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Thread: Lupus Meeting in Perth, Saturday June 18

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    Default Lupus Meeting in Perth, Saturday June 18

    I feel as though I am repeating myself ... but ... There is a Lupus question and answer sessions with some doctors at Royal Perth in the morning, I will post the information in a few minutes when school finishes. You need to phone a RSVP
    Last edited by Linda From Australia; 06-15-2011 at 12:20 AM.
    Diagnosed with Lupus - 22 June, 2010

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    LUPUS GROUP OF WA
    14/Jun/2011
    Comments:
    THE Lupus Group of WA will hold a Questions and Answers session on July 18 at Royal Perth Hospital from 8:30am until noon.

    Lupus patients, relatives and friends of lupus sufferers are welcome to ask a panel of specialists and a GP questions about the disease.

    At the meeting, details of a new online education module to assist GPs in diagnosis and management of lupus will be explained.

    The module was funded by the Lupus Association of NSW, who conducted a survey of NSW.

    The lecture will be held in the Bruce Hunt Lecture Theatre, at the Wellington Street entrance.

    Email admin@lupuswa.com.au or call 9224 3144.

    http://stirling.inmycommunity.com.au...OF-WA/7593629/




    OR click on http://www.lupuswa.com.au/

    then click on What's on

    Last edited by Linda From Australia; 06-15-2011 at 12:25 AM.
    Diagnosed with Lupus - 22 June, 2010

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    How wonderful for all of you!

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    Jammy i call it linda...we've got none of that here plus you'll most likely meet some members off the group but i do hope it goes well on the day.

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    Linda,
    Give us a report on what you learn from these docs. I would love to be there, asking some of the difficult questions that we discuss here.
    It will be interesting to hear about it.
    Hugs,
    Marla

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    rob is offline Super Moderator Super ModeratorEmperor of the World
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    This sounds really interesting. I would also love to be there.

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    I am not sure if I will actually attend now, things are pretty tough for me at the moment, and apart from that, I have a cold. I will see how I go after school tomorrow. If anyone else is planning to go, I might reconsider. BUT it does sounds pretty interesting.

    I am not sure about sitting in an uncomfortable chair for approx 4 hours, my principal let me buy a super dooper chair for school, and all the other chairs are just not the same.
    Diagnosed with Lupus - 22 June, 2010

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    Linda it would be a shame not being able to go but i can well understand your feeling about 4hrs on an hard chair...i would'nt be able to move at all.

    All the best with your cold mate and i hope it heals quicker than mine. xxx

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    I cant believe I forgot about this!!! I saw it advertised a while ago and definitely wanted to go...shame i forgot. I think I'll blame that on the lupus
    Linda, if you went - how did it go??

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    Yes it was good, met a few people and chatted. There was a immunologist, GP, Nephrologist and a Research Scientist on the panel. It was basically an open question forum. Very informative, and the panel were very easy to talk to and explained things pretty un-doctor like.
    Diagnosed with Lupus - 22 June, 2010

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