Archive for April, 2010

Pulmo Appt, Attempt TWO…

We’ll try this again on Monday. Her appt time is horrible, 11:30AM. Early enough that it doesn’t make sense to send her to school for the morning, and late enough that it won’t make sense to bring her afterward. Since she’s in kindergarten, after lunch is taken up by rest time, and Centers. So, I guess we’ll go to the appointment, then maybe have a mommy daughter lunch afterward.

So, on my list of things to ask him is about PFT’s, the blue crap she keeps doing, airway clearance, and what to do about the night coughing, and general lack of control.
I’m just not sure where we can go from here. She’s tried and failed SO many medications…She did great on the QVar for about 2 weeks. She was like a new kid. She ran around and played, even my mom commented on how DIFFERENT she was. We got 2 good weeks.
I’ll be sure to update after our appointment. Hopefully, we’ll have a good plan of action.
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UGH, flaring….

and not Mariella this time.

I seem to have hit a wall. I’ve actually done really well…I didn’t flare badly over the winter…just a few times did I need to hit the albuterol after going out in the cold, or whatnot. What’s going on right now? Totally different than I’ve ever experienced before. Totally short of breath, air pocketing, and generally feeling lousy. I’ve gone to bed at 8:30, 2 nights in a row…and that’s SO unlike me. I’m also waking up in the middle of the night, needing an albuterol puff, or 2.
I resorted to Mariella’s neb last night, and again this morning. It really does just work better. It’s keeping me from needing the puffer every 2 hours…so that’s good. (actually, it’s been 6 hours, and a gym trip, and I still don’t need more)
Sure, I should probably skip the gym when I’m feeling icky…but, I LIKE going to the gym. I only did 10 minutes on the elliptical, rather than trying to do 20…and I did the rest of my cardio on the easier treadmill.
Mariella, on the other hand…is doing pretty well. She hasn’t been blue in about 3 days. She still needs her rescue puffer at least once, usually 3 times every day…BUT, she hasn’t need a neb overnight in 5 days. Probably a good thing, since I don’t know if I’d wake up to give her one.
So, I’m hoping that Mariella doesn’t crap out before I get better…no room for 2 flaring people in one house. (and really, I just want to feel better…I don’t like this SOB feeling. I can handle the coughing [sort of] but the wheeze and SOB…totally not a fan)

We love the Wii

It’s allergy season here in New England (and everywhere else, from what I’m hearing) Abby has seasonal allergies that make her pretty darn miserable. She takes Zyrtec and Flonase every day, but this year, she’s suffering more than usual.

This puts a huge cramp in her “I must be outside at all times” style. She WANTS to be outside, but the pollen count is through the roof, and I’m a little concerned with triggering her RAD with the stuffy, nose and post nasal drip. Quite a few of her pneumonia’s have been in the spring and the summer, likely triggered by her allergies. I let her go out for a little while, but I’m hesitant to let her spend ALL day out there, though that would make her extremely happy.
Yesterday, after she had been outside for a while, she came in and still had a ton of energy to burn. (It’s school vacation week) I had her play Wii Sports for a while…she opted for boxing. After playing for about 20 minutes (and kicking the rears of all her computer opponents) she looked at me and said…”Momma, I’m all sweating, and my heart is beating REALLY fast…is that OK?”
Of course, she still didn’t get to sleep until well after 10PM last night, but that was MY fault entirely. I haven’t been keeping a good eye on her Clonidine script…so we only had 2 left…I’m not sure the refill will be in before Sunday…and she needs to get sleep before school…I’m not so worried about late nights on vacation…especially since she was IN bed, and reading for that whole time.
She’s back on the Wii today…playing Sports Resort…Fencing…she’s getting quite a workout with that too.

