organic bronze

  • small brain: The rise of agriculture started us down the evil path of domination and hierarchy.
  • medium brain: lol primitivism is dumb.
  • bigger brain: Primitivism as an ideology is built on an enlightenment edifice, and buys into both a Rousseauian notion of the "childhood of man" and a debased, vulgar Marxist view of staged historical development, it does not represent a new epistemic break. And its base presumption is not something that is borne out in historical or anthropological evidence. One might look to the Inuit, and how in the seasons during which they lived as small groups of hunter gatherers used a system of social relations that was highly hierarchical, but came together in larger groupings that lived in a more horizontally organized manner. Additionally bronze age archaeological sites in Asia Minor indicate sedentary, agricultural populations living under remarkably egalitarian conditions, as reflected in the exacting equality of house size and the presence of communal areas, wells, and enclosures. Or one might look to the phenomenon of nomadic pastoral steppe empires which ruled over numerous sedentary societies on their periphery and held to a strict hierarchy during most times but reverted to a rather egalitarian system when selecting a new leader. The presence of a city, or a sedentary settlement does not, prima facie, indicate a hierarchical way of enacting social relations. Human societies have a remarkable tendency to explore and play with their systems of political and societal organization. It could be argued that a part of the left's role in our critique should be to regain that sense of play and willingness to explore, modify, and transform our organizational structures.
  • biggest brain: lol primitivism is dumb.

anonymous asked:

What are some of your holy grail products

ooh um makeup or skincare? or just in general?

  • inglot ysm foundation (matte foundation w/ medium coverage looks natural and good for everyday!)
  • hourglass mineral veil primer
  • clear brow gel (i have one from australis is amazing!)
  • mario badescu rosewater facial spray
  • sugarbaby sheet masks (you can get 4 for $20 at myer!)
  • indie lee brightening cleanser
  • lush ultra balm - i use it to heal tattoos, eyebrows, lips, elbows, everything!
  • juvia’s place palettes - the formula is amazing!
  • agonist parfum in isis
  • french girl organics lumiere bronzing oil
  • ouai hair oil (another multipurpose product i love)
  • may lindstrom ‘the problem solver’ face mask
  • may lindstrom ‘the blue cocoon’ face balm
  • stila lipgloss in kitten
  • red lipstick! my fave is hourglass opaque rogue liquid lipstick in raven atm
6

Carillon Tower at Stanley Park in Westfield, Massachusetts.

It dates to 1949 and features both English and Flemish bells, plus an electronic organ. The two bronze doors have fourteen relief sculptures featuring scenes and symbols from the lives of Frank Stanley Beveridge (park founder) and his wife.

I don’t keep up with the blog much anymore, but every once in a while I come across something I have to share!

Rare Hannu Ikonen Black Enamel Bronze Necklace Reindeer Moss Finland Modernist

A beautiful and unusual pendant by Finnish designer Hannu Ikonen. The necklace is one of his iconic “Renmoosblüte” or Reindeer moss pieces and was produced by Finnish firm Valo Koru. Its organic quality and rich bronze patina make the piece warm and appealing. Enamelled detailing is rarely seen in his designs. (via)

anonymous asked:

Hey, what body products do you use/recommend? I'm running out of body moisturiser and wash and scrub..

i’m highly allergic to certain essential oils, so i mainly play it safe and use unscented body products. so might not be too interesting for you. for my body wash, i use sukin soap-free body wash. it does the job. as a body moisturiser, i use an oil. the sans ceuticals activator 7 oil is amazing. otherwise, i recommend the french girl organics lumiere bronzing oil (it has a slight tint and shimmer) for summer. For a scrub, i don’t use one that often but i like the vice & velvet called 12 days of crumble (smells like christmas). i also use coffee scrubs! and i bought this sponge from the body shop which also helps exfoliate and i have this muji shower brush thingy. it’s actually nice. indie lee had an unscented body lotion which i wanted to try but unfortunately they sold out :( that’s all i can think of for now! sorry not too interesting with the scents!

