Mike's Neurodivergent Toolbox

Mike's Neurodivergent Toolbox I am a late-diagnosed autistic with ADHD. I continue to struggle with a lifetime of unaddressed disabilities, but advocacy has enabled me to find my voice.
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I hope that my efforts provide help and understanding to others with similar stories.

04/23/2025

Wow! It's almost like scientific research made a difference and we got better at recognizing the condition in people! 🤦‍♀️🤦‍♀️🤦‍♀️

For the newer people, I am one of those relatively rare people on the spectrum who likes to cook and isn’t especially ch...
04/22/2025

For the newer people, I am one of those relatively rare people on the spectrum who likes to cook and isn’t especially choosy about food, as long as it doesn’t get too complicated and I can loosely follow my established routines.

So this is Mexican/south of the border night. Pupusas (I tried the loroco variety this time), plantain tostones and since I had avocados to use, guacamole.

In addition to regularly hosting European exchange students we are a fairly mixed and blended family. My wife speaks fluent Spanish and taught in the local school system for most of her career.

04/22/2025

Wise words from a fellow traveler:

04/22/2025

I do not think that I am exaggerating when I say that for the first time in my life, the overall trajectory is that of things getting far worse, rather than incrementally better, for those of us who do not fit the norm.

I have had my trauma, as have so many of you. I will continue to experience trauma despite some much-needed adjustments and some wonderful people in my life.

How bad it gets for any of us depends upon policies being determined in the near future. I don't want to be a doomsayer but in my experience keeping the worst case scenario in mind and adjusting to more favorable than expected events is better than assuming that things are just going to work out.

This is why I feel that we are doing our young people an enormous disservice when we offer feel-good philosophies based on the assumption of ongoing support and acceptance. Of course we want this and do our best to provide such a life for them.

But we can't guarantee anything despite our best efforts. People will be the opposite of understanding and accommodating. There are those who like to take advantage of those who are different, and may be able to do so with increasing impunity. There are those who will approach any challenge they see others facing by being harsh and demanding, the list goes on.

This is why I think that hyper-positive perspectives are well-intentioned but so harmful. "You are awesome, just be yourself" is something that we want for our younger people. But the reality is that it's not always safe to take that assumption, and we may be placing them in threatening situations if they assume that the understanding and support that they have found among us exists everywhere.

I say this as a parent of a neurodivergent teen. At this point I don't take anything for granted. My project over the next several weeks is is to draft an address to the younger crowd along these lines.

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My lucky weekend with my friends in the community! I hope you enjoy the book!
04/20/2025

My lucky weekend with my friends in the community! I hope you enjoy the book!

So excited to read this and love that it’s a short book too.
Thanks Mike's Neurodivergent Toolbox for sending this. Looking forward to dig in - so nice to see a book for middle-agers. :)

The affirmations from friends continue. I thank Jade Farrington - Counsellor and Therapist for this thoughtful and detai...
04/20/2025

The affirmations from friends continue. I thank Jade Farrington - Counsellor and Therapist for this thoughtful and detailed review.

You know when there's something you really mean to do, but things happen, and you forget. Then see something reminds you, but you can't do it right now... Rinse and repeat?

I've been meaning to read and post about this book since Mike from Mike's Neurodivergent Toolbox so kindly emailed it to me months ago. It was seeing a review from Brian at Autism Support Community that finally gave me the right shunt at the right time. So, with the sincerest of apologies to Mike, here's my very late review…

Michael Howard is a late identified AuDHDer who lives over in North Carolina in the USA. He's the author of 'Not Me, Us: The Story of a Middle-Aged Autistic and the Quest to Empower Others with Similar Stories' and was diagnosed autistic aged 50.

When people discover their autistic identity in their 50s or 60s, there's often a lot to process around being poorly treated, and thoughts of what could have been.

Mike begins his very personal story by highlighting the struggles of finding community as a middle-aged autistic who has only recently had this key part of his identity confirmed. He has a newfound sense of purpose as an advocate seeking to increase representation of late-identified autistic elders.

These difficulties parallel the challenges experienced in his younger years, with difficulties making friends and unscrupulous people keen to take advantage.

Mike excelled academically, but struggled when he moved away from his support network. He threw himself into his philosophy studies, then lost interest. There will be more than a few other AuDHDers nodding along.

Mike’s journey into discovering his neurodivergence began when a radio show covered Asperger’s, as it was then known, and he realised he met all the diagnostic criteria. He booked an appointment with a professional but was dismissed because he had done well academically. Mike endured this for another 20 years whenever he attempted to broach the idea: “In one instance, a therapist told me that since I came to her, and autistics do not like to interact with others, I could not be autistic. She added that even if I had been autistic at one point I would have grown out of it by my age.”

