www.6500redroses.com

[hbendz]

Hello! My name is Holly Bendz and I have a 6 month old daughter (Maggie-Faye) with Cystic Fibrosis. My husband has started a photography project to raise money for Cystic Fibrosis Research, Inc. You don't have to donate to be a part of the project (especially if you are dealing with the cost of CF directly - $$$$$$$-eek!!).

Please take a moment to view the website www.6500redroses.com and, hopefully, participate. Please share the information with other friends and family. Our local children's hospital (Lucille Packard in Palo Alto, CA) wants to promote the project via the media and a display at the hospital. However, they want to wait until there are 50-60 pictures posted. It really doesn't take long to post a picture thanks to the digial age we live in!

I would also love to hear your feedback on the site so I can share it with my husband.

Love and strength to all!

Holly

 

[hbendz]

Hello! My name is Holly Bendz and I have a 6 month old daughter (Maggie-Faye) with Cystic Fibrosis. My husband has started a photography project to raise money for Cystic Fibrosis Research, Inc. You don't have to donate to be a part of the project (especially if you are dealing with the cost of CF directly - $$$$$$$-eek!!).

Please take a moment to view the website www.6500redroses.com and, hopefully, participate. Please share the information with other friends and family. Our local children's hospital (Lucille Packard in Palo Alto, CA) wants to promote the project via the media and a display at the hospital. However, they want to wait until there are 50-60 pictures posted. It really doesn't take long to post a picture thanks to the digial age we live in!

I would also love to hear your feedback on the site so I can share it with my husband.

Love and strength to all!

Holly

 

[hbendz]

Hello! My name is Holly Bendz and I have a 6 month old daughter (Maggie-Faye) with Cystic Fibrosis. My husband has started a photography project to raise money for Cystic Fibrosis Research, Inc. You don't have to donate to be a part of the project (especially if you are dealing with the cost of CF directly - $$$$$$$-eek!!).

Please take a moment to view the website www.6500redroses.com and, hopefully, participate. Please share the information with other friends and family. Our local children's hospital (Lucille Packard in Palo Alto, CA) wants to promote the project via the media and a display at the hospital. However, they want to wait until there are 50-60 pictures posted. It really doesn't take long to post a picture thanks to the digial age we live in!

I would also love to hear your feedback on the site so I can share it with my husband.

Love and strength to all!

Holly

 

[Samsmom]

Hi Holly!! What a cute baby. I read your post and I will be looking at the web site soon. You might try putting your thread under the topic of families or something like that to draw more attention to it. I have a 13 yr. old daughter who was diagnosed with cf last year. Fund raising is so important for research to continue, so any ideas are good ideas. Best of luck with the project and I just wanted you to know that someone out there was reading. We are in Kentucky, so look how far you have reached allready!!! <img src="i/expressions/rose.gif" border="0">

 

[Samsmom]

Hi Holly!! What a cute baby. I read your post and I will be looking at the web site soon. You might try putting your thread under the topic of families or something like that to draw more attention to it. I have a 13 yr. old daughter who was diagnosed with cf last year. Fund raising is so important for research to continue, so any ideas are good ideas. Best of luck with the project and I just wanted you to know that someone out there was reading. We are in Kentucky, so look how far you have reached allready!!! <img src="i/expressions/rose.gif" border="0">

 

[Samsmom]

Hi Holly!! What a cute baby. I read your post and I will be looking at the web site soon. You might try putting your thread under the topic of families or something like that to draw more attention to it. I have a 13 yr. old daughter who was diagnosed with cf last year. Fund raising is so important for research to continue, so any ideas are good ideas. Best of luck with the project and I just wanted you to know that someone out there was reading. We are in Kentucky, so look how far you have reached allready!!! <img src="i/expressions/rose.gif" border="0">