why we do what we do: my mother’s crone ceremony

ebcmp quilted banner

It’s been very emotional for me to reemerge from the darkness of lockdown to return to building community through music-making. In my conversations with folks, it becomes clear that a younger generation of families don’t know about some of the ways we connected before, and don’t necessarily remember many of the ways things were different then.

In going through my instrument collection to decide what to bring to my family music classes, I brought out the box that contained the EBCMP banner. For those who don’t know, EBCMP was the East Bay Community Music Project, the organization I founded in 2012 to cultivate community music-making opportunities for people of all ages, ethnicities, faiths, economic access, neurotypes, and abilities, and any other way one might sort people into categories. I now continue that work as imeetswe, for reasons I won’t cover here. But I believe at this point in history, part of my job as a facilitator and advocate is to remind people of what once was, and what is possible again, and this banner is a powerful reminder for me.

We used to meet on second and fourth Sundays, and at this particular time we were meeting in the multi-purpose room at Malcom X Elementary in Berkeley. My mother would often drive over from the Peninsula where she lives, and join us. She was usually the oldest person in attendance, just because not so many older folks would join us often, but she did. Our second gathering in August of 2014 coincided with my mother’s 70th birthday, so we planned a ceremony to honor her entry into the crone realm (which, whatever your association with the word might be, is an honor and a privilege, and an important place in the community).

We got together in the morning, and ate potluck breakfast. We had asked folks to bring pieces of colored fabric that could be torn or cut into strips, and some of us had taken some time in the morning to cut the many colors and textures of fabrics into strips. We sang some songs together as usual. Then, we had my mother sit in a chair in the middle of the space. As my mother sat in the middle, on her chair, each family in attendance, in turn, approached her (her name is Susan, or Grandma Sue), and gave her a kind reflection, and handed her a piece of the torn fabric. She had been instructed to tie the strips together as she was handed them. I don’t remember exactly how many families were in attendance, but there were enough that when each family had shared their kind reflections, she had a long, long rope of tied together fabric strips.

Then, as she held one end of the fabric, all the rest of us sang Que Sera Sera, a song that my mother loved (it was originally sung by Doris Day, and my mother was about 12 when it was on the radio, in a time when we were all connected by the songs that came over the radio).

My mother stood. We all sang, and wound the fabric around my mother, until she was all wrapped up in the kind reflections that folks had given her. And then, we unwound her, still singing, and then she walked around the families gathered and wound the fabric around the community, and it was long enough to encircle us a couple of times.

I wonder how many people remember that crone ceremony for my mom, or any crone ceremony for anyone’s mom, for that matter. She still remembers it, I’m sure, and I do too. For some, becoming a crone, or welcoming one into the community, is an important rite of passage–a recognition of having lived life fully, and of having a certain kind of wisdom that only comes from living a long time, and the importance of that wisdom to the community.

And what, then, was done with the fabric? Was it discarded? If you know my mom, you are fairly certain it wasn’t discarded. No, my mom proceeded, over the course of several months, (when she was also consumed with the many sewing and knitting and crocheting projects that she’s always consumed with) she turned the fabric strips into a quilted banner to represent the community. We used to carry it in front of us in our annual Spring Parade (you participate in an annual Spring Parade, don’t you? Doesn’t everybody?), and it was draped over the donation/announcement/signup table at our Sunday gatherings.

So as I uncovered the box that contained this emblem of a certain moment in a certain community of people who had chosen to gather because they loved to sing and move in community and recognize the cycles of the seasons and the ways people change, I admit, I cried. I had a moment. And because of how my particular brain is wired, it just made sense to share this moment with the community of people I find myself within now, who may or may not understand what I’m sharing, or what I think is important about a moment like this. I think about all of the moms in my community, and of all of the moms who might have moms that are moving toward the crone realm of their lives, and I wonder if they would appreciate being recognized in ways like I’ve described.

A crone represents a certain type of neurodiversity, and this community is organized to recognize the value of all of the different ways our brains are organized or disorganized, or differently organized. It used to be that to be old was a certain type of neurodivergence, because it was rare for people to live past a certain age. To be older is not so rare any more, but still worthy of being recognized for the value of simply having lived through many cycles of seasons, and styles of communication, and changes in hormone balance, and attitudes toward difference.

