***Want to win a free print of my latest image, The Blue Ribbon? Read on to find out how you can enter!!***
It’s been an emotional week for me; not surprising since ME is something I deal with firsthand. Since we’ve all walked through the more difficult parts of this disease, let’s take a break with some levity and fun!
From constantfuckingshit.wordpress.com
From idelhearts.com
This actually does happen to me. From invisibleillnessweek.com
From memgenerator.com
From icanhascheezburger.com
And lastly, one poignant one:
From PostSecret.com
Now go tweet some facts so you can win a print!! 🙂
To do my part in raising awareness about ME, for the month of May, I am donating 50 percent of profits from all my sales to The Microbe Discovery Project, a group working to solve the mystery of ME and find a cure for those afflicted.. And what do I sell? Well, what do you want? Because my images come from the frameable to the wearable and in every price range.
– museum-quality, fine art prints
– iPad/iPhone/iPod covers
– stickers
– blank greeting cards
– post cards
– shirts and hoodies
– wearable art
– throw pillows
– INTROSPECTIVE: my eight-week, on-line, course of self-discovery through photography
Also, in honor of this day of raising awareness, I’m holding a contest to win a beautiful, 10″ x 15″, museum-quality print of my latest image, The Blue Ribbon; an underwater representation of the struggle that living with ME can be. Your print will come on beautiful, shimmering, pearlized, archival paper. And all you have to do is tweet!
The Blue Ribbon, model: Katie Johnson – enter the giveaway to win a print of this image!
Ready to tweet? Use any of the following!
Curing baldness gets 4x more funding than ME/CFS, but no one ever died of baldness http://wp.me/p17spB-EX #MEAwareness #CFS #SAPrintGiveaway
*****
ME/CFS can be just as deadly as MS, HIV and AIDS, yet it is largely ignored. http://wp.me/p17spB-EX #MEAwareness #CFS #SAPrintGiveaway
More exercise and a better attitude will not cure ME/CFS. http://wp.me/p17spB-EX #MEAwareness #CFS #SAPrintGiveaway
We’re not chronically fatigued, @CDCgov. We have myalgic encephalomyelitis. http://wp.me/p17spB-EX #MEAwareness #CFS #SAPrintGiveaway
Tweeting multiple statements will count as extra entries, so enter as many times as you like. However, tweeting the same statement multiple times will not count. And that will probably just annoy the people reading your feed, so don’t do it. 😉 I will choose a random winner from all entries on May 20th and announce the winner here!
Mythic Pictures 
[…] I wrote a blog entry for each day of the week and held a print giveaway for those who helped spread awareness about it. The Microbe Discovery Project asked for people to share their ME stories, so I recorded a short […]
[…] my life for the last eight years. How I have not had a single day since late May of 2008 that was free of pain or its constant, overwhelming exhaustion. How it has progressively gotten worse each year. How […]