home *** CD-ROM | disk | FTP | other *** search
-
- The International Rogues Guild/
- ShadowNet
- IRG Newsletter #4
- 1/18/91
- Written by: Haywire
- Edited by: Haywire
-
- 1. Table Of Contents
- --------------------
- 1......................................Table Of Contents
- 2......................................Disclaimer
- 3......................................More About IRG
- 4......................................CyberPunk Follies
- 5......................................Letters From Prison
- 5a.....................................How To Make LSD By Haywire
- 5b.....................................Trashing By Control-S
- 5c.....................................Interesting Places By Control-S
- 6......................................BBSs From Hell
- 7......................................VMBs From Hell
- 8......................................Running The ShadowNet
- 9......................................Hellos & Goodbyes, Greets, Etc.
-
-
- 2. Disclaimer
- -------------
- All items in this newsletter are meant for informational purposes.
- It is written to encourage illegal activities, I hope the reader is inspired
- to go out and break the law after reading all IRG Information. Of course the
- authors of this newsletter cannot be held for anything that the reader goes out
- and does.
- WARNING: Remember ALL explosives are dangerous, DO NOT, I repeat, DO
- NOT mess around with any of the recipes for explosives, EVER! These recipes
- are real, they can kill you, and anyone else. Make sure you know what you're
- doing. Otherwise its your fault.
-
- 3. More About IRG
- -----------------
- IRG is slowly taking off. It took a while but now its getting going
- this issue I am planning on spreading around the world. This issue is
- dedicated to all the Forgotten Heros, and the new ones that will be left over
- from the Iraq and US war.
- IRG is hoping to educate the world to make it a better place for us
- hackers. I have to admit the feds don't seem to be doing much but one day I am
- sure they will take us all down. I just don't understand why someone would
- care what a bunch of kids are doing on the computer while people are getting
- murdered all over the place. So fuck it! Join IRG the following are the members-
-
- IRG Members Rank
- ----------- ------
- Haywire IRG and ShadowNet Leader
- The Spectral Demon Part Time Editor and Hackin' Help
- Dr. Digital ShadowNet Member
- Wasteland Warrior Part Time Programer and Game Winner
-
- People who write IRG articals
- -------------------------------
- Haywire
- The Spectral Demon
- Control-S
-
- Thats about it, if you feel like becoming a member of either IRG or
- ShadowNet. Please call one of the IRG nodes. If you would like to become and
- IRG node again contact one of the IRG nodes.
-
-
- 4. CyberPunk Follys
- -------------------
- Heres that household substitues list I promised I would give you last
- time. How to make TNT will also be in the issue.
-
- Household Substitutes:
- Chemical Name: Household Substitute:
-
- Acetic Acid Vinegar
- Aluminum Oxide Alumia
- Aluminum Potassium Sulfate Alum
- Aluminum Sulfate Alum
- Ammoninum hydroxide Ammonia
- Carbon Carbonate Chalk
- Calcium Hypochloride Bleaching Powder
- Calcium Oxide Lime
- Calcium Sulphate Plaster Of Paris
- Carbonic Acid Seltzer
- Carbon tetrachloride Cleaning Fluid
- Ethylene Dichloride Dutch Fluid
- Ferric Oxide Iron Rust
- Glucose Corn Syrup
- Graphite Black Lead (pencil lead)
- Hydrochloric Acid Muriatic Acid
- Hydrogen Peroxide Peroxide
- Lead Acetate Suger Of Lead
- Lead Tetroxide Red Lead
- Magnesium Silicate Talc
- Magnesium sulfate Epsom Salts
- Naphthalene Mothballs
- Phenol Carbolic Acid
- Potassium Bitartrate Cream Of Tartar
- Potassium Chromium Sulfate Chrome Alum
- Potassium nitrate Saltpeter
- Silicon Dioxide Sand
- Sodium Bicarbonate Baking Soda
- Sodium Borate Borax
- Sodium Carbonate Washing Soda
- Sodium Chloride Salt
- Sodium Hydroxide Lye
- Sodium Silicate Water Glass
- Sodium Sulfate Glauber's Salt
- Sodium Thiosulfate Photographer's Hypo
- Sulfuric Acid Battery Acid
- Sucrose Cane Suger
- Zinc Chloride Tinner's Fluid
-
- Thats it folks. Now for How to make TNT!
