Enzyme replacement therapy is an approved treatment strategy used in Pompe disease. Learn more about available ERTs and current research.
Because late-onset Pompe disease (LOPD) causes muscle weakness, patients may experience respiratory challenges and breathing difficulties.
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Learn about strategies to make your daily routine with late-onset Pompe disease easier and more manageable.
There are many things to consider before undergoing enzyme replacement therapy. Learn more about preparation, treatment, and aftercare here.
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Pompe disease is a genetic disorder caused by mutations inherited at conception from an individual's biological parents.
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There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
Because late-onset Pompe disease (LOPD) causes muscle weakness, patients may experience respiratory challenges and breathing difficulties.
There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
Pompe disease symptoms can vary depending on age of onset and disease type. Common symptoms include muscle weakness and breathing issues.
Pompe disease is a genetic disorder caused by mutations inherited at conception from an individual's biological parents.
Enzyme activity tests and genetic testing are used to diagnose Pompe. Learn more about diagnosing Pompe and what to expect after diagnosis.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
Pompe disease is a genetic disorder caused by mutations inherited at conception from an individual's biological parents.
Pompe disease carriers and patients have some reproductive options available to ensure their child does not inherit the genetic condition.
Learn about strategies to make your daily routine with late-onset Pompe disease easier and more manageable.
Pompe disease affects life expectancy according to the severity and progression of the symptoms, and is often fatal.
Learn about strategies to make your daily routine with late-onset Pompe disease easier and more manageable.
Pompe disease is caused by GAA gene mutations leading to the toxic buildup of glycogen inside cells, causing weakness and poor muscle tone.
There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
Gene therapy is currently being investigated for Pompe disease. Learn more about gene therapies in clinical and preclinical development.
Pompe disease treatment costs require financial plans for health insurance, social assistance programs, and special-needs trusts.
There are many things to consider before undergoing enzyme replacement therapy. Learn more about preparation, treatment, and aftercare here.
Gene therapy is currently being investigated for Pompe disease. Learn more about gene therapies in clinical and preclinical development.
Pompe disease carriers and patients have some reproductive options available to ensure their child does not inherit the genetic condition.
There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
Living with Pompe disease means lifelong enzyme replacement therapy, healthcare specialists, and adaptations to daily life.
There are many things to consider before undergoing enzyme replacement therapy. Learn more about preparation, treatment, and aftercare here.
There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
April is National Parkinson's Awareness Month, a time dedicated to increasing understanding and
Setting up a healthcare team for late-onset Pompe disease (LOPD) involves connecting with medical specialists and therapists.
Living with Pompe disease means lifelong enzyme replacement therapy, healthcare specialists, and adaptations to daily life.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
While ERT is the only treatment option currently approved for Pompe, enzyme stabilizers are being investigated as a potential additional treatment.
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There is no cure for Pompe disease, but some treatments can slow its progression. Learn more about ERT and other supportive therapies.
Learn about strategies to make your daily routine with late-onset Pompe disease easier and more manageable.
Pombiliti + Opfolda (cipaglucosidase alfa/miglustat) is an approved treatment for adults with late-onset Pompe disease.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
Gene therapy is currently being investigated for Pompe disease. Learn more about gene therapies in clinical and preclinical development.
Learn about strategies to make your daily routine with late-onset Pompe disease easier and more manageable.
Pompe disease is a genetic disorder caused by mutations inherited at conception from an individual's biological parents.
Late-onset Pompe disease is an inherited disorder that leads to muscle weakness, breathing difficulties, and reduced life expectancy.
A number of adaptive devices are available to help maintain quality of life for people living with Pompe disease. Learn more about them here.
Coping with fatigue in late-onset Pompe disease includes using assistive devices, getting adequate sleep, exercise, nutrition, and support.
