Rainbow Colored Glasses
Monday, July 29, 2024
Reality of Masking 072924
Thursday, June 27, 2024
Different Processing System 06272024
I had a long conversation this morning about my brain and how it works differently. It was a compliment not a criticism. It really helps balance my team and helps us be successful. In some areas it is amazing, In personal relationships and feelings, it is not.
Math is one area I have always thrived in. The rules stay the same. They are logically and even if you do
something a different way you can get the same result.
I am also very detailed oriented. I have to have a process set up and all the
details worked out in my brain before I can even focus on the big picture. This can be very annoying to some.
Luckily my brain works very fast on figuring out the steps
to things. The problems come in when I there
isn’t a concrete solution or I can’t explain my steps to someone else.
I have spent my whole life this way. And I treated all my relationships this
way. It does not work for most
people. For example, I worked very hard
to be the best mom so there were certain
steps in my brain that made me a good mother.
I kept them in the same school. I
let them do whatever activities or sports they wanted to do. I coached teams. I volunteered. We did fun activities.
Lately as my children have gotten older, they felt like they
didn’t matter. In my logic, every decision
I made from where we lived to where I worked was made off the premise of what
was the best decision for my children.
I did not do a good job of explaining it. I didn’t allow break time so in their minds I
didn’t care about them. It is the farthest
from the truth but their reality.
While dad could take them fishing or fix the breaks when
they wanted, I had to make sure homework was done and they were growing to
adults. That down fun time was limited.
I’ve also realized that many of the times there was no right
decision. Accepting that neurotypical
people can have different ideas of perfect is baffling to me. Having 6 kids I was trying to make happy,
also left me feeling like a failure.
I am still working on it and allowing their feelings to be
valid even when they are not supported by facts.
Memories is another area that drives me crazy. My brain is pretty photo memory. I keep text messages and emails. I document everything to a fault. So I really struggle when someone claims a
memory I know to be false. I’ve had to
teach myself to just let it go. I logically
know memory is a construct and trauma based.
But for me it isn’t. Life is
exactly what happened.
I’m constantly having to adjust and see others point of
views. While not feeling like anyone
else does the same for me.
But I’m trying.
Thursday, June 13, 2024
Wardrobe Change
Tuesday, June 11, 2024
Product Review: Flatsocks
Rarely do I find a product I can tolerate, let alone enjoy. As someone on the spectrum with fibromyalgia, my skin is a major sensory issue for me. If I could tolerate it, I would be barefoot all the time. Socks are horrible for me. The seam sits in the wrong spot, They get twisted or they simply aren't very soft after a few washings. Smell and temperature is also a sensory thing so for me it is typically a hard decision between options for foot wear.
I typically cannot wait for spring and summer so I can throw away the socks for a season. The older I get, the more comfortable my shoes have to be due to constant pain. By the end of season, I have worn out a couple pairs of nice, comfortable sandals simply from wearing them barefoot. Because I now have to go comfortable, that can be a hundred or so a pop.
Earlier this year, I saw an ad for Flatsocks somewhere. Yes they seem expensive but I figured I would give them a try. I must say it has been night and day. Very absorbent and easy to wash. I've washed about 8 times and there has only been minor color change.
I actually ended up buying to more pairs. I cannot feel them at all other than they feel like a normal tennis shoes.
I do not receive any promotional funding or incentives for this review. Nor do I receive any income from purchases. However, I always want to share things I find that work especially for someone with sensory issues. You can also find them on amazon.
Saturday, June 1, 2024
Spectrumy
Relationship Dumpster Fire
Relationships
as a woman on the spectrum has always been a war zone. I desire the
meaningful connections that everyone else does but have no clue how to achieve
them. For a long time, I defined sex as
love and forever. That has caused me
more pain than you can imagine. It took me
20 years to realize the difference and I still struggle.
I also have
the tendency to be too trusting and forgiving.
I assume everyone has good intentions but as we have all seen in the
dating nightmare that is the farthest thing from the truth.
In my 20s, I
had this dream of recreating the childhood I had so I would forgive anything to
be able to achieve it. I got pregnant
with my oldest son at 17. For me it was
a life changer. I immediately went from
young, rebellious, youth to what I defined as motherhood. My boyfriend at the time dumped me of
course. Even when I begged him to take
me back, he refused. I felt broken and ashamed.
