<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dcterms="http://purl.org/dc/terms/">
<rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17756">
    <dcterms:title><![CDATA[Oral history interview with Roy Arruda]]></dcterms:title>
    <dcterms:subject><![CDATA[Arruda, Roy]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Roy Arruda was born in 1960 in the Azores<br />
<br />
His older brother, who also had hemophilia, died of complications from AIDS in 1995. Roy, who is not married, works as a nursing assistant with people who have AIDS. He is an avid hiker on the Appalachian Trail and a recreational all-terrain vehicle driver. Roy has often spoken publicly about his and his family’s experience coping with AIDS. He has severe factor VIII deficiency, HIV and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of an oral history interview with Roy Arruda]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience<br />
]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 23]]></dcterms:created>
    <dcterms:contributor><![CDATA[Arruda, Roy<br />
Harland, Christine]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007,  H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (64 pages) and 1 .mp3 file (134 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17757">
    <dcterms:title><![CDATA[Oral history interview with Avida]]></dcterms:title>
    <dcterms:subject><![CDATA[Avida]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Avida was born in Massachusetts in 1964. At the age of nine he moved to Michigan<br />
<br />
He has an advanced degree in psychology and is currently working to grow a nonprofit community arts and wellness center in Massachusetts<br />
<br />
He has severe hemophilia, is HIV positive, has Hepatitis C and is healthy and happy (5-H Club)]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript of oral history interview with Avida (pseudonym) for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Christine Harland, October 20, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:available><![CDATA[2025]]></dcterms:available>
    <dcterms:created><![CDATA[2004 October 20]]></dcterms:created>
    <dcterms:contributor><![CDATA[Avida<br />
Harland, Christine]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (45 pages)]]></dcterms:extent>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17758">
    <dcterms:title><![CDATA[Oral history interview with Wendell Bourne]]></dcterms:title>
    <dcterms:subject><![CDATA[Bourne, Wendell]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Wendell Bourne was born in 1948 in Cambridge, Massachusetts<br />
<br />
He is married and has four children and one grandson with<br />
hemophilia<br />
<br />
Mr. Bourne is the director of multicultural education for Kindergarten through 12th grade in the Cambridge school system. He is an African-American whose faith has been an enormous resource in handling life’s challenges. He has severe Factor VIII deficiency and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with Wendell Bourne for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Laura Gray, July 29, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004  July 29]]></dcterms:created>
    <dcterms:contributor><![CDATA[Bourne, Wendell<br />
Gray, Laura]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 document (48 pages) and 1 .mp3 file (131 MB)]]></dcterms:extent>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17759">
    <dcterms:title><![CDATA[Oral history interview with Clifford Deschenes]]></dcterms:title>
    <dcterms:subject><![CDATA[Deschenes, Clifford]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Cliff Deschenes was born in 1954 in Lawrence, Massachusetts<br />
<br />
He works in electronics at Wang Laboratories and is married with two children. One nephew has hemophilia<br />
<br />
He has learned to take one day at a time so as not to get too frustrated. Cliff has severe Factor VIII deficiency, HIV and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with Clifford Deschenes for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Laura Gray, September 15, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 September 15]]></dcterms:created>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 document (40 pages) and 1 .mp3 file (85.2 MB)]]></dcterms:extent>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17760">
    <dcterms:title><![CDATA[Oral history interview with Michael Donovan]]></dcterms:title>
    <dcterms:subject><![CDATA[Donovan, Michael]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Michael Donovan was born in Boston, Massachusetts <br />
in 1962. After his father left the family, Mr. Donovan’s mother moved to Houlton, Maine and, later, to Whitman, Massachusetts, where Mr. Donovan went to school<br />
<br />
He has a degree in electronics and has worked for many years in auto repair at a dealership<br />
<br />
One of his two brothers passed away from HIV. He is not married, travels at every opportunity and enjoys competing in poker tournaments. He has moderate factor VIII deficiency and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with Michael Donovan by Christine Harland for the Boston Hemophilia Oral History Project, October 10, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 October 10]]></dcterms:created>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 134 KB .pdf document, and 1 .mp3 file (79 MB)]]></dcterms:extent>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17761">
    <dcterms:title><![CDATA[Oral history interview with Michael Dowling]]></dcterms:title>
