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From: mhollowa@epo.som.sunysb.edu (Michael Holloway)
Newsgroups: bit.listserv.transplant,sci.med,sci.bio,sci.answers,news.answers
Subject: bit.listserv.transplant FAQ, Organ transplantation newsgroup (Part 1 of 2)
Followup-To: bit.listserv.transplant
Date: 20 May 1994 20:57:45 GMT
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Reply-To: mhollowa@epo.som.sunysb.edu (Michael Holloway)
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Summary: This is a description of the bit.listserv.transplant newsgroup
	and its parent mail list, TRNSPLNT.  Frequently asked
	questions regarding organ transplantation are addressed.
	A list of resources for transplantation patients is provided.
Originator: mhollowa@csws3.ic.sunysb.edu
Xref: bloom-beacon.mit.edu bit.listserv.transplant:1034 sci.med:42480 sci.bio:10720 sci.answers:1165 news.answers:19775

Posted-By: auto-faq 2.4
Archive-name: medicine/transplant-faq/part1

5/19/94

Modifications since 3/31/94:
 
Added information on bone marrow donation and the (800)MARROW-2 
  number of the National Bone Marrow Registry. (section XI)
Added sections on brain death and Latin American baby snatching 
  myth to section V.
Added Partnership for Organ Donation to section VII.
Added UNOS's self-introduction to section VII.
Added Jack Batterson's information of the 800 number for Prograf 
  (FK506) reimbursement to Part 2.

Contents

Part 1:
I. The TRNSPLNT mail list
II. Organ and tissue transplant info via gopher
III. Organ donation, frequently asked questions
IV. The organ donor shortage
V. Transplant and organ donation myths
VI. Organ donor awareness postage stamp campaign and other awareness 
    materials
VII. Sources of information on organ and tissue donation and 
     transplantation
VIII. Transplant fund raising (BMT Newsletter)
IX. Live kidney donor information
X. Renal transplant specific sources and information
XI. Blood marrow transplant specific sources
	Bone marrow donation info

Part 2: 
National Transplant Patient Resources Directory


About this FAQ
 -------------- 
This FAQ is archived at rtfm.mit.edu and available by gopher or ftp 
under usenet/bit.listserv.transplant.

The subjects treated in this FAQ are, for the most part, specific for the 
state of organ and tissue transplantation in the United States.  If 
anyone would be interested in providing information that might be helpful 
to people of other countries please let me know.  If anyone has other 
information they would like to have included in this FAQ please send it 
along.

Many thanks to the people who have contributed information and 
otherwise helped with the FAQ: Alex Bost, Dan Flasar, Kimberly 
Montgomery, Arthur Flatau, Katherine Eberle, Anne Treffeisen, and 
Joel Newman of UNOS.  Part 2, the National Transplant Patient 
Resources Directory, lists information on organizations providing 
support (financial and otherwise) to transplant patients.  It is 
taken largely from a pamphlet published by Stadtlander Pharmacy and 
The Transplant Foundation, a copy of which can be found on Yale 
biomedical gopher site.

Mike Holloway
mhollowa@epo.som.sunysb.edu

=========================================================================
I. Description of the TRNSPLNT mail list and bit.listserv.transplant 
=========================================================================

bit.listserv.transplant is a bi-directional echo of the listserv mail 
list TRNSPLNT.  If you have an interest in transplantation, and think 
that the posted news and discussions are of interest, it may be more 
convenient for you to subscribe.  This also provides a way to see who's 
listening since a list of subscribers and their addresses can be accessed 
through the listserv.  All posts to TRNSPLNT or bit.listserv.transplant 
are archived by the listserv system at Washington U.  You can get an 
index of the archive by following the directions below.  To have a list 
of listserv commands sent to you, send mail to LISTSERV@WUVMD.WUSTL.EDU 
and place either HELP or INFO REFCARD on the first line of text.

Below is the introduction to TRNSPLNT written by Dan Flasar.  Since Dan 
started the group early in `93 the posts have been on everything from 
copies of news and information to recipes for low salt diets.  It has 
been a useful electronic support group for some participants who are 
either waiting for a transplant, recovering from a transplant, or just 
getting on with life after a transplant.  We encourage recipients, 
caregivers and medical professionals to introduce themselves to the 
group.  The list is also a tool for organ and tissue donor education.

-------------------------------------------------------------------------
TRNSPLNT on LISTSERV@WUVMD.WUSTL.EDU
         or LISTSERV@WUVMD.BITNET

   TRNSPLNT is a discussion list for organ transplant recipients and
   anyone else intested in the issues, experiences and realities of
   living with an organ trasplant.

   Over the last 30 years, the number of transplants performed each year
   has grown steadily in both absolute numbers and type of organs
   transplanted.

   Though there are hospital, clinical and pharmaceutical
   industry-sponsored newsletters, there are few, if any, completely
   independent discussion forums for those who have experienced this
   oftentimes dramaticaly effective therapy.

   There are many life issues for the transplant patient that are simply
   not covered in medical literature or by medical personnel.  TRNSPLNT
   will provide a way for members to share information on such things as
   as travel, both domestic and abroad, how to deal with a compromised
   immune system, stories about transplant experiences, and anything
   that the members feel is worth discussing.

   Archives of TRNSPLNT postings can be listed by sending an
      INDEX TRNSPLNT
   command to LISTSERV@WUVMD.BITNET (or LISTSERV@WUVMD.WUSTL.EDU).

   To subscribe, send the following command to LISTSERV@WUVMD.WUSTL.EDU
   or LISTSERV@WUVMD.BITNET via email:

      SUB TRNSPLNT Your Full Name

   where "Your Full Name" is your name.  For example:

      SUB TRNSPLNT Billy Rubin

   Owner: Dan Flasar SYSFLASAR@WUGCRC.WUSTL.EDU

   NOTE: This is NOT a medical forum!  Though advice may be offered, you
   should, as with any medical issue, check with your physician before
   you accept anything said in this forum as a basis for doing anything
   that might affect your physical condition!


=========================================================================
II. Organ and tissue transplant info via gopher
=========================================================================

The Yale biomedical gopher is accepting information related to 
transplantation for presentation at their gopher site.  As of this 
writing, issues of UNOS Update, UNOS ethics committee and statistics 
reports, Stadtlanders list of support groups for transplant patients 
and excerpts of the National Kidney Foundation newsletters are 
available.

Point your gopher at: 

                Hostname:       yaleinfo.yale.edu
                Port:           7000

The "Organ and tissue transplant information" submenu is under "Biomedical 
disciplines and specific diseases/diseases and disorders".

Any organization that has information, newsletters, or papers that 
they would like posted are invited to send an ASCII file to Susan 
Grajek at Yale, email: grajekse@medpo1.med.yale.edu, phone: 
203-785-5181.  Other file types can be accommodated but please check 
with Ms. Grajek ahead of time.  If you need help with e-mail or 
preparation of the file, please contact Michael Holloway at 
mhollowa@epo.som.sunysb.edu, phone: 516-444-3090.  Most word 
processors have a simple command for making an ASCII, or plain text, 
file from anything created in that program.

=========================================================================
III. Organ donation, frequently asked questions
=========================================================================

contributed by Alex Bost, alex@unx.sas.com

*** Commonly Asked Questions About Being an Organ Donor:

- Where can I get an Organ Donor Card?

  Many organizations, including the NKF and AAKP will provide donor
cards free of charge.  Many physicians, pharmacies, and hospitals will
also provide them.
[Free cards and pamphlets also available from (800)24-DONOR]

- Should I mention being an Organ Donor in my Will?

  No.  Your will may be read too late to take your organs.  However,
you should definitely mention Organ Donation in your Living Will.

- What is a Living Will?

  A Living Will is a document where you stipulate what kind of medical
attention you will receive if you are unable to make decisions for
yourself.  You may state your wish to become an organ donor in a Living
Will.

- Who pays for the medical costs of being a donor?

  The transplant recipient is responsible for all costs involved in
organ procurement.  The donor's family will not pay any of the cost.

- Does organ donation disrupt funeral arangements?

  No.  Organ donation will not disfigure the body.  A donor may still
have an "open casket" funeral.

- Will becoming a donor mean a doctor will let me die?

