
It was extremely uplifting to feel supported by the community. I felt like not only did we raise some money for 2 terribly underfunded diseases, we raised some awareness. Perhaps that is even more important? I know that some people ended up there for a fun NYE party and maybe didn't know or care about the why. But some of them left with a cute little boy's smile in their heads -- maybe even heard the words "SMA and Menkes" for the first time. I appreciated every person who came. Sometimes just "showing up" speaks VOLUMES to me. It shows you care and I loved seeing our supportive friends and family.
Thank you is not "good enough" to express how grateful we are to every person who gave of their time, money, services to make this event so successful. Specifically Trent and Carrie. for carrying out this vision into a reality.
I knew i should've written this right after the gala, but wanted to wait to get a better idea of the amount raised. Now i am afraid I don't have the right words to convey what a special night this was but I must not put this off any longer... please take a minute to read Baker's mom's journal recapping the evening...http://www.caringbridge.org/visit/bakerdemeyer/journal


Taysen is our 7 year old ray of sunshine living with Spinal Muscular Atrophy type 2. He has a spunk and zest for life like no other and inspires everyone he meets. He has a huge imagination and a great sense of humor...he feels it is his purpose to make people laugh. Taysen loves to drive his powerchair at speed 5, watch movies, play with his toy animals and eat junk food.
River is our 5 year old little sweetheart. He has a sensitive soul, patient and protective of his brother. He is a huge blessing to our family, always ready to give and recieve a hug. He is sometimes called "Running River" as he is always on the go! River likes to play outside where he swings, climbs and gets dirty. He loves books, watching "The Berenstain Bears", and cookies & hot chocolate




WOW! Your words were perfect! Thanks to everyone!
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