Freedom in Fetters#
Fig. 28 The five networks described in the essay, mapped to Uganda’s and Africa’s identity negotiation, unfold as follows: First, the Pericentral network (sensory-motor) governs reflexive responses, reacting to “nonself” threats like colonialism with immediate, physical action. Second, the Dorsal Frontoparietal network (goal-directed attention) focuses on detecting and prioritizing nonself entities, potentially faltering in Africa’s blurred boundaries with foreign influence. Third, the Lateral Frontoparietal network (flexible decision-making) navigates ambiguity, reflecting the continent’s struggle to balance tribal diversity and imposed systems. Fourth, the Medial Frontoparietal network (self-referential identity) turns inward, emphasizing self-coherence over external rejection, perhaps overly so in Africa’s history. Fifth, the Cingulo-Insular network (salience optimization) integrates these, ideally balancing self and nonself for efficiency—a convergence Africa might yet achieve. The order—from reflex to attention, ambiguity, identity, and optimization—mirrors a progression from instinctive reaction to reflective synthesis, suggesting a natural arc of development, though not necessarily a hierarchy; Africa’s “error” may lie in stalling at ambiguity or self-focus, short of full convergence.#
See also
European aid is now moving away from aid to defense
Strategically target Bill & Melinda
Look out for George Bruce Kaiser and his foundation
Vulnerability of my original targets makes these more key
Infrastructure and government might be dead (EY & Danz; Restructure Team; Deloitte mostly consulting; pivoted to tech)
Show code cell source
import numpy as np
import matplotlib.pyplot as plt
import networkx as nx
# Define the neural network layers
def define_layers():
return {
'Suis': ['DNA, RNA, 5%', 'Peptidoglycans, Lipoteichoics', 'Lipopolysaccharide', 'N-Formylmethionine', "Glucans, Chitin", 'Specific Antigens'],
'Voir': ['PRR & ILCs, 20%'],
'Choisis': ['CD8+, 50%', 'CD4+'],
'Deviens': ['TNF-α, IL-6, IFN-γ', 'PD-1 & CTLA-4', 'Tregs, IL-10, TGF-β, 20%'],
"M'èléve": ['Complement System', 'Platelet System', 'Granulocyte System', 'Innate Lymphoid Cells, 5%', 'Adaptive Lymphoid Cells']
}
# Assign colors to nodes
def assign_colors():
color_map = {
'yellow': ['PRR & ILCs, 20%'],
'paleturquoise': ['Specific Antigens', 'CD4+', 'Tregs, IL-10, TGF-β, 20%', 'Adaptive Lymphoid Cells'],
'lightgreen': ["Glucans, Chitin", 'PD-1 & CTLA-4', 'Platelet System', 'Innate Lymphoid Cells, 5%', 'Granulocyte System'],
'lightsalmon': ['Lipopolysaccharide', 'N-Formylmethionine', 'CD8+, 50%', 'TNF-α, IL-6, IFN-γ', 'Complement System'],
}
return {node: color for color, nodes in color_map.items() for node in nodes}
# Define edge weights
def define_edges():
return {
('DNA, RNA, 5%', 'PRR & ILCs, 20%'): '1/99',
('Peptidoglycans, Lipoteichoics', 'PRR & ILCs, 20%'): '5/95',
('Lipopolysaccharide', 'PRR & ILCs, 20%'): '20/80',
('N-Formylmethionine', 'PRR & ILCs, 20%'): '51/49',
("Glucans, Chitin", 'PRR & ILCs, 20%'): '80/20',
('Specific Antigens', 'PRR & ILCs, 20%'): '95/5',
('PRR & ILCs, 20%', 'CD8+, 50%'): '20/80',
('PRR & ILCs, 20%', 'CD4+'): '80/20',
('CD8+, 50%', 'TNF-α, IL-6, IFN-γ'): '49/51',
('CD8+, 50%', 'PD-1 & CTLA-4'): '80/20',
('CD8+, 50%', 'Tregs, IL-10, TGF-β, 20%'): '95/5',
('CD4+', 'TNF-α, IL-6, IFN-γ'): '5/95',
('CD4+', 'PD-1 & CTLA-4'): '20/80',
('CD4+', 'Tregs, IL-10, TGF-β, 20%'): '51/49',
('TNF-α, IL-6, IFN-γ', 'Complement System'): '80/20',
('TNF-α, IL-6, IFN-γ', 'Platelet System'): '85/15',
('TNF-α, IL-6, IFN-γ', 'Granulocyte System'): '90/10',
('TNF-α, IL-6, IFN-γ', 'Innate Lymphoid Cells, 5%'): '95/5',
('TNF-α, IL-6, IFN-γ', 'Adaptive Lymphoid Cells'): '99/1',
('PD-1 & CTLA-4', 'Complement System'): '1/9',
('PD-1 & CTLA-4', 'Platelet System'): '1/8',
('PD-1 & CTLA-4', 'Granulocyte System'): '1/7',