  Absolutely not!  Medical personnel must follow very strict guidelines
before a donor can be pronounced dead.  You can expect the same quality
of health care as you would if you weren't a donor.

------------------------------------------------------------------------
The following was written by Anne Treffeisen of the Long Island Chapter 
of TRIO (Transplant Recipients International Organization) 
(516-421-3258).  The week of April 18th to the 24th has been proclaimed 
National Organ and Tissue Donor Awareness Week by the US Congress.  She 
asks that pastors or rabbis include mention of the gift of life in their 
sermon or bulletin during this week and provides this message as a guide.

ORGAN DONATION AND TRANSPLANTATION FACT SHEET

The donation of organs is a unique opportunity to save lives.  
It is possible for the organs, tissues, and corneas of a single 
donor to save or help as many as 25 people.

Transplantation works.  As of 1993, over 160 thousand people 
have been transplanted, and the majority are living full 
productive lives more than five years after surgery.

Over 28,000 people in the United States, many of them children 
under 10 years of age, are currently waiting for transplants, 
and someone is added to the waiting list every 30 minutes.  
Many will die waiting.

All potential recipients are listed on the United Network for 
Organ Sharing, UNOS, computer.  Organs are assigned as they 
become available considering the severity of a patient's 
condition, medical requirements (such as blood type, size, and 
tissue match), proximity to the available organ, and time on 
the waiting list.

More organ donors are needed.  Only about 20% of the potential 
donors actually have their organs donated.

Organ donors are healthy people who have died suddenly, usually 
through accident or head injury.  They are brain dead.  The 
organs are kept alive through mechanical means.

No one involved with the life saving care of an individual is 
involved in the transplantation or organ recovery process.  No 
one on the transplant team has any role in the diagnosis, 
treatment or declaration of death of a patient.

Organs for transplant must be made available soon after death.  
Organ removal will not take place without the permission of the 
next of kin.  Therefore, the decision to donate should have 
been discussed earlier and the next of kin should understand 
and be prepared to carry out their loved one's wishes.  This is 
the heart of DONOR AWARENESS.

There is no cost or payment to the donor family or estate.  All 
normal funeral arrangements are possible.

All religious groups approve of organ and tissue donation as 
charitable acts toward one's fellow human beings.

Organ donation is a true gift.  In general, the donor family 
will never know the recipient.  They do know that out of their 
tragic loss, they have given others life and health.


==========================================================================
IV. The organ donor shortage
==========================================================================

UNOS statistics reveal that in 1992, on average, 7 people a day died in 
the US while on the waiting list.  As organ transplantation has passed 
out of the experimental stage, the number of people with end stage 
diseases seeking a transplant has slowly but steadily increased.  The 
number of donations however, has not increased.  Sadly, this is not 
because there are not more potential donors.  Various estimates are that 
anywhere from 60 to 80% of potential donations are either refused by the 
next-of-kin or are never requested.  These estimates take into account 
the criteria for brain-dead, heart-beating donors and other 
contraindications.  Roughly half of the missed donations appear to result 
from failure of physicians to either declare brain death in a timely 
manner, or their failure to notify their Organ Procurement Organization 
of potential donors.  This is despite enactment in all 50 states of 
"required request" legislation that mandates that all potential donations 
be sought.  Apparently, there is no enforcement of these laws.

There are a variety of proposals to increase the number of 
donations, for example: public and professional education, giving 
people who have registered their support for donation additional 
points on the waiting list should they ever need a transplant 
themselves, and changing the structure of donation from a required 
opting-in to a required opting-out strategy.  These and others have 
all met with resistance from sectors of the medical community, 
public and government that don't seem to realize that the present 
system, and the people trapped in it, are in a crisis situation.

References:

Wolf JS 
The role of the United Network for Organ Sharing and designated 
organ procurement organizations in organ retrieval for transplantation. 
Arch Pathol Lab Med 1991 Mar;115(3):246-9

Prottas J  Batten HL
Health professionals and hospital administrators in organ
  procurement: attitudes, reservations, and their resolutions.
Am J Public Health 1988 Jun;78(6):642-5

Annas GJ
The paradoxes of organ transplantation [editorial]
Am J Public Health 1988 Jun;78(6):621-2

Evans RW  Orians CE  Ascher NL
The potential supply of organ donors. An assessment of the efficacy
  of organ procurement efforts in the United States.
JAMA 1992 Jan 8;267(2):239-46

Spital A
Mandated choice. The preferred solution to the organ shortage?
Arch Intern Med 1992 Dec;152(12):2421-4

"Solving the Organ Donor Shortage", The Partnership for Organ Donation, 
Inc. (617)330-8650.

UNOS Ethics Committee Reports on alternatives for organ donation:
"Financial Incentives for Organ Donation"
"Preferred Status for Organ Donors"
"An Evaluation of the Ethics of Presumed Consent and a Proposal Based on 
Required Response"
- available from UNOS (804)330-8500
- also available through the Yale biomedical gopher, yaleinfo.yale.edu 
  port 7000


==========================================================================
V. Transplant and organ donation myths
==========================================================================

As with any new technology, rumors, myths and misunderstandings about 
organ transplantation are wide spread.  Frustration produced by the high 
cost, the effect of the organ donor shortage, and the unavailability of 
transplantation throughout most of the rest of the world have probably 
contributed to this.  Since rumors can often be more entertaining than 
the truth, tabloid media will often pick up and help spread them, despite 
the great harm they cause.  Urban legends about organ transplantation are 
uniquely dangerous since organ transplantation can not succeed without 
the participation and support of the majority of the population.  Bad 
press, urban legends, even fiction portraying organ transplantation as 
somehow evil, all have prevented full support for donation and led to the 
death of people who might otherwise be leading productive and happy lives 
now. 

Another factor fueling the proliferation of myths is the unfortunate 
institution in India of payment for unrelated live kidney donation that 
preys on the poor in that country.  While it may be true that the Indian 
medical community is not required to abide by western standards of 
ethics, neither is the US medical community required to interact with 
them, train their physicians, publish their research, etc.  Its past time 
that the US medical community started taking visible responsibility for 
influencing transplantation ethics in foreign countries.

Mani, M.K., Renal Transplantation in India. (1992) Transplantation 
Proceedings, 24:1828-9.


The "rising from brain death" myth
----------------------------------

One of the requirements for solid organ donation from cadavers is 
that blood remain circulating for a number of hours.  This requires 
a patient that has been declared brain dead, total loss of brain 
stem function, but whose heart can be kept beating.  Unfortunately, 
the media, and even, apparently, some medical professionals, are in 
the habit of using the term "brain dead" to describe other 
conditions that are properly referred to as vegetative state and 
coma.  A patient can recover, to one degree or another, from a 
vegetative state or a coma.  As a result, when next of kin are 
approached with a request for organ donation after being told that 
the patient is brain dead they often mistakenly believe that the 
patient might recover and insist on waiting till the heart has 
stopped beating and the patient is no longer a candidate for 
donation.  

Myths are widely circulated of patients declared brain dead who 
recover just as they are about to be used for organ donation.  This 
has never happened.  Inaccurate use of terms has probably 
contributed to myths of resurrection from brain death but the 
linkage to organ donation is simply malicious.

The Partnership for Organ Donation (see section VII), a volunteer 
organization active in altering the way donation requests are made, 
is urging professionals to avoid the use of the term "brain death" 
when discussing the declaration of death with the family since its 
unrealistic to expect that the term can be explained to them, and 
misinformation corrected, while they're in a grieving process.

Freeman JW
Confusion and misunderstanding of some of the terms and practices
  readily employ in medicine [editorial]
S D J Med 1991 May;44(5):123

Pallis C
ABC of brain stem death. The position in the USA and elsewhere.
Br Med J (Clin Res Ed) 1983 Jan 15;286(6360):209-10

Young B  Blume W  Lynch A
Brain death and the persistent vegetative state: similarities and
  contrasts.
Can J Neurol Sci 1989 Nov;16(4):388-93

Oboler SK
Brain death and persistent vegetative states.
Clin Geriatr Med 1986 Aug;2(3):547-76


The black market myth: 
----------------------

In all the time that the rumors of a black market, kidnapping and 
murder of children, organ-swiping, and other atrocities have 
been circulating (since at least 1982), there has never been any 
evidence to substantiate any of them.  

