Somethings you just have to tell.
Three weeks ago I had my blood draw and after being told early on that my white cells probably would never come up because a few of us take a little harder beating on our blood cells. Well after 4 1/2 yrs. this time they were normal! I told my son and he never forgot what the Dr. said and my son says "Mom did you say "IN YOUR FACE DOC!" and I said no "IN YOUR FACE CANCER!"
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Re: Somethings you just have to tell.
I love it, thanks for sharing. It gives all of us hope that one day we will see normal CBC's again....
Best wishes Fern |
Re: Somethings you just have to tell.
Great news! Thanks for posting!
Carol Ann |
Re: Somethings you just have to tell.
Good to hear! Hoping you are feeling correspondingly better as well.
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Re: Somethings you just have to tell.
That's great! Thanks for telling us.
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Re: Somethings you just have to tell.
Congrats and well done! Normal is wonderful!
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Re: Somethings you just have to tell.
So pleased to read this!:)
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Re: Somethings you just have to tell.
Thank you everyone! I feel like I just received an award in Cancer kicking! lol
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Re: Somethings you just have to tell.
In your face cancer!!!! Love it
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Re: Somethings you just have to tell.
Good for you!!!
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Re: Somethings you just have to tell.
That is nice news :) I have just been going through treatment. One dr. visit I asked just that...will WBC counts go back up, to the normal range...and the dr. was kinda quiet...replied...some do/we will just have to wait and see....I was like, huh? So you are saying they just may not? All I could think was...why don't the drs. just say these things...so we don't just wonder? I sure have learned over these past months...that the phrase they use "everyone is different, so we just can't say" is true :/ But I feel the drs. could say a bit more...I just have been trying to wrap my head around it all... and have a general idea of things ! Reading, reading and reading about it all...well...at times I just must quit. It gets to be too much. One day at a time...w/ HIS help/grace : )
Thank you for any comments. |
Re: Somethings you just have to tell.
Cld14, I'd say your right where we all were at your stage of treatment! It Is frustrating on the other hand the times it is most fustrsring we force our selves to move on a bit hang in there your almost done hoot hoot
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Re: Somethings you just have to tell.
Thank you Pray : )
Yes, most treatment accomplished : ) I noticed most of the gals have their stats posted. I had not done that....need to figure that one out. I was 63 yrs. at diagnosis...Stage III C , IDC lymph nodes in armpit and near collarbone involved. I had chemo for 5 mos., break, lumpectomy, break, then rads 33 treatments Apr/May. Herceptin began in Oct. and I continue w/ it until one year complete...getting close :) Am just beginning to take the daily tab Arimidex. It is so interesting how each of us has a bit of a different story. I have neuropathy in fingers/toes/feet and that somedays is hard to take...taste buds still out of whack...I have done well, eating, even tho not enjoyed. Have been doing walking/ and some strengthening exercise to help w/ my stamina/fatigue. |
Re: Somethings you just have to tell.
Great! Thank You, Lord!
:-) Penny |
Re: Somethings you just have to tell.
Great news, thank you for sharing.
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Re: Somethings you just have to tell.
CLD14, I agree with you. I wish they would just lay it out in all the draconian depths of purgatory but I guess they are afraid we will all run for it. Who knows, maybe we would. Anyway, my husband keeps reminding me that not everyone can handle that level of honesty - a bit like the difference in dipping your toe in the pool & gradually going deeper to jumping in the deep end and swimming for it. I have decided he is one of the dippers and I am a deep diver; I think he wants to believe that there are just minor temporary problems and, as soon as treatments are over, we will be back to our old selves, minus a few body parts in my case. It's why I depend on all the folks on this web site to let me know the truth since I know most doctors I have met try to sugarcoat things. I finished radiation on Friday and start chemo on Wednesday. Radiation was a piece of cake for me. I think it must help to have a dead chest ( my double mastectomy was a year ago) and a numb underarm and side (my axillary lymph node removal was in June). Wish I thought chemo would be the same.
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Re: Somethings you just have to tell.
Hi Pat 94...thank you for you thoughts. My hubby said more or less the same...in that not all folks want to hear everything : /
My hubby went through cancer treatment a few years before me...so he does realize what it is all about...one good thing overall/altho in typical male style he didnt talk much/nor does he still...sees no point. He just has had his 5 yr. post treatment annv. and will see his oncologist next month for his final post treatment followup...thankful he is well...he lives w/ permanent side effect damage....his tumor was on his tonsil and in some lymph nodes in his neck...he had chemo/rads/surgery/feeding tube for 14 mos. It leaves all stiff in the neck, swallowing function...salivary glands damaged..thus affecting teeth/mouth health/eating is a slow process...quite an ordeal ! I will be glad to talk about the chemo if you wish...mine lasted 5 mos....I was ill at the beginning...w/the first mix of two drugs...second mix no nausea...so much better...as far as that goes... it was the second mix w/ Taxol that led to the neuropathy for me. Radiation was fine for me as well. My skin held up great...my dr. recommended aloe vera gel and I faithfully put it on a few times daily. I know a few other gals that have had mastectomies but they have not spoken in much detail about it. Talk to you later. : ) |
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