X-Message-Number: 15436
Date: Tue, 23 Jan 2001 12:39:12 -0500
Subject: A Reply To Mr. Grimes
From: 

Mr. Jeff Grimes has been favoring us with a couple of posts lately, in
one of which he mentioned me personally.  Well -- call on The Devil and
he will appear, as the old Russian proverb goes.  I thought I would take
the opportunity to respond to his points.

1.  Mr. Grimes says:  "I didn't mean to start a new debate here, I was
just pointing out that no one (at least on Cryonet) seems to show much
interest in what Cryonics Institute procedures are. And if we don't know
what the procedures are, it's impossible to make comparisons."

This is a very good point -- which is why CI has written a very lengthy
page on comparing policies and procedures.  Or at least comparing them
insofar as other organization's procedures are sufficiently explicit for
let us make comparisons.  I am afraid that Mr. Grimes  last sentence
there may give people the impression that 'we' don t know what CI
procedures are at all   ie, that there is no information whatsoever about
CI procedures on CI s web site.  Tastes vary greatly, so there may indeed
not be enough to satisfy Mr. Grimes (though from his remarks I do believe
he simply had to have missed a couple of passages).  But surely Mr.
Grimes cannot be saying that there is *no* information *whatever* about
CI procedures there.  He seems to, at times.  He says:  "Mr. Ettinger
says there's no secret. If there's no secret, why can't I find a specific
description of the procedure currently being used on human patients at
Cryonics Institute? This information does NOT seem to be on their web
site."

No?  Well, to take just one (1) paragraph from an article by Robert
Ettinger available through the CI site:   Heparin is used as feasible, up
to 30,000 units, or 40,000 for a very large person. (The heparin will not
do much good unless circulation can be maintained by CPR. If intravenous
injection is difficult, peritoneal or other injection may be used. If
heparin cannot effectively be introduced otherwise, you may want to add
it to the washout solution.) The right and left common carotid artery and
the right and left internal jugular vein are used for the
washout/perfusion site. The use of these vessels will allow the head to
remain packed in ice. The Cryonics Institute washes out first the head
then the rest of the body. The Cryonics Institute use one pass on open
circuit ie, first the washout fluid, and later the perfusate go into the
artery, and the blood and the other fluids flow out of the jugular vein,
to be disposed of in any convenient way. If feasible, it might be helpful
to occasionally collect a small vial of effluent, labelling it as to time
and stage of procedure. Both arteries are raised and cannulated, and both
veins opened. The fluids are injected up the arteries, the left side
being washed first then the right. Next the right side is perfused (it is
already connected), then the left. A low pressure 5 lb/in2 or less, and a
medium rate of flow is used, adjusting as indicated. 

Is this not a specific description of procedures?  Readers can judge for
themselves by reading the article at
http://www.geocities.com/HotSprings/Sauna/3748//funerals.htm.  They can
also read other materials touching on procedures at the Comparing
Procedures and Policies page at http://www.cryonics.org/comparisons.html,
the Phases of Suspension page at http://www.cryonics.org/phases.html, the
FAQ at http://www.cryonics.org/prod.html, the Becoming A Members FAQ at
http://www.cryonics.org/become.html, the student information FAQ at
http://www.cryonics.org/studentinfo.html, the research updates and some
full fifty or so pages of research reports at
http://www.cryonics.org/research.html, plus Mr. Ettinger s
procedure-related remarks on the Viewpoints page at
http://www.cryonics.org/news.html.

I note in passing that Mr. Eugene Leitl -- striving to make the point
that CI is secretive -- elected to prove this in an odd way by pointing
readers to Mr. Ettinger s 305 posts (854 KB of cloaked silence) on
Cryonet from 1993-1996.  These too are available for viewing at the
Cryonet Archives via http://www.cryonics.org/links.html, and, yup, CI
procedures are definitely addressed there too.  Besides this, the CI site
has an  Ask Us Anything  page where readers are invited to, well, ask CI
anything; and a Suggestion Box page where readers who feel that more
specific information should be put on pages can do so; and of course
there are people like Robert Ettinger and even me fielding the occasional
question online.  

