When I was first diagnosed with Parkinson's, I was overwhelmed by the amount
of information available, but I had so many questions:
- What did I need to know?
- What was with all these different Parkinson’s foundations?
- Who could help me navigate?
- Where do I find exercise?
- Where do I find a support group?
I also noticed that not everyone had
same facility with internet. From the
questions that I see on patient forums, it’s clear that some PWP (people with Parkinson's) and caregivers just
don’t Google things.
So my mission is to help PWP and their caregivers, especially
those recently diagnosed, to identify what they need to know, and show them
where the information is.
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