Colby is definitely doing better. Hooray, giddy up, 2 thumbs up, atta boy, hells yeah and way to go sweet boy. Around 4:30 yesterday they came and told me Colby's test confirmed pseudomonas. Boooo. That's on top of "a little spot" of pneumonia and "some" bronchitis. Damn, no wonder we couldn't care for him at home! So, he is currently on 3 antibiotics. Clindamycin will treat the pneumonia and also hopefully ward off any MRSA is it's lurking around. Zosyn will fix the pseudomonas, along with putting Cipro drops in his trach to help with this also. Good grief, he's bound to get better after all that!
I do see that Colby is definitely starting to improve. Thank goodness, he had me super worried. Yesterday he took a 2.5 hour nap. His body needs the rest for sure, since we've been doing cough treatments on this boy every 4 hours around the clock since September 18. Of course he didn't fall asleep last night until after midnight, the big stinker. Then he slept in late this morning. His cough treatments are going much better. We're not getting near as much "gunk" out as before, so his lungs are finally clearing up. Instead of doing cough treatments every 4 hours, we're going to try and move them to every 6 hours. He was on 30% oxygen. Yesterday we bumped it down to 28% and this morning we moved it down again to 26%. Baby steps. If he continues to improve at this rate, we'll be looking at discharge soon. I have my sights set on Friday. We'll see.
My dad has been with us since Sunday morning. My mom is driving up now and he'll be heading home for a couple of days. Can you say world's best parents/grandparents?!?! Don't know how in the world Colby and I would survive without them. I've been struggling with being sick, too. Actually I got a head cold before Colby started getting sick. Now the dry, hacking cough has been lingering on. I finally started a steroid pack yesterday, and just let me say, wheeeeeeeee, steroids! I've been up since 6:30. Our room is organized and spotless. I still have a little wheezing and a bit of a hacky cough, but can tell a big improvement. This being sick is for the birds. Going to have to make some lifestyle changes when we get back home and start taking better care of myself.
But for now, I get to eat what I want. I'm 100 miles away from home with my sick kid, stuck in a hospital room, getting over illness myself. Comfort food much needed. Let me tell you what they had in the cafeteria yesterday, a macaroni and cheese bar. Holy crapoly are you kidding me? Yummy, gooey, cheesy mac and cheese, then you could get add ins such as broccoli, chicken or BACON!! You bet your buns I had some. I at least ordered the half portion. That makes it ok, right? OMG it was so good. I could have taken a bath in it.
That's the scoop for now. Colby is on tons of drugs, doing better. I'm on steroids, doing better. And we're going to go home soon. Time to put this nasty illness behind us and move on with our lives. There is much fall decorating, Halloween costume choosing, pharmacy test studying and more fundraising to do. Time to start blogging about the fun stuff, not his old nasty hospital stay stuff. More later. Toodles.
Tuesday, September 30, 2014
Monday, September 29, 2014
MONDAY - FINALLY GETTING SOME ANSWERS/RESULTS
There seems to be some confusion as to what's going on with Colby. That's probably my fault, sorry. I'm not exactly hitting on all cylinders lately. So let's see if I can provide clarification. Read below and pay attention.
Saturday afternoon we went via ambulance to Kosair, the local children's hospital. There they did a chest x-ray, nasal swab to test for viral illnesses, a trach aspiration test to test for other things and drew blood work. Then we were taken via the Kosair transport team to Cincinnati Children's, late Saturday night. It always takes lab results at least 24 hours to complete, if not 36-48 hours. So it doesn't do me any good to start asking what the lab reports are until 24-36 hours after they were taken. X-ray showed small amount of pneumonia on Colby's lower left lobe. Well of course it did. Does Colby get sick without getting pneumonia?! Apparently if the pneumonia is "streaky" that indicates viral. If it is a "patch/spot" usually means bacterial. Who knew? So they started him on IV Clindamyacin (probably spelled incorrectly.)
That's really all I knew until this morning. In rounds we discussed everything going on with Colby. His CBC looked good. His renal panel was normal. His PCR is negative. That's the viral panel they run. The attending doctor here said Kosair said they test for about 20 viruses including flu, rhinovirus, etc. His nasal sample shows no nasty growth. However, keep in mind there are about 150 nasty viruses out there, and they only test for about 20 of them. His trach sample is growing gram negative. What does that mean? Probably means he has pseudomonas (probably spelled incorrectly.) Great, super, fantastic. Guess this will be Colby's arch nemesis. We have to wait for sure for the gram negative result to keep "growing" to further define what he has. They will probably keep him on his current antibiotic and add another one to treat the pseudomonas if that is in fact what Colby has. So, as of now, Colby's official diagnosis is bronchitis and pneumonia. We're going to try some hypertonic saline and maybe some Xopenex (spelling?) to try and break up the gunk in his lungs. Colby is on 30% oxygen, room air is 21%. So as he starts to improve, we will wean his oxygen down as he tolerates.
