Cindy and Jenni's Story   Bernadette's Story: Cloacal Exstrophy
Heather's Story: Infertility   Joshua's Story: Limb-Body Wall Complex
Francis' Story: Undiagnosed   Emiline' Story: Fetal-Hydrops
A Family Faces Dwarfism   Kseniya's Story: Amniotic Band Syndrome

Gabriella's Story: Walker Warburg Syndrome


Andrew's Story: Early Loss


Angelica's Story: Chiari 111


Tristan's Story: Thantaphoric Dysplasia

Karinne's Story: Acrania   High E Antibody
Aaron's Story: Early Birth   Ben's Story: SMA
Rose's Story: Agenesis of the Corpus Callosum   Carly's Story:
Angelman Syndrome
A Letter tp Parents facing Agenesis of the Corpus Callosum   Kellen's Story:
Epidermolysis Bullosa
Jonah's Story   Von's Story
Gavin's Story   Raphael's Story


The support, information and encouragement provided by the PPFL parents is not meant to take the place of medical advice by a medical professional. Any specific questions about care should be directed to a health care professional familiar with the situation.