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The Petersens

 

Eugene W. Petersen

Photograph taken approximately 1985-86 at Gallaudet College.

[I believe the following biography of Gene Petersen to have been written by him for inclusion with his manuscript. GK]

Eugene Petersen was born in 1920 in a small town in south Utah. The family moved to Salt Lake City when he was two years old. He lost all his hearing at age eight, the summer after completing second grade. After a year's convalescence, he resumed his education in the public schools and remained there until his sophomore year, when he attended the Utah School for the Deaf for one year. He returned to the public schools, graduating in 1938, and found work as an apprentice printer--a trade he followed for the next 25 years. In 1967, he left printing and moved his family to Indianapolis to accept employment as a counselor/evaluator in a developing program for the deaf at Crossroads Rehabilitation Center, where he is currently program director, program for the multiply disabled, severely handicapped deaf. This program is now one of the largest and most comprehensive of its kind in the U.S., with clients coming from 24 states.

A few years after graduating from high school, Mr. Petersen got involved in community services for the deaf. He served as a board member of the Utah Association of the Deaf for 23 consecutive years and was secretary, vice president and president. While on the UAD Board, he served on two committees made up of hearing and deaf community leaders that studied the needs of the adult deaf in detail and then the most feasible avenues for improving services to this population. This eventually led to greatly improved rehabilitation and social services for the adult deaf in Utah.

After moving to Indiana, he matriculated at Butler University, where he is currently working toward his degree. He was a member of a committee that studied the need for and secured seed money for the Indianapolis Community Services Agency for the Deaf, a committee that studied the problem of providing more adequate mental health services for the deaf in Indiana and eventually secured seed money to set up the Unit for the Mentally Ill Deaf at Central State Hospital and continues on the advisory committee. He is also on the Indiana Rehabilitation Services Board Committee on Deafness. He has been active in the National Association of the Deaf, the Indiana Association of the Deaf, the American Deafness and Rehabilitation Association and has been feature editor and associate editor of The Deaf American since 1962, when it was called The Silent Worker. He has received the Deafness Research Foundation's Distinguished Public Service Award and the Sertoma Service to Mankind Award.

 

Eugene (Gene) and Inez Petersen.

[I believe the following biography of Inez Petersen to have been written by either Gene or Inez for inclusion with Gene's manuscript. GK]

Inez Petersen was born in eastern North Carolina in 1926 and received her education at the North Carolina School for the deaf at Morganton. Always keeping her role as wife and mother first, she had still found time for a variety of church, civic and community activities. For many years, she was a member and later director of the Winston-Salem St. Paul's Episcopal Church Deaf Choir, served on the Board of directors of the North Carolina Association of the Deaf from 1968-74, including two terms as secretary.

She and her first husband, Ralph Crutchfield, were honored as the Outstanding Deaf Persons in North Caorlina by the National Fraternal Society of the Deaf in 1970. She served in many capacities in the North Carolina School for the Deaf Alumni Association and was NCAD's delegate to the 1976 convention at Houston. When her first husband died, she was appointed to complete his term on the Governor's Advisory Committee for the three North Carolina Schools for the Deaf and was a member of the Winston-Salem Mayor's Committee on the Handicapped and Elderly.

She was honored as Winston-Salem's Handicapped Citizen of the Year in 1976. She is a member of the Registry of Interpreters for the Deaf, was on the Board of directors of the Winston-Salem Deafness Center and was active as a volunteer at Winston-Salem Goodwill. Since moving to Indiana, she has been teaching sign language on both a volunteer and paid basis and currently has five beginning classes going.

 
Eugene (Gene) and Inez Petersen
   

[The following article is from the Indianapolis Star, Monday, July 29, 1985. GK]

Gene Petersen helps others to hear needs of the deaf

By Kathy Whyde, Star Staff Writer

Gene Petersen's friends know that once he latches on to an idea, it's difficult to pry him loose. When he sets his mind on a notion, the conversation follows his agenda; he won't let go until he's sure his point has been made.

For example:

"People are always referring to 'the deaf,' as if we're a herd of sheep or something." Petersen talks and uses sign language at the same time. But his speech is difficult for a hearing stranger to understand, so an interpreter translates.