Colby does not have the Enterovirus everyone keeps asking about. Here's some helpful info. The pulmonologist said 2-3 weeks ago they were swamped in the TCC with patients testing positive for it. He said it was so bad he felt schools should have been closed down. He said it's not that bad right now. I do know there is another patient on our unit that has it, but this patient is down another hallway, thank goodness.
What's the plan for Colby? Wait to see what else the trach culture grows. Treat accordingly, maybe add another antibiotic. Continue cough treatments every 4-6 hours for airway clearance, trying to finally get his lungs clear. Maybe use hypertonic saline or Xopenex to help with that. Colby is feeling better I think. He got lots of good sleep last night, more than in the last several days. His heart rate if finally down where it should be. We gave him a bath last night. He was needing one really badly. Stinky Poo! Hadn't had a bath in several days.
That's the plan, Stan. Hold tight. Watch for Colby to improve. Wait for further culture results. Give Colby kisses and hugs and more kisses and more hugs.
And don't forget!! The Origami Owl jewelry fundraiser is still a GO. We're still having it!! I know you were just thinking this morning, man, I need some new, uniquely designed and original jewelry. I just know you were thinking that! Taking orders from now until Tuesday (tomorrow) at noon.
I'll update when I know more. Colby is amazing! How in the world do you battle bronchitis when you have no cough?! He's such a trooper! What a strong-willed young man he is. Gooooo Colby! Kick some bronchitis/pseudomonas/pneumonia ass.
Saturday afternoon we went via ambulance to Kosair, the local children's hospital. There they did a chest x-ray, nasal swab to test for viral illnesses, a trach aspiration test to test for other things and drew blood work. Then we were taken via the Kosair transport team to Cincinnati Children's, late Saturday night. It always takes lab results at least 24 hours to complete, if not 36-48 hours. So it doesn't do me any good to start asking what the lab reports are until 24-36 hours after they were taken. X-ray showed small amount of pneumonia on Colby's lower left lobe. Well of course it did. Does Colby get sick without getting pneumonia?! Apparently if the pneumonia is "streaky" that indicates viral. If it is a "patch/spot" usually means bacterial. Who knew? So they started him on IV Clindamyacin (probably spelled incorrectly.)
That's really all I knew until this morning. In rounds we discussed everything going on with Colby. His CBC looked good. His renal panel was normal. His PCR is negative. That's the viral panel they run. The attending doctor here said Kosair said they test for about 20 viruses including flu, rhinovirus, etc. His nasal sample shows no nasty growth. However, keep in mind there are about 150 nasty viruses out there, and they only test for about 20 of them. His trach sample is growing gram negative. What does that mean? Probably means he has pseudomonas (probably spelled incorrectly.) Great, super, fantastic. Guess this will be Colby's arch nemesis. We have to wait for sure for the gram negative result to keep "growing" to further define what he has. They will probably keep him on his current antibiotic and add another one to treat the pseudomonas if that is in fact what Colby has. So, as of now, Colby's official diagnosis is bronchitis and pneumonia. We're going to try some hypertonic saline and maybe some Xopenex (spelling?) to try and break up the gunk in his lungs. Colby is on 30% oxygen, room air is 21%. So as he starts to improve, we will wean his oxygen down as he tolerates.
Colby does not have the Enterovirus everyone keeps asking about. Here's some helpful info. The pulmonologist said 2-3 weeks ago they were swamped in the TCC with patients testing positive for it. He said it was so bad he felt schools should have been closed down. He said it's not that bad right now. I do know there is another patient on our unit that has it, but this patient is down another hallway, thank goodness.
What's the plan for Colby? Wait to see what else the trach culture grows. Treat accordingly, maybe add another antibiotic. Continue cough treatments every 4-6 hours for airway clearance, trying to finally get his lungs clear. Maybe use hypertonic saline or Xopenex to help with that. Colby is feeling better I think. He got lots of good sleep last night, more than in the last several days. His heart rate if finally down where it should be. We gave him a bath last night. He was needing one really badly. Stinky Poo! Hadn't had a bath in several days.
That's the plan, Stan. Hold tight. Watch for Colby to improve. Wait for further culture results. Give Colby kisses and hugs and more kisses and more hugs.
And don't forget!! The Origami Owl jewelry fundraiser is still a GO. We're still having it!! I know you were just thinking this morning, man, I need some new, uniquely designed and original jewelry. I just know you were thinking that! Taking orders from now until Tuesday (tomorrow) at noon.
I'll update when I know more. Colby is amazing! How in the world do you battle bronchitis when you have no cough?! He's such a trooper! What a strong-willed young man he is. Gooooo Colby! Kick some bronchitis/pseudomonas/pneumonia ass.
Sunday, September 28, 2014
ORIGAMI OWL FUNDRAISER STILL HAPPENING
The Origami Owl jewelry fundraiser planned for tomorrow is still a GO!! Just because I won't be there doesn't mean a thing. You can still shop for beautiful, personalized, unique jewelry! The Origami Owl consultant/designer, Nancy, will be set up at my apartment from 6P to 9P just as we originally planned. Come one, come all. Grab a friend, come on over and see all the wonderful possibilities Origami Owl jewelry has to offer.
