Me?Breast cancer? nooo
Im 38 yrs old and was told on the27th "yes it is cancer the tumor and the suspicious cells around it" that's pretty much all that was said...I have an mri schedule on the 3rd and an oncologist on the 9th...n ot sure what stage what treatment..a little overwhelmed to say the least I know my tumor is 3cm but I'm not what happens next.... what's the next step for me.I know I'm always fatigue but yet can't get a good night's sleep anxious to say the least... Im trying to deal with what I know and not if the UN known but it's very difficult...
Comments
-
i am sorry to hear of your diagnosis. It is very difficult - overwhelming. The beginning is the worst. I was diagnosed 3 months ago. You've got appointments scheduled to find out exactly what you're dealing with so that is good. If the anxiety is too much as it was for me ask for Xanax or Ativan to help. I was a mess and it did help me. I still take ativan at night. Hang in there we all know what you're going through. It stinks and it's not fair, but we are here for you
Big hugs to you
Nancy
-
Thank you Nancy..im very happy I found this site because I have so many emotions and thoughts and im trying to stay positive. my family has been very supportive however I feel if I hear omg my baby sister has cancer again I may just explode...im still trying to absorb and except this and as much as I love my family I feel like no one knows what I am going threw mentaly...is this selfish that ide rather speak to strangers...
-
When I was first diagnosed, I was crazy with grief and anger. Then someone told me that I would live through it, that I would be happy again and that I'd look forward to the future. And that turned out to be so true. The first three months are the hardest, then it seems to get more manageable, then you get to the point where it isn't on your mind constantly. It's been 15 years since I was first diagnosed and really I never thought I'd live so long.
If I could offer a recommendation, it would be to consider antidepressants if you feel unable to cope and also antianxiety drugs if your life is disrupted by anxiety. It's tough enough to go through cancer treatments and be depressed & anxious too. Be good to yourself too.
Vent to us. We've all been through it.
-
Lynette I received my biopsy results this past Tuesday, appointment with surgeon on Friday. I have no idea how this is going to play out, and feeling like I can't plan anything for the foreseeable future is driving me nuts. I do not get sick, day of my biopsy was the first sick day that I have taken in 8 years! I'm not afraid of dying from this any time soon, but I do know that no matter what happens, I will never feel as physically well as I do right now. I am mourning that more than anything else. I'm also afraid of all the decisions that will need to be made.
-
I was diagnosed last year in September 2013. My first diagnosed was in my left breast, then after my second mri, they found it in the right breast as well. At 46, I had a double mastectomy. I forgot to mention that this was going to be my first major surgery in my life. (October 2013) I was not depressed, upset or going crazy over the doctor's result. I just keep thinking...I was given this for a reason...I have a story to tell. After my first chemo treatment, my hair began to fall out, so I told my husband to shave it all off...it's just hair. I AM NOT MY HAIR!!! When my hair fell out, I began to walk around with confidence, bald headed and smiling because I was STILL ALIVE! During this time, I was attending school. Upon my returned to work, I was still bald, going to school, (only missed one day of school, because I just had surgery the night before class) attending church and doing my normal routine. This month, I wll be celebrating my one year diagnosis, finishing up my college courses (BA in Business Administration), and everyday LIFE! All I have to say is, don't let the word 'CANCER' take control over your life. I AM FIGHTING CANCER LIKE A GIRL AND WINNING!!!!
Enjoying Life One Day at a TIME!!!
-
I also agree with alexgram. About a month ago I asked for lexapro. Never in a million years did I ever think I needed lexapro and Ativan. I still fight with myself about the Ativan, but it's helping me to sleep so I go with it. Anyway in no way at all am I trying to push these things on you, but know they can be helpful to you if you need them.
I too enjoy talking to others besides my family about BC. My husband thinks I just have to go through treatment and it will all be over. Um no it will never be over but you and I both will be able to move on. Nobody knows what you are going through mentally except someone who has or is going through it. That would be all of us and this board is super supportive
PM me anytime if you need to talk.
Nancy
-
I guess the worse part is I don't know my actual diag. yet stage kind etc..treatment. is it in my nodes my other breast...I feel once I know all this I will be able to have my mind at ease....till then I guess ill just continue to take my nappys..