"Almost everything that's been written about deaf people has been from only two perspectives: the success stories and the troubled people. There is not anything about the ordinary grassroots people.

"Deaf people tend to be like hearing people: Some are great, some are so-so, some are bastards.

"There are rich people, athletes, people on welfare and unwed mothers.

"To me, the world is full of deaf people. To you, there aren't all that many."

The interpreter interrupts. "I think you've made the point," he signs and smiles.

At 65, no task seems greater than Petersen's single-minded energy, whether it's building a cabin in the woods, digging up money for community services for deaf people or writing a book he's been thinking about for almost 15 years.

Tentatively titled, Deaf America, Petersen hopes the book will fill the literary gap between accounts of deaf "superstars" and accounts of "low-functioning" deaf people. He wants to travel the country, talking to "everyday deaf people," about their lives.

Until now, progress on the book has been slow. Petersen has had trouble finding the time for writing, what with his duties as director of deaf services for Goodwill Industries of Central Indiana and his work for the American Deafness and Rehabilitation Association and other deaf advocacy organizations.

But his appointment book has been cleared for the next year. He has been named to the Powrie V. Doctor Chair of Deaf Studies at Gallaudet College, the country's most prestigious school for deaf people. He and his wife, Inez, will move to the school's Washington D.C. campus in mid-August.

The appointment will allow him to work on the book uninterrupted. Gallaudet will provide him with a salary and traveling expenses while he gathers material for his book.

The Gallaudet appointment committee was so impressed with Petersen's project that it picked him over several candidates with doctoral degrees. No matter that Petersen has yet to complete his undergraduate studies. With five children to raise, there wasn't much time or money for him to continue his schooling.

I think the novelty of someone without a doctorate applying for the chair got their attention," Petersen says.

After that, his experience did the talking. For many years, Petersen worked with severely handicapped deaf clients at Crossroads Rehabilitation Center. He was a member of a committee formed to investigate the need for community services for the adult deaf in Indianapolis, which led to the establishment of the Indianapolis Community Services Agency for the Deaf. He studied the need for better mental health services for the deaf and was involved in efforts to establish a special unit for the deaf at Central State Hospital.

In 1983, he became president of the American Deafness and Rehabilitation Association for a two-year term. Over the years, he managed to squeeze in one or two classes a semester at Butler University.

Colleagues who wrote letters of support for him cited his experience with and knowledge of the lives of ordinary deaf people. It's a perspective to which the Gallaudet community may not have had much exposure, Petersen believes.

Because of his deafness, Petersen will have to employ unusual interview methods to gather material for his book. "When you're deaf, you can't look down at your notes while you write," he explains. "You have to be watching the person's hands."

He plans to videotape his interviews, then go back and transcribe the tapes. Still, he anticipates problems, because American Sign Language is its own distint language; an exact English translation is impossible.

As an added precaution, he plans to have a speaking person translate the videotaped sign language into a tape recorder, then have a written transcription made of that tape.

He hopes his book will be useful to people who have "a casual interest in deafness. They really need this information. They can mix socially with deaf people. But it will take them a longer time to learn what their lives are like."

Petersen hopes to have the book finished by December 1986, "before I'm so old I can't do anything but rock."

Then he'll be back at his desk at Goodwill to continue his crusade to develop programs for severely handicapped deaf people. He believes there are now ample educational opportunities for average and higher functioning deaf people, but that people on the other end of the spectrum are left out of the picture.

He knows that, the more Goodwill accepts these people who need help most, the agency's success rate may falter. But he's up to the challenge. "In vocational rehabilitation, they want successes. We know we're never going to have a high number of successful closures."

But offering training skills to the truly needy deaf people is the best way to serve society, he says. "It costs so much money to keep these people in institutions and on welfare. If we can successfully rehabilitate only 1 out of 10 of our clients, the state will make a profit. And our success ratio is 50 percent."

Government cutbacks in funding rehabilitation programs "is just lousy economics," he says.

"I really want to make that point. Do you understand?" he signs and smiles.

