At the age of 2, after a minor bump on the head, Sam Buck was diagnosed with a very rare, terminal brain disease called Vanishing White Matter Disease (VWM). There is no treatment or cure for VWM and there are only 250 cases worldwide.
This is the story of how Sam's family started the VWM Families Foundation and how they need your help to save Sam's life. There are treatments on the horizon but we need $2 million to get these drugs to clinical trial as soon as possible.
We have raised $175,000 so far but need your help to get to our goal.
Please watch, share and donate.
Follow us at www.vwmff.org
on facebook and instagram @vwmff
and on twitter @vwmfamilies
Thank you to Good Vibes Productions for telling our story so perfectly. https://www.goodvibesprod.com/
You can follow Sam's story @samvsvwm on facebook, instagram and twitter.