Discover Top Posts Tagged with #2073

Who asked for Xhekovsky cat girl art ? once again... ME OF COURSE !!!

#montreal canadiens #arber xhekaj #juraj slafkovský #xhekovsky #2073 #hockey fanart #hockey rpf #juraj x arber #digital art #GO HABS GO #this is canon

#Latvia #Latvija #Art #Riga #2073

RE-ANIMATOR 1985 (+ audiobook HP LOVECRAFT)

EN ESPAÑOL: EL REANIMADOR (+ audio-libro de HP Lovecraft)

Re-Animator (also known as H. P. Lovecraft's Re-Animator) is a 1985 American comedy horror film loosely based on the 1922 H. P. Lovecraft serial novelette "Herbert West–Reanimator". Directed by Stuart Gordon.

The film stars Jeffrey Combs as Herbert West, a medical student who has invented a reagent which can re-animate deceased bodies. He and his classmate Dan Cain (Bruce Abbott) begin to test the serum on dead human bodies, and conflict with Dr. Carl Hill (David Gale), who is infatuated with Cain's fiancée (Barbara Crampton) and wants to claim the invention as his own.

WATCH FILM BELOW

Go to settings for English subtitles and quality.

Re-Animator Extended Integral Cut - Horror 1985

link https://ok.ru/video/6779739245066

AUDIO BOOK

SECCIÓN EN ESPAÑOL

Re-Animator es una película de terror de 1985 dirigida por Stuart Gordon y basada en el relato de H. P. Lovecraft "Herbert West: reanimador". Protagonizada por Jeffrey Combs como Herbert West, un estudiante de medicina transferido de Europa a la Facultad de Medicina de la Universidad de Miskatonic para continuar desarrollando su suero de reanimación corporal. Las pruebas que realiza no son las que él esperaba y traen consigo una serie de fatídicas consecuencias para él y la vida personal de su compañero de cuarto, Dan Cain. La película se volvió de culto, entre fanes del cine gore combinando el terror con la comedia. Wikipedia

VEASE A CONTINUACION LA PELICULA DOBLADA

Herbert West estudia en Europa métodos regenerativos junto a un conocido científico, que muere en extrañas circunstancias. Herbert viaja a E

LINK https://ok.ru/video/5412764453612

Escuché el cuento

link https://youtu.be/fAYwSa6qkRs

IMAGINES: https://www.tumblr.com/gradexmovies/795567791371665408?source=share

#2073 #film #re animator #en español #reanimador #doblada #1985 #Dir. Stuart Gordon #2026-01-15

we are about an hour into rare disease day in my timezone! (it's always the last day of february, whether that's the 28th or the 29th.) the true prevalence of mast cell disorders is unknown, as they are often misdiagnosed or ignored. and mast cell activation syndrome, the most prevalent kind of mast cell disorder, only had diagnostic criteria laid out for the first time in 2010. so whether or not it's truly rare is really up in the air!

(personally I suspect it is just aggressively underdiagnosed but I'm not a research scientist or diagnostician right now. and even if it is rare, it's gonna be a lot less so than it was 5 years ago as certain respiratory infections are known to trigger it into visibility. that's what happened to me when I got mono at the end of 2015, further compounded when I got covid in 2022.)

all chronically ill people face a lot of hurdles when it comes to seeking diagnosis, accommodation, and treatment (all of which can be severely complicated by any intersecting marginalities), but rare diseases present a special challenge.

for example, I have an immune disorder. my immune system does not like being alive, my mast cells are way too jumpy and throw a tantrum over every little thing. you'd think an immunologist would be the one to treat me, right?

I've had 6 immunology referrals rejected in the past 9 months alone. multiple major immunology clinics in my major city tied to a major research university outright refuse to see patients with "mcas" written anywhere in their chart.

after 8 years of being debilitatingly ill, and suspecting it was immune mediated for 6, and getting it confirmed beyond a shadow of a doubt by the bone marrow biopsy last month, I will have my second ever appointment with an immunologist. another 2 1/2 months from now. the first immunologist lied to me about the reliability of the one available blood test, when I first came up with the hypothesis by myself 6 years ago, and forced me to abandon my (correct!!! now proven!!!) hypothesis for 3 entire years while we wandered around lost and got nowhere other than even more thorough process of elimination.

okay, well if my immune system is attacking me, maybe it's technically autoimmune? that's the rheumatologists instead of the immunologists, what do they have to say? dick all my dude, I don't have rheumatoid arthritis so they just shrug at me and go "idk, fibro? I don't know why you're here" and send me home with nothing. (I literally had a rheumatologist say to me, verbatim, "I don't know why you're here." buddy it's your job to read the chart and decide if I get seen or not, you tell me. at least he had a snazzy outfit.)

being chronically ill can be a terrible struggle no matter what, but a disease that is perceived as rare, accurate or not, adds a whole new layer of bullshit. (and of course there are much much rarer diseases out there, with even more hoops and dead ends and struggles and all-new layers of bullshit that even I don't have to deal with!)

anyway I'm having a shit time and using this awareness day as an excuse to productively bitch about it 👍