First holiday since dx
Thanksgiving was my first holiday since I was diagnosed with DCIS-MI. It was the first time some of us were together in person. Some would come in and just start crying. Some continued to tear up and cry when they would look at me. I tried to reassure them that it was alright. I know they care but it was exhausting. I have another family gathering this weekend. Any suggestions on how to handle this?
Comments
-
Gosh, I'm sry you are having to go thru this. It is hard. Do you have a significant other? If you do, maybe that person could be your "buffer" and tell everyone beforehand, that you appreciate their concern, but that you don't want anyone's sympathy or tears. They need to do their crying on their own time, not in front of you. You have enough to deal with keeping yourself going to not have to pick them up, too. ((HUGS))
-
``It`s so hard, isn`t it... That first Christmas after treatment (I was Stage 2), I found myself comforting more people. They were basket-cases; I was doing all the reassuring even though it was way too early for me to feel anywhere near assured that I was going to be okay. It was so hard.
I don`t have any advice `cause I never figured out how to deal with it. I just kept hugging and patting people`s backs and saying that I would be just fine. Just wanted you know... I get it. -
Honestly, you are a better person than I am. I let my family know ahead of time that I did not want to talk about health issues around the holidays. I have been dealing with a mother going through chemo for colon cancer (good news is that she has had two separate breast cancers without mets) and now me and I did not want to have a family gathering that focused on cancer or anything negative. My first grand child was born in August so I asked my daughter-in-law to say a grace for dinner that focused on the baby. I did not want to see quivering lips or anything else. I think I would have walked away from the gathering if anyone got maudlin. We were also at a mountain house for the holiday and I cut my holiday short by a couple of days because I knew my family could only keep their lips zipped for a finite period. (I tried to get my brother to bring his new boyfriend to the family get together to deflect the tongue wagging about me but he wouldn't oblige.) Good luck and remember, it really is about what you need right now. -
Unless it was my mom, dad or sister I would have wanted to slap the hell out of anyone who was self-indulgent enough to cry like that. When I was going into a surgery with a very poor prognosis even they didn't do that because they knew it would make things worse, even though I knew they were struggling not to. What is wrong with people? -
Oh, mouse9587 - that was probably the hardest part for me. After I got my diagnosis, it would be three months til my surgery, so there was plenty of time for well-meaning folks to come up and tell me their horror stories ("My neighbor's cousin's sister had...") or just hang on me and weep and sob.
The people that were closest to me, I tried to understand their fear, and write off their reactions to the fact that they loved me and worried about me. (I wasn't worried, my faith carried me through.)
But those who WEREN'T close to me, just irritated me. I would think "What part of this is about YOU?"
There were many times I just stepped back, gave them the unwavering stare, and asked them "Exactly how is this supposed to help me?" and of course, they'd sniffle and change the subject or walk away.
Here is an article that appeared in one of the threads here. Since I can't remember which one it was, I'm linking to the original article. It describes how not to say the wrong thing to a person with a serious illness. It's called the "Ring Theory" and the person who has been diagnosed is in the center of the circle, along with their immediate families if appropriate. That person can say anything they want to anyone outside the circle. But those outside the circle can only offer support to those inside the circle. When you see the diagram, you'll understand.
http://articles.latimes.com/2013/apr/07/opinion/la-oe-0407-silk-ring-theory-20130407 -
Declare a "Cancer free" zone. Let folks know that you are doing well and are hopeful but not discussing for the day. It does suck that we have to reassure others when we need all the assistance we can get.
Be Well
Nel -
I get the pat on the back, your tough, 2 weeks after last chemo you will be fine. Or certain friends that sob the whole time I see them. Both are annoying. The first month after dx, it was too much, the phone calls & food. Now I am supposed to be over it! I had last chemo yesterday, I have avoided holiday get togethers already. Saving my energy to heal & exercise when I can.. -
Thanks, everyone! You're a great support! -
Blessings - love the Ring Theory - Comfort In, Dumping Out. I had a friend like that - every time she looked at me she burst into tears. I finally ended up avoiding her until active treatment was over and my hair had pretty much grown back. I had the same feeling about her you had about the people who did that to you - "Just what part of this is about YOU??" And for those people who felt the need to tell me all the horror stories about aunts, mothers, first cousins' best friends' mothers who died of B/C! It finally got to the point when someone would start saying, "My aunt had breast cancer . . ." I'd cut them off saying, "If this doesn't have a happy ending I really don't need to hear about it right now." Usually they'd be chagrined enough to shut up.
Mouse - at least I could avoid people who did that to me. Not really an option when it comes to family. It should NOT be your job to comfort them! You may have to be blunt. I like Blessing's idea: "And exactly how is this supposed to help me??" Or you could just state flatly: "I don't need tears and pity right now - I need laughter and fun, and need to be treated just like you always treated me. If you must be a Negative Nelly, don't do it around me. Please leave the room until you have composed yourself. I don't need to see that." Also, it may get better with time. If last week was the first time they've seen you, then maybe it's a bit understandable. As they get more used to you, their reaction might get less strong. Find the fun outrageous people in the family and hang with them as much as you can. -
Do you have a family member who could act as a go-between? What I mean: is there someone who could diplomatically mention to the other relatives that you would prefer everyone not become so overly emotional when they see you?
I have a bunch of siblings. One sister left such a sad, depressing "I'm sorry" message on my answering machine after learning of my diagnosis that it scared and depressed my husband and I. It was awful. I asked another one of my sisters to please tell her not to leave those kinds of messages. She is the diplomatic sort, and did it tactfully. She was able to convey to other family members from time to time the sort of approach I preferred, and it helped and took the pressure off of me. Relatives mean well, but don't always act appropriately. -
I'm writing an article about how people living with cancer deal with the holidays. I've spoken with a social worker and she has tons of good ideas about how to do what's best for you - whatever that may be - whether it's talking about how you're feeling, starting new traditions (simpler ones!), celebrating what's important to you, all the while accepting that this year will be different because it will be impacted by cancer. How do you feel? Are you worried about the holidays? Will you be glad when they're over? Do you have any special plans? If you have any thoughts you'd like to share, please email me @ laurie@dailyRxstaff.com. I will honor you wishes about how you want to be described - either anonymously as a member of a breast cancer forum, your first or full name. Thank you in advance for helping me share ideas with our readers about how to best cope with the holidays.
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