Hi my favorite readers! Recently, something came to my attention that I believe is worthy of sharing with everyone. It applies to public misconceptions. The topic is living with double vision. I started experiencing double vision as a result of a head injury I sustained almost 40 years ago.
Years ago I learned to not discuss certain things about myself until I knew someone rather well. One topic in particular was double vision. In medical terms it’s known as strabismus (â€œlazy eyeâ€) which results in diplopia. I found that whenever I talked about it with â€œthe general publicâ€, jokes were everywhere. And…all types of misconceptions existed.
Popular songs used double vision as a sign of being so in love you â€œcouldn’t see straight.â€ As an example that immediately comes to mind…Foreigner does one song, I believe it’s titled â€œDouble Vision.â€
Movies have regularly depicted this condition as entertainment. â€œDouble Visionâ€ is used to define looking at twins, having a fungus taking over an evil mind and other depictions.
In real life, there’s nothing funny about living with double vision. Period. As much as I believe in the importance of finding humor in every situation, when someone finds out I have double vision and then asks me (while laughing) how many of them I can see…I go along with it at first. Then, if they ask again …it’s not funny. My eyes have to work to focus on anything. Sometimes it can be tiring. It can be frustrating. I can feel it. This applies even with my prism.
Depending upon the severity, double vision can result in loss of balance, nausea, headaches, mental confusion and other ailments. What’s funny about that?
Anyways, thank you for listening to my rant. I only wish the general public was more understanding about living with double vision. Those living with vision concerns completely understand. All I can do is spread the word to hopefully increase awareness among the misinformed.
Find interesting? Kindly share…Thanks!
AUTHOR NOTE: Booktoots’ Healing helps total knee replacement patients find support throughout recuperation and beyond. Its mission is for patients to understand they are not alone in their ordeal with either a tkr or other physicality concerns. The site is owned and operated by Marie Buckner, a published author and tkr patient who has been living with various physicalities for over 30+ years. She enjoys sharing her experiences to help others going through the same thing.