| # | Name | Comments |
|---|
| 151 | Karen Jenkins | |
| 152 | Pam Shorter | For Cole Campsey ~ my VERY SPECIAL nephew. |
| 153 | Donna Easley | |
| 154 | Cortnee Burkhour | |
| 155 | lorraine mccorry | |
| 156 | Lisa Lawson | |
| 157 | Judye Nazareth | As a parent who has lost a baby to this severe birth defect, the fact that an organization that supposedly supports me is seeking to copyright the awareness term is abhorrent. What is motivating this move? I feel betrayed by a group that is supposed to be helping people like me. Is there a profit here or a stab at other organizations? |
| 158 | janet Vignes | |
| 159 | Kara L Hess | |
| 160 | Michele Keating | why would anyone want to put a trademark on a phrase like CDHA, it disgusts me that considering this defect has had such an impact on so many, and so many beautiful lives have been lost, that anyone would want to own the awareness, that has helped us all. |
| 161 | Rachael Oliver | |
| 162 | Anonymous | |
| 163 | Anonymous | |
| 164 | Stephanie Proper | |
| 165 | Narelle Blakeley | |
| 166 | Susan Hall | |
| 167 | Troy Miller | Father of Non-Survivor Dallas Miller |
| 168 | Stephanie Boyer | |
| 169 | Nancy Rogers | |
| 170 | Jyl Albertson | |
| 171 | Anonymous | |
| 172 | Karen Blandford-Anderson | What purpose would it serve to have one organization hold a patent on this phrase when it would hurt so many other organization and individuals who are trying to make a difference, not a profit. |
| 173 | marie Brown | |
| 174 | Pam Callow | |
| 175 | Anonymous | |
| 176 | Freedom Green | |
| 177 | Anonymous | |
| 178 | Kelli Blakeley | |
| 179 | Gabrielle Majstorovic | My niece died 16 years ago of cdh.
We desperately need awareness so that others can be saved. |
| 180 | Tammy Jones | on bealf of Cole Campsey. |
| 181 | Karen Brown | |
| 182 | Anthea Kirk | |
| 183 | Tanja Hodgson | Cherubs was there for me when by newborn was diagnosed with CDH six years ago. They helped me so much through a difficult time. |
| 184 | Lori Leclair | |
| 185 | Cathy Willhite | Proud grandmother of the late Vito Robert Pensavecchia, born with CDH on November 12, 2005 past away January 20, 2006. We were lucky to have him for almost 10 weeks before his suffering ended and his heavenly life began. He is always in our prayers and will never be forgotten. We love you Vito.
Grandma Cathy |
| 186 | Linda A. Ryan | |
| 187 | Jeanette M Peracchio | |
| 188 | Anonymous | |
| 189 | Tammi Duzan | |
| 190 | Terra Sechrist | Bless you Asher!!! |
| 191 | Karla Holt | |
| 192 | Tami Traficante | How does such an idea get started to - own an awareness??? I'm having a hard time understanding what benefit could come from it? I can only see the limitation of other organizations trying to raise awareness. |
| 193 | Anonymous | No one has the right to own the name of a medical condition. No one. |
| 194 | Tamara Niebrugge | |
| 195 | Jeanne Mapes | Shame on such a soulless entitiy. |
| 196 | Brenda Johnson | |
| 197 | Anonymous | |
| 198 | Tammy & Ricky Riggs | To our very special nephew Cole Campsey who holds a very special place in our heart. We love you Cole |
| 199 | Bettina Haase | |
| 200 | Nicole Padgett | |