AGSD-UK Conference 2010

The Conference will be in central London on weekend of 20th-21st November. More details soon.

 

Walk over Wales... every step counts
2 July to 2 August 2010
Sponsored walk raising money for AGSD-UK. 210 miles. Details.

 

Walking with McArdle's - Wales
An opportunity to enjoy a week's walking holiday in Snowdonia and learn how best to cope with McArdle's. July 2011. Details.

 

 


 

AGSD-UK Conference 2010

The Conference will be in central London on weekend of 20th-21st November. More details soon.

 

Walk over Wales... every step counts
2 July to 2 August 2010
Sponsored walk raising money for AGSD-UK. 210 miles. Details.

 

Walking with McArdle's - Wales
An opportunity to enjoy a week's walking holiday in Snowdonia and learn how best to cope with McArdle's. July 2011. Details.

 

 

Glycogen Storage Disease Type V

Also known as McArdle disease or myophosphorylase deficiency.

McArdle disease is a rare metabolic disorder which causes muscle pain in everyday activities and exercise. If activity is prolonged despite the pain then muscle damage ensues with the risk of muscle breakdown and kidney failure.

Symptoms are usually apparent during the first decade of life but many people do not manage to obtain a diagnosis until the third or fourth decade. Later in life some people with McArdle disease experience fixed muscle weakness, possibly from cumulative muscle damage. It is important for those with McArdle disease to take regular aerobic exercise such as walking and avoid anaerobic activities such as lifting heavy weights.

 

About the disease

 

Exercise and McArdle Disease

 

Background information

 

Type V summary
Symptoms Muscle pain on everyday activity and exercise.
Fatigue. Fixed contractures with rhabdomyolysis.
Secondary symptoms Raised urate level. Possible muscle wasting.
Treatment No specific treatment. Maintain healthy diet,
control weight, take gentle aerobic exercise.
Outlook Good with gentle aerobic exercise and
avoidance of anaerobic activity.

Glycogen Storage Disease Type V

Also known as McArdle disease or myophosphorylase deficiency.

McArdle disease is a rare metabolic disorder which causes muscle pain in everyday activities and exercise. If activity is prolonged despite the pain then muscle damage ensues with the risk of muscle breakdown and kidney failure.

Symptoms are usually apparent during the first decade of life but many people do not manage to obtain a diagnosis until the third or fourth decade. Later in life some people with McArdle disease experience fixed muscle weakness, possibly from cumulative muscle damage. It is important for those with McArdle disease to take regular aerobic exercise such as walking and avoid anaerobic activities such as lifting heavy weights.

 

About the disease

 

Exercise and McArdle Disease

 

Background information

 

Type V summary
Symptoms Muscle pain on everyday activity and exercise.
Fatigue. Fixed contractures with rhabdomyolysis.
Secondary symptoms Raised urate level. Possible muscle wasting.
Treatment No specific treatment. Maintain healthy diet,
control weight, take gentle aerobic exercise.
Outlook Good with gentle aerobic exercise and
avoidance of anaerobic activity.