Tomorrow is the BIG day!!!
I, of course will have plenty of video clips. Austin is even coming with to help tape, Shhhh he gets to ditch school.
This whole process of deciding to even go ahead with the pump trial, has been very long & stressing. The talk of the Baclofen pump has been for about 3yrs & with his two parents not agreeing on whats best for him, it becomes a struggle to figure out who's right.
So lets just hope it's me LOL I wouldn't be able to live with myself if something happens to him.
Caradie & Corbin
At 14 month Corbin had a choking accident that left him with significant brain damage
Sunday, November 30, 2008
Comments
When ever there's a comment, I will comment back, right in the comments.
I tested it and it worked so that will be an easier way to get you comment &/or questions answered, instead of me having to write a new post :-)
Thanks everyone
Caradie & Corbin
I tested it and it worked so that will be an easier way to get you comment &/or questions answered, instead of me having to write a new post :-)
Thanks everyone
Caradie & Corbin
MacGyver at it again...
Corbie's onsies are getting to small & they don't make bigger sizes. So, I had to come up with a way to make his shirts into onsies.
Well....
Well....
Caradie & Corbin
Monday, November 24, 2008
Old floppy discs
Friday, November 21, 2008
More practice w/a spoon
Updating with videos to the blog takes to much time for tonight so please check out http://www.dropshots.com/BabyCorbin
Corb has been practicing eating pudding with his teacher every Tues & he totally knows what to do, it's just his hands/arms don't do what he wants them to do but he's trying sooooo hard.
As you will see I got some scraps of carpet that I patched together to make a softer spot for Corb to play & he loves it. He also loves his new toy rack.
Corb also got a walker he gets to try out for a few weeks. I won't be posting the videos of him in it until I get many days first. I will need proof that he will be able to use it for medical assistance. It's only been two days & he's AMAZING!!!!!!!!!!!
Caradie & Corbin
Corb has been practicing eating pudding with his teacher every Tues & he totally knows what to do, it's just his hands/arms don't do what he wants them to do but he's trying sooooo hard.
As you will see I got some scraps of carpet that I patched together to make a softer spot for Corb to play & he loves it. He also loves his new toy rack.
Corb also got a walker he gets to try out for a few weeks. I won't be posting the videos of him in it until I get many days first. I will need proof that he will be able to use it for medical assistance. It's only been two days & he's AMAZING!!!!!!!!!!!
Caradie & Corbin
Saturday, November 15, 2008
Jammies & a new invention
Friday, November 14, 2008
Real update
Sorry is something doesn't make since LOL I don't feel like rereading it again.
Since Corbie's Nissen Fundoplication surgery there has been a few bumps in the road, his g-tube site got very irritated & one of the little incisions got infected, he was hurting pretty bad, now his tummy is totally healed & he's feeling great but he has started this weird snorting/gagging issues, I won't get into details but after some work I finally got the doctor to listen to me. He's now on Zytec, also less stool medication but that has nothing to do with the gagging. The Zytec is to help loosen up the secretions, so he can swallow them easier. The snorting is still there but the gagging is gone.
Corb has also been doing very well with his home therapies. We started brushing & joint compressions-SI (sensory integration), spinning, swinging, floor time & practice eating different foods again. It feels great to be back in a routine.
Monday 11-3, we had an appt with one of Corbie's doctors & we have decided to go ahead with the Baclofen Pump trial. The trial is scheduled for Dec 1st I'm VERY excited & a little nervous, the trial is around here but the doctor wants the actual pump placement to be be done in the Cities (3 hours away). On Monday 11-10, I decided to call the doctors office, I left a message stating that I wouldn't be able to make it to the cities ever, because on Wednesday 11-5, we went to Hudson (3 hours away) & the check engine light came on & was on just about the whole ride home so I won't be driving that far away anymore, well the doctor personally called me, we talked about why I couldn't make it down there & he said he wants whats best for Corbin & the doctors in the cities are whats best so he said I promise you, I will get a ride there & back. WOW!!!!!!!!!!!!!!!!!!!!! (the family & child social worker from the hospital in the cities already found us a ride when ever we need it)
The reason we went to Hudson on Wednesday was because a very special lady, we know was able to get Corbie a special fund & we choose to use the funds to go back down to Hudson for evaluations, home programming & then some therapy equipment, that would help with the home program the therapists come up with. I haven't ever posted about this yet because I wanted everything to play out first. So the evals are done, now we just wait to find out about the equipment.
