Summary “so far”

This blog is already almost 2 years old!

2020 was one of the most confusing years yet.
Covid19 and its fallout have changed everything forever. Lots of us are scrambling in so many ways just to get from day to day. We know we are not alone in this.

Sorting my autism and finding ways to compensate or accommodate my neurological struggles has continued to be helpful.
Old painful memories are seen in a new understanding and finally put to rest. New ways are being learned, how to do things differently to make my every day life easier. I am having more insight and understanding of others and seeing how my own autism has worked and is still working in my life.
Self forgiveness and healing of old emotional wounds is in there too.

My goals to find and reach local undiagnosed autistic elders has failed miserably.
In our area there are few medical resources, let alone psychologists or therapists. My search for diagnosis showed me how few there were. I guess that is understandable because our area is so rural and such low population. Covid 19 set in, about the time I began my “awareness campaign”.
I began to contact local agencies, places that serve the elderly, the mentally ill, the homeless, the needy, medical/psychological groups, the local newspaper, substance abuse recovery, shelters for homeless or abused folks… I do not do well on the phone, so I generated an “autistic elders” email and began emailing these groups. I probably sent out 50 carefully worded emails. I got not even one response.

I wondered if there was anybody in these offices to sort emails. My email name might have backfired and never been opened due to the name and people’s thinking I was spamming to ask for donations. I hope to contact radio and tv stations next.

I was able to present a “webinar” through the local college which drew only 3 interested new people but at least as many supporting me through friendship. It was not recorded or saved for the internet. I am learning what works. I may take out classified ads in the local paper or on the radio. I have very few funds available for advertising, being a retired person with no income.

I am steadily gaining followers here, which is very gratifying since I am not attempting to self promote. So glad you found me and are here with me! I am grateful for all your messages of support and your interest, and hope you will share when possible, and hope that insights I have written have helped. If you have read some of the blog, you know nothing I have said is in copyright and that I want you to share freely anything I have said that helps!
Just don’t use my words as your own, OK?
Knowing each of us is different in so many ways, I do realize there will be “if’s, ands, and Yeah-buts” regarding any suggestions or thoughts I post here. I find that interesting too!

I have no idea what the future will bring. It is difficult to figure out what one person can do to make a difference for others. “think globally, act locally” was something I took to heart.
I can not change the world, but I can keep trying to find others in my own area and offer insights and suggestions to help the unsuspecting, curious, newly diagnosed older adults right here where I live. I know what a difference finding out about my autism has made in my life. I want others to experience that too!
As always, I will keep you posted.
Thanks so very much for your interest and your support. ❤ I am truly grateful!
Sending best wishes for a better 2021. Stay safe, self care always first! ❤

The Lost Generations

Since figuring out my autism, I have spent countless hours reading scientific papers, autism websites, personal blogs, and also I have joined a few online autism forums. One of these is especially for older people who have gone undiagnosed until recently. For those of us to finally learn we have autism, there is shock, relief, and a whole array of reactions. Many of us seem to go through the stages of grief. Denial, bargaining, anger, depression/sadness, and acceptance… back and forth. It is so wonderful to have the understanding and appreciation of others who have also experienced so many similar things.

I have been fortunate to get advice, insights, education and counsel from the members of the online group. Most precious to me is to know I am not alone, that i have a neurological condition which makes it much more difficult for me to navigate my world, especially socially and emotionally. I am so blessed to have the internet. I can communicate with ease and not be confused by body posture, eye contact, facial expression, tone of voice…not having people put off by my own oddness and appearance. Most of the people I communicate with are very direct without guile or manipulative behavior. What they say is for the most part what they mean. All of us grew up in a time where nobody knew about autism. We are able to share experiences and understand each others’ frustrations, concerns, struggles of understanding and coping, and share strategies to overcome the many ways in which our autism gives us trouble. Simply a miracle which could not happen without the internet.

What about those who went before? My mother was born in 1929, a child of the depression and in poverty. She too had autism, although I did not figure that out until I learned of my own autism. People with autism in earlier generations were the street people, the crazy uncle , the bachelor brother, the hermit, or the local cat lady. My mother’s family called her a simpleton, or said she was simple.

Autistic people in earlier generations were the quirky professors or music teachers, or the obsessive archeologist or scientist. They were manual laborers, odd job people, those assigned to simple back room tasks in domestic or industrial, or farming roles. They were folks in the poor house and housed in institutions because so many of their behaviors were not understood, and were assigned to severe psychiatric disorders. Originally autism was thought to be a form of schizophrenia.

Autism has always been with us. Statistics show we are much more prone to anxiety and depression, although that is not considered diagnostic of autism. Statistics also show our lifespans are considerably shorter than average.

What of those in nursing homes and institutions being medicated and labeled as intractable, hopeless, confrontational, combative, etc? My mother’s experience in nursing care could have been much better if we had known of her autism and asked for accommodations for her care. So many of the ways she was approached by staff and how she reacted to them could have been helped by simple understanding. I may talk of this more in another blog. It makes me quite emotional to think of how she suffered and how helpless I was to make her life better.

There are thousands of undiagnosed adults who have found their own way through life, never understanding that they had a condition that made everything in life so much more difficult, feeling like a failure, lonely because they don’t know how to reach out, frequently working low paid jobs or not working at all because of the social hurdles to overcome in society in order to perform even the most menial labor. How much better it could be to understand, to learn what has happened to oneself, and to know it was not your personal failings or lack of character which left one full of frustration, anger, sadness, and shame.

How much better to learn to cope in better ways, to learn to communicate effectively. How wonderful to have those around you understand your upset at sudden touch, loud sounds, flickering lights, sudden demands to change whatever you are doing to something else. How freeing to escape demands to sit in groups in classes or craft groups or social tea parties and the like when it is all overwhelming and difficult to deal with.

I started this blog hoping to help older people find and recognize themselves if they are autistic. My own personal discovery of my autism has led to final understanding of so much emotional pain, so many fears and anxieties which developed because I did not understand I had autism, and how it affected everything in my life. 65 years of emotional pain, deep anxiety and depression.

Pain has for the most part dissipated now that I understand what happened, and how . I will always wonder what might have been, but of course that is all speculation. Reality is where i spend most of my time, not fantasy.

Perhaps you have somebody you care about, even care for in a medical situation, nursing home, home care, or maybe it is the odd duck in church or a co worker at your place of business. We are in all walks of life from the greatest to the smallest. What a relief to finally know and understand, and to learn that you are not alone, that there are others like you, and for those in care- that people caring for you will try to make your struggles a little less severe, help keep you from anxiety and depression, and to feel finally, understood.