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57
When you think of LEGO, whom would you imagine as their clientele? Perhaps a White male child? WRONG!!! Single black women professionals are their target demographic now (media.kotakuinaction2.win)
posted 4 years ago by GimmeFuelGimmeFire 4 years ago by GimmeFuelGimmeFire +57 / -0
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– RealDrJester 1 point 4 years ago +1 / -0

Wow! An inbred who can't debunk the information! Wow!

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– DomitiusOfMassilia 1 point 4 years ago +1 / -0

Comment Reported for: Rule 15 - Slurs

Comment Approved: I wouldn't really consider "inbred" to be a slur.

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– deleted 1 point 4 years ago +1 / -0
▲ 1 ▼
– RealDrJester 1 point 4 years ago +1 / -0

Wait, are you actually triggered by the word inbred?

Well, that's something inbreds do. You lie, swindle, cheat, weasel out of things, blame Jews for everything under the sun(like SJWs do with whites), and then when I fight back, you cry foul play?! HAHAHAHAHAHAHAHA

You are pathetic!

PATHETIC! I have nothing but contempt and disdain to socialists such as yourself.

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▲ 1 ▼
– BigPedeEnergy 1 point 4 years ago +1 / -0

I'm not triggered, I'm pointing out how jews (factually more inbred than whites) always code southerners as inbred without much statistical support to divert from their own inbreeding and baby-dick-biting

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– RealDrJester 1 point 4 years ago +1 / -0

You sound super triggered.

List of genetic disorders of the white populace:


Thalassemia, Sickle-cell anemia, Cystic fibrosis, Tay–Sachs disease, Hereditary hemochromatosis, Amyloidosis, Finnish type Lethal arthrogryposis with anterior horn cell disease Aspartylglucosaminuria Autoimmune polyendocrinopathy syndrome, type I, with or without reversible metaphyseal dysplasia Cartilage–hair hypoplasia Ceroid lipofuscinosis, neuronal, 1 Ceroid lipofuscinosis, neuronal, 3 Ceroid lipofuscinosis, neuronal, 5 Ceroid lipofuscinosis, neuronal, 8, Northern epilepsy variant (Synonyms: Northern epilepsy; Epilepsy, progressive, with mental retardation) Choroideremia Cohen syndrome Cornea plana 2 Diarrhea 1, secretory chloride, congenital Diastrophic dysplasia Epilepsy, progressive myoclonic 1A (Unverricht–Lundborg) Glycine encephalopathy (Nonketotic hyperglycinemia) GRACILE syndrome Gyrate atrophy of choroid and retina Hydrolethalus syndrome 1 Infantile-onset spinocerebellar ataxia (Mitochondrial DNA depletion syndrome 7) Lactase deficiency, congenital Lethal congenital contracture syndrome 1 Lysinuric protein intolerance Meckel syndrome Megaloblastic anemia-1, Finnish and Norwegian type Mulibrey nanism Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3 Nephrotic syndrome, type 1 (Finnish congenital nephrosis) Ovarian dysgenesis 1 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (Nasu–Hakola disease) Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy RAPADILINO syndrome Retinoschisis 1, X-linked, juvenile Sialuria, Finnish type (Salla disease) Tibial muscular dystrophy, tardive Usher syndrome, type 3A

https://en.wikipedia.org/wiki/Race_and_health#Race_and_disease

https://en.wikipedia.org/wiki/Finnish_heritage_disease

https://en.wikipedia.org/wiki/Cystic_fibrosis#Epidemiology

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