    <dcterms:subject><![CDATA[Dowling, Michael]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Michael Dowling is a single man who was born in 1960 in St. Albans, Vermont<br />
<br />
He has been very active in the HIV and hemophilia<br />
community. He learned of his positive HIV status when a public health official told him from his car in a parking lot “You’re positive and have a good day!&quot; He owns his own business and is in love. He has severe factor VIII deficiency, HIV and Hepatitis C<br />
]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with Mike Dowling for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Laura Gray, September 24, 2004  ]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 September 24]]></dcterms:created>
    <dcterms:contributor><![CDATA[Dowling, Michael]]></dcterms:contributor>
    <dcterms:contributor><![CDATA[Gray, Laura]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (68 pages) and 1 .mp3 file (140 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17762">
    <dcterms:title><![CDATA[Oral history interview with Jeryl Drummey]]></dcterms:title>
    <dcterms:subject><![CDATA[Drummey, Jeryl<br />
<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Jeryl Drummey was born in 1941 in Brighton, Massachusetts <br />
<br />
Married with one daughter, he worked for ten years in a bookstore and then for twenty-five years for a distributor of women’s clothing. Jeryl feels strongly that health providers must treat the person and not just the disease. He has moderate Factor VIII deficiency]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of an oral history interview with Jeryl Drummey]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2005 March 17]]></dcterms:created>
    <dcterms:contributor><![CDATA[Drummey, Jeryl<br />
Gray, Laura]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (41 pages) and 1 .mp3 file (88.8 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17763">
    <dcterms:title><![CDATA[Oral history interview with Andrew Flagg]]></dcterms:title>
    <dcterms:subject><![CDATA[Flagg, Andrew<br />
<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Andrew Flagg was born in Massachusetts in 1959. His father was a plant manager at a plastics firm and his mother was a bookkeeper. He has two older sisters. His grandfather died from complications of hemophilia when Mr. Flagg was eight years old. Mr. Flagg took his Bachelor’s degree in Biology in Boston and his Master’s in Biology in Ohio. Married with two step-children, he works as a medical writer. Mr. Flagg has severe Factor VIII deficiency, HIV and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript of interview with Andrew Flagg]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2005 March 17]]></dcterms:created>
    <dcterms:contributor><![CDATA[Harland, Christine<br />
Flagg, Andrew]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (60 pages)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17764">
    <dcterms:title><![CDATA[Oral history interview with Theodore Frost]]></dcterms:title>
    <dcterms:subject><![CDATA[Frost, Theodore]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Theodore Frost was born in Haverhill, Massachusetts <br />
in 1915. Theodore, who was married but had no children, worked as a carpenter most of his life. He has many memories of years spent in the hospital when he was a child and the miracle of Factor VIII when it arrived. He has mild Factor VIII deficiency]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of an oral history interview with Theodore Frost]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 26]]></dcterms:created>
    <dcterms:contributor><![CDATA[Frost, Theodore<br />
Gray, Laura]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (22 pages) and 1 .mp3 file (67.1 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17765">
    <dcterms:title><![CDATA[Oral history interview with Robert Jarratt]]></dcterms:title>
    <dcterms:subject><![CDATA[Jarratt, Robert<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Robert Jarratt is a married man who was born in 1943 in Tennessee<br />
<br />
He is married and has a daughter. Bob was diagnosed when he was in the Air Force and the confirmation of his diagnosis ended his military career. After open- heart surgery in the mid-1990s, Mr. Jarrett volunteered for the New England Hemophilia Association because he wanted to give something back for all the support and care he received from the hemophilia community. He has moderate Factor IX deficiency]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of interview with Robert Jarratt]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 November 1]]></dcterms:created>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (37 pages) and 1 .mp3 file (81.6 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17766">
    <dcterms:title><![CDATA[Oral history interview with Christopher Kucinski]]></dcterms:title>
    <dcterms:subject><![CDATA[Kucinski, Christopher<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Christopher Kucinski was born in 1949 in Brockton, Massachusetts <br />
<br />
Married with four children, Chris grew up in a family of ten, seven of whom had hemophilia <br />
<br />
Chris was loved deeply by his family and was a beacon of hard work and positive thinking. He died in 2005. He had severe Factor IX deficiency, HIV and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of oral history interview with Christopher Kucinski]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 November 23]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Kucinski, Christopher]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (52 pages) and 1 .mp3 file (89.5 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17767">
