As I see it, what is the point of being on a medicine when there is no clear answer as to if he truly has Lyme's. Specially when the side-effects of the Medicine are what he already is experiencing prior to taking it and ultimately making his symptoms 100 times worse.
We did talk about him going off majority of the medicine that he's on to try to figure out which medicines are truly helping and which ones aren't. But it's a lot of medicine. 😒
I took Ezy to the pediatrician yesterday and it turns out that he could have a milk intolerance. His lungs are clear but his nasal pathways. We already struggled with formula and his spitting up but never thought that could cause the rattling and what he's going through. The doctor explained it to this way that due to him spitting up from having a sensitive stomac, the spit up is getting caught in his nasal pathways and causing the overactive mucous secretions. The doctor did give us the nasabulb to try:
Haha I'm not sure how I feel about sucking mucous from my child's nose from my own mouth...but supposedly this thing works better then the suction bulb you get from the hospital or first aid kits.
I have a sleep study next Wednesday, and to be honest I'm a little nervous about. This will be the first night away from all three littles and Anthony. Not saying that Anthony can't handle it or anything but I worry how the kids are going to react with their momma gone for a night. Yeah, I'm freaking out over one. night...I'll take a shower before I go and go to be early and maybe I'll ACTUALLY sleep! Because being a mom of three under 6 makes me a zombie and then going to school full time on top of that. I can't really remember the last time I was actually able to sleep without someone needing something in the middle of the night.
-Annie