"I talk and talk and talk about the need for rehabilitative services. But I don't seem to have made much impact. That's my big disappointment."

Petersen figures another five good years in him to keep making his point, to government representatives, to Sertoma clubs, to anyone who will listen. He doesn't plan to retire until age 70, at the earliest. "I don't feel like stopping now. I'll keep going as long as my mind will let me. I can't imagine just staying home day after day."


[The following interview was conducted by Bob Jacobsen, Supervisor, Office of Vocational Rehabilitation in the State of Indiana Department of Human Services. The interview occurred on April 17, 1987, but was not published until August and December of 1988. The first part of the interview was published in The Hoosier Beacon, of the Indiana Rehabilitation Association, Vol. XII, Number 5, August 1988. GK]

Part I. A Deaf American: An Interview with Gene Petersen

By Bob Jacobsen, M.S., C.R.C., President of IRA

Gene Petersen is an extraordinary person. He is a man of talent, energy, commitment, words and action. Born in 1920, deaf at age eight because of illness, he finished school and two successful careers while not only pursuing his writing but also working to improve the country for deaf Americans.

Gene is a large man, nearly 6'2" and over 200 pounds. He is hunched over at the shoulders, with powerful arms and strong hands. The physical strength is the result of working thirty years as a printer. With his bald pate, light complexion and piercing blue eyes, his feelings are easily discernible. When he speaks with excitement, his face reddens and the arteries in his temples and neck stand out. With the total communication he uses, oral and sign, the words are hammered out like a typesetter pounding on lead.

His soon-to-be-published book is an oral history of deaf America, written in the words of ordinary, grassroot, deaf Americans. This book will have sociological, anthropological and rehabilitative significance lasting well into the twenty-first century. It will be on a par with Terkel's Working and Xinxin and Ye's Chinese Lives.

Because of his disability, Gene has lived in two worlds. He has seen both sides: the hearing and the deaf, blue and white collar, printer and author. Now he wishes to communicate to the hearing world what he has learned about ordinary deaf folks. Like Eric Hoffer, the longshoreman/philosopher, Gene became disabled at age eight. As young men they worked with their hands and backs. As mature adults, writing became their passion. And like Hoffer, Gene has an undying belief in the value of work and the triumph of the human spirit.

(It is maintained that a society is free only when dissenting minorities have room to throw their weight around. As a matter of fact, a dissenting minority feels free only when it can impose its will on the majority: what it abominates most is the dissent of the majority. (Eric Hoffer, Reflections on the Human Condition, p. 29.)

H.B. [Hoosier Beacon] - Tell us about the early years?

G.P. [Gene Petersen] -When I was eight years old, in the summertime, I got spinal meningitis which left me profoundly deaf. I was pretty sick and I missed school for about a year. When I got well enough I went back to the public school, and from that point on I just read my way through school. Now-a-days they call it "Mainstreaming," but I just drifted with the stream. I could never really communicate with my parents. If my mother wanted to make sure that I understood her, she would write me a note and stick it on my face. She didn't trust my lip-reading. If she did, I might be a better lip-reader now. It was just easier to write it down. Then there would be no misunderstanding.

That one year at the school for the deaf opened the world for me. The world of real communication, not just superficial communication.

H.B. - What was school like when you were young?

G.P. - I just read and figured things out myself. I had no social life, very little peer interaction. Some, but really nothing like normal, hearing children do. I went on to my second year of high school and one teacher talked to my mother and father about sending me to the school for the deaf. He thought I'd be better off there, so I accepted it. But I didn't adjust. The other kids in my sophomore class were all older than me, a lot more mature, and I couldn't sign at all. But, little by little, I learned to sign and I really started to enjoy the interaction with other deaf kids--more than I admitted. At the end of the first year, I told my parents I wanted to go back to the public school. I think maybe they wanted to hear that. It made them feel that their son was smart, smart enough to keep up with the hearing kids.

H.B. - Did your one year at the Utah School for the Deaf change your life?

G.P. - That one year at the school for the deaf opened the world for me. The world of real communication, not just superficial communication. Later I met some deaf people and I started to go around with them.

