Question about monocular enucleation and perception
Hi all,
I am looking to virtually connect with people who have experienced monocular enucleation and are open to learning about how their sensory perception may have changed over time. It's for a good cause that could help others with your condition. The goal is to better understand how people process what they see and hear, which could help improve knowledge and support for others with this condition.
If you are comfortable, feel free to DM me or comment and I can reach out privately with more info.
I have made a similar post about this and am re-posting in case anyone is still interested in this discussion.
Thanks!