I thought no one would ever want to be with me.
In order to
compensate, I “fell in love” with the first man that even showed an interest. It didn’t matter if we had nothing in common. He “loved” me so that’s all that
mattered. I instantly jumped into a
relationship. There were red flags of
course but I ignored them. I thought we
would be together forever so I went all in.
We got married. Had 2 more
children in 3 years. (Yes I had 3
children under 3 before I was 21.) I
worked my tail off. We bought a house at
21. Had the 2 car payments, and I
thought my dream was coming true. But
wanting something to be true did not make it true.
We struggled
the entire time. He still wanted to be a
20yr old hanging out with friends. I was
in 100% mom zone. Everything and
anything I did was focused on my children.
He’d disappear or not come home and I’d forgive him because creating
that family was most important. It literally
took being thrown a shake in my face to see the reality. He was still the same person he was when we
got together, multiple girlfriends and no responsibility. I tried a few more times, but it got to be
the point I could no longer handle so I got out.
This pattern
would continue. Red flags glaring and I would
stay in trying to make the dream come true.
I would give my all while the other person barely cared. While I’ve given up on the dream, those urges
are still there and I struggle to this day.
Sure this
could be the story of any woman’s life even if they were not on the spectrum but
I have found I attach those actions and feelings much stronger than neurotypicals. If I just made the right choice or worked
harder, someone would love me. I blamed myself
for every failure. The reality didn’t
matter because in my head even their bad actions were caused by me. I wasn’t good enough to deserve love and faithfulness.
This is
something I really have been working on.
But those communication barriers still make the dumpster fires
happen. I ask questions to understand,
the other person takes it as accusations or blaming. I give 100% and get frustrated when the other
person doesn’t do the same. I didn’t
value you myself unless I was in that committed relationship.
Now I am okay
with just being Jill
Friday, May 31, 2024
Late to the Game
As an 80s baby, Autism was barely discussed and definitely never was related to girls. It lead to many of my generation getting a late diagnosis. I personally was in my mid 30s before it was even considered that I may be on the autism spectrum let alone diagnosed. Once I got my diagnosis, it was a huge relief however in many ways I am glad I was not diagnosed younger.
I was always the weird kid. My mom used to love to tell about my prep
work for getting ready to attend school.
I was reading sentences at a very young age. Honestly I had to be around 2-3. I was so excited when I found out I was
attending school. My mom always used the
term “Nursery School” instead of Preschool.
So what did her early reading child do? Practice and memorize a majority
of Mother Gooses Nursey Rhymes for the entire summer before school
started. I was going to be ready to say
them all on day one from memory. It was
always laughed about as one of my quirky tendencies.
Before school started, we did the
traditional school clothes shopping. We
were pretty limited on resources. My mom got me a brown dress with buttons and
white flowers on the collar. I’m sure
she meant it for me to use for school picture day and first day of school. But I defined my school dress as my school
dress. I’m pretty sure I wore it 90% of
the days that first year and I had severe anxiety when it was not clean, even
refusing to go. I now know those were
meltdowns.
I was always the kid with my hand
held high in the air on any question the teacher had. I remember in detail the first time I gave a
wrong answer. It set me spinning for
the rest of the day and probably week.
The teacher asked what color light do we cross the street on. I raised my hand high and said “red because
it means stop.” My little brain could
not comprehend that it did not mean stop for all directions. Stop means stop so every car should stop
right?
I’m sure I have a hundred more
examples of how my spectrum brain worked.
I honesty had no clue that anyone else’s brain worked differently.
I grew up in a family that my brain
function was so different than everyone else’s that it really made me struggle.
I learn to mask at a very young age. My
mother and older sister were always the life of the party. They had a million friends and made new ones everywhere
they went. I was lucky if I had 1 or 2
friends. They could spend hours on the
phone. I had high anxiety and still do
if I have to make a phone call. I could
barely understand emotions in person.
You put someone on the phone and I was completely lost.
Emotions are another thing. I hate when individuals on the spectrum are
characterized as being emotionless robots.
I am the farthest from that. I
have emotions, big emotions. Sometimes
it seems like I feel them much harder and internalize them more than other
people. Teasing I hated because I took
whatever those words were very literally.
