Every day. Twice a day. At least.
I miss the one photo a day, this is what we do, document our lives, one day at a time mentality around here.
Every day. Twice a day. At least.
I miss the one photo a day, this is what we do, document our lives, one day at a time mentality around here.
What a sweet boy! How is he doing with his treatments? Are they helping? My friends’ little one had terrible asthma when he was Teagan’s age and I remember his mom always having to do those treatments for him. I remember how scared Holly always was and how she would hover over him just to make sure he was breathing well. He is now almost 11, and I can’t remember the last time he had to have a treatment. I pray the same for Teagan, that this to will eventually pass.
You’re a great mama Lynds!!
We do the same thing with my sweet Addie. She was diagnosed with Asthma when she was two. We spent several trips to the ER and find out that not only does she Asthma but allergies to nuts. We do her breathing treatments once a day so I can say that is does get better! Hang in there!!!
That is our daily routine-twice a day-as well, so I feel your pain. Poor sweetie.
I am so impressed he does them. Both my children need the treatments and my 3 year old will do them just fine, but my little boy that is just a few months younger than Teagan will NOT do them. It’s hard. I try, give up…try again, give up. Tell me your tricks!!
Yep- us too. My 3.5 year old now has RAD and just today we were able to start an inhaler via a spacer chamber thingy. Love it and no more nubu’s!
Looks like he’s doing a great job with it…and I’m sure it makes him feel so much better!
This is what we’re doing this week, too. =(
little guy…what a trooper! we do these treatments daily with my 2 year old and with a “fish mask.” have you seen those? makes it a tad more exciting, well, ok- interesting. i will have to post a pic. of “the fish!” ha ha. you are so fun! always very fun to read about your life and your work! great stuff.