My CT scan was clean; everything looks good. Did the taxotere - no allergic reaction to it. The nurse told me that since I'm only doing 3 rounds of this, I shouldn't have any of the uncommon side effects. It's folks who have to do six or more doses that generally get the weird side effects. So I'M GOOD. Will have another CT scan in 3 mos but am positive that all will be clean with that one too.
Just a brief note to let you all know that I'M CLEAR OF ANY TUMORS (and hopefully cancer) at this point. And plan to stay that way. I have to get a shot tomorrow to help keep my red and white counts at an acceptable low over the next 10-11 days. But shouldn't get nauseous from any of this. Keeping my thoughts positive (and my fingers crossed).
March 29, 2010
2:33 pm
Monday, March 29, 2010
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I'll save you time and money: as I live in CT, I've scanned you and I'm here to tell you - you're fine.
ReplyDeleteNo charge.
WOOHOO - Your Taxotere went F*A*S*T - Mine is every 3 weeks - I've had 7 doses so far (Abraxane) so that's why I have no toenails - but if I get the same result, it'll be worth it. And congrats on getting through this close to summer! You're down to your fighting weight and ready to hit the beach in a floppy brimmed hat. I'm sooooo happy for you! (I'm one that gained 25 lbs on the steroids - yuk!)
ReplyDeleteMy next chemo and scan is April 14 - keep me in mind as you send out happy thoughts and good wishes.
Love, Kaysey
Kaysey, my next round is April 19. The steroids I'm taking for three days (one day before chemo, the day, and the day after) make sleep hard. Whereabouts do you live in Indiana? I'm sorry for your toenail loss. I've been understanding that I may have that side effect, or neuropathy, or even (God forbid!) permanent hair loss. One day at a time; sometimes just one hour at a time, and then stop and rest (can't sleep, but can certainly enjoy a stretch on the couch). The hair loss is the hardest, most devastating side effect (besides the acid reflux and emesis and not eating...okay, so it was the thought of the hair loss; now that my hair is pretty much history, it's easier to live with. You can email me directly at skokott@mchsi.com. I'd love to talk to you more personally.
ReplyDeleteDear Susie,
ReplyDeleteWhat wonderful news! I am so glad to hear that things are going in your favor. You have fought a hard fight, and I am so proud of you, your determination, and all your strength throughout this ordeal.
All of our prayers are being answered. Hang in there, as 3 more rounds will go quickly.
Enjoy the downhill ride from here on out!
Love you, Debbie
Okay, it says:
ReplyDelete"your comment will be visible after approval"
Are you weeding out some of your followers?
The hair is a pain - my wigs are still goofy looking - and I'm just not a hat person - scarves are it for right now, but they just scream "cancer". I'm in a wig today because I'm at work, but I drove the convertible, so I may end the day in a ball cap. I have a pink one in the car. The steroid I was on was dexamethasone and it does make it hard to sleep - but it really helps with the aches and pains. Start taking some B-6 now for the neuropathy - it's supposed to help - and N-acetylcystein - both are available at the health food store - They gave me these at Cancer Treatment Centers of America when I saw their naturopath. I didn't lose my toenails until after treatment #5. If you only have 3, you may miss that side effect. I'll email you, too.
ReplyDeleteHave a fun day and Hoppy Easter!
Love, Kaysey
I'm just moderating because I've had some pretty harsh comments made that are untrue and way off topic. I don't need that poison in my life right now. My own fault for feeling abandoned and then posting about it. Damage control.
ReplyDeleteSusie,
ReplyDeleteHow totally awesome! That is the greatest new I have heard in such a long time. I weep tears of joy! I love you, and can't wait to see you this summer! xoxoxoxo
Stephanie