Friday, April 17, 2009

A Slight Change

If you know the recent Heather this is very different from normal. Her sleep schedule has been put the kids to bed at 8:00, brush her teeth and sound asleep by 8:15. She then will sleep until about 8:00 or so in the morning. It is almost like in the recent months she has been afraid of the dark, and when the sun thinks about going beneath the horizon she thinks about being in bed until the sun comes out in the morning.

Flash forward to Monday, and the beginning of treatment. The tide has turned and Heather has began to sleep a lot during the day and up more during the evening time. It is almost like the exact opposite of her previous self. I think that she is becoming scared of the daylight. Even our doctor today came into the room and asked if we ever turn the lights on here as had never seen the lights in our room.

This has started to make me wonder, Heather was/is a big fan of the Twilight book series, and we own and she has watched the movie many many times. I am thinking that the medicine they are giving her is not really cancer medicine, but instead is vampire morphing serum.

After the 6 courses of treatment will Heather be a full blood vampire and only roam the nights? Will I have to fear the evil bite that might come my way. I am starting to wonder if readers of the Twilight series will all eventually become vampires of sort and those who don't get involved in the book are the only ones who are safe. Please beware of any medications that you might have and take, especially those that cause drowsiness. I think all medicinal therapies, now, are part of some master vampire serum scam. Please Beware! I will hope and pray that Heather will overcome the vampire drugs during the two weeks off and the vampire only returns when we are in this building.

Anyway, today started off well, and we thought we would make a day of it. It turned south quickly after 10:00ish. The way the dosage schedule is set up she gets the highest dosage on the first few days and then the dosage is lowered each day. by the time the worst of the side effects hits she is on a lower dosage and it supposedly lowers what I would call the "medicinal recovery time" (Don't quote that to anyone as that is a made up term by me). So basically the hard stuff she had early in the week is catching up with her yesterday and today, and theoretically/hopefully the days get better. She did finish the chemo section of this treatment at 9:00 today (Friday) and they have given her a medicine that should help with any fluid she has retained. I believe that we are drug free starting tomorrow, and if all is well we will be discharged on Sunday.

It has been fun, but I think that my course on the blog is done until the next return visit to Houston.

With Love and God Bless,

No comments:

Post a Comment