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# NameComments
6351 Jacquetta Sanyet
6352 kayla byrdwtf???
6353 Josh Freely
6354 Megan Freely
6355 Anonymous
6356 janice cooperthis woman needs some mental help!
6357 Kimber Reynolds
6358 Anonymous
6359 Dawn Garratt
6360 Bernadette Gengler
6361 Melanie WoodDisgusting
6362 Martin Jordan
6363 Rhonda Woodall
6364 Barbara Lewis
6365 Kyle Reynolds
6366 Mary Richards
6367 Anonymous
6368 Eric Downey
6369 Heather Mills
6370 francesca vlasakmy cousin died from this..... and to think that an org. can own this????? makes me sick to my stomache
6371 Charlene Cassese
6372 Sharronda H. Waldrop
6373 Vicki Purcell
6374 Heidi
6375 Anonymous
6376 Sherri Nichelson
6377 Hayley batemanwhy should any one own it. We have all been affected by cdh, my son nathan died 27 hours.! its so ahrd losing some one so precious and now this , why ..whats the point??,, why is it only your trademark! is affetcs so many people, my life has been turned upside down by it, if anyone would like to chat or know more bout my son his sites www.piczo.com/angelnathanlee
6378 Brandi Shobe
6379 Paul and Lisa Vallins
6380 Anonymous
6381 Jordan Griffin
6382 Peter Bechtold
6383 Rachel Amundsonmy sister Sarah Joy died of this.
6384 Julie Younce
6385 Natasha StevensonFocus Focus, help these children and their families breath of hope, stop being stuoid and worring about trademarks. The more people helping the better let us all own the right to help.
6386 Jessica SchmaltzPlease do not take away this name, without this name, I would not have found out what my daughter had. She passed away after 7 hours of life. If this gets taken away, you have taken another life away.
6387 Tina Meeker
6388 Sara Middleton
6389 Gary KellyDisgraceful and distasteful attempt at profiteering. Those responsible should hang thier heads in shame. CDH awareness belongs to my dead nephew Rhys and his memory.
6390 AnonymousPoor
6391 Heidi Fenn
6392 Kathy Juenke
6393 Joy Faber
6394 Todd Fenn
6395 vicki collinsmy grandson was born june 2005 with rightsided cdh your web site was our only link to cdh thanks to the staff at duke for informing us .camerons defect was so severe he was on ecmo and given a ten percent chance to live .god answered our prayers heis 4now still has feeding issuses but is doing great.this is a devastating birth defect and not much awareness on it thanks so much for your site .
6396 Shelly Zarbock Fenn
6397 Christine PaynePlease stop this insanity!!!!! Some people are not involved for the right reasons, this should be all about the babies and how to help them survive. This is a terrible defect and the word needs to be spread so we can help these precious babies. With GOD all things are possible!!
6398 LAURIE NOVARK
6399 Sheryl Cooper
6400 Anonymous

 

 

 

 

 




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