Hello everyone and sorry for the delay in updates. Days have been blending together and I've been pretty exhausted driving back/forth to Boston and spending the nights at the hospital. Scott is doing well after day three of chemo. He had some issues with the pain meds causing intense hallucinations so they changed them today and he's been zonked out all night. He has also been having really bad hiccups and they've tried to cure them with different things and nothing seems to work. Oddly tonight, as soon as the nurse gave the new pain meds they stopped, so we may be on to something.... (imagine having hiccups straight for 48 hours, poor guy!!!!) It is confirmed that there are nodules in his lungs and some in his liver which has caused it to swell pretty large. He is also very swollen in his surgical area. He's been experiencing serious fluid buildup in his legs and it's being monitored. He's on blood thinners in case there are some blood clots and I believe tomorrow they are going to see if they can work around chemo and do some tests to see what's going on. There are still some tests they have to do like to check his stomach once the swelling goes down. We are taking it day by day. We were told that on day three he would start to feel the nausea and sleepiness and such symptoms of the chemo. Luckily he has not been experiencing any nausea yet, and I pray to God that continues. He is so strong and he is surrendering to the treatment bravely and I'm so proud of him. I admire his grace through all of this. If chemo goes well the next two days, he will go home on thursday (possibly). There are other complications that could arise in the next few days and they need to keep a close eye on him. From there he will be 3 weeks off at home and then come back to Boson for 5 days on. That will continue 3-4 times and then he will be rescanned. Before he's discharged he'll receive an immunity shot but he will be susceptible germs so when you plan your visits, please make sure you are healthy and haven't been around germs that you can spread to Scott that could compromise his health. I think that's the best I can do for an update for now. It's been a long week I'll tell ya... and there is just no such thing as sleeping in hospitals. Today i got to go home and sleep on the hammock for a while which was really nice. I'm doing the night shifts and his amazing family is doing the day shifts. He is surely loved (and you all have made that obvious with your texts, phone calls, facebook messages, cards, etc) I apologize I have not been able to connect with you all one on one but I really am trying to put all my love and energy into Scott right now! If you have any questions please write back! I hope you're all well, and once this craziness is over we're going to get together to celebrate! Oh, one more thing! We're all wearing the yellow LIVESTRONG arm bands in support of Scott. I believe you can buy them at Bobs for $1. Once he is cured, we will all add the survivor band, which ironically is Scotty's favorite color: purple! And as if I need to remind you, PRAY, PRAY, PRAY! He's got a tough road ahead of him but he's going to do it, he needs the power of prayer and positive thoughts, so keep them flowing. Send me anything you want me to tell him, a joke, a picture, anything! and when he's coherent I'll share it with him. I know you all want to help in some way, but just thinking of him, praying and envisioning healing is what he truly needs! peace, x, o, jax please pass on to your own distribution lists or to anyone i accidentally forgot.
Updates for all of Scotty's friends and family and a way to keep everyone connected as Scotty BEATS cancer!
Wednesday, June 29, 2011
Email from June 21, 2011
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