I wanted to tell you about the time I graduated from high school. It was in the middle of the Great Depression and we were really poor. My mother and father didn't go to the graduation. Maybe the reason was they didn't have good clothes or didn't have the bus fare; I don't know for sure. They found an old suit, a second-hand suit. My father was a tailor, and he altered it to fit. They gave me $5.00. So I went and got my diploma. The other kids went out to dance or parties or whatever they do. And I walked uptown alone and I met some of those people that I had remembered from the school for the deaf. And I had $5.00 so I gave one of the older kids some money and he went and bought beer for all of us. So we spent my graduation night playing pool and drinking beer. It was okay--not normal--it didn't kill me.

H.B. - What kind of work did you do? Did V.R. help?

G.P. - After graduation I got a job on my own as a printer's devil. I did all the dirty work. Like washing windows, sweeping the floors, delivering things. And, little by little, I learned the trade. Shortly after that I got married and became active in the deaf community. I was elected secretary for the Utah Association for the Deaf. After I got involved with the deaf community I saw I needed more education. By then, I had heard about V.R. At the school for the deaf, you know, I had never heard about it. So I went there and asked for help to go to the University of Utah. The V.R. counselor asked, "Why do you want to quit printing?" I said, "I don't plan to quit printing, but I want to improve myself. Maybe do more to help deaf people." "Oh no! I think you should stick with printing." I said, "Yes, I plan to stay in printing." Well, we went around and around and about the third time I gave up. I just gave up.

H.B. - How did you get to Crossroads Rehabilitation in Indianapolis?

G.P. - In 1966 there was a V.R. counselor named David Myers. He was the only counselor for the deaf in Indiana. He was sort of a coordinator plus a counselor; he covered the whole state. He did a good job of that. David knew there was a big need for special programs for lower-functioning deaf people. So he asked them if they would think about hiring someone who could really communicate with deaf people, who could act as a counselor. He knew they needed a degree, but I was recommended by highly-placed people in Washington. So I was offered the job without an interview and without a visit.

I find it interesting that the deaf community in the U.S. is like a small or medium-sized town, even though it starts in Maine and goes to California. The deaf community is very close-knit, word spreads fast and there is a warm feeling of belonging.

H.B. - You also worked at the Indianapolis Star?

G.P. - Yes, I worked nights as a printer. At that time it was very easy to work as a sub at the newspaper, you know. Twenty years ago, if you had an International Typographical Union card, all you had to do was go up to a newspaper, put your slip in and they would hire you. There was all the work we wanted. You could travel all over if you wanted to, and some deaf people did that.

H.B. - Tell us about your soon-to-be-published book.

G.P. - About ten years ago, I began to dream about writing a book about ordinary deaf people. I had done a series of interviews for The Deaf American magazine using the usual question and answer format, then I read Studs Terkel's book, Working, in which he got a variety of hearing people to talk about their jobs and life styles with a minimum of questions. I thought that was what we needed in the area of the deaf. Too many demographic studies focused on problems and deviance, and the questions they asked deaf people were designed to show how deaf people were different from hearing people and highlighted their problems more than their ordinary life styles.

I hope my book will be well received, and I hope that it will help people like you, and all of those new people who are thinking of becoming counselors for the deaf, and psychologists and teachers to understand the deaf world and culture better.

From September 1985 to August 1986, I had the honor of occupying the Powrie V. Doctor Chair of Deaf Studies at Gallaudet University. It was a great year. Inez and I travelled around the country. We worked as a team from beginning to end. Inez is one of those people with a God-given talent for making comfortable friends out of strangers in about ten minutes. She was also my camera-woman.

I find it interesting that the deaf community in the U.S. is like a small or medium-size town, even though it starts in Maine and goes to California. The deaf community is very close-knit, word spreads fast and there is a warm feeling of belonging.

Most of my focus is on the middle-class deaf, but many of those higher-functioning people are very proud of their grassroots beginnings. I think the book is a good balance to all of the negatives and all the studies of deviance in the deaf world. I hope my book will be well received, and I hope that it will help people like you, and all of those new people who are thinking of becoming counselors for the deaf, and psychologists and teachers to understand the deaf world and culture better. That is my goal.

