Going back to work
I am 49 and was and still am in excellent health. I consider myself to be so fortunate to have been diagnosed and treated at Stage 1. Everybody in my life has been incredibly supportive. This experience has been an emotional roller coaster. The hardest part has been seeing how if effects my husband and father. I’ve seen my dad cry because of it and that is painful for me. I reassure them that I am fine. On to the point of my post. I have not worked since surgery April 17th. I am an occupational therapist in a nursing home. My job is bothering physically Andy mentally demanding. I am currently receiving 16 radiation treatments. I just received the 8th. I would like to return to work but have hesitated since people say the fatigue and skin issues get worse at the end. I am currently receiving short term disability which would stop if I return to work. I’m afraid if I return to work and start to feel unwell I may have to take more time off. So far side effects have been minimal. Could someone who had similar work demands give me advice? My work is very supportive.
Comments
-
Hi Amybb, yep, it's a roller coaster! Glad to hear you're coming to the end of the "active treatment" phase. I work at a desk job which is not physically demanding, so it's not so entirely the same. I did find my fatigue was deep for several weeks after radiation. Then it lessened a bit but it was a few months before I felt back to normal levels of energy entirely. It's probably some combination of the cumulative physical toll and emotional toll (my DX was in January and I completed radiation mid-December, was in some phase of treatment the entire year). My skin was fine throughout radiation and then peeled off for a few weeks after. I sense that skin SE's vary a lot among women and it's hard to predict. Sounds like you may want to stay out on disability until you're sure you can handle it, if the current setup is working well? I do find my work was a nice distraction during treatment and I worked throughout as much as I could (I was on intermittent FMLA), including all through radiation, but I had a week of vacation after radiation ended during which I slept a lot.
-
Amy- I agree so much with the emotional roller coaster comment! It is so true. I am sorry you are going through this. I work in an ER as a tech and went back 6 weeks after my UMX and just as I started rads. I am single so I needed the income. I did convert my FMLA to intermittent just in case. It was really not easy some days when the fatigue was hitting hard. I got pretty red and irritated as well but was able to push through. Would your job let you ease back in with partial shifts to see how it goes? If I could have afforded it I think I would have stayed off work looking back now. I wish you the best, be gentle with yourself and rest when needed
-
Thank you Dani. I am fortunate that the duration of my treatment will be 2 months so the financial impact will not be too bad. My radiation oncologist is concerned that my ability to be there 100% for my patients may be compromised. Your statement about staying at home if you could have is especially helpful. I only have 7 treatments left. I just always feel guilty when I am out of work. I am beginning to be more cranky which could be fatigue or just a response to bad weather
-
Thank you so much for your reply. I have found staying busy during treatment to beso important. I find it to be so therapeutic. I have been walking a lot and doing as much house and yard work as possible. Since I am almost at the end of the active treatment I just may stay home.
-
I would say if your job lets you stay out, might as well. I worked through 32 treatments, but my job has a flexible workload.... meaning I could put stuff off until later if I needed to. I wouldn't say the fatigue got worse at the end, but my skin certainly did. I had weird allergic reactions to the miaderm though, so maybe if that hadn't happened it would have been easier. In hindsight it might have been easier to just FMLA the whole thing, I don't know why I didn't. I just kept working. Oh well!!
-
Thank you gb, I feel like we are so programmed to work, and it’s hard to give it up even when we are ill. Routine is important to me so once I am out of one I start to doubt myself. It’s been hard because I have felt almost normal physically throughout everything. I am starting to feel a bit more fatigued and who knows how I would feel if I was working. Thanks again this forum is very helpful.
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