S.,
I have 3 kids (12-G, 2-G and 1-B) and one due in June, the two girls both have asthma. We found out with both of them when they were just over 2 years old. Things have changed a lot in the last 10 years for treatment.
The oldest was given a nebulizer and Albuteral (which you had to mix yourself), but even though we had the home machine – she was seen in the ER often. She was never put on any preventative medications. Recently we have started giving her the over the counter cingular with has helped her in her “peek” seasons. But she is now old enough to know when she need her inhaler.
My youngest had gone through allergy test and part of her issues stem from her allergies. She is on Zertch (before bed), Cingular (in the morning), Flovent - inhaler (2x a day) and Albuteral (inhaler/nebulizer - we have both) when needed. She was seen in the ER 3x and hospitalized 2x within a month before they got all her meds right and it took almost 2 month to get her completely under control.
It is a very scary thing, but it is something you learn very fast how to deal with. We were given a class at Akron Children’s Hospital before we were aloud to take her home and home medicate her. That way they were certain we knew when and how to give her her meds.
One thing I was told is a child with asthma shouldn’t be treated the same as a child without it when it comes to colds. In every other aspect they are the same… can run, play, and just be kids – as long as you can keep the breathing under control. But as for colds… we were told at the first site of a runny nose, watery eyes, or even a cough to start giving the Albuteral inhaler/nebulizer. Reason being is it is difficult to know what is an attack or what is a cold, plus most colds affect the lungs which affects the breathing. So, it is always better to be safe and use the inhaler then wait to long and even up at the ER for treatments. But if you do end up at the ER don’t look at is as you messed up… it happens to all of us with kids with asthma.
I know the class wasn’t where I wanted to be when I was there, but I’m glad it was monitory to take her home. I’m not sure where you live or if something similar is available around you, but if it is and you have questions about it… it might be a good idea to look into a class or something. They are educated to know the answers, give you more understanding of when he is going through, what meds are available and what the different is between them. They also let us know what kind of things can help to trigger is and what you can do around the house to help reduce the attacks.
Most of all know that you are doing everything that you can to care for you little ones… this is just one of the bumps in the road. Work with your son, he is a bit older and should be able to tell you when his lungs hurt and when they don’t. He will learn to tell you when he needs it – give it time. You both will adjust to it and will find your way!
J.