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When someone in your family is diagnosed with Multiple System Atrophy (MSA) you may have lots of questions. If you are 11-17 years old and not sure how to find the answers you need, use this Web Hub to get you started.
If you have other questions or concerns about MSA and how it is affecting the person you know, you can contact the MSA Trust by phone or email. One of our MSA Health Care Specialists will get back in contact with you. Their contact details can be found by clicking here.
If you are younger than 11, take a look at our Activity Book for children.
We have taken every care to ensure the accuracy of the information contained in this publication. However, the information should not be used as a substitute for the advice from appropriately qualified professionals. Speak to your doctor, qualified health care professional or legal professional before taking any action. Please note that personal views and opinions expressed are not necessarily endorsed by the Trust. The resource is produced independently, is not influenced by sponsors and is free from endorsement. References for this resource are available by contacting support@msatrust.org.uk. Your feedback helps us ensure we are delivering information to the highest standard. If you have any comments or suggestions, please contact us at support@msatrust.org.uk.
