Peyton Grace
Peyton is our smart and joyful daughter who is full of spunk and a ton of fun. She brings happiness to everyone that is lucky enough to know her. All of these things trump her DDX3X diagnosis.
Peyton has difficulty with every aspect of her development as well as 3 types of seizures, extreme sleep difficulties and struggles to regulate her body temperature. She also does not process pain as intensely as others. With a lot of hard work, Peyton has made HUGE developmental progress thru OT, PT, DT, ST and developmental preschool. She also has gained seizure control thru the ketogenic diet and AEDs. Everyday, she does something that amazes us and we have so much hope for what her future holds!
Receiving the DDX3X diagnosis has brought us a lot of mixed emotions, but the knowledge and support shared from the other DDX3X families has been wonderful.
Braylee
Braylee was born February 2, 2014. Pregnancy was normal, but she decided to make her appearance at 36 weeks. She spent 3 weeks in the NICU due to failure to thrive, low blood sugar, breathing abnormalities and two different CHDs.
Lena
We finally got her diagnosis in November 2015. We have since become part of an amazing group of families and caretakers. Lena recently celebrated her 2nd birthday by learning how to crawl!
Kate
Kate is globally developmentally delayed, non-verbal and has autistic characteristics. She attends school in a severe/profound program where she continues to make slow but steady progress.
Donate
Help further our efforts to find a cure for DDX3X Syndrome, and support those affected by it.
DonateRegistry
Register today to help expand what we know about DDX3X Syndrome and stay connected to our community.
Registry