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
Jackson's Story   Von's Story
Gavin'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.