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   Jonah'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.