Being realtively new to advocacy and support groups I've wondered what it takes to encourage other psoriasis patients to become a part. I have been all over the net and while there are millions of people who suffer from psoriasis they also seemingly suffer from chronic lack of participation.
I don't mean the proactive kind of activity, even if it is just registering and following what is going on, get the lastest patient perspective on treatments, encouragement etc. How do we reach other patients and bring them into the fold where they can be encouraged, understood and helped?
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