Tuesday, June 16, 2009
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This blog is dedicated to my daughter Kayla, who was diagnosed at birth with congenital myotonic dystrophy (cDM1). She spent 105 days in the neonatal ICU, 9 months on a ventilator with a tracheostomy and using a feeding tube. Her doctors did not expect her to live to see her first birthday but she lived 13 years and 8 months filled with amazing adventures. She loved defying the odds with love and care from her family, friends, therapists, teachers, and medical team. This is her story...
2 comments:
Your family album is our family album . . .Michelle was born with Myotonic Distrophy (DM 1) in 1975.
Kayla' & Michelle could have been sisters. Same face & hair.
Don't let the school system put road blocks in front of you.
Michelle went through Middle School and High School & 2 years of College. We demanded and pushed for Inclusion in all classes. She graduated with an IEP diploma. Our adventure continues. Good luck to you.
Thank you for making this website and sharing your story. It made me very emotional to watch the video and read about all you have been through as a family. We also have myotonic dystrophy in the family.
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