01/21/09 - Intrathecal Chemo #4
Last Tuesday, 1/13/09, I received my 4th dose of intrathecal chemotherapy. Besides that, I had my blood counts checked and MRIs of my head and spine. Including travel time of roughly an hour each way, I left the house at 11:45AM and got home at 7:45PM. A long day...
That was my last dose of "once every two weeks" chemotherapy. Now, it goes to once per month for 6 months. Better because I take a type of steroids (dexamethasone) twice per day for five days around chemotherapy and they cause me to not sleep much. At least now, that time should be limited to one week per month.
Intrathecal Chemotherapy Treatment #4
For intrathecal chemo, they must make a "withdrawal" of cerebrospinal fluid (CSF) before they "deposit" the chemo drug (50mg of Depocyte - 0.00179 ounces by my calculations). The chemo has to be administered this way because the CSF resides in a small space (in and around your brain and spine). One nice advantage of this technique is my CSF that is withdrawn at each chemo treatment is microscopically examined for signs of disease spread (cancer cells). These tests have been negative (no spread). This process is detailed in my post about Intrathecal Chemo #2...
"Neck" MRIs, previous tumor location circled
The doctors also said that there wasn't any sign of disease spread in my MRIs. More good news!
Blood counts. I haven't updated them since mid-October. Needless to say, they are updated now, including details about my intrathecal chemotherapy doses. Since my intrathecal chemo is confined to my CSF, it should not have any effect on my blood counts. That is good because my counts (especially my platelets) still remain low, even though my last dose of traditional chemo was back in March of 2008... It doesn't make sense to me that they are still low...
Prior to my Ommaya Reservoir surgery on 11/25/08, my platelets were at 62,000. The brain surgeon wanted to see them at a minimum level of 100,000 before the operation. The morning of the operation, I was tranfused with two units of platelets. The first one brought my counts up to 90,000, and the second one brought my counts up to 115,000, so the surgery was performed.
Since I spent a while updating them please look at my blood count plot here, or at the link to the right... Thanks!
That was my last dose of "once every two weeks" chemotherapy. Now, it goes to once per month for 6 months. Better because I take a type of steroids (dexamethasone) twice per day for five days around chemotherapy and they cause me to not sleep much. At least now, that time should be limited to one week per month.
For intrathecal chemo, they must make a "withdrawal" of cerebrospinal fluid (CSF) before they "deposit" the chemo drug (50mg of Depocyte - 0.00179 ounces by my calculations). The chemo has to be administered this way because the CSF resides in a small space (in and around your brain and spine). One nice advantage of this technique is my CSF that is withdrawn at each chemo treatment is microscopically examined for signs of disease spread (cancer cells). These tests have been negative (no spread). This process is detailed in my post about Intrathecal Chemo #2...
The doctors also said that there wasn't any sign of disease spread in my MRIs. More good news!
Blood counts. I haven't updated them since mid-October. Needless to say, they are updated now, including details about my intrathecal chemotherapy doses. Since my intrathecal chemo is confined to my CSF, it should not have any effect on my blood counts. That is good because my counts (especially my platelets) still remain low, even though my last dose of traditional chemo was back in March of 2008... It doesn't make sense to me that they are still low...
Prior to my Ommaya Reservoir surgery on 11/25/08, my platelets were at 62,000. The brain surgeon wanted to see them at a minimum level of 100,000 before the operation. The morning of the operation, I was tranfused with two units of platelets. The first one brought my counts up to 90,000, and the second one brought my counts up to 115,000, so the surgery was performed.
Since I spent a while updating them please look at my blood count plot here, or at the link to the right... Thanks!
posted by Mark at 1/21/2009 08:21:00 AM
7 Comments:
Hey, great news, Mark! What about the iffy area in your head that they are monitoring?
It was good to see you and Laura last week. The chemo certainly isn't hurting your appetite. 8-)
Carson
Carson,
Thanks! They are watching the "iffy area." I continue to ask them about it, but they tend to explain it away, so I'm not going to continue to put details about it on my blog. I won't lose track of it, though...
Appetite. Hmmm... I have a theory that the steroids increase it. So does good food and company, and I couldn't pass up the opportunity...
-Mark
Wow, wow, and more WOW!!!!! Now that's a report with good news and MORE good news. Not only that, you look GREAT, and your attitude is even better!! What more can one say, except that continual prayers are being said for the doctors to continue their wonderful work and the good Lord will do the rest!
Love to everyone there, from everyone here....keep in touch!
The Gregorys
Mary,
Thanks! I'm sure I keep my doctors on there toes, and they have MANY other patients as well. So kudos to them also...
-Mark
Great news! and...you arent half as iffy as Scott so...no need to worry!
Looking good Suter! Glad to see the good news and the hair all grown back. Melvin will be jealous how easily your hair grows.
Rico,
Thank you! The hair's not all back from my Ommaya surgery... They have to shave it each time I receive chemo. At least it will grow back...
-Mark
Post a Comment
<< Home