Autosomal Recessive Diseases List
  • Abetalipoproteinemia: decrease ApoB-48, Apo B-100; pigmentary degeneration of retina, acanthocytes, steatorrhea, cerebellar ataxia.
  • Acute Fatty Liver of Pregnancy: microvesicular steatosis in the liver, mitochondrial dysfunction in the oxidation of fatty acids leading to an accumulation in hepatocytes
  • Alkaptonuria: homogentisate oxidase deficiency, increase homogenistic acid, ochronosis, dark blue urine.
  • AcylCoA Dehydrogenase deficiency (MCAD): fasting hypoglycemia, no ketone bodies, dicarboxilic acidemia.
  • Bernard Soulier Sd: gp1b deficiency, prolonged bleeding time
  • Bloom Sd: chromosome 15, Ashkenazi Jews, BLM gene.
  • Carpenter Sd: craniosynostosis, acrocephaly, craniofacial asymmetry, increased ICP, cutaneous syndactyly, polydactily, mild-profound MR.
  • Chediak Higashi Sd: Lyst gene mutation, microtubule polymerization defect, no phagolysosome formation, albinism.
  • Chondrodystrophy: normal-sized trunk and abnormally short limbs and extremities (dwarfism)
  • Congenital Adrenal Hyperplasia: 17alpha or 21beta or 11 beta hydroxylase deficiency; enlargemente od adrenal glands due to increase ACTH
  • Congenital Hepatic Fibrosis: hepatic (periporta) fibrosis, irregularly shaped proliferating bile duct, portal hypertension, renal cystic disease.
  • Cystic Fibrosis: CFTR gene, Phe508, defective Chloride channel, chromosome 7.
  • Dubin-Johnson Sd: direct hyperBbnemia, cMOAT deficiency, black liver
  • Endocardial Fibroelastosis: restrictive/infiltrative cardiomyopathy, thick fibroelastic tissue in endocardium of young children, <2yo
  • Familial Mediterranean Fever: chromosome 16, recurrent autoinflammatory disease, characterized by F°, PMN disfx, sudden attacks pain/inflammation (7 types of attacks (abdominal, joints, chest, scrotal, myalgias, erysipeloid, fever). Complication: AA-amyloidosis
  • Fanconi Anemia: genetic loss of DNA crosslink repair, often progresses to AML, short stature, ↑incidence of tumors/leukemia, aplastic anemia
  • Friedreich’s Ataxia: GAA triplet repeat, chromosome 9, neuronal degeneration, progressive gait & limb ataxia, arreflexia, hypertrophic cardiomyopathy, axonal sensory neuropathy, kyphoscoliosis, dysarthria, hand clumsiness, loss of sense of position, impaired vibratory sensation.
  • Gaucher’s disease: glucocerebrosidase deficiency, glucocerebroside accumulation, femur necrosis, crumpled paper inclusions in macrophages.
  • Ganzman’s thromboasthenia: gpIIbIIIa deficiency, deficient platelet aggregation.
  • Hartnup Disease: tryptophan deficiency, leads to niacin deficiency, pellagra-like dermatosis
  • Hemochromatosis: HFE gene, C282Y MC mutation, chromosome 6, unrestricted reabsorption of Fe+ in SI, iron deposits in organs, bronze diabetes, DM1, malabsorption, cardiomyopathy, joint degeneration, increased iron, ferritin, TIBC. Complications: liver cirrhosis, hepatocelullar carcinoma
  • Homocystinuria: due to B6 deficiency (defective Cystathionine synthase) or due to B9,B12 deficiency (defective Homocysteine Methyltrasnferase), dislocated lenses (in & down), DVT, stroke, atherosclerosis, MR.
  • Krabbe's Disease: Galactocerebrosidase deficiency, galactocerebroside accumulation, gobloid cells, optic atrophy, peripheral neuropathy.
  • Leukocyte Adhesion Defect (LAD): CD-18+ deficiency, omphalitis in newborns, chronic recurrent bacterial infxs, increase WBC count, no abscess or pus formation.
  • Metachromic Leukodystrophy: Aryl-sulfatase A deficiency, sulfatides accumulation, Demyelination (central & peripheral), Ataxia, Demantia (DAD)
  • Niemann-Pick Disease: sphingomyelinase deficiency, sphingomyelin accumulation, HSM, cherry-red macula, foam cells.
  • Phenylketonuria (PKU): phenylalanine hydroxylase deficiency, Phe accumulation, MR, microcephaly, diet low in Phe!!! also in pregnancy, avoid aspartame, musty odor.
  • Polycystic Kidney Disease (children): ARPKD, rogressive & fatal renal failure, multiple enlarged cysts perpendicualr to renal capsule, association with liver cysts. Bilateral palpable mass.
  • Rotor Sd: direct hyperBbnemia, cMOAT deficiency, no black liver
  • SCID: ADA def. & rag-1, rag-2 def, bubble-boy
  • Shwaman Diamond Sd: exocrine pancreatic insufficiency (2°MCC in children after CF), bone marrow dysfunction, skeletal abnormalities, short stature.
  • Situs inversus: assoc w/ Kartagener sd
  • Sicke Cell Disease and Trait: Hb S, beta globin chain, chromosome 11, position 6, nucleotide codon change (glutamic acid --> valine), vaso-occlusive crisis (pain), autosplenectomy, acute chest pain sd, priapism, hand-foot sd, leg ulcers, aplastic crisis, drepanocytes & Howell-Jolly bodies, hemolytic anemia, jaundice, bone marrow hyperplasia
  • Tay-Sachs Disease: Hexoaminidase A deficiency, GM2 accumulation, cherry-red macula, onion skin lysosomes.
  • Thalasemia: alpha (chromosome 16, gene deletion), beta (chromosome 11, point mutation)
  • Werner Disease: adult progeria
  • Wilson’s Disease: Chromosome 13, WD gene, ATP7B gene (encondes for Copper transporting ATPase), copper accumulation in liver, brain (putamen), eyes (Descemet membrane - Kayser-Fleischer ring), decreased ceruloplasmin.
  • Xeroderma Pigmentosa: defective excision endonuclease, no repair of thymine dymers caused by UV radiation, excessive freckling, multiple skin cancers.