Thursday, December 18, 2008

some christmas cheer

As much as I hate to post on top of that lovely ode to the Griz, as a offspring of MSU grads, I had to. Just wanted to let you all know of some news our family received. Some of you may have seen this already on facebook, but the least technically savvy (read: old) family members, I thought you should be filled in too. Nate was diagnosed with Myotonia Dystrophy which apparently is a (very in comparison) mild form of muscular dystrophy. So it's a very slowly progressive disease that affects your muscles. He went in because his grip strength was bothering him. He wasn't able to play golf because he couldn't grip the clubs hard enough. The neurologist said he won't regain this strength and likely will lose other muscle strength throughout his body, including legs, eyes, and heart. But again, this is likely YEARS down the line. He's feeling fine and taking this surprising well. I'm personally still a little leary of the diagnosis because it's a strictly hereditary disease that one of his parents would have to have and neither of them have symptoms. I have no doubt that he is somehow diseased, though! If this is his diagnosis, it is a little worrisome because it's a dominant trait and so our kids have a 50% chance of having it. But I'm not really sure exactly what the prognosis is. We will be going to see a specialist after the first of the year.

On another note, Emma had her first Christmas program tonight with her daycare class. Only 3 other kids showed up, but it was pretty cute. She's the one second from the left. Emma's friend Ava is the last on the right and she was so hilarious and really got into it! Sorry about the jerky picture. What an amateur! You also can't hear the song very well, but it's the Chipmunks singing Santa Claus is Coming to Town. Enjoy and Merry Christmas!

6 comments:

Hannah said...

That video is so stinkin' cute! I love how Emma got her foot a-stampin a few times there. And it was also lovely to hear your sweet laugh, Randa, especially in a time with difficult news. Our prayers will be with Nate as we hope for the best prognosis possible.
All our love,
Hannah

Anonymous said...

i will definitely be keeping you and your family in my prayers. i hope that i will be able to see you guys while you are in great falls. i think emma gets more adorable every time i see her!!!

love,
jen

Jan said...

Cute!! Cute!! Cute!!
You and Nate are in our prayers! This too will pass. We have faith that Nate will not show any more signs of this disease and progress will be made!!
Love you, The Buyskes

Desiree said...

Randa,
So sorry to hear about the bad news, but glad Nate is tough. Your family is in our thoughts and prayers. Hope we can see you over the holiday. Emma is super super cute.
Abe&D

Kayla's Mom said...

Hi,

You don't know me but I wanted to say hi and introduce myself to you. My name is Lisa and our family got the shocking news of this diagnosis 3 years ago when my daughter was born with the severe congenital form. I had no symptoms at the time and am also very mildly affected right now. If you would like more information about myotonic dystrophy or just want to ask questions of someone who has dealt with this disease for the last 3 years, send me an email: lisa@global.t-bird.edu. PS, the video of your daughter is adorable.

Happy holidays,

Lisa Vittek
lisa@global.t-bird.edu

Meghan said...

Our prayers are with you and Nate, Randa!

And keep up the cute-babymaking! Emma is adorable!

:)