I really don t think that this constitutes no information about CI
procedures.  I mean -- really:  it's there.  Go look.  I'd cut and paste
it all for readers, but there's a text limit.  

Mr. Grimes is quite correct on one point.  There has not been (as of yet)
one single page on the CI web site -- or any organization's web site --
where all this information has been collected together.  But that doesn t
mean that no information is there, or that it isn t available.  CI has
never collected it on one page because   seriously!   in the nearly four
years that the page has been up, no one until Mr. Grimes ever said that
the information up there already is insufficient.  However, since he has,
Robert Ettinger -- ever willing to serve the cryonics public -- is
willing to pull it all together and devote a special additional page to
just this one subject online.  (For which he has of course gotten no
thanks or approval.)  I ought to point out, though, that the unlit and
impenetrable dungeon that is CI is going to be lit and penetrated by a
three separate film crews in succession TV after that.  Hence things are
a trifle busy at the moment.  I would imagine it may take a couple of
days for to get the page pulled together and edited, since things are
pressing and human fingers can only type so quickly.  If CI might be
allowed a grace period of several days, and let its lack of a unified
page be ignored as it is with other organizations, that would be nice. 
Readers who would like to check out the descriptions of procedures that
are there already online (such as the passage and links I quoted) are
free to do so.  Really, I do not think the result can accurately be
described as zero.

2.  Said Mr. Grimes:  "...there's no way of knowing what the differences
are between the lab work and the treatment of human patients, especially
since the lab work used three different procedures. Which one is the same
as you use on people? Is any of them the same?" 

I confess I don t quite understand this one.  Does Mr. Grimes mean by
 three procedures  stepped, one-pass, and experimental control?  The
procedure CI uses is the one that gets the best results, as evaluated by
qualified outside professionals.  (CI could merely go the way of other
organizations, of course, look at it themselves, and go,  That s great!  
But it doesn t.)   It is true that CI is extrapolating from its research,
ie, assuming that the results on freshly killed, cooled, perfused, and
evaluated sheep brains will yield similar results on humans.  What else
can it do?  Kill living human beings, and perfuse them and see what
happens?  I believe that Mr. Mike Darwin once suggested on Cryonet that
cryonics organizations remove a tiny chunk of their members  brains
(their cryopreserved members' brains) and see how stuff was going.  To my
knowledge no relative of a patient ever volunteered their wife, child, or
mother for this experiment.

3.  Mr. Grimes:  "Oops, I just read this statement by Mr. Ettinger a bit
more carefully:  "If anyone wants a summary of the procedure used on the
sheep heads, which became the CI temporary standard, and doesn't want to
bother with the detail on the web site, here it is in brief: The CPA is
75% V/V glycerol in a base of buffered Ringer's with Mannitol, at about
45 deg F. One pass."   Hey! What's that little word "temporary" doing in
there?! Does it mean that this "standard" isn't actually the standard any
more, because it was only temporary? What's going on here? Is the
temporary standard still being used or not? If not, why are you telling
me what used to be used in the past? If it is still being used, why is it
"temporary"? Or why was it temporary in the past?"

All medical procedures everywhere are  temporary  because they are all
discarded once superior ones come into feasible use.  CI s latest round
of tests show that stepped ramping is (*very* slightly) superior to
one-pass.  Therefore stepped is in and one-pass is out.  CI should soon
have results as to whether continuous as opposed to stepped is better,
and if it is, CI will of course then adopt it.  Why mention it at all if
we re throwing the entire old procedure out?  Because we re not throwing
the whole procedure out.  It has gone from  75% V/V glycerol in a base of
buffered Ringer's with Mannitol, at about 45 deg F. One pass  to  75% V/V
glycerol in a base of buffered Ringer's with Mannitol, at about 45 deg F.
Stepped.   One builds on old research, one does not make a complete
rupture, or discard it.

