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Old 02-12-2008, 06:50 AM   #1
HavahJ
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I'm really scared, can't stop crying

I'm so frantic about the liver mets and waiting to see if the chemo is working. I don't know how to figure out all the death stuff. I'm so alone. I had a single met for so long - I just didn't expect this. How do all of you stay so positive? Your religion thing? Anyway, I really need just pain support. Most people in my shape will be dead within a year, 2 at most. You people on the boards are the lucky ones. I guess I'm falling completely apart. HavahJ I don't know where or how to post it. I'm from Minnepolis, Minnesota and my email is HavahJ@aol.com.
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Old 02-12-2008, 07:14 AM   #2
suzan w
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Dear Havah,
I wish I could jet myself to your side and give you a great big hug and let you cry your heart out!!! Take a big breath and breathe.... this is all really scary stuff. I am also a recovering alcoholic and have incorporated into my life the "one day at a time" philosophy...and that is my 'religion'!!! You hang in there,,, hugs to you and a kiss from my little dog, Mel!!! xox
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Suzan W.
age 54 at diagnosis
5/05 suspicious mammogram-left breast
5/05 biopsy-invasive lobular carcinoma with LCIS,8mm tumor,stage 1 grade 2, ER+ PR+ Her2+++
6/14/05 bilateral mastectomy, node neg. all scans neg.
Oncotype DX-high risk
8/05-10/05 4 rounds A/C
10/05 -10/06 1 yr. herceptin
arimidex-5 years
2/14/08 started daily self administered injections..FORTEO for severe osteoporosis
7/28/09 BRCA 1 negative BRCA2 POSITIVE
8/17/09 prophylactic salpingo-oophorectomy
10/15/10 last FORTEOinjection
RECLAST infusion(ostoeporosis)
6/14/10 5 year cancerversary!
8/2010-18%increase in bone density!
no further treatments
Oncologist says, "Go do the Happy Dance"
I say,"What a long strange trip its been"
'One day at a time'
6-14-2015. 10 YEAR CANCERVERSARY!
7-16 to 9-16. Extensive (and expensive) dental work done to save teeth. Damage from osteoporosis and chemo and long term bisphosphonate use
6-14-16. 11 YEAR CANCERVERSARY!!
7-20-16 Prolia injection for severe osteoporosis
2 days later, massive hive outbreak. This led to an eventual dx of Chronic Ideopathic Urticaria, an auto-immune disease from HELL.
6-14-17 12 YEAR CANCERVERSARY!!
still suffering from CIU. 4 hospitilizations in the past year

as of today, 10-31-17 in remission from CIU and still, CANCER FREE!!!
6-14-18 13 YEAR CANCERVERSARY!! NED!!
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Old 02-12-2008, 07:29 AM   #3
MJo
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I don't think you need to figure out the death stuff yet. In fact, nobody has been able to figure out the death stuff. Are you alone like no husband and kids -- like me. That's rough. Even with a support system we feel alone, because nobody is going through this but us. It's okay to fall apart -- I did -- as long as you look for help to prop you up until you are back to yourself again. Posting on this board is getting help. Keep posting, posting and posting. If there is a Wellness Community in your city, try it. I walked in, fell into the arms of the receptionist and started howling. They could hear me all over the building. I also called the Cancer Care Connection helpline in my city almost every day for a while and talked, talked talked about how terrified I was and how I felt I was going crazy. This is my prayer for you -- that in a month or two you will look back on this time and think "Whoo, I was really breaking down, but now that my liver mets are shrinking, I feel hopeful again." Please ask for help -- demand it in fact. Take more anti anxiety medication, eat a gallon of ice cream. Whatever gets you thorugh this period of uncertainty, which is the absolute worst! ! Love and hope to you.
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IDC, Stage I, Grade 2
Oncotype DX Score 32
Her2++ E+P+, Node Neg.
Lumpectomy 11/04/05 Clear Margins
3 Dose dense AC (Couldn't tolerate 4)
4 Dose dense Taxol & Herc. (Tolerated well)
36 weeks Herceptin (Could not complete one year due to decrease in MUGA score)
2 years of Arimidex, then three years of Femara
Finished Femara May 2011
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Old 02-12-2008, 07:41 AM   #4
Mgarr
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(((Havah))) Sending you healing vibes, we're not counting on you going anywhere soon! With this disease, I think even negative thoughts creep into the most positive people and yes many tears but this is a great place to vent. You will move forward with good news about shrinking mets. Wishing you peace.

