The Family

The Family
07/26/2015

Thursday, December 31, 2015

Merry Christmas and Happy New Years!

Dad had a couple of doctor appointments yesterday which included a CT scan. The CT scan came back good, the swelling has gone down since his hospital visit and the CT was looking more like the MRI he had around Thanksgiving. His blood work is still coming back normal and we are continuing the clinical trial with Disulfrum. He started his second round of chemotherapy today; they doubled his dose from 200 mg to 400 mg however this is normal since he tolerated the last increase so well. They have decided to decrease his steroids (which was increased after his hospital visit) and will be slowing decreasing the dosage over the next couple of weeks.

Dad and I went to a Blues game a few weeks ago and had a great time! We had fairly decent seats and the Blues were able to bring home a win!!!!



We had a very busy Christmas Eve, Dad's extended family came over for Christmas lunch and then we had Christmas dinner with Mom's side of the family. Christmas day we were able to have a breakfast of cinnamon rolls with just the four of us, exchange gifts and then had the traditional meal of clam chowder before I had to leave for work. It was a very calm and relaxing morning!





Thursday, December 17, 2015

Weekend Getaway

Mom and Dad were able to enjoy a weekend trip to Branson with some family friends over the past weekend and were able to stop and have lunch with Mikayla in Springfield on their way down. Other than some rain, they had a great trip and were able to do everything they had planned. Dad's slowly eating more and more, he said food is starting to taste better. He still drinks a couple Ensure's every day but is eating more than he was a few weeks ago.



Monday, December 7, 2015

Back to Barnes

Yesterday early morning Dad woke up with a headache. He took some Tylenol and put an ice pack on his head and started feeling better and went back to sleep. When he woke up in the morning, he had a headache again and was vomiting. Mom got a hold of one of the oncologists who wanted him to go to the ER and get checked out. At the ER, they did a CT scan which showed more swelling on the brain compared to his last CT scan although I'm not sure which CT scan they compared it to because he hasn't had one in a long time. They decided to transport him by ambulance to Barnes downtown, mainly because all of his doctors are down here and they have a little bit better technology. Dad said the ambulance ride was TERRIBLE, 45 minutes of bouncing around with a full bladder was not his idea of a good time.

They've increased his steroids for now and he seems to be responding well to that. He's feeling much better, has not had any more headaches and his stomach has settled down. We're still in the hospital, just kind of waiting for the doctors to decide what they want to do. Dad hates hospitals and waiting so he's just ready to go home but he has a private room this time around and has been watching war movies all morning.





5:32 pm-- They finally made the decision to discharge Dad. He will stay on the increased dose of steroids until all of his doctors are able to get together and decide what the best course of action will be. They do not want him on steroids for too long, there are only three types of steroids that cross the blood-brain barrier and once he becomes immune to those steroids, there won't be any that would be beneficial. He's still feeling fine and is just ready to be back at home!

Wednesday, December 2, 2015

Family Photo and Some GOOD News!

I just got off the phone with Mom, she said that her and Dad went out to Applebee's with some friends for dinner and Dad ate his entire club sandwich as well as the mashed potatoes. This is the first meal he's eaten in about a week!!! He said it actually tasted pretty good and it was nice to be able to eat like a normal person. Hopefully his appetite keeps up and he can gain a little weight.

Dad and Mom also picked up Dad's medication for the next round of chemotherapy as well as the clinical trial. His next MRI is January 11th and depending on how that MRI looks, we may or may not have an appointment with Dr. Chicoine a few days after. An appointment would mean there's something on the MRI that concerns the doctors so we're hoping for no appoinment.

Here is the picture of the whole family on Thanksgiving! Dad brought it to my attention that it was never posted, it completely slipped my mind! I love this picture, surprisingly we got such a great looking picture in just one try! This is Dad's side of the family, we're missing quite a few of the cousins and some uncles but this is everyone that was in town!! Love them so much!!