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Very strange white fibrous clots — Transcript

by Dr. John Campbell · 3,039 words · 564 segments · language en · Watch on YouTube

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  1. 0:01You're very welcome to this talk. Now,
  2. 0:02today we want to carry on thinking about
  3. 0:04these anomalous white fibrous clots
  4. 0:07that are being found by embalmers, not
  5. 0:09really identified by pathologists yet as
  6. 0:11far as I know, but the embalmers are
  7. 0:13certainly flagging them up. They seem to
  8. 0:15appear in 2021, different from clots
  9. 0:17which occurred before 2021. So, just
  10. 0:20what is going on here? Now, there's a
  11. 0:22trickle of reports coming out on these
  12. 0:24in the scientific literature.
  13. 0:26Not a lot, but it is starting. So, we
  14. 0:28are starting to learn a bit about them.
  15. 0:30Now, just before we look at the content,
  16. 0:31YouTube are quite happy for me to talk
  17. 0:33about white fibrous clots, but they're
  18. 0:35not so happy for me to show pictures of
  19. 0:37them.
  20. 0:38So, at the very top of the description
  21. 0:40under this video, I'll put the link to
  22. 0:41the Substack Substack article I've done
  23. 0:43on this where there's a lots and lots of
  24. 0:46high-resolution pictures that
  25. 0:47definitively prove
  26. 0:49uh the existence of these clots,
  27. 0:51including some being withdrawn actively
  28. 0:53from various blood vessels in the body
  29. 0:55by embalmers. So, we know that these
  30. 0:57things are real. That's how I was
  31. 0:59convinced because of the photographic
  32. 1:00evidence.
  33. 1:02Check it out. Now, this video is about
  34. 1:05the what what these clots are made of.
  35. 1:07So, there's a some pharmacologists and
  36. 1:09biochemists have analyzed these clots
  37. 1:11and they've worked out partly what
  38. 1:13they're made of. Not entirely, it's not
  39. 1:15completely an exhaustive study,
  40. 1:17but what are they actually made of?
  41. 1:18Because this is the first point first
  42. 1:21thing we need to know. We need to know
  43. 1:22were these clots forming when people are
  44. 1:24alive, were they forming during the
  45. 1:26dying process, were they forming after
  46. 1:27the people were dead?
  47. 1:29We know they were there very shortly
  48. 1:31after death and we're going to look at
  49. 1:32evidence to show that they do actually
  50. 1:33form in life today as well.
  51. 1:36But, that's what this is about. Um
  52. 1:38it turns out they're made of abnormal
  53. 1:40proteins, very unusual proteins. So,
  54. 1:43they're a bit like amyloid protein,
  55. 1:45which is a pathological protein in the
  56. 1:47body, although it can be part of normal
  57. 1:48structures.
  58. 1:49But, they're a bit like that, but not
  59. 1:51quite like that. They're a bit
  60. 1:52different. And they're a bit like the
  61. 1:54clotting protein uh fibrinogen and
  62. 1:56fibrin, the sticky strands that that
  63. 1:58form blood clots, but not quite like
  64. 2:00that either. So, not only are the
  65. 2:02anomalous clots that made of anomalous
  66. 2:04non-typical proteins. So, that's what
  67. 2:06this is about if you haven't got time to
  68. 2:08watch. But if you have, the detail
  69. 2:10really is quite uh quite interesting,
  70. 2:12really.
  71. 2:13So, this is the first paper we're going
  72. 2:15to be looking at here.
  73. 2:17Um I'm not going to Yeah, I will read it
  74. 2:19out now. Raman spectroscopic
  75. 2:21characterization of characterization of
  76. 2:23anomalous intravascular fibers discuss.
  77. 2:26Evidence for stage-dependent beta sheet
  78. 2:28enrichment protein maturation. Now,
  79. 2:30that's pure gobbledygook, of course,
  80. 2:32unless you're a biochemist, but we will
  81. 2:34unpack that in a minute. Uh just to show
  82. 2:37you the way this paper was done, it's
  83. 2:39it's basically spectroscopic as it said.
  84. 2:41You know what spectroscopy is. It's it's
  85. 2:43analyzing light
  86. 2:45to infer things about the nature of
  87. 2:46matter. So, you can either shine a light
  88. 2:48at it like these researchers did. They
  89. 2:50They shone a laser light on the samples
  90. 2:52and they looked at the way it bounced
  91. 2:53back and did stuff.
