This is our son Hunter Wilhite, he is 9 years old. He was diagnosed with Fragile X at an early age, and we were devastated. After years of grieving and feeling sorry for ourselves, we [...]

Evyn is 9 and full of life. His favorite hobby is puzzles. He loves to swim and ride his bike and go to church. Life is a new adventure every day. Fragile X Syndrome is [...]

Zac is an amazing 13 year old who can do anything he sets his mind to. He loves so unconditionally it's amazing. He was diagnosed when he was a little over 3 years old after [...]

Ryan, 13 years old with FX, Autism and ADHD has a lot of challenges, including sensory, social awareness and other things that he really doesnt like to do. But Mom and Dad inspired him to [...]

I have three sons my two older sons are affected by FXS , Kyle is 14- he just graduated from middle school and will be attending our local high school next year. He is also [...]

Ben was a born entertainer. The idea of becoming a voice impressionist was suggested by many, but it wasn't until Ben's first business flopped, that he looked at the possibility seriously. He wrote down all [...]

I'm Chelsea Owens and I'm 19, soon to be 20 in September and I was diagnosed with the full mutation of FX when I was 7 years old. I'm not severely affected by it. I attended [...]

I was a young mother of a beautiful baby boy name Brendan. I started noticing at a young age Brendan was not the same as other kids. He was taking a lot of meltdowns a [...]

My brother, Albert Guerrero was born on January 23, 1943 and was a treasure to our family and everyone who knew him. He was not diagnosed with Fragile X until 1988. He was diagnosed with [...]

Lauren was born 6 February, 2007, our firstborn, and it would have been impossible to have been prouder parents. I cried when I went to the waiting room to tell my in-laws that they had [...]

Nathan is 26 and was diagnosed with Fragile X the same year the National FX Foundation was established. There was no internet or information at that time and no one (even most Dr.'s) had ever [...]

Nathan is 26 and was diagnosed with Fragile X the same year the National FX Foundation was established. There was no internet or information at that time and no one (even most Dr.'s) had ever [...]

Jack was diagnosed with FXS a little over ten years ago when he was just shy of his second birthday. The first signal that something was up was his lack of talking. He still can't [...]

My son, Ryan, who will be 4 July 26, was diagnosed with Fragile X Syndrome in October 2009. Ryan is full of energy and life. Every day is full of smiles and laughter and everyone who [...]

My brother Zachary loves is 22.  He loves swinging outside when the Mississippi weather isn't too hot.  He watches vintage cartoons, listens to country music, and enjoys being in control of every TV in the [...]