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Old 02-01-2007, 01:03 PM   #1
kat in the delta
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Location: MS Delta in Clarksdale="Home of the Blues" (near Memphis,TN)by Misssissippi River/levee's highest pt.
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Thumbs down kat in the Delta

How do or did you feel after all treatments?? My 3 grown sons and husband think I should be back to normal, but I am not....chemobrain has taken its toll on my life...I am so much slower getting ready to go anywhere. My orginizational skills flew out the window...and my house is a wreck .....As a result, I get looked upon with scowling faces and frowns and the 3rd degree!! My family of men tell me NOT to talk about "anything" related to cancer-How can they understand me??.... I feel alone, but is there anyone else like me ?, If so, How do you deal with this????????? kat in the delta
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Old 02-01-2007, 09:23 PM   #2
rinaina
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Your men in your family are not being fair to you. Perhaps some sensitivity training classes are in order for them! No seriously, someone other than you, someone they view as credible, needs to talk to them about breast cancer, chemo and post chemo. There is nothing wrong with you. All you are experiencing is valid and normal and part of the territory with cancer and chemo.
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~Rina~
Dx:3/06 had a lumpectomy April 19, 2006
Her2+ er/pr- Stage I Grade 3 tumor size 1.4 cm, node negative
AC 4 dense doses
34 radiation treatments including booster doses
receiving herceptin every 3 weeks since late August 2006 for 12 months
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Old 02-01-2007, 09:57 PM   #3
Sandy H
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I hear you!!!!

They just don't understand. Its normal what you are going through. I have the same problems. It does get frustrating and I feel at times what you feel. An example for me was just the past four days. I am in Florida and we just spent 4 days in Mississippi. Drove into New Orleans to see some of the hurricane damage. Well, I could not read the map and keep up with my husband driving-I was so slow at finding the streets. The map we had, was small, the streets were in fine print so had to use a magnifying glass because of vision problems from chemo. Many streets were one way and so we rode around the city three hours trying to get to the bus where my husband wanted to take the disaster tour. Guess what we missed the tour and so I felt bad because it was my fault I couldn't read the map, look at the signs, and tell him when to turn. He was very upset, hallowing at me saying all I had to do was read the map and tell him to turn right, left or go straight. I just could not do it. After it was all behind us and we were waiting to take the city tour he showed me the map and said its this easy this is what you do. He said I don't listen. How do you tell them, you listen, you hear, but you you don't comprehend it? So if anyone asks us how our trip was to New Orleans I will simply say it would have been better if the driver could have read the map and drove. Don't feel its your fault that is what I have to keep telling myself its not my fault my brain is chemical killed!! Cancer isn't the only issue here there are lots of others. I am sure you will hear from others. Don't get me wrong my hubby is a wonderful person and would do anything for me but for him to understand some of the things we go through when he is under stress, such as driving in lots of traffic, with one way streets coming at him, and meeting a time line really upsets him. Sending you a big hug, that is why we are here on this board. Right?? Sandy
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Dx. 03/01, Rt. IBC
AC/Taxatere
Rt. MRM-with graft Lt. simple
5 rads-skin mets
Herceptin, taxol, carboplatin (taxol seem to be the magic drug)
Navelbine & xeloda (did not work)
topical miltex for skin mets
Tykerb/xeloda
thoracentesis x 2 left lung fluid shows cancer cells
Port removal (4 years) with power port replacement
Doxil
Updated 05-07 Scans show no bone or organ involvement we shall see!




I shall not pass this way again. Any good I can do or any kindness that I can show let me not defer or neglect it for I shall not pass this way again.
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Old 02-01-2007, 11:28 PM   #4
StephN
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Thumbs up Get him a GPS!

Dear Sandy -
Nothing more frustrating than trying to be the "navigator" when you feel handicapped and the place is just as strange to you as it is to your other half.
It is always MY job to read maps - we got into that habit long ago when I was younger, had better eyes and a quicker mind.

Just get your hubby a Global Positioning device. They are great. You program in where you want to go and it tells you exactly where to turn. That way you only need to look for the signs or signals. A couple of my friends have them and they are named with female names and always referred to as "she"!

It will save you both a LOT of grief in the future when you go exploring.

KAT - Your men miss the "old" you, and it is hard to accept the "new" you. I just kept telling my family, there is no turning back and we all have to make some adjustments. When I need help in the house I hire someone in to take away the stress and get things done. Once you can "see daylight" it gets easier to manage.
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"When I hear music, I fear no danger. I am invulnerable. I see no foe. I am related to the earliest times, and to the latest." H.D. Thoreau
Live in the moment.

