[2]
DES Action USA has created a DES Health History Survey. They have put it online so that DES-exposed individuals around the world can participate. The more surveys turned in, the better the possibility they have of identifying health trends.
To get to the survey go to: desaction.org [3]/
There is no membership requirement for any organization.They are looking for participation from individuals who believe they were exposed to DES. No actual proof is required because that is something most people cannot get. They are hoping to hear from DES Mothers, DES Daughters, DES Sons and DES Grandchildren.
Please share this survey with individuals within your DES communities via newsletters, email alerts, Facebook posts, and any way you deem best.
If language is a problem perhaps you could help by using a translation service like Babblefish or Google Translate.
On the website there is also a link to get a hard copy version of the questionnaire that can be printed. You can make copies and have them mailed in to the address at the bottom of the print version of the survey. If mailed, the survey must go to the researcher and not the DES Action office.
June 15th is the deadline for all surveys to be completed and returned.
Please don’t hesitate to ask if you have any questions.
While not a scientific study, the anecdotal information they gather may identify trends that need follow-up by other researchers.
DES Action USA
Website: www.desaction.org [4]
Facebook: http://on.fb.me/jcqIii [5]
Email: info@desaction.org [6]
Toll free: 800-337-9288