-
- How To Make TNT:
- Probably the most important explosive compund in use today is TNT
- (trinitrotoluene). This and other very similar types of high explosives are
- all used by the military, because of their fantastic power - about 2.25 million
- punds per square inch, and their great stability. TNT also has the great
- advantage of being able to be melted at 82 degrees F., so that it can be poured
- into shells, mortars, or any other projectiles. Military TNT comes in
- containers which resemble dry cell batteries, and are usually ignited by an
- electrical charge, coupled with an electrical blasting cap, although there are
- toher methods.
- Preparation:
- 1. Take two beakers. In the first, prepare a solution of 76% sulfuric
- acid, 23% nitric acid, and 1% water. IN the other beaker, prepare another
- solution of 57% nitric acid and 43% sulfuric acid (percentages are on a weight
- ratio rather than volume.)
- 2. Ten grams of the first solution is poured into an empty beaker and
- placed in an ice bath.
- 3. Add ten grams of toluene, and stir for several minutes.
- 4. Remove this beaker from the ice bath and grently heat until it
- reaches 50 degrees C. The solution is stirred constantly while being heated.
- 5. Fifty additional grams of the acid, from the first beaker, are added
- and the temperature is allowed to rise to 55 gegrees C. This temperature is
- held for the next ten minutes, and an oily liquid will begin to form on the top
- of the acid.
- 6. After 10 or 12 minutes, the acid solution is returned to the ice
- bath, and cooled to 45 degrees C. When reaching this temperature, the oily
- liquid will sink and collect at the bottom of the beaker. At this point, the
- remaining acid solution should be drawn off, by using a syringe.
- 7. Fifty more grams of the first acid solution are added to the oily
- liquid while the temperature is slowly being raised to 83 degrees C. After the
- temperature is reached, it is maintained for a full half hour.
- 8. At the end of this period, the solution is allowed to cool to 60
- degrees C., and is held at this temperature for another full hour. After this,
- the acid is again drawn off, leaving once more onlt the oily liquid at the bottom.
- 9. Thirty grams of sulfuric acid are added, while the oily liquid is
- gently heated to 80 degrees C. All temperature increases must be accomplished
- slowly and gently.
- 10. Once the desired temperature is reached, 30 grams of the second
- acid solution are added, and the temperature is raised from 80 degrees C to 104
- degrees C., and is held for three hours.
- 11. After this three-hour period, the mixture is lowered to 100 degrees
- C, and is held for a hlaf hour.
- 12. After this half hour, the oil is removed from the acid and washed
- with boiling water.
- 13. After the waching with boiling water, while being stirred
- constantly, the TNT will begin to solidify.
- 14. When the solidifications has started, cold water is added to the
- beaker, so that the TNT will form into pellets. Once this is done, you have
- good quality TNT.
- NOTE: The temperatures used in the preparation of TNT are exact, and
- must be used as such. Do not estimate or use approximations. Buy a good
- centigrade thermometer.
-
- And there you have it. Thats all for CyberPunk Follys this time!
-
-
- 5. Letters From Prison
- ----------------------
- This issue of IRG News we have a bunch of things, write by Control-S
- and myself. First is the rest of how to make LSD. The end of the patent and
- with some easy recipes that can be make in YOUR kitchen!
-
- 5a. The Rest of How To Make LSD
- -------------------------------
- This is were I left off last time.
- The mixture is allowed to stand at room temperature for several hours, the
- alkali is neutralized with acid, and the lysergic acid amine is then isolated
- and petrified.
- It should be understood that, as used herein, the term "lysergic acid"
- is used generically as inclusive of any or all of the four possible
- stereoisomers having the basic lysergic acid structure. Isomers of the
- lysergic acid series can be separated or interconverted by means known to the
- art.
- This invention is further illustrated by the following specific
- examples.