Any rumor regarding a black market in organs, or organ piracy, needs 
to be evaluated in light of the necessity of matching the organ and 
recipient in order to avoid rejection by the recipient's immune 
system.  One can not take any old organ and just put it anywhere 
you please.  A rather complex system has been set up in the US to 
handle matching and distribution.  Its unlikely that any number of 
evil people in the US or abroad will be able to duplicate such a 
system in secret.  Adding these simple facts with the necessity of 
having many highly skilled medical professionals involved, along 
with modern medical facilities and support, makes it plain why 
rumors of the involvement of murder, violence and organized crime in 
organ procurement can not be given any credence.  

These stories have done great damage to the public's appreciation of 
the need for organ donation.


The Latin American baby snatching myth
--------------------------------------

These myths have been traced back to at least 1986 when Pravda in 
the Soviet Union carried allegations of children being taken to the 
US for adoption and then being murdered for their organs.  There are 
several variations and they've become quite popular in countries 
where the civil unrest they foster tends to favor one political or 
military faction.  As described above, all of them require an 
ignorance of what's involved in transplantation.  No evidence is 
ever produced, just the assertion that its being investigated.  

Within the last two years some individuals concerned about human 
rights violations in Latin-America have become infatuated with these 
rumors, apparently because one Central-American government official 
or another had told them that they were true, though again no 
evidence is produced.  This is very unfortunate since Amnesty 
International has started to quote some of their more irresponsible 
writings on the subject.

Further information is available from Todd Leventhal at the US 
Information Agency.  E-mail: tleventh@usia.gov Phone: (202)619-5673. 
Fax: (202)205-0655.  
They've been following the body parts rumors for seven years.

References and additional information:

Leventhal, THE "BABY PARTS" MYTH: THE ANATOMY OF A RUMOR.  
(available from Todd Leventhal tleventh@usia.gov and the Yale 
biomedical gopher after 6/1/94)

Pierce, Burdick face accusers in baby parts allegations, UNOS Update, 
June 1993 (available at the Yale biomedical gopher)

UNOS Update, April/May 1994 (available from UNOS, see below)

Organ Trafficing perspective from UNOS, UNOS press release available 
from UNOS and soon to be posted at the Yale biomedical gopher site.

Foreigners Attacked in Guatemala. New York Times, 4/5/94, pg. A10.


The racism myth: 
----------------

The chance of getting a good organ or tissue match is more likely within 
an ethnic group.  Since minorities in the US have traditionally been less 
likely to participate in organ and tissue donation, the chances of a 
patient from one of these groups finding a match is decreased.  The urban 
legend, of course, is that organ distribution discriminates by race and, 
therefore, donation should be refused since it will punish the 
oppressors.  The tragic reality is that the people they are hurting the 
most by doing this are the people within their own ethnic group.

References:

Kallich JD.  Wyant T.  Krushat M.,   The effect of DR antigens, race, 
sex, and peak PRA on estimated median   waiting time for a first cadaver 
kidney transplant.   Clinical Transplants.  :311-8, 1990.

Pike RE.  Kahn D.  Jacobson JE.,  Demographic factors influencing 
consent for cadaver organ donation.   South African Medical Journal.  
79(5):264-7, 1991 Mar 2.

Arnason WB.,   Thomas Jefferson Memorial Church, Unitarian Universalist, 
Charlottesville,   Va.   Directed donation. The relevance of race.   
Hastings Center Report.  21(6):13-9, 1991 Nov-Dec.

Plawecki HM.  Plawecki JA.,   Improving organ donation rates in the black 
community.   Journal of Holistic Nursing.  10(1):34-46, 1992 Mar.

Mozes, Hayes, Tang
Impediments to Successful Organ Procurement in the "Required Request" 
Era: An Urban Center Experience
Transplantation Proceedings 1991 October; 23(5):2545


The preferential treatment on the US waiting list myth
------------------------------------------------------

Since patients are not listed by name in the regional and national lists, 
its hard to imagine how this is supposed to take place.  

It is likely that people taken in by this myth are having a hard time 
distinguishing preferential treatment on the list (which doesn't exist) 
with the problems of simple access to health care in general.  This is a 
problem with the entire US health care system and has nothing to do with 
how patients are treated once they are on the transplant waiting list. 


==========================================================================
VI. Organ donor awareness postage stamp campaign
==========================================================================

A petition is being circulated for a postage stamp to promote 
organ donor awareness.  A similar stamp promoting blood 
donation had a large impact on increasing blood donation.  
Copies of the petition are available from the address below but 
any sheet of paper with names and addresses will do.

The following appears at the head of the petition sheet:
-------------------------------------------------------------------------
December 31, 1993         Revision No. 11    225,859 signatures secured

Ed Heyn, Chairman of Organ Transplants of Southwestern Michigan Support 
Group, has begun a campaign to create a United States postage stamp to 
promote organ donor awareness.  Eds's group must receive a positive 
recommendation from the Citizen's Stamp Advisory Committee before they go 
to the Postmaster General.  Please sign this support signature sheet and 
pass it around.  Upon completion please return it to the address on the 
bottom of this sheet.  This stamp will encourage donor awareness, donor 
awareness saves lives.

Please return to Ed Heyn, 8637 Ruggles Rd. Baroda, MI 49101
--------------------------------------------------------------------------


Sources of the "Don't take your organs to heaven.  Heaven knows we need 
them here" bumper sticker and other materials:

The Aurora Group in Arkansas: 501-2-CHANCE.  
The New York Regional Transplant Organization: 212-870-2240 and 
  212-861-7370
UNOS (see below).

========================================================================== 
VII. Sources of information on organ donation and transplantation 
==========================================================================

UNOS 
---- 
From UNOS quick info sheet:
------------------------------------------------
The United Network of Organ Sharing, located in Richmond, Virginia, 
administers the national Organ Procurement and Transplantation Network 
(OPTN) and the U.S. Scientific Registry for Organ Transplantation 
under contracts with the US Department of Health and Human 
Services.  UNOS is responsible for promoting, facilitating and 
scientifically advancing organ procurement and transplantation 
throughout the United States while administering a national organ 
allocation system based on scientific and medical factors and 
practices.

UNOS members include every transplant program, organ procurement 
organization and tissue typing laboratory in the United States.  
Policies governing the transplant community are developed by the 
UNOS membership through a series of regional meetings, deliberations 
at the national committee level and final approval by a 32 member 
board of directors, equally represented by physicians and 
nonphysicians.

UNOS has formulated policies to ensure equitable organ allocation to 
patients registered on the national waiting list.  These policies 
forbid favoritism based upon political influence, race, sex of 
financial status; they rely, instead, upon medical and scientific 
criteria.
------------------------------------------------

"UNOS Update" June '93, July/August `93 and Sept/Oct `93 issues,  
the UNOS Ethics Committee whitepaper reports on alternative organ 
donation and tables of recent UNOS statistics on organ 
transplantation, are available through the Yale biomedical gopher 
(see above).

The UNOS 800 number for organ donation information, pamphlets, organ 
donor cards, bumper stickers, etc., is: 1-800-24-donor. 

To request transplantation statistics, UNOS Update, or ethics 
committee reports call (804) 330-8500.  UNOS Update gratis 
subscription requests can also be made by writing  to Esther 
Benenson, Managing Editor, UNOS Update, P.O. Box 13770, Richmond, VA 
23225-8770.  A list of educational material is also available.  Some 
of these require a fee.

You can also send a request for information or donor education 
materials to newmanjd@comm5.unos.org.

TRIO
----
The Transplant Recipients International Organization is a network of 
local support groups that meet for the benefit of members and to promote 
organ donor awareness.  Their national headquarters can put you in touch 
with your local chapter: (412) 687-2210.  They also have pamphlets and 
organ donor cards available.

The Partnership for Organ Donation, Inc.
----------------------------------------
From "Solving the Organ Donor Shortage":

	"The Partnership for Organ Donation, Inc. is an independent 
nonprofit organization dedicated to solving the desparate shortage 
of organs available for transplantation in the United States.
	"The Partnership believes the gap between eligible and actual 
donors can be closed, and donation substantially increased, by 
implementing an organized, proactive, and systematic program which 
focuses on three key audiences: health car professionals, organ 
procurement organizations, and the American public."