If you live out of town or are unable to attend the fundraiser, don't panic. You can shop online. Go to this link to place your order:
www.windowtomysoullockets.origamiowl.com/parties/AmyBagshaw451375/collections.ashx
You must use this link in order for us get get credit for the purchase. All orders are due no later than noon on Tuesday, September 30.
Thanks so much for your continued support as Colby and I start the journey of owning a handicap accessible house. Time to kiss apartment life bye-bye!
If you live out of town or are unable to attend the fundraiser, don't panic. You can shop online. Go to this link to place your order:
www.windowtomysoullockets.origamiowl.com/parties/AmyBagshaw451375/collections.ashx
You must use this link in order for us get get credit for the purchase. All orders are due no later than noon on Tuesday, September 30.
Thanks so much for your continued support as Colby and I start the journey of owning a handicap accessible house. Time to kiss apartment life bye-bye!
GOOD MORNIN FROM TCC
Yesterday was one of the longest days. I was asked the same questions about Colby over and over. And over. If one more person asked me what size trach he had, I was going to lose it. Don't they write that shit down in the computer?! Good thing I was too worried and exhausted to go cray-cray on anybody.
I called 911 about 2:45PM Saturday. First the firemen show up. Hello boys, I'm single BTW, wink wink. Then the ambulance ride to Kosair. Ugh, we tried so hard to keep Colby out of the hospital!! While in the ER, I continued Colb's feeds. Also had his IPV and CoughAssist with us. Lord knows they don't have that equipment at that insufficient, non-SMA hospital! So I was able to give Colby his treatments. They did a chest X-Ray, which shows pneumonia. I could've told them that. We are waiting for the other lab results. Kosair's Transport Team came and got us around 7:00. Took us to Cincinnati Children's. Went to that ER. First to a triage room for assessment. Then to another room for holding until his room was ready in the TCC. I'm so thankful they had a room for a Colby. That was another big worry I had when deciding whether or not to take him to the hospital. Got up to the TCC room at 12:10AM. Colby is such a trooper! And he was way overdue for a cough treatment, so we did that as soon as we got him settled and the RT got the orders. Can't wipe Colby's behind without orders. Drives me up a wall. I said just bring me the equipment and I'll do it! But we didn't have to wait too long. Colby's nurse and RT (respiratory therapist) were very good. I watched the RT closely, she had her shit together. Good thing for her. If not, she'd probably have my footprint embedded in her backside. By that time, I was NOT in the mood for any goofball ding dongs.
I already know who Colby's nurse is today, and I'm pleased. She has worked in the TCC forever and took care of a Colby a lot when we were here in June for surgery. For now Colby is on IV Clindamyacin. We'll have to wait for lab results to see if he needs another and/or different antibiotic.
Colby is snoozing away. I should be probably. It will take a very long time for us to get caught up on our rest. I told my parents just to stay home last night. It was getting so late. Plus Colby is stable and we weren't having a true OMG Colby needs help now emergency. Just thought we would head to the hospital before it became that type of situation. My dad is on his way up now. Think I'll lay back down for a few minutes. I guess we're in a holding pattern until lab results come back. Hurry up and wait as they say. More info/updates as I have them.
I would like to give a shout out to Colby's rock star nurses. They all went above and beyond this past week helping me with Colby. They did anything I asked them to do. Wipe down this, let's try this with Colby's treatment, could you stop on you way here and grab me some lunch, rinse the snot out of this, answer the phone while I'm in the shower, help us pack for Cincy, etc. they all sent texts checking on him and are truly concerned about Colby. We're blessed to have the group of nurses we currently have. Because trust me, I know a loser nurse when I see one. We've had our share of those, too. But the ones we have now are awesome. Thanks guys and gals for helping me take care of sweet boy. Hope to be home soon!!
I called 911 about 2:45PM Saturday. First the firemen show up. Hello boys, I'm single BTW, wink wink. Then the ambulance ride to Kosair. Ugh, we tried so hard to keep Colby out of the hospital!! While in the ER, I continued Colb's feeds. Also had his IPV and CoughAssist with us. Lord knows they don't have that equipment at that insufficient, non-SMA hospital! So I was able to give Colby his treatments. They did a chest X-Ray, which shows pneumonia. I could've told them that. We are waiting for the other lab results. Kosair's Transport Team came and got us around 7:00. Took us to Cincinnati Children's. Went to that ER. First to a triage room for assessment. Then to another room for holding until his room was ready in the TCC. I'm so thankful they had a room for a Colby. That was another big worry I had when deciding whether or not to take him to the hospital. Got up to the TCC room at 12:10AM. Colby is such a trooper! And he was way overdue for a cough treatment, so we did that as soon as we got him settled and the RT got the orders. Can't wipe Colby's behind without orders. Drives me up a wall. I said just bring me the equipment and I'll do it! But we didn't have to wait too long. Colby's nurse and RT (respiratory therapist) were very good. I watched the RT closely, she had her shit together. Good thing for her. If not, she'd probably have my footprint embedded in her backside. By that time, I was NOT in the mood for any goofball ding dongs.
