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Hi Mary (& George);

> Now, about your plan.  I think your idea of compiling a packet of information
> is a very good one but, thinking back to the way I felt when I left the
> neuro's office, I would have been even more devastated to have been given info
> about pallidotomies.
>
This subject is obviously inappropriate for anyone dealing with the
initial stress.
>
>  I think a newly diagnosed patient needs to have an
> explanation of what PD is, main symptoms, encouraging news of current
> research, and information on support groups, PD organizations, exercise
> classes and that's all.  I think, above all, that newbies need to hear that
> there is research going on with encouraging results and there's a good
> possibility of a cure in the future.  It's important to keep hope alive.
>
My thoughts precisely.
>
> Good luck on your project.  It's wonderful that you're out there educating
> people about PD.
>
> Mary
>
Good health.....Best regards..................Murray
.
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