Carrie's Treatment Version 2.0

Carrie talked to her Oncologist this morning and instead of having a treatment on Friday, they have moved it to this Thursday. Carrie's doctor appointment has also been moved to Thursday as well. Also, we found out this morning that Carrie will be having treatments everyday next week. I actually talked to her Oncologist this afternoon and the treatments will be every four weeks. Carrie will get a CT scan after every 2 treatments. Other than that we don't have any information right now but hope to have some more info after Thursday.

Carrie's Treatment

On Friday Carrie talked to her Oncologist here in Birmingham and on next Friday Carrie takes her first treatment of infusion chemotherapy. We do not know the strength of the dosage or how long Carrie will have to have treatments. We plan on getting more information once we get to Birmingham on Friday. I will try to keep everyone updated as much as possible. Please keep us in your thoughts and prayers.

National Lampoon's Cruise Vacation

Okay, by now most of you have heard the news that Carrie and I got last Friday (1/29). Well that was just the beginning of a long weekend. Backup one week, our plans were to go to B'ham and get good news from the doctor on Friday and then leave for a cruise to Jamaica on Saturday. On the Tuesday before the doctor's appointment, we got word that something was wrong with our cruise ship and that it would not be able to make to Jamaica and back in 5 days. So they decided to move the cruise to Cozumel and Costa Maya Mexico. Now fast forward to Friday afternoon after the doctors appointment. We were planning on driving to Nashville and fly out with Carrie's parents on Saturday morning to Miami. Problem was that Nashville got hit with a very nasty ice storm Friday night we drove into. We slid off the road at one point due to the ice and spent 20 minutes getting the car out of the ditch. So if that wasn't enough Southwest started cancelling flights Friday night. At 9pm Friday night we decided to drive to Miami to catch this boat. The latest time we could check in to get on the cruise was 2:30pm on Saturday. We arrived at the cruise terminal at 2:15pm. So after a Friday to forget and a 16hr drive we made it on the boat and were able to spend a week in 80+ degree temps and catch some sun. As Jeff Foxworthy says, "You can't make this stuff up."

3 Month Check-Up

We returned to UAB today for Carrie's 3 month check-up. She had a PET scan done last thursday, and today, she had a CT scan done as well. We then met with her oncologist and was informed that the cancer has returned. There is a 2 cm spot next to her vena cava, exactly where they original tumor entered the vena cava and was repaired during the surgery in August. In addition, they found a few spots on her LEFT adrenal gland that they assume are traces of the tumor as well. One of the spots on the adrenal gland is about 3 cm, the others are smaller. As of right now, the doctors are unsure what they are going to do. They cant risk another surgery right now since the tumor is in the same place in the vena cava as it was before - to do surgery would bring too many complications and be even more life threatening than the first one. The only option they are considering as of right now is radiation. The oncologist is waiting to get in touch with a few other doctors to decide for sure the next step, but they should have an idea sometime next week. We will keep everyone up to date as soon as we know more details.

Short Update

Carrie met with an Oncologist today at MD Anderson in Houston and he agrees with our Oncologist at UAB with the method of treatment that has been recommended to us. We meet with a specialist on Monday just for another confirmation of the treatment.

Good News

Carrie met with the Oncologist this afternoon and today's CT Scan came back clean. Woo Hoo!!! We go to M D Anderson in Houston on the 29th of October just to make sure that we are following the right course of action. Carrie will get CT Scans every 3 months for the next 2 years and then every 4-6 months for 3 more years. Carrie's status for taking chemo is still undecided and we are waiting to hear what M D Anderson says before proceeding with any treatment. Carrie has been released for work and plans on starting back on the 21st of October.

And the journey continues

Carrie met with her Oncologist, Dr. Mollie DeShazo, yesterday at UAB. Dr. DeShazo is considered the "expert" for Carrie's form of cancer and Carrie's case is the third case Dr. DeShazo has seen, EVER. Carrie has been prescribed a drug called Mitatane. It is a different type of chemotherapy in that it doesn't kill the white blood cells like the typical chemo treatments and it is in a pill form. The side effects of the medicine, include nausea, diarrhea and vertigo. They are going to start Carrie on a very low dose(500mg) and it increase it to 2g over the next few weeks. She will have to take the drug daily and continue to take it for 6 months to a year. Due to the rarity of the cancer Dr. DeShazo is trying to contact other doctors at other clinics to get some info on how to handle this.