Starting chemo Dec 2007
Comments
-
Same here,was hoping she'd post a bit this weekend?
Hope she's found something to occupy her mind and time and just is having fun
No scans here at all other than the bone density which I had my pcp do when I started on arimidex, b/c the onco never did. new onco now, so that hopefully will not be a problem to redo it this april.
-
Hello my Friends,
Thank you so much for your caring concern! Im feeling better, less anxious and much more capable of dealing with whatever I have to deal with. Ive had a really nice weekend.... Friends took me out for a belated b day dinner then dh and I went shopping on Saturday and bought a monster snow blower for the business and a new (almost new) car for me. Lol its the first time in my life that Ive picked out and bought a car for just me...... All the trucks dont count
they are nice, but they are all work trucks. So I insured it today and will be scooting around town tomorrow just for fun after work in MY first car.
I'm supposed to alternate from MRI to Mammogram every 6 months but this mammo is almost 4 months from all the last tests (MRI, Mammo & Ultrasound) but whatever, Hopefully the results will be normal and I'll carry on. I really am ok, I had a low moment and came back from it as it does noone good. Im a pretty tough cookie and crumble just a bit once in a while. Thanks for all the love and support, Love and Hugs Suz
-
Sounds like that car lifted those spirits well!
Enjoy it and dear, we're here, whether you need us to rejoice in a clear report or for support if its a concern. You know that,but still keeping you in good thoughts and close to the heart with a prayer.
So? What type of car did you get? I have to live vicariously through others. Mine is a 1990 and no sense for a future newer one till it's 20 years old
LOL
-
Hello ladies,
It has been a very long time, I have been extremely busy with working day and night
and life in general (when I can squeeze it in, lol).
Suz, big hugs to you, I am sorry you are in this waiting mode with these issues. It is SO unnerving......I hope and pray everything will turn out to be nothing to worry about! You mentioned a belated b day dinner - did you have your b-day? If so, HAPPY BIRTHDAY to you!!!! Enjoy the new wheels!
I'm sorry I can't be around much these days, I hardly ever even look at facebook too....I am just TOO busy.
Hugs to all
Laura
geez I really MUST change that photo - I actually do have hair now, lol! When I have time.....
-
Please know we wish you well, even if we are low on your priority list LOL...J/K of course!
Hope all is going well and things settle enough to catch with us on occasion. All the best till then1 looking forward to seeing an avatar on you too! Do you like your new do?
-
Thanks my dears, Yes the car was a moment to remember as my whole life has been purchasing vehicles (trucks/equipment) for the business. Ive never bought something for me. It was odd as I had no input from anyone, it was all about me and I think that was a first EVER. Lol I love the car and it was a very good distraction from "stuff" you all know what I mean. I have a few more weeks till I get the results, but am not worried...... why worry right. It will be what it will be. I love you all and Laura I would be really happy to see the new you in your pic. Geeze I bet you have a beautiful crop of hair by now. So will wait for your updated avitar.... It really sucks that your too busy for anything, but your living life and really it doesnt get any better than that right! Sooo Love and Hugs to Everyone.... I couldnt have done it without you all, Suz
-
And us without you Suz
We'll be waiting along with you for those results, so let us know and keep us up on it, k? Enjoy that new car .....mine better be good this weekend....long trip to a wedding and time withfamily and sooooooooo looking forward to it
-
Hey dear Suz--
I'm so sorry I haven't been keeping up here so I could chime in with lots of hugs and encouragement. I think you need to INSIST that somebody tell you what they are seeing. At my breast center, because I am a bc survivor, they read it right there--even the techinician is very open, showing me what they are looking at, why they need more or a close-up, etc. It was a little unnerving when they found a couple of micro-calcs that first time, but I would SOOO much rather know what's going on than to wonder. You have a complete right to know what's going on in your own body!!! "Not wanting to scare you" is absurd--what bc survivor isn't scared the second she steps in the door!?
Anyway--I'll be thinking of you, and please let us know how it goes.
