Being Assertive with Healthcare Professionals

Adele
Adeleon Monday, June 15 2015
5 Comments

Hey all,

My stroke experience involved a lot of appointments with healthcare professionals such as GPs, neurologists, neurosurgeons, physiotherapists, ophthalmologists, etc. Sometimes I have felt that there can be a tendency for doctors to rush through providing information or not provide enough information for me to make an informed choice or feel that my needs, wishes, feelings and beliefs are not heard. To help me make the most of my appointments I like to write down any questions that I have, take notes and repeat back what I have heard to check that I have understood their meaning. Are there other strategies that you use to make the most out of your appointments? Here's a link on how to be assertive from Better Health Channel.  http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/assertiveness

5 Responses

Hi Adele, that's a really good strategy, so long as you remember to look at your notes.  I try to make sure I'm only dealing with one issue at a time with the doctor etc. or I go in with a list and make sure it's all done before I leave.   I still forget things by the time I walk out of their office.  I've found getting the health professional to write things down for me helps.  And repetition is needed before I remember reliably.

Post stroke The list is your friend.  I do this for my work schedule too.  I have a monthly to do list in excel that I colour code at the end of each day with comments on what's still to be done if needed.  That's work not doctors etc.  but it would work for both.

-Heather

Hi Adele,

Great resource you've added on assertiveness. I have many callers to StrokeLine who feel uncomfortable being assertive if they aren't used to communicating this way. It is essential though to get your needs heard and met. Everyone has the right to accurate information and have it explained in a way they can understand.

The My Stroke Journey resource has some useful sections to write down questions and names of health professionals depending where you are at in your journey. See page 15-20 and page 24. https://strokefoundation.com.au/what-we-do/support-programs

The Post Stroke Checklist may also be helpful for some, again depending on where you are at in your journey. https://strokefoundation.com.au/what-we-do/support-programs

Jude's blog is a fantastic resource as are lists as suggested by Heather. Writing things down, using the notes in your phone and other 'to do list' apps with reminders I find helpful in my own life and reduce stress and overwhelm.

Simone (Occupational Therapist for StrokeLine)

This post is very interesting and helpful. My mother in law used to use her phone to record doctors meetings but she wasn't always allowed to do so. My advice is to seek permission to record a meeting in advance, and explain why you want to do so. Also, taking another person who takes notes during the meeting is helpful, I have not have a stroke myself, but when I go for appointments, I often ask my partner to take notes about what was advised/said in a meeting (e.g. physiotherapy session where I'm given exercises to do that Im likely to forget).

This post interested me a lot. I have found that there is no real one stop shop and dependent on where you are at and what you want to focus on will depend on what and who you should deal with. I know that I don’t take no for an answer and I can see that others too have experienced what I have. I have written a stroke diary which not only includes my thoughts and fears but also notes about what therapy and contacts I’ve made so that if I should want to go back and focus, say for example on my balance (at the moment my focus is getting my left hand to work) I know who I can contact. The one main problem I have is the medication prescribed to me but again, that’s a constant balance so that I can do therapy without chronic pain.

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