- Example One
- Preparation of the mixed anhydride of lysergic and trifluoroacectic
- acids:
- 5.36g. of d-lysergic acid are suspended in 125 ml. of acentonitrile and
- the syspension is cooled to about -20 degrees C. To this suspension is added a
- cold (-20 degrees C) solution of 8.82 g. of trifluoroacetic anhydride in 75 ml.
- of acetonitrile. The mixture is allowed to stand at -20 degrees C. for about 1
- 1/2 hours during which time the suspended material dissolves, and the
- d-lysergic acid is converted to the mixed anhydride of lysergic and
- trifluoroacetic acids. The mixed anhydride can be separated in the form of an
- oil by evaporating the solvent in vacuo at a temperature below about 0 degrees
- C.
- Example Two
- Preparation of d-lysergic acid N,N-diethyl amide:
- A solution of the mixed anhydride of lysergic acid and trifluoroacetic
- acid in 200 ml. of acetonitrile is obtained by reacting 5.36 g. d-lysergic acid
- and 8.82 g. trifluoroacetic anhydride in accordance with the procedure of
- example one. The acetonitrile solution containing mixed anhydride is added to
- 150 ml. of acetonitrile containing 7.6 g. of giethylamine. The mixture is held
- in the dark at room temperature for about two hours. The acetonitrile is
- evaporated in vacuo leaving a residue which comprises the "normal" and "iso"
- forms of d-lysergic acid N,N-diethyl amide together with some lysergic acid,
- the diethylamine salt of trifluoroacetic acid and like byproducts. The residue
- is dissolved in a mixture of 150 ml. of chloroform and 20 ml. of ice water.
- The chloroform layer is separated, and the aqueous layer is extracted with
- four 50 ml. portions of chloroform. The chloroform extracts are combined and
- are washed four times with about 50 ml. portions of cold water in order to
- remove residual amounts of amine salts. The chloroform layer is then dried
- over anhydrous sodium sulfate, and the chloroform is evaporated in vacuo. A
- solid residue of 3.45 gm. comprising the "normal" and "iso" forms of d-lysergic
- acid N,N-diethylamide is obtained. This material is dissolved in 160 ml. of
- 3-to-1 misture of benzene and chloroform, and is chromatogramed over 250 g. of
- basic alumia. As the chromatogram is developed with the same solvent, two blue
- fluorescing zones appear on the alumina column. The more rapidly moving zone
- is d-lysergic acid N,N-diethylamide which is eluted with about 3000 ml. of the
- same solvent as above, the course of elution being followed by watching the
- downward movement of the more rapidly moving blue fluorescing zone. The eluate
- is treated with tartaric acid to form the acid tartrade of d-lysergic acid
- N,N-diethylamide which is isolated. The acid tartrate of d-lysegic acid
- N,N-diethylamide melts with decomposition at about 190-196 degrees C.
- The di-iso-lysergic acid N,N-diethyl amide which remains absorbed on
- the alumina column as the second fluorescent zone is removed from the column by
- elution with chloroform. The "iso" form of amide is recovered by evaporating
- the chloroform eluate to dryness in vacuo.
- Example Three
- Preparation of d-lysergic acid N-diethylaminoethyl amide:
- A solution of the mixed anhydride of lysergic acid and trifluoroacetic
- acid is prepared from 2.68 g. of d-lysergic acid and 4.4 g. of trifluoroacetic
- acid anhydride in 100 ml. of acentonitrile by the method of Example One. This
- solution is added to 6:03 g. of diethylaminoethylamine. The reaction mixture
- is kept in the dark at room temperature for 1 1/2 hours. The acetonitrile is
- evaporated, and the residue treated with chloroform and water as described in
- Example Two. The residue treated comprising d-iso-lysergic acid
- N-diethylaminoethyl amide is dissolved in several ml. of ethyl acetate, and the
- solution is cooled to about 0 degrees C, whereupon di-iso-lysergic acid
- N-diethylaminoethyl amide separates in crystalline form. The crystalline
- material is filtered off, and the filtrate reduced in volume to obtain an
- additional amount of crystalline amide. Recrystallization from ethyl acetate
- of the combined fractions of crystalline material yields d-iso-lysergic acid
- N-diethylaminoethyl amide melting at about 157-158 degrees C. The optical
- rotation is as follows:
- [x] d^26<that is an exponet>= +372 gedrees (C. = 1.3 in pyridine)
-
- There has been in the last few years a great deal of discussion about
- the correct treatment for victims of bad LSD trips. When an individual does go
- into a panic on acid, it is an extremely delicate situation. Although it has
- been said that tranquilizers, such as thorazine, will help to calm the person
- down, be very careful, as certain drugs react violently with tranquilizers
- (STP). My advice in a situation of that sort is just to attempt to create an
- atmosphere of reasurance and sympathy. In no circumstances, except real
- uncontrollable panic, should a person on acid be taken to a city hospital. If
- you want a freaky experiance, spend a couple of hours at any city hospital and
- watch the people die in the halls!
