October 28, 2009, Wednesday
Wednesday, October 28th, 2009October 28, 2009, Wednesday
I have found out more information about my treatment coming up next week.
First of all, it will take about 4 hours each day Monday through Thursday. Maybe you noticed it is not starting on Tuesday but has been changed to start on Monday.
On Monday before treatment starts at 9 a.m,, I will be seeing Dr. McCroskey at 8 a.m. I’m only guessing, but any bets they will take blood samples then as well? On Tuesday I will only be getting the 4 hour treatment (infusion) starting at 10:30 a.m, On Wednesday it will start at 9 a.m and on Thursday it will also start at 9 a.m. The person who called me said to be sure to bring things like a nice warm blanket, a pillow (I will be in a chair that lays back pretty good), something to read or keep you busy and be comfortable for 4 hours.
I was also told (and asked for the spelling of each) drug that was included in the treatment. From what I understood Ireta, the schedular at the clinic, to say was it would include velcade, cisplatin, adriamycin, cytoxan, and etopside (VP16). I asked about revlimid and she said that was an oral drug I will be taking. I wasn’t sure, and didn’t think to ask, but it seems like that is what they will give me the following 3 weeks. I’m not sure of that completely, but the others are all infusion drugs and the revlimid is an oral pill (which I have had previously - that’s why I’m thinking it would be what I take when not in the clinic. She also said that next week on Monday I would be coming in for velcade (which is what I have been doing every other week as an infusion already).
And then I will go through the same things again after the three weeks as I am going to be doing on Monday.
I was told I will get a complete schedule when I come in on Monday.
Had a bit of a negative mood this morning thinking about going through this as I am wondering if I will again be extremely tired and feel very weak, spending a lot of time sleeping, lose my ability to taste things correctly. If I will again get a rash. If I will be intense and not nice to be around again, as Dr. McCroskey said the treatment will include decadron (dexamethasone) again which is a steroid. He has already given me a prescription that is supposed to counter that. But then I believe we tried that previously, and it made me real tired and feeling groggy and brain dead. I guess that is better than not being very nice to Jane as a result of the dexamethasone by itself. Of course, most of the time she will be at school teaching - which is good! The one person I don’t want to treat poorly is my wife. She has been so very supportive and understanding and loving, but wrong words can really hurt. I seem to have trouble keeping my tongue under control - talk too much, and say hurtful things - believing those things have to be said. Not good! Lord, help me!
I did get past that negative thinking quite quickly this morning and again remembered that God is in control, and He will not put me through more than I can handle - or Jane either. So as usual, the flesh wants to go negative, my spirit through the power of the Spirit of God needs to take control and stay positive! Inch by inch, step by step, brick by brick; as my brother, Dick, kept telling me four years ago (Oct 2005) when this all started. Maybe go sideways on occasion, but never backward!!!
So for those of you who wanted more detail. That is what I know for know!
I know you will be praying and that means a lot to me.
Dan