
A lot of people have asked what Odette's treatments are like, if she needs an IV each time she gives blood and what is chemotherapy anyway. Well, here is my very best explanation how I understand it...any of you technical doctor types can correct me later.
Two days after Odette was diagnost with leukemia-cancer of the blood, they put in her chest what is called a central line. It is a permanant IV tube that goes directly into her heart. Through this line, they are able to make blood draws without having to poke her each time they need blood, which is every day at least once while in the hospital, and about once a week when we are home. Through this tube is also where they put any medicines that they want to work quickly since it goes right through her veins and doesn't have to digest in her stomach. Here is also where they put fluids to keep her hydrated and the chemo drugs-that hopefully kill off the cancer cells.
For chemotherapy there are many chemicals/drugs that are used. I can barely say them, so there is no way that I will be able to spell them! Some are put in through this central line for short periods of time, and some run in over long periods of time, up to 24 hours like the one that she just got. Other chemotherapy comes in the form of shots into her thighs or they will put her out and she will get a back poke/spinal tap where they shoot the chemo drugs directly into her spinal fluids. Once they have administered the chemo, they will then send in a "rescue drug". (Not all chemo drugs have a rescue drug.) These drugs, (include steroids and bone marrow transplants and others) are meant to help rescue the body from the negative effects of the chemo. So, they are to help neutralize the chemo drug or fight adverse affects, such as protect the kidneys and liver or help to make the stomach stronger so ulcers are avoided or lessened, or to help jump start your bone marrow into producing the good kind of white blood cells. (This is what we want since ALL is cancer of the blood and is seen in the white blood cells having a mutation and growing at a way to fast of a rate.) Obviously there are still side effects that aren't "fixed". Odette will not have any hair after the next week or so since the next chemo drug affects the hair. She also is very sick to her stomach because she has sores there, so she doesn't want to eat and pukes frequently. (This is why we have the feeding tube.) She will also have fevers, not just because she is sick, but as a reaction to a drug or even the cancer. A lot of the drugs can cause irritability, which is rough because normally she is a happy, calm baby. Hopefully next week, she will be getting the steroids and this makes her hungry, then maybe she will start to eat some baby food or anything again!
So, that is basically chemotherapy in a nutshell. I am glad she doesn't have to get poked often and even though it is gross looking and a pain to keep clean and limits her time in the bath tub, I know the central line is helping her to get the treatment that she needs. If anyone has other questions feel free to ask and I will see what kind of answer I can come up with!