4.  Mr. Ettinger said, "There is indeed considerable mystery about the
Alcor procedures, parts of which are still secret, which prevents us
testing them ourselves," and Mr. Grimes replied:  "Well, this may or may
not be true. But here you go talking about Alcor again! I want to talk
about CI! Why change the subject?" 

To answer the first, it is not  may or may not be true :  it is quite
true.  We do not know   merely to restrict ourselves to vitrification  
what the formulae used are, what the cooling rate is, what concentrations
are being used on human patients, etc. .  I don t want to get away from
the subject of CI research, but I do hope that at some point Mr. Grimes
will extend his researches to other organizations and not merely CI
exclusively and share his results.  Mr. Grimes says    I want to talk
about CI!    OK.  But if we genuinely want to have a comparison, we must
at some point compare something to something.  It cannot be Mr. Grimes 
position that CI and only CI should be completely and painstakingly
explicit about every last conceivable detail, and that other
organizations should be given complete carte blanche and ignored.  Does
Mr. Grimes feels that that everyone is equally open about everything? 
I m sorry to say the facts don t support it.  There is no mystery about
what sort of perfusate CI is using, and there is total mystery about what
Alcor's vitrification solution is.  I m sorry that that s the case, but
it just is, and if Mr. Grimes is serious about wanting an honest open
comparison, he ought to distibute his inquiries and criticisms equally. 
Otherwise he will only get what he is now transmitting:  a distorted
picture. 

4.  Mr.  Ettinger said, "On our web site are extensive reports by the
cryobiologists/microscopists who repeated our sheep head work and
evaluated it in the Ukraine a few years back, with a great deal of
detail."  Mr. Grimes replied:   But what does this have to do with CI
procedures being used on people today? 

Apart from the use of stepped over one-pass, the other variables are the
same, and that is relevant, is it not?  I might add, it does make a
difference to people -- at all organizations -- whose spouses or
relatives might have been prepared similarly.  There's an impression that
'better techniques today' means 'worthless techniques yesterday'.  That
is not the case.  CI's earlier techniques -- like it's current techniques
-- demonstrably reduced freezing damage, and therefore give patients
better hopes for revival.  That is worth mentioning.  Should we burn all
Mike Darwin's BPI Tech Briefs (available at -- well, you know where,
don't you)?  After all, they're different -- probably; we don't know --
from what Alcor is doing today; I think; maybe. 

5.  Mr.  Ettinger said, "If anyone wants a summary of the procedure used
on the sheep heads, which became the CI temporary standard, and doesn't
want to bother with the detail on the web site, here it is in brief: The
CPA is 75% V/V glycerol in a base of buffered Ringer's with Mannitol, at
about 45 deg F. One pass."  This was not enough for Mr. Grimes, who
replied,  I'm sorry but this is not a proper description. I wish you had
spent as much time giving me the details as you spent on all the
political rhetoric. Then we would have some better information. What is
the Ringer's solution buffered with? If you have 75% glycerol and 25%
water by volume, and then you mix it with Ringer's solution, I assume
this means the actual amount of glycerol decreases. Is that what you're
saying here? So, what is the final concentration of glycerol?And how much
Mannitol is used? I have some knowledge of chemistry, and have completed
part of an emergency med tech course, but I don't understand why you need
Mannitol. Can you explain this? Also you don't give any indication of how
length the "one pass" is. Ten minutes? Ten hours?  Also you don't say
anything about the volume of the solution which is passed through the
person, or the temperature, or any methods for measuering temperature. 

The washout solution is Ringer s solution (KCl 0.3 gm/liter, CaCl2 0.33
gm/liter, NaCl 8.6 gm/liter).  It is buffered with sodium bicarbonate
(NaHCO3), 2.6 gm/liter, plus mannitol 4 gm/liter. Heparin may (in some
cases, depending on the patient s circumstances) be added.  The perfusate
is 75% glycerine by volume, the rest washout solution:  CI does not add
 25% water by volume .   Mannitol is used because it reduces or
eliminates the problem of edema or swelling.  Solutions are cooled by
being kept in a refrigerator beforehand, where the temperature is about 7
degrees C or 45 degrees F.  Solutions are fine-filtered and sterilized
before refrigeration.  

