Today I was just observing clients. The first was in their 80s, who had had an extremely severe stroke. This was my first experience of stroke in the acute phase. The client was globally aphasic, had a dense hemiplegia, fluctuating consciousness, and was unable to initiate a swallow when food was placed on their tongue. My CE and my partner were going to review their swallowing, as they had been displaying small signs of improvement throughout the week, but were foiled by an ultrasound. I did have an opportunity to talk with a family member, which I think revealed a deficit in my counseling skills.
What I did:
- I talked about the beautiful weather outside
- I said they seemed to be coming from a high-baseline (they were fit and active before the stroke)
- I said the family seemed to be doing helpful things (having pictures of familiar people, talking to them in their home language)
What I should have done:
- Listened more! Allowed the family member more time to talk
- Reflected the family’s members thoughts back
One of my colleagues said it was natural to offer solutions when listening to the problems of others, but sometimes they really don’t need your input. Instead, they just need to be heard.
The second client was also in their 80s, and had entered the health system a few weeks ago upon the discovery of a serious metastasised cancer. I felt overwhelmed on many fronts: medically, the client was complex, with multiple systems involved in confusing (for my poor Speech Pathologist’s brain) ways; and emotionally, as I tried to imagine how quickly this person’s world had changed. We observed an instrumental swallowing examination, where it became apparent that the client was unsafe on all consistencies and thicknesses. One of my Clinical Educators (CEs) showed the client the results and explained them to them. It was difficult to watch, as the client clearly had difficultly coming to terms with the news. I was amazed at the language my CE used, and how she was able to distill the deficit in layman’s terms without being condescending. When the client asked if she thought his swallowing would improve, she didn’t directly answer the question, but pointed towards the next steps – making sure they were comfortable in their feeding.
When it comes to the end of the road like this and palliation is on the horizon, I thought about what one’s goals might be as a Speech Pathologist in this situation. SP involvement in palliative care is relatively new but I found this helpful article from 2004, which distilled the goal to:
To assist in optimizing function related to dysphagia symptoms in order to improve patient comfort and eating satisfaction, and promote positive feeding interactions for family members
I’m unsure if I could top that.
Pollens, R. (2004) Role of the speech-language pathologist in palliative hospice care. Journal of Palliative Medicine, 7(5), 694-702. doi: