Yesterday was our first Buddy Walk. It was really a short walk as an excuse to get people together. I loved being in a place where there so many people with DS and those that loved them. I've talked to a few family members but this outpouring support for the whole community was great to see. I almost cried a few times when I saw the following shirts and when I really thought about what was going on there.
Love doesn't count chromosomes
Friends don't count chromosomes
My daughter rocks her extra chromosome
A few people talked to us and were really nice. They gave me hope that Russell could lead a wonderful life. I know he can, I just have to overcome my initial thoughts and get the truth of what is possible for him ingrained in my head.
There were booths from a pediatric dentist to Young Life. The dentist said people with DS can have a lot of oral health problems. His daughter has DS too. YL has a ministry just for those with special needs. How great is that? The local group is at the high school nearby in Shoreline.
Next year, I think I'll get more involved, maybe volunteer and/or get more people to join us.
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