Catch an insiders view on what its like to be in the final stages of moving a family of 7 out of a house and into a camper/storage unit.
Take the opportunities you have and MAKE MEMORIES HAPPEN.
You can do BIG things too!!
♡ About our Family:
We are a Ranchin', Life Living', Grace Givin', Full out Lovin'- Kinda family. We enjoy being together, and doing life together. Our kids were born within 5.5 years of each other, so they are a tight knit crew, and we are always fixing a problem, laughing at their comedy acts, breaking up a fight, or holding a couple of them in our arms.
Our oldest and youngest daughters were born with a rare Genetic disorder called Spinal Muscular Atrophy (SMA type 2). This is a progressive muscle weakening disease similar to the onset and progression of ALS (Lou Gehrig's Disease). When we first heard the diagnosis- we were told to make the most with what we had, because they were not promised tomorrow....
So- this is us, living life full out- while we have it to live. Big things are possible... you just have to figure out a way to make them happen.
What would you like us to do a video on next? Leave a comment in my video and let me know!
FOLLOW US AT:
♡Website: This Life UNLIMITED https://www.NatoshaMae.com/
♡ Instagram: ThisLifeUNLIMITED https://www.instagram.com/the_NatoshaMae
♡ Facebook: The Natosha Mae
https://www.facebook.com/theNatoshaMae
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♡ Email
[email protected] for any inquiries.