|
Donate Contact
us Home |
 |
|
|
 |
About
the Support Group |
 |
How
to join |
 |
Newsletters |
 |
Annual
Report |
 |
Information
|
 |
Meetings |
 |
Research |
 |
Fundraising |
 |
Donations |
 |
Community |
|
The
Myositis Support Group is a UK charity providing
advice and support to individuals and their families affected by
Dermatomyositis, Polymyositis, Inclusion Body Myositis and Juvenile
Dermatomyositis. We also raise funds and promote medical research to improve the diagnosis, treatment, management and understanding of these rare illnesses. » Read more about the Support Group. |
|||
|
|||
Latest
News |
|||
| |
MEETINGS AGM & mini-conference - Sunday 13th July. We hope you enjoyed the day. More»  RESEARCH We have awarded the Letitia Rawson Fellowship to Dr Zoe Betteridge to continue her research at Bath University into novel antibodies associated with myositis. read more about their work in the research and information pages. More »  NEWSLETTER UPDATE Newsletter 64 and Annual Review 2007-2008 now online We would love to hear of your "Good News" stories for the Newsletter. Have you just got married, celebrated the birth of a baby, has your child returned to school full time, have you passed your driving test, graduated, gone back to work, off all medication and discharged from hospital? Please send your story to the office of email les@myositis.org.uk and if you wish to include a photo that would be great. For it is this information that makes the Newsletter interesting reading. More »  Latest Fundraising NewsPlease visit the Just Giving website for details on our fundraisers www.justgiving.com/myositis. Tracie and Chris Dunn are taking part in a 10K from Warwick to Kenilworth Castle. Lynne Nazer is on a sponsored diet. Shelly Egan is "Going Blue". More » CHRISTMAS CARDS The 2008 Christmas card order form is now on line -More » |
||
|
|||
|
||