- Talk to a person and remind him that he is under the influence of acid.
- Try to calm him down. Even a change of environment can effectively reverse a
- bad trip.
-
- Making LSD in the kitchen:
- For those readers who couldn't make head or tail of the last recipe for
- acid, there is a much sipler one. It basically extracts the lysergic acid
- amide either from morning glory seeds or Hawaiian wood rose seeds. It can be
- prepared in the kitchen.
- 1. Grind up 150 grams of morning glory seeds or baby Hawaiian wood rose
- seeds.
- 2. In 130 cc. of petroleum ether, soak the seeds for two days.
- 3. Filter the solution through a tight screen
- 4. Throw away the liquid, and allow the seed mush to dry.
- 5. For two days allow the mush to soak in 110 cc. of wood alcohol.
- 6. Filter the solution again, saving the liquid and labeling it "1".
- 7. Resoak the mush in 110cc of wood alcohol for two days.
- 8. Filter and throw away the mush.
- 9. Add the liquid from the second soak to the solution labeled "1".
- 10. Pour the liquid into a cookie tray and allow it to evaporate.
- 11. When all the liquid has evaporated, a yellow gum remains. This
- hould be scraped up and put into capsules.
- 30 grams of morning glory seeds = one trip
- 15 Hawaiian wood rose seeds = one trip
-
- Many companies, such as Northop-King, have been coating their seeds
- with a toxic chemical, which is poison. Order seeds from a wholesaler, as it
- is much safer and cheaper. Hawaiian wood rose seeds can be ordered directly
- from:
- Chong's Nursery and Flowers
- P.O. Box 2154
- Honolulu, Hawaii
-
- LSD Dosages:
- The basic dosages of acid vary according to what kind of acid a
- available and what medium of ingestion is used. Chemically the potency of
- LSD-25 is measured in micrograms, or mics. If you're chemically minded or
- making your own acid, then computing the number of micrograms is very
- important. Usually between 300 to 500 mics is plenty for a five- to eight-hour
- trip, depending on the quality of the acid, of course. I have heard of people
- taking as much as 1,500 to 2,00 mics. This is not only extremely dangerous, it
- is also wasteful.
- LSD comes packaged in amny diffrent forms. The proverbial suger cube
- is pretty passe', in the sense that other more feasible methods have taken its
- place. The most common are listed below.
- 1. The brown spot, or a piece of paper with a dried drop of LSD on it, is
- always around. Usually one spot equals one trip.
- 2. Capsuled acid is extremely tricky, as the cap can be almost any color, size,
- and potency. Always ask what the acid is cut with, as a lot of acid is cut
- with either speed or strychnine. Also note dosage.
- 3. Small white or colored tablets have been known to contain acid, but, as
- with the capsuled acid, it is impossible to tell potency, without asking.
- 4. I have heard about some charaters who attempted to choot acid. Shooting any
- drug is a bad scene. Stay way from it. I cannot imagine what their rush was
- like, but would certainly adivse against this form of drug abuse.
-
-
- 5b. Trashing Tips & Tricks By Control-S
- ---------------------------------------
-
- Disclaimer: This phile is for information purposes only, the author
- will not be responsible for any actions the reader takes as a result
- of reading this, and/or printing it out and eating the paper.
