Phoenix Rising tells QMUL: release the PACE trial data
Mark Berry, Acting CEO of Phoenix Rising, presents the Board of Directors’ open letter to Queen Mary University of London (QMUL) urging them to release the PACE trial data, and hopes that other non-UK organisations will join British charities in the same request...
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Chronic longterm tonsillitis - anyone else?

Discussion in 'Immunological' started by Tulip, Mar 27, 2011.

  1. Tulip

    Tulip Guest

    I have had this for years, most of the 18yrs I have had me/cfs infact. It has ranged from mild to severe with pus on the tonsills :eek: . But the worst is it effects my spine, heart, ears and gives me night sweats. I am going to see an ENT soon and will beg him to take the damn things out.

    I am wondering how much having them removed could improve my health/ability to function?!.
  2. sickness


    Western Australia
    Hi Tulip,

    Just today I started a thread about my recent tonsillitis, I am wondering if it is actually a reactivation of my EBV. I can relate to the pus on the tonsills, I had that last week! I haven't really had it before (that I know of anyway). I don't think I actually looked at them when I had Glandular fever.
    Sorry, I don't have any useful advice about it. I'll be interested to see what other people have to say about it.

    goodluck, ness

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