I’m excited! My post on Low-Dose Naltrexone was selected for the Patients for a Moment (PFAM) Blog Carnival.
The carnival is being hosted by ChronicBabe this month. And actually, I was more than a little surprised that it was selected. LDN isn’t so much controversial as it just doesn’t seem to be on anyone’s radar at the moment. Research in heading in the direction of the XMRV retrovirus and what it means to those of us with Chronic Fatigue Syndrome and Fibromyalgia. I still think that LDN will be found to be a useful tool and I appreciate the nod from the blog carnival.
If you haven’t checked out the Chronic Babe website, and you happen to be a chronically ill young woman, you should take a look. Lots of useful articles and podcasts, but best of all; The Chronic Babes Forum. It’s nice to talk to people who’ve been there and done that.
And that’s pretty much all I got to say about that. Other than, go vote for Jennifer! Unlike being selected for a blog carnival, voting for Advocacy for Patients on Facebook could help them win hundreds of thousands of dollars to continue their legal advocacy for people with chronic illnesses. Seems like a GREAT use of your mouse potato time!