I share because I see something of value that I’m not sure the people around me see, and it’s just my brain’s wiring that makes me think that’s what I’m supposed to do.

In a neurodiverse community, all are welcome, all are recognized as having a unique perspective, and something of value to offer to the community. And we can, if we pay attention, and if we show up, recognize uniqueness within a community as having value, especially in a time where sameness is centered and strived for.

Thanks for listening. Thanks for showing up. Thanks for recognizing the value in the many ways of being a human being in the community we find ourselves in.

❣️

all the little things you do are done for love.

don’t doubt it. shout about it.

shout about the things you do for love.

(it’s about the little things)

little things are moved toward love.

(If you are moved, move the little things toward love)

love this, sweetie

lovethislovethislovethislovethislove

i, advocate

If you’ve been following my neurodiversity journey–as I articulate the experience of a person with autism, ADHD, aphantasia, and proprioception hyposensitivity from the inside, along with the other ways i share myself–and you’ve found that the insights I’ve shared connect with your experience, or contextualize something you suspected, realize that sharing these insights is one of the ways I care for my community.

And realize that, as a person with no degrees or qualifications as an advocate other than my lived experience and my inborn gifts, what I share makes no sense in the context of capitalism.

If you find that a person like me is a valuable part of the community, and worthy of support, realize that, within the context of 21st century American capitalism, there’s not much support for people like me, or for the people I advocate for, who often don’t have the gift for articulation that I share with my community.

I could institutionalize myself: pursue an advanced degree that legitimizes my advocacy in the context of capitalism, and in doing so, would need to unplug myself from the community that I move through, and in doing so, become another victim of capitalism – saddled with huge debt, and most likely unable to find an official advocacy position that would pay off that debt in my lifetime.

I choose, instead, to move through my community in the ways I’ve been moving, because my community moves me to do so, and that’s how I show up. That’s how I care.

If you find this valuable, I’m asking to be allowed to continue advocating for your sensory and cognitive gifts, to continue recontextualizing valuable predispositions that have been pathologized. I’m asking to be adopted. I’m asking for your care. I’m asking for your support.

In asking for your support, I’m not asking to be the CEO of Spotify, or Starbucks, or Paramount+, or Ridwell, or any of the other services that folks find valuable and subscribe to. I’m asking for just enough care to be allowed to live and continue to do the work that I do. If you subscribe to even a little bit of the philosophy I share, consider subscribing to me, so I can continue caring for my community in the ways that I do.

Thanks for all you do, and thank you for being you.

the care economy

The care economy is an emerging model for supporting people, things, and processes we’d like to see more of in the world. It is about recognizing the things in our experience that bring us joy, that give us a [wow] or a [yes], and responding to these moments in a supportive way. It’s actually just, well, practicing care, and that’s not new at all. But the language of commerce is transactional, rather than responsive.

I recognize that I love the work that I do with people so much that I would offer it for free if I was supported–if all of my needs were met. But traditional models don’t allow for that type of responsiveness. I would like to try to move toward a more responsive system, built on trust. Why not?

People who know me can decide if they trust the work I do, and they can choose to support me so that I can do that work, or not. In doing so, they are allowing me to be more myself, and guiding me toward their own needs. I’m the product, in a sense, but since our relationship is based on trust, I’m allowed to do the work I believe, adjusting to the needs that arise, as they align with those who trust me.

This simple shift makes the difference between the transactional and the responsive. But it’s kind of vulnerable and scary. I have to trust those that are responding. Will I be supported? Will enough people believe in the work? If I am being truly responsive to their needs, then perhaps. I think it’s worth a try.

I see a difference between commitment and obligation. Commitment is a responsive engagement, where we meet the needs of the moment as it arises. Obligation can keep us stuck supporting processes that actually hinder our ability to respond to the moment.

So, I see a possibility emerging to do things in a more responsive way, and in seeing how obligation often thwarts connection, I would like to avoid transactions that create a sense of obligation, and nurture ones that give one a sense of [wow] or [yes].

