Best Practices Involves Multi-Center Cooperation for MD Care
by |
In this video from Muscular Dystrophy UK, patients, caregivers and medical professionals talk about some of the best practices that should be adopted when it comes to the treatment and management of muscle-wasting diseases such as muscular dystrophy (MD) and spinal muscular atrophy (SMA). They explain how many different departments need to work together to offer a care package for patients and their caregivers.
MORE: This animated video explains Duchenne muscular dystrophy to children
The approach to care is multi-centered and requires geneticists, nutritionists, nurses, doctors, physical therapists, occupational therapists and support groups to come together to offer families the best care possible.
In addition, participating in research and clinical trials is important to help advance treatments in this field and to work towards finding cures for neuromuscular diseases.
MORE: Five tips for emotionally coping with Duchenne muscular dystrophy
Muscular Dystrophy News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
About the Author
