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For those of you with MS, do you rely on your doctor for information and what is current in research or do you find it on your own? Do you get a lot of support from your health care provider?
COMMUNITY LEADER
From my understanding of today's patients, no matter the medical condition, the majority of knowledge dxed patients have is from their own pursuit for information about their condition. In Australia the MS society is typically more individually supportive and also a valuable source of MS related information for patients and family.
Cheers....JJ
Cheers....JJ
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