-
- WARNING: reading this file may cause mental instability.
-
-
- Trashing:
- --------
-
- Trashing is one of the best ways to obtain information not readily
- available to you. You can find many interesting things in other
- people's garbage, the trick is knowing what is good trash and what
- is useless trash. "One man's trash is another man's goldmine", words
- to live by!
-
-
- 1.0 - Intro to Trashing
- 1.1 - What you need
- 1.2 - Where to Trash
- 1.3 - How to Trash
- 1.4 - What to do with your trash
-
-
-
-
-
-
- 1.1:Trashing Tools:
-
- Attire: You should wear the most grungy outfit you can put together.
- (for some of you, this means 'dress as if you had a date' -heh.)
- Ripped jeans are alwayz a plus, and a large overcoat is a nice touch.
- If you have a t-shirt that sayz 'Recycle or Die' or any other social
- activist type slogan, wear it, it will make you look like a social
- activist type. (People rarely fuck with social activists, as they
- are for the large part quite fanatical and prone to be unstable).
-
- Carry alongs: You should have 2 large garbage bags, fill one with about
- 20-30 aluminum cans (it may be noisy, but its a good cover!), leave
- the second bag empty, this is where you're going to stash your goodies.
-
- Other: If you're planning on trashing someplace were you could come
- across some discarded floppy disks, you should have an array of programs
- at home to help you recover data from these disks, as most will either
- be formatted, or riddled with bad sectors. Utilities for undeleting,
- uncopyprotecting, recovering sectors and editing sectors are available
- practically everywhere (even in the Public Domain!).
-
-
-
- 1.2:Where To Trash:
-
- Depending on what you're interested in, you have to decide where you're
- going to look. Dept. stores are good for credit card carbons, and TRW/
- CBI accounts. Office buildings can have just about anything, from office
- memos to logins and passwords. Likewise, buildings occupied by a software
- or hardware company can have logins, and discarded reference manuals.
- Schools/Universities are one of the BEST places to find great stuff,
- there is a problem with the amount of garbage you'd have to go through
- at a school, because they really generate a lot (of the worthless kind!)
- so if you're going to do a school, you should hit the inside trash cans
- of the Library, and the Computer Lab (if you can get in). You should also
- scan desks in both, as many students, being the lazy student types, will
- write passwords on desks! (I've gotten internet accounts using this method).
- TelCo buildings are both hard to find, and dangerous. They are almost
- universally unmarked buildings with darkened windows, absolutely no way
- to tell what the building is. (typical gestapo headquarters!) They also
- will be alert for people dumpster diving -- itz certainly nothing new!
-
-
-
-
- 1.3:Trashing:
-
- Okay, now that you're suited up and have bags in hand, at the right
- location, you're ready to get to buisness. Its good to bring a car,
- or someone with a car, this will provide both a base of operation, and
- a quick getaway. Ideally, you'll want the car withing a quick sprinting
- distance of where you'll be trashing, if you have a few people with you,
- someone should stay in the car to keep lookout and be ready for whatever.
- In the dumpster, things will usually be fairly orderly, (suprising as that
- may sound). You'll problably come across bunches of smaller bags, look for
- any that have papers, printouts or even shorthand. Keep an eye out for
- diet coke cans too, this is a favorite of fat secretaries and usually
- an indication of something good to come. Look for for anything
- resembling a binder or notebook, many refernce manuals are discarded
- but still incredibly useful. A good time to trash is around tax time,
- as many companies will do a severe office cleaning and put some of their
- records in archives after they've filed income tax reports -- as a rule
- of office cleaning, many interesting things get chucked. Try and grab
- things already bundled into smaller bags, its easier to carry, and if
- you get one say from a computer room or office, all the excelent stuff
- will be in one catch - making life easy for the trasher. After you've
- gotten a few small bags and stuffed you're large garbage bag with
- junk, throw it all in the trunk and head home, (stop off an turn in
- the aluminum cans you had, because recycling really is IMPORTANT).
