We received our diagnosis in 2010 and at that time we were completely unaware of what Fragile X was or how we could help two of our children that have the full mutation. A couple clicks later and I found the National Fragile X Foundation and I am so glad I did. We have received non-stop support and encouragement along with information on valuable resources that we have been able to utilize for our children. In 2014 we took on a more active role and are helping to raise awareness in our own community and reaching out to our community members who have received this diagnosis. Without the NFXF we would be lost on this journey, but thanks to their support we have a plan and a goal in sight.
Without the National Fragile X Foundation, I can't imagine where we would be today. I've become connected with so many families who understand and live lives like ours. From day to day tips, to research participation to advocacy and awareness, the National Fragile X Foundation truly does it all and is always here for everyone.
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