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Holly was born on 3/11/08 with Fragile X. I started keeping a daily journal when she began an experimental drug treatment through the UC Davis Mind Institute with Dr. Randi Hagerman. Holly recieved early intervention services. Thankfully she has only show very mild delays. I so enjoyed keeping her treatment journal, I decided to create a blog to chronicle our journey.
Mostly big and some little stuff related to Fragile X: grief, joy, work, marriage, community
Our blog. :)
A blog devoted to finding the answer to my daughter's disability. Fragile-X? Autism? Or just something we never heard of?
My blog about living life with FXS.
Brody and his service dog, Millo. Come join us in a day to day adventure with adopted "triplets"
This is blog about the everyday happenings with our son, Cale, who was just diagnosed with Fragile X Syndrome.
This site is to remind us that we were chosen to be the parents and family of a child with special needs, it didn't just happen. Because of that, we know we can handle whatever is thrown at us. We just need to remember to laugh along the way!
The true story of identical twins with Fragile X Syndrome, their unaffected big sister, and their loving and devoted mom & dad.
Lessons learned from my three children with fragile x and autism. I hope that sharing my lifes experiences will help another family out along the way.
This is news coming from the National Fragile X Foundation, including articles about Fragile X, local events, tips, and Foundation news
About "Our Life" mixed with our three children who all have Fragile X Syndrome. The funny, sweet and not so funny moments.
Musings of a mom with 2 fx kids, and one without fx, life with a diabetic kid, and a quilting hobby...just whatever else pops in my head.
Blog about the development and education of a girl with Fragile X from the perspective of a Speech Therapist Mom.
Life as "Me" in all my many roles...mother, teacher, police officer, equine therapist, adventure seeker... Come along and join the ride.
This blog is simple everyday stories about our family's joys and challenges associated with having a son with Fragile X and autism. The intent is to tell simple stories, with easy to understand facts weaved throughout, in an effort to help raise awareness among our family and friends. If anyone else is helped along the way, so be it.
Red Letter Living: Living the words of Christ out loud through all the ups and downs each day brings.
Our journey through parenthood with a curve ball thrown at us: Fragile X Syndrome.
I hope that by documenting our experience with FXS that maybe we'll be able to help others along their journey as well.
eXtraordinary - thoughts about life with fragile X.
We are the Strattons. Our oldest was adopted from Russia. Our middle son came to us as our foster child. It took two years and a big custody trial before his adoption was finalized. No plans to have biological children as I am a Fragile X carrier but then... surprise! Along came our youngest son who was diagnosed with Fragile X at two months old. The husband is a missionary pilot and I'm in charge of all things groundspeed. Here's our family journal of just what's going on down here on the ground!
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