Summer camp can be an incredible time of learning, growing and fun for our kids with CF. But it can also be a time of stress for us parents! Will they get the proper medications? What about dehydration? Will their needs be attended to?
Problems can be avoided by setting up the expectations early on with both our child and the camp staff. Here are some tools to help you, and your child, prepare for a great summer vacation.
This website is the sole property of Lisa C. Greene, BS CCP. Lisa is a certified parent coach, parenting educator, public speaker, and the mother of two children with cystic fibrosis. She is also the co-author with Foster Cline, MD of the award-winning Love and Logic® book “Parenting Children with Health Issues.” For more information, visit visit www.PCWHI.com.
The information published on this website or in any connected material is the opinion of Lisa C. Greene dba Happy Heart Families only and is not meant to replace professional medical or mental health care. Persons should always seek the advice of a medical professional when making decisions about personal healthcare or treatment.