H.B. - You are a product of a mainstream education. In your view, what are the pros and cons of mainstreaming for the deaf?

G.P. - If my children had been born deaf, I would not mainstream them. If my grandchildren happen to be deaf, I would tell my daughters and sons, "Forget about mainstreaming, put them in residential schools for the deaf." But some places schools for the deaf are closing down. Utah is down to about 35 and they are all for the multiply handicapped. Parents visit the schools with their children and all those obviously multiply handicapped children don't look normal. So the parents think mainstreaming is better than that. The deaf schools need a mixture of smart kids, some average kids and low-functioning kids. The smart kids will pull up the lower-functioning kids.

If my children had been born deaf, I would not mainstream them. If my grandchildren happen to be deaf, I would tell my daughters and sons, "Forget about mainstreaming, put them into residential schools for the deaf."

In mainstreaming there is a problem with interpreters. I think interpreters are wonderful. But many times children up to high school will look up on the interpreter as the teacher. That is not a healthy thing. Their interpreter becomes the teacher, not the teacher over there.

After school these mainstreamed kids go home on the bus. Most have no communication in their home, no peer interaction. Neighbors don't sign and they can't talk or read lips. They sit and stare at the T.V. without understanding or trying to talk to their parents. They will go home at night and their education stops. Well, that is not part of rehabilitation. But it makes them what they are when they get old enough to go to rehab for help. But I know that some do wonderfully. Some are just fantastic and do really well in mainstream programs and talk very well. I am really impressed at how well they can lip-read. It impresses the hell out of me. But not many do that. The few get all the attention, though.

END OF PART I.

Editor's Note: Part II will contain comments on sign language, Counselors for the Deaf, and other deaf issues.

Special thanks to Phil Hess, Carl Garner, Carolyn McCutcheon and Goodwill Industries of Central Indiana. Mr. Petersen was interviewed on Good Friday, April 17, 1987. On May 27, 1988 Gene retired from Goodwill Industries.

Gene Petersen has published dozens of articles. He is a former associate editor of The Deaf American. His professional activities include: Board Member of Indiana Association of the Deaf; Past-President, American Deafness and Rehabilitation Association; Mayor's, Governor's, and Indiana Rehabilitation Service's Advisory Committees on the deaf and handicapped. Appointed Powrie V. Doctor Chair of Deaf Studies at Gallaudet University for 1985-86. He has received two Sertoma Service to Mankind Awards.


Part II. From the Bottom of the Barrel to the Bottom of His Heart: An Interview with Gene Petersen

By Bob Jacobsen, M.S., C.R.C., President of IRA

Helen Keller has written: I am just as deaf as I am blind. The problems of deafness are deeper and more complex, if not more important, than those of blindness. Deafness is a much worse misfortune. For it means the loss of the most vital stimulus--the sound of the voice that brings language, sets thoughts astir and keeps us in the intellectual company of man.

She has also written: ... I have come to regard hearing as the key sense. If I could live again I should do much more than I have for the deaf. (The Quiet Ear: Deafness in Literature, 1987.)

Born in 1920, deaf due to illness at age 8, Gene Petersen has completed two successful careers, one in printing, the other in rehabilitation. Now he looks forward to the publication of his first book, Visits with Deaf Americans. It is Gene's hope that the book will increase the understanding of the social and cultural influences of deafness on the individual.

H.B. - Tell us about your family.

G.P. - My first wife, Kay, and I had five children, three boys and two girls. In 1967, when I came to work at Crossroads Rehabilitation Center, two daughters stayed in Utah, one boy was away from home and two teenagers came with us. Today my two daughters work for a computer company. My oldest son has a Ph.D. He works at the Jet Propulsion Lab. Another works for Blue Cross/Blue Shield and the other for Pittsburg Testing Lab. All three boys have been on church missions for the Mormon Church. One went to Sweden, another to Japan and the other to the Northwest. They are all married now. I have 15 grandchildren. Kay died in 1968.

Inez, my second wife, attended the school for the deaf in North Carolina. Her first language was ASL (American Sign Language). Inez has a wonderful talent for making friends. She was a great help with the interviews for the book.

