
Disability and Loneliness
Over half of disabled people report feeling lonely. I am one of them. I left the work world in 2012 on disability. My condition continues to deteriorate and keeps me away from social interactions (pre-COVID 19), and family gatherings. Since COVID 19, things are worse. Totally quarantined due to a lowered immune system, my outings consist of only those pertaining to medical visits which are necessary and can’t be done via telehealth.
What friends I had have disappeared from my life. My current life revolves around the family members inside of my home. I miss out on anything fun or stimulating and if I could I probably wouldn’t enjoy myself for long. My stamina is low, and my pain levels are high. I know I am not alone. I would like to find a way to communicate with others with the same problems, but the online forums seem lonely as well as typing on a screen to a faceless “other person” seems fruitless. I don’t think I’d like it as much as I feel I would some days, and fear I’d start and never go back. The connections are too meaningless and most people only want to complain. I do enough of that myself.
Lost friendships are a painful reminder of what my illness has cost. It hurts to feel lonely. Creating a blog that no one cares to read-only makes me feel lonelier. I know there are ways to combat loneliness. I can increase family ties or find new friends. I deserve to remain connected to those I love. By reaching out, thinking ahead, and recognizing my needs, perhaps I can find happiness and a greater sense of social connection again.
Join My Newsletter! It's Free!
Join my mailing list to receive the latest news and updates in my newsletter. Don't miss out! You may unsubscribe at any time.
You have Successfully Subscribed!
Your personal information will only be used for the express intent of sending you the monthly newsletter of Kathryn M. B. Johnson. Your privacy is important to me!