Over the years, MultipleSclerosis.net has lost powerful voices in the MS community. Hear the stories of those who are no longer with us as we celebrate their lives and messages.

Patrick Leer

Over a quarter century ago in the beginning of “living with MS as a family” there was nothing available about MS spouse caregiving. I would bundle up our toddler daughter and transfer Patti out of her wheelchair and into our car to drive to our local library where I poured over hardback volumes of the New England Journal of Medicine. Read more

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