H.B. - Does it sadden you that none of your children work with the deaf?

G.P. - Many people assume that if your mother and father are deaf, you automatically become an interpreter, but it doesn't work that way. We communicate very comfortably with our children. They grew up with signing. But interpreting is not their cup of tea. The fact that they do not work with the deaf does not sadden me. They are doing fine.

We need to do more to train counselors and to train more deaf counselors.

H.B. - How important are signing skills for counselors for the deaf?

G.P. - Deaf people appreciate it when counselors can sign a bit. Really, it opens doors and I push that all the way. But deaf people never really feel comfortable with those hearing counselors with just the basic signing skills. And the counselors are not very comfortable with their deaf clients. Some hearing rehab counselors for the deaf will have the basic aptitude to learn to sign well, but the older you get the harder it is to learn a new language. Also, the sign language that people learn from classes is not what they see with the clients.

I'm not saying that deaf people always make better counselors. There are some mediocre deaf counselors and some wonderful. But there is no way you are going to know what it means to be deaf and what it is like in the deaf world and what deaf people are doing after taking a ten hour class in sign language. I'm really concerned about that. We need a lot more training. We need more deaf people in rehabilitation.

But then the grant money was gone, and that good staff started to wonder about job security.

H.B. - It takes money to train people. It also takes money to provide quality services to the severely disabled. Was there a time when more grant money was available for training and programs?

G.P. - Back in the seventies there was money all over. We had already developed a good fee-supported program for severely handicapped deaf adults at Crossroads when a large grant was more or less dropped in our laps. It was about $150,000 a year for three years. With this extra money we developed an even better program. Our success rate, working with the most severely disabled deaf clients, attracted national attention. But then the soft grant money was gone and the good staff started to wonder about job security. All over the United States there must have been 20 to 24 programs like that started up with grant money. It was a wonderful era for rehabilitation of the deaf. But I believe 80% of the programs went down the drain after the grant money was gone, while the need is still there. Today, all the hard money is going to programs for the real smart deaf kids. Kids who go to Gallaudet University, the National Technical Institute for the Deaf, etc. For the severely handicapped deaf, it has gotten to the point where there is no money except the V.R. fee for services and a few start-up grants. At Gallaudet, four-fifths of the money is hard Federal money, one-fifth is V.R. tuition and lodging. Severely handicapped deaf adults need more individual help and more comprehensive services than those bright young students. This is hard to provide with just V.R. fees for services. But given the history of soft money grant programs, I think the way to go is to negotiate fees for services high enough to cover the extra expenses and give rehabilitation programs time to do the job right. Also, preparing these people to live independently in the community is just as important as vocational training.

H.B. - Tell us about the special program for the deaf mentally ill patients at Central State Hospital.

G.P. - In 1967, about six months after I came to Indiana, David Myers made a survey of State psychiatric hospitals and found a sizeable number of deaf patients who were more or less being "warehoused" due to lack of appropriate services and treatments. Myers left the state to continue his education but Alan Parnes, a new rehabilitation counselor for the deaf took up the campaign and with the help of Jess Smith, assistant superintendent at the Indiana School for the Deaf, and seed money from the Lilly Foundation, a program for the deaf was set up at Central State Hospital. It was very successful. But the grant money ran out and the superintendents have changed several times. New people come in and they don't know a damn thing about deafness and don't understand why the deaf patients need special services and professional staff who can communicate with them in their preferred language at their level. The program has become another "white cross," like the many soft money rehabilitation programs.

I remember a man who was placed in a State psychiatric hospital at the insistence of his hearing sister. He wasn't crazy, he wasn't mentally ill; he just had a communication problem on top of a personality conflict with his sister, who did all the talking when arranging commitments. After talking to him, Myers arranged to have him transferred to Crossroads with housing in the community. He had had so little contact with other deaf people, in the rural area where the family lived, that he was overjoyed to have someone to talk to and progressed very well. We put him in a job and he's still there and still living independently in the community. Hell, all I did was let him talk to me. That was all he needed.

