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PARKINSN  January 1997, Week 2

PARKINSN January 1997, Week 2

Subject:

SET PARKINSN DIGEST NOMAIL

From:

bernardo klainberg <[log in to unmask]>

Reply-To:

PARKINSN: Parkinson's Disease - Information Exchange Network

Date:

Thu, 9 Jan 1997 20:54:24 -0500

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (1354 lines)

At 05:00 AM 1/8/97 +0000, you wrote:
>  7. Happy Birthday
>  8. Feet (2)
>  9. Public Perception (7)
> 10. I'm new    referal to PDF & PAN
> 11. listmembers - please ignore my 1/5/96 message "re:New Year's Greeting."
>     (3)
> 12. NEW MEMBER (2)
> 13. Dear President Clinton (2)
> 14. Fwd: new member needs a good neurologist referral
> 15. Letter to the President
> 16. Dennis-no biggee
> 17. Beth Leslie's reply to Happy Birthday
> 18. Drug Database Info Available
> 19. Pallidotomy & Hydergine
> 20. Well-know PWPs (4)
> 21. Letter to the President   response to Jim Cordy
> 22. Dear President Clinton by Dale Severance (3)
> 23. AMGEN GDNF CLINICAL TRIALS (4)
> 24. This Is War... (4)
> 25. Ginger
> 26. Depression (2)
> 27. Lecture-Pittsburgh
> 28. Letter to the President response to Jim Cordy
> 29. Message to Barb Marling (3)
> 30. Pain in feet and toes (3)
> 31. I'm new      (an effort to give contact info re PSP)
> 32. hello to all PDs (4)
> 33. Muscle spasms
> 34. Pres. Address Wrong?
> 35. SURVEY: Reactions to PD Drugs
> 36. Not real famous PWP's
> 37. no biggee
> 38. Health and Medicine
> 39. Dear President Clinton by Lil Honey and Dale's response
> 40. PD \ Eye Position Sensor (adaptive technology) (2)
>
>----------------------------------------------------------------------
>
>Date:    Tue, 7 Jan 1997 00:08:55 -0500
>From:    David Boots <[log in to unmask]>
>Subject: Holiday Music (Drug)
>
>* This can be sung to your caregiver and/or stash of PD-meds
>
>I'm Through With Sinemet (Happy Holiday!)
>(to the tune "Don't Get Around Much Anymore")
>
>Fell down Saturday night
>On my way to the floor
>Knew I can't live without you
>Don't get around much anymore
>
>Tried to exit the tub
>Couldn't step on the floor
>Life's quite different without you
>Don't get around much anymore
>
>Funny I guess
>I used not to be (so)
>Unhappy?...YES....(but)
>Why stir up memories?
>
>Been immobile all day
>Could have dressed but what for?
>It's awfully different without you
>Don't get around much anymore
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 00:22:02 -0500
>From:    "JONES, BRYCE" <[log in to unmask]>
>Subject: Ginger for nausea?
>
>A while back several people mentioned taking crystalized ginger
>to lessen the nausea caused by sinemet.  How do you find this
>ginger?  Is it in ginger snaps?  Has it helped many?
>Thanks.
>Bryce Jones
>
>------------------------------
>
>Date:    Mon, 6 Jan 1997 22:31:42 -0500
>From:    Barbara Mallut <[log in to unmask]>
>Subject: Re: AMGEN again
>
>Joy... I spoke with AMGEN right after the word about the GDNF trials came out.
>  What little (and I stress the word "little") I was able to find out was that
>the trials will take 2 to 3 years, are being done with 50 persons, in
>unknown-to me locations, and the drug is inserted or injected in a pallidotomy
>like hole.
>
>That's not a lot to go on, and it was a frustrating phone call, to say the
>least.  It's possible that more information is now available as several months
>have passed since my call to Amgen.
>
>Barb Mallut
>"Lil_Honey" onthe PD chat
>[log in to unmask]
>
>
>
>----------
>From:   PARKINSN: Parkinson's Disease - Information Exchange Network on behalf
>of Bob & Joy Graham
>Sent:   Monday, January 06, 1997 6:47 PM
>To:     Multiple recipients of list PARKINSN
>Subject:        AMGEN again
>
>Either no one read my question or no one knows... I will ask again: Does
>anyone have any information about the AMGEN trials with GDNF?  Where are
>they happening, has anyone received any GDNF yet?
>Thanks
>Joy Graham
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 00:36:55 -0500
>From:    Lee Heck <[log in to unmask]>
>Subject: I'm new
>
>My name is Lee, and I am new to this list.  I am 33, live in Seattle, =
>and am a fundraiser for the Northwest AIDS Foundation.  My mother was =
>diagnosed with PD after a trip to Mayo and a couple of years of =
>unanswered questions.  At one point, she was diagnosed with PSP.
>
>Working in HIV, I understand the limitations of the medical community.  =
>It has been, though, a tremendous mental battle for my parents.  It has =
>been a god send for my Mother to name her disease.=20
>
>I have read a couple days of postings on this list, and I realize I need =
>lots more information before I can truly understand PD.  I began =
>searching for answers on the Net, but was soon overwhelmed by the =
>incredible amount of information. =20
>
>Can someone direct me to comprehensive web-sites, newsgroups, or books =
>which will be a good starting place for me as I begin to learn about =
>this disease?
>
>Feel free to post to the list, or if this is a really common questions, =
>please feel free to e-mail me directly.
>
>Thanks.
>
>Lee
>[log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 01:05:56 -0500
>From:    Gaylon Johnson <[log in to unmask]>
>Subject: Parlodel supply
>
>New Year Greetings list members,
>
>A week or so ago I called the local Walgreens pharmacy to have my
>parlodel prescription refilled. When I went to pick it up I was told
>they were out, but would have it in a couple of days. Checked back and
>they still didn't have it. The pharmacist asked me to call back today,
>which I did. Now I'm told they can't get parlodel and don't know when it
>will be available. Not real cheery news when your supply is about to run
>out.
>
>Has anyone else encountered this problem? You would think that if the
>drug was available a company the size of Walgreens should be able to get
>it somewhere. Sandoz is the manufacturer. Any input or suggestions would
>be welcome.
>
>Cordially,
>Gaylon
>--
>                ***************************************
>                            Life is GREAT!!
>                         Try doing wothout it.
