It's time

It's time to begin educating about the disease MSA. It's not fun, it's not pretty, but I feel I can't keep what I know to myself because I need and will continue to need your support. If not physically, then in prayers and the hope all of you give Keith and I.

I began by posting a link (I think that's what I did ) on facebook about a couple with living with MSA. Please watch that if possible, difficult as it may be and has been for me.


I watched it about a year ago and only shared it with Keith yesterday. He was sad watching it as am I each time I do. Also if you type in Miracles for MSA on your facebook page you will see other families dealing with MSA. It's a beginning. If you are like me, I have to stay away from the page for the most part though I am constantly drawn to it.

I appreciate any information about MSA you gain.

Now on a lighter note. I told Keith about Clint's suggestion of what to watch that was humorous as was suggested by the wife in the video. So, we turned the channel to what we thought was the old funny sitcom shows. The first thing we heard was a man who had just been told he had cancer and was running through a senario in his mind about dying. We looked at each other and then back to the tv. The next picture we saw was of a woman who had fallen down and couldn't get up. We looked at each other and started laughing. Just what we needed, a commercial that addresses two of probable outcomes of MSA, falling and death. It was ironically funny, but we turned the channel. We are now taking suggestions as what to watch that is funny.

Enough hard stuff for now.

Thanks everyone for being in our lives. We love you. =)