Psychological Support in MS
What has been your experience of psychological support in MS?
What kind of psychological support would you like for living with MS?
Tell us by completing this online survey here by clicking the ‘start’ button at the bottom of the page. https://research.reading.ac.uk/neurodegenerative-diseases/multiple-sclerosis/
I sought Help from the Brain Injury Clinic, who said that they didn't need to see me Anymore since I was diagnosed with MS. During the Pandemic, I was put in the hospital Psychiatric Care. My husband did not understand why my poor communication led to me holding a knife. It took being arresting me to Calm Down. I am now attempting a PHD in Interdisciplinary Care of people who are suspected of having MS.
Wow. You have been through quite a bit,
. Does your husband now understand what was going on back then? How scary for you both! Your PHD sounds fascinating and necessary. So much about MS and its psychological impact is misunderstood. I hope you are able to finish your degree and put it to good use. Best of all wishes! - Lori (Team Member)
Unfortunately I just need a supervisor Who agrees. Know any one at UBC?
I wish I did,
! - Lori (Team Member)
