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Being diagnosed with MND

Posted By Platignum

"Being diagnosed with MND"

About: Forest Holme

(as the patient),

After a series of tests I was informed that I had MND.

I was shocked and dismayed, did not understand the true effect of the diagnosis.

Do you have a similar story to tell? Tell your story & make a difference ››

Responses

Response from Annemieke Fox, MND Advanced Healthcare Practitioner Co-ordinator for Poole area, Forest Holme Hospice, University Hospitals Dorset NHS Foundation Trust 2 years ago
Annemieke Fox
MND Advanced Healthcare Practitioner Co-ordinator for Poole area, Forest Holme Hospice,
University Hospitals Dorset NHS Foundation Trust

Support people living with motor neurone disease and their families

Submitted on 22/11/2021 at 12:34
Published on Care Opinion at 14:22

picture of Annemieke Fox

Thank you for your comment Platignum. The diagnosis is often a very difficult time for people, especially if it is unexpected. We would love to hear from you if you have any ideas about how this can be improved, or how we could help people to feel more supported around this time? Please feel free to get in touch with me if you feel you need any further support, or if I can do anything else to help you. My email is annemieke.fox@uhd.nhs.uk, mobile 07387041914.

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