I am dancing with Ned
We met in his office after along with my mom and my cousin. Dr explained that there is sn 80% chance of recurrance but 20% chance it will never come back. He said I am in remission, no evidence of disease. I prefer no evidence of disease. Remission sounds like it is lurking while no evidence of disease sounds like it's gone! He said it will take 6 months to a year for all symptoms from chemo to go away. I told him I feel like my old self already. I just need to gain more stamina and my legs feel weak. I will only see him once a year while I will see my oncologist and have a CA 125 every three months.
He gave me a hug and I thanked him. My mom hugged him and thanked him for saving her daughter's life.
So I am dancing with Ned. I hope I let him lead. I will be putty in his hands so he can keep me safe. Today is a great day.
Thank you all for sharing this with me. Love, Karen
Comments
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Fantastic!
So pleased for you, I hope your dance in neds arms lasts forever xxx0 -
Ain't it grand? You keep
Ain't it grand? You keep right on dancing, hon. We aren't jealous of NED; he can have as may girlfriends as he wants and none of us will mind a bit. In fact, we hope every woman on this board will get a chance at a long-term relationship with NED.
Remission and NED are exactly the same thing, but if you like "no evidence of disease" better, then by all means, that's the one you should use.
I had to have my port removed because it eroded thru my skin, but after much deliberation, I had another one put in, so I could use it to finish my year of Taxol (consolidated therapy....AKA maintenance). Now I have matching scars on my upper chest. Lovely.
Carlene0 -
Dance , dance, dance !
Great
Dance , dance, dance !
Great News !0 -
Dance on! Dance on!Cafewoman53 said:Dance , dance, dance !
Great
Dance , dance, dance !
Great News !
Great news!!
"I could have danced all night; I could have danced all night, and still have danced some more! I could have spread my wings and done a thousand things I'd never done before"...
Do the 1000 things you never did before!! BE JOYOUS!
(now I'll be humming that tune all day in my head....)0 -
Wonderful news... keep onkellyh33 said:NED
Amazing news Karen! Keep on dancing and keep on celebrating and know we are celebrating with you
Wonderful news... keep on dancing!0 -
Karen....I was just
Karen....I was just wondering about the decision to have your port removed....was this something that had to be done, because of problems with it, or is this your doctor's standard procedure?
Will you have a new port placed, if you have a recurrence?
My port eroded thru my skin, after my initial treatment, but while I was on monthly Taxol consolidation therapy. My choices were to (1) have the port removed and finish the Taxol via IV, or (2) remove the port and discontinue the Taxol, or (3) have a new port placed, so I could finish the Taxol and leave it for any possible recurrence. I chose door number three.
I am NED, too, but I had planned to leave the port in place for at least two years, just in case.
Carlene0 -
I guess it is standard procedure. I didn't really have a problem with the port. During my second to last infusion I started getting pain and they could not find a reason. I made it through but it hurt a lot. I was apprehensive the next time so they had me take a vicodin and also gave me ativan so I basically slept through it.Hissy_Fitz said:Karen....I was just
Karen....I was just wondering about the decision to have your port removed....was this something that had to be done, because of problems with it, or is this your doctor's standard procedure?
Will you have a new port placed, if you have a recurrence?
My port eroded thru my skin, after my initial treatment, but while I was on monthly Taxol consolidation therapy. My choices were to (1) have the port removed and finish the Taxol via IV, or (2) remove the port and discontinue the Taxol, or (3) have a new port placed, so I could finish the Taxol and leave it for any possible recurrence. I chose door number three.
I am NED, too, but I had planned to leave the port in place for at least two years, just in case.
Carlene
I am not sure if a port would be used for a recurrence. My veins are pretty well shot at this point but I'm hoping they get back to normal or better at least. I had taxol(day 1) intravenously, then carboplatin(day 2) through the port and then taxol(day 8) through the port.
My understanding was chemo given through the port in my abdoman gave me the best result. The surgeon asked how many infusions I completed. I told him 8 and he said that was icing on the cake.
Karen0 -
so happy for youkikz said:I guess it is standard procedure. I didn't really have a problem with the port. During my second to last infusion I started getting pain and they could not find a reason. I made it through but it hurt a lot. I was apprehensive the next time so they had me take a vicodin and also gave me ativan so I basically slept through it.
I am not sure if a port would be used for a recurrence. My veins are pretty well shot at this point but I'm hoping they get back to normal or better at least. I had taxol(day 1) intravenously, then carboplatin(day 2) through the port and then taxol(day 8) through the port.
My understanding was chemo given through the port in my abdoman gave me the best result. The surgeon asked how many infusions I completed. I told him 8 and he said that was icing on the cake.
Karen
thanks great0 -
so happy for youkikz said:I guess it is standard procedure. I didn't really have a problem with the port. During my second to last infusion I started getting pain and they could not find a reason. I made it through but it hurt a lot. I was apprehensive the next time so they had me take a vicodin and also gave me ativan so I basically slept through it.
I am not sure if a port would be used for a recurrence. My veins are pretty well shot at this point but I'm hoping they get back to normal or better at least. I had taxol(day 1) intravenously, then carboplatin(day 2) through the port and then taxol(day 8) through the port.
My understanding was chemo given through the port in my abdoman gave me the best result. The surgeon asked how many infusions I completed. I told him 8 and he said that was icing on the cake.
Karen
thanks great0 -
so happy for youkikz said:I guess it is standard procedure. I didn't really have a problem with the port. During my second to last infusion I started getting pain and they could not find a reason. I made it through but it hurt a lot. I was apprehensive the next time so they had me take a vicodin and also gave me ativan so I basically slept through it.
I am not sure if a port would be used for a recurrence. My veins are pretty well shot at this point but I'm hoping they get back to normal or better at least. I had taxol(day 1) intravenously, then carboplatin(day 2) through the port and then taxol(day 8) through the port.
My understanding was chemo given through the port in my abdoman gave me the best result. The surgeon asked how many infusions I completed. I told him 8 and he said that was icing on the cake.
Karen
thanks great0 -
so happy for youkikz said:I guess it is standard procedure. I didn't really have a problem with the port. During my second to last infusion I started getting pain and they could not find a reason. I made it through but it hurt a lot. I was apprehensive the next time so they had me take a vicodin and also gave me ativan so I basically slept through it.
I am not sure if a port would be used for a recurrence. My veins are pretty well shot at this point but I'm hoping they get back to normal or better at least. I had taxol(day 1) intravenously, then carboplatin(day 2) through the port and then taxol(day 8) through the port.
My understanding was chemo given through the port in my abdoman gave me the best result. The surgeon asked how many infusions I completed. I told him 8 and he said that was icing on the cake.
Karen
thanks great0
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