The VDM Project is launching a YouTube channel for you to share your story with eye floaters.
This is the chance for the community to let researchers and other professionals understand how VDM affects a person day-to-day, from a personal perspective.
In addition, we hope these videos can provide a positive message of hope for the community – and give advice to sufferers about the best way to cope with the condition.
The videos will remain anonymous will only be used for this purpose in the VDM Project. You do not need to share your name or location or any other personal details. We will not gather any personal information or share this content anywhere else. We just hope to gather many testimonials to demonstrate the reality of this condition.
Disclaimer “The information provided here in is general and not specific to any given individual. The availability of this information on the VDMresearch.org website does not constitute individual medical advice. Visitors to this website and subscribers to the VDMresearch.org project/movement should not construe the available information as individual medical advice, but rather should consult a physician for evaluation and care. VDMresearch.org and VMR Research Foundation assume no responsibility or liability for the use of the information provided on the VDMresearch.org platform with respect to individual medical care.”
“Subscription/membership fees are collected for the purposes of supporting education and research by VDMresearch.org and the VMR Research Foundation. All materials that appear on VDMresearch.org website are in the public domain and are accessible via various other routes. As a service to VDMresearch.org subscriber members, interviews and publications are organized in convenient resource centers. Subscription fees are paid only to support research. The convenience of organized resource centers is provided as a courtesy to subscribed members of VDMresearch.org.