Mary
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Diagnosed 11/04 @39yrs. young
Stage IIB
2.5 cm, ER/PR- Her+++, grade 3
Partial Mast., 1/3 pos. node
1/05 full node dissection
4 A/C 4 Taxol DD, Herceptin 1 yr.
30X rads.
BRCA Negative
NED

Hope is the thing with feathers
That perches in the soul,
And sings the tune without the words,
And never stops at all -Emily Dickinson

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Old 02-12-2008, 08:07 AM   #5
ita
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Thinking of you. Although I am not in your shoes I wanted you to know that you WILL find love and support here. YOU are NOT alone.

Regards,
Gricel
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Old 02-12-2008, 08:19 AM   #6
Karen W
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Havahj,

Where do you live? Why don't you pm me and I can look into some resources for you in your area. In Northern California we have the Wellness Community... maybe there is something like that were you live. I know you are really scared and we, on this board want to help, so please pm me so I can help you.

Hugs,
karen
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Old 02-12-2008, 08:45 AM   #7
Audrey
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Havah, I'm sorry you're going through such a rough time right now, but please don't give up, many people survive years and years with liver mets--I met a woman at the CURE conference last year that was going on year seven with liver mets. She was trying a variety of treatments and taking milk thistle as a supplement. Sounds like you could really use a support group, I agree with the other posters that you might want to check out wellness centers in your area or support groups at your local hospital. When I was first diagnosed and the prognosis was "poor" I fell apart, too...planned my whole funeral, gave stuff away, walked around in a cloud of doom. One day I walked into our local wellness center and just poured my heart out and found so much comfort there. I also started taking really good care of myself--getting massages, etc. to relax and feel better. Finally, I know you're not a religious person, but I have to admit I did find a lot of peace and strength in believing that God was there with me for me to lean on & that we are never really alone. Finally, my doctor recommended an anti-depressant/anti-anxiety medication that really seemed to help me with my feelings of doom. (Paxil) Don't stop reaching out for help, I know you will find something that works for you.
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diagnosed July 2001, at age 36
large tumor, 11+ nodes
Stage IIIb, er/pr-, Her2+
treated with A/C, weekly Taxol
radiation, + year of Herceptin
on clinical trial. double mastectomy
followed by reconstruction
NED!!
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Old 02-12-2008, 08:59 AM   #8
SoCalGal
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Where do you live?

Maybe you live close to one of us. Right now - until you feel more steady - you need to be with someone most of the time. It's really hard to ask friends for what we truly need but most of our friends are happy to give it to us.

The panic at the realization that we might be dying is overwhelming and unmanageable. BUT BUT BUT those feelings will calm down. Everyone is dying. We are just painfully aware of our limited time and it's scary. I struggle against the fear every day of my life. I try different things on different days. Sometimes I am able to remain present and feel faith and hope in the power of healing. Sometimes I melt down like a small child filled with fear and wanting my mommy.

When I am at my worst I reach out to my friends or my guy - sometimes just needing to cry endless tears and have someone just be with me until the grief passes. That is really what we are going through - grief. Grief is a powerful emotion - it comes in giant waves often when we least expect it.

Havah - NO ONE knows what tomorrow holds for them.
My disease is not yet under control and it has been almost a year of stage 4. I too am greatly worried at times - what if - what if - what if? But I fight those fears everyday trying to focus on what IS. I feel fine. I look fine. The sun is shining. My children are healthy. I am surrounded by love and light. It's all a game of the mind. There are many wise words posted here. Print them out and tape them up. Remember you are not alone...

Please post where you live. A her2 friend may be near by.

Flori
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1996 cancer WTF?! 1.3 cm lumpectomy Er/Pr neg. Her2+ (20nodes NEGATIVE) did CMF + rads. NED.
2002 recurrence. Bilateral mastectomy w/TFL autologous recon. Then ACx2. Skin lymphatic rash. Taxotere w/Herceptin x4. Herceptin/Xeloda. Finally stops spreading.
2003 - Back to surgery, remove skin mets, and will have surgery one week later when pathology can confirm margins.
‘03 latisimus dorsi flap to remove skin mets. CLEAN MARGINS. Continue single agent Herceptin thru 4/04. NED.
‘04 '05 & 06 tiny recurrences - scar line. surgery to cut out. NED each time.
1/2006 Rads again, to scar line. NED.

