Starting Chemo in December 2013
Comments
-
There are so many "hidden" places on this cancer journey. People are really unaware. It stinks, but we do have this place! That part rocks, because I know all of you understand the place I am coming from when I post. Char, we definitely get it. I just saw something on Facebook that relates. I will edit and link it here. ---> Good article
I am up 30 lbs, and while my MO does not seem concerned, I sm freaked out. Even when I work at losing I gain...
BTW...never lost a nail until last night. My nails did become paper thin and razor sharp, but held on. The sheets caught my baby toenail...silly me pulled it off...didn't even think about it this far out.
Love you all!
-
love you all....thank you for being in my pocket today.
-
why did they chooses TC in lieu of ACT? Just curious and trying to learn
-
post from my facebook page I thought I would share
Hiding from Cancer-
My battle with cancer always reminds me of Harry Potter. Cancer is like voldermort and you do not think of it or it gains power. I find myself basically hiding away from Cancer as much as I can. But, time is ticking..and I must go back soon...
It seems like yesterday I left MD with the NED report. Praying that report stays the same. However, so much has happened since the beginning of October. We lost Amy, and I have met or have known four others who are now fighting Breast cancer. It seems my personal facebook is full of prayer request for Cancer reasons. There is no escape. I will never get off this team.
People always have told me that they knew I wasn't feeling well when I was quiet. Seriously, my whole life I have been like this. So, I noticed how quiet I have been about my fight lately and it is because I am not well. This isn't a physical illness but a mental one. I am having a hard time wrapping my brain around the last year. My motto of "just keep
Swimming" worked- I got through it. But now seems harder because I am not actively fighting (besides my daily pill I take). So I avoid-
I avoid:
- medical smells like rubbing alcohol
- the hall bathroom at school because there is a "beep" in there that is exactly like the ending beep of chemo,
- calling Pilots for Patients for my January trip because I haven't flown since I had chemo. Contacting them brings me back- although I must do this lol! This week!
- wearing my hair short because all I see is Cancer there.
- making any vacation plans with the kids because I am scared I'll have to cancel them.
Hiding is not good. I wish I could hide away from all of this, but that is not an option. I just wanted to put this out there in case anyone else feels like I do. It is time for me to come back out and fight again. I had my break, but honestly I did better as a fighter than a survivor. I'll just keep that title in my head because even if you are NED you still are fighting cancer's memory or taunting everyday. Come out and fight now.
-
michelle, good luck with your tests today. Love your post!
jodi, hang in there.
char', good to hear from you. Vent away...
I think I am finally where I can take each day as it comes and really only stress when I have an up-coming appt. Yesterday marked my one yr, first chemo anniversary. Whew!!! Celebrate the milestones. We have all come a long way!
((HUGS))
-
Michelle, I love your post!
-
NED the three best letters in the alphabet. Passed my PET scan yesterday. Never happier to say stage 3 then yesterday. I wa so afraid my cough was indicative of being stage 4. Now I can stop being anxious until May when my next Breast MRI is scheduled. Celebrated tonight with a great steak dinner.Michele love the poem you posted. It is so true. Hopefully some day we can look each other in the eyes .
Char we get you. Some days it is just too much to keep sane Hope things settle down for you. This is a safe place to vent away
Jodi, so happy to hear NED for you too. Still life is so scarey, everything reminds us of this terrible past year's trauma.
Robin , gaining the weight stinks and seems so unfair with everything else you have gone through. You will work at it and lose it eventually off the steroids.
Keep the faith, when will we be able to not stress at upcoming scans and tests? I decided the next 6 moths are to be spent doing things I could not do last year. I now think about 6 months of living at a time and plan on enjoying the time each and every day .
Hope everyone is surviving the weather and not having to stres about weather and getting to chemo appointments
-
Michelle, you've been in my thoughts all day. Hoping for the best
Char, good to hear from you. We are here for everything, ups and downs.
Jodi, thanks for expressing what we all think. You look great...that great hair!
My iPad keeps freezing up and I loose everything I've typed, has happened so many times so will post this quickly with this picture that I've also put on the hair thread. Keepthefaith- here's my recent hair collage pics. It's good to see how far I've come. First is 7 wks post and top R is today. Bottom R is old from 2001 but my style is almost like that. Keep it gray? I think so or I'll be coloring every 3-4 wks
t
-
Thank you Lisa! My pockets are full of love from you all! I am waiting for my results from the biopsy yesterday, should have them by tomorrow. Scared doesn't even begin to describe what i'm feeling, but no matter what it is, i'll get through it. Yesterday I had my first official meltdown since this all began......I went back to work between my ultrasound and the biopsy and i'm in the classroom all this week with 8 of my closest friends/co-workers doing a Europe refresher course, and they asked how it went and when i mentioned that the first doctor said there is a chance of a recurrence I just started sobbing....not the pretty sob, but the ugly gasping snotty sobs. I had 16 arms around me holding me tight and just letting me cry and you know what? it really felt good to finally let it out and even to just let some people see that i'm really not as strong as I let on to be.
