Cystic Life Network

Well, I have just joined a CF netwrok, called Cystic Life.  What an amazing site.  You can read posting that other with Cf put up, like reading their blogs, and help them figure things out.  It's what i have eben trying to do here for some time now, and never really thought I was making a difference.  No one knows about my site, and no one really reads it but be.

Not only that i have found a site that will publich my blog for $40 some odd dollars, and it's tempting, oh so very temping.  i might consider it, but I still blog my heart out.  I tell eveyone what's going on, and whant to tell the whole world ina book.  Well okay, for selfish reasons, I want a book.  I want to think that I am capable off making a difference in what I write.

So maybe I am a skeptic, and think it will work, or is that an optimist?  I never really understood the difference, and still don't.  At 30 years old, you would think i have learned that stuff by now.  But, no, I have not. lol

Well, there really isn't much to report... I'll let you know about Emily when I hear nore.  but your prayers are working, and i couldn't believe it when i read the last entry.  I am so proud of you Em, I hope things will keep working out for you.

Loving you always