Hi to everybody--loving your 25 random things
!! (I did one, but I don't think I tagged ya's--feel free to read!)
cheers -- A
-
Sorry I've been absent too. Sorry I haven't been supportive, Suz. I'm thinking positive thoughts for you... hope you get some definite answers today!!
Luv, Sal
-
I don't know why, but its in my head you will get the results today, Suz? If so, best wishes and prayes for that B9 report on that. Please let us know how you are doing. Been gone a while but still thinking about you and keeping up a prayer dear lady!
-
OK... Rough day, no really rough few weeks. I had my Oncologist appointment before the ultrasound. So I arrived way too early and then sat in her office for what seemed like forever.... when she walked in all chipper with "so how are you" I broke down in tears...I mean really broke down! She was really sweet but didnt understand what was wrong. When I finally composed myself and told her that my gut was wound up like a spring as Ive heard nothing from anyone, and noone was willing to inform me of anything..... so of couse I thought the worse. She was horrified and just gave me the biggest hug and said she would be right back. She came back with all the paperwork and results from all the tests so far and the reasons for retesting and went over every single detail before doing my check up.
Basically they were looking into a really small 2mm mass on my good side that they thought was a cyst, but wanted to make sure.... hence the ultrasound. She was horrified that no one had talked to me at that point and said it wouldnt happen again..... The ultrasound tech was also very informative (she was not supposed to be) and also said it looked like a cyst, but was not supposed to say anything to me.
So Im very relieved, but think it was so wrong for them to put me through this hell for no reason....
Sorry for the vent, but thanks for the ear and support my friends, I couldnt say this even at home....you know what I mean. So Im gonna say thumbs up, Im good... besides being really really stressed out. I dont have to go back till August, so I need to get back into that real people mode (not the cancer one) Love and hugs and thanks so much for being there....Suz
-
SUZ!!!!!!!!!!!!!!!!! I am so releived to read your posts, and feel horrible thinking about how you felt while waiting for results....Lord knows we all know how much the waiting game sucks! Drive on my fellow BC warrior!
Dec 207 friends,sending love and cyber hugs to all of you wonderful ladies.........I check your posts often, and feel so connected when I read them.
Had yet another bump in the road....surgery to remove some necrotic tissue in my belly as a result of my hysterectomy in Nov 08, which also triggered appendicitis! All done laproscopically, so piece of cake recovery, thank goodness.I am running out of body parts to lop out!
Praying for our continued health in 2009 and beyond! Bring on SPRING !!! xoxox cindy
-
I already cheered for you on FB but doing it again here hip hip hoooorayyyy!!
Breathe my friend breathe!
-
Suz,
So relieved to hear things turned out ok in the end. I'm glad they explained everything to you (finally!). Hopefully this will make someone think twice next time they keep information from someone... like you said before, it's info about your body, why shouldn't you hear it. Anyway, so very glad it turned out ok for you, buddy.
Cindy,
Sorry to hear about your problem. You sound like you plowed ahead and took care of it, in typical Strong Cindy fashion. Am laughing at your comment about running out of body parts to lop off:-) Glad you're doing well.
Hugs to you all,
Sal
-
Just sayin' howdy. Hope everyone is doing well:-)
-
Just saying hi
-
Hi to everyone from me too. I know some of us keep up with each other via FB but there are others who we don't. Hope everyone is doing well and moving forward.
-
OK my first post here in ages. Im just trying to find a place to be comfortable to talk again on this board. So far Ive tried posting on a few threads but deleted them, Im just not that comfortable here yet. After all its been a while and I didnt plan on coming back
. Life doesnt work the way we plan. So Im gonna just talk here for this post and see where it takes me.
I figured once I had my tubes and ovaries removed last Sept I was done, went on an incredible vacation with dh in Nov. Life was finally returning to normal!
