Living with MND Just diagnosed
Just diagnosed
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If you, a member of your family or a friend has recently been diagnosed with motor neurone disease it is likely that you are experiencing many confusing and confronting emotions. You may also be feeling overwhelmed by too much information or worried that you do not have enough information. Some people like to take time to think about what is going on before they want more information. Other people feel the need to talk to someone straight away. When hearing about a diagnosis of motor neurone disease, the only certainty is that everyone will react and respond in their own way. You might like to: Talk to a person who knows about motor neurone diseaseDo you have a question about motor neurone disease? Have you just found out that a friend or colleague has motor neurone disease and you don't know what to say? Are you thinking about attending a motor neurone disease information session but want to find out more before you make the decision about going? Phone the MND Info Line
Attend an information session about motor neurone disease for people who have been recently diagnosed with motor neurone disease, their family and friends. Information evenings for people who are newly diagnosed with MND ensure that help is available at a time when many questions need to be answered.
Read about motor neurone disease Do you need more information about living with motor neurone disease? MND NSW publishes booklets, information sheets and a quarterly member newsletter. Many are available free online for you to read, print or download
Find out about accessing services You can get support from the MND Association, MND Clinics, government agencies, local healthcare services and community services. You can find out how to access these services here
Contact us and ask for an information pack to be posted to you You can read the information pack when the time is right for you |
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