  92. 2:55Uh or or you can um look at stars, for
  93. 2:58example, and do spectroscopic analysis
  94. 3:00of stars, and that's
  95. 3:02that's how we know what little stars are
  96. 3:03made of. Um twinkle twinkle little star,
  97. 3:06we now know exactly what you are.
  98. 3:08But that's a separate topic. So, we know
  99. 3:09what they are because of looking at the
  100. 3:11light. It's analyzing matter from the
  101. 3:13light.
  102. 3:14That's what it means. Now, this is the
  103. 3:16results from the paper here. Now, these
  104. 3:18are the spectroscopic analyses. Now, I
  105. 3:20do not pretend to understand these. Only
  106. 3:22biochemists and
  107. 3:24specialists do, really.
  108. 3:25But all the data is there. It is a
  109. 3:27peer-reviewed paper from the
  110. 3:30one of the most reputable European
  111. 3:31agencies
  112. 3:33as we'll look at. So, basically, I'm
  113. 3:35more than happy to trust what the
  114. 3:37authors are telling me these things
  115. 3:39mean. Although I don't fully Well, I
  116. 3:42don't
  117. 3:43hardly understand them at all.
  118. 3:45Anyway, that that doesn't matter. We can
  119. 3:47trust that it's a proper interpretation,
  120. 3:49and it is peer-reviewed by other people
  121. 3:50who know what they're talking about. So,
  122. 3:52we can be pretty sure
  123. 3:54this this is good scientific data. Now,
  124. 3:56let's just unpack it a little bit.
  125. 3:58That's the title there. Raman
  126. 4:00spectroscopy um
  127. 4:02what compounds are present by reading
  128. 4:05the vibrational fingerprints of the
  129. 4:07molecules in the sample. So, that's what
  130. 4:08it is. Shining light, bouncing light,
  131. 4:11non-destructive means of probing
  132. 4:13molecular architecture of proteinaceous
  133. 4:15materials. So, this is a way of
  134. 4:17analyzing proteins by shining lasers on
  135. 4:19it, looking at what comes back and what
  136. 4:21happens to that light spectroscopically.
  137. 4:24Just spectro- we've said what spectros-
  138. 4:27spectroscopy is. So, next bit, what is a
  139. 4:30beta sheet protein? Um
  140. 4:32a protein where a lot of its structure
  141. 4:34is made up of beta sheets.
  142. 4:36And what are beta sheets? Uh flat
  143. 4:38pleated segments form when strands of
  144. 4:40the proteins line up
  145. 4:44side by side. So, it's a secondary
  146. 4:46structure of a protein, really.
  147. 4:48And hydrogen bond together. So, we end
  148. 4:49up with a sheet of these things.
  149. 4:51And just to give an example, um silk
  150. 4:55um it it is is a beta pleated sheet.
  151. 4:58This is what gives uh silk its strength
  152. 5:01and stability
  153. 5:02and uh elasticity.
  154. 5:04So,
  155. 5:06the same thing the these beta pleated
  156. 5:08sheets in these um anomalous white
  157. 5:11fibrous clots giving them very unusual
  158. 5:13characteristics.
  159. 5:14What does the protein maturation bit of
  160. 5:16the title mean? It means as proteins
  161. 5:18progress through different stages of its
  162. 5:19development or aggregation,
  163. 5:21so I as they are clumping together, its
  164. 5:23structure becomes increasingly rich in
  165. 5:25in beta sheets.
  166. 5:26So, these beta sheets become more
  167. 5:28common,
  168. 5:29basically replacing what's called the
  169. 5:31alpha helical state,
  170. 5:33which is the more normal native state of
  171. 5:35proteins.
  172. 5:37Um
  173. 5:38Sorry if that's a bit of a stretch, but
  174. 5:39you've just exhausted my knowledge of
  175. 5:40biochemistry, so we won't be saying much
  176. 5:43more about that in terms of protein
  177. 5:44chemistry. But, the secondary structures
  178. 5:46in proteins,
  179. 5:48the first structure is the way the amino
  180. 5:49acids come together and the way that
  181. 5:51these fold into sheets and fold into
  182. 5:53helices is the secondary structure of
  183. 5:55the protein.