"Solving the Organ Donor Shortage" is a very concise and detailed 
description of the shortage, the problems contributing to it, and 
how the Partnership believes it can be combatted, complete with 
bibliography.  A copy can be obtained from: 

The Partnership for Organ Donation
100 Oliver St. International Place
Boston, Massachuetts  02110

telephone:(617)330-8650.
fax:(617)330-8651


Long distance love
------------------
The Sept/Oct `93 issue of UNOS Update carried a story about a pen-pal 
support network for transplant recipients.  The address is: Long Distance 
Love, P.O. Box 2301, Ventnor, NJ 08406.  A $6 donation is requested.

Encore: Another Chance at Life
------------------------------ 
A slick magazine published by Chronimed Pharmacy "exclusively 
for organ transplant patients, their families and friends."  
Apparently published 4 times a year.  "This publication 
provides a broad look at many issues surrounding organ 
transplantation and encourages personal stories and feedback 
from readers."  For a gratis subscription write to: Chronimed 
Publishing, P.O. 46181, Minneapolis, MN, 55446-9920

Local transplant centers and OPOs
---------------------------------
Local Organ Procurement Organizations (OPOs) often have education and 
promotion activities.  A local transplantation center will be able to 
give you information on this.

============================================================================
VIII. Transplant fundraising (BMT Newsletter)
============================================================================
(see also the National Transplant Patient Resources Directory, part 2 of 
the FAQ)

The following is from the BMT Newsletter, November 1993, and reproduced 
by Kimberly.A.Montgomery.1@ND.EDU with the publisher's permission.  

        Copyright 1993
        BMT Newsletter
        1985 Spruce Ave.
        Highland Park, Illinois   60035
        708-831-1913

The information is applicable to any kind of transplant 
fundraising.  Two other excellent articles from the BMT Newsletter 
on organizing fundraising and support are available in the TRNSPLNT 
archive and at the Yale biomedical gopher (see above).

Agencies Provide Fundraising Help
---------------------------------

What do you do when you need to raise $10,000 for a bone narrow transplant,
but have no fundraising experience? Some BMT patients have turned to groups
such as the Organ Transplant Fund in Memphis TN or the Children's Organ
Transplant Association in Bloomington IN for help.

The Organ Transplant Fund (OTF) was founded in 1983 to raise funds for
organ transplant recipients. Since its inception, the group has
orchestrated more than 500 successful fundraising campaigns including 100
for bone narrow transplant patients. On average, $200,000 is raised per
patient, says national director Suzanne Norman.

Initially, a staff person from Organ Transplant Fund meets with the family
to identify a fundraising chairperson, and to set up a committee of local
volunteers. "We then meet with the volunteers, help them develop a
fundraising plan, and show them how to tap into resources in their
community quickly and effectively. We provide them with a fundraising
packet and ideas for events, as well as access to low-cost products they
might want to sell to raise funds such as cookbooks, candy bars, etc."

Funds raised through OTF are used solely to pay transplant-related
expenses. OTF controls the funds and administers payments directly to the
health care provider. In the event of death, funds remain in the patient's
account for up to one year to pay transplant-related bills. Thereafter, the
funds are transferred to a general account that provides emergency grants
and support services for future patients.

"Since contributions to the Organ Transplant Fund are tax-deductible.
working with us expands the universe of potential contributors," says
Norman. "Large corporations, for example, will simply not make a
contribution to an individual but they will contribute to a tax-exempt
organization."

Fundraising guidance is not the only help Organ Transplant Fund provides.
'"We offer our families a multitude of support services such as arranging
for lodging and transportation to the transplant center, identifying BMT
centers that do transplants for their particular disease, negotiating a
reduced down payment at the BMT center so the transplant can begin quickly,
etc." says Norman.

Organ Transplant Fund retains 5 percent of the funds raised to cover
administrative costs. "Many patients have told us that our support
services, alone, are worth the price," says Norman.

The Children's Organ Transplant Association (COTA) also provides
fundraising assistance to organ transplant patients, both children and
adults. Founded in 1985, the group has conducted more than 150 fundraising
campaigns on behalf of organ transplant patients, approximately half of
which have been for bone marrow transplant patients, according to COTA
executive director David Cain.

"The amount of money varies according to the number of volunteers working
on the fundraising campaign and the size of the community." says Cain.
"Typically, $75,000-$100,000 can be raised in a period of 60-90 days."

Like OTF, COTA asks families to identify a network of volunteers who will
orchestrate fundraising activities in the community. "We provide them with
a fundraising kit, ideas for events, and help with publicity," says Cain.
"Depending on the amount of money to be raised, COTA staff may meet with
the family or simply provide guidance over the phone."

All contributions are deposited in a tax-exempt COTA fund and are used
strictly to pay medical expenses. "It's important that the public have
confidence that their contributions will be used only for necessary medical
expenses," says Cain. "Having the funds controlled directly by COTA rather
than the family provides that assurance."

COTA's administrative expenses are covered by the interest earned on the
accounts into which funds raised for patients are deposited. All funds are
invested in government securities, says Cain.

"Our goal is not only to raise funds for transplant patients, but to get
the community educated and involved in the process," says Cain. "Our
emphasis is on having friends and neighbors help each other."

To contact the Organ Transplant Fund, phone 800-489-FUND. To contact the
Children's Organ Transplant Association, phone 800-366-2682. Life-Core
(Oregon), 503-366-9125, also provides fundraising assistance.


============================================================================
IX. Live kidney donor information
============================================================================

The following is a summary of "Donating a kidney to a family member- How 
primary care physicians can help prepare potential donors"

Authors:  Michael L. O'Dell, MD
       Kristi J. O'Dell, ACSW
       Thomas T. Crouch, MD

VOL 89/NO 3/February 15, 1991/Postgraduate Medicine . Kidney
Donation

Summarized by Katherine Eberle, eberle@gdls.com for the
TRNSPLNT FAQ Jan 1994.

Preview

When a relative needs a kidney to survive, family members often 
impulsively offer to donate one without stopping to consider the 
physical, emotional, and financial ramifications, which can be 
considerable.  The family's primary care physician can be very 
helpful in guiding and educating potential donors and, by arranging 
for screening to be done in the community, can ease the financial 
strain. The authors discuss the things a potential kidney donor 
should consider.

The desirability of transplantation is increasing and the supply of 
cadaveric kidneys falls far short of the demand. So searching for a 
possible living related donor is becoming more and more common.  
Much of the preliminary testing required to identify a donor can be 
easily performed in the potential donor's community, under the 
direction of the primary care physician in communication with the 
transplant team.  Additionally, the donor's care is aided when the 
evaluating physician serves as an advocate.

Evaluation for Immunologic Match

Usually, the first test performed is determination of ABO blood type 
compatibility.  Many physicians follow ABO compatibility testing 
with HLA typing.

Tests required by most centers and a description of results that may 
prohibit transplantation:

TESTS                         Potential Disqualifying
                              Factor
                              
History and Physical          Age under 18 or over 55 yr
Examination                   Obesity
                              Hypertension

                              Systemic disorder with
                              potential to impair health
                              Psychiatric disorder
                              Deep vein thrombosis
                              Family history of polycystic
                              kidney disease,
                              diabetes in both parents,
                              hereditary nephritis,
                              systemic lupus erythematosus
                              
Laboratory Studies            
Blood typing                  Poor match with recipient
Complete blood cell count     Anemia or blood dyscrasia
Automated biochemical         Abnormalities indicating
analysis                      significant disease state
Screening for diabetes        Evidence of diabetes
Serologic tests for syphilis  Evidence of current
                              infection
Hepatitis B surface antigen,  Evidence of current
antibodies, core antigen      infection
Human immunodeficiency virus  Evidence of current
testing                       infection
24-hr urine collection for    
     Creatinine               Diminished clearance
     Protein                  Significant proteinuria
     Calcium                  Hypercalciuria
     Oxalate                  Hyperoxaluria
     Urate                    Hyperuricemia
Urine osmolality after        Inability to concentrate to
overnight thirst              >700 mOsm/L
Urinalysis                    Unexplained hematuria and/or
                              other abnormality
                                 (eg, proteinuria)
Urine culture                 Evidence of urinary tract
                              infection
Pregnancy test (where         Positive for pregnancy
applicable)
HLA typing                    Poor immunologic match with
                              recipient
                              
Radiographic Studies          
Chest x-ray film              Evidence of significant
                              disease
Intravenous urography         Anatomic abnormality
Renal arteriography           Anatomic abnormality
                              
Other Studies                 

                              other significant
                              abnormality
Tuberculin and Candida skin   Evidence of active
tests                         tuberculosis or anergy
Multiple gated acquisition    Evidence of ischemic heart
stress test (in men over age  disease
45 yr and women over 50 yr)
Pulmonary function testing    Significant abnormality in
(in smokers)                  lung function
                              

If the potential recipient is a reasonable match, renal angiography 
is performed to determine which of the donor's kidneys is the more 
accessible and the better anatomic match and to screen for 
abnormalities that might preclude uninephrectomy.  In general, the 
left kidney, with its longer renal vein, is selected.

