Shelly Crane's Blog, page 3
July 3, 2019
So...
So...yeah.
Significance has been re-optioned for film! I'll be moving forward with https://www.optxent.com So much more coming soon!
I'll just leave you here with that.
You guys!Best wishes and happy endings,
June 12, 2019
Undeniably Fated Teaser!
Happy birthday to me! I'm 29 again. Thank you guys for all the birthday wishes!! And to celebrate, here's an Undeniably Fated Teaser! Mwah!!
June 4, 2019
Undeniably Fated Teaser Tuesday!
“You are way too calm for someone about to meet a roomful of Jacobsons,” I muttered, more to myself than to him. He was calmer than I was.
“I’ve met a couple of them before. And I don’t know,” he stopped me by grabbing my hand, “you’re kind of stuck with me, right? Can’t get away. It’s not like I have to make a good impression on your family or anything. Really takes the pressure off.”
I punched his stomach lightly with the side of my fist. “Oh, shut it. You better be Mister Perfect. I have a reputation to keep up, pal.”
“So do I,” he said cheekily before he grinned, taking a step closer. “Good thing you’re pretty cute.”
Coming Soon!Still working guys. Thank you so much for your understanding and sticking with me! You rock my socks.
March 30, 2019
You're invited...
Leave the shoes at home... You're invited to a Jacobson wedding, baby.
#SignificanceSeries #LittleRedDress #JacobsonWedding #EmberAndLandonSittingInATree #ImWorkingOnItIPromise
Original Photo Credit : Bruno Salvadori
March 24, 2019
March 21, 2019
The Significance series BOXSET is HERE!
The Significance Series Boxset for the first five books—Significance, Accordance, Defiance, Reverence, Independence, Consequence—is LIVE and now available on all sites and platforms.
For a limited time, you can get it for $5.99!
AMAZON: https://amzn.to/2UOZ96oiTUNES: https://apple.co/2umS2XeB&N: https://bit.ly/2UKjQAxSMASHWORDS: https://bit.ly/2Tm7m0AAMAZON UK: https://amzn.to/2ToI41QAMAZON AU: https://amzn.to/2FlKjhrAMAZON DE: https://amzn.to/2TppuXg
These are the same books as before but have gone through a little “brush up” for old editing and formatting issues, etc. The next boxset will contain the new books from the Significance sort-of spin-off but not really, which starts with Undeniably Chosen.
I’m currently working on Undeniably Fated. I hope to have more updates for you soon! For those of you who haven’t seen an update from me in a while, because social media is silly like that, I did give a lengthy update about me and the books, including UF, if you’d like to go give it a read HERE, it can hopefully help you feel a little better about things.
March 19, 2019
Undeniably Fated Teaser Tuesday!
It's an Undeniably Fated Teaser Tuesday!#SignificanceSeries #UndeniablyFated #EmberAndTrouble
There's still no release date, as you guys know. I'm working! Mwah!!!!!
Best wishes and happy endings,
March 15, 2019
Cashmere Writing Glove GIVEAWAY
Hi, guys! As you know, I've been freezing my writing fingers off in Montana the past couple months, (LOVE it!) as we've been here with hubby's job, and was contacted by the AWESOME Literary Book Gifts to pass this amazing pair of cashmere
March 5, 2019
March 3, 2019
March is MULTIPLE SCLEROSIS awareness month. Also kn...
March is MULTIPLE SCLEROSIS awareness month. Also known as MS Sucks, But Life Doesn’t Have To Month.What about MS Gets On My Nerves Month. Or Keep Calm, It's Only Brain Disease Month.
Whatever you want to call it, I let you guys know recently that I was diagnosed a few years ago with MS and how it has affected me.
2015 and 2016 were my worst years, by far. And a few people in my life at the time did the MS Walk in my name those years. (Because Stephanie and Tessa are AMAZING people). I got one of my readers, Kendra’s Creations, to make a logo for our team shirt. We won Best Team shirt BOTH years at the HUGE Jacksonville city MS walk. This is one of the logos she made that we came up with and you are more than welcome to share.
But what IS MS? Before I was diagnosed, I certainly didn't know.
MS is defined as a chronic, auto-immune, usually progressive disease involving damage to the sheaths (myelin) of nerve cells in the brain and spinal cord, whose symptoms may include numbness, impairment of speech and muscular coordination, vision problems, severe fatigue, pins and needles, pain, and more. Almost all cases progress to a place, in some form, of a loss of bodily function. Though there is no cure for MS, there are medications to slow the progression of the disease.
I know, that still tells you nothing, really, of what MS is. But it IS awareness month and you can look it up and find some people telling their stories of MS and other brain disorders all over the web right now. I encourage you to do so. It can be truly inspiring, and perspective-inducing, to see someone work twice as hard for the simple things that others do without even thinking about it.
You guys just have to look past that uggo awareness orange and share please. :) For MSers and brain injury havers everywhere, we thank you.
Best wishes and happy endings,
For info and research:
http://youdontknowjackaboutms.com/
https://www.nationalmssociety.org/
https://www.abovems.com/
Whatever you want to call it, I let you guys know recently that I was diagnosed a few years ago with MS and how it has affected me. 2015 and 2016 were my worst years, by far. And a few people in my life at the time did the MS Walk in my name those years. (Because Stephanie and Tessa are AMAZING people). I got one of my readers, Kendra’s Creations, to make a logo for our team shirt. We won Best Team shirt BOTH years at the HUGE Jacksonville city MS walk. This is one of the logos she made that we came up with and you are more than welcome to share.
But what IS MS? Before I was diagnosed, I certainly didn't know.
MS is defined as a chronic, auto-immune, usually progressive disease involving damage to the sheaths (myelin) of nerve cells in the brain and spinal cord, whose symptoms may include numbness, impairment of speech and muscular coordination, vision problems, severe fatigue, pins and needles, pain, and more. Almost all cases progress to a place, in some form, of a loss of bodily function. Though there is no cure for MS, there are medications to slow the progression of the disease.
I know, that still tells you nothing, really, of what MS is. But it IS awareness month and you can look it up and find some people telling their stories of MS and other brain disorders all over the web right now. I encourage you to do so. It can be truly inspiring, and perspective-inducing, to see someone work twice as hard for the simple things that others do without even thinking about it.
You guys just have to look past that uggo awareness orange and share please. :) For MSers and brain injury havers everywhere, we thank you.
Best wishes and happy endings,
For info and research:
http://youdontknowjackaboutms.com/
https://www.nationalmssociety.org/
https://www.abovems.com/