- Don't try and look for goodies at the site, it takes to much time and
- you'll prolly be in to much of a hurry and might miss something good.
- Once you get home, find a good place, like the kitchen floor, spread
- your trash out and start seperating it. Look for everything, you never
- know what you might find, so be alert for the most atypical type of
- information. Use a little common sense and ingenuity and you're set.
-
-
-
- 1.4:Trash Use:
-
- For the most part, you should be able to distinguish what might be
- useful and how to use it, however there may be cases where you could
- get an accountname/password or such, and not know what its to or how
- to use it. If this is the case, look up the # of the place you trashed
- in the phonebook, and scan the entire exchange for carrier signals.
- This sounds like a pain in the ass, but really its not, scanning is
- a great way to find computers, and one of my personal favorite pastimes.
- Scanning a single exchange takes less than a week, and you'll prolly
- find a lot of other carriers while you're at it.
-
-
- Well, thatz about all there is to it, you're set to trash. Have phun!
-
-
- Questions? Comments? Keep them to yerself! -hah! j/k, I can be contacted
- on The Corrupt Society, and Insanity Lane, for whatever.
-
- Look for my scan files to be comming out soon.
-
- This phile may be reproduced, as long as the credits are left intact.
-
-
-
- ^S
-
- 5c. Interesting places to telnet to on the Internet:<Ctrl-S>
- -----------------------------------------------
- Note: This is by NO means an exaustive list, merely tid-bits. The
- internet is so huge, and complex, one would shutter at the mere
- magnitude to trying to put together anything like a 'complete'
- list of interesting things found there, so I've weeded it down to
- a very few. (for infomation on anonymous FTP's, and Inet bbs'es,
- there are other text files available many places, again, this list
- is of only a few, and in my opinion, some of the more interesting
- internet sites.
-
- Mars Hotel: mars.ee.msstate.edu (130.18.64.3)
- login: bbs
- notes: Phrack/cud/ATI/PHun/LOD/lots more, good messages, (VERY good bbs)
-
-
- Dawg House: ra.msstate.edu (130.18.80.10)
- login: dawg
- notes: lots of files
-
-
- IRC: fairhope.andrew.cmu.edu
- notes: busy chat system
-
-
- IRC: tilley.cc.umanitoba.ca
- login: guest
- notes: type 'IRC' (just an alternate route to fairhope)
-
-
- Merit Gateway: (35.1.1.6)
- notes: many gates (compuserve, sprintnet, 313 dialout, others)
-
-
- TAC: (192.67.67.20)
- login: tacnews
- notes: CERT bulletins available
-
-
-
- The following is a list of dialouts, reachable via telnet. Most
- have been compiled from various bbses, and a few I hunted out
- myself. Please don't abuse these, there are only so many lines
- on each modem, and if you piss off the administrators, they will
- simply disconnect them.
-
-
- DialOut Address NPA Format/Comments
- ----------------------------------------------------------------------
- 128.54.30.0 619
- (dialin.ucsd.edu)
-
- 129.72.1.59 307
-
- 128.120.2.251 916 Service? dialout / D9,XXX-XXXX
-
- 128.143.70.101 804 'connect hayes'
-
- 131.212.32.110 218
- (modem.d.umn.edu)
- aa28.d.umn.edu 218 cli/rlogin modem/modem
-
-
- 35.1.1.6 313 'dial2400-aa'
-
- 18.26.0.55 MIT?
-
- 128.146.6.127 614
-
-
- 128.101.232.31 612
- 128.101.231.31 612
-
- dca.utk.edu 503 'dial2400'
- dca.ntk.edu 503 'dial2400'
-
- 128.112.88.0 ??? (in NJ - 201?)
-
- 128.249.27.153 ???