>
>***************************************
>[log in to unmask]
>                      "On the Suncoast of Florida"
>                ***************************************
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 01:26:42 -0500
>From:    Elizabeth Southwood <[log in to unmask]>
>Subject: Re: Ginger for nausea?
>
>Hi Bryce:
>
>I don't know where you live, but I buy crystallized ginger in California at
>Trader Joe's.  It is a product of Australia.  I don't
>know about the efficacy of ginger snaps.  The crystallized ginger comes in
>cellophane bags.  Good luck!   Liz S
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 02:51:40 -0500
>From:    "Joseph W. Duggan" <[log in to unmask]>
>Subject: Re: Pycnogenol
>
>I've just caught up on reading about 30 PD digests and read some of the
comments
>about pycnogenol. I'm interested to know if anyone has given it a fair 90 day
>trial to see if it does improve PD symptoms. My understanding is that much of
>the aging and destruction of cells in the brain is due to abnormally high
levels
>of free radicals. Apparantly, PD patients have an unusually high level of free
>radicals in their brains. This could be due to poor diet, toxic metals or
>chemicals as well as indiviidual biochemistry. If pycnogenol is able to
>penetrate the blood-brain barrier and is 50 times more active than vitamin C or
>E, perhaps it can do some good and stop the progression of PD as well as
>moderate the side-effects of L-dopa therapy, one of which is elevated levels of
>free radicals in the brain. Has anyone given pycnogenol the same fair trial
that
>seems to be so freely given to new drugs which always seem to have negative
>side-effects?
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 03:11:40 -0500
>From:    elizabeth leslie <[log in to unmask]>
>Subject: Happy Birthday
>
>Jacqueline Winterkorn!  And thank you for sharing it - and os muxh of
>yourself - with us.  As a 'newbie' I read it all with interest bordering
>on gruesomefascination bordering on terror!  But I'll cope.  With my
>friendds from the list.
>
>You do raise one issue I've not seen discussed here before, that is
>particularly bugging me just lately.
>
>On Thu, 2 Jan 1997 you wrote:
>
>>        We might also record our experiences with social prejudice against
>> people who move or look funny: assumption--worst of all among doctors--  is
>> that the shaking hand means either you're drunk or demented, or both.
>
>
>I'm finding simple things like shopping and paying my bills more and more
>embarrassing.  I feel such a goon when I can't put away my change; when
>my left hand refuses to release the goods when it - and I! - arrive at
>the checkout; when things just won't go into the silly bags I'm sometimes
>left to stuff them into; and when staff give me 'that' look that is
>somewhere amongst impatience/exasperation/frustration/pity.  And when they
>bark at me to speak up.  I feel like I need a big T with a list of 'rules' for
>approaching Parkies.  Somebody did suggest a card for social situations
>(just something else fiddly to bother with) ... and anyway, truthfully
>I'm not so bad yet for it to be a real NEED.  But let's just say I'm
>feelin' it.  And I don't like it.
>
>I began to think  about devising a short educational program to offer to
>retailers; of suggeesting marked checkout lanes with attendants wise to
>disabilities. There is a superficial awareness of the need to be aware of
>people with disabilities.  But it is just that.
>
>Of course I've spesnt most of my almost 53 years pretty unaware of all
>this, too, and shudder to think of whwat damage I might have done others
>over time.  Makes you think.
>
>And,did anyone else notice how fast the world goes now?  what a rush
>everyone is in?  on the roads, in the aisles, on the footpaths?  And
>suddenly I not only can't but can't be bothered trying to keep up.
>
>Hope to hear more on this.
>
>Hope you had a great Birthday, Dr. Jacqueline
>
>Beth Leslie
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 03:19:39 -0500
>From:    elizabeth leslie <[log in to unmask]>
>Subject: Feet
>
>I'm amazed at what I learn here.  Now I cvan begin to believe that my
>groiwng 'useless shoe' collection is part of a much bigger problem, and
>not otherwise unexplainable fetishism.  Thanks friends.
>
>Beth Leslie
>
>
>
>On Mon, 6 Jan 1997, Barbara Mallut wrote:
>
>> Dale.....
>>
>> I've noticed severe foot swelling (even after my pallidotomy) twice with the
>> past 3 years.  Each time it lasted for about 5 to 7 days.  Not painful, just
>> scary... I used a diuretic herbal tea... very common blend made up of juniper
>> berries.. An over the counter product in any health food market.  It's under
>> the well known "Weightless" brand, and'll cost ya maybe $3 for a box of
10 tea
>> bags.
>>
>> BTW... IF you or any of our list members are tea drinkers such as I am (never
>> drank coffee after my first taste of it at 16!) <smile>, Weightless puts out
>> several other very tasty herbal teas, with a heavenly spicy smell to the
>> brewed tea.  And if I can taste 'em and smell 'em, well, ANY Parkie could!
>> ('cause there ain't a whole helluva lotta stuff that's tasty and/or pleasant
>> smelling to THIS Parkie-type-gal) Enjoy.......
>>
>> Barb Mallut
>> "Lil_Honey" on the PD Chat
>> [log in to unmask]
>>
>> ----------
>> From:   PARKINSN: Parkinson's Disease - Information Exchange Network on
behalf
>> of Dale Severance join list
>> Sent:   Monday, January 06, 1997 12:41 AM
>> To:     Multiple recipients of list PARKINSN
>> Subject:        Re: Tricks of the Trade  a response by Dale Severance
>>
>> In a message dated 97-01-05 15:08:29 EST, [log in to unmask] writes:
>>
>> << TRICKS OF THE TRADE >>
>>
>> Hi Folks:
>>
>> I just read Sam's article and learned something new abour PD that is why this
>> list service is so dam good.
>>
>> I never new that swelling feet was a PD symptom and Sams article was the
>> first time I have noticed it mentioned. I have been on a shoe buying spree
>> never quite getting a comfortable shoe even though I buy larger than pre PD.
>>
>> Is swelling feet a common PD related ailment?
>>
>> Dale Severance
>> [log in to unmask]
>> Brooklyn, NY.
>>
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 03:32:53 -0500
>From:    Marling McReynolds <[log in to unmask]>
>Subject: Re: Public Perception
>
>I noted in a book in my Neurologist's office the statement that PDers seemed
>more embarressed by their tremor than any other tremor suffers.  The author
>could not understand this.  I thought about it for quite a while, and came to
>the conclusion that the reason I get upset about my tremor in or out of public
>is that it is a reminder of what I have--PD.  It is a reminder that this is not
>just a tremor, but a progressive condition and that it will get worse.  It is a
>reminder of where I will end up eventually and I hate to be reminded of it,
>especially in public.