I wish I could say I hadn’t heard this dozens of times before, but the level of ignorance about autism amongst many professionals is legitimately shocking, and even now autistic people are turned away for an absurd array of reasons – including some doctor’s ‘not believing in it’.

An ADHD diagnosis came for Mike in 2006, an autism in 2021. He understandably talks of his disappointment at the sense of feeling lost, and the fact that accommodations and adjustments didn’t automatically follow. But Mike acknowledges the sad reality that for many, formal identification in the past meant harsh interventions designed not to support, but to try to make autistics appear more allistic – as is often still the case today.

I’ve yet to meet an autistic person who is ‘only’ autistic. Co-occurring neurodivergences and health conditions are the norm. An autistic who is also apraxic and has a learning disability (known as intellectual disabilities in the USA), for example, is likely to have a very different experience to an AuDHDer like Mike. He discusses the challenges that can come from this combination, describing it as sometimes putting him at odds with himself, while at other times traits amplify one another. Sometimes much can be achieved, but there are also a trail of unfinished projects and discarded interests. Mike also touches on his mental health difficulties; the loss of his friend at his own hand; and the stark reality of the su***de statistics for autistic people.

If you’re wondering whether to pursue a formal diagnosis later in life, Mike lays out what it’s meant for him, including self-acceptance, vindication, and accommodations at work and at home.

Mike dedicates a chapter to his work history and challenges, including the familiar autistic experiences of being unemployed and underemployed. He also shares the specific accommodations he has in place.

The book raises the important point of the lack of resources for older autistics. The vast majority of those approaching retirement age or older remain unidentified. We are only beginning to see more understanding and wider recognition in the youngest age groups, in part due to recategorisations in diagnostic criteria; understanding of different presentations; and increased screening. People like Wenn Lawson are leading the drive for more research into the experiences of older autistics, and bringing their needs to the table.

Thank you Mike for sharing your story!

Not Me, Us is available now on Amazon.

Happy Spring celebration of your choice. That includes Easter or in some denominations Resurrection Sunday. Or if the ev...
04/20/2025

Happy Spring celebration of your choice. That includes Easter or in some denominations Resurrection Sunday. Or if the event of another holiday brings anxiety that’s an attitude affirmed here too. I never want to give the impression that only people of certain religious beliefs are welcome—or unwelcome.

04/19/2025

I stand firmly against bigotry in all forms. If I don’t emphasize intersectionality that’s because I don’t pretend to speak from experience I have not had, not because it is not a concern. All those who affirm others are welcome.

Pet pic Friday! Add yours in comments.
04/18/2025

Pet pic Friday! Add yours in comments.

I am getting used to odd contradictions. This has never been about success by conventional standards or money. But since...
04/17/2025

I am getting used to odd contradictions. This has never been about success by conventional standards or money. But since last month I have had some encouraging developments: a conference appearance, a fantastic independent review, the first anniversary of the page, the scheduling of my first public address as an advocate and a profile with an established vlogger. But this is the first month that I have not sold any copies of my book. Not one. Not in any market. Any thoughts?

04/17/2025

This week's excerpt from the book (link in comments):

Afterword

The recurring theme of this book has been that my situation is not unique. I do not know the exact statistics, but increasing numbers of people are being diagnosed as autistic later in life. And frequently, while the diagnosis may provide personal vindication and enhanced self-understanding, we continue to be misunderstood by others and can have difficulty getting the help we need. Even worse, too many people remain undiagnosed for lack of resources or access. And for those of us who have internal wiring that makes us prone to confusion in unfamiliar settings, knowing where to start in terms of pursuing a diagnosis can seem impossible. I can attest to having had my share of false leads.

I, of all people, have difficulty affirming myself as part of “us.” Even with some wonderful people in my life, I have remained mostly on my own in finding ways to function in a world that is not is not geared toward someone of my neurotype. My attempts to find a community beyond the family are only beginning to show results, and I am thankful for my growing number of online friends. This is not to say that people have not been welcoming. Rather, having spent decades with unrecognized autism, making connections with others in any context has become very challenging, though I am hopeful.

Yet I affirm the title of this book, “Not Me, Us.” I do not have to know another late-diagnosed autistic person to have a good idea of what their life has been like because I have lived that life as well. Those diagnosed late in life tend to have less access to guidance and resources, yet face a much longer journey toward wholeness than those who have been diagnosed in their youth. As I have already mentioned, there may be some benefits to having been diagnosed later in life and I could have hardly expected a much earlier diagnosis given my situation. But many of us are literally dying before we get meaningful help. Others will never know the source of their alienation and inability to function. And if they happen to find out that they are probably autistic, such individuals are often unable to achieve subsequent aid or inclusion.

