Lymphedema and cellulitis
Hi my sister,Joan, has just been dx'd with lymphedema and cellulitis. She is taking an antibiotic for the cellulitits..and waiting to find a LE specialist in her area.She had a bmx in December and is doing well otherwise. She has 3 more tx of taxol. I have not had lymphedema so I am not sure how to help her.
My questions: Have you or anyone you know had or have both lymphedema and/or cellulitis? She cannot find an LE specialist in her area. She lives in South Jersey. How does she take care of herself at this time ? Any helpful hints? Any feedback or suggestions would be greatly appreciated.
Thanks and hugs and prayers to all!
Comments
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Yes, I have LE, and I am recovering from my third bout with Cellulitis! I highly recommend getting a good LE therapist and possibly going to an infectious disease doctor! I now have a standing script, in case I get it again! Your sister is in my thoughts and prayers! There are other good threads on this board that address Lymphedema and Cellulitis, lots of knowledgeable ladies that can help you!! Since moving to CA, I found a good therapist and doctors that are knowledgeable about these two conditions!!!! Please keep us posted!!!
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Hello, Candle, and thanks for taking on the research for your sister. Finding a well-qualified lymphedema therapist is important. Here's how to find one near her:
http://www.stepup-speakout.org/Finding_a_Qualified...
It sounds like she's doing what she needs to about the cellulitis for now. Getting therapy for the lymphedema will help reduce her risk of future episodes, but as Kathy suggests, many of us keep a filled prescription of antibiotics so we can start treatment immediately in case of future infections. Here's more information about cellulitis:
http://www.stepup-speakout.org/Emergencies_and_Med...
Please do greet her for us and let her know we're thinking of her. And please keep us posted on her progress.
Gentle hugs to you both,
Binney -
Hi there, I live in central jersey
not sure where you are but I do know that the hospital in Freehold has a good LE program so if that is close, perhaps to check! dang if I can remember the name but it starts with a C!
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Thank you Kindergarten, Binney4 and proudtospin.....I will let you know how it goes.
hugs and prayers
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Hi I'm in the South Jersey area as well, I have a mild case of lympherdema, and Im goign to therapy twice a week for it. I have to say it has really helped alot. Freehold do have a few Lymperdema's therapist.. Good luck!
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sloyd66..thanks for the info. We found one in Mays Landing. She has an appointment on Tuesday.....but at least now we know if the Freehold area. Hugs and prayers
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Candie. Wishing a speedy recovery with sis.Tell her about the fantastic LE website and us girls too. We would love her to join in when she can. More the merrier
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Candie, Lots of prayers for your sister on Tuesday, that everything goes well!! So glad you found a therapist!!!
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What sort of medication is suggested for LE? I carry penicillin but I am thinking this may not be the drug of choice anymore.
Thanks so much! (flying in a few months so I need to be ready)
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Dear Crystalphm!! I take Clindamyacin!
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I carry Keflex. Some women us Cipro. Hope you have a great trip and never need to use it, but best to have it handy in case.
Be well, and happy travels,
Binney -
Thank you both so much!
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I carry keflex, too.
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500 mgs? twice a day? My family doctor won't know, that is for sure.
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I have taken Clindamyacin 600mg 4times a day!
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I have keflex . Can't recall. Is it 500mg twice a day for that drug? Haven't used it for LE but I have used it for PS reconstruction and it was great.
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