Post Diagnosis
When I was diagnosed with FND, I was basically given a website (to remember) and shown the door
Speaking to people in various interviews, for a variety of different conditions this is common place
How could this be improved?
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jschulz9 jschulz9- Daisy Hunter
guyheather1959 guyheather1959Ettie Bailey-King Ettie Bailey-King- kittenweb
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My take would be for the NHS to offer 4-6 counsellor session on how to process a diagnosis
Wouldn’t be experts in our particular diagnosis, but they would be able to support us in finding out what we need
A lot of signposting, but giving the autonomy and ownership to the individual