Hi everyone,
I'm back at Emory for 5 days. We had some communication problems and I thought that I was not going back till after Christmas. Well, it seems that I will be hear every 21 days from the start of day one. Day one being today, so I will come back the next time around Jan 7th or so. Right about when Jonathan starts back to school. It's ok, if it was not that week, it would be soon enough. When I get home, we will all have 2 and half weeks or so to be together, with no where to be (except some doc visits), no school, and no work. Just kidding, I have to work. As I said on FB earlier, this 5 days in the hospital is going to cost the insurance company $20,000, so for me to try my best to keep it isn't so bad.
I like my new job ok, it's just taking some getting use to. I don't have the interaction with my people and their caregivers so it's all just paper work. I have the hang of it for the most part, it's just hard to concentrate for long periods of time. Now that I know what the schedule is going to be like, I can start lining up some sitters like I did before. The only thing now is that I need to get my Papa Bill a wide screen monitor so when I work over there I can see all the forms. Maybe I can just carry mine back and forth. hee hee Jonathan probably is saying "nooooo!" Those of you that know me, know that I break a lot of phones and computers. I break a lot of stuff, not hearts, never broke any hearts. At least I hope not.
I'm on the A treatment schedule this time and yes, I will be getting a LP this week. I have expressed my anxiety over this and they seem to think it will be alright. I'm starting the oral chemo again tomorrow morning. Please pray that it's doesn't give me migraines again. I've been waiting all day today to start my IV chemo but it still has not arrived. I heard a rumor that the pharmacy didn't get the orders. Funny, since the pharmacist came up around 6 pm and gave me a copy of the treatment plan for the week. Oh, my patience really must have been bad for me to have to learn this one. About my Chemo Treatment
My cousin Shanna helped to change the flyer today. Please help out by printing them, placing them at yours or someone you know business, and giving them to family and friends that you will see over the holidays. I still need a match and so do so many other people. I think if you right click it then save it to your computer, then print it out. Thank you for your help!
We received a check in the mail yesterday that is going to be a big help. This person has helped two other times and don't think would want me to share names. In the card, they wrote "I don't know how you do it." Well __________, I don't either. People like you that are supporting us whether its money, food, prayer, encouragement, baby sitting, letting me keep a job, bringing a Santa to Evalyn since we can't go to the mall, etc, etc. and most important the grace and mercy of God. God has a plan, it is unfolding as I write this. I know that, so that helps me keep going. I can't say this is easy because believe me it is so much harder than I thought it would be. But is anything easy worthwhile in the long run. Not really. I could see God working that very first week. So that in turn increased my faith. He said that just a mustard seed is enough, I'm pretty sure that I have that, and so do you.
Jeremiah 29:11-13
For I know the plans I have for you,” says the LORD. “They are plans for good and not for disaster, to give you a future and a hope. 12In those days when you pray, I will listen. 13If you look for me wholeheartedly, you will find me. 14I will be found by you,” says the LORD
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