Had my routine mammo & ultrasound in Feb. 09. they called me back for a MRI core biopsy,on my right (good) side. They never did it as as soon as I was in the mri machine they said not cancer just a very small cyst. My next set of appointments were set for August 28 MRI and Sept 10, 09 with my Oncologist. Great.. I was free and clear for 6 more months. Well the beginning of May I found a noticible lump on my right breast. At first I though naw its just that cyst and maybe it has more fluid in it. made a routine call to the Cancer Agency got voice mail... stated my concern and asked to have my oncologist call me or set up an appointment. Called again that same day. No response! About a week later it seemed bigger... Made a call again ( f-----g voice mail) with all the details and stated I was extremely concerned and I needed to speak with someone about it. no response again. I got busy and had to set my worries aside for a while. It was the beginning of july and I made another call stating it was urgent I get a sooner appointment with my Oncologist. No response!!!!! So around the 1st week of August I ranted on the phone and FINALLY got someone to call me back only to say they couldnt fit me in earlier and my best bet was to wait till my Aug 28 MRI... at this point its no longer a lump but a mass and in my heart I know its cancer. Had the MRI and as my Oncologist was on vacation they wouldnt give me the results. Now in the meantime I have found out my mom is being tested for an Ovarian mass and they were 90 % possitive (maybe more like 100% but couldnt say) that it was cancer. They even booked her chemo date before the results were in. I told her I would be there for her for her first chemo (she's a 3 hr flight away) and I was hoping my would end up being nothing..... So I got on the phone and harrassed every person I could to push the mri results through and have ANY doctor give me the results on the phone. I finally got to the right person (my oncologists personal secretary) and had her working on it. They pushed for the results and then I got the call. A Dr at the Cancer Agency called me late in the afternoon of Sept 2 They were sure it was cancer and they wanted to do a whole ton of tests immediately.
Sept 3rd I kept my appointment with my hairdresser as this was my first real hairstyle cut I had since my last Chemo A really cute layered bob that got ris of all the scraggy chemo curls. It made ME feel better & thats all that mattered. I would have nice hair for a month (maybe)
Sept 4th Ultrasound guided core biopsy on the large tumor
Sept 9th Full body CT scan
Sept 10 Bloodwork saw my Oncologist,went over treatment (chemo, rads, then maybe surgery) went back to cancer agency to have a needle biopsy on a node or lump in my neck then straight to have my heart rythm tested.
Sept 11 The needle biopsy the day before is cancer. I go for a full body bone scan. I phone over to my Oncs receptionist and asked if they had faxed in my port request yet (umm no) but chemo is tenatively booked for monday. I asked her to get it faxed immediately as I was going over to the pre op area for ports and was gonna get one come hell or high water. Went over there and explained my situation. The receptionist said no the earliest they could get me in was the END OF OCTOBER..... Ummm no, I need it today and I can wait all day if needed. She thought for a sec sat me in a chair and said wait right here Im making some calls. 5 minutes later she came running out asking if I had eaten today (no as I had the bone scan really early) She had found a vascular surgeon, 4 nurses and an operating room for right this minute. So I was signing the paperwork as I was stripping down for a lovely hospital gown and was rushed by wheelchair to the operating room for the port.. there was a few minor complications, I think they had to reset the tube/wire 3 times also I dont think they really gave the freezing time to set in as I could feel a lot of what they were doing (nothing like the last port I had) but whatever, Im thinking it might have been more difficult cause that side was radiated in 08. Had my son come to the hospital to drive me & my car home. My Oncologist calls me in the evening to tell me she had changed her mind on my chemo cocktail after consulting with many other Oncs online
Sept 13, I start my Dexamethasone (2 pills 8am & 2 pills 8pm) So am now hopped up on steroids and will go for my first chemo 9am tomorrow.
Sept 14 will be chemo 9am
Sept 15 Mammo & ultrasound for markers (also my mums first chemo)
Sept 18 Mugga scan
So Now Ive vented
DX so far is not all in yet.. so this is tenative
Stage 3 ER weakly possitive (10%) PR negative and her2 equivical (all need retesting)
Dont know tumor size yet, but mass in breast is about 1/3 of my breast (im a D) definately one node under arm and one above the colar bone in my neck
So here I am again! Im also posting this on the main chemo board.
