Hip
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Swollen lymph nodes are linked to chronic fatigue syndrome, and are one of the characteristic symptoms of ME/CFS (tender lymph nodes, especially in the neck or armpit, are listed in the CCC and CDC Fukuda criteria for ME/CFS).
In my case, I developed some mild (but permanent) swollen lymph nodes at various locations – in the neck, under arms, chest and groin areas – long before I developed ME/CFS from a respiratory virus I caught many years later.
I had swollen lymph nodes as a permanent feature for over a decade, but only descended into ME/CFS once I'd caught a respiratory virus (that started as a nasty sore throat).
So my thoughts are that pre-existing swollen lymph nodes could be a factor that predisposes individuals to developing ME/CFS when they later catch a viral infection, or when they later are exposed to some other ME/CFS-triggering event (such as a mold exposure, a vaccination or surgery).
I'd like to hear other people's experiences regarding swollen lymph nodes.
My question is:
(a) Do you have swollen lymph nodes as part of your ME/CFS symptoms?
(b) Were these swollen lymph nodes present before the triggering event or infectious agent that you believe precipitated your ME/CFS, or did they only appear after your experienced your triggering event / infectious agent?
EDIT Jan 2016: I have just added a poll to this thread as well. So you can answer via the poll, and if you like, also answer by posting a comment in this thread.
In my case, I developed some mild (but permanent) swollen lymph nodes at various locations – in the neck, under arms, chest and groin areas – long before I developed ME/CFS from a respiratory virus I caught many years later.
I had swollen lymph nodes as a permanent feature for over a decade, but only descended into ME/CFS once I'd caught a respiratory virus (that started as a nasty sore throat).
So my thoughts are that pre-existing swollen lymph nodes could be a factor that predisposes individuals to developing ME/CFS when they later catch a viral infection, or when they later are exposed to some other ME/CFS-triggering event (such as a mold exposure, a vaccination or surgery).
I'd like to hear other people's experiences regarding swollen lymph nodes.
My question is:
(a) Do you have swollen lymph nodes as part of your ME/CFS symptoms?
(b) Were these swollen lymph nodes present before the triggering event or infectious agent that you believe precipitated your ME/CFS, or did they only appear after your experienced your triggering event / infectious agent?
EDIT Jan 2016: I have just added a poll to this thread as well. So you can answer via the poll, and if you like, also answer by posting a comment in this thread.
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