So tomorrow we shall know.....love you all.
Michelle
-
Warning. PUI. (posting under the influence) I had my lat flap and exchange at noon. Home by 6 pm. ..my drycleaner should do so good! I came home with a pain ball. It continually delivers a lidocaine agent to my spine and along my ribs in the back I'm completely numb there and have no pain on either incision. I do have pain,however, in my left arm ...I'm sure that arm was manipulated quite a bit and pulled on. I've been dealing with quite a bit of stiffness and cording since my last fill after radiation so that arm is quite painful. I requested pain meds in recovery and later even took a Percocet just to manage that pain.
This paintball is freaking amazing. they sedated me in pre op and the anesthesiologist placed a small catheter in my back under an ultrasound guide. I have zero pain and I will keep it for 3 to 5 days. Once it's empty I will remove it myself it's like this thread under the skin:
-
Oh Missy, sending you another virtual hug! Praying for "it's nothing" results.
Jodi, never heard of a painball (I had lumpy) but wow, sounds cool. Hope you are recovering well.
Well, I've arrived at my last Herceptin infusion. This is it. One year ago this day seemed so far away. Thank you all for helping me get here! I think it's never really "over" (great article, by the way, Robin) but this is a big milestone for me.
My husband & I are going out to celebrate tonight, but pretty low key. My mom (who is 71) fell at home on Wed. night. She broke her arm in a terrible way (she had surgery last night that took 3 hours, had to put in 2 plates and titanium screws). Had to me taken to the ER by ambulance. The surgery went well & the surgeon says she should recover full use of her hand. But, upon arrival at the ER, they discovered she had afib (atrial fibrillation). They're keeping her in the hospital at least another day to run tests on her heart. She is 500 milles away so not so easy to visit.
-
Hi ladies - I have been reading posts on my tablet, but hate typing on it. My son has hijacked my laptop in the evenings to work on school work..... so he says. Anyway grabbed it this morning.
Holli & Mikesgirl- Chemo brain - great post. Decorated the xmas tree last night and my daughter says, "Are you going to put your ornament up that I got you last year." Luckily I saw the box, I didn't have the heart to tell her that I didn't remember receiving it. My memory is horrible, this is very frustrating for me.
Drank and ate way too much over Thanksgiving. Had my colonoscopy that following Monday. I had this picture in my mind, my getting knocked out for the procedure, my waking up with my husband and doctor in the room. My husband having tears in his eyes and the doctor telling me that I have colon cancer.... This was not the case, I was never knocked out completely, and my colonoscopy was clear. Our minds can be our worst enemy. I too am trying to enjoy my life to the fullest in between tests.
Michelle - I have been praying for you. I just had tea with a group of breast cancer survivors. These ladies are older than us, some have fought this more than once, but are still here today. There was a younger lady in attendance who is BRCA positive who has battled this several times. She highly recommended a drug that she is taking and is cancer free today. I need to find out the name of the drug and will pass this on to you ladies. I thought that I would remember the drug....but not with this chemo brain.
Lisa - Your hair looks great. I will be keeping you in my prayers. So many of us have had some type of lung issue from either the chemo or rads. I blame it on the rads.
Oranje - I was accepted into an exercise program for cancer and former cancer patients. I start in a couple of weeks, I will have a personal trainer 2x a week for a few months. I am looking forward to this. I am so glad to hear that you are swimming again.
Robin & Barbara - So glad to hear that your scans are clear. Robin sorry for the loss of your friend....every loss to this friggin disease is heartbreaking.
jbok - ouch! Glad they are giving you good drugs. Hoping you have a speedy recovery.
I need to get off the computer and get to work. Hugs to you all.
Kim
-
Christmas ornament from my daughter last year.
-
Thinking of you Michelle
Kim- LOVE the ornament. How does it make you feel to hang it up this year?
Lisa- love the hair progression photos. You look amazing at every stage.
Jodi - don't stop girl... Just keep swimming. You may been closer to the end of the physical healing but the emotional healing is just beginning. I think we fight so hard physically that everything else is on the back burner.