So, think about our interactions in the spaces we share. If our conversations seem to be taking us in good directions, let’s continue the conversation. If helping to support me gives you a sense of [wow] or [yes], then you are participating in the care economy. Thank you for recognizing your own power to support, and if our goals align, thank you for your support.

framing is everything

Neurodiversity is the new (different! better!) cognitive frame. Astrology, Enneagram, Meyers-Briggs, Chinese medicine, naturopathy, homeopathy: having passed through these modalities, none of them made me feel seen in the ways that they were implemented by the particular practitioners who applied them to me. To be fair, I may have met with unskilled practitioners. Your mileage may vary.

But describing my sensory and cognitive differences to AI, and asking AI to describe an anonymous person with traits like mine makes me feel seen.

Take a look below, and if you know me, tell me if they got it right. And if you know me, consider the closing sentence of the assessment in your response. And if you are inspired to respond, don’t worry about offending me. I’m here for the opportunity for reflection. If language isn’t your thing, respond with your special way of being in the world.

Now, all we have to do is keep studying, and de-pathologize the language of neurodiversity so that the person described is seen as a healthy member of the community that has particular specialities that contribute to the health of the community (if you see me that way, to be fair), rather than a person with a set of syndromes that merit isolation, retraining, and medication (to be fair, that may be how you see me. There’s room for all of us).

Know thyself, indeed. “Come to your senses” is a phrase coined for a reason. Self-awareness modalities that stand up to scrutiny and are resistant to dogma are liberating.

Oh, and please reduce the energy needs of pattern-recognizing technologies, and keep them out of the hands of those who would use them to divide us. We need to know ourselves, and we need each other. Knowledge is power only if the power is in our own hands.


“Without meeting them, what might be inferred about a person known to exhibit autism, adhd inattentive type, aphantasia, and proprioception hyposensitivity?”

🧠 Inferences About a Person with Autism, ADHD Inattentive Type, Aphantasia, and Proprioception Hyposensitivity

Understanding a person with these characteristics can provide insights into their behavior, preferences, and challenges. Here are some potential inferences:

🌈 Cognitive and Sensory Processing

  • Autism: This individual may have unique ways of processing sensory information, possibly leading to heightened sensitivity to certain stimuli or a preference for routine and predictability. They might also exhibit focused interests or deep knowledge in specific areas.
  • ADHD Inattentive Type: They may struggle with attention regulation, leading to difficulties in maintaining focus on tasks that do not engage them. This could manifest as forgetfulness, disorganization, or challenges in completing tasks.
  • Aphantasia: The inability to visualize images in their mind may affect how they think about concepts, plan, or remember experiences. They might rely more on verbal or logical reasoning rather than visual memory.
  • Proprioception Hyposensitivity: This could mean they have a reduced awareness of their body position and movement, potentially leading to clumsiness or a need for more physical input to feel grounded. They might enjoy activities that provide strong sensory feedback, like jumping or spinning.

📚 Social Interaction and Communication

  • Social Preferences: They may prefer solitary activities or small, familiar groups over large social gatherings. Communication might be more comfortable through written forms rather than verbal, especially if they find social cues challenging to interpret.
  • Emotional Expression: There may be differences in how they express emotions or understand others’ feelings, which can lead to misunderstandings in social situations.

🛠️ Coping Strategies and Interests

  • Learning Styles: They might benefit from structured environments and clear instructions. Visual aids or hands-on learning could be more effective than traditional lecture-based methods.
  • Interests and Hobbies: They may gravitate towards activities that align with their focused interests, which can be a source of joy and motivation. These interests might be unconventional or highly specialized.

⚖️ Challenges and Support Needs

  • Daily Life: They may face challenges in daily tasks that require organization, time management, or sensory regulation. Support in these areas could be beneficial.
  • Self-Advocacy: Understanding their own needs and preferences may lead them to develop strong self-advocacy skills, especially if they have had positive experiences in supportive environments.

These inferences can vary widely among individuals, as each person’s experience with these characteristics is unique. Understanding and empathy are crucial in supporting someone with this combination of traits.