Welcome!

Thank you for visiting our website. We hope you find this site educational and inspirational as we search for a cure for Fragile X Syndrome affecting our two sons, Graham and Reid Pierce.  

Please watch the video to get to know us; learn about Fragile X Syndrome and understand what you can do to help.

Visit our News & Events page to catch up on what we’ve been doing.

Thank you!

Michael & Kathan Pierce / Parents and Founders                                

 

Kathan's Korner

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Hello 2017!!
Hello 2017!!

Wow 2016. You made it reeeeeealllllly hard to like you. Like real hard. You took a cue from the end of 2015 when we received Graham’s Fragile X diagnosis and you kept the hits on coming. We were only 4 days in, just getting to know you, and you delivered the hardest news we’ve ever gotten: Reid had also tested positive for Fragile X. .

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IEPs & ABCs
IEPs & ABCs

“School day, school days.  Dear old Golden Rule days.”

Happy Fall everyone!  This time of year just flies by….we will blink and it will be the holidays!  I can’t believe that Graham has been in preschool for a month and a half! 

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Visiting Santa in June
Visiting Santa in June

Traveling with toddlers is not for the faint of heart and, when you add the challenges due to Fragile X that the boys face, one could easily talk themselves right out of going anywhere that’s not within walking distance! But we really try not to let these issues stop us.

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Hope Floats

“Out of difficulties grow miracles”

- Jean de La Bruyere

...

that glimmer of hope that we hold onto so dearly has gotten brighter thanks to the overwhelming support from all of you – our village. We have been so humbled by the outpouring of kindness, compassion and generosity from our families, friends and community.

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“Five hundred twenty-five thousand six hundred minutes"
“Five hundred twenty-five thousand six hundred minutes"

I’m in planning mode for my son Reid’s first birthday party and it has caused me do some reflecting on the past year.  Wow – what a year this has been for us.  

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