Dawn Torrence Ireland
04-10-2011, 04:53 PM
**** YOU DON'T GO ANYWHERE ****
April 19 - celebrating Congenital Diaphragmatic Hernia Awareness DAILY
♥ This is the ONLY non-trademarked day set aside for CDH that ALL CDH families, charities and researchers can participate in! ♥
WHAT DO YOU DO? Just raise CDH Awareness! Be involved as much or as little as you want to be! Wear a shirt, hand out fliers, light a candle, let balloons go, send out an e-mail, wear a ribbon, hold an event, tell at least 1 person what CDH is - just do at least 1 thing to raise CDH Awareness!!!
Every family affected by CDH has their own Congenital Diaphragmatic Hernia Awareness day - the day their child was diagnosed. The day that they became personally aware of CDH. We honor that and we promote CDH Awareness Daily.
On April 19, 2010, after 2 years of a very unnecesary trial, led by 7 caring CDH organizations, 4 compassionate pro bono attorneys and 1000's of CDH families Congenital Diaphragmatic Hernia Awareness was restored to it's rightful owners - the babies, families and medical care providers affected by CDH. Now, ALL families affected by CDH can raise awareness freely without harrassment, threats of lawsuits and other negative behavior. Now, ANYONE can say and raise "Congenital Diaphragmatic Hernia Awareness" and help the babies!!!!! :)
http://ttabvue.uspto.gov/ttabvue/v?pno=92050284&pty=CAN&eno=2
On the 1 year anniversary of this triumphant accomplishment for our children and the future of CDH Awareness and Research, we will celebrate with balloon releases, candle lighting ceremonies and more to raise more CDH Awareness, honor all children affected by CDH.
This is the only non-trademarked day specifically for CDH and we hope that you will join us and over 3600 members + 6000 supporters in this very important day!
April 19 - celebrating Congenital Diaphragmatic Hernia Awareness DAILY
♥ This is the ONLY non-trademarked day set aside for CDH that ALL CDH families, charities and researchers can participate in! ♥
WHAT DO YOU DO? Just raise CDH Awareness! Be involved as much or as little as you want to be! Wear a shirt, hand out fliers, light a candle, let balloons go, send out an e-mail, wear a ribbon, hold an event, tell at least 1 person what CDH is - just do at least 1 thing to raise CDH Awareness!!!
Every family affected by CDH has their own Congenital Diaphragmatic Hernia Awareness day - the day their child was diagnosed. The day that they became personally aware of CDH. We honor that and we promote CDH Awareness Daily.
On April 19, 2010, after 2 years of a very unnecesary trial, led by 7 caring CDH organizations, 4 compassionate pro bono attorneys and 1000's of CDH families Congenital Diaphragmatic Hernia Awareness was restored to it's rightful owners - the babies, families and medical care providers affected by CDH. Now, ALL families affected by CDH can raise awareness freely without harrassment, threats of lawsuits and other negative behavior. Now, ANYONE can say and raise "Congenital Diaphragmatic Hernia Awareness" and help the babies!!!!! :)
http://ttabvue.uspto.gov/ttabvue/v?pno=92050284&pty=CAN&eno=2
On the 1 year anniversary of this triumphant accomplishment for our children and the future of CDH Awareness and Research, we will celebrate with balloon releases, candle lighting ceremonies and more to raise more CDH Awareness, honor all children affected by CDH.
This is the only non-trademarked day specifically for CDH and we hope that you will join us and over 3600 members + 6000 supporters in this very important day!