The questions about volume and the length of the one-pass are good ones,
incidentally, because they
point up the variable nature of actual treatment.  Mr. Grimes asks how
much CPA does CI use and how fast do they put it in.  The *rough* answer
is, we need enough to replace all the patient s blood possible, and we
try to do it as quickly as we can, and *generally* doing so in an actual
perfusion of a patient takes perhaps an hour and a half.   I say  rough 
and  generally  because, as simple common sense will tell you, patients
vary:  A 300-pound man will have more blood to replace, need more CPA to
replace it with, and require more time to have it done, than a 90-pound
woman will, or a thirty-pound child.  People in accidents or with cancer
or vascular disorders do not necessarily perfuse at some abstract perfect
rate.  It would sound nice and authoritative if CI could say  10 liters,
72 minutes, always and everywhere .  That might be ideal for some
patients, inadequate and disastrous for others.

In actual practice, circumstances very often dictate the procedures used.
 Normally, for instance, CI prefers to use the jugular vein for
perfusion.  But what if the patient has fallen and broken his neck and
the entire neck is swollen?  Normally, CI uses (as does Alcor) heparin as
an anticoagulant.  But what if the patient dies alone and is not
discovered for two days?  What is the point to adding anticoagulant when
the blood has coagulated?  It is easy and tempting to give a snap
response.  But it is misleading.

6.  Mr. Ettinger said, "I doubt that any critic, including Mr. Grimes,
really does want to know the exact details, except to look for debating
points."  Mr. Grimes replied:   Well, I took the trouble to send two
emails to CI asking for details, and now I am taking the trouble to ask
questions here. So far, all I have from you, answering my question
specifically, is one sentence, followed by a lot of PR about your
organization. 

Again, interested readers who wish to find out whether CI s descriptions
of it s procedures are restricted to one sentence may check out my brief
quote of several of Mr. Ettinger's sentences above, plus the Comparing
Procedures and Policies page at http://www.cryonics.org/comparisons.html,
the Phases of Suspension page at http://www.cryonics.org/phases.html, the
FAQ at http://www.cryonics.org/prod.html, etc., etc., etc.  (again, see
above).  Or simply read keep reading Cryonet, where questions like Mr.
Grimes  are (obviously) responded to.  I think one will find more than
one sentence on the topic.  Nay -- more than two!

7.  Mr. Grimes:   All right, I suppose I have got myself into this, so I
will continue. I have spent a lot of time going through the web site for
CI, and find some statements that seem flat-out wrong, or at least
misleading, and I am really surprised that other organizations have not
objected (maybe they haven't bothered to look at the web site). 

Actually, about a year ago, Mr. Charles Platt reviewed our Comparing page
in some detail and sent a series of quite lengthy emails to myself and
Mr. Ettinger and (to brighten his day) to Mr. Fred Chamberlain of Alcor
in which he made several suggestions in his colorful and inimitable
manner.  Where they were felt to be correct and justified, CI made
changes.  Where they were not, the reasons were explained in a reply
posted to Mr. Platt.  Mr. Chamberlain, I believe, had no comment on the
exchange.  Maybe he didn t bother to read it, lucky fellow. 

8.  Mr. Grimes wrote,   I am interested in the Cryonics Institute partly
because it seems to be the only organization providing service in the UK
these days. The web site is VERY large so I will just pick a small piece
to start with, relating to some recent discussions here,  and so saying,
Mr. Grimes then quoted this passage from the CI page:  "Also, and more
importantly, the cryoprotectants used in vitrification are toxic. Thus,
vitrification kills cells: it poisons and injures them to the point of
actually disintegrating cell membranes in some cases. Indeed, the damage
done by vitrification has been so immense and so much worse than
conventional suspension treatments that, on balance, every last cryonics
organization has throughout cryonics history opted for the less
destructive option of conventional glycerol suspension and cooling and
liquid nitrogen storage."  