3/07 Heartbreaking news - mets! lungs.sternum. Try Tykerb/Xeloda. Tykerb/Carbo/Gemzar. Switch Oncs.
12/07 Herceptin.Tykerb. Markers go stable.
2/8/08 gamma knife 13mm stupid brain met.
3/08 Herceptin/tykerb/avastin/zometa.
3/09 brain NED. Lungs STABLE.
4/09 attack sternum (10 daysPHOTONS.5 days ELECTRONS)
9/09 MARKERS normal!
3/10 PET/CT=manubrium intensely metabolically active but stable. NEDhead.
Wash out 5/10 for tdm1 but 6/10 CT STABLE, PET improving. Markers normal. Brain NED. Resume just Herceptin plus ZOMETA
Dec 2010 Brain NED, lungs/sternum stable. markers normal.
MAR 2011 stop Herceptin/allergy! Go back on Tykerb and switch to Xgeva.
May-Aug 2011 Tykerb Herceptin Xgeva.
Sept 2011 Tykerb, Herceptin, Zometa, Avastin.
April 2012 sketchy drug trial in NYC. 6 weeks later I’m NED!
OCT 2012 PET/CT shows a bunch of freakin’ progression. Back to LA and Herceptin.avastin.zometa.
12/20/12 add in PERJETA!
March 2013 – 5 YEARS POST continue HAPZ
APRIL 2013 - 6 yrs stage 4. "FAILED" PETscan on 4/2/13
May 2013: rePetted - improvement in lungs, left adrenal stable, right 6th rib inactive, (must be PERJETA avastin) sternum and L1 fruckin'worsen. Drop zometa. ADD Xgeva. Doc says get rads consultant for L1 and possible biopsy of L1. I say, no thanks, doc. Lets see what xgeva brings to the table first. It's summer.
June-August 2013HAPX Herceptin Avastin Perjeta xgeva.
Sept - now - on chemo hold for calming tummy we hope. Markers stable for 2 months.
Nov 2013 - Herceptin-Perjeta-Avastin-Xgeva (collageneous colitis, which explains tummy probs, added Entocort)
December '13 BRAIN MRI ned in da head.
Jan 2014: CONTINUING on HAPX…
FEB 2014 PetCT clinical “impression”: 1. newbie nodule - SUV 1.5 right apical nodule, mildly hypermetabolic “suggestive” of worsening neoplastic lesion. 2. moderate worsening of the sternum – SUV 5.6 from 3.8
3. increasing sclerosis & decreasing activity of L1 met “suggests” mild healing. (SUV 9.4 v 12.1 in May ‘13)
4. scattered lung nodules, up to 5mm in size = stable, no increased activity
5. other small scattered sclerotic lesions, one in right iliac and one in thoracic vertebral body similar in appearance to L1 without PET activity and not clearly pathologic
APRIL 2014 - 6 YRS POST GAMMA ZAP, 7 YRS MBC & 18 YEARS FROM ORIGINAL DX!
October 2014: hold avastin, continue HPX
Feb 2015 Cancer you lost. NEDHEAD 7 years post gamma zap miracle, 8 years ST4, +19 yrs original diagnosis.
Continue HPX. Adding back Avastin
Nov 2015 pet/ct is mixed result. L1 SUV is worse. Continue Herceptin/avastin/xgeva. Might revisit Perjeta for L1. Meantime going for rads consult for L1
December 2015 - brain stable. Continue Herceptin, Perjeta, Avastin and xgeva.
Jan 2016: 5 days, 20 grays, Rads to L1 and continue on HAPX. I’m trying to "save" TDM1 for next line. Hope the rads work to quiet L1. Sciatic pain extraordinaire :((
Markers drop post rads.
2/24/16 HAP plus X - markers are down
SCIATIC PAIN DEAL BREAKER.
3/23/16 Laminectomy w/coflex implant L4/5. NO MORE SCIATIC PAIN!!! Healing.
APRIL 2016 - 9 YRS MBC
July 2016 - continue HAP plus Xgeva.
DEC 2016 - PETCT: mets to sternum, lungs, L1 still about the same in size and PET activity. Markers not bad. Not making changes if I don't need to. Herceptin/Perjeta/Avastin/Xgeva
APRIL 2017 10 YEARS MBC
December 2017 - Progression - gonna switch it up
FEB 2018 - Kadcyla 3 cycles ---->progression :(
MAY30th - bronchoscopy, w/foundation1 - her2 enriched
Aug 27, 2018 - start clinical trial ZW25
JAN 2019 - ZW25 seems to be keeping me stable
APRIL 2019 - ONE DOZEN YEARS LIVING METASTATIC
MAY 2019 - progression back on herceptin add xeloda
JUNE 2019 - "6 mos average survival" LMD & CNS new single brain met - one zap during 5 days true beam SBRT to cord met
10/30/19 - stable brain and cord. progression lungs and bones. washing out. applying for ds8201a w nivolumab. hope they take me.
12/27/19 - begin ds8401a w nivolumab. after 2nd cycle nodes melt away. after 3rd cycle chest scan shows Improvement, brain MRI shows improvement, resolved areas & nothing new. switch to plain ENHERTU. after 4th cycle, PETscan shows mostly resolved or improved results. Markers near normal. I'm stunned but grateful.
10/26/20 - June 2021 Tucatinib/xeloda/herceptin - stable ish.
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Old 02-12-2008, 09:11 AM   #9
sarah
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Dear Havah,
BIG hug. Everything that the others have said is great advice. Don't give up. Cry and then go out and find a local support group as well as all of us on this site. I've met several amazing people in my life who had been given 2 months to live (brain caner, cancer everywhere, ALS) and guess what, 10 years down the line, they were still around. A best friend of ours has inflammatory cancer and is having serious treatment problems and we all though she would die first but her husband died suddenly in a freak accident, so it's the old, we could be hit by a bus tomorrow theory. we just don't know how long any of us have. Sso get back on the positive train and keep on fighting with the rest of us. However much time you have and I bet you have more than you think you have, you can still have a good life. Get that pain worked out - tell them to give you whatever you need for that. Also are you taking anti-depressants? that might help. Where in the world are you? You might just be near another member.
Big hugs and love
sarah
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Old 02-12-2008, 12:04 PM   #10
chrisy
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Who's positive?

