Like you to meet Baryden Janetzke and his mom Christina. We're a little short on time for this one, and I'll explain why in a minute, but I am going to quote what Christina sent me in advance so we can get to work. -
"Brayden Janetzke was born with a genetic disease called Spinal Muscular Atrophy (SMA for short).
SMA is a neuromuscular disease that limits voluntary muscle movement. SMA has NO cure but there is currently ONE form of treatment that Brayden is receiving every two weeks at Helen DeVos Children’s Hospital.
Click for Braydensvoyage.com |
We appreciate the opportunity to spread awareness and let Brayden’s story be heard."
So there is that part. Now, here's where we come in. Michigan Mortgage is offering to help the cause out. They have made a cash donation already and are giving a $1 donation for every check in on their Facebook page between now and the end of the month...which is Thursday November 30th. Time to get clicking. You can find the link to their Facebook page on the right. Click on it, and click on that check in!! Let's see if we can raise a few bucks for the little shaver.
Check in @MichiganMortgage and #mmgivesback |
While you're clicking and checking in take a listen to our chat with Brayden, Christina and Tracey Kiel who was the employee of the month who nominated Brayden's Voyage! Take a Listen!
There's the scoop! Click on the Michigan Mortgage Facebook Link above and check in! Given them the #mmgivesback and $1 goes to help Brayden and his family along in the journey. We are always on the hunt for great people, and great companies who are out to make a difference in our community. It was a pleasure and honor to meet Brayden and his family today and the folks at Michigan Mortgage were first class from the minute we walked in the door until we left. What a great place to do so much for the Janetzke's. Our best wishes to all. To visit Michigan Mortgage online, click on the image below.
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