Potential donors should also be screened for psychosocial risk 
factors.  An evaluation of the stability of the individual and the 
family and the financial impact of donation should be undertaken.  
This is often performed by social workers.  An important 
consideration is psychosocial evaluation is whether the potential 
donor is being coerced into the donation.  Purchase of a kidney is 
illegal in the United States.  Occasionally, evaluators discover 
potential donors who are unwilling to donate and yet are being 
significantly pressured to do so by family members.  Such persons 
should be skillfully assisted in resisting such coercion, perhaps by 
honestly describing them as "not an appropriate match."

Potential Disqualifying Psychosocial Factors in Kidney
Donor:
Evidence of significant coercion to donate
Evidence that donation would cause extreme financial
hardship
Evidence that spouse is strongly opposed to donation
Evidence of significant psychiatric disturbance

Often, family members spontaneously decide to donate a kidney before 
they have had an opportunity to consult medical personnel.  They 
make their decision on moral rather than technical grounds, often 
describing it as "the right thing to do" or their "calling."

Effects on the Donor

PHYSICAL EFFECTS - The actual risks to the donor from uninephrectomy 
may be divided into short- and long-term. Short-term risks are those 
typically seen with this major surgical procedure (ie, pulmonary 
embolus, severe infection or sepsis, renal failure, hepatitis, 
myocardial infarction, splenic laceration, pneumothorax).  Estimates 
of the mortality rate are generally less than 0.1% and of 
significant complications less than 5%.  Less than 1% of donors have 
any permanent disability.  Long term risks are controversial and 
largely unknown.  In one third of all donors, nonprogressive 
proteinuria develops.  This finding has led to a recommendation that 
donors restrict their protein intake after uninephrectomy.  In 
addition, donors experience a slight rise in the serum creatinine 
level, which is also nonprogressive.

PSYCHOSOCIAL EFFECTS - These risks to potential and actual donors 
may also be short- or long-term.  Potential donors who choose not to 
donate may experience guilt about their decision or be ostracized by 
the family, although detailed studies of potential donors who choose 
not to donate are few.

About one fourth of those who choose to donate experience moderate 
to severe financial difficulties.  Even though the cost of the 
evaluation and procedure is borne by the federal End Stage Renal 
Disease Program, unreimbursed financial losses resulting from job 
absence and travel can be significant.  Most authorities cite a 
return to work 4 weeks after uncomplicated uninephrectomy.  Some 
centers use donor- specific blood transfusions as a means of 
enhancing graft survival.  This requires blood donation from the 
potential donor several days before the actual procedure, which may 
extend the time away from home and work.

Troubled marriages may fail when the added stress of a kidney 
donation is introduced.  According to one study, one third of the 
couples whose marriage failed cited the kidney donation as a major 
factor in the failure.

Although much attention may be lavished on the donor in the 
perioperative period, it may be short-lived and tends to quickly 
refocus on the recipient.  The recipient may, paradoxically, 
criticize the donor's decision or become distant or angry toward the 
donor.

However, the increase in self-esteem gained from the altruistic 
action of donating a kidney may counterbalance such losses.  
Donation of  a kidney has provided many donors with a sense of deep 
satisfaction.

In view of the potential risks to donors, some centers refuse to 
perform transplantation from a living related donor.  With effective 
immunosuppressive therapy, cadaveric transplantation is quite 
successful, and these centers argue that the benefit to the 
recipient is not greatly enhanced by transplantation from a living 
related donor.  However, cadaveric organs are scarce.  In contrast, 
proponents of transplantation from a living related donor argue that 
thwarting legitimate altruistic behavior by denying the procedure is 
paternalistic, particularly since enhanced graft survival is noted 
in such recipients compared with recipients of a cadaveric 
transplant.

Conclusion

Although the use of living related donors will remain controversial, 
everyone involved should be struck by the courage of those willing 
to donate a kidney to a relative. For physicians providing care to 
these families, an exceptional opportunity for guidance exists.  

============================================================================
X. Renal transplant specific sources and information
============================================================================
(see also the National Transplant Patient Resources Directory, part 2 of 
the FAQ)

contributed by Alex Bost, alex@unx.sas.com

*** Periodicals (Magazines) Available to Renal Patients:

RenaLife
Semi-Annual Publication
Publisher:  American Association of Kidney Patients
Cost:  Free with Membership
Contact:  See AAKP in "Associations" Section


For Patients Only
Bimonthly Publication
Publisher:  Contemporary Dialysis, Inc.
Cost:  $17/year; $27/two years; Canada, $22/year; Foreign, $32/year
Contact:  For Patients Only    6300 Variel Ave. Suite I.
          Woodland Hills, CA  91367.


*** Do I need a Hepatitis B Vaccine?

Hepatitis B is a serious viral disease that attacks the liver.  It is
highly contagious and is potentially fatal.  While there is no cure for
the dangerous Hepatitis B, there is a vaccine available.

Immunization is recommended for persons of all ages, especially those
who are in a high-risk category:  healthcare workers; abusers of
injectable drugs, sexually active individuals (including heterosexuals
with more than one partner in a six month period; homosexuals;
bisexuals), patients on dialysis or those receiving frequent blood
transfusions, and patients waiting for organ transplantation.

If you fit into any of these categories, you should ask your physician
about the Hepatitis Vaccine.


*** Should I get a Flu Shot?

Yearly immunization for the influenza virus is recommended for anyone
who has a chronic condition.  If you are a transplant recipient or on a
donor list, ask your physician about the Flu Vaccine.  Starting in 1993,
Medicare will pay for the influenza vaccine.

===========================================================================
XI. Blood marrow transplant specific sources
===========================================================================

Become a marrow donor
---------------------

Bone marrow transplantation (BMT) is an effective treatment for some 
forms of leukemia and is being evaluated in treatments for other 
kinds of cancer.  A donor is needed who matches the patient's tissue 
type in order to make the transplant work.  Since the odds of any two 
people matching are small, a large number of possible donors is 
needed in order to find a match.

Information about how to be registered in the database for tissue 
type matching and bone marrow donation can be obtained from the 
National Bone Marrow Registry at (800) MARROW-2.  They'll answer any 
questions and provide you with local centers for testing.  To 
register, a small amount of blood is needed for typing.  The 
operation to remove marrow is simple and only slightly discomforting.  
Within days, a donor regenerates the marrow.


Resources
---------

The BMT Newsletter is published bi-monthly by a former BMT patient for 
BMT patients.  It is free, although they also accepts contributions.  The 
address is: BMT Newsletter, 1985 Spruce Ave., Highland Park, IL 60035, 
phone 708-831-1913.