Love & Hugs Suz
-
This really sucks Suz. I am sorry. Back into the ring again.I'll pray for you to have a fighting spirit and able to handle well all that is coming and for you to win again. Good for you for being so firm in getting the procedures you needed. You are in my thoughts and prayers.
-
I know how angry I am, having read all that you went thru... I can't imagine how angry (completely weak word) you must be.
But in typical Suz fashion, you are moving onwards and upwards. Taking it one step at a time and doing what needs to be done to get this thing going.
Love ya, buddy.
-Sal
-
Sorry its not stage 4 its 3 I need to edit that I mixed my mums up with mine
-
Suz, we love you. If this is where you feel best talking about all of this, you can have the whole forum for all I care--we can be your personal cheering section/shoulder to cry on. Am feeling so powerless about this--I imagine this is how those close to me felt when I was doing it--I want to be there, to help, to fix it, to go in and yell at that stupid office for you... But I know you will do what needs to be done, and that you have wonderful people around you to help you with what you need.
That said--can I send you my old wig (cute, brown bob), hats, scarfs, etc? What could you use?
Thinking of you, lots and lots--A
-
You know I knew that you had some issues with moving up an MRI and I do remember the February cyst issue now after reading this..what I didn't know, and this makes me so friggin' angry as I know everyone else is and especially you.. what the hell is with the not calling you back after all your voice mails. I would say that is such poor patient care. They could have at least called you back why take so long.... this scares me because you know we all believe our doctors what choice do we have I hear so many stories where women are told oh it's nothing and then a few months later .. oh sorry it's cancer now .. there are several in my YSC support group. But it is no use me ranting about this as now you are in the fight and things are moving!!! Good for you pushing with the port, I was the same the first time. Actually my friend was my advocate as she had a sil that was going through the same thing as me. I had my port in before my first chemo which was scheduled for a week later as well.
Anyway... my friend you talk away here! If this is your comfortable place then cool... I wish I could do more for you.. I wish I could make it all go away. I cried when you talked about your haircut, it is such a milestone but you know you did this once you can do it again!!!! I have a wig too that is just sitting in a box.. however mine is singed in the front a bit as I leaned a little to close to the oven once!!
I will be thinking about you tomorrow at 9am and beyond. Actually doing some volunteer work for breast cancer tomorrow
-
The thing that's impressive to me about your port story, reading through this again, is that you did that by yourself. You are one kick-ass chick, my dear. I'll check in later. love, hugs--A
-
Dear Suz,
I had so deeply hoped we'd never have to post again on this forum. But as said by everyone else - we are here for you and standing alongside you in this battle. You are doing so well, pushing for what you need! Hats off to you for being so persistent. I'm so sorry you had to fight so hard just to get SOMEONE to call you - good heavens! I can't imagine the frustration with all the delays!!!! I hope things go well today - you're probably just finishing your chemo now. Best wishes for you mom also.
Much love,
Laura
FUBC
-
Kept my wig too (just in case I ever...). Great idea, Amy... could you use a spare wig or two? You could have your own fashion show of wigs to choose from. No clue what size it is, but if the fashion was something you liked, it's yours!
Hope today went as well as could be expected. Looking forward to hearing from you once you get "settled in" and feel better.
Hugs, Sal
-
Morning my friends! Well that was my last night on the steroids and I did sleep again. Ive been taking the last 2 pills at 7:30 instead of 8:00 and Im thinking thats helping along with maybe getting used to them.
So I got a LOT more details yesterday (unofficially) from the techs. Sept 15,09
Mammo not so much just that it wasnt one large mass but a whole lot of small ones. Now when I went to the ultrasound, since I already had much more info than her and was already on chemo, she answered all the questionds they normally dont.
In the right breast a quarter of it center upper inside has 7-8 tumours most about 1 cm + & -. One looks bad as it has a blood source feeding it which is why it grew and spread so fast.