>
>Sometimes people stare when my hand starts to tremor, but for the most part I
>live in a small community.  The people here are my friends and long time
>acquaintences.  When they ask, I tell the truth, and they feel sorry, but want
>to help.  And usually ignore it from then on.  Worse than my hand tremor is my
>leg.  I go to many meetings, and almost everytime my right leg will begin to
>tremble.  I must hold it with my other leg, or let it tap.  Sometimes, people
>must think I am listening to music they cannot hear.
>
>Oh yes, one more thing.  Congratulate me.
>I have developed my FIRST EVER Hemroid!
>My depression is back, with a vengence.  I have been thinking of not taking
>anything and letting the PD get me now, rather than waiting.
>Any suggestions as how to keep my spirits up,or whereever they are supposed to
>be.??..
>
>PD forever or until a cure is really found>>>>>>
>
>Marling McReynolds
>Director SHCRC the People Center
>mail: Box 2017, Redway, CA 95560
>77 Avenue of the Giants
>phone: 707-923-5220 fax:  707-923-5221
>e-mail:  [log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 04:31:24 -0500
>From:    Dale Severance join list <[log in to unmask]>
>Subject: Re: I'm new    referal to PDF & PAN
>
>Hi Lee:
>
>Glad you joined this list you will get a lot of info from this group.
>
>You can also contact the Parkinson Disease Foundation,at 710 West 168th St.
>New york, NY at 1-800-457-6676 or since you have email I suggest you contact
>them at   PDF [log in to unmask]  They have a packet of info for new members
> without charge.
>
>If you would like to subscribe to a free monthly publication by our political
>action arm ( Parkinson's Action Network ) send me your snail mail address and
> I will forward your name to their mailing list.
>
>Welcome to the group
>
>Dale Severance
>
>[log in to unmask]
>
>Brooklyn, N.y.
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 04:33:31 -0500
>From:    Bernard JOLY <[log in to unmask]>
>Subject: Re: listmembers - please ignore my 1/5/96 message "re:New Year's
>         Greeting."
>
>Maryhelen,
>
>I hope you will not blame me if I question the need to be so apologetic about
>a simple mistake.
>
>After all, this group is about PD, not PC-user talent. It gives all
>subscribers a unique opportunity to communicate with others. It allows each of
>us to listen and learn. It should also allow each of us to take an active part
>in the ongoing discussion.
>
>This is a concern to me : we don't hear about several hundreds of subscribers
>who never post anything. As far as I am concerned, I have no problem with
>receiving the same post twice, or mistyped or whatever, if only one subscriber
>thus feels encouraged to post instead of only listening. One post too many is
>no big deal ; one post to few, I hate the idea !
>
>Bernard JOLY
>[log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 06:15:56 -0500
>From:    "W.S." <[log in to unmask]>
>Subject: NEW MEMBER
>
>        I am a new member to your group, I am looking
>for information on parkinsons for my mother, I am interested
>in the ups and downs of sinemet cr, could anyone tell me what
>the usual dose of sinemet cr is ? just for comparison, we are
>not changing it without the doctor's say so...
>
>        I have gained a lot of helpfull information from this
>group in my first 24 hours, I thank you all,I am in the prosess
> of changing doctors, we need more info than " take 2 sinemet and
>see you in three months" It is good to see such an active group
>sharing information, and it is helpfull to know the symptoms that
>are parkinsons and not unusual. If I am actualy sending out this
>message, like I think I am, ( I'm new to computers and Internet)
>I wish you all well, and thank you for your help.
>        [log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 06:35:54 -0500
>From:    Dale Severance join list <[log in to unmask]>
>Subject: Dear President Clinton
>
>January 7, 1996
>
>Office of the White House
>Washington, DC.
>
>Dear  President Clinton:
>
>Over the last five years I have supported  your political objectives and
>stood up to vote for you at election time.
>
>Now I would request your assistance for a minority group in this country
>whose numbers are estimate at one to one and a half  million.
>
>I am referring to our fellow Americans who have or will contract Parkinson's
>Disease. This disease is one which gradually wares away our bodies to the
>point that we have to stop working, and eventually we deteriorate to the
>point that others must care for us.
>
>The cost to society is tremendous in lost wages,  Federal taxes, State taxes
>local taxes and Social Security withholding. Most of us qualify for Social
>Security  Disability and Medicaid earlier than the average American.
>
>I just turned 56 and have had to stop working. I was a small business person
>employing thirteen people. I estimate that the eleven years lost ability to
>work will cost society over two million dollars in lost income taxes, lost
>social security contributions to the system with the employers matching
>payments, the loss of sales tax paid for goods purchased, the early payment
>to me of Social Security Disability, Medicaid Coverage and the cost to
>private disability and medical insurance companies.
>
>To offset this great loss the Federal government is allocating $ 26.00 per
>person with Parkinson's Disease for research. I think this is a short sided
>view of the situation by Congress  bordering on a national shame that so
>little is being done for our minority group.
>
>I therefore respectfully request that you stand by our side and vocally
>support the Parkinson's Disease Community when a bill is offered to raise the
>funding level for Parkinson' s Disease Research in the next Congressional
>session.
>
>I thank you on behalf of your fellow Americans who desperately need your
>help.
>
>Thank you,
>
>A. Dale severance
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 07:06:53 -0500
>From:    Dale Severance join list <[log in to unmask]>
>Subject: Fwd: new member needs a good neurologist referral
>
>In a message dated 97-01-07 05:31:21 EST, [log in to unmask] (W.S.)
>writes:
>
><< My mother has had parkinsons for about 3yrs. and her DR.
> is not a wealth of information, to say the least, I made
> a call today to Lahey clinic and set up an appointment with
> a new DR. I hope we can get more info than just take sinemet
> and see you in three months.her DR. had her on 1 1/2 sinemet cr
> and tells me "I" can go up to 3 a day, I did increase to 2 but,
> I would like to know what the usual dose is.