BONE MARROW TRANSPLANT SUPPORT NETWORK (800-826-9376)
A telephone support network for Bone Marrow Transplant patients & 
families.
Path: bloom-beacon.mit.edu!hookup!usc!howland.reston.ans.net!gatech!newsxfer.itd.umich.edu!zip.eecs.umich.edu!panix!cmcl2!newsserv.cs.sunysb.edu!ysics.physics.sunysb.edu!mhollowa
From: mhollowa@epo.som.sunysb.edu (Michael Holloway)
Newsgroups: bit.listserv.transplant,sci.med,sci.bio,sci.answers,news.answers
Subject: bit.listserv.transplant FAQ, Organ transplantation newsgroup (Part 2 of 2)
Followup-To: bit.listserv.transplant
Date: 20 May 1994 20:57:51 GMT
Organization: Institute For Theoretical Physics
Lines: 716
Approved: news-answers-request@MIT.Edu
Distribution: world
Expires: 06/19/94
Message-ID: 
References: 
Reply-To: mhollowa@epo.som.sunysb.edu (Michael Holloway)
NNTP-Posting-Host: csws3.ic.sunysb.edu
Summary: This is a description of the bit.listserv.transplant newsgroup
	and its parent mail list, TRNSPLNT.  Frequently asked
	questions regarding organ transplantation are addressed.
	A list of resources for transplantation patients is provided.
Originator: mhollowa@csws3.ic.sunysb.edu
Xref: bloom-beacon.mit.edu bit.listserv.transplant:1035 sci.med:42481 sci.bio:10722 sci.answers:1166 news.answers:19776

Posted-By: auto-faq 2.4
Archive-name: medicine/transplant-faq/part2

Last update 5/20/94

Part 2 of bit.listserv.transplant FAQ

The following is a list of financial and support resources that are 
copied primarily from a pamphlet provided by Standtlanders Pharmacy 
and The Transplant Foundation, with additional information from a 
list provided by American Preferred Plan and people on the TRNSPLNT 
mail list.  Inclusion of pharmacy companies here is not an 
endorsement of their services.  In fact, it is recommended that 
patients very carefully examine whether their services are worth the 
added cost to your medication expenses.  The word on the TRNSPLNT 
list is that they are convenient, but expensive.

March, 1994
Mike Holloway
mhollowa@epo.som.sunysb.edu
==========================================================================
===============================================
National Transplant Patient Resources Directory
===============================================
provided by Stadtlanders Pharmacy and The Transplant Foundation
(with additional information from American Preferred Plan)

The Transplant Foundation

The Transplant Foundation is a national, non-profit volunteer organiza-
tion providing resource information and direct grants to post-transplant
recipients to offset the costs of immunosuppressive medications. The
number of individuals who can receive assistance and the grant
amounts are determined by total contributions received each year. The
Foundation serves as a clearinghouse for information as well as an advo-
cate for the rights of transplant recipients. For more information on The
Transplant Foundation call 800-285-5115.

Stadtlanders

At Stadtlanders we witness the miracle of transplantation everyday
through the 10,000+ transplant recipients we serve. As the first pharmacy
dedicated to serving the needs of the transplant community, Stadtlanders
provides individuals with medication delivery and insurance billing
services nationwide. The Social Services Department offers financial
and emotional counseling as well as resource information. To learn
more about Stadtlanders services call 800-238-7828.

American Preferred Plan

APP is the leading free membership organization delivering prescription 
medications, directly to you home or office & providing linkages to 
community resources & national support networks. Call your APP membership 
specialist for a confidential planning consultation.  800-227-1195


Other companies offering pharmaceutical delivery services:
----------------------------------------------------------

Express Pharmacy Services.  800-826-8850 
PO Box 94999
Birmingham, AL
35220-9989

CHRONIMED PHARMACY
                P.O. BOX 47945
                MINNEAPOLIS, MN.55447
 (THEY PUBLISH ENCORE MAGAZINE FOR ORGAN TRANSPLANT PATIENTS)
800-888-5753

HOMECARE MANAGEMENT, INC.
   			80 AIR PARK DRIVE
   			RONKONKOMA, N.Y. 11779
800-637-5633 (NY)
800-927-4642 (TX)
800-927-4643 (CA)
800-927-4644 (PA)
800-829-4645 (FL)
800-637-5633 (DC)

---------------------------------------------------------------------------


                              INDEX


NATIONAL RESOURCES
COVERAGE FOR HEALTH CARE/MEDICATIONS
   Prograf (FK506) reimbursement				1
   COBRA							1
   High Risk Insurance Pools					1
   Medicaid Coverages						2
     SSI - Supplemental Security Income
     Medicaid
     QMB - Qualified Medicare Beneficiary
   Medicare										3
   Medicare Supplemental Insurance (Medigap Policy)		3
   State Kidney Programs					3
   State Pharmaceutical Assistance Programs			4
   Veterans Administration					4
   Drug company payment assistance				4

NATIONAL RESOURCES
EDUCATIONAL INFORMATION, FINANCIAL GRANTS,
FUNDRAISING INFORMATION, MEDICATION GRANTS
   
   American Association of Kidney Patients			5
   American Cancer Society					5
   American Diabetes Association				5
   American Heart Association					6
   American Kidney Fund						6
   American Liver Foundation					6
   American Lung Association					6
   American Organ Transplant Association			7
   Children's Organ Transplant Association			7
   Juvenile Diabetes Foundation International			7
   The National Heart Assist and Transplant Fund		7
   National Kidney Foundation					8
   National Organization For Rare Disorders (NORD), Inc		8
   Organ Transplant Fund, Inc					8
   Pharmaceutical Manufacturers Association			9
   The Transplant Foundation					9
   TRIO								9

RESOURCES BY CATEGORY INDEX							10

---------------------------------------------------------------------------
pg. 1

=======================================================
National Resources Coverage for Health Care/Medications
=======================================================

The following resources may provide coverage for your health care and 
medications. Please contact these resources to determine if you meet the 
eligibility requirements for such coverage.

Prograf Reimbursement Hotline

Jack Batterson (mulbattj@mizzou1) writes (5/19/94):
I got a notice from Stadtlanders Pharmacy stating that FDA approved on
April 8, 1994, FK506 for liver transplants. The new brand name for this
will be Prograf. Patients who were receiving the drug in clinical studies
will eventually be responsible for the cost of this drug. Questions about
this transition program and patient's insurance coverage for this can call
Prograf Reimbursement Hotline at 1-800-4-Prograf (1-800-477-6472), and
those in Wash. DC area can call 202-393-5563. 
                                                

COBRA
Consolidated Omnibus Budget Reconciliation Act

If you have separated from a full-time place of employment recently, you 
may be eligible for COBRA coverage. The exception to this is an employee 
who enrolls in Medicare. In this case, the employer is not required to 
offer COBRA coverage, but the employer can choose to offer COBRA coverage.

Under COBRA, an employer with 20 or more employees must offer 
continuation of the group health plan for approximately 18 or 29 months 
to an employee whose employment is terminated, if certain eligibility 
standards are met. The employee would be responsible for payment of 
premiums at the same cost (plus 2%) that the employer was paying. A 
dependent of the employee may be eligible for 36 months of coverage.

To determine whether you might be eligible for COBRA coverage, contact 
your employer's employee benefits office. In addition, you can contact:

U.S. Department of Labor--202-219-8776
Contact regarding non-public employment.

Public Health Service--301 443-1886
Contact for state and local government employees.

Internal Revenue Service--202-6224695
It takes approximately 3-5 working days to have a response to your request.



HIGH RISK INSURANCE POOLS

A directory of high-risk insurance policies available state-by-state has 
been put together by an organization called Communicating for 
Agriculture. These policies are rather expensive, not available in all 
states, and need to be carefully considered to determine if they meet 
your needs. However, when available, they may be an excellent way to 
obtain necessary health coverage.

For information as to whether your state has such a high risk pool, call 
800-445-1525.

-------------------------------------------------------------------------
pg. 2


MEDICAID COVERAGES

Medicaid often provides coverage for outpatient medications. There are 
several ways to become eligible for Medicaid benefits.

A. SSI - SUPPLEMENTAL SECURITY INCOME

Provides a minimum income level for aged (65 or over), blind, individuals 
with disabilities, and couples with limited income and limited resources. 
If you are eligible for SSI cash payments, you are likely to also be 
eligible for Medicaid coverage for medications. To determine if you are 
eligible for SSI, call the Social Security Office at 800-272-1213.

B. MEDICAID
There are two possible categories of need under the Medicaid program.

1. Categorically Needy - Individuals who fall at or below the income and
resource level designated as the "poverty line" by their state must be
covered by Medicaid for their health care, assuming all other eligibility
criteria are met.

