From this phase will slowly create what I call Participatory Medicine: based on information, interaction and a joint process between caregiver and patient they arrive at an “attack plan” for diagnosis, treatment and care possible. Here comes the role of e-health “around the corner, where efforts by the patient can be addressed.
If you add to Participatory Medicine the vital role of family and informal caring and also about the opportunities for prevention on this side, I like to talk about Participatory Health Care, which is the “2.0-thing for my. Because the patient has the disease not alone since his environment is part of the process surrounding it. ‘Health’ means here literally “health” as a total approach. What is not there, you do not have treat, it is an attempt to prevent diseases.
Soon we look back as caregivers to what we’ve built. And we will see in the care process things have changed and improved, sometimes “with velcro”. Maybe then we conclude that have reset the process . How would you design it all over again when you should draft ? If you could start with a white sheet of paper ? We call this process ‘REshape’. Then we would like to talk about Service Design phase (health 3.0), where everything is designed from the perspective of the patient.
It will start to let care institutions disappear, and care networks in varying composition around and with the patient to occur. In that e-health, or (part of) m-health will play a major role for me is a given.