>
> Thank you for the info on the parkinsons disease foundation,
> I will send off a note today! see, your info helped more people
> than you thought!   Thank You  [log in to unmask]
>
>  >>I have a feeling that if you give the group your city and state someone
>here will be able to recommend a good physican for your family based on
>personal experience
>
>So happy you joined;
>
>Dale Severance
>[log in to unmask]
>Brooklyn, NY.
>
>
>---------------------
>Forwarded message:
>From:   [log in to unmask] (W.S.)
>To:     [log in to unmask]
>Date: 97-01-07 05:31:21 EST
>
>        Hi Dale;
>I am also a new member, as a matter of fact less than
>24 hrs, I have gained more info from this group in 24hrs.
>than I have recd. from my mother's doctor in 3 yrs.
>
>I am also new to the computer and internet, I thought I
>sent a message to the group asking about the ups and downs
>of SINEMET, but, I must have done something wrong! I will
>try again,
>
>My mother has had parkinsons for about 3yrs. and her DR.
>is not a wealth of information, to say the least, I made
>a call today to Lahey clinic and set up an appointment with
>a new DR. I hope we can get more info than just take sinemet
>and see you in three months.her DR. had her on 1 1/2 sinemet cr
>and tells me "I" can go up to 3 a day, I did increase to 2 but,
>I would like to know what the usual dose is.
>
>Thank you for the info on the parkinsons disease foundation,
>I will send off a note today! see, your info helped more people
>than you thought!   Thank You  [log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 07:18:19 -0500
>From:    John Cottingham <[log in to unmask]>
>Subject: Re: I'm new
>
>--=====================_852646722==_
>Content-Type: text/plain; charset="us-ascii"
>
>At 12:36 AM 1/7/97 -0500, you wrote:
>>My name is Lee, and I am new to this list.  I am 33, live in Seattle, and
am a fundraiser for the Northwest AIDS Foundation.  My mother was diagnosed
with PD after a trip to Mayo and a couple of years of unanswered questions.
At one point, she was diagnosed with PSP.
>>
>
>Lee, a good place to start is the archives....attached are directions to
get specific articles.
>
>
>--=====================_852646722==_
>Content-Type: text/plain; charset="us-ascii"
>
>
>THIS IS THE REVISED CURRENT PARKINSON'S TOPICS BY E-MAIL MESSAGE.
>DISCARD EARLIER POSTINGS BY THE SAME NAME.
>
>Current Parkinson's Topics by E-Mail
>
>Welcome new subscribers and those who have found the address to the
>Parkinsn Archives through out the World Wide Web!
>
>Two services are available at [log in to unmask] One is the ability to
>request a search for information. Another service is the availability
>of this message, which catagorizes messages that have previously posted
>to the Parkinsn list and now reside in the archives. These messages
>may be ordered.
>
>For those not acquainted with the Parkinsn list, it is a e-mailing list
>of Parkinson's patients, care-givers, family members, neurologists,
>psychologists, family practice doctors, and manufacturer representatives
>that represent the pharmaceutical industry and equipment manufacturers.
>We currently have about 1400 members in 34 countries around the world.
>The language of the list is English.
>
>Postings to the list are only accepted from subscribers. If you join us,
>you will have that privilege also. The Parkinsn list is a high volume
>list, having from 20 to 30 postings a day, some quite long.
>
>If you wish to join us, send an e-mail message to:
>
>[log in to unmask]
>
>In the body of the message put ONLY FOUR WORDS:
>
>subscribe parkinsn Yourfirstname Yoursurname
>
>Within a short while you will receive acknowledgement and a welcoming
>message.
>
>Subscription is not required to receive the archival material mentioned
>in the rest of this message. This is a public service.
>
>
>Everything ever discussed on the Parkinsn list is in our archives.
>Periodically, a message called, "New Parkinsn Archives Information
>by E-mail" is posted on the Parkinsn list.
>
>"New Parkinsn Archives Information by E-mail" gives instructions on
>the kinds of searches available, examples, and information on how to
>request them.
>
>Many of you have learned about the Parkinsn list from friends
>or reading the Wall Street Journal and New York Times articles about
>pallidotomy.  This message gives answers on how to directly use the
>Parkinsn archives and get information NOW while you are "coming up
>to speed".
>
>
>MSG      Finding Answers to Frequently Asked Questions:
>order
>number
>
>                       ARTICLES
>
>001 New Study links Eldepryl/Deprenyl With increased Mortality
>
>This study from the UK raises some controversial questions on how often
>Parkinson's patients die from long term Eldepryl/Sinemet treatment.
>
>002 Article on Information on Aging
>
>This article was posted posted by Alan Bonander, ELDER CARE: THEY'RE AGING,
>AND YOU'RE WORRYING  8/26/94 When children grow up, and parents grow old
>Published: Aug. 22, 1994 By KATHLEEN DONNELLY Mercury News Staff Writer
>
>If someone you know and love needs help, this article will give you a
>starting point to look for social agencies that help the elderly.
>
>003 Young Onset PD
>
>This article was posted by Alan Bonander entitled: THE YOUNG
>PARKINSON'S PATIENT By Erwin B.  Montgomery, Jr., MD
>
>This article appeared in the Parkinson News & View, Southern
>Arizona Chapter APDA, June / July 1994.  It is reprinted with
>their permission.
>
>Young onset Parkinson's patients and caregivers need to read
>this article.
>
>004 Medicare/Medicaid...Congress wants your Home/Car
>
>Article posted by John Cottingham. An editorial by Christopher
>Matthews from the San Francisco Examiner on attempts in Congress
>to take the cars and homes of those family's with serious illness.
>
>005 Tai Chi Exercise Reduces Falling in the Elderly
>
>Newspaper article posted by John Cottingham, Tai Chi Keeps the
>Doctor Away, Research Says / Chinese exercise helped elderly keep
>from falling by Paul Recer
>
>006 Wall Street Journal article on pallidotomy
>
>Margaret Monty's posting of David Stipp's article in The Wall
>Street Journal entitled Hope From a Knife-----Surgery for Parkinson's
>Brings Success Stories In Face of Skepticism
>
>007 News on the Parkinson's Front
>
>Several articles compiled into one message...interesting reading.
>
>008 The Scientist: Brainstorms Abound At NIH's NINDS
>
>An article from The Scientist magazine outlining where research is
>going at NINDS.
