ALS- Neuro Note #5
For my post I read the blog post titled "The Diagnosis", this blog is written by a woman who shares her life experiences after she was diagnosed with Amyotrophic Lateral Sclerosis (ALS). In this post the author, Rachel Doboga, recalls what the weeks and months were like after her initial ALS diagnosis. To begin her story, she shares with her readers the message she sent her family and friends and tells them how she is hopeful that she will outlive the typical 2-5 year prognosis because of her lower motor neuron function being preserved in her case more than in typical cases of ALS. What stuck out to me the most from this message is that even though she was sharing with her loved ones how she was diagnosed with a terminal disease, she still was able to divert attention from herself and show gratefulness to the people who were taking care of her. She then goes on to write more of what life was like after those first fateful weeks; including how she was directed to go to a ALS clinic every three months where she then met her new care team consisting of a doctor, social worker, occupational therapist, and physical therapist. What caught my attention from this part of her story is the relationship that bloomed with her occupational therapist, Deb.
Doboga, R. (2016, May 21). The Diagnosis. How I Live Now: Life With ALS. August 21, 2023, https://howilivewithals.com/2016/05/21/the-diagnosis/
Comments
Post a Comment