So, I woke up with celluitis
Crap,
I woke up this morning and my LE arm hurt like I really slept on it wrong . After my shower, I noticed that the top of my hand was splotchy and felt bruised. I called my onc's office let them know and in the meantime starting running a fever. I kept an eye on it (starting to spread) and finally on antibotics this evening. I will be on them for 10 days.
My question is - other than elevating the arm and drinking lots of water, what do I need to do?
Thanks,
Trish
Comments
-
Oh, Trish, bummer! Yes, elevate and drink lots of water. Lots. You might want to draw a line around the reddened area with a permanent marker so you can see if it's spreading or retreating as you begin the antibiotics. No MLD, wrapping, or compression until it's definitely retreating and no longer actively raging around. Take it real easy and heal quick!
And when you're all better, ask your doctors for an antibiotic prescription to fill and keep on hand so you can get the jump on it if it should ever rear its ugly head again. (Of course if you ever do have to start them, you'd call the prescribing doctor and let him/her know as soon as possible).
Keep us posted! Real gentle hugs,
Binney -
I recently had cellulitis in my arm. While the infection is active only elevate as you do not want to any bugs making it into your systemic system by use massage or compression garment right now.
I did notice that after the infection was gone that the swelling went down with massage and compression garment much easier.
-
Trish,
So sorry you're dealing with cellulitis - I just got over a bout that took 2 rounds of antibiotics to be rid of it.
Nothing new to add here other than to echo what Binney said - for those of us with LE, a bottle of 'in case of emergency' antibiotics is a necessity.
Cellulitis makes me feel very odd...I get very emotional and down, and it's almost a relief when I realize that I'm not losing it, but in fact have cellulitis. I know this sounds nuts.
Hope you're feeling better very soon!
S.
-
Thank you everyone for your help. Right now it is looking better (not bright red any longer) but still there and warm/painful/swollen.. I do know that I have been very emotional these past tow days. Really not wanting it to be celluitis as now I know I will be prone to having it in the future. Crap, Crap, Crap.
Thank you and thanks for listening to me whine.
Trish
-
Trish, I have nothing to add, but just want you to give you hugs. Cellulitis... and lymphedema in general certainly take their toll. Hang in there.
-
Trish, you jumped on it right away, and you'll be prepared if it ever dares to recur.
LE just plain stinks, and I'm sure there was a sense of horror when you woke up to the sore, red hand.
Hope it never,ever happens again.
Kira
-
I give my thanks to this website, SUSO and in particular all the women in this forum for the heads up on celluitis. If it wasn't for you, I would not have caught it for what it was as early as I did. I would have thought it was some sort of rash or bad reaction (I did just have my hair trimmed the night before and almost thought it was from the salon I had been to).
Thank you all!!
Trish
-
I am so sorry to hear this.....sometimes I wake up and have slept on my arm wrong too, what a bad feeling to wake up with it bigger than before I went to sleep.
What is the suggested antibiotic to keep on hand? I travel often and probably sould get this...
Thanks.
-
Prayrv, thanks for checking in, and I'm so glad it's looking better!
Hope the pain level (not to mention the depression and panic) is better too. Get well quick! Congrats on jumping on this so quickly
Binney -
Crystal: it will depend on if you have allergies--the usual antibiotics are
1) keflex 500 mg --take 4 a day, either every 8 hours or 2 twice a day (cephalosporin)
2) Augmentin 875 mg--take one twice a day with food (penicillin derivative)
3) Amoxicillin 875 mg--twice a day (or some version of Amoxicillin dosing) (penicillin derivative)
4) Levaquin 500 mg once a day (quinolone)
5) Cipro 500 mg twice a day (quinolone)
6) Bactrim/ Septra DS one twice a day (sulfa drug)
7) Clindamycin 300 mg three times a day (lincomycin)
And there are others, like doxycycline, azithromycin, dicloxacillin. Somewhere we had a reference for it.
Kira
-
Crystal, I have augmentin, but I'm allergic to a lot of things. Some women have keflex or cipro. What you need is a broard-spectrum antibiotic, and --YES!-- if you travel it's a huge help to have it along. Keep it in its original pharmacy container for travel, so you don't have a TSA hassle. Be sure to ask your prescribing doctor for instructions about how to know when to self-start it, and how to notify him/her if you do. Hope you never need it, but best to have it on hand. (And mark your calender with the expiration date so you can re-order in a timely manner).
LE is an education, yes?
Stay well!
Binney -
Kira,
I am on Clindamycin 150 mg every 6 hours. I only wonder why the dosage is different. Thoughts?
Trish
-
Trish, that's a standard dose for clindamycin, when my husband was put on it at Mass Eye and Ear, it's the first time I ever saw people use it as a three times a day drug. I did just look it up on uptodate, and they recommended clindamycin 300 or 450 mg three times a day.
The dose you're on is standard for it.
Here's the dose range from epocrates:
Clindamycin:
infections, bacterial
[150-450 mg PO q6h]
Max: 600 mg/dose IM; 4800 mg/day IV; Alt: 600-2700 mg/day IV/IM div q6-12h; Info: use IV for severe infxnsSee, big range, so a moderate infection will respond to the lower dose, but some people start higher--it's just clinical judgement.
Kira
-
I'm very allergic to sulfa.........are any of those antibiotics sulfa based?
-
Yes Sharon, Bactrim/Septra are sulfa based, and used more often lately as it works against MRSA--methicillin resistant staph.
I'm allergic to sulfa also.
