Just a quick update on yesterday's visit to Dr. Frenette's office...
Stuart and I saw Dr. Frenette for about 15 minutes for an exam. The only issue he responded to was the numbness / tingling in my feet. He said it was a side-effect of the Vinblastine and that he wanted to keep going for one more treatment and then assess whether my dosage needed to be reduced. Other than that, he was ok with the other issues I reported. We scheduled the interim PET scan for Monday December 6th at CMC Main hospital...big day for me.
Treatment today went almost flawlessly. In the midst of the treatment, the nurse came over to break the bad news that there is a nationwide shortage of Adriamycin (the red stuff). The doctor recommended a substitute drug in the same "family" called Epirubicin. I signed the waiver and moved on.
I am feeling ok today and will try my best to pound down some Turkey and fixings...I will be saying a big thank you to each of you during my pre-meal blessing.
4 down...8 to go...
Musings to keep friends and family updated on my condition as I progress through treatment and life beyond.
Showing posts with label Vinblastine. Show all posts
Showing posts with label Vinblastine. Show all posts
Thursday, November 25, 2010
Monday, November 22, 2010
22nd - John Larroquette...From a Distance
Thank you to the Kerrins' for bringing us an absolutely delicious pot roast over the weekend. I will be enjoying the left-overs for days. Thank you to Stuart's parents, Bill and Cathy, for coming down to keep us company and help out around the house. Thank you to Shelley Typrin for the good-luck amber necklace.
Time has flown by over the last couple of weeks. It is hard to believe that I am headed to see Dr. Frenette on Wednesday for my fourth treatment, which is the end of my second "cycle". This one carries some additional significance, as it is protocol to follow the second cycle with a PET scan to check treatment progress. The scan is not scheduled yet, but I suspect it will be next week at the hospital. I am optimistic about it, but I would be lying if I did not admit to being nervous as hell.
As I mentioned in my last (very short) post, my third treatment went "fine". I have come to expect a new experience (or more) each time I visit Dr. Frenette's office and this trip did not disappoint. As I was sitting in the treatment chair waiting for my blood tests to come back, I found myself getting nauseous over just being there. Apparently it is a pretty common phenomenon called "anticipatory nausea", which is when you get sick over the thought of something that has not even happened to you yet. Next time, I will be taking the anti-nausea medication before I go into the office. That said, the "hangover" from treatment was a little longer this time and I ranked the days following it as:
Friday: 5
Saturday: 3
Sunday: 4
Monday: 5
Tuesday: 6
Wednesday: 8 (fyi, I consider 8 "back to normal")
Since then, I have been feeling much better and my activity level has been pretty good. I have done some work off and on from the house and have been walking regularly. The walking is getting a little slower though, as I have developed tingling in both my feet. Apparently, this "neuropathy" is a common side-effect of the Vinblastine (the "V", in ABVD), and there is not much you can do about it, other than stop that part of the treatment if it gets to be too much to handle. I will certainly mention this to Dr. Frenette on Wednesday, but if history is any indication, he will not be impressed.
During my last visit to Dr. Frenette, I complained of continuous pain in my groin, which I was afraid was lymph nodes acting up. Rather than examining my groin, he carefully studied my neck...from his chair which was four feet away...and said I was fine. Works for me. Stuart has told me multiple times that Dr. Frenette reminds her of John Larroquette, of Night Court fame. I can see it, from a distance, and his good sense of humor probably adds to the comparison.
Time has flown by over the last couple of weeks. It is hard to believe that I am headed to see Dr. Frenette on Wednesday for my fourth treatment, which is the end of my second "cycle". This one carries some additional significance, as it is protocol to follow the second cycle with a PET scan to check treatment progress. The scan is not scheduled yet, but I suspect it will be next week at the hospital. I am optimistic about it, but I would be lying if I did not admit to being nervous as hell.
As I mentioned in my last (very short) post, my third treatment went "fine". I have come to expect a new experience (or more) each time I visit Dr. Frenette's office and this trip did not disappoint. As I was sitting in the treatment chair waiting for my blood tests to come back, I found myself getting nauseous over just being there. Apparently it is a pretty common phenomenon called "anticipatory nausea", which is when you get sick over the thought of something that has not even happened to you yet. Next time, I will be taking the anti-nausea medication before I go into the office. That said, the "hangover" from treatment was a little longer this time and I ranked the days following it as:
Friday: 5
Saturday: 3
Sunday: 4
Monday: 5
Tuesday: 6
Wednesday: 8 (fyi, I consider 8 "back to normal")
Since then, I have been feeling much better and my activity level has been pretty good. I have done some work off and on from the house and have been walking regularly. The walking is getting a little slower though, as I have developed tingling in both my feet. Apparently, this "neuropathy" is a common side-effect of the Vinblastine (the "V", in ABVD), and there is not much you can do about it, other than stop that part of the treatment if it gets to be too much to handle. I will certainly mention this to Dr. Frenette on Wednesday, but if history is any indication, he will not be impressed.
During my last visit to Dr. Frenette, I complained of continuous pain in my groin, which I was afraid was lymph nodes acting up. Rather than examining my groin, he carefully studied my neck...from his chair which was four feet away...and said I was fine. Works for me. Stuart has told me multiple times that Dr. Frenette reminds her of John Larroquette, of Night Court fame. I can see it, from a distance, and his good sense of humor probably adds to the comparison.
Can you see the likeness?
Talk to you soon and Happy Thanksgiving!
Labels:
ABVD,
anticipatory nausea,
Bill and Cathy Clarke,
Dr. Frenette,
John Larroquette,
Kerrins,
PET scan,
Vinblastine
Thursday, October 7, 2010
7th - Learning About Chemo
With almost all of my test results back, with the exception of the bone marrow biopsy, it is time to start seriously planning for chemotherapy. As I have mentioned previously, the standard of care in the US for Hodgkin's Lymphoma is ABVD chemotherapy. For me, it will be a 6-8 month regime, with treatments given every two weeks.
In order to learn more about ABVD and the potential side effects, Stuart and I spent the better part of the morning with Lindsay D. Griffin, Oncology RN extraordinaire. Lindsay was great and gave us a lot of detail, which I'll summarize for those of you who are interested.
ABVD is an acronym using the first letter of each of the four chemotherapy drugs used.
A = Adriamycin/Doxorubicin (a.k.a. "The Red Devil")

