How did u tell to family & friends?
I would like to know how did you manage to tell your friends & family about your BC. In my case since i found out having BC it's only my husband and my close sister knew about it. My parents have no idea at all. I'am asian, my family are all living in asia. I' am planning to keep it to them till i can, to avoid them to worry about me here living in the U.S. with my daughter. My husband works oversea, he travel a lot for his job.
Next month, i will start doing all the necessary check to my doctor while my husband is home for home leave. It made me think what if i have to do surgery... of course all my close friends will be surprise. I don't want to be treated like a ill person, i don't like attention and would like to avoid questions. Mostly, when i'm with friends at least i forget all about it. I feel like i'm still the old me. What it's gonna be if they find out? Also i have 11 yr old daughter, she's the most i am concern with, it make me worried how she's going to affect her once she know about my situation. She's with me everyday & knows nothing. I love her so much. I want to provide her the mother that she always knew. Strong & never get sick.
I find it hard to start how to tell friends & family.... please advice.
Comments
-
We told most of our family (my husband's family, I have none) on the computer using Skype. It is free and all you need is a web-cam. It helped because they could see me, and see that I was ok. I Skype my in-laws regularly and have found it a great way to keep in touch, and we can talk as long as we like.
-
Sagita ~ I think it's wise to wait to tell friends & family, as you're doing, until you have more information and a treatment plan in place. That avoids sharing news that might be shocking and create more fear than it would if you can also share your treatment plan.
Another thing I found helpful when I told people was being sure to add something positive about my prognosis. Saying something like, "... and my doctors assure me we've found it early and it's very treatable, and that I should be fine after I go through this treatment." That way, you are answering everyone's natural concerns about your prognosis, which I think is often the awkward elephant in the room.
As far as your 11-year old, she will look to you for her cues on how scared or worried to be. Let her know that you have excellent doctors who are taking very good care of you, and that you have an excellent prognosis for a full recovery. Let her know that any sickness you may experience from treatments will be temporary, and that it's all part of a healing process. Life won't be exactly the same as you go through treatment, but she will learn how to cope when life throws her unexpected challenges through the strength and courage she'll see you demonstrate in this situation. Deanna
-
I waited until I had all pathology reports, MRI reports, consults with doctors, and a surgery date before I told anyone (only my husband and one friend knew). First, my husband and I told our 3 daughters all together. We focused on the positive, telling them exactly what the game plan was. There were some tears, but basically children take their cues from their parents, and they ended up having a positive attitude about the whole process. I gave some thought as to how I would tell my sisters - I have 4 sisters, and no bc history in our family. Since we all live in different areas of the country, I knew it would be difficult to tell them all at the same time. Plus, it is kind of shocking getting the news over the phone, out of the blue. So I sent an email, briefly stating that I had bc, and that I was comfortable with talking about it and answering any questions. One by one, my sisters called (when they were over the initial shock), and I had a nice conversation with each.
-
Don't feel like you have to tell anybody until you are ready. It is your personal choice who you tell and feel comfortable talking to and who you don't. It is often better to wait until you know what your treatment entails. I personally was not going to tell my family at all until it was done (they don't live close by) but, when my test results were all in and it got at little more complicated to treat I ended up telling them sooner than I would have liked. I was pressured into it by good meaning people. I wish I hadn't. They haven't been the pillar of strength for me I would have liked. Actually its added a lot more stress to my situation than I needed. You likely know better than anyone what to expect from them so trust your gut.
My friends and co workers however were my surprising strength. I'm sent good wishes by someone almost daily. You never know for sure where you are going to find support and we definitely need it when going through this. The ladies on this board are awesome if you have any concerns while you are waiting to tell your friends and family, afterwards as well. It's a very hard thing to just say out loud at first but it will get easier after you've done it a few times. Good luck to you.
-
Thank you for taking time to share your advices. I thought i was strong enough to handle about BC. Had a couple of trusted friend i have but still i had'nt figure out how to start. Will work on it once i find my treatments how it gonna be. Like my husband says that i may need help in some days specially when he's is not home. Hopefully i will get by with all this ok and be more strong to face my new battle in life & with my family.
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