I think this is a fabulous idea PJH. Just within my own experience and experiences that other women have shared with me, it seems like there is a huge loss of "attention" to survivors once their hair grows back and begin to look "normal" again. The general public think that you have finished all treatment and that's it.... You are cured and it's all gone and you do not need support any more. Little do they know... hey!
Which is why I am so grateful that I have been served up "Breast Cancer" because the worldwide support that we have is truly fantastic. We are able to touch base with so many other women. In fact I am in a mothers group of 9, since our little ones started pre-school 5 years ago and I am the 4th to be diagnosed with Breast cancer. So for me, I am extremely lucky to have a sounding board of my ongoing inner journey regarding survivorship. So many do not have that. and what if you hade a rare cancer?
So I think your idea of "Patient Navigators" is super.
Love your work.
Maz.
As a survivor myself, facing many of the issues, 1 of my biggest problems is probably looking at other survivors who appear to be doing well, managing to get on with thier lives, while I am fighting post mastectomy syndrome 3 years out of chemo from a bi-lateral mastectomy and being forced to medically retire, and having to jump thru those hoops. How much easier it would be if I had a navigator to help me thru all of this.