-
definitely the worst part is not knowing the full picture yet. My obgyn felt a thickening and ordered a mammo and ultrasound. After the ultrasound the radiologist/dr walked in and said she thought it was cancer. That's when my world fell apart. A biopsy four days later confirmed it but I still didn't know all of the details. I would say I didn't start calming down until I knew what I was dealing with and treatment started. You are in the hardest part right now, but take it one day at a time.
-
Welcome Lynette. Sorry you joined our club. I was diagnosed in July (at 39!) and it is a whirlwind emotionally. I'm not one to take meds ever, but I have to say Xanax helped me get through the first few weeks of the unknown and to sleep! I don't take it all the time, just when I felt panicky or had to be in social situations where my Dx might come up. (We live in a tiny town and word got around fairly fast.) I'm grateful that my 3 kids and back to school provided a huge distraction!
That said, for me, it's all about being in control of my life. I felt better when I decided which surgery I wanted, I felt even better once the surgery was scheduled, better when it was done and better so when I received my full path report. Today I meet with oncology and we decide where I go from here. I know I'll feel better after this appointment and I know what's next. Try and not let yourself get caught up in the what ifs and just focus on what you need to do to take control. Don't feel bad if you need medication to help sleep or keep anxiety at bay. Your body needs to be rested and your mind clear, so you can face this and have the best possible outcome. You can beat this! Best of luck to you!
-
thank you all for all the supportive words..today I go for an mri to see if and what nodes and also my left breast..I know after this ill feel better. its been about 4 weeks since I felt my tumor and it feels like 4 months..i really just want to get a move on and get this this conquered..
-
Hi, Sjacobs--
I hear what you are saying now, soon after your diagnosis, and can tell you that I had the same I'm-feeling-too-good-and-too-healthy-to-have-breast-cancer feeling, when I was in your shoes almost two years ago. But I found it useful all through treatment to use my good health to my advantage rather than to lose it or mourn its potential loss, even at 71.
Yes, you and I were diagnosed with early-stage breast cancer, and yes, the diagnosis can shake up our world (if we let it). BUT the sooner we decide to not let the diagnosis itself undermine us, the stronger we can become. Surviving the diagnosis is, in my opinion, the first step toward surviving the disease! The medical team takes care of our diseased tissues, pathologies and treatments, but we are the caretakers of our attitudes and feelings that accompany the disease.
Example: After my initial "diagnosis shock" wore off and my treatment plan was in place a week later, I returned full steam to my usual schedule, including 3 weekly 90+ minute resistance and cardio workouts at the gym and walking on non-gym days. Since my surgeon said I could return to the gym as soon as I felt like after the lumpectomy (provided I skipped arm work for a while to help the healing and avoid lymphedema), two days after surgery I was back there doing my non-arm routines and the treadmill--and felt great--and continued exercising right through 35 days of radiation, with no fatigue at all. For me, working out was normalcy and a reminder that I am a whole, strong person (just missing some excised, diseased tissue); your activity may be different, but I expect its healing effect on you to be similar.
So instead of mourning a perceived loss of your good health, use your good health to maintain your usual pre-diagnosis activities, and to keep yourself strong during treatment. While radiation will keep you close to home for 5-7 weeks, it should not keep you from planning a vacation for sometime after your one-month follow-up with the rad onc and between other follow-ups with the surgeon or med. onc. Part of our attitudinal caretaking
Best of luck to you on Friday when you see the surgeon--I'll be thinking of you. TG
-
so I went for a mri and was told that thet found another tumor so I will have to have another biopsy to see if its on the same cell.line? does A ny one know what that
-
Thank you for your kind words tgtg. I've been feeling my age lately, and wishing I appreciated my youth more when I was young, bc is just adding insult to injury. I am feeling more positive after talking to the surgeon. I have been focusing on the worst that can happen, and not the best. Thx again!
-
sweetie, most of us remember those feelings and will always, so I,m here to help u get thru and encourage you with HOPE, once all is in place u won,t feel so overwhelmed. remember also not being able to sleep brain wouldn,t turn off, doc gave me script for meds for that, u need rest, so hang in there an come back often we are here for u, stay Positive too I am a lont time Survivor (Praise GOD) and am here to Inspire those going thru. msphil(idc,stage2, 0/3 nodes, L mast chemo and rads and 5 ys on Tamoxifen and all while planning our wedding)
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