Dear HavahJ,
You're wrong if you think "we all stay so positive". It is a daily, even moment by moment effort to keep that glimmer of hope alive and to focus on what IS (I am still living) in between worrying about the what if's (was that my last Christmas?). I can't even touch Flori's eloquence in expressing this, but I could sure relate to what she said.

You're not alone, although I sure understand why you feel that way. Even with support it is a lonely road. As for the unexpectedness I can relate: the diagnosis of extensive liver mets was completely unexpected following a pronounced "cure" of Stage 0 DCIS, then after 2 years of complete remission, I had dared to hope it would last forever - but it didn't. So now I'm working to get it under control again, hopefully for a long time. I still believe this is possible and for me, keeping that hope alive is important. In the meantime, guess what, I'm still alive and I choose not to spend ALL my time thinking about death. Because I'll sure feel stupid if I live another 20 years and waste every minute of it in fear and grief. Neither of us KNOWS how much time we have.

I agree with what others have said about seeking company of people who can relate, but if I were feeling as you do, I would also consider getting counseling from professionals who deal with this situation.

I really don't know what I can say to help how you feel, but I will share this. My husband and I were seeing the 2nd opinion doctor, reeling from the shock of the fresh diagnosis of extensive liver mets. He asked her "how can people live with facing this diagnosis" meaning, the horrific fear, grief, and everything else entailed. Her answer, in retrospect, was very wise. She said "you just do".

Your fears are valid, maybe you just need some help working through it.
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Chris in Scotts Valley
June 2002 extensive hi grade DCIS (pre-cancer-stage 0, clean sentinal node) Mastectomy/implant - no chemo, rads. "cured?"
9/2004 Diag: Stage IV extensive liver mets (!) ER/PR- Her2+++
10/04-3/05 Weekly Taxol/Carboplatin/Herceptin , complete response!
04/05 - 4/07 Herception every 3 wks, Continue NED
04/07 - recurrence to liver - 2 spots, starting tykerb/avastin trial
06/07 8/07 10/07 Scans show stable, continue on Tykerb/Avastin
01/08 Progression in liver
02/08 Begin (TDM1) trial
08/08 NED! It's Working! Continue on TDM1
02/09 Continue NED
02/10 Continue NED. 5/10 9/10 Scans NED 10/10 Scans NED
12/10 Scans not clear....4/11 Scans suggest progression 6/11 progression confirmed in liver
07/11 - 11/11 Herceptin/Xeloda -not working:(
12/11 Begin MM302 Phase I trial - bust:(
03/12 3rd times the charm? AKT trial