Mr. Grimes  response was:   This is a bit "controversial" isn't it? We
saw a post on CryoNet not long ago by one of the scientists developing
vitrification, who stated flatly that the chemicals used are LESS toxic
than the 75% glycerol which Cryonics Institute says it uses now. Does he
know what he's talking about? One problem I have with the CI page is that
it includes hardly any references for any of the things it says about its
competitors. Where does their information come from? Surely it cannot be
very ethical to state outright that "damage done by vitrification has
been so immense and so much worse" if you don't have a really solid
source for your statement. 

The really solid source for that statement is available through the CI
link to the INC web site, where one of the scientists developing
vitrification has a full article posted which states that in earlier
results (not the current ones), quote,    vitrification was only possible
by combining the cryoprotectant with 1,000 atmospheres (atm) of
hydrostatic pressure. Unhappily, we found that these high pressures could
not be tolerated. We therefore raised the concentration to a
concentration that required only 500 atm of applied pressure, resulting
in a drop in survival from 100% to virtually 0%. Given a couple of years
of effort, this survival rate was boosted to 75%, but when we combined
this concentration with 500 atm, the survival rate again fell to zero.
Raising concentration still more, so that no pressure would be needed,
also resulted in a 0% survival rate. 

0% survival seems to me to be kind of not so great.  Can one fairly
describe total wipeout as  worse , nay, 'immense'?  I think so, but I
will grant that some more verbally stringent might not.  (Readers wishing
to view the entire article may go to the CI s web page at
http://www.cryonics.org/links.html and click the INC link.)

I might add that according to Fred Chamberlain's article (available at --
you guessed it -- http://www.cryonics.org/comparisons.html), he states
that Alcor is using its vitrification solution in higher concentrations. 
How much higher we do not know, though we do know that higher
concentrations are more toxic.  More toxic than glycerol?  Maybe.  Mr.
Grimes is not asking, and I can't help but notice that no Alcor official
is volunteering the information.  Assuming any comparison tests have been
run at all.  But so what?  We want to know what mannitol is for, so we
can be sure that CI is not just slipping goop in to impress people, but
also not telling them about it to keep it secret.) 

9.  Mr. Grimes:   Since Robert Ettinger complains that the procedures
used by competitors are "secret" how can he know that they are so bad? 

The use of quotations above suggest that those procedures are not in fact
secret.  They are.  If Mr. Grimes knows of a place where 21CM formulae
(or even the full names and mixes of medications used by Alcor in
glycerol suspension) are publicly available, please, by all means tell us
where.  Inquiring minds want to know.

How does Mr. Ettinger know they are so bad?  He doesn t.  Maybe they re
not so bad.  We just have no way of testing, and therefore no way of
knowing.  I should point out, however, that I m not aware that Mr.
Ettinger has ever said  vitrification is bad .  The CI site   if I may
quote from it directly -- says:   Please note carefully: in pointing out
the many practical difficulties of developing and applying vitrification,
we are not saying that vitrification as such is bad or that research into
it is inappropriate. On the contrary. We admire the energy and effort
that many people at various organizations have invested in the new
research. We fully agree that much more research and development is
needed. Indeed we are ourselves conducting ongoing new research, with
fresh reports from time to time on this web site. And, of course, we are
glad to point people to the article and let them make their own
judgments: the article in question is available at
http://www.alcor.org/eventsb.html, and some further commentary on it is
available at http://www.cryonics.org/vitcomm.htm. Nonetheless, we think a
close rather than a casual and uncritical reading of the article in
question will demonstrate that its somewhat grandiose promotional claims
plainly go much much further than the evidence presented justifies.  Let
us be clear, though: CI believes that patients who undergo vitrification
(like those who don't) should be recoverable by future technology, that
research into the technique should definitely continue, and that such an
option should be made available to members who want it. However, people
reading the article in question, upon seeing phrases like 'no structural
damage' and speculations about 'pharmacology' restoring vitrified
patients, may be led to assume that no damage whatsoever occurs to
vitrified patients, and that reversible suspension has essentially been
achieved. Nothing could be further from the truth."