What keeps her breathing…

These are the medications that keep Mariella breathing. The machine is a compressor for a nebulizer (the plastic cup thing with the snazzy “Bubbles the Fish” mask attached.) Her albuterol rescue medication goes in there, as well as her Pulmicort, when she’s sick. Her Prevacid is sitting on top of her compressor. That is for her “GERD” (for lack of a better diagnosis) We hope that by keeping the acidity of her “reflux” down, it might help her lungs. She also has 2 inhalers she uses every day. They are not in actuators, because the spacer we use doesn’t need the actuator. The blue puffer is Xopenex. It’s also a rescue med, but easier to bring out and about than a nebulizer. The 2 liquid bottles are prednisone, which we keep in the house at all times, and a codeine cough syrup that we also keep in the house at all times. I didn’t add the multivitamin or the probiotics that she takes daily.

Mariella takes medication at least 3 times a day. More often when she is flaring. She takes dosages of adult medications that make pharmacists (and insurance companies) call the doctor to verify that what they faxed over was really what they meant. That little bottle of Prevacid, that’s supposed to hold 2 weeks worth of pills? We go through them in a week…and will probably start going through 2 a week soon.
Parenting a child with a chronic illness isn’t for the faint of heart, that’s for sure.

We had a great time at the Dance For Dominic!!!

Today was the 2nd Annual Dance For Dominic. It’s a fundraising “Kids Prom.” The purpose is to help raise money for my friend’s son, Dominic’s medical expenses, but a portion of the proceeds goes toward the Cystic Fibrosis Foundation, and research towards a cure.

Just like last year, it was a great time…the children had such a fabulous time, dancing…watching a magician, eating. It appears that we were at least as successful as we were last year. We are searching for a new venue, as we seem to have outgrown the hall we used last year and this year.
Mariella was fully recovered from her stomach bug, so she was allowed to go. She was very droopy, just sitting on a chair, watching all the activity. At first, I thought that she was just tired. Until I looked at her fingernails. They were tinged with blue. So, I puffed her. Literally in seconds, she was like a new kid. I think that unless she’s actively coughing, or experiencing a tight chest…she doesn’t always realize if she’s not exchanging her air well. She hasn’t figured out that feeling. We talked about listening to her chest and her body. That her teachers at school aren’t looking at her fingernails and lips to see if she is getting blue. I’m not able to ask the teachers to look for that…it’s really not their job. Since they already think she has ADD, I hesitate to tell them that if she is lethargic or lacking attention, to send her to the nurse. This blue thing has been happening more often, and it’s concerning me. I hate that we have to wait until May 3rd for her appointment.

On the upswing!!!

After a full day of feeling crummy, with a scary high fever to boot. Some Tylenol and a good nights sleep seemed to do a world of good.

Mariella has been eating applesauce, saltines and rice all day. She was a little upset that Abby got pizza for supper, and she didn’t, but I told her I would save her a piece for Monday. I’ll have to remind Rob not to eat it. Otherwise, we’ll have a very unhappy girl.
Tomorrow is the Dance for Dominic! We’re so excited, and we’re hoping for as good a turnout, and a successful fundraising effort. Mariella was quite worried that she wouldn’t be well enough to go…but she seems to be nearly 100%, so she will be there with bells on. I’ll post how much we were able to raise, as soon as I know.

I swear, the forces of the universe are out to get me!

It all started at 2AM. The Cough. Up I got, started the neb. I snuggled in bed, and took the backdraft off the nebulizer (you know…a good 2 for one deal)

I got back in to bed and had JUST gotten to the point of sleeping again, when Mariella came RUNNING out of the bedroom, kind of crying that she had to pee really bad. I got up with her, because though she can use the bathroom on her own, she seemed agitated.
Good thing I did, because the next thing she said was, “my belly hurts, I have to throw up!” and before I could get the bowl, she threw up, all over the bathroom floor. Good thing we hated the bathmat, and wanted to replace it anyway.
So, at 3 AM, I was giving her a bath. I wasn’t thrilled with how she looked, so I “slept” on her bedroom floor…helping her with the pukes several times. She also needed 2 more nebs in this time. I think we’ve got a 2fer going on…a tummy bug AND a good asthma flare.
I’m bringing her in to the walk in this morning, because often, the vomiting accompanies an ear infection, and she’s running a temp of 101ish.
Of course, we were supposed to see Dr. Duda this afternoon, which of course can’t happen now. Hopefully, they can squeeze us in sometime next week, but I don’t think they will, I guess we’ll just keep that May 3rd appointment.

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