MY STORY SO FAR ~~~~
Found suspicious lump 9/2000
Lumpectomy, then node dissection and port placement
Stage IIB, 8 pos nodes of 18, Grade 3, ER & PR -
Adriamycin 12 weekly, taxotere 4 rounds
36 rads - very little burning
3 mos after rads liver full of tumors, Stage IV Jan 2002, one spot on sternum
Weekly Taxol, Navelbine, Herceptin for 27 rounds to NED!
2003 & 2004 no active disease - 3 weekly Herceptin + Zometa
Jan 2005 two mets to brain - Gamma Knife on Jan 18
All clear until treated cerebellum spot showing activity on Jan 2006 brain MRI & brain PET
Brain surgery on Feb 9, 2006 - no cancer, 100% radiation necrosis - tumor was still dying
Continue as NED while on Herceptin & quarterly Zometa
Fall-2006 - off Zometa - watching one small brain spot (scar?)
2007 - spot/scar in brain stable - finished anticoagulation therapy for clot along my port-a-catheter - 3 angioplasties to unblock vena cava
2008 - Brain and body still NED! Port removed and scans in Dec.
Dec 2008 - stop Herceptin - Vaccine Trial at U of W begun in Oct. of 2011
STILL NED everywhere in Feb 2014 - on wing & prayer
7/14 - Started twice yearly Zometa for my bones
Jan. 2015 checkup still shows NED
2015 Neuropathy in feet - otherwise all OK - still NED.
Same news for 2016 and all of 2017.
Nov of 2017 - had small skin cancer removed from my face. Will have Zometa end of Jan. 2018.
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Old 02-02-2007, 10:20 AM   #5
KathyH
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sorry

Hi Kat

I have 3 young sons and a grown husband. He is tremendously supportive. I can, however, completely relate to your difficulty in facing the expectations of other people. They want me to be a person that no longer exists. That is not a bad thing, in many ways it is a good thing, but it is a fact. We don't live very far from each other. If you would like to e-mail me, I would love to chat or maybe even have lunch if that is a possibility.

Blessings, Kathy H
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Old 02-02-2007, 10:48 AM   #6
mslinda
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Hi Kat:

I can associate with you. I am two years out from treatment, and the more I read about chemo brain, I think that is me. I am no longer organized, and it takes me forever to get anything done. Unless I write it down immediately, I won't remember it. I feel like I am in a fog all the time. I have a really great husband, but he is tired of hearing about bc. So I usually keep it to myself. I don't know what to tell you, but hopefully this group is a big help. I know it is for me.

Best of luck from Linda in Lumberton, MS.
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Diagnosed 12/23/04
Biopsy 12/28/04
Lumpectomy 1/04/05
IDC, ER-PR-, HER2Neu+++
7mm tumor, Stage 1, Grade 3
6 CAF's
38 Rads
Finished 10/05

"Worry looks around. Sorry looks back. Faith looks up."
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Old 02-02-2007, 11:15 AM   #7
tousled1
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I'm with the rest of you on this one. I really have a problem remembering things. My 2 daughters get so frustrated with me because they will tell me something and before you know I'm asking the same question again. They yell at me and say I've already told you that. Also I have trouble remembering if I called people. I've learned that keeping lists is helpful. I'm hoping that this stuff going on in my brain will ease up because I used to be the most organized person. Now I feel like a scatter brain. You are not alone. I think what happens is that once you start to look more like your old self people around you think that everything is back to normal. Little do they know!
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Kate
Stage IIIC Diagnosed Oct 25, 2005 (age 58)
ER/PR-, HER2+++, grade 3, Ploidy/DNA index: Aneuploid/1.61, S-phase: 24.2%
Neoadjunct chemo: 4 A/C; 4 Taxatore
Bilateral mastectomy June 8, 2006
14 of 26 nodes positive
Herceptin June 22, 2006 - April 20, 2007
Radiation (X35) July 24-September 11, 2006
BRCA1/BRCA2 negative
Stage IV lung mets July 13, 2007 - TCH
Single brain met - August 6, 2007 -CyberKnife
Oct 2007 - clear brain MRI and lung mets shrinking.
March 2008 lung met progression, brain still clear - begin Tykerb/Xeloda/Ixempra
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Old 02-02-2007, 12:06 PM   #8
KellyA
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Hi Kat,

