Cellulitis Questions
Hello,
Because lymph nodes were removed from my right armpit, I have lymphedema in my right arm. The breast cancer was in the right breast. I had a double mastectomy in April 2013.
I have had cellulitis in my right arm 8 TIMES - been admitted as an inpatient 3-4 times. My last bout with cellulitis was in Nov. 2018.
I take the normal precautions - hand sanitizer, etc. I do not wear a sleeve.
I have in fact become complacent and a bit careless. There have been several times when I was shocked I didn't get cellulitis. For example, scraped my right arm at a waterpark and the scrape was open the rest of the day.
What makes a person get cellulitis? Is it when your arm swells? Do you have to touch bad bacteria with your affected arm? What is the BIGGEST risk factor for getting it?
Biggest 2 questions: What is the "incubation period" for cellulitis - meaning after you have come in contact with the bad bacteria, how long before you see signs of cellulitis on your arm (red spots for me) ? Also, is my right arm the only part of my body that is at risk for cellulitis?
I would greatly appreciate any input that you might have...
Thanks so much!
Comments
-
Hi max2111...you might have moved on from this question but I am newly diagnosed and scanning the boards and saw your question.
My mom was dx with BC in 2006. Right mastectomy and multiple lymph nodes removed. From 2006 - 2012 we had no issues with lymphedema. We moved to South Carolina in 2012 and cellulitis started aggressively. She has had about 13 episodes since then. The last one landed her in ICU for 5 days.
Honestly, I cannot figure out the rhyme and reason for when she will get it. She filleted her forearm one time, just peeled back about an inch of skin. I treated that at home with the top of a tube sock holding the dressing on because I could not use tape. The ICU visit had no identifying starting injury or cut.
Couple of things we have started doing are AM and PM inspections to check for any redness or swelling. I am able to wrap her arm so if any swelling begins I wrap instead of her normal compression sleeve. We also keep antibotics at home so if anything starts I begin treatment right away and monitor every 30 minutes.
The timing varies but one of my moms signs it is starting is getting the chills. Within a few hours of that complaint the redness will start. Then it moves fast for her. I mark it with a sharpie and check every 30 minutes after starting treatment.
I also measure pretty often and have been told that swelling can be a risk factor.
Hope some of that helps.
-
Hi,
I'm new here and new to BC. This is so scary about cellulitis. I developed a seroma and cellulitis following lumpectomy and sentinel node removal.. seroma had to be drained twice. Post op I took Keflex, followed by Cipro and now on Clindamycin. Finally now the cellulitis is smaller , fading and much less redness.. I never had fever but occasionally experience a chill that moves thru rapidly. Do you know how this will effect my radiation treatments ? What antibiotic works well for your mom? Thanks for all the tips
-
Hi Margo53,
Sorry, I lost this thread!
We keep a prescription of SMZ-TMP and Cephalaxon (sp). She used to do fine with just the SMZ-TMP but after a few bouts her docs added the other antibiotic. I can usually keep her out of the hospital if I catch it quickly but there are times the infection just moves quick.
Keep in mind my mom is 80 so we are all in for quality of life. If she were younger I might question the frequent use of antibiotics for fear of resistance developing. But she is healthy and active and wants to stay that way so we weigh how she feels versus the risks and this is one she is willing to take.
My mom's did not start until about 6 years after active treatment so I can't comment on radiation treatments.
-
everything I read says to not put any lotions , etc on it. Mine is just about gone. Is there anything I can safely put on the area? Coconut oil or other non-alcohol base product? I just used to using lotion because my skin is dry . I also would like it to be in good condition before RADS. Thanks y’all for all the responses
-
Margo,
I've never had cellulitis, but I have taken Clindamycin for an abscessed tooth. It is a very powerful antibiotic. No one told me how hard it is on your body. I ended up getting C-Diff, which is a miserable, and possibly life threatening condition caused when the antibiotic destroys all the good bacteria in your gut, allowing Clostridium difficile bacteria to overgrow. It took me two years of another antibiotic, Vancomycin, (which costs over $4,000 per month) to get rid of the C-Diff.
Of top of the misery of the C-Diff itself, is the possibility that the lack of good gut bacteria caused (or exacerbated) my breast cancer.
I'm not trying to scare you, but I wish someone had warned me about Clindamycin. It would saved me from two years of sheer hell.
If you continue with Clindamycin, please take every prebiotic and probiotic you can get your hands on. Yogurt, fermented food. Everything. It's better to prevent C-Diff than to have to treat it.
Good luck. Hope all works out for you.
Trish
-
Margo...everyday my mom usually uses Avenno for babies, no fragrance. LE therapist uses lotion as well but it is always fragrence free. My mom is experimenting with a few drops of ginger oil in sunflower oil. I am not sure she is doing this regularly though so dont know the results.
When she is in a bout of lymphagitis we do not put any lotions on. We also do not do compression garments or wrapping. I will keep her arm covered if outside and out of direct sunlight. If very hot to touch I will use cold, not freezing, cloths.
Trish...c-diff is no joke. I am sorry you had to go through that. We do keep my mom on a probotic regularly and certainly after a round of any antibotics. I am just learning that so many of our health issues go back to our gut.
-
I’ve not had cellulitis, but, like Trish, was a C Diff sufferer that started from Clindamycin. Margo you might ask your doc about taking Florastor which is a probiotic that doesn’t get destroyed by taking antibiotics with it. I took it the first time I had C Diff. Couldn’t take it the last two times I had it because I was on chemo.I have mild truncal LE and my biggest fear is infection, and needing antibiotics because I’ve had C Diff three times. Haven’t needed an antibiotic in almost seven years (knock on wood), and that was Vancomycin for my last bout of C Diff. Trish, I thought I had it bad, but wow, having to be on Vanco for two years to get rid of the C Diff is just horrible! So sorry you had to endure that!
-
Thanks, luvmydobies. It really did suck. I had Florastor as well. I think that helped finally clear things up. It's amazing that something as simple as probiotics can make such a huge difference.
Trish
-
wow thanks for all the CDiff info. I’m so sorry y’all had to go thru that. I am taking a probiotic, a generic from Walgreens. It’s a little round, pearl looking pill and I take it once a day.... is that enough? I’m not a big yogurt fan but can eat it if I need to. I will be finishing the Clindamycin this week. Cellulitis is much better also. Thanks so all the info
-
wow thanks for all the CDiff info. I'm so sorry y'all had to go thru that. I am taking a probiotic, a generic from Walgreens. It's a little round, pearl looking pill and I take it once a day.... is that enough? I'm not a big yogurt fan but can eat it if I need to. I will be finishing the Clindamycin this week. Cellulitis is much better also. Thanks so all the info
-
Margo - both my dermatologist and my LE therapist recommend CeraVe. It is non-comedogenic, fragrance free and lightweight. Definitely not greasy. One application will usually last through a couple of hand washings. I just use the original "moisturizing lotion" in the pump bottle but purchased the cream for when my hands & feet get really dry in the winter.
I also do travel with an antibiotic - Amoxocillin - so that I can catch it early if I'm away from my regular doc.
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