March 24, 2012
Back in 2010, during a routine ultrasound, I was informed the newest addition to our family would be born with a cleft lip and possibly a cleft palate. I was terrified and felt so isolated. I found the foundation in an online search and joined their facebook page. They had not only a WONDERFUL webpage with all the resources and information, but programs like Weimer Bottle program who help moms get special needs nipples and bottles if we need them and can no afford them. With all that said, the GREATEST part of this foundation is their actual support network. The administrators are personally active and outright offer support as well as hundreds of other cleft parents. I have never gone more than 15 minutes without a response to a question or concern. Also, the support I have gotten from the group was the biggest factor in me staying calm through my son's surgeries. This group is truly amazing and definately one of a kind!
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MY ROLE:Client Served