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    United2EndMND

    Many of you are aware of the Β£50m new commitment to Targeted MND research made here in the UK by our government in November 2021.

    We all hope it is a major inflection point in the fight against our disease. When implemented this would also represent a tripling of government funding yearly for our cause.

    We have been working along with researchers and the charities since and our focus for early 2022 is guaranteeing the release of the full funds in a sustainable manner to our researchers and their plan.

    Please consider subscribing to our website for monthly updates including our latest (below) on the vital need for a single grant application. What exactly is this? Have a read.

    In addition, perhaps have a look at, and perhaps bookmark, our open documentation page which includes the full strategy plan that was submitted simultaneously at the same time as the request for funds.

    https://patientsunited2endmnd.org/documentation/

    It was not just an ask for cash. All the funds in the world won’t help us if there is no strategy.

    The #united2endmnd coalition have submitted a 5 year plan of work.

    https://patientsunited2endmnd.org/20...leapplication/

    best wishes all
    Lee

    #2
    Onein300 many thanks Lee πŸ‘πŸ»πŸ™βœŠπŸ»
    Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.​​​​​​

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