All prices below include shipping within the United States. International shipping costs will depend on the country and method of shipment utilized. These titles are not yet available for credit card purchases.
Quest for Dignity. Personal Victories Over Leprosy/Hansens Disease -- $25
This 11 x 13, 112-page book with 100 museum-quality black and white photographs, was published in association with the launch of the Quest for Dignity exhibit at the United Nations in 1997. Through quotations, short life stories and powerful images, Quest for Dignity illustrates how people affected by leprosy around the world are challenging the stigma and defying old stereotypes as they transform the traditionally negative image of leprosy into a positive message of hope and triumph.
Freeing Ourselves of Prejudice -- $6.00
This 32-page booklet contains empowering quotations and dignified images from IDEA members around the world, illustrating a strong determination to end prejudice and misunderstanding.
"We will no longer bow our heads. We'll hold them high. By our strength of purpose we will no longer feel ashamed or guilty. We will no longer have the fear of rejection. Most important, we will not be denied our human rights. We will maintain our esteem and dignity. -- Francisco A.V. Nunes, Brazil
The Texture of Our Souls -- $8.00
This 48-page booklet contains inspiring quotations, poetry and powerful images, largely chronicling the challenges faced by the older generation of individuals who were diagnosed with leprosy prior to the advent of a cure. Sample quote:
"A man can survive a cataclysm, suffer the loss of his nearest and dearest; see the whole pattern of his life smashed to pieces, and yet remain basically unchanged; the inner texture of his soul untouched. -- Peter Greave, England
VIDEO: Olivia and Tim: Very Much AliveNTSC format, 50 minutes, 1994 -- $25.00
Olivia Breitha is a 75-year-old woman who was diagnosed with leprosy in 1934 and isolated on the remote Kalaupapa Settlement in Hawaii. Cured since the early
In addition, IDEA also has copies of the following books available for purchase:
The Walls Crumble. The Emancipation of Persons Affected by Hansen's Disease in Japanby Dr. Fujio Ohtani (hard cover, English) -- $25.00
To deny the basic human rights of someone who is ill is totally unconscionable.
I believe that the fact that the Leprosy Prevention Law has, in the name of law,
in fact made de facto prisoners of those who suffer from this disease by forcing
their isolation in the name of public welfare. In banishing a group of people
from the rest of society, the law has condoned the way that society has both
despised, ignored and discriminated against these people. This was not merely
wrong, this indicated a conscious intent to cause harm. From both the social
and ethical perspectives these are acts which cannot be permitted to continue
or be forgotten. This book is an attempt to analyze what effect the Leprosy
Prevention Law (through its several stages of amendments) has had on this
country and how it was terminated.
-- From the Foreword, by Fujio Ohtani
Alone No Longerby Stanley Stein (paperback) -- $10.00
Originally published in 1963, this is the inspiring autobiography of
Sidney Levyson, who took the name Stanley Stein upon entering the
U.S. Public Health Service Hospital in Carville, Louisiana in 1931.
I was case number 746. Henceforth I would always be No. 746,
a number identified not only with my case history but with
everything I would do at Carville for the next third of a century,
from seeking laxative tablets to making a laundry list . . . . We
were no more entitled to individuality than a convict in a
penitentiary . . . At ten o'clock that Sunday morning, March 1, 1931, I became
an exile in my own country. -- Stanley Stein
Olivia. My Life of Exile at Kalaupapaby Olivia Robello Breitha (paperback), is also highly recommended and available from the Arizona Memorial Museum Association.
In June of 1937, I received my bad news. I mean bad. I got a letter telling
It really was bad news. First the letter said that treatment would benefit me no longer. That killed any hope I had of ever getting well. Second, Kalaupapa seemed to me to be the end of the world, the very end. In public, I tried to be cheerful, mostly in front of my family. In the privacy of my room, my pillow was soaked with tears . . . -- Olivia Breitha
Replacing Old Images with Modern Day Realities
IDEA Scholarship Fund
Museum of Hansen's Disease