The red drug, Adriamycin, is usually given first. It is administered via a slow IV push over 10 minutes or so. Common side effects include:
B = Bleomycin/Blenoxane (a.k.a. Bleo)

Bleo is a clear fluid given via IV push, or mixed in 100ml normal saline solution and infused over 10 minutes or so. Common side effects include:
V = Vinblastine/Velban/VLB

Vinblastine is another clear fluid given via IV injection/infusion. Common side effects include:
D = Dacarbazine/DTIC

Dacarbazine is a clear liquid or may have a faint yellow tint. It is typically mixed in 250ml or more of D5W and infused over 30 minutes or longer (more of a drip). Common side effects include:
That is ABVD...3-5 hours and you are done and on your way.
In order to learn more about ABVD and the potential side effects, Stuart and I spent the better part of the morning with Lindsay D. Griffin, Oncology RN extraordinaire. Lindsay was great and gave us a lot of detail, which I'll summarize for those of you who are interested.
ABVD is an acronym using the first letter of each of the four chemotherapy drugs used.
A = Adriamycin/Doxorubicin (a.k.a. "The Red Devil")

The red drug, Adriamycin, is usually given first. It is administered via a slow IV push over 10 minutes or so. Common side effects include:
- Reduced blood counts, possibly leading to fever, chills, etc.
- Hair loss
- Nausea and vomiting
- Discolored (red) urine - no shock here
B = Bleomycin/Blenoxane (a.k.a. Bleo)

Bleo is a clear fluid given via IV push, or mixed in 100ml normal saline solution and infused over 10 minutes or so. Common side effects include:
- Fever and chills, which may occur after treatment
- Skin and nail changes, typically involving brown, yellow or pink discoloration and brittle texture.
V = Vinblastine/Velban/VLB

Vinblastine is another clear fluid given via IV injection/infusion. Common side effects include:
- Nerve changes or muscle cramping, which may occur within two weeks of the first treatment or after several doses have been given. Numbness, tingling or burning in the fingers and toes is common.
- Constipation
D = Dacarbazine/DTIC

Dacarbazine is a clear liquid or may have a faint yellow tint. It is typically mixed in 250ml or more of D5W and infused over 30 minutes or longer (more of a drip). Common side effects include:
- Flu-like syndrome
- Reduced blood counts
- Nausea and vomiting
That is ABVD...3-5 hours and you are done and on your way.
Labels:
ABVD,
Adriamycin,
Bleomycin,
chemotherapy,
Dacarbazine,
Dr. Hellner,
hodgkin's,
Lindsay D. Griffin,
lymphoma,
Vinblastine
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