Jbokland - I had an "on cue ball" with my DIEP last November. Was cut hip to hip and the abdominal pain was minor. Much less then my C-Sections. They are awesome.
So... No endometrial cancer. Yea!!
Are y'all still having pain? Mine my be from weaning off the steroids, but my shoulder and neck and arm (the side they took all the nodes) hurts so bad. I go to PT twice a week. I hope once my my surgeries are done the pain will go away.
Anyone have a hysterectomy? I'm scheduled for February. But my hubby and I were looking for pictures of female anatomy before and after hysterectomy, we came across a YouTube video that scared the &@$* out of us. About how removing the uterus basically causes everything to cave in- spine, bladder, bowels. Oh my!!
-
Holli, I had a hysterectomy in 1999. I had a bladder tack surgery done at the same time. There is a website very simar to this called Hystersisters. I found them prior to my surgery and stayed on as a Hostess(moderator) for a couple of years. I have not caved in
There has been so much going on here! I am happy that everyone seems to be doing well. We have our issues, but overall doing okay. Michelle, still praying for clear results.
-
Michele, so hard to wait those few days for the biopsy results.thank God for friends both in person and in the ether of the web. Keep chanting.
It will be normal, It will be normal , It will be normal
Oranje big congratulations for finishing out the year of herceptin. Wishes for your Mom's recovery. Will you be able to go see her?
JB awsome the pain all and being so comfortable except for your arm, heal fast
Kim, love the Christmas ornament. How nice of your daughter to have gotten it for you. Yah, I get you about chemo brain. I am getting really good at making lists. Discovered SIRI on my iphone is great. Just dictate a note to myself. Of course I often forget to look at the notes.
Holli, great news on the endometrial biopsy results. Are they going to do the hysterectomy robotically or laparoscopic surgery. Recover is really quick that way. I get periods of pain in my lumpectomy site still, off and on. Also pain in the muscle along the from of my armpit when I really stretch it. I keep massaging the edge of the muscle there and stretching but it is still much more firm then the other side.
Robin. Glad you have never "caved in". LOL.
Everyone have a great weekend, I guess I do not have an excuse this year to not Christmas shop.
-
Wow, I feel like a response slug...
Do you all write down the thread stuff? I cannot remember it all. I, unfortunately, find my attention span missing in action and scrolling has become a frustration. I lose track and when I get back on track and back to my response I have lost track again. I need a notepad when I log on. Now if I can remember to do that
-
I scroll up and down on the iPad... Could not remember it all otherwise.
I forget, Robbin, did you get a new puppy? My son just got a new Great Dane puppy, 8 weeks old and already 23 lbs. he lost his GD a year ago.
-
Lisa love the hair pictures! I like the color now. It's so pretty!
Jbokland, ouch. I'm glad you have the drug ball. What a great idea.
Ornge_mama, YAY! Last herceptin. Congratulations!!! I know that is a relief. Mine is January 23rd. I've already rented a place for a January 24th "F#ck Cancer...no pink allowed" party! I've already ordered the banner. I will be dancing on tables that night. The place I rented waved the rental fee because they love my party theme.
Robin & Barbara - YAY your scans are clear.Phew!
Jodi, I think we all have a long way to go on the emotional aspect of this looong year. I keep myself non-stop busy. I'm having a ton of fun but sometimes when I slow down the thoughts start to creep in and I wonder if I'm keeping myself so busy to keep the thoughts at bay.
Michelle, love the poem. And I just read your facebook post....YAY!!!!
Holli, my sister had a hysterectomy yesterday and said that she is feeling fine with little pain.
Kim, knock on wood but I haven't had chemo brain. But still have the friggen neuropathy. Although it is getting better my hands kept me awake last night. They get so hot sometimes but they don't buzz anymore.
I had chemo one year ago tomorrow which also happens to be my birthday, it was the worst birthday ever! Tomorrow I will not even think about it! I am going to work on decorating my new home and then Greg (aka rock hard chest guy) is taking me out for a romantic dinner. From now on I'm going to cherish every birthday and not worry about getting old. Every new wrinkle will be a welcome gift....don't get me wrong, I'm still going to use Retin A
-
NO CANCER!!!!! I feel like I can breathe again.....nothing worse than the fear of the doctor saying that from what he is seeing it appears there is a recurrence ......glad i could prove them wrong!!
First time I actually said out loud that I was scared. I couldn't imagine going through chemo again but knew if i had to i would. I am heading back to Mayo on Monday to get my new right boob deflated and then inflated with saline in the expander....taking one of my best friends with me so we will make it a fun trip!
