

 Thanks to my doctors’ faith in me to not only turn up but give it my best shot I found myself sitting in front of a room full of doctors who were attending a weekend clinical skills training session, a preliminary to commencing 2 years training to become pain management specialists.

 I had 2 anxieties, firstly ‘what if I went into a massive flare and could not think?’, secondly ‘what if I was so nervous I could not speak and froze?’ Fortunately neither of these things happened and I had no trouble finding my voice!

So what was discussed? Empathy featured strongly and I had read about this topic following a link sent to me by my doctors. When asked if I had any thoughts about empathy I said I believed it was something that you felt deeply inside with the heart and also that it was something you could run out of. The course incorporated a section that covered the need for doctors to prevent burn out and how to look after themselves.

 I was also able to talk about my bad experiences from a bullying doctor and my vulnerability at the time; how in order to be taken seriously by doctors in the past I had learnt to hide my emotions so I would not be judged as an ‘hysterical woman’ and my pain would be believed. Then through my art that was projected onto a large screen I was able to illustrate what my shooting pains felt like to me and the deep physical impact of these pains when severe. Through some of my paintings and drawings I was able to show how I visualise my world, how in my own personal universe severe pain is ever-present, lurking somewhere ready to strike at any moment.

 The end of the session was all a bit a blur, my husband/carer John and I were invited to share a buffet lunch, my doctors seemed pleased with the discussion and I was thanked by many of those in the audience. Upon reflection I believe that from what I read in the weekend curriculum for the course that the general direction of the training is going to produce more empathetic and knowledgeable doctors who recognise the importance of strong doctor patient relationships. We can only hope this is the case and that more of these graduates make their way into the public system to help those who have no choice.
Sharon Munday
13/9/2017 08:04:50

What a great post. I'm so happy you were able to share this with us Ro. We patients rely so heavily on opportunities like this where one of us with this horrible disease can advocate and be a voice. Thank you so much for being so brave to get us there and do your stuff. It certainly gives me hope that the next generation of pain doctors coming through will be getting into this field for the right reasons. They need to be able to hear each and every one of us and find what works for this 1 patient and not just wave their hands and blanket everyone the same treatment. Thank you again for being our voice💜

Rosemary Eagle
13/9/2017 08:47:59

Thank you for your comment Sharon, I really appreciate your thoughtful words. 🌞


Comments are closed.

    Author

    Rosemary Eagle
    I am an artist www.rosemaryeagle.com
    I also have CRPS. The life of CRPS pain & disability and my life as an artist are intrinsically entwined
    . I look forward to your feedback and comments.
    Rosemary Eagle

    Sign up to Receive Blog Notifications

    * indicates required
    Email Format
    Click below to see my  Privacy Policy and Disclaimer

    RSS Feed

    Categories

    All

    Archives

    September 2021
    March 2020
    November 2019
    April 2019
    October 2018
    April 2018
    January 2018
    September 2017
    May 2017
    March 2017
    February 2017
    December 2016
    October 2016
    September 2016
    July 2016
    June 2016
    February 2016
    October 2015
    August 2015
    April 2015
    December 2014
    August 2014
    April 2014
    December 2013
    May 2013

Powered by Create your own unique website with customizable templates.