Saturday, 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

Thursday, March 21, 2019

The Significance series BOXSET is HERE!


The Significance Series Boxset for the first five books 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/2UOZ96o
iTUNES: https://apple.co/2umS2Xe
B&N: https://bit.ly/2UKjQAx
SMASHWORDS: https://bit.ly/2Tm7m0A
AMAZON UK: https://amzn.to/2ToI41Q
AMAZON AU: https://amzn.to/2FlKjhr
AMAZON DE: https://amzn.to/2TppuXg

These are the same stories as before but have gone through a little “brush up” for old editing and formatting issues, etc.

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. ๐Ÿ˜Š
I continue to be amazed by you guys and how awesome you are. You are THE best readers in the world and I don’t care who knows it! Mwah!

Best wishes and happy endings,



Tuesday, March 19, 2019

Undeniably Fated Teaser Tuesday!


It's an Undeniably Fated Teaser Tuesday!

There's still no release date, as you guys know. I'm working! Mwah!!!!! 

Best wishes and happy endings,



Friday, 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 ๐Ÿงค writing gloves along as a giveaway to a lucky WINNER!
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To ENTER, you can do any and or all of the following:
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1) Tag an author you love (On Twitter or Instagram) in the comments or a tweet that you'd like to WIN these awesome gloves and I'll enter them to win AS WELL as you!! .
2) Go check out Literary Book Gifts' awesome website here 
They have a TON of goodies for the whole fam: t-shirts, totes, book gifts. Just go look. ๐Ÿ“š๐Ÿ‘•๐Ÿงค
(This one is obviously on the honor system. I'm ๐Ÿ‘€ you...not really.)
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3)Go on over to Instagram/Twitter and follow me there if you want! It does get an entry. Just sayin' @AuthShellyCrane
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I'll choose one WINNER next Friday, one week from today, March 22! Good luck!
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Go forth and get your write on! 
Best wishes and happy endings,
Shelly Crane

Sunday, March 3, 2019

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/