Searching for a cure, Improving lives

Accident and Emergency Pack

 

Action Duchenne developed the Emergency pack for patients living with Duchenne, in partnership with Professor Kate Bushby and Dr Tracey Willis , from the Centre for Life in Newcastle.

 

Why is the pack necessary?

 

  • You are likely to know more about Duchenne than the doctors in the emergency room.
  • Most people living with Duchenne muscular dystrophy (DMD) never need to visit an emergency department, however if someone with Duchenne is unwell and needs to go to hospital this file contains vital information that you can pass on to the emergency doctors.
  • The pack contains information on the different areas of care, such as respiratory and cardiovascular care, gastrointestinal problems specific to Duchenne, fracture care and appropriate anesthesia and surgery management.
  • Recent  test results such as FVC (breathing muscle strength) and LVEF (heart function) along with everyday medications should be updated regularly. This gives emergency doctors information about your son’s normal status.
  • Chronic steroid use needs to be made clear including how long your son has been taking steroids and if he has missed a dose.
  • Boys with Duchenne are more at risk of broken bones – if a break occurs in an ambulatory boy then walking can become compromised if not delt with properly; surgery is often a better option than casting.
  • Information about giving oxygen therapy in Duchenne patients is very important.

 

You can now download the A and E pack from the following link http://duchenneemergency.co.uk/

 

This was made possible from the collaboration of all UK Duchenne Charites, and a grant from the QBE Foundation secured by the Duchenne Children’s Trust.

 

The A and E pack is also available for Android from the Google Play Store.

 

You can also download the link from the Apple store by searching for ‘Duchenne Accident and Emergency Pack’

 

To order a hard copy of the  Accident and Emergency pack please contact Angela Stringer – angela@actionduchenne.org or call the office on 0208 556 9955 .

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