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mamawof4 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote mamawof4 Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 11:43am
Rebecca,
I live in the Cincinnati area and all of my treatments have been through Bethsda Hospital and my ong is Dr. Bechhold . A very nice doctor her office is close toReed Hartman. Good luck and God bless you.
dx 4/9/09 with stage 2a grade 3,one node cancerous, lumpectony,10 radiation treats via mamma site,8 chemo treat with 4 a/c and 4 iexempra thur clinical trial finished 11/25/09 PALB2 gene+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote rebecca lynn Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 11:55am
Thank you so much....I will write that down so I have it when I move ..
 
HUGS
Rebecca
rebecca
stage 3 grade 3A
Dx 12/08
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mamawof4 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote mamawof4 Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 12:06pm
My pleasure if you got any questions send me a personnal message and I can give you more details. How soon are you moving to town?
dx 4/9/09 with stage 2a grade 3,one node cancerous, lumpectony,10 radiation treats via mamma site,8 chemo treat with 4 a/c and 4 iexempra thur clinical trial finished 11/25/09 PALB2 gene+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote kaycee Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 12:41pm
Hi Ellen,

You and I are following an almost identical path. I'm 54, had my biopsy on May 18, and also was told that I would need radiation following lumpectomy, no chemo. I didn't learn of my triple negative status until I had my wire insertion and was being taken over to outpatient surgery for lumpectomy on May 25.

I had not received my copy of the pathology report prior to surgery, and the nurse kindly stopped on our way over to outpatient and got me a copy. I had no idea what triple negative cancer was at that time, but from the careful way the nurse chose her words about the status, I realized it might be a worse cancer than I had thought. I was home from surgery by noon, and immediately started searching the internet. A little knowledge really can be a dangerous thing -- I spent the next few days in total terror. I really wish I would have consulted with an oncologist immediately following the biopsy. I also wish that I would have stumbled across this website in the beginning, because the ladies here are a font of wisdom and have helped me enormously in finding perspective on this disease.

I don't want to minimize the seriousness of a TNBC diagnosis, but I believe that managing the fear of recurrence is important for living a quality life right here right now. This is the only life I have and I don't want to spend it in dread of what might happen later. I still have my moments where I get freaked out but at this point in my journey, I am finding it helpful to concentrate on the task at hand, which is getting through treatment and maximizing my chances to prevent recurrence, and am pretty much living in the moment rather than worrying about what comes next. I just keep repeating the mantra "Let Go and Let God". Somehow, it's working for me and I hope it will work for you too.

Hugs,
Kaycee




Edited by kaycee - Jul 26 2010 at 12:44pm
DX age 54, lumpectomy, IDC,10mm, 0/10 nodes, Stage 1 Grade 2, ER-/PR-/HER2neu-, Ki-67 74%, BRCA negative, TCx4, 6 weeks rads
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Post Options Post Options   Thanks (0) Thanks(0)   Quote guygirl Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 12:54pm
It's been a couple of days since the port went in and it is starting not to feel so uncomfortable.  Had to go and have blood taken so that they would have a baseline before chemo.  They used the port and it worked ok, but it still hurt.  So now I am 7 days and counting til the start of chemo.  Did have a ray of light this past week.  I was driving to work and was having my own personal pity party (one of many) and all of the sudden the guardian angel that is on my sun visor fell right into my lap.  I took it as a sign that my mom was telling me to stop feeling sorry for myself and get myself together that it was all going to be all right.  My husband and I celebrated our 28th anniversary on Saturday.  I got my hair cut, colored and highlighted and he hated it, said it was too short.  I told him, you think it is short now, just wait a couple of weeks.  Anyway, thanks to all of you for you encouragement and kind words. 
Age 50 DX: 6/3/10 IDC, Stg 1A Grd 3 1.9cm, KI-67 85%, lump. w/SNB, clear margins, lymph node 0/1, 4 cycles A/C (dose dense) every 2 wks, 4 cycles Taxol(dose dense) every 2 wks, 33 rads, BRCA 1/2 neg.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote kirby Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 2:05pm
great story guygirl.
kirby

