After 5 years of being very ill and having to give up work I am finally with some Drs who are listening. Slowly getting diagnosis. Was diagnosed with connective tissue disease last summer. Now I am being tested for myotisis. After reading about the condition symtoms certainly fit.
Anyone have any information that would be useful on this long journey?
Thank you in advance.
Written by
Muff20
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Head over to Facebook myositis Uk community forum, bit more active than here , load of info very lovely group of mixed ages men , women and children ( their parents). Good luck
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Hello to every sufferer fighting his/her way back to a kind of normality
Inclusion myositis conclusion 
How do you get a firm Mysiotis diagnosis? What scans will show affects on muscles? 
Diagnosed with Polymyostis 
