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Seven-year-old Jack Laidlaw, the oldest of three boys, is upbeat and friendly to everyone he meets, according to his parents, Anna and Richard Laidlaw. But Jack faces challenges due to a rare disorder he cannot yet comprehend. His parents are determined to remain hopeful and create a better future for him despite his diagnosis of hereditary spastic paraplegia type 4 (SPG4).
🎧 Listen and subscribe to all episodes of Rare Diseases, Real Storie: umassmed.edu/rarediseasesrealstories
đź’ś Learn more about the Laidlaw family and their efforts to support SPG4 research.
BluGenes
SPG4 research and treatment for Jack
Additional information about Jack
đź’ś To learn more about hereditary spastic paraplegia, patient advocacy and research, visit the following resources:
UMass Chan Medical School
Boston Children's Hospital, Spastic Paraplegia – Centers of Excellence Research Network
Cure SPG4 Foundation
Spastic Paraplegia Foundation, Inc.
Mauray Koduri Foundation
The Lilly Blair Foundation
đź”— Share Jack's story using the following hashtags: #RareDiseasesRealStories, #RareDiseases, #podcast
Interested in learning more about gene therapy research? Email us at: [email protected]
By UMass Chan Medical School5
55 ratings
Seven-year-old Jack Laidlaw, the oldest of three boys, is upbeat and friendly to everyone he meets, according to his parents, Anna and Richard Laidlaw. But Jack faces challenges due to a rare disorder he cannot yet comprehend. His parents are determined to remain hopeful and create a better future for him despite his diagnosis of hereditary spastic paraplegia type 4 (SPG4).
🎧 Listen and subscribe to all episodes of Rare Diseases, Real Storie: umassmed.edu/rarediseasesrealstories
đź’ś Learn more about the Laidlaw family and their efforts to support SPG4 research.
BluGenes
SPG4 research and treatment for Jack
Additional information about Jack
đź’ś To learn more about hereditary spastic paraplegia, patient advocacy and research, visit the following resources:
UMass Chan Medical School
Boston Children's Hospital, Spastic Paraplegia – Centers of Excellence Research Network
Cure SPG4 Foundation
Spastic Paraplegia Foundation, Inc.
Mauray Koduri Foundation
The Lilly Blair Foundation
đź”— Share Jack's story using the following hashtags: #RareDiseasesRealStories, #RareDiseases, #podcast
Interested in learning more about gene therapy research? Email us at: [email protected]

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