Life During Covid

Today is the first time since Covid that I have made an entry on the web site. I want to share my experience in what I call life during Covid. When the virus first started and the stock market made a quick adjustment I thought the virus would last just a couple of months. As a person on the spectrum I have lived most of my life with fear and anxiety. I am very routine orientated by nature.
For the first 6 months of Covid I was very anxious because the rules were changing in the world and the places I often go to like retail stores and the coffee shop. Because I could not wear the standard mask issue due to anxiety issue, glasses fogging up, and breathing my own carbon back in, I purchased a face shield that sits on my neck called Z shield which helped me meet the needs of protection and society. I found myself in conflict with the so called mask police at times, being told I was not meeting the standard to enter an establishment. I would say that I have on the Z shield due to Asbergers and anxiety issues, but most of the time there was just no understanding. Our way or leave. I would get angry at first but as this wore on I just by limiting the number of places I went to. I just did online ordering for any needs I had. I found it frustrating with the coffee shop I went to. One day I can sit inside and now for the past 6 months have to sit outside in any kind of weather. The restaurants were different. Things need to be more consistent in my area of the country. I know a lot of it was driven because of the fear of lawsuits.
I stopped watching the news to keep my anxiety down, and my mood leveled out. My volunteer work just went to zero and the places made it so hard I was discouraged.
 I attend my Asberger support group on a weekly basis,12 step meeting several times a week, and various other seminars. I sometimes feel I am getting more done this way instead of driving all over town. To give me more to do I even joined several dating sites. For me, dating sites give me a chance to meet people I would normally not meet. This gave me the chance to practice some social skills with people. I was glad I was kind of isolated from meeting people to some degree in person.  When I tell a person that I have Aspergers they generally lose interest. I have not been on an airplane since this started because I could not sit for hours with the mask the airlines require you to use.
Yesterday I was in my small pharmacy checking on medication instead of driving an hour away with big crowds. They said they were doing testing giving the vaccine and would I be interested in it. I said yes and felt like I had 10 Christmas gifts. I wanted to pinch myself. I have felt like I have been in a prison cell for the last year.

A Late Diagnosis, Questions Answered, and Self-Acceptance

by Sam Farmer 

I can relate to a late in life diagnosis .  I still struggle in the dating world with acceptance from others and  do feel some low self esteem because to the reactions  I get from ladies.  I have a much better experience in being valued and accepted in my volunteer work.    I still struggle with fitting in society box on what is normal to do.  I try to honor the people that supported me over the years by being the best person I can. – Greg

As an adult living with a late autism spectrum diagnosis, I have come to view my life up to now as embodying three phases: partially informedenlightened, and paying it forward.

I refer to the first stage of my life as “partially informed” because I was aware of my learning disability but not of my spectrum profile. Better one than none, though the missing puzzle piece did not help matters. While living for 40 years in a partially informed state of mind, the degree of self-unawareness, compromised self-esteem, and all of the unanswered questions as to why I faced the challenges and adversity that I did arguably left me in a fog. I had no idea that I was as unaware as I actually was. I did not understand the meaning of self-esteem, much less understand that my own was not far from hitting rock bottom.