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UND and EOT numbers for triple Tx
I am 7 days post EOT. 12 weeks Triple Tx Sovladi, Pegasys, Ribavirin.
Just got back from my EOT meeting with my doctor today—and I am also UND!
For those who like stats and numbers:
The HCV RNA QN test using COBAS® TagMan® HCV, v.2.0 (limit of detection (LOD) and LLOQ is 15 IU/mL)
HCV Not Detected.
ALT is 41, AST is 50.
HGB 10.3 / Platelets 139 / WBC 2.4
I went walking at the zoo for the first time in 12 weeks today, and wasn't exhausted at the end. My mental energy is improving all the time, physical energy is improving slowly, really just the last 2 days. Appetite is returning too.
My skin is really giving me a lot of problems this week it seems hyper sensitive. Like it really hasn't healed at all in 3 months. But that should subside as the drugs exit my body, and my blood levels even out. Will go to dermatology if it drives me crazy. Have a follow-up with opthamology later this month too. Will have a 1, 3 and 6 month follow up blood and viral load tests. My doctor will be retiring in 2 months, but will turn me over to a new doc, whom I will meet, next month for follow-up consults, and for yearly monitoring.
I do want to let people know that the treatment really wasn't that bad, (though it was interesting that my doctor was surprised when my husband and I were telling him that each and every time I got the Interferon shot, it would just knock me out for a day or two, not just the first time or two, but every shot).
He said that the Navy was now starting off-label with Sovaldi and Simeprevir for the more seriously ill patients. I thanked both him and his nurse for believing in me that I could do this.
Thank you fellow dragon slayers on this website for you support. You were more help than you will ever know. Knowledge really is power!
Sandi
Just got back from my EOT meeting with my doctor today—and I am also UND!
For those who like stats and numbers:
The HCV RNA QN test using COBAS® TagMan® HCV, v.2.0 (limit of detection (LOD) and LLOQ is 15 IU/mL)
HCV Not Detected.
ALT is 41, AST is 50.
HGB 10.3 / Platelets 139 / WBC 2.4
I went walking at the zoo for the first time in 12 weeks today, and wasn't exhausted at the end. My mental energy is improving all the time, physical energy is improving slowly, really just the last 2 days. Appetite is returning too.
My skin is really giving me a lot of problems this week it seems hyper sensitive. Like it really hasn't healed at all in 3 months. But that should subside as the drugs exit my body, and my blood levels even out. Will go to dermatology if it drives me crazy. Have a follow-up with opthamology later this month too. Will have a 1, 3 and 6 month follow up blood and viral load tests. My doctor will be retiring in 2 months, but will turn me over to a new doc, whom I will meet, next month for follow-up consults, and for yearly monitoring.
I do want to let people know that the treatment really wasn't that bad, (though it was interesting that my doctor was surprised when my husband and I were telling him that each and every time I got the Interferon shot, it would just knock me out for a day or two, not just the first time or two, but every shot).
He said that the Navy was now starting off-label with Sovaldi and Simeprevir for the more seriously ill patients. I thanked both him and his nurse for believing in me that I could do this.
Thank you fellow dragon slayers on this website for you support. You were more help than you will ever know. Knowledge really is power!
Sandi
I want to wish all the moms on this website to many more Mothers's Days, now that we have these new treatments leading to (hopefully) cures! And hopefully for me future Grandmother's Days too! Thank goodness there are researchers and companies willing to search for cures for this disease.
11 days post Tx, and I wanted to let you all know I am really feeling good! My appetite is returning, my skin is calming down finally (using a little Benadryl cream on the worst spots), and my energy is returning! Almost feel normal again—but maybe only about 80% energy, but that is improving every day! I felt so energized this morning I got up early and wanted to start the day. So hang in there (if you are almost done), because the reward is not far off at all.
4 week EOT report:
Hi! Still UND! Yay! My doc says SVR4!
WBC: 5.7 (1000/uL)
HGB: 12.5 (g/dL)
Platelets: 199 (111/uL)
ALT: 10 (L) (17-63) U/L
AST: 19 (<40) U/L!
I feel fine! What a relief! Thank you for your continued support! I love you all and you are in my thoughts and prayers!—Sandi
Will get an additional viral load test in at end of July for my 12 test. Will let you know the results. My doc said with the UND at 4 weeks, it is a good indicator that I am cured. The 12 and 24 week tests will just reconfirm it!
Hi! Still UND! Yay! My doc says SVR4!
WBC: 5.7 (1000/uL)
HGB: 12.5 (g/dL)
Platelets: 199 (111/uL)
ALT: 10 (L) (17-63) U/L
AST: 19 (<40) U/L!
I feel fine! What a relief! Thank you for your continued support! I love you all and you are in my thoughts and prayers!—Sandi
Will get an additional viral load test in at end of July for my 12 test. Will let you know the results. My doc said with the UND at 4 weeks, it is a good indicator that I am cured. The 12 and 24 week tests will just reconfirm it!
You are going to have to change your ID (grin). Great news...live well nohepc4 sandi....live well! Jo
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I'm not surprised to hear of you reactions to the interferon shots. My past treatments all involved some kind of interferon, and I took it on Fridays knowing I would be out of commission all weekend!
-Mark