MRI brain scan is CLEAR!
Houston skies are clear.
Houston traffic at 5:30 is not clear.
2 out of 3 ain't bad.
Finally saw the Dr and got good news about the MRI. We have instructions and the trial medication and are on our way home after a quick bite to eat in beautiful Sealy.
Thank you for praying!
Please continue to pray for
1. Safe travels 🚗
2. No side effects 🤢
3. Total annihilation of this stupid cancer 🔫
Thank you for loving us!
Thursday, April 26, 2018
New plan part 2
They just took David back for the biopsy. They said it will be about an hour.
The biopsy is only for research purposes for this new study. They want to see how the cancer has evolved and how this new regimen will effect it. He will have another biopsy in 2 weeks and then again in 6 weeks. I think that is all. He is thrilled. 😒
The Drs appt is at 3. Hopefully. We might be out of here just in time for Houston 5 o'clock traffic. Yay!
If all goes as planned, he will start the trial drug orally tomorrow and add the Opdivo infusions every two weeks, starting in two weeks.
More later.
Thank you for your prayers.
Thank you for loving us!
The biopsy is only for research purposes for this new study. They want to see how the cancer has evolved and how this new regimen will effect it. He will have another biopsy in 2 weeks and then again in 6 weeks. I think that is all. He is thrilled. 😒
The Drs appt is at 3. Hopefully. We might be out of here just in time for Houston 5 o'clock traffic. Yay!
If all goes as planned, he will start the trial drug orally tomorrow and add the Opdivo infusions every two weeks, starting in two weeks.
More later.
Thank you for your prayers.
Thank you for loving us!
Wednesday, April 25, 2018
New plan part 1
Here is our day:
So far everything has gone smoothly.
David is in the process of the MRI. He's being a good sport. I have never had an MRI, but he said it's not that fun. I am in the 3rd or 4th waiting room of the day.
Tomorrow is the biopsy (insert anxiety here) and Dr. visit. He will get the oral medication tomorrow that he will take for 2 weeks before he starts the immunotherapy infusions. The drug for that is Opdivo. You may have seen a commercial for it. You know the one where everyone looks happy as the voice over reads the list of side effects and warnings. Yeah, that one. So that's the plan right now anyway.
Please pray for:
1. A clear scan
2. A clear plan
3. My friends battling and families of those that have lost the battle.
More tomorrow.
Thank you for loving us.
So far everything has gone smoothly.
David is in the process of the MRI. He's being a good sport. I have never had an MRI, but he said it's not that fun. I am in the 3rd or 4th waiting room of the day.
Tomorrow is the biopsy (insert anxiety here) and Dr. visit. He will get the oral medication tomorrow that he will take for 2 weeks before he starts the immunotherapy infusions. The drug for that is Opdivo. You may have seen a commercial for it. You know the one where everyone looks happy as the voice over reads the list of side effects and warnings. Yeah, that one. So that's the plan right now anyway.
Please pray for:
1. A clear scan
2. A clear plan
3. My friends battling and families of those that have lost the battle.
More tomorrow.
Thank you for loving us.
Tuesday, April 10, 2018
Time to move on
Thank you for all your prayers yesterday and today. I know I could feel them, and I'm sure David did too.
Funny thing about prayer. Funny in a kind of annoying way honestly. Sometime God says no. I was really praying for at least stability so we could just continue with what we know. But that's not what we got. There has been growth in several of the lung nodules and some new ones are present. Also the lymph node has grown. We saw the PA and Dr. T, they are both in emphatic agreement that we are done with the current treatment and it's time to move on. They are very encouraged that David was able to do so well on this drug and think that that will be a positive going into the next treatment.
So the new study is another trial. David will be only the 13th patient in this study. It is a combination of an approved immunotherapy drug and a new oral drug. Their thought is that David will have a great response to combining these two drugs. There is even hope of remission with this treatment. It will be more time consuming as far as trips to Houston, but weighing all the options, we think it's worth the trips. It will be every 2 weeks for maybe 2 months, then every 4 weeks. The good thing about it is that most of the appts will only be 1 day long, not overnight each time. The travel up and back in one day will be tiring but we won't be away from home as long. Got to look for the silver, right? We originally thought the infusions could be done locally, but that was if we chose only the FDA approved drug and not the study. They were very frank with us that while we could continue treatment at MDA not in a trial, that the best care and best chance of success, is under a trial.
So we press on. We won't be seeing our research nurse, Marisa anymore. We were actually her last patient, as she is now the head of all the research nurses, working in a more admin role and not directly with patients. We will miss her very much, we've spent almost 5 years with her! She said we'll see her around!
It was a lot to wrap our heads around today, like starting over. They told us at the beginning that this cancer would eventually find a way around the current treatment and we would have to switch. We are buying time and hoping for a cure eventually. So here we go...
Please pray for
1. A smooth transition
2. Less side effects
3. Effectiveness in slaying this dragon
4. Laura who just lost her mother and whose sister is battling.
5. Holli who continues to fight
6. Lorraine who has the best smile through it all
7. Bobby
8. an undiagnosed disease
9. Family. This is not fun for anyone
Thank you for loving us.
Funny thing about prayer. Funny in a kind of annoying way honestly. Sometime God says no. I was really praying for at least stability so we could just continue with what we know. But that's not what we got. There has been growth in several of the lung nodules and some new ones are present. Also the lymph node has grown. We saw the PA and Dr. T, they are both in emphatic agreement that we are done with the current treatment and it's time to move on. They are very encouraged that David was able to do so well on this drug and think that that will be a positive going into the next treatment.
So the new study is another trial. David will be only the 13th patient in this study. It is a combination of an approved immunotherapy drug and a new oral drug. Their thought is that David will have a great response to combining these two drugs. There is even hope of remission with this treatment. It will be more time consuming as far as trips to Houston, but weighing all the options, we think it's worth the trips. It will be every 2 weeks for maybe 2 months, then every 4 weeks. The good thing about it is that most of the appts will only be 1 day long, not overnight each time. The travel up and back in one day will be tiring but we won't be away from home as long. Got to look for the silver, right? We originally thought the infusions could be done locally, but that was if we chose only the FDA approved drug and not the study. They were very frank with us that while we could continue treatment at MDA not in a trial, that the best care and best chance of success, is under a trial.
So we press on. We won't be seeing our research nurse, Marisa anymore. We were actually her last patient, as she is now the head of all the research nurses, working in a more admin role and not directly with patients. We will miss her very much, we've spent almost 5 years with her! She said we'll see her around!
We have a new research nurse. Her name is Shedani. I think. We will love her too. Our whole team is so great, so caring, and so compassionate. They really are incredible and we know it's the best place to be. There were some tears all around today.
It was a lot to wrap our heads around today, like starting over. They told us at the beginning that this cancer would eventually find a way around the current treatment and we would have to switch. We are buying time and hoping for a cure eventually. So here we go...
Please pray for
1. A smooth transition
2. Less side effects
3. Effectiveness in slaying this dragon
4. Laura who just lost her mother and whose sister is battling.
5. Holli who continues to fight
6. Lorraine who has the best smile through it all
7. Bobby
8. an undiagnosed disease
9. Family. This is not fun for anyone
Thank you for loving us.
Subscribe to:
Posts (Atom)