Please follow the link and respond to the survey from the MS Society.
Some of the issues you may want to address are:
- your perception of whether they have been acting in the best interests of persons with MS
- the quality of the "educational information" they have provided regarding CCSVI
- the amount of support you have been given with respect to desired (non pharma) treatments and / or follow up medical care
-your level of satisfaction with how they have influenced the govenment with respect to health care for persons with MS
-how the society might act in the best interest of persons with MS in the future.
Here's the link:http://www.surveymonkey.com/s/Listen2012