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"All fixed up" - so I thought...

Mchapp
CSN Member Posts: 95
Well, I have taken a break from here - hope all of you are doing well and on your way to a better 2011!
I am not there yet... - since my chemo (folfox etal) and raditation were finished in March 2010 - and my reversal went well with out a glitch in May (2010) - but my lovely white counts are YUCKY!!! And not so good...
Has anyone else had their white counts take over 8 months to be "normal"?? Mine are bouncing from 2.9 to 3.6...the highest they have been is 3.9
I can't seem to hit the 4's...I don't feel bad - I am still fatigued at a higher level than what I would like...but this is bothering me that they are not re-bounding...the doctor said if they are not in the 4's by November - bone marrow biopsy...I want to avoid that at all costs!
Thanks in advance for your thoughts and suggestions and others...
Michelle
I am not there yet... - since my chemo (folfox etal) and raditation were finished in March 2010 - and my reversal went well with out a glitch in May (2010) - but my lovely white counts are YUCKY!!! And not so good...
Has anyone else had their white counts take over 8 months to be "normal"?? Mine are bouncing from 2.9 to 3.6...the highest they have been is 3.9
I can't seem to hit the 4's...I don't feel bad - I am still fatigued at a higher level than what I would like...but this is bothering me that they are not re-bounding...the doctor said if they are not in the 4's by November - bone marrow biopsy...I want to avoid that at all costs!
Thanks in advance for your thoughts and suggestions and others...
Michelle
Comments
-
Hi Michelle
It is good to hear from you! I am sorry you are having the white counts issue. I hope they are in the 4s soon so you don't need that biopsy (3.9 is awfully close!), but if you do, they will figure out what is going on. I am still undergoing chemo, so I can't comment on what is normal after treatment. -
Fours
Hi Michelle
I never rebounded with my WBC's after chemo treatments....they would stay in the high 3's but they won't go back to minimum....pretty close to 2 years now.
Since getting back into treatment (had recurrence #3) since you were last here, they have been as high as around 3.9 but in two treatments, they are about 3.1 now. I'm doing Folfiri now.
I take Neulasta shots every cycle to boost counts to do the chemo.
Don't know how it will all turn out - hope things get better for you, but the point of my story is if they stay high 3's, that may be the new you - if you have a bone marrow test, will be interesting to see if they see anything at all.
Best wishes!
-Craig -
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