Aa
THE FINISH LINE with Victrelis
This is gonna be long…
It’s 7pm and I feel like I should be doing something. What oh what could it be?? My cell phone alarm is ringing, but……I have no more tx pills to take!! Wuuuu Huuuuuu!! The Victrelis bottles are empty, the Monday – Friday pill case of Ribavirin is empty, and the fridge doesn’t have any syringes of Interferon waiting for the Friday Night Darts Club injections. I am done! I have survived. I am nauseous and exhausted today, relieved and happy, grateful and humbled. The last 2 months have been extremely draining for me and I have missed many a post on UND and otherwise.
How do I even begin to thank everyone in this forum? For once, I am ‘almost’ at a loss for words. Almost. Where else could I make 43+ friends, have over 650 posts (to date) and receive 100 notes…in 10 months…from total strangers?? In the Hep C Community on Med Help, I have encountered the most supportive, honest, and knowledgeable problem solvers. I have felt GUILTY for enjoying my time here but it gave me such a safety net and sense of purpose at the same time. While family grows weary of the week by week details (of which I am certain I gave too much), this is full of members willing to listen and lend encouragement. THANK YOU AND MAY GOD BLESS YOU & YOURS, right where you are.
This process has taken me through many stages: DENIAL – How can I have this?? I have no idea how I got Hep C; ACCEPTANCE – Okay, my tests keep showing my Viral Load is chronic; FEAR – My life just got shorter; DECISION – being African American, it made no sense to me to treat, as odds were so low, but the new P.I.’s offered much more hope, so I finally agreed; TREATMENT – September 1st, 2011 – March 16th, 2012.
I don’t have any labs to report at this time (UND at week 21) but expect to in one month.
For all my cyber-friends, official and otherwise…….YOU ROCK!! I will always appreciate you more than you can ever know. Wishing the very best for EVERYONE, and giving a special shout out to those who started this journey in September/October with me, just as scared to walk through that door:
Aj7538! Arlenedupee! Brianmo! Cieritaqt! Coeric! Dee1956! Dreamcat! Hondapatches! Jillybean! Indy531! Libzo2! Livingontheedge! Mykids247! Needinghelp213 (wishing you well) PJHep! Pooh55811! Screaming48! Starshine1ca! Vannh9!
Special thanks MUST also go to Frijole, for maintaining spreadsheets, from which I got most of the start dates.
Thank you to ALL the experts here for sharing your journies and advice, and also to the volunteer moderators (Claire and Emily). And most, most of all, I give thanks to God, for whom I could never have done this without. Time will tell if I am off and running to SVR-land (as ElPasolady would say)!
Blessings Always,
Bee :)
It’s 7pm and I feel like I should be doing something. What oh what could it be?? My cell phone alarm is ringing, but……I have no more tx pills to take!! Wuuuu Huuuuuu!! The Victrelis bottles are empty, the Monday – Friday pill case of Ribavirin is empty, and the fridge doesn’t have any syringes of Interferon waiting for the Friday Night Darts Club injections. I am done! I have survived. I am nauseous and exhausted today, relieved and happy, grateful and humbled. The last 2 months have been extremely draining for me and I have missed many a post on UND and otherwise.
How do I even begin to thank everyone in this forum? For once, I am ‘almost’ at a loss for words. Almost. Where else could I make 43+ friends, have over 650 posts (to date) and receive 100 notes…in 10 months…from total strangers?? In the Hep C Community on Med Help, I have encountered the most supportive, honest, and knowledgeable problem solvers. I have felt GUILTY for enjoying my time here but it gave me such a safety net and sense of purpose at the same time. While family grows weary of the week by week details (of which I am certain I gave too much), this is full of members willing to listen and lend encouragement. THANK YOU AND MAY GOD BLESS YOU & YOURS, right where you are.
This process has taken me through many stages: DENIAL – How can I have this?? I have no idea how I got Hep C; ACCEPTANCE – Okay, my tests keep showing my Viral Load is chronic; FEAR – My life just got shorter; DECISION – being African American, it made no sense to me to treat, as odds were so low, but the new P.I.’s offered much more hope, so I finally agreed; TREATMENT – September 1st, 2011 – March 16th, 2012.
I don’t have any labs to report at this time (UND at week 21) but expect to in one month.
For all my cyber-friends, official and otherwise…….YOU ROCK!! I will always appreciate you more than you can ever know. Wishing the very best for EVERYONE, and giving a special shout out to those who started this journey in September/October with me, just as scared to walk through that door:
Aj7538! Arlenedupee! Brianmo! Cieritaqt! Coeric! Dee1956! Dreamcat! Hondapatches! Jillybean! Indy531! Libzo2! Livingontheedge! Mykids247! Needinghelp213 (wishing you well) PJHep! Pooh55811! Screaming48! Starshine1ca! Vannh9!
Special thanks MUST also go to Frijole, for maintaining spreadsheets, from which I got most of the start dates.
Thank you to ALL the experts here for sharing your journies and advice, and also to the volunteer moderators (Claire and Emily). And most, most of all, I give thanks to God, for whom I could never have done this without. Time will tell if I am off and running to SVR-land (as ElPasolady would say)!
Blessings Always,
Bee :)
GREAT job, bee. i wish you nothing but the best for your future. i have 9 1/2 weeks more and i'll be stoked like you are. congratulations cyber friend. best of luck for SVR. belle
Well done Bee...!
Hope you feel better soon and looking forward to hearing an SVR from you...
Will
Hope you feel better soon and looking forward to hearing an SVR from you...
Will
nice going bee! keep in mind it might take a while to feel good...right after tx new symptoms started...i got really achy and bad headaches...at 6 weeks post things turned around big time...every week i noticed a change up until 3 months post..now theres not much going on..i'm getting stronger...and feeling better still but i'm almost out of the woods....looks like by 6 months post tx i'll be doing better then 10 years ago...just don't be disappointed if things take a little time...good luck....billy
THANK YOU!!! You are all such a blessing. Once I get my energy back, I will surely be doing my happy dance. In the meantime, I will settle for doing it on the inside:
http://www.youtube.com/watch?v=mYP4MgxDV2U
Still tired but feeling better today!!
Hugs,
Bee :)
http://www.youtube.com/watch?v=mYP4MgxDV2U
Still tired but feeling better today!!
Hugs,
Bee :)
Absolutely wonderful news! I finished about 3 weeks ago, and life is slowly getting better. I'm so happy for you and look forward to seeing you post UND here shortly! There were quite a few of us that all started around the same time. It would be nice if we could all get together this fall for like a weekend somewhere. And truly, people that haven't done treatment, just can't understand.
CONGRATUATIONS FOR A JOB WELL DONE!!!
Jilly
CONGRATUATIONS FOR A JOB WELL DONE!!!
Jilly
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