dx Feb. 2001. Age 44
Lumpectomy

2cm. no nodes stage 1 grade 3

4 rnds AC, 35 rads
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Post Options Post Options   Thanks (0) Thanks(0)   Quote tnbcsucks Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 2:36pm
overwhelmed....Hi, I also have had some bad headaches after my first two rounds of A/C...they seemed to disappear for rounds 3 and 4...not sure why.  My eyes have been the most irritating ofit all.  They seem to water a lot.  I did get some drops to help, and they do for the most part...just a pain, but I was told it was a side effect of the chemo...so I guess I live with it and move on...  Good Luck wiht your treatments.  I just finished my A/C and going to start my Taxol x12 on August 2nd.
TNBC DX April, 2010,Lumpectomy May 3.5cm with clear nodes,Stage 2, Grade III Started Chemo on June 7: 4 A/C every other week and then 12 weeks of Taxol. followed by 6 weeks of radiation.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Katastrophe Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 9:43pm
Hi Guygirl, I know when I had my port put in it was shocking. I had to stay in hospital for the night. My blood pressure went so high they said I was bordering on a stroke. I complained for sooooooo long about it, and the docs all said is is unusual as most people have no probs with it. I personally think they dont listen to MOST people. I went to a Rheumatoid specialist about pain in my shoulder (the same side as the port, and hip pain). She gave me cortizone injections to both areas. The guys that did my ultrasound told me I had a rather large build up of fluid in my right shoulder in the same place he put the needle. You would not believe it, but after the initial couple of weeks settling time after the injection, I have had no problems with the port. The docs cannot explain to me why this is so! Maybe the operation to insert the port had caused the fluid build up in the first place, who knows. Certainly not the doctors.
Overwhelmed .... I got some stuff from my chemist called "liquid tears", it did help with my eyes to some extent. gl luv Kat
Age 49. Stg2 gr3 19mm lump in L/br 1 lymph node in L/br 3/14 lymph nod under left arm full clear bil/mast 6rds Chemo 3wkly 25rds Rad 18rds of Avastin finished treatment on 19th August 10.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote dmwolf Quote  Post ReplyReply Direct Link To This Post Posted: Jul 26 2010 at 11:04pm
Hey, Sharon.  How's it going?  Did you decide on a chemo protocol yet?
Thinking of you,
Denise
DX 2/08@43 stg II IDC; gr2,0 nodes. Neoadj chemo, first ACx2 (fail) then CarboTaxotereX6(better). Lump, Rads done 11/08; Clodronate. False alarm queen: PetCT lung & TM marker. NED. PBM w/recon 9/10.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Jul 29 2010 at 10:27am
Hello guygirl and welcome to our community,
 
Be sure and check out our "chemo tips" in the TNBC News/Resource section.
 
Also the Resource link near the top has some helpful information for you.
 
This is a wonderful brochure about TNBC, the first ever published which came out the end of last year.
 
Congratulations on your anniversary!
 
I think that you can do whatever you want with your hair.  Getting our hair done makes us feel better, a positive in a stressy situation.  Good for you, it sounds pretty. 
 
There are links for headwear in the TNBC News/Resource section.  If you have trouble finding them let me know.
 
Best wishes
Stage 2 2003
Stage 1 2007
BRCA 1+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Carol (Tenn) Quote  Post ReplyReply Direct Link To This Post Posted: Jul 29 2010 at 11:15am
Welcome Guy/Girl, it's good to have you here. Not so good you have to be here but glad you found us. We are all in this together and give each other all the loving support we can muster.
I do love your angel story and I know it that God does work in His own way. Please visit our Spiritual Support thread if that's something you might be interested in. It's just a clk away.
Kaycee,
I love that saying but being human it's the hardest thing to do for me but it's the best advice.
Love and Prayers,
Carol
St 2 Gr 3, A/C/T, DD
Radiation x35
Rec chest wall 07/09
Radiation x28
NED 10/24/11
NED 10/5/12
NED 03/15/13
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Post Options Post Options   Thanks (0) Thanks(0)   Quote staceydooley Quote  Post ReplyReply Direct Link To This Post Posted: Jul 30 2010 at 12:51am
Hi Sharon,
I haven't been on the site for awhile. I just signed on and read your letter. The same thing happened to me, I had horrible pain in my breast.
My Dr told me cancer does not hurt, but it seems TNBC does.
Just wanted to say that.
Take care.
http://www.youtube.com/watch?v=0Nvx7vFE2fs
Stacey, 43 years, TNBC
Double mastectomy 04-01-10
BRCA 1, porto cath put in
no nodes
chemo to start June 3rd
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Post Options Post Options   Thanks (0) Thanks(0)   Quote staceydooley Quote  Post ReplyReply Direct Link To This Post Posted: Jul 30 2010 at 1:01am
sorry to hear about your headaches. I have them also. They say its the chemo.
http://www.youtube.com/watch?v=0Nvx7vFE2fs
Stacey, 43 years, TNBC
Double mastectomy 04-01-10
BRCA 1, porto cath put in
no nodes
chemo to start June 3rd
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Post Options Post Options   Thanks (0) Thanks(0)   Quote staceydooley Quote  Post ReplyReply Direct Link To This Post Posted: Jul 30 2010 at 1:03am
just wanted to share my hair cutting video with you
http://www.youtube.com/watch?v=0Nvx7vFE2fs
Stacey, 43 years, TNBC
Double mastectomy 04-01-10
BRCA 1, porto cath put in
no nodes
chemo to start June 3rd
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Post Options Post Options   Thanks (0) Thanks(0)   Quote tnbcsucks Quote  Post ReplyReply Direct Link To This Post Posted: Jul 30 2010 at 11:37am
not sure how scientific this is...but I  had a runny nose and sore throat when I was taking A/C...so my onc. said to take my claritin for it....I did...after I took that...I had no more headaches from the chemo treatments....not sure if it is related...but I'm not willing to give up the claritin if it is as those headaches sucked!!!
TNBC DX April, 2010,Lumpectomy May 3.5cm with clear nodes,Stage 2, Grade III Started Chemo on June 7: 4 A/C every other week and then 12 weeks of Taxol. followed by 6 weeks of radiation.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote gobluegirl90 Quote  Post ReplyReply Direct Link To This Post Posted: Jul 31 2010 at 1:42am
Welcome Guy/Girl,
I too am a newbie and I can so remember that day I was told, it was CANCER!! As do we all, I rolled into a ball on my husbands lap and cried like a baby for 2 days and then set up took a shower and pulled myself together and got on the treatment train and I am going to hit this beat head on and know him off the of my train tracks.
You will do the same thing.
Your angel story game me goose bumps...God is very powerful, I am learning more so just how power full everyday.

