Jodey&Eddie&Blue
Member Since 2021
Good morning, finally!
Eddie and I have been in Victoria at the VCA clinic since October 23rd. Eddie was on 27u Levemir BiD at the time and had been on it for awhile (see SS). While in Victoria Eddie received three fractions of SRT for his acromegaly and actually came through the entire process with flying colours.
I cannot attribute the same flying colours to my experience of the clinic. It was almost impossible to get any information on his BG or for that matter what dose of insulin they were giving him. The "homecare" instructions I received at the end is equally mysterious. It says he had a hypo event the first time they gave him insulin and appears to say that they didn't give him insulin for a day or so, at all. Somehow, they have him on 10u and apparently that was the case for the last few days (he was in clinic for 5 nights: our arrival, his CT scan and then 3 separate days for SRT, one each day). If this sounds confusing to you, believe me, I am even more confused as I tried so many times to get information and even when I did it was contradictory.
The long and short of it (I just can't adequately describe the stress and the confusions over the past week), is that we are now home. Eddie's SRT will probably result in a decrease in his insulin requirements (recall he was on 27u and is now on 10u [Go figure. How did they come up with that number?] or even cease insulin altogether.
What I am dealing with right now is the question of dose. I have to be mindful of his numbers because too much insulin can be dangerous if the SRT starts to put the boots to the tumour and it no longer secretes GH (which makes him insulin resistant). But I also see that his insulin dose is too low at the moment.
I've started recording again as I had to give Eddie a day or so at 10u just because we did all that travelling. Moreover, because he had SRT, he needs to take a high dose of Prednisolone (10mg/once daily) until November 11th and then reduce (5u/once daily) "until otherwise directed". I understand Pred raises BG so there's that balancing act as well.
So, what am I asking? @Wendy&Neko what do you think? Should I increase 1u/2u? Again, he's on Prednisolone until Nov 11th and onwards. Prior to all this he was on .625 mg Prednisolone once daily...
The good news is that Eddie is doing really well. He tired of course but he's got the 5Ps happening. He even jumped up on the bed and slept in the crook of my arm, something he hasn't done for over a year...
I might add, which has nothing to do with VCA but while in Victoria my friend and I took a daytrip drive to offset the stress of worry about Eddie and on the way to Port Renfrew the wheel of my car was damaged. I was told it may be the CV joint when I brought it to Victoria Nissan; they said no parts until October 31st and I was freaking out because what was I going to do with Eddie and getting back to Kelowna. It turned out to need ball bearing replacement and they actually fixed the car within 3 hours even though they said they were so busy they would not be able to get to it until Friday, which is when we were to return home. I told them about Eddie and somehow it got through to them and they fixed the car.
There is so much to this story but I'll leave it at getting Eddie at home again. I am so relieved to be home with him.
Eddie and I have been in Victoria at the VCA clinic since October 23rd. Eddie was on 27u Levemir BiD at the time and had been on it for awhile (see SS). While in Victoria Eddie received three fractions of SRT for his acromegaly and actually came through the entire process with flying colours.
I cannot attribute the same flying colours to my experience of the clinic. It was almost impossible to get any information on his BG or for that matter what dose of insulin they were giving him. The "homecare" instructions I received at the end is equally mysterious. It says he had a hypo event the first time they gave him insulin and appears to say that they didn't give him insulin for a day or so, at all. Somehow, they have him on 10u and apparently that was the case for the last few days (he was in clinic for 5 nights: our arrival, his CT scan and then 3 separate days for SRT, one each day). If this sounds confusing to you, believe me, I am even more confused as I tried so many times to get information and even when I did it was contradictory.
The long and short of it (I just can't adequately describe the stress and the confusions over the past week), is that we are now home. Eddie's SRT will probably result in a decrease in his insulin requirements (recall he was on 27u and is now on 10u [Go figure. How did they come up with that number?] or even cease insulin altogether.
What I am dealing with right now is the question of dose. I have to be mindful of his numbers because too much insulin can be dangerous if the SRT starts to put the boots to the tumour and it no longer secretes GH (which makes him insulin resistant). But I also see that his insulin dose is too low at the moment.
I've started recording again as I had to give Eddie a day or so at 10u just because we did all that travelling. Moreover, because he had SRT, he needs to take a high dose of Prednisolone (10mg/once daily) until November 11th and then reduce (5u/once daily) "until otherwise directed". I understand Pred raises BG so there's that balancing act as well.
So, what am I asking? @Wendy&Neko what do you think? Should I increase 1u/2u? Again, he's on Prednisolone until Nov 11th and onwards. Prior to all this he was on .625 mg Prednisolone once daily...
The good news is that Eddie is doing really well. He tired of course but he's got the 5Ps happening. He even jumped up on the bed and slept in the crook of my arm, something he hasn't done for over a year...
I might add, which has nothing to do with VCA but while in Victoria my friend and I took a daytrip drive to offset the stress of worry about Eddie and on the way to Port Renfrew the wheel of my car was damaged. I was told it may be the CV joint when I brought it to Victoria Nissan; they said no parts until October 31st and I was freaking out because what was I going to do with Eddie and getting back to Kelowna. It turned out to need ball bearing replacement and they actually fixed the car within 3 hours even though they said they were so busy they would not be able to get to it until Friday, which is when we were to return home. I told them about Eddie and somehow it got through to them and they fixed the car.
There is so much to this story but I'll leave it at getting Eddie at home again. I am so relieved to be home with him.