  184. 5:57So that's what we're talking about. Now,
  185. 5:58what method was used in this paper? Now
  186. 6:01this is the uh Wigner Research Center
  187. 6:03for physics in Hungary. Now this is part
  188. 6:07of the Hungarian National uh physical
  189. 6:09network. In fact, it's probably the main
  190. 6:11um research center in Hungary.
  191. 6:14And it's got a very, very high
  192. 6:15international reputation. So this is uh
  193. 6:17absolutely definitive uh research
  194. 6:20institute uh for physics.
  195. 6:23Uh so
  196. 6:24the the quality of the work there is is
  197. 6:26uh is is second to none. It's absolutely
  198. 6:28world-class.
  199. 6:30So we can trust that.
  200. 6:31Uh what did they do? White to pet what
  201. 6:34white to pet rubbery intravascular from
  202. 6:36within the blood vessels.
  203. 6:38Uh fibrous casts Casts because they were
  204. 6:41like molds on the inside of the blood
  205. 6:43vessels.
  206. 6:44Uh recovered during routine embalming
  207. 6:47were analyzed during using
  208. 6:49Raman spectrum.
  209. 6:52Micro Raman microspectroscopy so it
  210. 6:55shining a small laser beam at it and
  211. 6:57looking at what came out.
  212. 6:58Uh Raman spectra exhibited strong
  213. 7:00protein signature. So these things are
  214. 7:02full of proteins.
  215. 7:03Lots and lots of proteins. We know that
  216. 7:05bit.
  217. 7:08Uh now they they look they did other
  218. 7:09things as well as the spectroscopy.
  219. 7:11Yeah, the cast made of from
  220. 7:14atypical protein protein aggregates. So
  221. 7:16different types of unusual proteins
  222. 7:18clump together and they found 17
  223. 7:20different amino acids and there's only
  224. 7:2120 amino acids really present in the
  225. 7:23human body. So um
  226. 7:25they found quite a lot of them.
  227. 7:27Uh the amino acid profile departs from
  228. 7:29published composition of human fibrin
  229. 7:31fibrinogen. Now
  230. 7:34we had thought that these clots were
  231. 7:36made of amyloid and and fibrin.
  232. 7:38So fibrinogen clumps together to form
  233. 7:40fibrin which is the sticky strands and
  234. 7:42the red blood cells stick to that form a
  235. 7:43blood clot. And that is kind of true.
  236. 7:47But what what this is saying is um it's
  237. 7:50like fibrin and fibrinogen, but not
  238. 7:52quite. It's an abnormal type of fibrin
  239. 7:54and fibrinogen.
  240. 7:56>> [snorts]
  241. 7:56>> It's a bit like amyloid protein, which
  242. 7:57is a common pathological protein.
  243. 8:00Causes an Alzheimer's disease, for
  244. 8:01example, though probably not causal.
  245. 8:03That's a separate matter. Um
  246. 8:05so it's a well-known pathological
  247. 8:07protein, although it does occur in
  248. 8:09normal tissues as well.
  249. 8:10Um but it's not quite normal amyloid
  250. 8:12protein. So we've got to put it in the
  251. 8:15way I understand it.
  252. 8:17Uh kind of weird fibrin and kind of
  253. 8:19weird amyloid. Atypical ones.
  254. 8:22And uh
  255. 8:23the authors say that this supports
  256. 8:25interpretation of the non-canonical
  257. 8:27protein aggregate. So a canonical
  258. 8:29protein would be one which is
  259. 8:30well-known, well-identified.
  260. 8:32So healthy proteins would be a
  261. 8:34canonical. Uh these aren't. They're a
  262. 8:36bit weird. It's another way of saying
  263. 8:38kind of
  264. 8:39off-the-book or not quite off-the-shelf
  265. 8:41proteins.
  266. 8:42Exhibiting strong hetero-
  267. 8:45genic
  268. 8:47cons cons
  269. 8:48exhibiting
  270. 8:49exhibiting heterogeneous consistency
  271. 8:52with state with stage-dependent beta
  272. 8:55enhancement.
  273. 8:57So in other in other words, it's
  274. 8:58consistent with that. So in other words,
  275. 9:01there's a mixture of proteins. So
  276. 9:02there's some alpha helical ones.