I already know who Colby's nurse is today, and I'm pleased. She has worked in the TCC forever and took care of a Colby a lot when we were here in June for surgery. For now Colby is on IV Clindamyacin. We'll have to wait for lab results to see if he needs another and/or different antibiotic.
Colby is snoozing away. I should be probably. It will take a very long time for us to get caught up on our rest. I told my parents just to stay home last night. It was getting so late. Plus Colby is stable and we weren't having a true OMG Colby needs help now emergency. Just thought we would head to the hospital before it became that type of situation. My dad is on his way up now. Think I'll lay back down for a few minutes. I guess we're in a holding pattern until lab results come back. Hurry up and wait as they say. More info/updates as I have them.
I would like to give a shout out to Colby's rock star nurses. They all went above and beyond this past week helping me with Colby. They did anything I asked them to do. Wipe down this, let's try this with Colby's treatment, could you stop on you way here and grab me some lunch, rinse the snot out of this, answer the phone while I'm in the shower, help us pack for Cincy, etc. they all sent texts checking on him and are truly concerned about Colby. We're blessed to have the group of nurses we currently have. Because trust me, I know a loser nurse when I see one. We've had our share of those, too. But the ones we have now are awesome. Thanks guys and gals for helping me take care of sweet boy. Hope to be home soon!!
Saturday, September 27, 2014
GUESS WHERE WE ARE?! Dammit
This has been the strangest illness Colby has had. He was better he was worse. Better, worse. Friday the pulmonologist started Colby on a different antibiotic. He had a dose last night and a dose this morning. I really did think he was getting better. I just got off the phone with my mom at 10:45 this morning saying how much better I thought he was doing. I swear 15 minutes later the shit hit the fan. Oh Lord give my strength. And patience. And knowledge. And some more strength.
Within 15 minutes Colby's oxygen dropped a little and heart rate increased. I gave him a set of cough assist and there was thick yellow stuff. What the fuckity fuck?! Then there was blood coming from his trach. Too much suctioning/irritation I assume. I had to start his cough treatment early because he was struggling. I was like that's it, we're done, hospital time. This is the absolute LAST place I want to be right now. But I know we're fighting a losing battle trying to treat Colby's illness at home. I feel the nurses and I did EVERYTHING possible to help Colby get over this gunk. So, the nurse packed Colby's needed stuff, I packed mine. We did a double check and then I called 911. Again, NOT what I wanted to be doing today.
We took an ambulance ride to Kosair. We're in the ER. They have done a chest X-ray. Done a respiratory culture (collected spit basically). Have accessed port and drawn labs. Kosair has called Cincy and we're working on transport.
So that's the latest. Will update when I can. Thanks everyone for the concerns and prayers.
Within 15 minutes Colby's oxygen dropped a little and heart rate increased. I gave him a set of cough assist and there was thick yellow stuff. What the fuckity fuck?! Then there was blood coming from his trach. Too much suctioning/irritation I assume. I had to start his cough treatment early because he was struggling. I was like that's it, we're done, hospital time. This is the absolute LAST place I want to be right now. But I know we're fighting a losing battle trying to treat Colby's illness at home. I feel the nurses and I did EVERYTHING possible to help Colby get over this gunk. So, the nurse packed Colby's needed stuff, I packed mine. We did a double check and then I called 911. Again, NOT what I wanted to be doing today.
We took an ambulance ride to Kosair. We're in the ER. They have done a chest X-ray. Done a respiratory culture (collected spit basically). Have accessed port and drawn labs. Kosair has called Cincy and we're working on transport.
So that's the latest. Will update when I can. Thanks everyone for the concerns and prayers.
Friday, September 26, 2014
LET'S HAVE A GOOD, COLBY GETTING BETTER FRIDAY, SHALL WE
You know, if I had a brain in my head, I would just take it
easy today. But let's face it, that's a pretty big IF. I don't have anything
pressing that I "have" to do today. Yes, that's an excellent idea.
We'll be taking it easy around here. I could see me doing a couple loads of
laundry, making some phone calls, and just hanging out with kid. I may even
treat myself to Panera broccoli cheese soup because it is quite yummy and
delicious and one of my favorite things on the planet. This past week has drug
on and on, and on and on. Let's see if we can have some TGIF moments today.
I swear it's like Colby has been 2 different kids this week.
Tuesday he was so much better. He was able to sit up in his chair 2 different
times for an hour each. We had him outside practicing his driving. I was
thinking oh yeah, this is the turning point for him. Then Wednesday he had a
horrible day. What the what?! We tried to sit him up and it was a disaster.
