
7. The apple doesn't fall far from the tree - Emma Rennison's children both have her genetic condition Multiple Epiphyseal Dysplasia (MED)
Emma Rennison chats with host Lisa McKelvey about the difficulties her mum went through with getting medical assistance for what was originally thought to be hip dysplasia for herself as a child. Then years later, as a mother, Emma sits in medical appointments and by her childrens bedsides, while they have extensive orthopedic conditions as well.
Episode 7: The apple doesn't fall far from the tree
Emma Rennison's children both have her genetic condition Multiple Epiphyseal Dysplasia (MED)
Listen to Emma's powerful story about experiencing MED both as a patient and as a parent, and how genetic conditions can shape family bonds across generations.
About This Episode
Emma Rennison chats with host Lisa McKelvey about the difficulties her mum went through with getting medical assistance for what was originally thought to be hip dysplasia for herself as a child. Then years later, as a mother, Emma sits in medical appointments and by her childrens bedsides, while they have extensive orthopedic conditions as well. The Rennisons now know they have Multiple Epiphyseal Dysplasia (MED), a genetic skeletal disorder that affects the growth of bones, particularly at the ends of long bones.
Emma shares her unique perspective of having experienced MED both as a patient and as a parent of children with the same condition. She discusses the challenges of diagnosis, the physical limitations, and the emotional impact of watching her children face similar struggles to those she experienced growing up.
The conversation explores the complexities of genetic conditions, the advances in medical understanding and treatment over generations, and the special bond that forms when parent and child share a rare condition. Emma offers valuable insights for other families navigating hereditary health challenges and the healthcare system.
This episode highlights the importance of genetic counseling, early intervention, and building a supportive medical team who understands the nuances of rare conditions that affect multiple family members.
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