2. Medically Needy (Spend Down) - In some states, individuals who are
above the income and resource level designated as the "poverty line"
may be eligible for Medicaid through the medically needy program. In
the states where such a program is offered, individuals are allowed to
"spend down" their excess income (but not resources) to the "poverty
line over a period of time. The "spend down" is like a 'deductible."
It is the process of using medical expenses to reduce the income of an
individual to the level of eligibility for Medicaid.

C. QMB - QUALIFIED MEDICARE BENEFICIARY
You are a Oualified Medicare Beneficiary if you are:

...age 65 or over or a person living with a disability, AND

...entitled to Medicare Part A

...have income that is not over the Federal Poverty level

...have resources that do not go over the limit set for SSI eligibility.

If eligible, there is a possibility of Medicaid coverage for prescription 
medication and/or coverage of other Medicare premium costs.

To apply, contact your local public assistance of tics.

Note: For information regarding SSI, Medicaid, Spend Down, and QMB,
call the Social Security Office at 800-772-1213.

--------------------------------------------------------------------------
pg. 3


MEDICARE

Medicare currently covers heart, liver and kidney transplants in an 
approved facility. Bone marrow transplants are covered only under 
specific diagnoses.

Medicare Part B pays for immunosuppressive drugs for a period of one year 
from the date of discharge from the transplant admission.

On August 6, 1993, Congress passed the Omnibus Budget Reconciliation Act 
of 1993 which will extend Medicare coverage for immunosuppressant 
medications for those who meet the eligibility guidelines.

This extended coverage will be phased in by the following timetable:

... before 1995, coverage will continue to be for 12 months
           ... during 1995, coverage will be for 18 months
           ... during 1996, coverage will be for 24 months
           ... during 1997, coverage will be for 30 months
           ... during any year after 1997, coverage will be for 36 months


MEDICARE SUPPLEMENTAL INSURANCE (Medigap Policy)

Medicare does not always cover 100% of all medical needs. That is why 
there are medicate supplemental policies (Medigap), which are intended to 
cover some of the services that Medicare does not. In every state there 
are standardized Medigap policies which are created to fill these "gaps."

Generally, an individual must purchase one of these Medigap policies 
within six months of their Medicare B effective date.

There are three Medigap plans (H, I, and J) which offer LIMITED coverage 
for out-patient medications.

You are strongly encouraged to call your State Insurance Department to 
determine if you are eligible to buy one of these policies. They can also 
advise which insurance companies are selling Medigap plans H, I or J. For 
the number of your State Insurance Department call the National Insurance 
Consumer Helpline at 800-942-4242.


STATE KIDNEY PROGRAMS

Only Kidney Transplant or Renal Patients

There are approximately twenty-five states which have a state kidney 
program which may offer assistance with out-patient renal medications. To 
determine if your state has such a program, contact the National 
Organization for State Kidney Programs in Missouri at 800-733-7345.

--------------------------------------------------------------------------
pg. 4


STATE PHARMACEUTICAL ASSISTANCE PROGRAMS

The following states have programs with specific financial eligibility 
guidelines that offer assistance with out-patient medications to senior 
citizens andror persons with disabilities:

- Connecticut 	CONN PACE Program - CoMecticut Pharmaceutical
		Assistance Contract to the Elderly and the Disabled--
		800-423-5026

 Delaware      The Nemours Health Clinic Program
               New Castle County--302-429-8050
               Kent and Sussex County--800-292-9538

- Illinois 	Pharmaceutical Assistance Programs
  		800-624-2459 or 217-524-0435

- Maine 	Elderly Low-Cost Drug Program--800-773-7894

- Maryland 	Pharmacy Assistance Program--800-492-1974

- New Jersey 	PAAD Program - Pharmaceutical Assistance
  		to the Aged and Disabled--800-792-9745

- New York	EPIC Program--800-332-3742

- Pennsylvania  PACE Program - Pharmaceutical Assistance
  		Contract for the Elderly--800-225-7223


VETERANS ADMINISTRATION

If you have a military history with an honorable discharge, it may be 
possible to become eligible for VA benefits. However, it has become more 
and more difficult to become eligible without a service-connected 
disability. To determine your eligibility, contact your local Veterans 
Hospital or VA office.


PAYMENT ASSISTANCE

Ask your doctor to call for information and paperwork.

DRUG		Manufacturer			Telephone #
----		------------			-----------
BACTRIM		Roche Labs			800-526-6367
CALAN		Searle				800-542-2526
CARDlZEM	Marion Merel Dow		800-552-3656
DILANTIN	Parke-Davis			800-755-0120
EPOGEN		Amgen Inc.			800-272-9376
IMURAN/ZOVIRAX	Burroughs Wellcome		800-722-9294
NEUPOGEN	Amgen Inc.			800-272-9376
SANDIMMUNE	Sandoz				800-447-6673
VASOTEC,PRILOSCEC
			Merck, Sharp & Dome		800-637-2579
ZANTAC		Glaxo				800-452-9677
MICRONASE		Upjohn				(616)323-6004
* Abbott Laboratories/Ross Laboratories, (202)637-6889, (800)922-3255
* Adria  Laboratories Inc.  (614)764-8100
* Allegan Prescription Pharmaceuticals (800)347-4500, extension 6219
* Boehringer Ingleheim (203)798-4131
* Bristol-Myers Squibb (800)736-0003
* Burroughs-Wellcome (919)248-4418
* Ciba-Geigy (908)277-5849
* Genentech Inc. (800)879-4747
* Hoechst-Roussel (800)776-4563
* ICI/Stuart (302)886-2231
* Immunex Corp. (206)587-0430
* Johnston & Johnston (Ortho Biotechnology) (908)704-5232
* Johnston & Johnston (Janssen Pharmaceuticals) (908)524-9409
* Eli Lily and Co.  (317)276-2950
* Norwich-Eaton (607)335-2079
* Pfizer Pharmaceuticals (800)869-9979
* Sanoll Winthrop (212)907-2000
* Schering-Plough (800)822-7000
* Sigma-Tau (800)999-6673
* SmithKline Beecham (Program 1: all pharmaceuticals) (215)751-5760
* SmithKline Beecham (Program 2: Eminase and Triostat) (800)866-6273
* Syntex Laboratories (800)822-8255
* Wyeth-Ayerst Laboratories (215)971-5604

--------------------------------------------------------------------------
pg. 5

====================================================================
National Resources 
Educational Information, Financial Grants, Fundraising Information, 
Medication Grants
====================================================================

Listed in alphabetical order are agencies that may offer assistance with 
educational information, financial grants, fund raising information, and 
medication grants.

Please refer to the Resources by Category guide on page 10 of this 
directory to quickly determine which agencies offer the resource you 
need.

In addition, the following letters are noted after each agency name to 
indicate resources offered:

			E - Educational Information
                        F - Financial Grants
                        FR - Fundraising Inforination
                        M - Medication Grants


AMERICAN ASSOCIATION OF KIDNEY PATIENTS (E)

111 S. Park Street, Suite 405
Tampa, Florida 33606
800-749-2257

Purpose is to promote the welfare of kidney patients through education 
and advocacy. Self-help and patient education are key elements of local 
chapter activities.


AMERICAN CANCER SOCIETY (E, M)

1599 Clifton Road
Atlanta, Georgia 30329
800-227-23g5

Non-profit health organization that supports education and research in 
cancer prevention, diagnosis, detection and treatment, with special 
services available to cancer patients. Some chapters offer limited 
medication grants.


AMERICAN DIABETES ASSOCIATION (E)

1660 Duke Street
Alexandria, Virginia 22314
800-232-3472

Non-profit health organization that provides the general public, 
diabetics, and health-  care professionals with educational support 
including books, literature and seminars.

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pg. 6


AMERICAN HEART ASSOCIATION (E)

7272 Greenville Avenue
Dallas, Texas 75231-4596
800-AHA-USA1/800-242-8721

Callers are routed to a local American Heart Association office and can 
obtain infor- mation about heart disease and the type of support services 
available in local area. Also, callers can receive a free brochure, 
"About Heart Transplants."


