VWM Pie Face Challenge

Find a Cure for VWM
Sep 7, 2017 · 1 min read

It’s pie face challenge time! For the month of September and October VWM Families Foundation is running a pie face challenge to raise money to fund essential research to find a cure for Vanishing White Matter disease (VWM).

Please complete the challenge by posting a video of someone smashing a pie or plate of whipped cream in your face, nominate at least 3 people to complete the challenge, and most importantly donate a $7 to https://vwmff.org/donate/ or https://www.crowdrise.com/o/en/team/the-vwm-families-foundation-pie-face-challenge

Why $7? Because Sam turned 7 August 30th! Don’t forget to tag the VWM Families Foundation & Sam vs. VWM so we can see and share your videos and use our hashtags #VWMpieface & #7forSam

#VWMff #SamvsVWM #findacureforvwm

Listen to Radio Interview here:

Watch Team Reed do the #VWMpieinthefacechallenge

Please take the challenge and share these videos!!
#piefacechallenge #SmashVWM

Leukodystrophy Awareness

Raising Leukodystrophy Awareness while searching to find a cure for Vanishing White Matter Disease (VWM) -VWM is a rare genetic disorder that results from mutations in a gene known as EIF2B.

Find a Cure for VWM

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It is all about raising awareness for leukodystrophy called vanishing white matter disease (VWM) ~ while searching to find a cure...!

Leukodystrophy Awareness

Raising Leukodystrophy Awareness while searching to find a cure for Vanishing White Matter Disease (VWM) -VWM is a rare genetic disorder that results from mutations in a gene known as EIF2B.

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