Under my right arm there is one large and 2 small nodes infected, dont know thw size of these ones, But the larger did look noticable.
The US Tech wasnt going to do my neck as she said they normally dont... I asked a few times nicely and she just smiled it off. SO I finally said not quite so nicely that I was the one who found this one and even the once was brushing it off..untill I said it was painfull to touch (thats when they sent me for a plain needle biopsy on it and it was cancer... So in the end she did do it and found 2-4 nodes with cancer, One again being a bad one with a blood source to feed it. Glad I pushed. No more mrs nice gal! It just doesnt cut it.
Im not sure if this will change my treatment... But at least we have the full picture now!!
I dont neccesarily want this type of detail on facebook, so this gives me a good place to start logging it till I tranpose it or get all the proper paperwork back from them. Love & Hugs Suz
-
Oh I forgot about the wigs... So far I have the really good natural looking real hair one that I bought last time. Also picked up a new darker longer real hair wig for free from the cancer agency. Needs a good style and some bangs but will make a nice outdoor with a funky cap duo. Lol dh & ds laughed at me and called me a hippy chick. It does kinda look like that with the tam on, but its fun. Im donating any others that I didnt wear to the cancer agency. And maybe will find a funky shoulder length wavey synetic one.
Hats well I know how to gets tons of hats. Have about 15-20 new ones already But plan on sendind most to my mum. I already know what I liked to wear that was comfortable daytime & nightime. So am picking those out for myself. But most to send to her.
For now I think I have things under control. Being in that area of town so often these last few weeks gave me a chance to dig though a few boxes and find some nice stuff. We also now have a bin of new knitted & donated hats in every chemo room (lol for people with numb hands), snack rooms and family counceling room as well as across the street at the cancer lodge. This has expanded incredibly from my last round.
Time to run as I need to do a ton of chores & shopping today as this might be my last "good one" before" I crash (hopefully not) Love ya all, Hugs Sue
-
Hey Suz,
You are so right about "no more mrs. nice gal" - Still, I'm pissed off and think it's disgraceful that you have hadto fight so hard just to get things properly checked and diagnosed. It is a sad commentary on the state of our health system. Don't give up! (I know that of course you won't). Allow yourself to rest a bit, although I know that keeping really busy also helps psychologically. I really admire your ability to stay upbeat through all this. You are one tough lady and we are cheering for you!
-
My Dearest Bestest Buddies & Friends,
What would I have done without you all!
I was restless last night and since I've started posting here again on the stage IV forum, I thought I would read a few of our early posts. Well.. once I started I couldn't stop, I read the whole thing... my gosh, I spent the whole night here and laughed, cried, giggled, smiled & cried again like my heart was breaking when I got close to the end. Our Dec Angel Joy.
I cant believe its been 4 years since we started this ride and I couldn't be happier that most of us have continued to stay in touch on facebook and are able to keep in touch with whats going on in real life as well as life's bookmarks. You gals will always be so very special to me. I continue to pray that you will all have blessed lives as you so much deserve it.
This was probably one of the most difficult, emotional and rewarding things Ive done in a long time. To actually go there mentally & emotionally and live out that first year. I'm so very glad I did it. This is where I learned to truly trust.. and to lean on a safe shoulder as well as be embraced in the most heartfelt hugs. Finding that this was that soft place to land when things became to much. Vent our hearts out knowing we would not be criticized for it, as well as laugh & laugh & laugh as we got to really know each other, without ever meeting! That's pretty darn incredible if you ask me.
Being December I just want to say thank you, with all my heart! I could never have come this far without your support, love strength & laughter. Lol, My Dec 07 Sisters. I believe you made me a better, stronger & kinder person. I'm sending you all my love, wishing you all incredible health, strength and laughter. And of course it wouldn't be from me if I didn't send you the warmest heart felt hugs... because I believe in hugs.
Love & Hugs Suz
(aka, Susie, Suzy Q and formally Susan Holm)
Edited to say 4 years not 3
oops chemo brain says I cant do the math
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team