The other day I was looking at my blog traffic stats for the past few months, and they confirmed the obvious: You guys really like the posts focusing on treatments and tips to reduce fibromyalgia symptoms. And then I noticed something else that wasn’t as obvious to me: My weekly fibromyalgia news roundups get a lot less traffic than my treatment-related posts do.
So I’ve decided to switch things up. Starting next week, I will be reducing the weekly news posts to twice a month. Making this move will free up some time so I can write more of the posts that you all find useful. And of course, as always, I’ll be sharing any extra content that doesn’t make it into the bimonthly news posts on my Facebook page and on Pinterest!
I hope you’ll like the change.
Top stories …
Now this is funny (and I bet every single one of us has our own version of this script): “Why am I awake? Sleeping with chronic illness” from fellow blogger Chronic Mom.
“Must see” chronic fatigue syndrome documentary “Forgotten Plague” has been released to DVD, iTunes, Google Play and Amazon Instant Video.
Now who thought of trying this in the first place? Using human placental extract to treat ME/CFS
Why those of us with chronic illness should consider making a NOT to do list.
A lot of us with fibromyalgia and ME/CFS aren’t able to hold a typical 9-5 job due to the severity of our symptoms. My friend Julie over at Counting My Spoons gives us some alternatives for “working with chronic illness.”
Research & treatments …
Fibromyalgia News Today: “Younger adult fibromyalgia patients at increased risk of stroke, according to study”
Tonix releases more data on Tonmya, a sublingual form of cyclobenzaprine (Flexeril) that’s undergoing trials as a potential fibromyalgia treatment.
From HealthRising: Gluten sensitivity in ME/CFS sufferers leads to NIH-funded gut study.
How supplementing with vitamin B12 may make fibromyalgia symptoms more manageable
Personal stories …
NFL player Dominique Easley made the cover of this quarter’s PainPathways Magazine for his work in building awareness for fibromyalgia. Easley’s teen sister was diagnosed with fibromyalgia in 2011.
Team USA member John Nuyen gives us a first-person account of what it’s like to be a man living with fibromyalgia.
Odds & ends …
From Brainless Blogger: “5 reasons people give you advice about your illness.” (They’re really not trying to tick you off – at least most of them aren’t.)
Registration is open for the Third Annual U.K. CFS/M.E. Research Collaborative (CMRC) conference in Newcastle this September.
#MEAction will hold its first protest in Washington, D.C., on May 18.
In case you missed it…
Prohealth.com republished my post, “Playing the chronic illness blame game: Why you shouldn’t ignore that new symptom”
Off topic (an ode to St. Patty’s Day this week)…
Mother Nature Network: “7 surprising facts about St. Patrick’s Day”
I’d love to hear from my Irish subscribers if this article is accurate: “How to celebrate St. Patrick’s Day like the Irish”
In case you’re spending the day in front of the tube: “16 must-watch films set in Ireland in honor of St. Patrick’s Day” and a list of “10 great Irish films”
More fibromyalgia news …
If you’re interested in reading more fibromyalgia and ME/CFS news, then you might like these:
Twice a month, I compile the best fibromyalgia and ME/CFS news into one convenient post for subscribers. If you found this post helpful, please subscribe below. For subscribers, I share even more news and research on my Facebook page and on Pinterest.