I can completely relate to how you feel. I am the only woman in a house of five myself (we have three boys), and I was outnumbered and "misunderstood" before cancer, let alone now. My hubby has been my hero through all of this and my boys all pitched in to help, but I have noticed that since treatment is over, and now that I am looking a little more like myself, that they think everything is back to normal. Even my co-worker, who is like a sister to me is frustrated with the new me. I was always very quick and on top of things, and the one who kept everything in order and now I am like a senile, confused, aching, slow little old lady. She keeps saying, "what's wrong with you Kelly....."
Geeeee... I WONDER...... maybe it was the six months of getting poisoned, or the two months of frying......or the fact that I have been completely traumatized.....

While we are venting :-) , let me add one more thing. You know that annoying reference to "must be that time of the month" every time a woman is crying or angry? Well now that that doesn't apply anymore (chemopause- I don't dare let them know THAT word exists!), now its "Honey, have you been taking your Lexapro???" Can you believe it?! Men are pathetic. Sorry, I just had to vent.

Love, Kelly
__________________
dx'd 05/06, 37 years old
er/pr-, Her2+, grade 3
double mastectomy, immediate reconstruction- implants
Stage 2b, 2 tumors- 2.2 cm and 0.6 cm, 3/5 + nodes
all scans clear
genetic testing- negative
06/06 began dd A/C x 4, 12 weekly Taxols w/ Herceptin
30 rads
Herceptin weekly x 1 year
Herceptin completed 08/07
Port removed 12/26/07 MERRY CHRISTMAS!!!!!!
05/17/08 Two year anniversary NED

"We gain strength, courage, and confidence by each experience in which we really stop to look fear in the face... you must do the thing that you think you cannot do."

-Eleanor Roosevelt

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Old 02-02-2007, 12:30 PM   #9
Adriana Mangus
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Cool I hear you Kate..

Same situation here...My husband comes home after work and takes a nap, I came home after working six hours, rest a little (no nap), then dinner time. He does not like to eat out a lot, but we have been going out to dinner a lot, because I have no energy and my body aches; in addition to chemo (xeloda) I suffer from fibromyalgia. He wants everything to look "normal" and appear like nothing is going on.. But it does not change the fact that yes , am on chemo, I have mets bc, and my pain is real. Kate, you did the right thing by sharing your feelings with us; anytime you feel misunderstood by the men in your house, just write a line, we'll help you anytime. Note: I do like Stephanie's idea about the GPS. I think I will buy one for both, my husband and I this Valentine's Day. Also housekeeping help is great, do not negotiate! Stay strong.
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1994 - rt brst, .lump, underarm node dissection,chemo+rad 1.2 cms, Grade 3.
28 nodes neg
Er,Pr, Positive HER2 status unknown
2003- Recur to rt lung.July 16 ( B-Day!)
Her2+++ Er,Pr, Negative
2003 - Aug04--Navelbine + Herceptin
2004- 2007--
NED - Herceptin, only
2007 Feb-April Xeloda added to hereceptin
2007-May Back on Navelbine+Herceptin
2008-Feb-Mar 15 Ses Rad to Rt. Lung
2008- Oc 17 Add Tykerb to Herceptin
2009- June-- Discont Tykerb
2009 July 7--Current Taxol + Herceptin
2009 Dec--Discontinued treatment due to progression. Looking into cyberknife.
2010-Aug Accepted to TDM1, no SE, except liver count went up.
2010-2011 September got kicked out of the trial, due to a small spot found on lung.
2011- 2012 September thru early 2013 on Herceptin
2013- March Bone density shows small spot on 5th rib.
2013 - April 4th appt with onc. will post after discussing course of treatment.
2013-March-April Cyber knife to brain and radiation to rib. Chest --base line before chemo-CT-Scan stable for lung issue. CA2729 Normal.
2013 April Herceptin- TDMI
2013 Sept Herceptin + Perjeta . CA2729 within normal range. Brain and Pet scans October 31st. will post results.
2013 October Brain MRI- mixed response. Will see Onc/rad on Halloween.
2013 October/November Brain-MRI nothing new. Repeat MRI next year in May.

2013 December Continue Herceptin and Perjeta. Stable at the moment.
2014 February Brain MRI -clear!
2014 January Added Taxotere to Perjeta+Herceptin.
2014 March Stopped chemo-chest ct-scan next.