Another thing going on is that at St. Luke's where Corbin goes to for therapy, as of yet he still only gets OT. PT & ST have been trying to get coverage from Medical Assistance for a year now, with no luck. I talked to the ST that would have Corb if it ever gets approved & he said he wasn't comfortable doing feeding therapy anyway so Corb had an eval with the other ST there & we will see if she can get him approved.
And I also have been in contact with an advocacy place in WI & we now have an attorney to help fight the screwed up system. I have also decided that if this other ST can't get things approved, we are going to have to go to another facility.
One thing I learned in Hudson that I think will be a big help is, if Corb does get the pump, there's something called “New episode of care” that should make him more inclined to receive, more intensive therapies so we will be shooting for PT, OT & ST each 2x a week right away (after he feels better after the surgery). I'm going to demand he get better services because he will need to relearn everything he knows now & MORE & I'm only one person.
Now for sleeping...
As I said in my earlier post Corbie did great last night & just about every night now he might fuss a little but he totally falls asleep on his own. (Besides last night) he was still waking at least once a night. I'm hopeful that this awesome behavior will continue!!!!!
Oh one more thing our new worker seems to be a nice girl & I'm hopeful that she will work out.
Caradie & Corbin
Since Corbie's Nissen Fundoplication surgery there has been a few bumps in the road, his g-tube site got very irritated & one of the little incisions got infected, he was hurting pretty bad, now his tummy is totally healed & he's feeling great but he has started this weird snorting/gagging issues, I won't get into details but after some work I finally got the doctor to listen to me. He's now on Zytec, also less stool medication but that has nothing to do with the gagging. The Zytec is to help loosen up the secretions, so he can swallow them easier. The snorting is still there but the gagging is gone.
Corb has also been doing very well with his home therapies. We started brushing & joint compressions-SI (sensory integration), spinning, swinging, floor time & practice eating different foods again. It feels great to be back in a routine.
Monday 11-3, we had an appt with one of Corbie's doctors & we have decided to go ahead with the Baclofen Pump trial. The trial is scheduled for Dec 1st I'm VERY excited & a little nervous, the trial is around here but the doctor wants the actual pump placement to be be done in the Cities (3 hours away). On Monday 11-10, I decided to call the doctors office, I left a message stating that I wouldn't be able to make it to the cities ever, because on Wednesday 11-5, we went to Hudson (3 hours away) & the check engine light came on & was on just about the whole ride home so I won't be driving that far away anymore, well the doctor personally called me, we talked about why I couldn't make it down there & he said he wants whats best for Corbin & the doctors in the cities are whats best so he said I promise you, I will get a ride there & back. WOW!!!!!!!!!!!!!!!!!!!!! (the family & child social worker from the hospital in the cities already found us a ride when ever we need it)
The reason we went to Hudson on Wednesday was because a very special lady, we know was able to get Corbie a special fund & we choose to use the funds to go back down to Hudson for evaluations, home programming & then some therapy equipment, that would help with the home program the therapists come up with. I haven't ever posted about this yet because I wanted everything to play out first. So the evals are done, now we just wait to find out about the equipment.
Another thing going on is that at St. Luke's where Corbin goes to for therapy, as of yet he still only gets OT. PT & ST have been trying to get coverage from Medical Assistance for a year now, with no luck. I talked to the ST that would have Corb if it ever gets approved & he said he wasn't comfortable doing feeding therapy anyway so Corb had an eval with the other ST there & we will see if she can get him approved.
And I also have been in contact with an advocacy place in WI & we now have an attorney to help fight the screwed up system. I have also decided that if this other ST can't get things approved, we are going to have to go to another facility.
One thing I learned in Hudson that I think will be a big help is, if Corb does get the pump, there's something called “New episode of care” that should make him more inclined to receive, more intensive therapies so we will be shooting for PT, OT & ST each 2x a week right away (after he feels better after the surgery). I'm going to demand he get better services because he will need to relearn everything he knows now & MORE & I'm only one person.
Now for sleeping...
As I said in my earlier post Corbie did great last night & just about every night now he might fuss a little but he totally falls asleep on his own. (Besides last night) he was still waking at least once a night. I'm hopeful that this awesome behavior will continue!!!!!
Oh one more thing our new worker seems to be a nice girl & I'm hopeful that she will work out.
Caradie & Corbin
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