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    Grants

    Recently I was talking to a forum member about grants available through the association. The person was unaware of what might be available so I’ve dug out the link from a post earlier in the year that gives a few examples of the types of grants available. I would say this is not an exhaustive list so suggest you contact the connect team direct to get the up to date info.

    https://www.mndassociation.org/app/u...chart-2020.pdf

    I have also lifted this off the MND Association website, it’s a list of organisations outside of the association that maybe of use.

    https://www.mndassociation.org/app/u...of-funding.pdf

    #2
    Bowler thanks for the info....good to know👍
    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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      #3
      Thank you so much for posting this Phil...its really useful.

      Hugs to you x😘🤗

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        #4
        It's definately worth a go. Our MND coordinator (based at hospital) filled out the forms for us and we got a grant from the Doddie Weir Fund for my son (young carer) and I got a grant from the local MND association as for carer support (respite etc).

        So thankyou !!

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