Hi, I guess after today's app't I was in the wrong group!
I was diagnosed with IDC after scratching an itch the first week of July.
I had a lumpectomy with sentinel node removal on Aug. 11th. The first lymph node lit up and the surgeon removed it, the 2nd on didn't light up but looked strange so he removed it as well. I was told it was grade 3 but that's all I knew.
I had my first app't with the Oncologist today, I have stage 2, grade 3 IDC and he wants more lymph nodes removed. But first I am to have chemo, which begins on Friday. It seemed like wait wait wait now everything is rush rush rush, it's a lot to take in!
I have had my own home childcare for 10 years and love it. My Dr. told me I had to stop too many germs from the kids and I just won't be able to do it. I was really hoping to book the app't for a Friday and be sick over the weekend and back to work on Monday...guess not. I sent home letters explaining it all to my families today. It's especially worse because my dh had an excellent job for 20 years and they shut down. He is working now, but it's at 1/2 the pay and no benefits so without my income I just don't know how this is going to work
I am not enjoying this banner, it's nice that there's so much money donated, and I like pink.....I just don't like what it's doing to my life...
Comments
-
Wow, so many huge changes for you recently. This really is the club nobody wants to join...
It's probably a good idea to avoid the kiddie germs while you're having chemo. I took a 3 month leave from my job for similar reasons. Some gals actually manage to work throughout treatment because it can be nice to maintain some kind of normal routine (and keep getting a paycheck!) but you're wise to follow the doctor's advice.
Do something fun this weekend that doesn't cost too much. Having lost even a couple nodes, you are at risk for lymphedema so take it easy. I bet you'll have lots of people step up to offer assistance - make a list of things others can do and take advantage of whatever help you can get.
-
Lori -
I am so sorry that you have to join us. I remember feeling exactly what you are talking about...waiting to get the cancer out & come up with a plan...then boom everything slams into high gear and your whole life feels immersed in Cancerland.
I was in your spot right before Christmas. I stretched weird & felt a pull, and upon investigation found a lump...the rest is history. Like you I did the lumpectomy & SNB. Unfortunately for me, they could not get a clear margin on my tumor, so I too ended up with chemo...and then a second surgery.
It has been a difficult 8 months since then, but I finished AC chemo & Taxol, had my bilateral mastectomy, and am almost 1/3 of the way through radiation.
I am an anxious person so I have really had to make sure I keep that in check. I keep trying to remember small hurdles throughout each type of treatment so I do not get overwhelmed. I have learned to let go of things I cannot control (that has been the most difficult for me), and trust moving forward.
Like you, I had some struggles along the way...I couldn't work because of germs, my hubby got laid off & ended up having surgery too...etc. please accept help offered by friends, family, neighbors and even friends of people who care about you. Once I allowed myself to realize it helps them to help you &most people enjoy helping...my life got a lot easier.
It may feel now like this will never end, but I am a stage 2b, grade 3 person who was in a similar position, and I can tell you it does pass more quickly than you think. I wish for you kind caring nurses, helpful doctors and loving support of family & friends.
I hope you find a thread here with people who you connect with; who of course understand what you are going through.
Good luck.
-
Thank you Smartass......now that feels weird!
It is comforting that you have come thru this and starting to get your life back in order....I feel like by quitting work that I am giving in.
I know now, realistically they are right. Getting up at 7 every morning and looking after 5 toddlers isn't the easiest when you are healthy.....and I don't get sick, so I've never had to work while sick. I am thinking my days would be miserable.
I am the one who does everything. Hubby's job is exhausting and long hours. He works comes home and showers, takes a quick nap, has dinner and winds down to go to bed for 9pm. I feel guilty about asking him to do more. 10 years ago he fell and crushed his L1 vertibrae and was off work for almost a year, he still aches from that.
I'm not sure that I'm anxious, but I am a planner.....and my life isn't going as planned. Even my treatment isn't going as planned. I am not spontaneous at all, and yet I feel like I have to be with this.
We've had lots of offers to help, I just can't believe we've worked so hard over the years, overcome all of our obstacles and now this. We drew the short stick in this game of life....all we do is struggle. I had a lot of pride that we had come this far and never needed to accept help.....but now I know we will need it, we have no choice.
Thank you for your post, it has helped me see the light at the end of the tunnel. I guess if you made it thru, I will too...I won't promise to like the ride, but I'll hang on...
Lori
-
Lori
I totally understand what you are saying about independence and working hard to take care of your life and obligations. It makes accepting help hard.
My BS is the one who said something that got through to me. She said something like: you are a lot like me, you feel like a loser if you are not working. But you are not a loser. You are fighting a bad disease. Take care of yourself and you will be fine. This one time accept help.
It seems kind of silly, but it is how I feel. If I cannot take care of myself it means I need help & that makes me feel like a loser. In the past I would rather go without. At first accepting help with meals, or the few donations we got, made me hyperventilating. I decided to check my brain at the door & write thank yous for everything when I felt well.
As for your hubbys schedule & how to keep life somewhat normal for him...we switched to buying some pre-made things so it was easier for both of us. Fruit that is already chopped (fresh cuts from the grocery so no prep needed), canned soups, Lean cuisine (I know kinda gross), trader Joe's frozen pastas with red sauce that he could just heat up in the microwave, pizza, broasted chicken from the deli, etc. This worked better anyway, because smells of food bothered me a lot during chemo. That was during AC. I was able to actually cook sometimes, but not too much.
I had to send him to the grocery store as my immune system was pretty bad. We ended up with a LOT of snacks in the house because that is what he picked out...not on the list. I had to let that go and be happy we had groceries.
It will be hard, but hopefully you will feel as well as I did. After a couple of bad days, I usually would start to feel better. They give you lots of med options to control pain if you have it, prevent nausea, and help you sleep if you need it.
My husband had testicular cancer 20 years ago at age 22. My memory of his treatment & constant vomiting scared the crap out of me knowing what I had to look forward too. Things are so much better now. I did not vomit once, for which I am thankful.
Good Luck! You will get through it. I am glad people have offered to help. Please be honest with them about what you need & give them the gift of helping. Once you do, things will become easier.
Jo
-
Smurf is not just a Smartass but a wise one! Good advice on the shopping - I would never trust my hubby in the grocery store.
Hang in there Lori: since you survived hordes of wild toddlers, this ordeal might even seem easier in some ways...
-
There is no way I could have worked through chemo, and I'm only half done and the side effects of neuropathy, muscle twitches, muscle fatigue (like you over did it big time at the gym yesterday, so weird jello feeling and almost cramping after 4 stairs) and chemo brain. I keep a running list on the island for my husband to grocery shop. The symptoms change and some increase as you go along, chemo brain, fatigue, pealing burning feet. I'm offline for 7 days each cycle, as the computer makes me nauseous. This is your time to get better, it has been very hard for me to accept, as I am very active in volunteering, but have had to cut it all out. I figure I am totally out of it for 1 week each cycle, therefore I'm giving up at least 6 weeks of my life, so that I can live a longer life. I see it as a WIN.
-
Lori, so sorry for your situation - it sounds like the rug's really been pulled out from under your feet.
Take care of yourself and DO let others take care of you, too. I wish I could help!
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