Top Five Living Disability Activist

Too humbling. Not sure if I am deserving of mention in same space as Judy Human and Alice Wong. 

Eric Garcia: Ask me for my "Top five ____."

Solomon: Disability activists, 4 living, 5 all time

Eric: All Time: Judith Heumann, Brad Lomas, Ed Roberts, Justin Dart, Pat Wright

Living: @SFDireWolf (Alice Wong), @JustStimming (Julia Bascom), @Cal_Montgomery, @HariSri108 (Hari Srinivasan)


Getting Real

Attended my first PhD Dissertation Defense session by a Vandy PhD Student on Enlarged Vascular Spaces. 

Its getting real...., classes start in 2 weeks!!! Excited and also terribly nervous. 



Henry Ford Museum of American Innovation

History of the Industrial Age - Trains, cars (including presidential cars), planes, tools, steam engines, farm equipment, art glass, furniture, clocks and more all under one roof. 



This week a year ago

A lazy summer day of just chilling on the Cal Campus








 

Move to Nashville

 Well I've officially moved to Nashville, Tennessee. First words that comes to mind - Green and wildlife. 

So far seen adult deer with antlers, without antlers, and fawns all in my backyard and front yard. Lots of turkey including baby turkeys, a few birds including cardinals. bluebirds and blackbirds. The baby deer did a happy dance on the lawn after the rains and ran back and forth on the lawn playing. Its  hot (kinda) but also rains quite a bit so everything turns green. Towering tall trees. Going for early morning hikes at Percy Warner Park near by. 

So far.... nice....






Good Job. You're so Brave


Sharing art made by students in my 1:54 Autism Spectrum Disorder Class.

Image Credit: Thanh Pham

Quote is from Stella Young's Ted Talk https://youtu.be/8K9Gg164Bsw


Conversations with God

Conversations with God


A feeling of lightness
Of bonds breaking free
I look down at my body below
And people that stand around it

Tears on their faces
Anguish in their hearts
They mourn the carrion of flesh and bone
While unshackled, flies my soul

Mourn me not my loved ones.
My words unheard by those below
My mortal body is Maya, mere illusion
Brahman, transcendent reality, is my soul

I will always be with you, dear ones
Grief at start will fade to distant memory
Your dreams and your memories
Are conversations with God really

I travel with angels all around me
Apsaras dance to heaven’s melody
Gloria in excelsis deo
Glory to God in the Highest

O Resplendent Light, Phos Hilaron
I see the face of God before me
Down there at His divine feet
I settle myself down in ecstasy

The Cosmic Director smiles down on me
Are you ready for the next act, asks He.
You may tarry a while in My company
Before I assign you, your next role

Kaala tithaya am I, beyond space and time
Siddha Sankalpaya, My will is instantaneous
I protect and nourish earthkind at all times
For I am verily the Embodiment of Love

Human existence involves, He explains
Births, deaths and rebirths
A karmic cycle of cause and effect
Free will of man plays a mighty role

Free Will I give to man, for I love you most
Use it well in the roles you lead
With spiritual evolution you will reach
Your ultimate destiny, mergence with Me

God recounts the roles of past played by me
Movie clip images, scenes flash before me
Countless colors, countries and lifestyles do I see
In the multitudes of lifetimes I have led.

Ignorant was I, now understanding dawns
Human life is transient at best
Death, a mere comma in the cosmic scheme
So why waste trifles over mortal emotions

To experience Happiness
One must know sorrow
Tests of the morrow
Are but a path to the end


Translations
Maya [Sanskrit]: Illusion
Brahman [Sanskrit]: Absolute Reality
Gloria in excelsis Deo [Latin]: Glory to God in the Highest
Phos Hilaron [Greek]: O Resplendent Light
Kaalatithaya [Sanskrit]: one who is beyond space and time
Siddha Sankalpaya [Sanskrit]: one who’s will is instantaneous and successful

Media Mention

Media Mention...

"...an alternative framework for understanding autism spectrum disorder outside the traditional “high functioning” and “low functioning” categories, offered by Hari Srinivasan in a Berkeley class on autism, inspired the theme. The zine format is great – approachable, fun, and cheap! – and I’ve found it’s an easy way to start a conversation about new ways to think and communicate about data." - Madeline Arnold. https://datasciencebydesign.org/blog/beyond-binaries 7/13/22


Regressive Autism

Regressive autism, also known as late-onset or acquired autism, is characterized by the loss of previously acquired developmental skills, particularly in social communication and interaction. This regression typically occurs between 15 and 30 months of age, where children may initially develop normally but then experience a decline in verbal communication, social engagement, and may exhibit decreased eye contact, along with an increase in repetitive behaviors. This regression often leads to significant distress for both the child and caregivers.

Explanations and Theories for Regressive Autism

  1. Genetic Factors: There is evidence suggesting a genetic predisposition to regressive autism. Children with this form of autism may have a family history of autism or other developmental disorders, indicating a potential genetic component (Zwaigenbaum et al., 2009).

  2. Environmental Triggers: Environmental factors, such as exposure to certain toxins, infections, or other external stressors, have been hypothesized to trigger regression in children who are genetically predisposed. However, clear causal relationships are not well established (Hertz-Picciotto et al., 2006).

  3. Immune System Abnormalities: Abnormal immune responses or autoimmunity have been linked to regressive autism. Research has identified irregularities in the immune systems of children with autism, which might contribute to the regression of skills (Ashwood et al., 2006).

  4. Neurological Factors: Changes in brain structure and function, including abnormalities in brain development and connectivity, are being explored as potential explanations for regression (Courchesne et al., 2007).

  5. Mitochondrial Dysfunction: Mitochondrial dysfunction, which affects energy production in cells, is another area of research in autism, including regressive forms. Dysfunction in these cellular processes could impact neurodevelopment (Rossignol and Frye, 2012).

  6. Neuronal Pruning: Abnormal neuronal pruning is a significant area of interest. Neuronal pruning is a natural process during brain development where excess neurons and synaptic connections are eliminated to optimize brain function. In autism, including regressive autism, either excessive pruning (leading to a loss of necessary neural connections) or insufficient pruning (resulting in too many synapses) could disrupt normal brain function and development. This disruption may contribute to the loss of previously acquired skills in regressive autism (Tang et al., 2014; Varghese et al., 2017). Genetic studies have linked mutations in genes involved in synaptic pruning, such as MECP2, SHANK3, and PTEN, to autism spectrum disorders (Penzes et al., 2011). [READ MORE ON NEURONAL PRUNING]

Citations

  • Zwaigenbaum, L., et al. (2009). The changing epidemiology of autism spectrum disorders. Canadian Journal of Psychiatry, 54(7), 533-540.
  • Hertz-Picciotto, I., et al. (2006). The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism. Environmental Health Perspectives, 114(7), 1119-1125.
  • Ashwood, P., et al. (2006). The immune response in autism: a new frontier for autism research. Journal of Leukocyte Biology, 80(1), 1-15.
  • Courchesne, E., et al. (2007). Mapping early brain development in autism. Neuron, 56(2), 399-413.
  • Rossignol, D. A., & Frye, R. E. (2012). Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Molecular Psychiatry, 17(3), 290-314.
  • Tang, G., et al. (2014). Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits. Neuron, 83(5), 1131-1143.
  • Varghese, M., et al. (2017). Autism spectrum disorder: neuropathology and animal models. Acta Neuropathologica, 134(4), 537-566.
  • Penzes, P., et al. (2011). Dendritic spine pathology in neuropsychiatric disorders. Nature Neuroscience, 14(3), 285-293.