I’ve learned over the years to dampen it down but to this day things
that hurt and bother me, are not the same as other people. And I hurt other people by stating what in
my mind is just facts while others take it as offensive and rude. I still at times want to scream just say what
you mean.
Now I know masking is now seen as a
negative in some components of the autism community but for me it was a
requirement and how I was able to survive and thrive. It wasn’t something that was forced on me or
even encouraged. It was my way of
navigating this world I did not understand.
I had to figure out on my own how to be ‘normal’. I still fail at it regularly. I sometimes wonder if I would have mastered
the skill of masking so well if I was diagnosed younger. Blending into any crowd has been by gift and
failure.
Being a female, my collecting
traits seemed to be more socially acceptable.
Having 15 dolls was completely normal.
Collecting books and rereading them over and over again was normal. Now when memorizing the star chart and able
to label them all in the sky, was not as ‘normal’. My interests would ebb and flow but whatever
my focus was, it dominated every aspect of my life. During my basketball phase, I lived and
breathed stats for pros and college players.
I always picked the weird one as my favorite.
My grades were amazing. My social skills were horrible. I came home every single day completely wiped
out and emotional about something that should not have been a big deal. I did not understand why I didn’t get invited
places or why someone was mad at me. I
was miserable in a majority of interactions that were not education
related. I was blessed to be able to do
sports. That was something I could understand.
There were clear rules and guidelines to follow. And I was lucky enough to be skilled enough
to exceed in it.
So like I said I was in my mid 30’s
and even in the field of disability services before it was ever mentioned to me
that I might be on the spectrum from an amazing boss. I had been diagnosed with Anxiety Attacks in my
early 20s and PTSD from trauma. But
never was a different processing system even mentioned.
I can do forced eye contact under
most circumstances. I could smile and
pretend just enough to get by. I was
still high achieving in my employment life as well. I had romantic and friend relationships but
none lasted long. I held roles such as
PTO President or Soccer Coach without any issues.
I would have record level
achievements in my work life and then get called in for a reprimand over
something like I didn’t say hi enough in the hallways. I didn’t acknowledge the CEO when he walked
into a room. My tattoo showed when I was
serving food for a room full of 200 people.
I was offered uniforms when no one else wore them because of one issue
or another. In my mind, they met the
dress code so who cared. I was passed
over for promotions for others while doing their job and mine. I had a hard glass ceiling due to my social
skills only. All of which was extremely
frustrating for me.
It was another complaint that I was
rude that left me in tears with a very compassionate manager. I was explaining why I was upset and how I
felt it was so unfair. I just didn’t
know how these people wanted me to talk to them or ask them to do
something. That’s when she mentioned if
I had ever considered I was on the autism spectrum. It was like a light bulb for me.
I had been providing Employment
Services for individuals on the spectrum as well as other disabilities for over
5 years at this point. It never even
dawned on me that why I was amazing at my job is also why I was struggling
professionally. I could teach other all
those stupid masking rules for certain circumstances because I had lived it my
whole life. I just did not see it in
my own actions.
Put me in a room full of
professionals talking about my passion and I thrived. Put me in a hallway or breakroom, I crumbled
and felt defeated.
Getting the diagnosis has helped me
so much. I still don’t always tell
everyone but it helps me realize why the rules are so important to others. It makes me keep candy in my office, so I am
softened to others. It forces me to say
hi or at least let people know in advance that I may not see them and feel free
to interrupt me. I am more accepting of
myself and my flaws.
Now my personal life is a whole
other can of worms we will open in a later podcast.
I’m glad I now know why I’m
different. But I’m also glad I was
forced by default to figure out ways on my own to navigate this crazy
world.
I do wonder at times how my life
would have been different if I was diagnosed younger. It sure would have been nice to realize I was
not an alien but I wouldn’t for a second want to change who I am. My challenges made me a better human.
Reality of Masking 072924
I had a friend introduce me to a new group of people, "Jill loves and accepts everyone except labels." This statement has been ra...
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Welcome to Rainbow Colored Glasses. This is a unique prospective on navigating this world around us. I have been told my life is too cra...
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Relationships as a woman on the spectrum has always been a war zone. I desire the meaningful connections that everyone else does but have...
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I spent a lot of my life thinking I was broken and something was wrong with me. I was not diagnosed until well into adulthood. There is so...

