Lifemoves - a peer support program for people with MS

Letter of invitation for Lifemoves (a peer support program) for MS
The rehabilitation department at the Royal Melbourne Hospital is working on a project that looks at the effectiveness of a peer support program called LifeMoves.
This program offers an opportunity for participants to support each other, listen and share strategies and has been offered at the Royal Melbourne Hospital since 2002.
Each program involves attending a weekly 2 hour session (with rest breaks) for 8 weeks (We recommend a minimal attendance of 4 weeks). Group members decide the issues to discuss and topics may include “coming to terms with the change” and “dealing with emotions”. There will be up to 10 people in each session, all of whom will have MS and two trained facilitators who will also have neurological conditions (generally at least one facilitator will have MS). Sessions will be held either in Blackburn or at the Royal Melbourne Hospital, Royal Park Campus (venue to be determined depending on which venue is more accessible to participants) and will commence on the 2nd of June 2010.
If you are interested in attending the peer support program, please return the attached form either by mail or by fax. I will also contact you by phone to answer any queries. I look forward to hearing back from you.
With regards,
Dr. Louisa Ng MB ChB FAFRM (RACP)
Rehabilitation Specialist. Tel: (03) 83872000 E-mail: Louisa.ng@mh.org.au
Dr. Louisa Ng
Rehabilitation Specialist
Royal Melbourne Hospital, Royal Park Campus
Poplar Road,
Parkville 3052
Fax: (03) 83872222
Under the dotted line can be copied and pasted into your email client so it can be filled out and sent to Dr. Ng
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Dear Dr. Ng,
I would like to hear more about the Multiple Sclerosis LifeMoves program.
Name:
Date:
Contact details:
Address:
Telephone number:
Disclaimer please read!
Disclaimer please read!
Please Note: Any advice given on OzMS must not be taken as medical advice, it's merely advice given by members from their own experiences of living with Multiple Sclerosis. Always check with your GP or Neurologist or other medical professionals, it's the smart thing to do and only logical! If you have something to contribute please do so, everybody has something to offer.