Do Alcor or INC or 21CM or Mr. Grimes believe that no damage whatsoever
occurs to vitrified patients, and that reversible suspension is here now?
  Again, this is a question Mr. Grimes does not ask, and that is why he
is not getting, or giving, a balanced view. 

10.  Notes Mr. Grimes:   I am also really surprised by the last part of
the quote stating that all other organizations have "opted for"
conventional glycerol. Did they have a choice? From previous posts it
seems that only one organization (Alcor) has been allowed a license to
use the vitrification system, which was only developed last year anyway.
But "throughout cryonics history" suggests vitrification has been an
option for years. It hasn't, has it? This seems intentionally
misleading."

From CI s link to the INC site, one can read an extended statement by the
scientist developing vitrification on this subject, in which he states,
quote:   In 1980, I decided to begin looking at a radical alternative. In
this alternative, which is called vitrification, no ice forms in the
organ regardless of how deeply it is cooled.    It would seem, thus, that
vitrification has been under serious consideration for at least twenty
years.

I should add that I don t believe that Alcor has been licensed to use
 the vitrification system .  My understanding (perhaps wrong) is that
Alcor was issued precisely one formula and given some instructions in how
to use it, but that (according to Mr. Chamberlain s article) Alcor is
cooling faster than 21CM suggests, and using higher (and therefore more
toxic) concentrations.  The procedure currently being applied on humans
is not (therefore) the procedure that is being applied on either INC s
two brain slices, or on 21CM s two rabbit kidneys.  What is being
applied, we don t know.   True, we don't know that it is 'bad'.  Maybe
it's not.  In all sincerity, I hope that it in fact is not.  CI would
like to find out by running tests evaluated (like its current tests) by
third-party researchers.  But it can't because neither BioTransport not
21CM will (for the moment) license anything to them.  I think that if
they would, the additional research results would be to everyone's
benefit.  But it just isn't happening.  Yet.

11.  Mr. Grimes:   Here's another part that bothered me:  [Ettinger:]
"What does 'viable' mean? It does not mean that half the cells were
cooled to a temperature that forestalled all decay and were then restored
to healthy life. It means that, in two experiments, about half the cells
managed to retain a potassium/sodium ratio that cells require to be
alive. About half did not, and were irrecoverably dead (by present
methods)."  Mr. Grimes:   But we saw a post here recently that absolutely
contradicted this and stated that the percentage viability measures the
overall ability of cells to do what they normally do, which is like
saying an athlete can only run 53% as fast as he used to (but he's still
running, not lying on the ground, with half of him paralyzed). How did
Cryonics Institute get this so wrong?  

To be quite precise, on January 9, the principal researcher at the
Institute for Neural Cryobiology reported 66% viability using a newer
cryoprotectant and longer equilibration time.  This scientist said that
the percentage referred to each individual cell, not an average over all
the cells in the specimen.  (This I have to confess sounded rather odd to
me, since I find it kind of tough to imagine both every last cell being
individually examined, *and* every last cell coming out exactly 66%
viable.  It is really rare that treated biological specimens come out
absolutely perfect straight across the board, though I do not say that it
didn t happen.  Merely that we cannot replicate the experiment, lacking
the solutions and formulae.)  

Now I don t read Cryonet every day (good grief, who could, and remain
sane!); however, I believe that six days later, on the fifteenth, in a
message to Cryonet, Paul Wakfer, President of INC, said that the 53%
viability (now 66%) is indeed a global or average percentage of
functionality by K/Na criterion, and did not apply to each individual
cell.  So I am not sure just what the particular line is on this subject
at the moment.   When there s a consensus, someone tell me.