('PD-1 & CTLA-4', 'Innate Lymphoid Cells, 5%'): '1/6',
('PD-1 & CTLA-4', 'Adaptive Lymphoid Cells'): '1/5',
('Tregs, IL-10, TGF-β, 20%', 'Complement System'): '1/99',
('Tregs, IL-10, TGF-β, 20%', 'Platelet System'): '5/95',
('Tregs, IL-10, TGF-β, 20%', 'Granulocyte System'): '10/90',
('Tregs, IL-10, TGF-β, 20%', 'Innate Lymphoid Cells, 5%'): '15/85',
('Tregs, IL-10, TGF-β, 20%', 'Adaptive Lymphoid Cells'): '20/80'
}
# Define edges to be highlighted in black
def define_black_edges():
return {
('DNA, RNA, 5%', 'PRR & ILCs, 20%'): '1/99',
('Peptidoglycans, Lipoteichoics', 'PRR & ILCs, 20%'): '5/95',
('Lipopolysaccharide', 'PRR & ILCs, 20%'): '20/80',
('N-Formylmethionine', 'PRR & ILCs, 20%'): '51/49',
("Glucans, Chitin", 'PRR & ILCs, 20%'): '80/20',
('Specific Antigens', 'PRR & ILCs, 20%'): '95/5',
}
# Calculate node positions
def calculate_positions(layer, x_offset):
y_positions = np.linspace(-len(layer) / 2, len(layer) / 2, len(layer))
return [(x_offset, y) for y in y_positions]
# Create and visualize the neural network graph
def visualize_nn():
layers = define_layers()
colors = assign_colors()
edges = define_edges()
black_edges = define_black_edges()
G = nx.DiGraph()
pos = {}
node_colors = []
# Create mapping from original node names to numbered labels
mapping = {}
counter = 1
for layer in layers.values():
for node in layer:
mapping[node] = f"{counter}. {node}"
counter += 1
# Add nodes with new numbered labels and assign positions
for i, (layer_name, nodes) in enumerate(layers.items()):
positions = calculate_positions(nodes, x_offset=i * 2)
for node, position in zip(nodes, positions):
new_node = mapping[node]
G.add_node(new_node, layer=layer_name)
pos[new_node] = position
node_colors.append(colors.get(node, 'lightgray'))
# Add edges with updated node labels
edge_colors = []
for (source, target), weight in edges.items():
if source in mapping and target in mapping:
new_source = mapping[source]
new_target = mapping[target]
G.add_edge(new_source, new_target, weight=weight)
edge_colors.append('black' if (source, target) in black_edges else 'lightgrey')
# Draw the graph
plt.figure(figsize=(12, 8))
edges_labels = {(u, v): d["weight"] for u, v, d in G.edges(data=True)}
nx.draw(
G, pos, with_labels=True, node_color=node_colors, edge_color=edge_colors,
node_size=3000, font_size=9, connectionstyle="arc3,rad=0.2"
)
nx.draw_networkx_edge_labels(G, pos, edge_labels=edges_labels, font_size=8)
plt.title("OPRAH™ aAPCs", fontsize=18)
plt.show()
# Run the visualization
visualize_nn()
#
Fig. 29 Musical Grammar & Prosody. From a pianist’s perspective, the left hand serves as the foundational architect, voicing the mode and defining the musical landscape—its space and grammar—while the right hand acts as the expressive wanderer, freely extending and altering these modal terrains within temporal pockets, guided by prosody and cadence. In R&B, this interplay often manifests through rich harmonic extensions like 9ths, 11ths, and 13ths, with chromatic passing chords and leading tones adding tension and color. Music’s evocative power lies in its ability to transmit information through a primal, pattern-recognizing architecture, compelling listeners to classify what they hear as either nurturing or threatening—feeding and breeding or fight and flight. This makes music a high-risk, high-reward endeavor, where success hinges on navigating the fine line between coherence and error. Similarly, pattern recognition extends to literature, as seen in Ulysses, where a character misinterprets his companion’s silence as mental composition, reflecting on the instructive pleasures of Shakespearean works used to solve life’s complexities. Both music and literature, then, are deeply rooted in the human impulse to decode and derive meaning, whether through harmonic landscapes or textual introspection. Source: Ulysses, DeepSeek & Yours Truly!#