  277. 9:04But as time goes on, they think there's
  278. 9:06more of these beta-pleated ones come up.
  279. 9:09It's consistent with that. Now, they
  280. 9:11don't know that for sure because they
  281. 9:12didn't follow it through a pathway. This
  282. 9:14is only based on
  283. 9:16uh basically a snapshot in time, but
  284. 9:17there's a mice from looking at two
  285. 9:19different samples that they're
  286. 9:20analyzing. That there was an evolution
  287. 9:22in the way that these things uh that
  288. 9:23these things develop.
  289. 9:25With the normal um
  290. 9:26alpha helical proteins being replaced by
  291. 9:28these
  292. 9:29uh
  293. 9:31tough, stretchy, but abnormal beta-sheet
  294. 9:33proteins, which is giving them the the
  295. 9:35elastic uh calamari kind of
  296. 9:38characteristics.
  297. 9:41Right, so what? Well, it's distinct from
  298. 9:43conventional postmortem thrombi. This is
  299. 9:45not what we normally wash out of the
  300. 9:47vasculature of dead bodies.
  301. 9:50So, unusual.
  302. 9:51The distinct physical and spectroscopic
  303. 9:53features of these casts may aid in their
  304. 9:55further recognition during embalming and
  305. 9:57postmortem examinations. Hint hint,
  306. 9:59pathologists, look out for these things.
  307. 10:02Hint hint, pathologists, again.
  308. 10:04This may aid pathologists in
  309. 10:05distinguishing atypical intravascular
  310. 10:07casts from conventional postmortem
  311. 10:08thrombi. These are not the usual
  312. 10:11postmortem thrombi.
  313. 10:13So, this is now scientific validation
  314. 10:17of what the undertakers were saying. The
  315. 10:18undertakers were saying way back in
  316. 10:202021, this is not what we normally see.
  317. 10:24Undertakers with sometimes decades of
  318. 10:26experience were saying, "No, we don't
  319. 10:28normally see these. These are new." And
  320. 10:30here we have the scientific confirmation
  321. 10:32of that.
  322. 10:34That these are not conventional
  323. 10:36postmortem, after death, thrombus. Nor
  324. 10:39is it similar to the thrombus that you
  325. 10:42get in pathological situations such as
  326. 10:44coronary arterial thrombosis formation
  327. 10:47or deep venous thrombosis. These are
  328. 10:49different.
  329. 10:51They're essentially new
  330. 10:52uh and they're not like all the other
  331. 10:54ones.
  332. 10:56What is causing these?
  333. 10:59Uh no causal link to any exposure,
  334. 11:02infectious agent, vaccine, or
  335. 11:03therapeutic intervention can be inferred
  336. 11:05from the present data. What they are
  337. 11:07saying is because these samples were
  338. 11:10given anonymously
  339. 11:11to maintain confidentiality,
  340. 11:14they don't know
  341. 11:16whether the patients that these clots
  342. 11:18from were vaccinated or not with COVID
  343. 11:21vaccines, for example.
  344. 11:22They don't know what their history is,
  345. 11:24so they can't make any
  346. 11:26uh intimation from that.
  347. 11:28Clearly, this is research which urgently
  348. 11:31needs to be done.
  349. 11:33If it were that these clots are caused
  350. 11:35by adverse reactions to some therapeutic
  351. 11:37intervention, boy, do we need to know
  352. 11:39about that quick.
  353. 11:41Because there's a we're seeing a lot of
  354. 11:42these clots.
  355. 11:43There's a lot of them.
  356. 11:46Sorry, that's the paper. We don't want
  357. 11:47to see that. There we go.
  358. 11:49Um these results underscore the need for
  359. 11:52systematic multimodal investigation. So,
  360. 11:54give it to the biochemists. Let them
  361. 11:56think of any technique they can. As many
  362. 11:58different modalities of investigation as
  363. 12:00they can.
  364. 12:01The clever people will think of dozens
  365. 12:03of ways of doing it.
  366. 12:05And we need further studies
  367. 12:06incorporating incorporating proteomics.
  368. 12:09That's analyzing the uh analyzing the
  369. 12:11proteins.