5/12 Scan shows reduction! 7/12 More reduction!!!!
8/12 Whoops...progression...trying for Perjeta/Herceptin (plus some more nasty chemo!)
9/12 Start Perjeta/Herceptin, chemo on hold due to infection/wound in leg, added on cycle 2 &3
11/12 Poops! progression in liver, Stop Perjeta/Taxo/Herc
11/12 Navelbine/Herce[ptin - try for a 3 cycles, no go.
2/13 Gemzar/Carbo/Herceptin - no go.
3/13 TACE procedure
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Old 02-12-2008, 12:22 PM   #11
Carolyns
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Havah,

I am sorry that you feel so alone. As the others have said, we all feel this way at times. I am a single parent with a 9-year old son so I must put on a happy face for him but I fall apart regularly. I have sought professional help when I need it. Please find out what resources your cancer center has for you. There is also medication...I use valium on rare occasions when I can not pull myself together. For me, it seems to pass. If I get to a point where these emotions don't pass I will go on antidepressants.

Best wishes, Carolyn
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Old 02-12-2008, 01:01 PM   #12
BonnieR
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Havah, I noticed that you posted at 5:50 am. I have found that it is, literally, "always darkest before the dawn". I have had most of my most dire thoughts in those early waking hours.
When I was first diagnosed I thought "well at least now I know what I am going to die from. Other people just don't know their destiny". But now I realize I don't even know THAT! I can get hit by a car tomorrow.
You have been given some really helpful suggestions here. Both practical and emotional. I hope that you no longer feel quite so alone and that you find comfort and support from some of the sources suggested.
Like Suzan, I am a recovering alcoholic and have found that our efforts to live "one day at a time" has been a real gift in this journey.
I know it is hard, but keep the faith.
Bonnie
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Bonnie

Post menopause
May 2007 Core biopsy, Rt breast
ER+, Pr-, HER2 +++, Grade 3
Ki-67: 90%
"suspicious area" left breast
Bilateral mastectomy, (NED on left) May 2007
Sentinel Node Neg
Stage 1, DCIS with microinvasion, 3 mm, mostly removed during the biopsy....
Femara (discontinued 7/07) Resumed 10/07
OncoType score 36 (July 07)
Began THC 7/26/07 (d/c taxol and carboplatin 10/07)
Began Herceptin alone 10/07
Finished Herceptin July /08
D/C Femara 4/10 (joint pain/trigger thumb!)
5/10 mistakenly dx with lung cancer. Middle rt lobe removed!
Aromasin started 5/10
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Old 02-12-2008, 02:38 PM   #13
tousled1
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Havah,

I feel the fear in your post. We are all afraid and it's perfectly normal to feel that way. I thought I had this dreadful disease beat and WHAM - mets to the lungs and brain! It's difficult to keep a positive attitude and stay strong but somehow we manage to put on a happy face and carry on. I wish I could just reach out to you and give you a big hug and let you have a good cry on my shoulder. I know what keeps me going and that's my one and only grandson. I look at him everyday and tell myself keep fighting. Perhaps an in person support group or even professional counselling would help you. Ask you oncologoist office if they have someone on staff that can help you deal with your fears. I know my oncologist has a physcologist on staff and I'm free to make an appointment with him at any time. I will keep you in my prayers.
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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 02-12-2008, 09:35 PM   #14
Joanne S
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My heart goes out to you Havah. It's horrible to feel so down, alone and scared and helpless with this disease. You sound so down, there is only one way to go and that's up. I glad you recognize this and are looking for support. Take it one step at a time. Many of us have felt just like you. Here's a big virtual hug!

May it comfort you to know that we understand and we care!

You are in my thoughts and prayers!
Joanne
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Old 02-12-2008, 10:03 PM   #15
Bev
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Havah, you've been around here for such a virtual long time. We all know the feeling. You have a tough road to hoe and it's OK to feel crappy about it.

