Hello MND Connect.

Maybe Iím being over sensitive but I donít agree with being bombarded by email and letters from MNDA appealing for donations for research.

Over the years living with MND my family, friends, former colleagues and me have raised 10ís of thousands of pounds for the charity. I am a member of a research advisory group and I actively campaign for improvements in support for people like myself living with the disease.

I fully support the association campaigning for funds but surely they have the technology to screen out those of us who have MND. Whilst I am listed as a volunteer, and that will never change whilst I am able, I hope you can see my point.