August 8th, 2016: Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis
Jody Smith joins with other ME voices in honor of Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis.
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Has anyone with CFS/ME had cellulitis ?

Discussion in 'General ME/CFS Discussion' started by Lucy1996, Aug 20, 2017.

  1. Lucy1996


    I have CFS/ PVFS (although am doing a lot better these days generally...)

    I've currently got cellulitis from an insect bite on my underarm. Has anyone with CFS had experience with cellulitis? I feel like my immune system is struggling to kick it, on a second course of antibiotics and my glands feel like they're going to burst out my neck head is pounding and can't concentrate , sleep is disturbed (feeling very CFSish)

    Just wondered if anyone else with CFS has had cellulitis ? How long did it take you to recover? Did your CFS symptoms get worse during the infection ?

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