Within half an hour his heart rate was over 130 and his oxygen was 87-90. Oh,
Colbster. Then once we got him back in his bed, it took a couple hours to calm
him back down. I finally called Cincinnati
yesterday. I said this is what has been going on with Colby, this is how we've
been treating it. They were like yep, good job, you're doing everything right,
call us if he gets worse. So we took it easy yesterday, no sitting up. Still
doing cough treatments around the clock every 4-5 hours. Colby did take a big,
fat morning nap yesterday, and honestly I think he needed that more than
anything else. So we'll see what today brings. May try to sit him up again. He
has missed 7 days of school so far, and I'm not really sure if he'll be going
on Monday or not. We just have to stick with it, "treat the symptoms"
as Cincinnati
said, and appreciate the progress Colby has made in kicking this cold. We're
not in the hospital and that's what matters! Being able to treat Colby's
illness at home - priceless!
Colby was well enough yesterday that I was able to do some
birthday celebrating. My BFF had bought Eric Church tickets months ago, the day
they went on sale. She got me my ticket as my birthday present. Earlier in the
week I was worried I wouldn't be able to go. No way I'd leave Colby if he
wasn't doing well. But it all worked out and we had a great time. We all met
for supper before the concert, and Eric Church puts on one helluva show. He played
for over 2 hours! It was awesome. His opening act was Dwight Yoakam. Now, some
of the youngsters in our group didn't like him too much. But he's had a lot of
hits through the years and I loved it. Had a blast. Can't wait until our next
concert.
I've been spreading the word on our fundraiser. Origami Owl
jewelry is the mack-bomb-daddy! It's so unique and individual to each person's
taste. You know you want some! You can come to our open house on Monday the
29th or you can shop and order online. All the proceeds from this fundraiser
will go straight into our "get us a house and out of this tiny
apartment" fund. I'm not sure exactly how much money we'll need for a down
payment, closing costs and/or handicap accessible changes, but I'm guessing A
LOT. Starting early. Doing lots and lots of fundraisers until we're out of this
apartment. Somehow, some way, I'm going to make it happen. Luckily I have
friends who are willing to help with fundraising and amazing support from many
who know us. I simply can't do it by myself. So let's get this fundraising
going. You know you're needing/wanting a new necklace or bracelet. Be sure to
check out what Origami Owl has to offer. I love this jewelry and would have one
of everything in the catalog if I could. If you would like to order, use this
link: www.windowtomysoullockets.origamiowl.com/parties/AmyBagshaw451375/collections.ashx
Feel free to
order online anytime using the above link above from NOW until September 30th. You
must use this link so that
your order is reflected under our fundraiser.
There's your
Friday update. The nurse is back there finishing up Colby's 9AM cough
treatment, which includes manual CPT, saline nebulizer, IPV and CoughAssist. Hoping,
praying Colby continues to improve today and over the weekend. Thanks again,
everyone, for asking me how Colby has been doing/feeling. Your texts and calls
really mean a lot to me. Keeps me going. Love ya!
Wednesday, September 24, 2014
LET'S GET US A HOUSE!!
- Amy and Colby Fundraiser - Origami Owl Open House -
Our next fundraising endeavor is to come up with the money
needed for a down payment on a house. Oh boy, that's a doozie! This is a huge
undertaking, with many fundraisers being held over the next few months. Here's
the first! I'm pleased to say my friend Nancy is an Origami Owl consultant/designer
and has offered to help with our fundraising efforts. Here are the details:
When
Monday, September 29th
6PM to 9PM
Where
Amy and Colby's place
Contact me if you need directions
More information
Come by anytime between 6PM and 9PM to check it all out!
If you cannot make it to the OPEN HOUSE, you can shop online
at:
www.windowtomysoullockets.origamiowl.com/parties/AmyBagshaw451375/collections.ashx
Feel free to
order online anytime using the
shopping link below from NOW until September 30th. You must use this link so that your order is reflected under our
fundraiser.
Nancy
is donating 25% of sales (before tax and shipping) that will go into our
"get a house and get out of this tiny apartment" fund. Everyone
who orders is entered in a drawing for a FREE rose gold dangle bracelet that
includes 2 dangles and a mini rose gold locket with charm. Also, everyone who
orders $75 or more (before tax and shipping) is entered to win a gold chain and
locket set which includes "beach" theme charms.
You are going to LOVE this jewelry because you personalize it just for you!
Bracelets, earrings, lockets, bridal line, charms and chains. If you've seen it
before, you will be surprised how much has changed...300 new items! Origami Owl
Living Lockets are unique to every individual and the options are endless!
Whether you are shopping for yourself or a gift for someone special - daughter,
mother, sister, friend - you are sure to find something truly personal that will
speak to your heart.
Many examples will be available for you to see exactly what Origami Owl is
all about!
Don't
forget about your Christmas shopping! This jewelry makes an awesome gift...so
unique and personal!
Light refreshments served! Children welcome! Bring a friend!
ALL are WELCOME!
