I'm Scared!!!
I'm going to quit the intellectualizing and just say it!
I'm scared!!!! I'm sad!!! and...feeling alone!!!
I've handled the 6 biopsys, Dx, and all the rest including the mystery of the floating clip, yet here I am at the first meeting with RO and it's hit. And yet, I take inventory of all I'm grateful for:
An early diagnosis....i mean it's 'just' stage zero...DCIS
my wonderful sister-in-law who has schlepped to all these appointments and took care of me after my lumpectomy and said nothing about my dog peeing on her new carpet...twice.
I'm grateful that my brother makes me laugh...
My loving nephews (9) and neice (1).....
I'm grateful that I have a mom I can vent to about everything!!
I am grateful I don't feel as weepy now after yoga as I did an hour ago.
I 'm grateful that an old family friend said to me yesterday, "I love radiated breasts."
There's probably more but right now I'm on my pity potty and ashamed that I am. I hate that I'm single without children of my own and struggle to find meaning...and still, ashamed that I do have much to be thankful for...
Lastly, I'm grateful for you guys....xo
Comments
-
What you are feeling is completely normal Lisa. It will get better...and then worse...and then better. I just caught a thread yesterday how less strong some people felt once all their treatments were past than they did while going through treatment. It's hard to come to terms with this, especially since we can't knock the cancer out and be assured we're done with this fight. It sucks. Period. If you can find times when the Big C isn't front and center in your life (delve into work, or take the weekend off from this [stop researching, talking about, etc.], that you can find some peace. I try to avoid reading, logging into discussion groups after 8 pm so I don't go to bed thinking about BC).
-
Lisa, you are not alone in feeling the fear........we have all been there and done that. I know that you move through the dx, the biopsies and the lumpectomy with a feeling of dread and numbness but there comes a point when the reality of it all sets in and that is right where you are now. Believe me, it does get better and you learn to accept it for what it is and the fact that you are doing all that you can to prevent it from returning.
This whole thing is a process and one that takes time.........please don't beat yourself up for having all these feelings and emotions........they are perfectly normal.
Love n hugs. Chrissy -
Thank you for your support and encouragement Chrissy! I guess I just feel like I'm falling apart today. I read yesterday that real strength is what you do after you've fallen apart...or something like that...
-
Renee...thank you! so right about getting off line...
-
Lisa we all have days like that but tomorrow is a new day.......look forward, never back.
Love n hugs. Chrissy -
Hi Lisa, of COURSE we get scared! We're not fools. We know this is a big deal even if we have a fabulous outlook. Just being linked to the word "cancer" is terrifying. That's when I start muttering, "Stay in the day, stay in the day, stay in the day." TODAY I am definitely not dying. TODAY I have nothing specificly terrifying happening to me. TODAY I can cope fairly easily with side effects. TODAY I am alive, in love with my family and loved in return. TODAY I will stay in the day! Works for me.
-
Thanks, Carolyn. One day at a time...:)
-
Love that, Carolyn!
-
I was a rock all through the diagnostic process and surgery. Couldn't wait to start chemotherapy, so I could really begin kicking some butt. Celebrated losing my hair 'cause it meant the chemotherapy was doing its job. Embraced the wigs. Knew deep in my gut that I could do this.
Then, part-way through radiation, I was blindsided by complete and utter panic. Lasted for months. Funny how that happens.
-
Scared is okay, sad is okay, mad is okay, it's all part,of this journey. I remember telling my husband I can't do this, I don't want to do this. But some time has passed and guess what, I'm doing it. Is is fun, no not always, but everyday is getting easier. Do I still have bad days, of course it's going to take time. You are entitled to your feelings, so have a pity party if you need to. Just know that tomorrow is a new day and that means you have a chance to start new.
-
Thank you selena and renee. Hearing your experiences/feelings really help. xo
-
Hi Lisa - I still have days and sometimes weeks like this 3 yrs out. I remember during treatment being so strong. I worked throughout, traveled (for work) during weeks two and three of each of my chemo cycles and then suddenly found myself in tears during a post infusion checkup. I just broke out sobbing and my favorite nurse, Derrick, looked at me and I just had to tell him I was feeling sorry for myself. I was scared and tired. It still happens from time to time even though I have been NED for 2.5 years. It isn't necessarily logical.
Try to show yourself compassion by not judging yourself.
Send happy, peaceful thoughts your direction. -
Woo woo woo ((((hugs)))
I get it.....I am down to only crying about 2-3 days a week now.... I am kind of seeing the light at the end of the tunnel, it just seems so far away. But I will make it and so will you.
Your sister in law sounds great!!!! You are lucky to have family near. I wish I had mine around but we're all in different states.
-
Hi Lisa
Just had a good 2 year check-up....and today I realized I have been on this site for 6 HOURS! Why I do not know....I should be off doing something fun! Altho this site is great - it sometimes can be obsessive if you let it. I am assuming that b/c the whole ordeal was front and center this week...this is how I came to spend my whole damn day here. Brought my scary feelings to the fore.....don't feel ashamed in any way. Tomorrow is a new day. One foot in front of the other for awhile.....
-
Thanks impatient...
and my heart goes out to you when you're having tougher moments...
I had a moment the morning of my RO consult which prompted this thread and tomorrow is my first day of radiation and I'm actually feeling positive. I'm prepared knowing some days I'll feel less encouraged and I'm letting myself of the hook to have a little pity party. But more and more I am really grateful for the days that are calm...xo Lisa
-
Thanks softness...you will make it...hugs and comfort for you!
Patti...Front and center you are so right. Need a new answer to What's new? Other than Cancer...:)
Congrats on your good 2 year report!!
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