>
>009 More: Physics and PD
>
>
>010 Drugs: From Compound to Pharmacy
>011 What Parkinsonians Should Know About Social Security Disability
>Insurance
>012 Disability Evaluation under Social Security
>013 Incontinence: What the Algorithm has to say, and More
>014 ADL and UPDRS Role in PD Treatment
>015 Pallidotomies or Thalamotomy on an Outpatient Basis?
>016 Chinese Influences in Western Medicine
>017 Can't Remember Your Name...How About Singing?
>018 RESTLESS LEGS
>019 Confusion , Cold Intolerance, Constipation...How i+
>020 Ability to regulate eating declines in elderly
>021 New Dystonic Tremor Case Study by list-member, T. Davis
>022 Mouse Gene May Lead To Clues by M.A.J. McKenna
>023 Surgery and transplants show new promise: by Judy +
>024 PALLIDOTOMY; A chance for a normal life by M.A.J. +
>025 Listmember Quoted in Toronto Pallidotomy Article
>026 Parkinson's Abstracts presented at AAN Convention 1995
>
>        WORLD-WIDE PARKINSONS CHATTING INFORMATION
>
>050 Parkinsons Chat Room
>051 Getting from AOL to the Undernet Parkinsons channel
>
>          PD HUMOR
>
>060 Wednesday PD-humor By David Boots
>061 HUMOR: Sinemet chain-letter
>062 can't get it up (a twisted pair variation on an ol+
>063 Fred Turner, Funny Glossary of Medical Terms
>
>
>          PALLIDOTOMY INFORMATION
>
>
>         PALLIDOTOMY FOLLOW-UP STUDY
>
>075 M. Dogali, E. Fazzini,E. Kolodny Pallidotomy Follow-up
>
>
>
>       STIMULATION, (PALLID AND THALAMIC) INFORMATION
>
>           STIM Clinical Trials in Progress
>
>080 Thalamic Stimulation at Vanderbilt, Dr. Thomas Davis
>081 Breaking News, Dr. W.C. Koller/Busenbark Pallid STIM
>
>           Technical Details, Patient Selection
>
>085 Thalamic Stimulation System
>086 Deep Brain Stimulation References
>087 Don Sandstrom's Thalmic Stimulation Experiences
>
>
>        CONTENTS OF CURRENT RESEARCH STUDIES
>
>090 What is Parkinson's Disease and how is it treated?
>090 What is Essential Tremor (ET) and how is it treated?
>
>           The following questions are answered in 0091
>
>091 What is Shy-Drager Syndrome (SDS) and how is it treated?
>091 What is SupraNuclear Palsy (SNP) and how is it treated?
>091 What is Multiple System Atrophy (MSA)?
>091 What is StriatoNigral Degeneration (SND) and how is it treated?
>091 What is OlivoPontoCerebellar Atrophy (OPCA) and how is it treated?
>091 What is CorticoBasal Ganglionic Degeneration (CBGD) and how is it treated?
>091 What is Diffuse Lewy Body Disease (DLBD)?
>091 What symptoms may or may not be present in Parkinsonism Plus Syndromes?
>    Table 3.
>
>092 Adverse Reactions to Sinemet CR in the Elderly : Joseph
>093 Drug-Induced & Tardive Movement Disorders Gwen M. Vernon
>094 Tremor: by Marjorie M. Gillespie
>095 Dose-response Relationship of Levodopa/Mood/Anxiety
>096 A Study of Hereditary Essential Tremor Bain et al.
>
>            DIET
>
>097 Dietary Factors in the Management of Parkinson's Disease
>098 Re: Fava Beans!
>099 Eating Fava Beans in Old San Francisco
>100 Three Fava Bean Recipes
>101 Mailorder sources for Dry Fava Beans
>102 Favism, Faba, Sinemet and Parkinson's
>
>            DRUG TRIAL ANNOUNCEMENTS
>
>103 NIH Study on Slowing or Stopping PD Progression
>104 NINDS Studying Postmenopausal Estrogen Replacement+
>
>
>           PARKINSON'S PLUS DISEASE ETIOLOGY AND DIAGNOSIS
>
>091 PD & PD+ Syndromes by Mark Stacy/J. Jankovic
>
>          RECOGNITION AND TREATMENT OF PARKINSON'S DISEASE
>
>090 Recog/Treat of Early PD & Other Tremor Disorders by Mark Stacy/D. Brownlee
>
>        NEW MEDICINAL APPROACHES TO TREATING PARKINSON'S-STUDY
>
>106 NADH--a new therapeutic approach to Parkinson's disease by Birkmayer JGD
>
>       MEDICATIONS USED IN THE TREATMENT OF PARKINSON'S DISEASE
>
>105 Medications in PD
>106 Quick PD Drug Glossary
>108 Constipation Protocol
>109 Corrections to Constipation protocol
>
>       CONTENTS OF ABSTRACTS IN THE ARCHIVE
>
>200 What Is DHEA?
>201 What is Melatonin and How Is It Helpful?
>202 NIH Grant to design and synthesize Co-factor of TH
>203 Vitamins E and C, Useful in Parkinson's?
>204 Gastrointestinal Problems Encountered With PD
>205 Does It Take You a Little Longer to Think Now?
>206 Are Melonomas Activated by Carbidopa/Levodopa?
>207 Has Aluminum Been Implicated in PD?
>208 Are Environmental Factors Implicated in PD?
>209 GM1, An Elixir of Life for a Damaged Dopamninergic+
>210 Cisapride References
>086 Deep Brain Stimulation References
>211 A Relationship between Diabetes and PD?
>212 fava beans and Mucuna pruriens Natural L-dopa in t+
>213 Cerebral Palsy with parkinsonian symptoms References
>214 Essential Tremor: Another use for GM-1 ganglioside?
>215 The 2 1/2 Hour Erection..How To..or..Not To
>216 Ganglioside GM1
>
>
>       RESOURCES
>
>    How do I make a Parkinson Alert ID Card which lists
>217 the medications I take and drugs that can hurt me?
>218 Care-Giver Handbook
>219 Algorithm for Managing Parkinson's Disease
>220 Blue Glasses Tech Info
>
>----------------------------------------------------------------------
>
>              ORDERING MESSAGES
>
>You are now ready to order messages from the Parkinsn archive at
>[log in to unmask]
>
>Prepare a message to:
>
>[log in to unmask]
>
>On the Subject: line put CT:220 Blue Glasses Tech Info
>
>(The CT: indicates that this is a Current Topics request. The 220 means
>message number 220 and following that is the name of the message.) ONLY 1
>Current Topics message request per message. I will reply to this message
and attach message 220 to it. Please limit your requests to 5 per day.