You have come to the right  place, the senior members are so full of helpful information and posting new information ASAP.

My thoughts are prayer are with you,
Jen
Age 38,Dx 4/8/10 IDC stage I, No Nodes, GradeIII, Brac I&II NEG lumpectomy, 2 nodes removed(neg)finished 4 AC& T on 10/1/10 33 Rads finished 10/2/10. Married 19yrs, 1 son 11yrs & 1 daughter 9yrs
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Post Options Post Options   Thanks (0) Thanks(0)   Quote SagePatientAdvocates Quote  Post ReplyReply Direct Link To This Post Posted: Jul 31 2010 at 6:35am
Dear staceydooley,

you wrote-

"My Dr told me cancer does not hurt, but it seems TNBC does."

48 years ago a doctor told my mother...regarding her painful lump in her breast..."don't worry about it, cancer doesn't hurt." WRONG, she had cancer...but she walked around for one year, with her painful lump before she had surgery. Even the night before she was told "we will remove the lump but not to worry it is not cancerous, because cancer doesn't hurt." She woke up with her breast gone because they found cancer.

6 years ago two physicians told my 36 years old cancer "don't worry about your tender lump. Cancer doesn't hurt." WRONG, again. This time she walked around for 3 months waiting for her lump to "go away" as the physicians suggested. But instead it grew, remained tender, and a needle biopsy showed TNBC.

Yes, sometimes breast cancer (and other cancers) don't hurt...maybe even most of the time, but sometimes cancer does hurt. Isn't it about time that a required course is given (perhaps a one hour seminar) in med school about how cancer can hurt with videos of men and women saying "my cancer hurt" and at the end of the seminar there is one question "can cancer hurt some of the times?" and if the medical student answers "no" he is thrown out of school and if s/he answers "yes" there is a short essay requirement..please explain your answer so if that is left blank and the "yes" was just a lucky guess that student can't become a doctor either..Smile..but this topic is not funny, huh?

I am really disgusted to read that physicians keep repeating inaccurate information to their patients, at times putting the patients lives at risk...Surely the medical schools can do a better job!!!!

Stacey, sorry you were given misinformation. Good luck to you!!!!!

all the best,

Steve
I am a BRCA1+ grandson, son and father of women affected by breast/oc-my daughter inherited mutation from me, and at 36, was dx 2004 TNBC I am a volunteer patient advocate with SAGE Patient Advocates
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Jul 31 2010 at 1:03pm
The only good lump is one in a jar.
 
Unfortunately we have to take the reins and tell docs we want the lump out and tested.  Alot of women have posted here saying their lump hurt.  It's obvious this happens.  I too get disgusted at some of the advice women are given just like I was given wrong information when I was diagnosed.  It has to stop.
We are our best advocate!
Stage 2 2003
Stage 1 2007
BRCA 1+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote guygirl Quote  Post ReplyReply Direct Link To This Post Posted: Aug 02 2010 at 7:29am
Getting ready to leave for my first chemo.  My sister is going with me.  I am very emotional this morning and just want this to all be over with.  Thank you all for being here and sharing your knowledge and experiences.  Hugs to you all.
Age 50 DX: 6/3/10 IDC, Stg 1A Grd 3 1.9cm, KI-67 85%, lump. w/SNB, clear margins, lymph node 0/1, 4 cycles A/C (dose dense) every 2 wks, 4 cycles Taxol(dose dense) every 2 wks, 33 rads, BRCA 1/2 neg.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Carol (Tenn) Quote  Post ReplyReply Direct Link To This Post Posted: Aug 02 2010 at 11:11am
Good morning everyone...
Guy/Girl...I hope you had a good day...it's really a very doable thing and you will get through it just fine in spite of the emotions. I was excited to get started, I thought I'm finally going to get to DO something. So hang in there...we are here to support you through the whole process.
The disturbing part of this forum is the number of young women who have to deal with this. Women in their thirties and forties ought to be concerned with raising children and having a good time doing it, not fighting this awful disease.
But hey, here we are and we are strong....we are women, watch us roar...LOL..now I'm getting silly...
 
My prayers are with each and everyone of you. Young and not so young.
If you would like to join us on the Spiritual Support thread as well as all the other threads, we're just a clk away.
Love and Prayers,
Carol  Heart
St 2 Gr 3, A/C/T, DD
Radiation x35
Rec chest wall 07/09
Radiation x28
NED 10/24/11
NED 10/5/12
NED 03/15/13
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