However, my intent is not to divide the autistic community into factions. I am happy for all resources we can attain for autistics of any age. We need organizations like Autism Over 18 (a group situated in the area in which I live) for young adults, though to my knowledge, there is no corresponding group, in terms of matching needs to resources, for those my age. I am not arguing for a bigger piece of the pie, but for a larger and better pie, one that will nourish us all. We need one another regardless of our respective stories or when we were born. So when I say “us,” I am referring broadly to everyone whose lives have been touched by autism. May we find the resources we need for a better life.

Copyright Š 2024, Michael Howard

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Another outdoor work project. As much as I love working alone and the satisfaction of the finished product my back is ki...
04/16/2025

Another outdoor work project. As much as I love working alone and the satisfaction of the finished product my back is killing me and I feel that I have lost a piece of my future well being.

04/15/2025

I just clipped a paragraph in the introduction to the book that more or less said "I don't go into the gory details, but I don't pretend to be perfect or blameless," something that can probably be implied. Instead, I substituted this paragraph, which I believe needs to be said, but before re-publishing, I thought that I would run it by you all:

I do not expect that my experience will match that of everyone on the autistic spectrum, though I hope that many can relate to much of my narrative and that non-autistics may gain a better understanding of what autism can look like at the ground level by reading my story. I acknowledge that without a fair amount of privilege I would not be in the position to write this book and I do not take any advantages I have for granted. Too many of my generation have been lost while others face layers of marginalization that I have never experienced. Others require support that far eclipses my own needs and can only be represented by proxy. I cannot claim to speak for everyone but I hope that my underlying desire to advance the interests of autistic people in general outweighs any variances in experience, perspective or preferred vocabulary without trivializing these important differences.

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As I have previously mentioned I am not much of a tag lister but when a trusted friend tags most of my favorite pages I ...
04/14/2025

As I have previously mentioned I am not much of a tag lister but when a trusted friend tags most of my favorite pages I am happy to share!

This is a post to my favourite 20 pages who have been just brilliant to me since meeting them. I want to shout out their names as they deserve more love and appreciation 💗

1. With All My Spiciness
2. Meg Stone Wellness
3. Out of the Box - Autism & Us
4. SEND at Heart
5. A Cup Full of Spoons
6. Unapologetically, Abi xoxo
7. Aspie Queens
8. Angela G. Williams - Author
9. Joy of Autism
10. Mike's Neurodivergent Toolbox
11. Callum Knight Autism
12. Asperger's Syndrome Awareness
13. I've been autistic all along?
14. Kaelynn’s Autistic Angle
15. Rosie Weldon's Autistic Life
16. The Autistic Teacher
17. The Bright Centre: Neurodiversity & Mental Health Coaching & Consulting
18. ASD with a G and T
19. Autism Support Community
20. Stop discrimination against special needs

These are 10 newer pages who I am grateful to know and am learning so much from 💗

1. Gentle Dragon Wellness
2. Spilling the Tea on ASD and ADHD
3. Ashra Louisa
4. Shawnicorn Mindshift Coaching- Trauma Recovery Coach
5. Multiply Neurodivergent
6. The Unmasked Zebra
7. Dear Future Sam
8. Healing Loudly - an Autism and Mental Health story
9. Sensory Stories by Nicole
10. Neurodiversity with Naomi

04/14/2025

To follow up on the hereditary nature of autism, yes, I do see it in my family.

Both my parents exhibit tendencies but I don’t know if either would meet clinical standards. Even fifty years ago both were completely uninterested in fads, trends and popular culture and I learned early in life that what was normal at home and what was normal elsewhere were not the same.

Dad is a retired engineer (as were both of my grandfathers) and has the classic nerd vibe, quiet and bookish. Mom is extroverted, but often blunt to the point of being contrarian, and with too many mysterious sensitivities to mention. Both hyper focus on interests and projects. But they both seem to enjoy many outings and social interactions that I find challenging. I believe the situation may be more clear cut with others in the family.

I don’t offer this in the spirit of criticism, and from what I gather they don’t follow the page. In their late 70s, they have accepted my diagnosis but I don’t know how aware they are otherwise.

I often get in hot water for saying this but I don’t like the armchair diagnosis of anyone living or dead. I strongly believe that individuals should have as much authority as possible over how they are identified. But noting tendencies and probabilities, if it helps us understand ourselves, can be very useful.

04/13/2025

ND people: My internal GPS does not work well and I get lost easily. Others have a near perfect recall of places and directions. Which are you?

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