Monday, September 22, 2014
SLOOOOOOW IMPROVEMENT, BUT WE'LL TAKE IT
Could it be? Dare I say? Is it possible? Colby is feeling
better!! Our weekend was miserable. Simply miserable. Yesterday I was toying
with the idea of taking Colby to Cincinnati Children's. His heart rate was
over-the-top high, and he was having difficulty keeping his oxygen above 91-92.
Colby's oxygen is usually 97-100. I'm not a fan of bleeding oxygen into his
vent, but really didn't know what else to do. I could hear/feel gunk moving
around in his lungs. Snot was pouring out of every orifice he has. Not to
mention the lovely brown-red runny diarrhea he has from the antibiotic. Oh
yeah, a barrel full of chuckles around here. Aren't you jealous?
So I've done little else around here except hover over and take care of sweet boy. Even though we had nursing Saturday morning and last night, as you can imagine, I'm very hands on when Colby isn't feeling well. Yesterday the nurse and I sanitized everything in this apartment that didn't move. Door knobs, remotes, surfaces. I told the nurse, if we touch it frequently, wipe it down. I've been spraying Lysol spray twice daily and have opened the windows trying to de-germ this place. Icky germs, be gone!
But finally, last night, Colby started to seem to feel
better. I gave him a full cough treatment at 10PM - nebulizer, IPV and Cough
Assist. I coughed and coughed and suctioned and suctioned that kid. His oxygen
and heart rate were stable/normal after that. He fell asleep immediately, and
his heart rate stayed nice and low. He didn't need extra oxygen through the
night to keep up his oxygen saturation. Ah, a little relief. His 2:30AM and 7:30AM
cough treatments have gone equally as well. The nurse is back there finishing
up his morning routine. Hoping we can get through the day with high oxygen, low
heart rate and overall Colby feeling, looking and acting more like his usual sweet,
funny self.
I called the bus drivers last night and the school this
morning. Basically I told them I didn't know when Colby would be back to
school. Colby hasn't left his bed since Wednesday afternoon. Maybe, just maybe,
if he continues to do this well, we could try to sit him up in his wheelchair tomorrow.
Maybe. Can't push it.
So I've done little else around here except hover over and take care of sweet boy. Even though we had nursing Saturday morning and last night, as you can imagine, I'm very hands on when Colby isn't feeling well. Yesterday the nurse and I sanitized everything in this apartment that didn't move. Door knobs, remotes, surfaces. I told the nurse, if we touch it frequently, wipe it down. I've been spraying Lysol spray twice daily and have opened the windows trying to de-germ this place. Icky germs, be gone!
My dad came over last night and made me supper. We try to
get together a couple times a month to do that. He usually brings the meat - fries
fish, grills a steak, etc, and I'll make the side dishes and/or dessert. Yesterday
I was like, yeah Dad, I've been really busy with Colby, you're in charge of all
of supper. He brought over 2 giant, beautiful T-bones as a late birthday gift
to me. He also brought potatoes from his garden, which I baked, and we had
salad from the Jay C salad bar. Yep, worked for me. The steak was delicious. I
ate the rib eye part last night and am getting ready to feast on some steak and
eggs for breakfast this morning. My mom is coming over in a bit to help out.
Get the apartment back in order, take home a load of laundry to do for us, etc.
It's not a total mess around here, but I could use some help. Then maybe I could
sneak in a nap later before the nurse leaves.
Thanks everyone for checking in on us since Colby and I have
had the feel-bads. Hoping Colby has turned the corner and continues to improve.
I'll keep you posted.
Saturday, September 20, 2014
JUST GIGGLES AND GRINS AROUND HERE. Well, maybe not
Oh wow, we've had so much fun around here the last 3 days, I
don't know where to start in telling you about it. Nah, just kiddin, it has
totally sucked. I was sick with a head cold and even worse, sweet boy got sick,
too. Breaks my heart to see him all puny and miserable. He just looks so awful.
Colby had gone to school Wednesday. That night he started with a high heart
rate, very high actually. It continued to get worse from there. Blaaaaaah. Colby
missed school Thursday and Friday. I cancelled my Endocrinology appointment on
Thursday and missed work Friday. I was up through the night giving Colby cough treatments,
and along with being sick myself was pretty much exhausted for a couple days. No
way in this world I could've gotten Colby to the pediatrician. We were both too
yucky to get it done. Luckily the pediatrician trusts me enough that when I
called and said hey, Colby is sick, please and thank you call him in an
antibiotic, he did. Good man. Colby had a much better day yesterday but has
struggled a little today. But his fever is gone and his secretions are back to
a nice clear color. Yellow/green secretions, not cool. So slowly but surely
he's getting better. What took me 3 days to get over will probably take Colby 7-10.
Another way SMA sucks. A little head cold can totally knock an SMA kiddo down
and out. "Not fair" is an understatement.
There you have it, our last few days. Oh yeah, my birthday
was Thursday. Woop-dee-doo. I could have cared less. All I wanted to do was nap
and breathe through my nose. Hoping to do some celebrating next week since I'm
feeling better. I got lots of nice cards, texts and phone calls. I've fortunate
to have so many people care about me and remember my birthday. My BFF stopped
by after work and brought me flowers, broccoli cheese soup from Panera and
bread pudding from The Café. She knows me well and yes, it made me feel better!