Thank you everybody for all your prayers and for hanging out in my pocket all week.....love you all.
Michelle
-
Whoo-Hoo Michelle! Happy Dance for you!!! That's the BEST news!
Lisa, thanks for sharing the hair photos. You look great!
Kim, LOVE the ornament.
oranje, congrats on your last infusion. YAY!!!
I'm posting this from another thread...
kind of says it all, doesn't it?
((HUGS))
Have a great week-end, ladies! I think of you all often~
-
-
hello robin?!
Must revisit this picture. We are awesome, every damn one of us, although missing a few even " awesomer" ones.
-
Michelle, great news, and it brought a big smile to my face today as I sure it did to yours. It is so feeking scary to get each and every test done. It wa great of your doc to let you know the results on a Saturday
Keepthefaith. A lot of truth in that poem.
Just not feeling much of the holiday spirit this year. With my husband in the nursing home now I will be home alone for the holidays. Weather permitting I may try to drive to New Hampshire to visit my older son. The younger one, in the SF Bay Area was here 3 weeks ago and so he will not be back. At least I did a lot of shopping on line the past week so gifts are all done including several form myself.
-
My phone ate my reply it appears! LOL!!
Barbara, yes we did get a puppy. I am happy that Moki is stable, I wish the tumor was gone though. The holidays can be tough.
Keepthefaith, I love that poem.
DJ, enjoy yourself!!
Michelle, so excited all was clear!
Oranje, so exciting you are done!
Lisa, we do need another collage I think!!
Jbok, I loved my pain ball.
-
Michelle!!!!!! Whoop whoop!!!! So so happy!
Want a laugh? I officially have an Afro ladies! I'm thinking about not wearing my wig to school soon and just wear some of LuLu's headpieces/bow bands to make the students laugh! I'll post pics soon lol
-
jodi, love fb post. See my response! Lol. Hairdresser Kim...you are needed!
Tomorrow is my bilateral mammo and us, nervous. R breast still feels weird (non Cancer side!) with occasional little zingers right through the nipple (?!) and the left is tender, I know the mamo will be painful, they always were. The thought of tugging, squishing, pulling on L girl is making me more anxious. And then they can never see much due to density. Pocket party for me girls
Marital issues creeping in again. Last year was just survival. Now I'm different but hes not. Tried counseling in the past but he says it doesn't help and its not for him. He's not a talker and difficulty expressing feelings. And I love to share and express and feel. More so now since BC. Ugh, what will be :-(
How have your marriages and relationships faired since BC? Many say it has brought them closer, I wish :-
-
Aw Lisa-so sorry to hear. Whatever happens, be true to yourselves. Relationships that are not nourishing are too depleting of your spirit.
-
Michelle, I am so happy for you! After much thought and deliberating I have chosen to stop going on this site. I love each and every one of you and will miss all your post. I just can't keep thinking about cancer. In order to move forward this is the best thing for me. I wish you all the best. I hope we never have to fight this again. Take care and God bless! Kathy.
-
Jodi - Regarding your very curly hair. My friend who is now a 6 year cancer survivor, had really tight afro curls when her hair was short. She ended up having to go to a hair salon for black people to get help with straightening it and learning how to work with it. Her hair is now straight, so this was a short term issue. Good luck, you always look pretty!
Oranje - I don't know if I said congrats..... So congrats on finishing up treatment. What a flipping long road for you ladies who had to have the Herceptin infusions.
Holli - My bc santa ornament ..... Santa is cute, but he is not my healer. Jesus is the reason for the season. I am praying and trying to get my kids to understand that.
Keep the faith - Great poem, thanks for sharing.
Barbara - I live near the bay area. If you ever get to CA, contact me. I hope that the weather is good so that you are able to get out of the house and go to New Hampshire to visit your son.
Robin - I agree that we should do a new collage, with our new hair, since we were all losing it last December.
Lisa - We are in your pocket.... Praying for a clear mammo. Regarding marriage, I have been married for 30 years this April and can tell you that it is not a walk in the park. I think that Eric and I are just so darn stubborn, that we have kept this marriage going for so many years. I agree with Jbok's post about the importance of being in a nourishing relationship, it is so depleting to be with someone with a lot of issues and who doesn't want to work on them.
I am sorry to see Kathy leave our group. I wish her well. I do not see this board as a reminder of cancer, I see this board as a group of ladies who have battled cancer together. We keep in touch, just as any friends try to stay in contact. We are here for each other through the ups and downs of life. Have a great day ladies....
Kim
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