Hello! We wanted to invite you to a very special Blog Hop being hosted by members of StampTV's Center Stage Alumni. This time around, we are participating in a card drive for four very special kids. As you go through the blog hop you will see a variety of cards designed for these special kids. We hope that this inspires you to participate in the card drive as well!
Here's a photo of the four adorable kids, please meet Madison, Logan, Tanner, and Rebekah.
Here are the details on how you can participate:
Card Drive for Kids
181 Perry Way
Yakima, WA 98901
In case you're wondering, here's a photo of some of the prizes with a list of all the prizes below the photo.
Are you ready to start the hop? Here's a list of all those participating:
Hope you'll be able to join us in making this card drive a huge success! You can find more details on the card drive over at Giovana's blog as well!
Have fun hopping!
Sandra....looks like she moved her blog and started a new one. You aren't doing anything wrong!
Wonderful hop ladies!!! It took a couple of tries to reach Joy Hadden's blog, but it finally worked. Not so much luck with Sue Morris's blog. I will keep trying.
Here is Sue's new blog:
Sue is really sorry about this, she has to change sites and lost her posts ans such. But you can see her cards now.
Hope this helps.
Here's Sue's direct link to her post:
She had to change providers because her previous blog provider lost all her posts and she had to start over. She feels horrible about having the broken link, but it was beyond her control. Thank you all for understanding and patience. Lee will be changing the link above as soon as she gets a chance.
Ok...her link is now updated!!
Also just an FYI......we don't require comments to be left on blogs....it's just a fun thing to do! =)
Our family is pleading for everyone we know to please pray for our new little grandson Toby who was born on October 12th with Myelomeningocele Spina Bifida and Chiari II Malformation. Toby is not doing well. Originally Dr's thought that Toby had the Asymptomatic form of Chiari II but are growing more and more convinced that it's the Symptomatic form. For those of you that do not know what these means, it means that Toby may not survive apart from a breathing machine. He is unable to breath on his own and does not appear to have the ability to swallow. These are indicators for the severe form of the Chiari II. Dr's are trying desperately to find other causes for his breathing problem but so far have been unsuccessful at resolving the issue. On Tuesday Toby underwent brain surgery to install a shunt for Hydrocephalus. Dr's were hopeful this would correct his breathing but in fact Toby has just gotten worse. If there is anyway that word could be spread to pray for Toby it would be greatly appreciated because apart from another surgery for decompression which is normally only done on adults, Dr's have run out of options so at this point we are praying for a miracle to save little Toby's life. You all have our family's permission to post a prayer request for Toby on Facebook and ask if you belong to a church that you please put this request on your church prayer chain.
Please Laurie never underestimate the power of prayer. You and Toby and your entire family are in ours.
Miracles happen everyday!
God Bless You All!
The winners have been announced! Thanks so much to all of you who participated.