  370. 12:12Uh histochemistry analyzing the
  371. 12:14histology and the chemistry. Electron
  372. 12:16microscopy, controlled comparisons, and
  373. 12:19well-documented provenance will be
  374. 12:20essential. So, the provenance means we
  375. 12:23need to know the medical history of each
  376. 12:24patient's clot.
  377. 12:26The patient or the the corpse that the
  378. 12:28body that the the clot was removed from,
  379. 12:31we need to know their medical history.
  380. 12:35That will be essential to uh clarify
  381. 12:37biochemical
  382. 12:39biochemi- biochemically identify
  383. 12:41structural evolution, prevalence, and
  384. 12:44potential clinical and postmortem
  385. 12:46significance.
  386. 12:48Um and as we've said, it may be that
  387. 12:51these are forming in life.
  388. 12:53Now, these huge clots
  389. 12:55like like if you look on the Substack
  390. 12:57Substack article, you'll see a clot that
  391. 12:59um
  392. 13:00>> [snorts]
  393. 13:00>> basically would occlude all the bottom
  394. 13:02of the aorta. Patients aren't going to
  395. 13:03live with that. The question is did that
  396. 13:05clot kill the individual or did the clot
  397. 13:08form after death?
  398. 13:10More on that in a minute.
  399. 13:12Um anyway, let's look at the other
  400. 13:14papers that we've got on few of the
  401. 13:16papers I've got on this. We've got this
  402. 13:17paper here
  403. 13:20uh from uh New Zealand.
  404. 13:22We've got this paper here also from the
  405. 13:24same authors in New Zealand.
  406. 13:25And this paper here. So, a trilogy of
  407. 13:27papers. So, what are these papers got to
  408. 13:30contribute to this is their consistency?
  409. 13:32Yes, basically there is consistency.
  410. 13:34So, if we take this first one,
  411. 13:36morphological and histological
  412. 13:37characterization of an
  413. 13:40characterization of anomalous
  414. 13:41intravascular casts, which are the white
  415. 13:43fibrous clots.
  416. 13:45Gross examination revealed elongating
  417. 13:47lumen-filling casts up to 25 cm in
  418. 13:49length, although on the
  419. 13:51on the sub stack we have got a longer
  420. 13:52one than that.
  421. 13:54Um [snorts]
  422. 13:55frequent branching as the blood vessels
  423. 13:57do, demonstrating elasticity of
  424. 13:58resistance atypical of conventional
  425. 14:01thrombi, not like conventional clots.
  426. 14:04These are different.
  427. 14:06These are different to what
  428. 14:08pathologists, doctors,
  429. 14:10embalmers are used to seeing.
  430. 14:13Histology demonstrates dense fibrous
  431. 14:16lamination with intermittent lines of
  432. 14:18Zahn. Now, these lines of Zahn
  433. 14:22uh basically form
  434. 14:26when there's a pulse.
  435. 14:28They show
  436. 14:29it's a bit it's a bit like the ripples
  437. 14:30on a beach.
  438. 14:32Uh the wave comes in and it forms a
  439. 14:34ripple.
  440. 14:36Comes in again, forms another ripple.
  441. 14:37Lines of Zahn are like that. So, the
  442. 14:39pulsatile nature of the blood forms
  443. 14:41these lines of Zahn.
  444. 14:43So, clearly
  445. 14:45if these if these lines of Zahn are
  446. 14:46confirmed and they're not they they
  447. 14:47haven't been confirmed by other studies
  448. 14:49yet, but if they're confirmed,
  449. 14:51that means the lines of Zahn formed
  450. 14:53during life. Therefore, at least part of
  451. 14:55this white fibrous clot formed during
  452. 14:58life and therefore was probably partly
  453. 15:00responsible for killing the
  454. 15:02individual. That means they're not
  455. 15:05purely a postmortem phenomena.
  456. 15:08That means they're an end-of-life or
  457. 15:09perimortem phenomena.
  458. 15:12We need that confirmed.
  459. 15:14We have the labs to do that really
  460. 15:15quickly and readily.
  461. 15:17Uh pity none of them are chomping at the
  462. 15:18bit to do it, but there you go.
