Just joined a forum specific to patients and family of MDS.
Hopefully connecting with others experiencing this will give insight to treatment, medications, side-effects, etc.
Definitely don't want information overload but other patient and family experiences will be helpful.
For anyone who also wants to use the forum, it can be found at http://www.mds-foundation.org/forums/ubbthreads.php?ubb=cfrm
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