Mr. Grimes has a point, though   albeit not one that sheds a good light
on vitrification.  He is right to the extent that he claims CI apparently
believed that the 53% of the cells treated were in viable condition and
that 47% were not.  This, however, was because the article by Mr.
Chamberlain did not specifiy which of the alternatives was the case, and
CI gave vitrification researchers the benefit of the doubt by assuming
they got good results with more than half the cells.  It seemed kind of
weird to assert that, using vitrification, every individual cell was  53%
viable .  I confess I find it kind of hard to figure out what that means
exactly in terms of individual cells -- 53% of pottasium and sodium in
each cell?  (No doubt I shall be violently enlightened, in between
numerous aspersions on my legitimacy, my IQ, etc.).  See, if my leg gets
vitrified, and 47% of it isn t viable (the lower leg, say), that means
the upper leg is, and so at least I ve got an upper leg.  But if 47% of
*every single cell* in my leg doesn t work   well, what does that mean? 
Mr. Grimes compares 53% viability with a runner running only 53% as fast.
 Does this mean that if we vitrify a runner s leg right now, it ll come
out walking half as slow?  I don t think so.  I think that if someone s
head gets vitrified and thawed, it will come out dead and not just
thinking at half-speed.  Again, it is easy to put that sort of thing to
the test and see, but no one who can is doing so, and CI (which would
like to) cannot.

I should note in passing that the only reason we found out about these
different versions of viability is precisely because Mr. Ettinger   alone
  raised the issue and so finally got someone to come out and clarify it.
 Sort of.  Would we be better off is *no* one asked any questions about
it at all ever?  This seems to be a strange position for Mr. Grimes to
hold, and I find it hard to believe he holds it.  It seems to me that if
he is justified in asking questions about CI procedures -- and he is --
Mr. Ettinger is justified in asking about vitrification procedures. 
Whereas in fact Mr. Ettinger is characterized as 'intentionally
misleading' for asking questions.  Why should Mr. Grimes be upset that
Mr. Ettinger is doing what he is doing?

12.  Mr. Grimes:  "Since these are VERY serious allegations, isn't there
a question of legal liability here? I mean if this was a pharmaceutical
company claiming that a new drug by another pharmaceutical company killed
its patients, and the company making the accusation did not bother to
back up this claim with some citations to literature, or even a phone
call to check the facts, I would expect the injured party to file a law
suit or restraining order ASAP."

I hate to have to quote the same passage twice in the same post,
especially since it s on the CI site and I am sure Mr. Grimes, quoting
from the section, must have read it, but:  Let us be clear, though: CI
believes that patients who undergo vitrification (like those who don't)
should be recoverable by future technology   and, far from having no
citations, this passage is preceded exactly two sentences earlier by a
link to Fred Chamberlain s own full article at
http://www.alcor.org/eventsb.html.   CI is quite explicitly not saying
that anyone is 'killing its patients', and quite clearly pointing to the
other side and letting it make its full stated case.  A courtesy that is
not now and never has been returned. 

13.  Mr. Grimes:  "I must say, the Cryonics Institute does seem to have
some advantages in its use of morticians to provide a faster local
response than other organizations, but its web site bothers me somewhat
because it is so full of negative comparisons, without references or
proof. When I first became interested in cryonics I assumed that in a
small field, there would be some need for people to support each other.
But it looks more like the Maoists vs the Trotskyites vs the Stalinists."

Not to be harsh, but I should note in passing that, for some reason I
don t quite understand, comments on the internet always seem to come out
ten times harsher than they do in real life.  This is something we all
ought to remember when posting.  I really don't think that Mr. Grimes
seriously intends to compare people posting on Cryonet to the greatest
mass murderers in human history.  Just as I don't really believe that
having answered his questions in private correspondence, in public
correspondence, having pointed to several online information sources,
etc., etc., Mr. Grimes really believes that there is zero information on
CI procedures available.  What question has he asked that hasn't been
answered?  I kind of feel that Mr. Grimes   understandably, maybe   would
like one single article where all CI s procedures are listed together. 
He does not want, apparently, to go hopping around reading this here and
reading that there and having to put the picture together himself.  Well
  OK.  If that s what he wants, CI will oblige.  It's a reasonable thing
to offer CI site readers.  (I wish all the organizations did, for that
matter.)  In fact, I'm not the webmaster or anything, and it does take a
little while to pull all this stuff together and edit it, but if he
really doesn't seem to want to read the web page in any depth, then if
he d like, I d be happy to email it to him personally once it s done   as
well as to anyone else.