>
>This is easy to do with the copy and paste function of your mail program.
>
>Again the example will look like this:
>
>To: [log in to unmask]
>Subject: CT:220 Blue Glasses Tech Info
>
>Only one message will be sent per each request with a 5 request per day limit.
>
>NOTHING IS REQUIRED IN THE BODY OF THE MESSAGE.
>
>Send the message.  In a short while, the requested document will be in your
>mailbox.
>I haven't set a limit on the number of messages you can request, I have
just adjusted the way of ordering them so that I can deliver them to you
using the least amount of time and labor on my part.
>
>
>PRINTING NOTES
>
>Many of the messages and studies contain information in columns. Print the
>messages using a non-proportional font. This will allow the items in
columns, to line up.
>
>Some of the studies were multi-part. For my convenience, I have recombined
>them into one package for sending. If you wish to print them, use your word
>processor to put the parts back together in the correct order. All of the
>parts, ie. pt 1/5, 2/5 etc are clearly labeled even though they may have
>been packaged out of order.
>
>Due to the size of some documents, simple text editors may not always work
>to view and edit them. Use the import function for ASCII files in your word
>processor to do this.
>
>THIS IS A TEST:
>
>1. What does the CT: that I put on the Subject: line of my message mean to
John?
>
>A: The CT: will tell him that your message is a request for a Current Topic
>message.
>
>2. What does that number mean that I put after CT: on the Subject: line?
>
>A: The number is the Current Topic message order number of that document
and is found in the left hand column of the listing of documents. It tells
John which message to attach to his reply to you.
>
>3. If I put the message number on the Subject: line, why put the name of
the message there also?
>
>A: The message name is a check to make sure that the message number wasn't
a typo and likewise when you get the message back, you will know what is
>contained in that message.
>
>4. How many messages can I request with each CT: message?
>
>A: One Current Topic message will be sent for each CT: request.
>
>5. How long should I keep this listing of Current Topic messages?
>
>A: Until the message is updated, usually monthly.
>
>John Cottingham    To search the Parkinsn archive, send search requests
>                   to [log in to unmask] with Archive Search as the subject.
>LibraryH           Search of the Subject: line, From: line and Body are
>                   possible. Look for "Current Topics...." message for
>[log in to unmask]    Articles and Studies available by e-mail.
>=========================================================================
>
>
>--=====================_852646722==_
>Content-Type: text/plain; charset="us-ascii"
>
>[log in to unmask]      That man may last, but never lives,
>                        Who much receives, but nothing gives;
>HomeBoy #Parkinsons         Whom none can love, whom none can thank,--
>                               Creation's blot, creation's blank.
>John Cottingham           Thomas Gibbons (1720-1785): When Jesus dwelt.
>
>
>
>
>
>
>
>
>
>
>
>--=====================_852646722==_--
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 08:28:43 -0500
>From:    Bob & Joy Graham <[log in to unmask]>
>Subject: Re: AMGEN again
>
>Thanks Barb Mallut for letting me know about AMGEN
>Joy Graham
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 08:34:23 -0500
>From:    Camilla Flintermann <[log in to unmask]>
>Subject: Re: I'm new
>
>Lee--I expectyou'll hear of websites etc.  Also, there are excellent
>materials available from thenational organizations, a couple of which
>are:          Nat'l.Parkinson Fndtn
>              1-800-327-4545
>
>             American Parkinson Disease Assn.
>             1-800-223-APDA
>
>Of many books, here are a couple--
>            "Parkinson's Disease ...One Step at a Time
>            Problems & Answers for Patients & Health Professionals "
>                by J.David Grimes, M.D.
>                   Peggy A. Gray, R.N>
>                   Kelly A. Grimes,B.Sc.
>           May be ordered from:Parkinson Soc. of Canada
>                  Ottawa Civic Hospital,1053 Carling Ave.
>                  Ottawa,Ontario,Canada K1Y 4E9
>
>           "Parkinson's Disease:A Guide for Patient & Family
>                by Roger Duvoisin, M.D.                     "
>           May be ordered from : RavenPress
>                   1140 Avenue of the Americas,New York,NY 10036
>
>There is also a sublist of the PD list especially for caregivers(CGs)
>of Parkinsonians(PWPs) and I will post the notice about it again today.
>You're right, there's a lot to learn--and different folks have different
>versions of this "designer disease" (Jeff Jones' term). Glad to have you
>aboard...
>Camilla Flintermann,CGfor Peter,78/7,Oxford,OH
>[log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 08:59:44 -0500
>From:    Jim Cordy <[log in to unmask]>
>Subject: Letter to the President
>
>Thank you Dale.  Your letter to the president got me off my duff.  Perhaps
>our two letters may motivate others.
>
>----------
> January 7, 1996
> Office of the White House
> Washington, DC.
>
> Dear  President Clinton:
>
>I am writing you to ask that you take a leadership position in the battle
>to cure Parkinson's Disease.  Last year a grass roots effort resulted in a
>bill increasing federal spending for Parkinson's Disease research amassed
>62 cosponsors in the Senate and 240 cosponsors in the House.  The language
>of this bill was amended to the NIH Revitalization Bill and passed by
>unanimous consent in the Senate.  Despite having a majority of cosponsors
>in the House, this bill never made it out of the Commerce Committee.
>
>This year we are back.  It is not enough for us who suffer from this
>dreadful disease to be told what they great job we did in raising
>awareness.    It is not enough to have my Senators and Congressman be
>cosponsors.  It is not enough to hear Zach Hall, director of NINDS, say
>they are doing what they can.  We want a cure for Parkinson's Disease now.
>The most frustrating part of this situation is that the majority of
>neuroscientists believe we are on the threshold of making a dramatic
>breakthrough if not a cure.  With a strong commitment from your office we
>could look forward to one day soon witnessing a Mohammed Ali absent the
>trembling hand the world saw as he lit the Olympic flame in Atlanta.
>
>This is a disease where the scientist say we have a real shot at victory.
>That translates not only into a reduction in suffering for those afflicted
>but also a real reduction in the budget deficit.  It is estimated that
>conservatively Parkinson's Disease costs society $6 billion per year.  It
>is that potential savings that has resulted in even the most fiscal
>conservatives such as Pennsylvania's Senator Santorum supporting this
>initiative.