Religion thing helps some, but it's not a get out of jail pass.

For me it's a you can't change what's happening but you can do everything you can to fight it. At least you go down fighting.

As others have said though, they're are people here that keep fighting with different treatments. "Someone" promised Cancer control by 2010. You can do it.

Keep us posted. Do reach out if there's a local Her2 gal, otherwise, it's your duty to contact your local cancer center. You're in our thoughts and prayers. Bev
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Old 02-12-2008, 09:39 PM   #16
Sherryg683
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You are not alone. My prognosis from the start was not good, stage IV also. Yet, here I am 2 year later NED and praying to stay that way, fearing that the cancer is waiting for me to get comfortable so that it can rear it's ugly head again. Fear of death, yes, I know that feeling too. It paralizes me sometimes. I have had such panic attacks that I could not hardly breath. We are not all brave, we are human and no one wants to die. I don't let anyone see what I go through in private, it's a battle I feel that I pretty much fight alone. My faith in God does help, but even that is a big unknown. I cannot be certain what awaits behind that curtain and I'm not ready yet to find out. Having a young child just adds to my desperateness to stay alive for her. I don't know how we get through these rough times...we just do. We have no other choice. I remember those days when I was on chemo and the not knowing whether it was working or not like it was yesterday, I call it the "black hole". I honestly felt like I had been swallowed by it with no signs of light. I am watching my brother go through what will probably be his last days. There has been nothing that has worked for his melanoma. I want to tell him something that will make him feel better, but I can't think of anything. All I can say is that hopefully there's a better place for us to go when this life ends, there must be. I'm sorry I don't know how to make you feel any better, it's hell that you are going through right now. I do hope that you have a good response to your chemo and that it puts the cancer back in check. In the end, that's pretty much all that we have ..our hope and our faith...never ever let go of that. On the medical side of things, are you on any sort of anxiety medicine. I know it's not the answer you want but it did help me get through many days I thought I would not make it through. I still rely on ambien to sleep, I couldn't get a wink without it. Please know that the women on this board do know what you are going through, it's the one thing we have in common that we would rather not have. ...sherryg
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Sherry

Diagnosed: December , 2005 at age 44
13+ positive lymph nodes
Stage IV , Her2+, 2 small mets to lungsChemo Started: Jan, 2006
4 months Taxotere, Xeloda, Hercepin
NED since April 2006!!
36 Rads to follow with weekly Herceptin indefinately
8 years NED now
Scans every year

Life is not about avoiding the thunderstorms, it's about learning to dance in the rain!
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Old 02-13-2008, 12:51 PM   #17
lilyecuadorian
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Smile

Havah ...I find this on a airplane magazine : " courage" sometimes is a little voice in the end of the day saying ...." I will try again tomorrow " and put it everything in the Lord hands ...that is my philosophy
__________________
Lily
Diag April/06 5 months after give birth my son Max
stage IV mets on liver (5 tumors) 38 year old,
her2+++ and ER+PR+ from32 nodes 4 positives
mastectomy right breast chemo before surgery herceptin/carboplatin/taxotere ,clear and surgery have radiation 20, `& then herceptin and tamoxifen
NED until Aug/07 body only then 'n June 04-06-07 .1 lesion of 1.6 cm on cerebellum ...novalis ,open sugery
5m.m brain met again novalis, 4mm.In the liver. Waiting 2 months now 3 tumors enroll on T-MCC trial start first infusion Nov 5/07 at Dec 17 scan show one tumor despair the 2nd and 3th diminish Doc said great results until March/08 ct scan show progression
03-05-08 start tykerb & xeloda
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Old 02-13-2008, 03:45 PM   #18
Andrea Barnett Budin
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Location: LAND OF YES! w/home in Boca Raton, Florida Orig from L.I., N.Y. Ever hovering IN THE NOW...
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I remember thinking I was dying. That my extinction was imminent. That my breast cancer had metastasized and spread throughout my liver in too many places to count. Tumors everywhere. What I had was inoperable and incurable and I would be on longterm chemotherapy for the rest of my life. What could be worse? Nothing. I sobbed, wailed and wept, grieving over my demise, the end of me.