Kira
-
Kira, thanks for posting this list. I was going to ask what's best. My primary gave me amoxicillin when I requested an in-case-of-emergency script, but it's time for a new one. My doc isn't too familiar with LE, and I wondered if there was something preferable. I guess you don't have to understand LE to know how to treat cellulitis. Looks like there are a lot of choices.
I am allergic to sulfa, too. I also took clindamycin after my exchange surgery, and that stuff is hard core. I swear it did something funny to my feet, as they did not feel right. It was toward the end of treatment, and the symptoms went away not long after I stopped taking.
By the way, I take a probiotic daily but double up on it when I'm on an antibiotic. I take at opposite times from antibiotic, and it really helps keep my tummy in check. My primary had me do that for all of my surgeries. -
ok - doing well in that the redness is starting to fade from its brightness (still red) . But now I am starting to see a few spots that look like an ant bite. They were NOT there earlier today and it is only on the red areas. Is that something that occurs with celluitis?
Thanks.
-
Trish, not exactly sure what an ant bite looks like--but I just figure it's a bug bite--is it like a blister?
When in doubt, best to have your doctor check it--as long as you're getting better, it sounds like you can wait until tomorrow.
Kira
-
The red spots look like a cross between an ant bite and a flea bite. I did google "red dots with celluitis" and it did come up with some hits. I'll see what they look like in the morning and go from there.
Trish
-
Which doctor is the best best to diagnose cellulitus? Radiologist / onco or would a GP be familiar with it? I have mild LE in my arm and breast and breast feels warm to the touch, mild red rash but it doesn't itch and breast feels hard compared to the other non le side. I finished rads last april...
-
Elaine, cellulitis is an emergency, so anything suspicious of cellulitis needs prompt attention from any doctor on your team. Or the emergency room, if they aren't immediately available.
Please get somebody to look at it and take it seriously right away. Mention the words "lymphedema" and "cellulitis" in case they don't pick up on the possibility themselves. Here's information about lymphedema emergencies:
http://www.stepup-speakout.org/Emergencies_and_Medical_Care_lymphedema.htmYou might draw a line with a permanent marker around the reddened area so you and your doctor can note any changes.
Please keep us posted.
Gentle hugs,
Binney -
Kira,
The every 6 hour dose keeps the blood level of the antibiotic at it's peek all the time. It's a smaller dose then the every 8 hours, but it all adds up and sounds good. If the half life is 6 hours and you take it every 6 hours, then very good. Half life means the time that it takes your body to get rid of half of the medication. When I was in the hospital with it they gave it to me every 6 hours.
Glad to hear it is getting better. My doctors would rather me go to the ER on weekends and get started on IV antibiotics. Then once it starts getting better I can go home on oral. After a week I started throwing up the oral. They sent a nurse to the house and she accessed my port and I gave myself the IV every 8 hours. I like that much better then going back to the hospital. A port can stay accessed for 1 week.
-
Binney4 thanks so much for that link, I am on the phone now taking care of this!! I had many of those same excuses, this has actually been going on for a few days. I am just so over going to the doctor but you made me snap out of it, thanks again!!
-
Good morning ladies!
Question, the cellulitis is resolving (yea!!), so when should I be able to start wearing my glove and sleeve again? I'm starting to see swelling in my hand again and I really don't want to see that happen. But I also don't want to aggrevate the cellulitis either...
Sigh.
Trish
-
Trish, as the infection wanes, you can go back to compression and MLD again. Glad you're feeling better.
Kira
-
Well, hey! So glad you're feeling better.
If you have a night garment that's a good way to start back to compression because it's gentler than the day garments. Or just try some self-MLD first, only remember it's REALLY gentle and REALLY slow (when I'm stressed out about new swelling I find myself going too fast and furious
-- have to work hard at remembering to keep that kitten-petting, slow-as-a-slug pace
).
Whew!
Binney -
Well, here I am, in the hospital with my second run in with cellulitis. I had the typical symptoms at onset but this time the arm went from slightly pink to a raging purple red w/ a temp of
104 in about 35 minutes. I have been on Rocefin IV--tomorrow will be the 4th dose. Being dosed with 2gms every 24 hours..Doc said he will probably send me home withi a script for Augmentin. It does look better but not where we want. This sucks!! Katiejane -
katiejane!!!
I hope you stay in as long as needed to beat this cellulitis back with the IV's---you sound like you got very sick, very quickly--I'm sure that was/is very scary.
Get better soon.
And yes, this totally SUCKS.
Gentle hugs and wishes for steady recovery.
Kira
-
Kira, thanks for the encouragement and hugs. I was discharged on oral Augmentin and am feeling pretty good. Even baked a batch of Chocolate Chip cookies. My arm is still swollen more that usual but that is to be expected & the redness is just a very subtle pink. And the fever is gone-hopefully all of this means I'm on the mend! I have always been encouraged to get to the ER with any sign of cellulitis but I'm still amazed at how quickly I went from a temp of 99 and being alittle achy to a raging temp of 104.0 and so very sick! Let this re-enforce to all of us who suffer from lymphedema-even if you just "suspect " you may be developing cellulitis, get to th closest ER ASAP. There really is no time to waste!! Katiejane
-
KatieJane, thank you so much for thinking of all of us in the middle of everything you're dealing with. It's scary to think how fast that got out of hand, but so important for us to keep in mind, so thanks for sharing. Get all better soon!
Uh...mind passing those chocolate chip cookies this way?
Very gentle hugs,
Binney
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