>
>We who have Parkinson's Disease were delighted when Dr. Freed was able to
>speak briefly to you during a campaign appearance in Colorado, and that you
>chose to mention subsequently, in several instances, the potential for
>dramatic breakthroughs  in Parkinson's Disease.  I know this disease
>touches you personally.  Your Attorney General courageously announced that
>she has Parkinson's Disease.  Retired Senator Pell suffered from
>Parkinson's Disease.    The fathers of Senators Wellstone, Robb, and Coats
>all had Parkinson's Disease.  Congressman Joe McDade from Scranton
>Pennsylvania has Parkinson's Disease.  Your new Secretary of Defense was
>last years recipient of the Mo Udall Award recognizing his support of this
>legislation.
>
>There seem to be two obstacles hindering passage of this legislation and
>neither of them stand up to an open minded evaluation:
>
>Concerns by the right to life supporters about fetal tissue research.  Our
>response is simply one does not choose to have an abortion in order to
>provide fetal tissue for research.   A simple analogy puts this issue in
>the proper perspective.  Pennsylvania's former governor Casey had a heart
>transplants.  The heart came from a murder victim.  No one is claiming that
>heart transplants increased the murder rate.
>
>Concerns about earmarking.   I believe that the NIH's policy of pursuing
>the "best science" is indeed the proper policy to follow in general.  But
>as a politician I'm sure you appreciate there are up always legitimate
>exceptions to even the best policies.  Such is the case with Parkinson's
>Disease.  As we are close in a number of different technological areas in
>Parkinson's Disease Research, it's makes sense from a humanitarian point, a
>scientific point and an economic point, to two additional resources to
>achieve that end.
>
>
>I am one of an estimated 1.5 million Americans diagnosed with Parkinson's
>Disease.  As the symptoms to this sinister affliction to not become
>apparent until over 70% of the necessary brain cells have died, it is
>estimated that another 1.5 million Americans have Parkinson's Disease but
>have not yet been diagnosed.   I am 49 years old and have had Parkinson's
>for nine years.  I had to go on disability 3 years ago from my position as
>Metallurgical Manager for Allegheny Ludlum.   I have been extremely active
>in promoting this legislation.  My wife and I have spoken personally to
>both Pennsylvania Senators and the majority of the Congressman.  I am
>convinced that if we allocate a modest increase in funding Parkinson's
>Disease research that we will realize a breakthrough.  But, there is a part
>of me that is terrified at the prospect of continually degeneration of my
>bodies ability to function.  Please help!
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 09:10:10 -0500
>From:    Camilla Flintermann <[log in to unmask]>
>Subject: Re: Public Perception
>
>Dear Marling McR---I can suggest that one very good way to "keep one's
>spirits up" is to DO something positive, like for example, get involved
>in legislative advocacy for the soon-to-be new Udall bill...we used to
>hear that the best way to relieve children's fears about atomic bombs
>was for them to know that their parents were actively working against war.
>I bet PAN (the Parkinson Action Network) would love to hear from you!
>You can call them at 1-800-850-4726....why not get plugged in ahead of the
>rush for the new Congress????  Hang in there-we need you!
>Camilla Flintermann,CG for Peter,78/7,Oxford,OH
>[log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 09:20:18 -0500
>From:    Kathie Tollifson <[log in to unmask]>
>Subject: Re: Pycnogenol
>
>Joe Duggan writes:
>
>. Has anyone given pycnogenol the same fair trial that
>>seems to be so freely given to new drugs which always seem to have negative
>>side-effects?
>>
>
>Hi Joe,
>
>I have been using pycnogenol for about 2 years, usually in the 60-120
>mgs/day dose range. I began using it for its anti-inflammatory properties,
>and was able to drop the prescription non-steroidal anti-inflamatory drug
>that I had been dependent on for years, and that was chomping holes in my
>stomach lining. I read the stuff about its anti-oxidant properties,
>penetrating the BBB etc and decided to continue its use.
>
>I am not aware of any actual direct effect on my PD symptoms, however I now
>take 1/2 the sinemet that I took a year ago, and consider myself very stable
>(little to no progression) after 8 years of battling the dragon. I could not
>say whether this is because of pycnogenol, or any of the other supplements I
>use, or purely the grace of God. Probably all of the above.
>
>In any event, I consider pycnogenol to be a vital part of my PD treatment, I
>would not consider dropping it for any reason, and I use it every day. BTW,
>there are 2 kinds, the grape seed extract, and the maritime pine bark....I
>can not tell the difference subjectively, but unless funds are very tight I
>opt for the maritime bark source. One reason is that no matter what the
>claims, I have trouble believing that there is a pesticide-free grape alive
>anywhere in the US.
>
>Cheers,
>
>Kathie Tollifson
>[log in to unmask]
>
>------------------------------
>
>Date:    Wed, 8 Jan 1997 00:01:36 -0500
>From:    Dennis Greene <[log in to unmask]>
>Subject: Re: Dennis-no biggee
>
>Joao,
>
>You wrote:
>----------
>> Dennis allow me to say that it is lets say a "funny" abreviation...
>> Living and learning,  :-)
>
>Its a funny language english. Thank God its my 'mother tongue',
>I'd hate to have to learn it as a foreign language.  Mind you it is
>such an alive language that some times my kids use it and it is
>a foreign language. Non fache mal,  or as you might say,'no biggee'.
>
>Keep the postings coming,
>
>Dennis
>
>Dennis Greene
>[log in to unmask]
>
>------------------------------
>
>Date:    Wed, 8 Jan 1997 01:15:31 -0500
>From:    Dennis Greene <[log in to unmask]>
>Subject: Re: Beth Leslie's reply to Happy Birthday
>
>Beth,
>
>This is WAR!!!
>
>You wrote in part:
>
>----------
>
>> I'm finding simple things like shopping and paying my bills more and =
>more
>> embarrassing.  I feel such a goon when I can't put away my change; when
>> my left hand refuses to release the goods when it - and I! - arrive at
>> the checkout; when things just won't go into the silly bags I'm sometim=
>es
>> left to stuff them into; and when staff give me 'that' look that is
>> somewhere amongst impatience/exasperation/frustration/pity.
>
>Beth.   PD is your problem,   Bad manners is theirs!!!!!
