
By harnessing the power of the Fiber Arts Community, #SocksForSam is raising awareness and funds to benefit the Vanishing White Matter Disease Family Foundation. You can help too. Continue Reading →
Greenwich Free Press (https://greenwichfreepress.com/tag/sam-buck/)
By harnessing the power of the Fiber Arts Community, #SocksForSam is raising awareness and funds to benefit the Vanishing White Matter Disease Family Foundation. You can help too. Continue Reading →
“”Don’t ever let anyone tell you that you can’t do something, or worry about how much time it will take or how much money it will cost. There’s always a way to do it. Always believe in yourself. Don’t let anyone tell you no. Trust your heart.” – Dr. James Brunetti DO Continue Reading →
All hats are hand made by Greenwich Schools staff and students and all proceeds benefit the VWM Families Foundation. Continue Reading →
On Thursday, April 28, get your shoes and socks ready, or not ready, for Mismatch Day for an important cause. Continue Reading →
During a time when close to 150 travel wishes have had to be postponed, Make-A-Wish Connecticut continues to grant all wishes that are safe to grant. Continue Reading →
Every 2 minutes a child is diagnosed with cancer. The Mane Event at Western Middle School raised funds for St Baldrick’s Foundation who seek to cure childhood cancers. Continue Reading →
The entire Glenville School community are knitting winter hats and key chains to benefit Vanishing White Matter (VWM) Families Foundation. Fourth grader Sam Buck has the rare disease. Continue Reading →
Also, Thursday VWM Families Foundation is organizing “mismatched shoes day” with a nod to Sam Buck who wears mismatched shoes to school as a way of expressing his personality.
Help VWM support Sam and all VWM kids on Thursday, April 4, the anniversary of Sam’s diagnosis by wearing your mismatched shoes or socks. Continue Reading →
Former NHL All-Star Theo Fleury enthralled visitors as the headlining motivational speaker to help raise money for medical research of an extremely rare brain disease during a recent visit to the Ridgefield Playhouse on Rare Disease Day. Continue Reading →