Sydney Taborelli - Born November 8th, 2008.
Welcome to the World, Little One!
Cloud Nyne Design is honored to feature little Sydney Taborelli.
Little Sydney arrived today - Happy Birthday! She is doing well and you can read all about it on her mommy's blog.
Just click her ultrasound photo to link there - her link can also be found on the "Expecting & New Arrivals" page (CDH link above).
Welcome to the world, little Sydney! It's already a better place because you're in it.....
October 17th, 2008
CHRISTMAS is peekin' round the corner!
I generally take orders until the 10th of December (first come, first created!) so if you're interested in a personalized keepsake DVD be sure to email me as soon as you collect the necessary items (you can find these on the "ORDER VIDEO" page).
The Congenital Diaphragmatic Hernia link above has been updated. Be sure to head that way!
........and please take the time to sign the guestbook. We'd appreciate it.
Cloud Nyne Supports The Parker Reese Foundation
Cloud Nyne creates beautiful keepsake DVD videos from your family photos. They are set to music and include 3D components to make your video truly unique.
That's not all we do....
We also support Congenital Diaphragmatic Hernia Awareness and those who are dealing with it. We support The Parker Reese Foundation. Won't you too?
While you browse Cloud Nyne Design, please be sure to click on the "Congenital Diaphragmatic Hernia" link or The Parker Reese Foundation logo above and see what it's all about.
See Who's Stopping By!
Want one? Click here: http://feedjit.com/
The Parker Reese Foundation Update: Parker's House In Need of Help.
The Parker Reese Foundation exists to fight the congenital diaphragmatic hernia birth defect. We are committed to funding research, advocating public awareness, supporting parents, children, family members and friends facing the diagnosis or who have been diagnosed with the congenital diaphragmatic hernia birth defect. We will carry out this mission by supporting the medical community, encouraging and funding research efforts to find a cause and to effectively treat those diagnosed with a congenital diaphragmatic hernia, sponsoring public awareness campaigns and supporting all who seek our organization.
The Parker Reese Foundation is an IRS approved 501c3 tax exempt public charity. Through donations, grants and future investments, The Parker Reese Foundation will become a central locator for information, support and referral for congenital diaphragmatic hernia.
This organization is run solely by volunteers who are working towards the achievement of our non-profit entity.
Parker's House is ready for a new family who will be moving in come September. This means that another baby is going to be born with CDH - and will have to fight. It will also mean a place for the family to call home and be closer to their baby while the fight is on. THAT means everything. That is why Parker's House exists.
If Parker's House can no longer pay the monthly bills (so far these bills are being paid by Jessica & Ashley - Parker's parents and from any donations received) we will be forced to close a very important aspect of The Parker Reese Foundation.
Parker's House needs donations. If you can find it in your heart to go to www.theparkerreesefoundation.com and at least read about what it is we do and why - that's all we ask. Then, if you feel inclined to donate - we would gratefully accept it on behalf of all CDH babies, angels, survivors and parents. So please head to The Parker Reese Foundation website and find out more information. It's the greatest thing you'll do today.
Thank You