2014- March Scans shows tumor's larger, CA2729 higher. Discontinue Herceptin.
2014 April Perjeta+ Halaven
2014 April CA2729 went down 60 points after one cycle. Cough does not want to go away.
2014 June Continue on Perjeta + Halaven-- no more cough. Stable
2014 June Back on Herceptin + abraxane
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Old 02-02-2007, 03:54 PM   #10
Donna
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Me too

Hello all,

There was a time when I thought the worst thing I would have to deal with in life was the disorganization that my ADD caused. hahahahaha! So, I didn't have those "stay on task, organization" skills to begin with - and now it's not much different. It has actually given me relief because my two guys, husband and son, expect chemobrain and point out to me all the time that I have a reason to be so forgetful and disorganized after all I have been through. Frankly, nothing has changed with my habits, just their idea of why it happens has changed and now suddenly it's expected and okay

I have hired a professional organizer, she comes twice a week and we now have a home that can be visited. The first week of my diagnosis I panicked that people wanted to visit me and I hired her and it's the most wonderful thing!

Pamper yourself, don't listen to the guys - get a housekeeper, an organizer or whatever it takes to get yourself comfortable. There is no way for them to understand what you are going through without experiencing it themselves so you just have to look to yourself for the understanding - treat yourself as if you were your own best friend and do what you would advise a close friend.

Have a great day!

Donna
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Old 02-02-2007, 07:49 PM   #11
Sandy H
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Steph, great idea!

As always Steph, you are right on top of things! I think my husband has a GPS and its home. I will ask him if he does and suggest he start using it. Now, he has a cell phone and most of the time its on the counter, or in the truck and so we are hunting for each other in the stores!! I did not mention he also has chemo brain and its from anti depressants and not chemo drugs but the same thing. He admits to that so he should understand my frustration right?? That is why one of us is from venius and the other from mars. Now, don't ask me which one is which. Life can be complicated. hugs, Sandy
__________________
Dx. 03/01, Rt. IBC
AC/Taxatere
Rt. MRM-with graft Lt. simple
5 rads-skin mets
Herceptin, taxol, carboplatin (taxol seem to be the magic drug)
Navelbine & xeloda (did not work)
topical miltex for skin mets
Tykerb/xeloda
thoracentesis x 2 left lung fluid shows cancer cells
Port removal (4 years) with power port replacement
Doxil
Updated 05-07 Scans show no bone or organ involvement we shall see!




I shall not pass this way again. Any good I can do or any kindness that I can show let me not defer or neglect it for I shall not pass this way again.
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Old 02-02-2007, 08:16 PM   #12
Bev
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Hey Kat, I'm too lazy to look it up, but there was a study that showed brain damage from chemo. The good news was the damage healed up after 3 years. There's hope. BB
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Old 02-02-2007, 08:42 PM   #13
Soccermom
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DITTO,DITTO,DITTO! Take my advice I'm not using it...in fact I can no longer remember what it was!
I actually accused my family of "Gaslighting " me...remember the old movie where the husband tries to make the wife think she is crazy??
I get hollered at ALOT and it ST*NKS! I get so stressed out I get sick to my stomache.THEY just don't get it...but WE do!

Thanks for the chance to vent!
Marcia in Mississippi
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Old 02-02-2007, 09:51 PM   #14
Catherine
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Cool Chemopause

Kelly, Chemopause is the best new word I have heard. Hats off to everyone for venting and venting with a little humor. I also, like don't negotiate. I too have a housecleaner. While I was going thru chemo she came once a week. Now I am back to twice a month. In general I have it very good. But when I can tell my husband is uptight and wants me to be normal, I try to disappear into a back bedroom or to the computer room and the Her2 site. Especially in the evening. Then I find him asleep on the couch and I have the house to myself. I keep reminding myself of all the support he has given me. People I used to work with keep saying "now that you are done with treatment....I guess your life is back to normal." Yeah right.

I always wonder who raises some of these insensitive men. I wonder what a chat room for men with prostate cancer reads like. Maybe I will try and invade one.

Keep the faith and keep the humor and keep up the fight,
Catherine in Oregon
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Catherine


Found my own lump in the shower
April 2006 at the age of 58
Stage IIB, ER- PR- HER2+++ multi focal tumors, largest 2.3cm
Chemo first: AC/Taxol over 16 weeks
Bilateral mastectomy Sep 06
33 rads after the surgery
1 year of Herceptin completed Dec 07
15 years and no recurrence as of April 2021
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