Another problem is the stigma of the hospital. There are many deaf people with mental health problems who would be better off with out-patient services, but very few out-patient services for the deaf exist around the state. Existing community mental health centers outside the Indianapolis area have not met the needs of deaf people. We need a lot more flexibility than we have today.

...he was overjoyed to have someone to talk to and progressed very well. We put him in a job, and he's still there and still living independently in the community.

H.B. - What is the cultural difference between American Sign Language and Signed English?

G.P. - I am very interested in language. Not much more than 25 years ago, we had speech and we had sign language. Period. But people began to notice that the sign language the teachers used in the classroom wasn't the same as the language the kids used on the playgrounds and in the dorm and deaf adults used in social situations. What the kids used was what we now call American Sign Language (ASL). Just as in France, where public schools for the deaf got started, they used sign language for instruction, but it wasn't the same as the adult deaf people in Paris used in social situations. They had French Sign Language and they had Signed French. In American today, we have ASL and Signed English (or more accurately "Pidgin Signed English"). The reason for this is because deaf people feel more comfortable with ASL and hearing people feel more comfortable with Signed English. There have been many attempts to modify ASL to make it conform more closely to the grammar of spoken and written English. ASL, like all living languages, is changing. I feel there will always be ASL because it's a good language with certain people in certain situations. Most older deaf people are bilingual, they switch from ASL to Pidgin Signed English as the situation calls for it. You can't change ASL into grammatical English; it's impossible. To put it another way, good English isn't good German and good German isn't good French, but each is a good language in its own right. When you try to translate ASL into English, you lose the flavor.

I hope I have made hearing professionals more aware of the need for more and better services for the deaf people at the bottom of the barrel.

One more thing. I've read that sign language is the fourth most used language in the U.S. I think that's a bit exaggerated, but it is still a very common language and as more and more hearing people learning basic sign language, they become more and more comfortable with deaf people and realize that except for the fact we can't hear, we are not really different.

H.B. - What would you like to be remembered for?

G.P. - I would like to be remembered for helping hearing people understand that except for the basic physical fact of hearing/not hearing, deaf people are more like hearing people than they are different. Deaf culture is based on the need for comfortable social communication, not on ethnicity, religion or region. The deaf community has great heterogeneity but remains a warm, friendly place in which to live. I hope I have made hearing professionals more aware of the need for more and better services for the deaf people at the bottom of the barrel.

THE END

 

 

This is the extended Petersen family, a photograph taken from a reunion in the early 1990s. The five Petersen children are Gene Petersen, Shauna Petersen Saddler, Lorraine Petersen White, Gary Petersen, and Blaine Petersen.

Gene and Suzanne Petersen have two daughters, Jeanette and Megan

Shauna and Edward Saddler have four children: Edward Dean, Steven, Brian, and Rebecca (Becky).

Lorraine and John White also have four children: Adam, Daniel, Nathan, and Jeffrey.

Gary and Linda Petersen have two daughters, Anna Kay and Katherine (Katie).

And Blaine and Becky Petersen have four children: Ryan, Jennifer, Jonathan, and Elizabeth.

Shown in the photograph above are (front row): Brian Saddler's wife, Heather, holding baby Andrew with McKenzi on her left shoulder; John, Becky, Elizabeth, and Blaine Petersen; Linda, Katie, and Gary Petersen; Lorraine and John White with Jeff (on John's right shoulder); Taylor (Steven Saddler's eldest daughter), Shauna, Sara (Dean's daughter), Ed, and Madison (Steven's youngest daughter) Saddler; Suzanne and Gene Petersen holding Jeanette's son Ethan, and Jeanette Petersen.

In the middle: Brian Saddler, kneeling to the far left; Jeff (on John White's shoulder); Steven and Brenda Saddler; and Becky Saddler.

Back row: Jennifer and Ryan Petersen; Anna Kay Petersen; Joan and Adam White; Nathan White; Shirene and Edward Dean, holding son Eric; Spencer and Megan Hall; Jeanette's ex-husband Zane.

 

Background Information About Eugene W. Petersen
and a Perspective on Why He Wrote His Book

Gene R. Petersen
June 19, 2000

 


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