Jocko has survivors of the USS Liberty on to tell their story
(jockopodcast.com)
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Indeed, for instance, if anybody asks about socialist inbreds I show screenshots of you. ( and some others)
You are the embodiment of inbreeding and why identity politics is retarded. And why being a low information idiot is detrimental to mental health.
Lmao nice projection. Why don’t you tell the class about Jewish genetic diseases.
I have a massive list of diseases affecting whites. Frankly all ethnicities and races have it. But I like to show your hypocrisy. Do you have want it?
Yes I “have want it.”
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
Dude, Jews have been interbreeding for thousands of years haha
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