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.