Hi all,
I'm sharing my study on the experience of seeking and having counselling due to symptoms of fatigue from ME/CFS or long covid. I am doing this for my master's dissertation in counselling.
I'll be doing interviews with questions about the impact of counselling on how people view themselves, their illness, and any influence on their relationships. If this sounds relevant to you and you are interested in participating and you are in the UK, please email me at [email protected].
Alt text: Research participants needed for Chronic Fatigue study
Have you received counselling for your Chronic Fatigue symptoms?
Have you struggled with fatigue, particularly after exerting yourself?
Did therapy impact your life, positively or otherwise?
What am I investigating?
Your experience (positive, negative or mixed) of seeking therapy, having therapy, and any life changes following therapy.
Changes in how you viewed yourself and your fatigue.
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What should I expect?
An online or in-person interview about 1 hour long, in which we talk in-depth about your experience.
Reasonable adjustments will be provided to accomodate your needs.
If interested, please contact Lyndsay: [email protected]
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Lyndsay Barwell
Calligrafae