>
>If you really need to take the offensive try  "I have Parkinsons Disease,
>Sorry if my disability has inconvenienced you." It usually gets you the =
>moral high
>ground.
>
>Better yet is knowing that if you are the biggest problem they are going =
>to face
>today they are really very lucky. This lets you look at them with a sweet=
> smile.
>That really throws them.
>
>>But let's just say I'm feelin' it.  And I don't like it.
>
>Question: What can't get its words out, and shakes with more than rage?
>Answer: A parkie with attitude!
>
>Beth it is all I can do to get my own head in the right place, but at lea=
>st that
>is a battle I can win.  I was recently invited to speak on PD to the stud=
>ents
>at my local TAFE college.  My address coincided with a meeting of the
>principals of all the SE district campuses.  These senior educators fille=
>d the 10+
>disabled parking bays thoughtfully provided by the college. Have you ever=
>
>tried finding parking in a TAFE parking lot at 10 am.
>
>My point is that as a rule society is happy to provide facilities to the =
>disabled
>AS LONG AS WE DON'T INCONVENIENCE ANYONE TO MUCH. Its going
>to take a long time to change society so we better get a grip of ourselve=
>s first.
>
>Hell, I'm no inconvenience, I'm a chance for a non parkie to shine.
>
>
>Go get 'em!!
>
>Dennis
>
>Dennis Greene
>[log in to unmask]
>
>------------------------------
>
>Date:    Tue, 7 Jan 1997 09:48:26 -0500
>From:    John Cottingham <[log in to unmask]>
>Subject: Drug Database Info Available
>
>The Parkinsn Archives located at [log in to unmask], now has
>the capability to send drug information by e-mail.
>
>The drug information was compiled from many sources by
>Kathrynne Holden. The information was formatted by Margaret
>Tuchman. Margaret Monty and Simon Coles were also members
>of this "GREAT!" team. Needless to say, this was done as
>meticulously as possible. Mistakes if found, were unintentional.
>The use of this material is intended for educational purposes
>only. Only you and your doctor have the final say in your
>treatment. "He who self-medicates, has a fool for a doctor."
>
>The following are names of drugs and the number beside the name
>of the drug is the Order number for ordering that information
>from the archives.
>
>ORDERING INSTRUCTIONS:
>
>Send a message to:
>
>[log in to unmask]
>
>On the Subject Line put:
>
>DDB: 1 20 30 40 50
>
>Nothing is required in the Body of the message.
>
>DDB:, signals me to send drug info on 1, 20, 30, 40 and 50.
>
>If you have an email only account that has limits on the sizes
>of messages you can receive, each one of the order numbers can
>be as large as 30 KB. Please limit your requests to no more
>than 5 drugs per day.
>
>
>DRUG NAME
>generic or Trade(R)-- Order #
>
>Acenorm(R), 26                       acetaminophen, 1
>acetazolamide, 2                     Adalat(R), 90
>Adapin(R), 49                        Adrenalin(R), 52
>Advil(R), 68                         Agon(R), 57
>Akineton(R), 17                      Aldazine(R), 126
>Aldomet(R), 3                        Aldopren(R), 3
>Alfprin(R), 12                       alpha methyldopa, 3
>alprazolam, 4                        amantadine,5
>Ambien(R), 139                       amiodarone, 6
>amitriptyline and perphenazine, 7    amitryptyline, 8
>amlodipine, 9                        amoxapine, 10
>Anatensol(R), 64                     Anpec(R),137
>Antivert(R), 77                      apomorphine, 11
>Aropax(R), 97                        Arrestin(R), 135
>Artane(R), 133                       Asendin(R), 10
>Aspergum(R),12                       aspirin, 12
>Astra(R), 94                         Atamet(R), 28
>atenolol, 13                         Ativan(R), 74
>Aurorix(R), 86                       Axid(R), 91
>
>baclofen, 14                         Bayer(R), 12
>Benadryl(R), 47                      benztropine mesylate, 15
>bethanechol, 16                      biperiden, 17
>bisacodyl, 18                        Bonine(R), 77
>Botox (R), 19                        botulinum toxin a, 19
>Brevicon(R), 38                      bromocriptine, 20
>Bronchaid(R), 52                     bupropion, 21
>Buspar (R), 22                       buspirone, 22
>
>cabergoline,23                       caffeine, 24
>Calan(R), 137                        calcium carbonate, 25
>Capoten(R), 26                       captopril, 26
>Carafate(R), 122                     carbamazepine, 27
>carbidopa/levodopa, 28               Cardcal(R), 46
>Cardizem(R),46                       Catapres(R), 35
>chlorpromazine, 29                   cholestyramine, 30
>ciladopa, 31                         cimetidine, 32
>Cinnarizine(R), 61                   cisapride, 33
>clonazepam, 34                       clonidine, 35
>clozapine, 36                        Clozaril(R), 36
>Cogentin(R), 15                      Colestid(R), 37
>colestipol, 37                       Compazine(R), 108
>conjugated estrogens, 38             Coras(R), 46
>Cordarone(R), 6                      Cordilox(R), 137
>Coumadin(R), 138                     Cylert(R), 98
>cyproheptadine, 39
>
>DDAVP (R), 43                        Demerol (R), 79
>Demi Regroton(R), 117                Demulen(R), 38
>Depo-Provera(R), 78                  Deprenyl(R), 120
>deserpidine, 40                      desipramine, 42
>desmopressin, 43                     Desogen(R), 38
>Destinex(R), 23                      Desyrel(R), 130
>Dexedrine(R), 44                     dextroamphetamine, 44
>Diamox(R), 2                         diazepam, 45
>Dilantin(R), 103                     Dilosyn(R), 82
>diltiazem, 46                        Diphedryl(R), 47
>diphenhydramine,47                   Dizac(R), 45
>domeperidone, 48                     doxepin, 49
>Dulcolax(R), 18                      Duvoid(R), 16
>
>Easprin(R), 12                       Ecotrin(R), 12
>Effexor(R), 136                      Elavil(R), 8
>Eldepryl (R), 120                    Emprin(R), 12
>enalapril, 50                        Enalaprillat(R), 50
>Endep(R), 8                          Enduronyl(R), 40
>Enovid(R),  38                       entacapone,  51
>Epifin(R),52                         epinephrine, 52
>Epipen(R), 52                        Epitrate(R), 52
>

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