- (bcm.tmc.edu)
-
- r596adi1.uc.edu ??? ATZ
-
- umnet.cc.umanitoba.ca 204/(Canada?) which host? dial24
-
- ns2400.ircc.ohio-state.edu which host? dial
-
-
- *New Jersey Dialouts (untested)
- 128.112.88.0
- 128.112.120.14
- 128.112.131.110
- 128.112.131.111
- 128.112.131.112
- 128.112.131.113
- 128.112.131.114
-
- 128.112.88.1
- 128.112.88.2
- 128.112.88.3
-
- *Florida: (untested)
- modem.cis.ufl.edu
- 128.227.224.27
-
- *Berkeley CA: (untested)
- 128.32.132.250
- dialer
- Annex132.berkeley.edu
-
- *Unknown: (untested)
- 128.249.27.152 - modem12.bcm.tmc.edu
- 128.249.27.153 - modem24.bcm.tmc.edu
-
-
-
-
- Thats about it for now, I'll probably be updating this file
- every now and then, so stay tuned to IRG for more interesting
- stuff found on the internet.
- Questions, Comments? - I can be reached at TCS and Insanity Lane
-
- I'd like to mention one more thing; code abuse and credit card fraud
- are lame, it only increases the wrongfully portrayed image of hackers,
- and harms EVERYONE. 'C0deZ' has NOTHING to do with phreaking, and
- 'carding' is just plain stupid. Don't be lame, and don't do them.
- (my $.02)
-
-
-
- Control-S
-
-
- 6.BBSs From Hell
- ----------------
- I have found that this part of IRG news is pretty worthless and most
- Elite users can find board numbers no problem. I have decided to descontinue
- this part. I will keep VMBs from hell since VMBs are rather hard to find.
-
-
- 7.VMBs From Hell
- ----------------
- Heres this issues VMBs check them out!
-
- VMB Number Box Number VMB Use
- -------------------------------------------------------------------------------
- 1-800-999-1380 215 IRG Code Line/Info Line
- 1-800-477-7691 4448 The Knights Code Line /Info Line
- 1-800-634-3455 999 + 138 L.o.L. Code line
- 1-800-633-3402 #15000 Code Line
- 1-800-633-3402 #15001 Code Line
-
- Well thats it for this installment of VMBs From Hell. If you would like you
- VMB in IRG News please leave mail at IRG/ShadowNet VMB #1 1-800-527-0543 Box
- Number: 8 + 158.
-
-
- 8.Running The ShadowNet
- -----------------------
- The first use of ShadowNet has gone and passed. As I told you last
- time ShadowNet would be working for free the first few times. Well We were
- hired to find out about some by the name of Casey ?????(his last name will be
- left out just in case you know him). ShadowNet found out his phone number,
- and his address. We procceded in cansuling his credit cards, turning his phone
- off, and bothering him most completely. We figure he will never bother our
- client again.
- If anyone else would like to hire us, please contact us. We are still
- going for free...
-
-
- 9.Hellos and Goodbyes
- ---------------------
- Thats all folks, for this IRG news, all people who have something to
- say about it can contact anyone who was writen or done anything for IRG at
- Insanity Lane IRG/ShadowNet Home. If you would like to join, contact us!
-
- Freedom Of Speech
- Remember: Big Brother Is Watching
- Snakeman where are you? If YOU have any info on Snakeman please e-mail
- me!
- THRILL/FIST you guys all suck and were doomed to die!
- Wizball Call my board!
-
- -------------------------------------------------------------------------------
- This Is An Offical IRG/ShadowNet Production All Rights Resevered
- Copy Write (C) Jan. 18 1991
- -------------------------------------------------------------------------------
-
- Call The IRG HeadQuarters:
- Insanity Lane
- Home Of IRG
- 619-591-4974
- NuP: Last Try
- Running Aftershock 1.21
- Call here for the latest in IRG Productions, and invaluable P/H/C/A
- information found anyware!
-
- The CorrupT SocieTy
- IRG Node 02
- 619-630-8450
- NuP: Defiance
- Running AfterShock 1.21
-
- Also Call These Fine IRG/ShadowNet VMBs
-
- 1-800-527-0543
- Box Number: 8 + 158
-
- 1-800-999-1380
- Box Number: 215
-
- Downloaded From P-80 Systems 304-744-2253
-
-
- Downloaded From P-80 International Information Systems 304-744-2253 12yrs+
-