sue robins

So sometimes I write and I don’t get paid for it.  But that’s ok, because I do that for organizations I volunteer for.  Like the Canadian Family Advisory Network (CFAN).  Of which I happen to be chair.

I wrote a piece for London Health Science Centre in Ontario about a family who frequents their Cystic Fibrosis Clinic and have two delightful little girls with CF.  We are trying to celebrate family centred care initiatives in Canada.  To learn more about family centred care, visit the Institute for Family Centered Care website.

Here’s the link to the London article, off our CFAN website.   If you click around the site, you will find all sorts of information about what’s happening at health facililites here in Canada to include a family voice in the care of their children.   Of which I feel pretty passionately about…