Add yourself to the ME/CFS & FM World Map - help build a picture of the global ME/CFS and FM community and see whether there are any "hotspots"


The website and blog that go along with the map seem to have some useful information. For instance, I had not heard that Annette Whittemore, who founded The Whittemore Peterson Institute (the private not-for-profit research organization that found the presence XMRV in blood samples from a high percentage of Chronic Fatigue (ME/CFS) patients and in small number of Fibromyalgia samples), has a daughter who suffers from ME.

Comments

  1. Thanks for posting this. I just added myself to the map. I also see that there are four people close to where I live who live with FM/CFS/ME like I do. This is a very interesting project.

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