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Compare your country's ME/CFS research funding with Canada's - similar?

Discussion in 'Action Alerts and Advocacy' started by waiting, Nov 28, 2012.

  1. waiting

    waiting Senior Member

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    Thanks to Kati for tweeting the following news story that appeared yesterday on the Canadian "National ME/FM Action Network" website about their recent meeting and subsequent letter to the "Canadian Institutes of Health Research": Network asks CIHR to address the ME/CFS and FM Research Deficits.

    It would be interesting to compare funding rates (per patient, per year) and # of citizens affected between all countries represented on this forum (note: the relevant categories are split into CFS, FM and MCS).

    (I thought I'd re-post it here on PR for everyone as Kati is extremely busy with fundraising and advocacy!).
    justinreilly likes this.
  2. Kati

    Kati Patient in training

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    Thank you Waiting, I appreciate you posting it. It is an article very worthy of sharing and targetting our canadian politicians. i have sent to Carolyn Bennett. MP who has instigated the recent order paper. we need things changing in Canada (and all around the world).
    justinreilly likes this.

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