Anxious to see what tomorrow brings. If Colby is doing okay,
I'll go in and work some. I don't know though. If he feels the way tomorrow that
he did today, I'll stick by close. So many times over the last couple of days
I'd walk into Colby's room and his heart rate would immediately drop 10 or so
points. Aaaaah, he wanted me in there with him, and that makes me feel warm and
fuzzy all over. He may be Mr. Big Shot 12-Year-Old, but at times he still needs
his mama.
Time to get kid in bed. I possibly see a nice hot bubble
bath in my immediate future. I think I deserve one, don't you?
Wednesday, September 17, 2014
PARTIES, POOLS AND FEELING POOPY
Colby's party was huge, wonderful, fantastic, special, and
all around freakin' fantastic! We're all still talking about it, and I have so
many people to thank. I had help deciding on the theme, sending out
invitations, decorating, making food, picking up the cake, paying for items, everything
that needs done for a party! Basically I bossed everyone around and told them
what I wanted, then showed up with Colby for party time, that was my job. And
the fireworks. Oh my, they were remarkable. These were not your average
sparklers, trust me. Giant loud fireworks that made that "thoomp"
sound when they were lit and shot off. Thank you, thank you to everyone who
helped. Thank you, thank you for all who took the time to come see Colby. I
don't want to list individuals because I would feel badly if I left someone
out. Again, for all who helped and for all who attended, THANK YOU for making
Colby's late-4th-of-July-belated-birthday-back-to-school-Colby-kicked-spine-surgery's-ass
party so amazing and memorable. The look on Colby's face when I rolled him out
of the van and he started looking around at all the people there. Priceless!
And the look on his face during the fireworks, doubly priceless! It'll be very
hard to top our surprise tie-dye fireworks party.
We've started another project with Colby. I contacted the
high school near our apartment in hopes of finding Colby a big
brother/peer/friend. Colby needs friendship and male interaction in his life, not
just his mama, grandparents and nurses around him all the time. It took a few
weeks to get the ball rolling, but I think it's going to work. Two students
came over Monday and "hung out" with Colby for about 45 minutes.
Colby and I showed them Colby's eye gaze and what all it can do. They were
fantastic with Colby. Next time they come over they're bringing pics of their
pets as a topic for conversation. Hoping these boys can encourage Colby to
communicate more accurately. Two more students are coming over tomorrow after
school. Very excited for Colby to make some age-appropriate friends.
We took Colby swimming yesterday for the first time in
several weeks. And today we are just plum tuckered out. Yesterday I started
sneezing like crazy. Then my head got stuffy, along with a little achiness.
Dammit, this mama ain't got no time for dat! We didn't have a nurse last night so
by the time I unpacked all our swimming stuff, got ready for school today and
got Colby in bed, I was exhausted. I took a swig of TheraFlu, rubbed a little
Vaporub on my nose. It's the bomb when you have stuffiness! I think it took me
all of 3 minutes to fall asleep. Felt better this morning but as the day has
gone on, symptoms are returning. Well hell. Colby is also a little
"off" tonight. Higher than normal hear rate and just a slight tinge
of color in his trach secretions. So it's doubtful he'll be going to school tomorrow.
Maybe we both need some TLC and rest. And Vaporub haha!
I did survive my dentist appointment today. A miracle
indeed. I hate going to the dentist with a passion. Terrifies me. Seriously, I
hate it. I went last month for x-rays and a consultation. I had a tooth that
was driving me crazy. And ta-da, now it's all fixed. And my teeth are super
clean and flossed. Good for another year. Then the dentist panic will hit
again.
Going to take another dose of Theraflu, rub some Vaporub around
my nose (sexy huh) and hit the sack. Tonight it will probably only take 2
minutes to fall asleep. We'll see what tomorrow brings. Hoping sweet boy feels
better in the morning. I'll blog tomorrow and let you know.
Sunday, September 7, 2014
WEEKEND WRAP-UP - Not much up with us
Not much to report since my last blog update. I was supposed
to go to an IEP meeting for Colby on Friday, but it got cancelled at the last
minute. It's rescheduled for Thursday of this week. Friday night I actually
went out with friends for dinner and then to see a band. Don't even know the
last time I did something like that. Had a great time. We're going to get
together and do it again in November. Whoever said hangovers get worse as you
get older sure wasn't kidding. I had a few drinks, didn't get totally carried
away/wasted, but still had a bit of a headache on Saturday morning. Just can't
throw them back like back in the old days. But I'm thinking that's probably a
good thing.
