A month after her surgery, Jo visits her surgeon and a specialist nurse to have her DBS device programmed for the first time. She knows it won’t be an immediate fix for her symptoms, but believes it will be worth it in the end.
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This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit [ Ссылка ].
