Petition Against Congenital Diaphragmatic Hernia Awareness Trademark Ownership Petition : [ powered by iPetitions.com ]

#	Name	Comments
201	Anonymous
202	Ramona Gallegos
203	Megan Bradshaw
204	Becky Howard	I sincerely hope this is blocked for all families and babies who are affected with this defect and also for all others families who have children born with any kind of defect. This could set a precedent.
205	Sharon Frechette
206	Anonymous	mother in honor of my CDH child
207	Suzanne Pierssene
208	Jessica Jackson
209	Deborah Albano
210	Tom Hargadon
211	rebecca miller
212	Marianne Link
213	jesse hubbard	aaron this is for you
214	Dave Retterer	This would be a travesty if you were to let this trademark go through
215	Anonymous
216	Elizabeth Randazza	This is for you James.
217	Kim Byers
218	wayne stevenson
219	Cathy Salesky
220	Sandra Richards-Vance	Mother of a surviving child who had a CDH. This is ridiculous. How can you claim patent to something that is used regularly by others. I have never heard of this group nor what their intentions are for the use of this patented phrase.
221	Barry J Smith	In memory of my granddaughter Kaitlyn.
222	Carole Olson	Raising awareness of CDH belongs to all family and friends of those whom have been born with this horrible defect. It cannot and should not be owned by a single entity, organization or person. Awareness began with each one us the day we found out about the person in our life that had/has CDH. That right and those words should not be allowed to be taken away or denied from another person.
223	Anonymous
224	Lindsey McClave
225	Anonymous
226	Anonymous
227	Katherine Lindsey
228	Natividad Osorio	This is for you Alexis.
229	Jay M Wilson MD	Give me a break! I and many other hard working physicians and surgeons around the world have been promioting CDH awareness for more than two decades. Promoting awareness is one thing and is admirable. Trademarking the phrase and concept as though it was an original idea is quite another and in the long run risks having exactly the oposite effect by hampering the efforts of others, some of whom have been doing this a hell of a lot longer than this group, to get the same message across.
230	Becky Shooter
231	Kara Enssle	They truely have lost sight of whats REALLY important in all of this. The children! Not the name!
232	Elaine DeSalvo
233	lillian ortiz
234	Rina Bahri	SInce my baby girl Mary passed away on June 3, 2008, CDH has become a way for me to teach others what these little babies have to go through. Taking this away from not be the right thing to do.
235	Judy Hart	In memory of Bethany Grace.
236	Charles Cloughen, Jr.
237	Renee Sandford
238	Christina Budriss
239	Nathan Nava	In memory of Gabriel Eric Nava who lost his battle with CDH. Let EVERYONE spread awareness for the sake of all the children who will have to fight for their lives.
240	Mary Setliff
241	Dawn Grady	It would be unthinkable that the Patent Office would approve this Breath of Hope's request. It should not matter WHO uses the phrase, as long as awareness is raised for our precious CDH babies. Please do not limit the awareness of CDH to one corporation.
242	Deborah
243	Anonymous
244	Lynn Tidy	cherubs helped me come to terms with the loss of my baby through cdh it helped me understand lots of things and realise there were lots of babies have this defect if this could help one person like me then it could help a lot more mothers of an angel
245	Cristin Russell
246	Daphne Parker
247	Libbie Miller
248	Margaret Thompson	As the mother of a surviving CDH child I am appalled by this request for ownership. Had more awareness been available when my son was born, he may have been identified and treated for this condition prior to his birth. The trauma and resulting effects of the day of my son's birth remain with us today, and will for the rest of his life.
249	Anonymous
250	Anonymous