No nurse yesterday. How many times have I reported that
lately? I would call the nursing agency and say hey, we need more weekend
coverage, but it wouldn't do a bit of good. I've called and said that I bet 20
times in the last couple of months. Don't get me wrong, I love it when it's
just Colby and me. But seriously, I couldn't tell you the last time all of
Colby's available shifts were covered in a week's time. We have 5 nurses on
Colby's case, one full time and 4 part time. Looks like we need to find us a
6th! My mom came over and helped me get Colby up. Then she helped me study my
pharmacy math/word problems for a while. Studying for that test is not going
well. Totally stressing me out! My dad came over last night. The Moose Lodge
had their annual member picnic and he brought me some grub. Best pork chop I
ever ate! Wish I was chowing down on another one right now.
We've been using the vocab builder on Colby's eye gaze. This
teaches him where specific words are. Hard to explain. Basically on Colby's
"home page" there are 84 pictures/words. Yes, he can navigate among
84 tiny pictures, and he does it with amazing accuracy. So you can go into
vocab builder and tell the eye gaze the words you want Colby to learn. Then
when you go back to the home page, only those words will show. Make sense? Right
now we're teaching him basic words like go, get, make, read, you, up, teacher
and a few others I can't remember. Then the teacher sent home the vocab words
they were going to use the next day in class. So the speech therapist showed me
how to do the vocab building thingy, and now I'll be able to do it any time the
teacher sends home a new list of words they're working on in class. Yesterday he
did a fabulous job focusing and working on vocab. Today, not so much. That's
okay though. Not forcing it on him, because we've learned the hard way that
just doesn't work with Colby.
You know what I've been doing all day. Yep, watching
football, along with trying to get some housework done. Basically all I wanted
to get accomplished over the weekend was to pick up stuff and get organized. I
spent the whole afternoon moving crap around from one room or corner of the
apartment to another. Great googly moogly we cannot get a house soon enough. Now
I'm just waiting for the Colts game to start. C-O-L-T-S Gooooo Colts!! So I'll
wrap this up for now. Need to get my nachos ready before kickoff. More soon.
Thursday, September 4, 2014
GIMME GIMME GIMME SOME NFL
Okay, this has to be a quick update because football is on!
Do you hear me? Football season, more specifically the NFL, has begun. So
stinking happy about that.
I've been studying my buns off for this nasty, icky, super duper hard state certification test they are making me take at work. At first I said, uh no, I'm not doing it. It's way too hard and none of this crap even applies to my job, so I'll quit before I take that test. Yeah well, that attitude didn't last long. There's no way I'd find another job making what I make per hour along with having the flexibility that I have at my current job. Dammit! I seriously don't have time for this. Too bad I suppose. Trying to find a little time every day to study. Quite honestly, my brain hurts.
Colby had his 5th day of school today. It's going okay,
considering all the newness going on there. Still a couple of issues that need
to be addressed. Won't go into too much detail on those just yet. Tomorrow I'll
be going to an IEP meeting at school. I share the feeling with many other SMA families,
we despise IEPs. They're horrible. Actually I've never met a parent that enjoy
IEPs. Nothing like having to fight tooth and nail for something you feel your
child needs/deserves. But what else is new? I've fought for that kiddo for 12
years now and see no need to stop any time soon. So look out school, Mama's a
comin'.
I do have a cute eye gaze story. The nurse was telling me
this when they got home from school today. About 20 minutes before it was time
to load the bus to come home, Colby looked at his eye gaze and said
"leave". As in, later taters, I'm ready to get the heck out of here.
Funny kid. Then a few minutes later he said "love home". Aaaaah. That's
my sweet boy. I guess at that point he was thinking he'd say anything if it
would get him out of class. He's a hot mess. His health has remained incredibly
stable. Words cannot describe how thankful I am for that. I'm still a nervous
wreck every time I watch that bus drive away. I'm hoping the more he goes to
school and the more good days he has, the less I will worry about him having a
choking incident.
Did I mention football is on now?! Holy crap on a cracker,
I'm totally geeked up about it. I won't be making it to Mass this Sunday I'm
sure, way too many games on. I'm sure Jesus will understand, right?
I've been studying my buns off for this nasty, icky, super duper hard state certification test they are making me take at work. At first I said, uh no, I'm not doing it. It's way too hard and none of this crap even applies to my job, so I'll quit before I take that test. Yeah well, that attitude didn't last long. There's no way I'd find another job making what I make per hour along with having the flexibility that I have at my current job. Dammit! I seriously don't have time for this. Too bad I suppose. Trying to find a little time every day to study. Quite honestly, my brain hurts.
I'll try to do better at blogging in September than I did in
August. No promises. In looking at my calendar for the month, it's pretty full.
I have done crap this month like lab work, a dentist appointment (pray for me),
etc. I haven't even looked at Colby's schedule yet. I know we don't have any
trips to Cincy this month, so that's good. Oh, and I'm planning a surprise party
for Colby. It's a combo July 4th, belated birthday, you're-an-awesome-kid-and-deserve-a-party
kind of party. So much to do, so little time. But it'll get done. It always
does.
Wrapping this up now. Need to watch the rest of the
Packers/Seahawks game. In case you were wondering, I love football!
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