awesome

people's

party

awesome people's party for down syndrome research

a 501c3

WE'VE POSTPONED DUE TO: COVID-19.

next event coming soon

MY STORY

Our daughter was born full term in 2010 with her fraternal twin brother.  All of the prenatal tests came back normal.  In the delivery room, the doctors asked me if I knew anything about Down Syndrome, and I was immediately caught off guard.  The room seemed so quiet that I could hear a pin drop, and time appeared to be standing still.  I felt as though I was unprepared for a special needs child, so I began researching Down Syndrome.  I found that most of the research was outdated and archaic.  Being that I am a can-do person, most of the research was depressing and not uplifting at all.  That's when I stumbled on to the LuMind Foundation's website.  The information posted there explained the abilities, strengths and positives of Down Syndrome.  After I made it my mission to learn all about Down Syndrome, I felt I should help to raise awareness and funds for Down Syndrome research through the LuMind Foundation.

 
 

awesome people's party for down syndrome research

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