I had rallied from my original diagnosis, mastectomy and reconstructive surgery (which was far more major than I had anticipated). I'd come back to life after eight months of chemotherapy (which left me weak and weary, shuffling my feet and I slowly managed to walk, feeling like I had the worst flu ever, every single day, feeling woozy and about to pass out often, feeling whipped and wiped out, and losing thirty three pounds, having no appetite). How could I do it again? Fourth stage (out of four) with little chance of recovery. I was doomed.

Friends called and offered me names of top liver surgeons in Manhattan, trying to help as best they could. I called. The first receptionist told me that doctor only dealt with colon cancer into the liver. Okay, not for me. Wow! They have doctors with such specific specialties? I was aghast. The next receptionist told me -- YOU HAVE BREAST CANCER INTO THE LIVER. YOU DO NOT HAVE LIVER CANCER! YOU DON'T WANT LIVER CANCER. IT IS BETTER TO HAVE WHAT YOU HAVE. YOU HAVE BREAST CANCER. INTO THE LIVER.

Okay then. I was reminded that -- it can always be worse. I had thought I now had liver cancer. I wasn't informed enough to even understand my diagnosis. I quickly rectified that. And -- I began tossing the bad statistics aside and focusing on books that empowered me. I have a list if you're interested.

I began to dwell in possibilities anyway, consciously choosing to ignore the realities of my condition. I sensed that I could be defeated if I concentrated on what happened to most people. I wanted to be in the little group that survived. I had to start thinking outside the box.

In our darkest hours, we can choose to become bitter and defeated. Or, we also have the ability to choose to become more than we were yesterday. To dig deep within ourselves and come up with some radical new realities we weren't previously aware of. We can awaken to miraculous vistas. And sacred summonings. I am not a religious person, but I have become spiritually enlivened.

I began to use the power of my thoughts to call my desired destiny to me. I believed what I read repeatedly. The energy of our thoughts goes out from us on frequency waves of varying vibrations. Positive thinking travels on higher, faster vibes. While negativity emanating from us leaves us on lower, slower waves. AND THE UNIVERSE BOTH SENSES THE ENERGY WE EMIT -- AND RESPONDS -- IN KIND. So, we have the power to draw positive manifestations of our thoughts to us. OR, we can unwittingly magnetize negative realities to become our own. WE ARE EACH PERSONALLY EMPOWERED.

KNOWING that I had the power to free myself from being caught in an unpredictable abyss of misery was exquisitely electrifying! My crisis became transformed as did I. Life, for everyone, is a bout with persistent unknowns. I was not as unique as I thought in this regard. So, I explored the possibilities, choosing one road over the other, using my power of choice given to me as my birthright. I began to script my thoughts, arduous though that is. Not only did I realize I was informing the Universe of my clear Intentions and passionate Expectations, but commanding my body to respond as *I* directed.

Yes, staying alive requires constant attention for some of us, but it can be an exhilarating venture as we confront the riddles of Being, I "perpetually imagine sublimities beyond reason" as author Eric Wilson expresses it so well in Against Happiness. I AWAKENED TO THE IDEA THAT WHAT WE THINK DETERMINES HOW WE FEEL AND HOW WE FARE. And, that we have the capability to rewrite our tormenting thoughts, for our benefit. I chose not to be taunted and tortured by my fearsome, uncertain, fragile, insecure thoughts of gloom.

This is what I wish all of us to discover on our own. To personally empower each and every one of us! Sending healing, loving energy...
Andi
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Andi BB
'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 02-12-2008, 11:01 PM   #19
hutchibk
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Hi all - does anyone know a good counselor or especially dynamic support situation in the Minneapolis area for cancer patients in distress?? Please post and/or PM me if you do. I am doing some research.
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Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
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Old 02-12-2008, 11:18 PM   #20
Jean
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Havah,

Give your treatments time to kick in and do their job. As the others have posted who have had liver mets "it can be done" and you can achieve NED also! Of course you are scared, each and every one of us on this site has the same fear no matter what stage.
But that fear cannot be allowed to force us to give up or give in. As Becky said so well, you have work to do and your job is to
work hard to get back to NED.

We are all here to support you and everyone has given you
great advice, but maybe contact with a professional would give you much needed comfort, please consider reaching out to a nearby professional. You do not have to be alone.

Please update us on your treatments.
Kind Regards,
Jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006

Last edited by Jean; 02-12-2008 at 11:29 PM..
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