But -- frankly -- at some point a serious seeker after truth has to
exercise a bit of self-criticism too.  I mean -- look, Mr. Ettinger says,
 The CPA is 75% V/V glycerol in a base of buffered Ringer's with
Mannitol, at about 45 deg F,  and  Mr. Grimes reads this, cuts it out,
pastes it into his post, and says in the very same paragraph carrying the
quote,   you don't say anything about the volume of the solution which is
passed through the person, or the temperature   

Well   yes, he does!  It s  45 deg F .  It's right there!  How can
someone *read* the temperature, and cut it and paste it and quote it, and
then ask what the temperature is?   The  volume of the solution passed
through the person ?  Well, isn t it simply obvious that a deceased six
foot five obese adult male will require  more , and a deceased one-year
old child  less , and that snap responses like 'six liters' simply cannot
be given?  In the very section on vitrification he quotes from, the CI
site says,  Please note carefully: in pointing out the many practical
difficulties of developing and applying vitrification, we are not saying
that vitrification as such is bad,  and Mr. Grimes, clearly having read
the section, nonetheless says,  since Robert Ettinger complains that the
procedures used by competitors are "secret" how can he know that they are
so bad? 

I m not saying that Mr. Grimes is badly motivated or that he s wrong to
ask.  I m sure he s well motivated, and he's quite right to ask.  But it
just seems to me that he's -- well, skimming in his reading rather than
reading closely and thoughtfully.  Hopping on certain points that strike
him as not being good enough, but not bothering to make a really thorough
check.  That's not a crime, of course.  And it's certainly not a problem
for CI.  Hey, it just gives CI another chance to make its case, show the
world that it s hiding nothing, and point everyone to the appropriate
information sources.  Me, I thank Mr. Grimes for doing his bit to drive
more people to CI's web site.  We need more people like Mr. Grimes,
showing the Great American Republic that CI responds and others don't. 
Web site readership is up and so are inquiries this week:  thanks, Jeff! 
I myself tend not to post much to Cryonet, but Mr. Grimes has managed to
drag even me away from my cough drops and Robutussin and gotten me
typing.  CI owes such folks much thanks.  I can only hope that once Mr.
Grimes is done asking questions about CI, he'll go on to ask them of all
the other organizations, and give them a boost too.  I think complete
openness would be a very good thing for the cryonics movement, and I am
both happy and sorry to say that it is only CI that seems to be the main
practitioner at the moment.

I d also like to say one thing before I go.  I do think Mr. Grimes 
exclusive concentration on CI procedures are a bit odd, and his comments
on Robert Ettinger a bit harsh.  But I think he has every right to ask
the former, and that he has come close but not stepped over the line that
constitutes  civilized discourse  in the latter.  But he has come close,
and that really isn't necessary.  People in cryonics are not 'Maoists and
Stalinists' and they don t hate each other, and they don t spend all
their time goring each other.  Yes, I have to admit that when Mr. Eugene
Leitl called Mr. Ettinger a  warty troll , he did some damage   to Eugene
Leitl.  But did the cryonics movement crumble and shake because of it? 
Of course not.  In everything cryonicists are doing and striving for,
there has been progress, and that progress is growing.  We are heading in
the right direction, and we are heading there together.  I think perhaps
the most graceful post of the past few weeks came from an Alcor member,
Kennita Watson, who responded to Mr. Leitl s  troll  post by pointing
out, with wit and a sense of humor,  that such language really was
neither accurate, substantive, nor kind.  Yes:  people in cryonics really
do act like grown-ups and come together and support each other   as CI
did, when it came to CryoCare s aid when it was beginning to crumble. 
Good will, generosity of spirit, love of truth:  all this is genuinely
out there, and I suspect is there even in the worse of us.  This is what
counts about the cryonics movement   this, and gestures like Ms.
Watson s, and the objective progress which CI in its way and no doubt
Alcor in its way is making too.  All the rest is just hot air.

David Pascal  

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