  463. 15:21Um so, it did contain these lines of
  464. 15:23Zahn according to this paper. Various
  465. 15:25intracellular inclusion inclusions, so
  466. 15:27you know, some white cells, some red
  467. 15:28cells, things like that. Suggesting
  468. 15:30antemortem, that means before death
  469. 15:32formation
  470. 15:34under atypical hemodynamic conditions.
  471. 15:37So, suggesting they formed when the
  472. 15:39patient was still alive
  473. 15:41but in an abnormal circulatory
  474. 15:44system
  475. 15:45is what these lines of Zahn would
  476. 15:47indicate.
  477. 15:49These structures uh
  478. 15:50features differ from
  479. 15:52physiological thrombi and postmortem
  480. 15:55clots. So, these these are different.
  481. 15:56This is a new phenomenon. It's not like
  482. 15:58normal blood clots.
  483. 16:01Indicating a distinct pathological
  484. 16:04phenomena in these white clots.
  485. 16:06And then the last paper So, remember
  486. 16:09that that was the first one. That was
  487. 16:11the second of this trio of papers.
  488. 16:13That was the third one there.
  489. 16:15So, um
  490. 16:19I've got those in the wrong order.
  491. 16:20Anyway, there's three of them. Yep,
  492. 16:22there's three of them anyway. Right, so
  493. 16:24just to look at the last one.
  494. 16:26Elemental characterization of anomalous
  495. 16:28intravascular casts reveals an abnormal
  496. 16:30biochemical matrix. So, everything about
  497. 16:33these is abnormal.
  498. 16:35The proteins, the biochemistry, all very
  499. 16:37strange.
  500. 16:38The elemental composition of anomalous
  501. 16:41intravascular casts, which is what
  502. 16:42they're calling the white clots,
  503. 16:44is inconsistent with kinetical thrombus.
  504. 16:47In other words, this is not like the
  505. 16:49thrombus that's studied. It's not like
  506. 16:51the thrombus that's in the book. It's
  507. 16:53not like the biochemistry that's in the
  508. 16:54book.
  509. 16:55And supports the presence of a
  510. 16:57non-kinetical
  511. 16:58intravascular matrix. So, this
  512. 17:04matrix structure within the blood
  513. 17:06vessels is not
  514. 17:08what we've seen before. We are dealing
  515. 17:10with a new phenomenon.
  516. 17:12So, uh thanks to those authors,
  517. 17:14especially of ones from the this one we
  518. 17:16haven't looked at before the Raman
  519. 17:17spectroscopy.
  520. 17:19Um we are hoping to talk to one or two
  521. 17:21of the authors at some point
  522. 17:23uh to get more detail and hopefully they
  523. 17:25can
  524. 17:26uh explain the biochemistry better than
  525. 17:28I have.
  526. 17:29But there we go. They are really weird.
  527. 17:31New abnormalous uh
  528. 17:34and clots very strange
  529. 17:37very strange biochemistry, very strange
  530. 17:40structures.
  531. 17:41What is going on here? I would have
  532. 17:43thought we need to find out fairly
  533. 17:45desperately.
  534. 17:47Big question of course remaining in my
  535. 17:48mind, why these being identified in a
  536. 17:50lot of patients, a lot of bodies
  537. 17:53by undertakers
  538. 17:55but it's not hitting
  539. 17:56the mainstream
  540. 17:59uh
  541. 17:59pathology journals.
  542. 18:01Uh these samples in this study here
  543. 18:05were provided not by pathologists
  544. 18:07but were provided by uh
  545. 18:10embalmers
  546. 18:12who anonymously donated these uh these
  547. 18:14these white fibrous structures.
  548. 18:17Why isn't this in the mainstream of uh
  549. 18:19pathology? Why isn't it in the Lancet?
  550. 18:21Why isn't it in Nature?
  551. 18:23American Journal of Medicine, all those
  552. 18:25other things.
  553. 18:27Journal of the American Medical
  554. 18:28Association, why is it not in there?
  555. 18:30Because we're dealing with a truly
  556. 18:31bizarre new phenomena that's relatively
  557. 18:33widespread and yet
  558. 18:35it [snorts] looks like the mainstream
  559. 18:36doesn't want to touch it, which is just
  560. 18:38really quite
  561. 18:40I can't I can't explain it, maybe you
  562. 18:42can.
  563. 18:43For now as always, thank you for
  564. 18:44watching.

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