Prior to Christmas I finally started undergoing a set block of 4 sessions devoted to CBT - prescribed due to anxiety significantly causing the symptoms of vestibular migraine to be out of control. I kept a diary and notes of each session for this newsletter, to lift the lid on what this has been like - this is the third and final entry in the series.
“What can I do to help?”
It’s such a simple question - and one rarely asked with the intent of understanding proactively. From the get go there has been an awareness that Cognitive Behavioural Therapy (CBT) may not be for me; it is something that does not necessarily work for an Autistic person, because of the difference of neurologies. That was the caveat at the start of each session - but this is usually the set pathway as a gateway to other treatments.
I’ve turned to nature meanwhile, and going slowly. Sugar is a vice, I’m also home based a lot. But isn’t this world a pretty place? I love to sit and watch people from a cafe. In March it will be two years since I caught Covid 19; I feel wasted, watching everyone I know off and living. And then I feel very guilty for such a thought.
Keep reading with a 7-day free trial
Subscribe to The Disabled Feminist to keep reading this post and get 7 days of free access to the full post archives.