CATEGORIES: Faces of CMT - Jaxson

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Jaxson’s Shotguns & Guitars

by Estela Lugo | Oct 16, 2022 | 0 comments

Thank you to everyone who attended this fun event with music, shoes, and plenty of shotguns, for Jaxson’s Cure.

For the entire photo gallery follow this link.

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HNF sheds Light & Research Funding on Mitochondrial Diseases Linked to CMT

HNF sheds Light & Research Funding on Mitochondrial Diseases Linked to CMT

by Courtney | Jun 13, 2023 | Faces of CMT - Jaxson, Faces of CMT - Zach, Research, Research and Critical Trials | 0 Comments

Mitochondria are the powerhouses of our cells. Think of them as our body’s batteries. Mitochondrial disease causes these batteries to run low.

Cambridge-led natural history study identifies MTRFR/C12orf65 deficiency to improve diagnosis and therapy development

Cambridge-led natural history study identifies MTRFR/C12orf65 deficiency to improve diagnosis and therapy development

by Courtney | Apr 17, 2023 | CMT Type - MTRFR-C12orf65, Faces of CMT - Jaxson, Faces of CMT - Zach, University of Cambridge | 0 Comments

This research will potentially show a method that may be quicker and better at identifying...

Battersby Lab Donor Story: Fighter Moms Donate to Vital Research into Mitochondrial Diseases

Battersby Lab Donor Story: Fighter Moms Donate to Vital Research into Mitochondrial Diseases

by Estela Lugo | Oct 4, 2022 | CMT Type - MTRFR-C12orf65, Faces of CMT - Jaxson, Faces of CMT - Zach, Research, University of Helsinki | 1 Comment

Battersby Lab Donor Story Fighter Moms Donate to Vital Research into Mitochondrial Diseases

Jaxson’s Clay Shoot 2021

Jaxson’s Clay Shoot 2021

by Courtney | Oct 23, 2021 | CMT Type - MTRFR-C12orf65, Faces of CMT - Jaxson | 0 Comments

Jaxson’s Clay Shoot 2021 Image gallery

Jaxson’s Spooky Shoot 2020

Jaxson’s Spooky Shoot 2020

by Courtney | Nov 23, 2020 | CMT Type - MTRFR-C12orf65, Faces of CMT - Jaxson | 0 Comments

Thank you to everyone who attended this family-friendly event with costumes. Check out the photo gallery!

HNF tackles the hidden mysteries behind the genetic diagnosis of CMT mitochondrial diseases

HNF tackles the hidden mysteries behind the genetic diagnosis of CMT mitochondrial diseases

by Estela Lugo | Jan 4, 2020 | Faces of CMT - Jaxson, Faces of CMT - Zach, Research | 0 Comments

C12orf65 gene, a rare form of CMT also known as Leigh Syndrome is robbing young children of a normal life even beyond the classic CMT symptoms.

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