AMERICAN KIDNEY FUND (ELF)

6110 Executive Boulevard, Suite 1010
Rockville, Maryland 20852
800-638-8299

Non-profit health organization that provides limited grants to needy 
dialysis patients, transplant recipients and donors to help cover the 
cost of health-related expenses, transportation, medications, etc. 
Provides information and support for kidney donation and transplantation 
as well as general education and information on kidney diseases.


AMERICAN LIVER FOUNDATION (E, FR)

1425 Pompton Avenue
Cedar Grove, New Jersey 07009
800-223-0179

Voluntary agency dedicated to fighting liver disease through research, 
education and patient self-help groups. Provides fund raising information 
and will act as trustee for monies raised.


AMERICAN LUNG ASSOCIATION (E)

1740 Broadway
New York, New York 10019
800-LUNG-USA/800-586-4872

Non-profit, voluntary health organization that offers information to 
people considering lung transplant, and to those individuals who are at 
any point in the lung transplant process. Callers can receive a fact 
sheet on lung transplantation and a list of trans- plant centers 
nationwide. This association can provide referrals to local support 
groups, as well as contacts with other people who have had a lung 
transplant or are waiting for a transplant.

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pg. 7


AMERICAN ORGAN TRANSPLANT ASSOCIATION
(AOTA) (E, FR)

P.O. Box 277
Missouri Citys Texas 77459
713-261-2682

Private, non-profit group that provides numerous services to recipients 
and their families. Including airfare and bus tickets, advice on fund 
raising and establishing trust funds. Will act as trust fund, no 
administrative fees collected. AOTA publishes a newsletter for members. 
Individuals needing airfare or bus tickets must be referred by their 
transplant center.


CHILDREN'S ORGAN TRANSPLANT ASSOCIATION
(COTA) (FR)

2501 COTA Drive
Bloomington, Indiana 47403
800-366-2682

National, non-profit agency helps organize local community in fund 
raising for the individualifamily in order to assist with pediatric 
transplants and related expenses. COTA also assists adults. All funds 
raised go to the individual, no administrative fees collected.


JUVENILE DIABETES FOUNDATION INTERNATIONAL (E)

432 Park Avenue South
New York, New York 10016
800-JDF-CURE/800-223-1138

Non-profit health organization supporting diabetes research. Provides 
information and brochures on diabetes. Offers referrals through its 
chapters.


THE NATIONAL HEART ASSIST AND TRANSPLANT FUND
(E,F,FR)

519 West Lancaster Avenue, PRO. Box 163
Haverford, Pennsylvania 19041
800-NHATF99/800-642-8399

Private, non-profit group dedicated to providing financial, social and 
emotional support to patients needing heart, heartalung, or lung 
transplants and their families. NHATF provides modest grants for 
transplant related costs. Provides information on centers, support 
groups, and materials.
(Continued)

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pg. 8


(continued....) Individuals may establish regional restricted funds 
through NHATF.

Assists heart, heartalung, and lung transplant patients with fund raising 
by providing expertise and by acting as a trust fund for monies raised.

NATIONAL KIDNEY FOUNDATION (E)

30 E. 33rd Street, 11th Floor
New York, New York 10016
800-622-9010

Voluntary health agency seeking the total answer to diseases of the 
kidney and urinary tract...including prevention, treatment, and cure. The 
Foundation's program brings help to people suffering from kidney disease 
through research, patient and community services, professional education 
and public information.


NATIONAL ORGANIZATION FOR RARE DISORDERS
(NORD),INC. (E,M)

P. O. Box 8923
New Fairfield, Connecticut 06812-2783
800-447-6673/203-746-8958

This organization manages a drug cost share program for individuals who 
cannot afford Sandimmune (cyclosporine). To inquire about the 
application process, call 800 447-6673 or 203-746-8958. Allow 8-10 weeks 
for eligibility to be determined.

Serves as a clearinghouse for information for over 5,000 rare disorders. 
This informa- tion is clearly written for the lay person. NORD can also 
connect patients with the same or similar illnesses with each other.


ORGAN TRANSPLANT FUND, INC. (FR, M)

National Office
1027 South Yates Road
Memphis, Tennessee 38119
800489-3863

Offices located in selected states.

Assists candidates/recipients nationwide in obtaining transplants and 
after care, as well as providing essential support and referral services. 
Provides clients with fund raising expertise and materials and assures 
that funds raised are properly dispersed. Limited emergency grants 
available for medications of not longer than 3 months duration. 
Administrative fee collected.

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pg. 9


PHARMACEUTICAL MANUFACTURERS ASSOCIATION (M)

1100 Fifteenth Street NW
Washington, DC 20005

This association publishes the "Directory of Prescription Drug Indigent 
Programs" from information provided by member companies. The directory 
currently lists 59 programs alphabetically by company. Each entry details 
how to apply, drugs that are covered, and basic eligibility requirements.

A free copy may be obtained by writing to PMA, at the above address. The 
request must be received on physician, health-care professional or agency 
letterhead.


THE TRANSPLANT FOUNDATION (E, M)

8002 Discovery Drive, Suite 310
Richmond, Virginia 23229
804-285-5115

National, non-profit volunteer organization providing grants to post 
transplant recipients to offset the costs of immunosuppressive 
medications. The number of individuals who can receive assistance and the 
grant amounts are determined by total contributions received each year. 
The Foundation serves as a national clearinghouse for information, as 
well as an advocate for the rights of transplant recipients.

TRIO
Transplant Recipients International Organization

        244 North Bellefield Avenue
        Pittsburgh, PA 15213
        412-487-2210

TRIO is an independent non-profit international organization committed to 
improving the quality of life of transplant candidates, recipients, and 
their families. TRIO, through a network of local chapters, serves its 
members in the areas of support, advocacy, awareness and education. TRIO 
awards $1,000 scholarships annually to transplant recipients wishing to 
pursue post-secondary education. Clearinghouse for educational materials. 
Referrals made to local chapters.

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pg. 10

	      =====================
              RESOURCES BY CATEGORY
              =====================


EDUCATIONAL INFORMATION

AMERICAN ASSOCIATION OF KIDNEY PATIENTS					5
AMERICAN CANCER SOCIETY							5
AMERICAN DIABETES ASSOCIATION						5
AMERICAN HEART ASSOCIATION						6
AMERICAN KIDNEY FUND.							6
AMERICAN LIVER FOUNDATION						6
AMERICAN LUNG ASSOCIATION						6
AMERICAN ORGAN TRANSPLANT ASSOCIATION (AOTA).				7
JWENILE DIABETES FOUNDATION INTERNATIONAL.				7
THE NATIONAL HEART ASSIST AND TRANSPLANT FUND				7
NATIONAL KIDNEY FOUNDATION						8
NATIONAL ORGANIZATION FOR RARE DISORDERS (NORD), INC			8
THE TRANSPLANT FOUNDATION						9
TRIO									9

FINANCIAL GRANTS

AMERICAN KIDNEY FUND							6
THE NATIONAL HEART ASSIST AND TRANSPLANT FUND				7


FUNDRAISING

AMERICAN LIVER FOUNDATION						6
AMERICAN ORGAN TRANSPLANT ASSOCIATION (AOTA)				7
CHILDREN'S ORGAN TRANSPLANT ASSOCIATION (COTA)				7
THE NATIONAL HEART ASSIST AND TRANSPLANT FUND				7
ORGAN TRANSPLANT FUND, INC.						8


MEDICATION GRANTS

AMERICAN CANCER SOCIETY							5
NATIONAL ORGANIZATION FOR RARE DISORDERS (NORD), INC			8
ORGAN TRANSPLANT FUND, INC.						8
PHARMACEUTICAL MANUFACTURERS ASSOCIATION				9
THE TRANSPLANT FOUNDATION						9



If you are aware of any other national resources that you would like to 
have reviewed for inclusion in the next printing of this directory, 
please call Stadtlanders Social Services Department at 800-238-7828 
and/or The Transplant Foundation at 804-285-5115. Thank you for any 
resource information you are able to contribute.

We hope that this information is helpful to you but, by no means is this 
an all inclusive list of resources. You are always encouraged to seek the 
support and direction of the social worker at your medical facility.