Focus on the positive.
Although your child needs to have an age-appropriate understanding of his illness, treatment time does not need to be an ongoing reminder of potential health problems. Instead of saying, "You'll get sick if you don't do your treatment" try reminding him that the breathing treatments help keep his body healthy.
Make breathing treatments fun.
Sitting alone attached to a machine can be an isolating experience. Properly using the nebulizer is the number one priority, but you can add some fun by doing low-key activities such as reading to your child, letting him play a video game, watch television or color during treatment time. Sometimes, simply staying in the same room may be enough to comfort him. Learn to read your child's mood to see if he needs more or less interaction during a particular breathing treatment.
Let him make decisions.
It can be empowering to let your child choose when to do treatments, but multiple medications and therapies do not leave much flexibility. Instead, let him take an active role by making other decisions, such as where to sit during breathing treatments or, if appropriate, which medicine to take first.
Make breathing treatments routine.
Even if your child has the luxury of choosing treatment times (within reason), help him understand prescribed nebulizer treatments are not optional. This can help eliminate those daily "Do I have to?" discussions.
Each child's unique personality and health considerations mean there is no one perfect formula for encouraging and completing nebulizer treatments. Your personal physician and child psychologist are the best sources of information for treating your child's illness. Never hesitate to ask for their advice.
Published by Drew Taylor - Featured Contributor in Arts & Entertainment
Drew Taylor writes about a variety of practical topics including TV, shopping, product reviews, cooking, holidays, crafts, pets and gardening. As a creative cook, her food coverage includes product revie... View profile
- Cystic Fibrosis: A Personal Story About Experiences with PortsMy friend "Eleanor" is one of the longest living survivors of Cystic Fibrosis. She has undergone many medical treatments, and has agreed to share her experiences with ports and stents with us.
- Common Signs and Symptoms of Cystic FibrosisThis article details the five most common signs and symptoms of cystic fibrosis.
- Your Help is Needed to Find a Cure for Cystic FibrosisThe Cystic Fibrosis Foundation (CFF) has plenty of events planned for 2007. Check out how you can get involved and help find a cure for this devastating disease.
- More Women with Cystic Fibrosis Are Becoming MothersOnce a fatal childhood illness, people with Cystic Fibrosis are now living longer than ever. Many women with this disease are now facing the question on whether or not they want to have children of their own.
- Coping with Home Infusion Therapy for Cystic FibrosisMany cystic fibrosis patients are well-seasoned professionals when it comes to managing the schedule of home IV therapy; for the newly diagnosed or parents who are learning the home IV routine for the first time, it c...
- A Day in the Life of an Adult with Cystic Fibrosis
- Treatment for Cystic Fibrosis
- Keeping Your Child Entertained While Giving a Breathing Treatment!
- How to Safely Use a Nebulizer on a Young Child
- Effective Pediatric Asthma Treatments, Including Treatments for Symptoms of Asthma
- Zafirlukast Treatment for Asthma and Allergies: People, Dogs & Cats
- Cystic Fibrosis: A Personal Story - Part One: The Discovery
- Focus on the positive and help the child understand the importance of breathing treatments.
- Whenever possible, let the child make decisions.




