You are not alone! FTD is a rare disease, so it may be unlikely that you will meet other teens who have a parent or other relative with it.
These videos have been made and submitted by teens who know what it’s like. They aren’t professionally done and may not have high technical production qualities, but the courage and generosity of the speakers make them priceless.
If you would like to create a video and share your experience with others visit Contribute Content or send an email to [email protected]