Recent content by breathinisbelievin

Good job all of you for raising money for great strides. It is definitley a good cause. With out them, we would not be where we are today. We started our oun Foundation to raise money for our local families for medical and travel expenses/educational and cultural opportunities and will also...

Good job all of you for raising money for great strides. It is definitley a good cause. With out them, we would not be where we are today. We started our oun Foundation to raise money for our local families for medical and travel expenses/educational and cultural opportunities and will also...

Good job all of you for raising money for great strides. It is definitley a good cause. With out them, we would not be where we are today. We started our oun Foundation to raise money for our local families for medical and travel expenses/educational and cultural opportunities and will also...

Hi u all. I have signed up for a blog, and our title is breathin is believin, however, i can not figure out how to get into it to post. i see the ones posted, but how do i post a blog. I am already signed up to so. I need a computer smart person out there to tell me how. thanks alot...

Hi u all. I have signed up for a blog, and our title is breathin is believin, however, i can not figure out how to get into it to post. i see the ones posted, but how do i post a blog. I am already signed up to so. I need a computer smart person out there to tell me how. thanks alot...

Hi u all. I have signed up for a blog, and our title is breathin is believin, however, i can not figure out how to get into it to post. i see the ones posted, but how do i post a blog. I am already signed up to so. I need a computer smart person out there to tell me how. thanks alot...

This is a very big need. We lost our daughter to Cystic Fibrosis April of 2005 at 23 years old. We formed The Cody Dieruf Benefit Foundation in her name to carry on her legacy and to raise funds to help famlies with financial and emotional help, and with educational and cultural opportunities...

This is a very big need. We lost our daughter to Cystic Fibrosis April of 2005 at 23 years old. We formed The Cody Dieruf Benefit Foundation in her name to carry on her legacy and to raise funds to help famlies with financial and emotional help, and with educational and cultural opportunities...

This is a very big need. We lost our daughter to Cystic Fibrosis April of 2005 at 23 years old. We formed The Cody Dieruf Benefit Foundation in her name to carry on her legacy and to raise funds to help famlies with financial and emotional help, and with educational and cultural opportunities...