    <dcterms:title><![CDATA[Oral history interview with David LePage]]></dcterms:title>
    <dcterms:subject><![CDATA[LePage, David<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[David LePage was born in 1963. David is single and lives alone. He has dealt with mental and physical challenges throughout his life. He has been a public speaker about his experiences living with chronic illness and has found that his faith has been an enormous support. He has severe Factor VIII deficiency, HIV and was successfully treated for Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with David LePage for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Christine Harland, August 23, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 11]]></dcterms:created>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (28 pages) and 1 .mp3 file (74.6 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17768">
    <dcterms:title><![CDATA[Oral history interview with William Lynch]]></dcterms:title>
    <dcterms:subject><![CDATA[Lynch, William<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[William Lynch was born in 1960 in Fall River, Massachusetts. <br />
He went to school in Fall River; his mother was a nurse and his father was a school principal. When he was diagnosed with<br />
 hemophilia at age one, it came as a surprise to his family because there was no history. He has two brothers, neither of whom has the disease. Billy attended Bridgewater State College, is single and works with the retarded. He feels that Factor manufacturers should have admitted that they made mistakes. He feels lucky to be alive and healthy and would never have imagined that he’d be this well in 2005. Billy has severe Factor VIII, HIV and Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with William Lynch for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Christine Harland, September 20, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 September 20]]></dcterms:created>
    <dcterms:contributor><![CDATA[Harland, Christine<br />
Lynch, William]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (67 pages) and 1 .mp3 file (151 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17769">
    <dcterms:title><![CDATA[Oral history interview with James Martinowsky]]></dcterms:title>
    <dcterms:subject><![CDATA[Martinowsky, James<br />
<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Dr. James Martinowsky was born in 1953 in Washington Heights, New York <br />
<br />
He has moderate factor VIII deficiency and hepatitis C. He is married and has one teenage son. James is a child, adolescent and adult psychiatrist teaching and practicing in the Boston area.. He attended medical school in New York City, training and practicing on the same wards and clinics where he was treated for his hemophilia as a child. He believes the long-term psychological damage from hemophilia often outweighs the physical.]]></dcterms:description>
    <dcterms:abstract><![CDATA[Interview with James Martinowsky for the Boston Hemophilia Center Oral History Project, A Gift of Experience, by Christine Harland, October 7, 2004]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 7]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Martinowsky, James]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (61 pages) ]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17770">
    <dcterms:title><![CDATA[Oral history interview with Robert Massie]]></dcterms:title>
    <dcterms:subject><![CDATA[Massie, Robert<br />
]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Robert Massie was born in 1956 in New York. His parents wrote the book Journey, an autobiographical account of their son with hemophilia <br />
<br />
Mr. Massie is an ordained Episcopal minister and also has an MBA from Harvard College. He is married and has three children. He speaks of the richness of his life even with all the challenges. Mr. Massie has severe factor VIII deficiency, HIV and hepatitis C. He is currently waiting for a liver transplant]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 files of oral history interview with Robert Massie]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 October 21]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Massie, Robert]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (76 pages) and 2 .mp3 files (105 MB and 94.5 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio files]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17771">
    <dcterms:title><![CDATA[Oral history interview with Stephen Place]]></dcterms:title>
    <dcterms:subject><![CDATA[Place, Stephen]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Stephen Place was born in 1954 in Oak’s Bluff on Cape Cod’s Martha’s Vineyard Island. Stephen is married and has two daughters. He has worked in sales. He has a nephew with hemophilia. He believes you must “know your limits and go to the limit.” He has mild Factor VIII deficiency]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of oral history interview with Stephen Place]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 September 14]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Place, Stephen]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (31 pages) and 1 .mp3 file (58.2 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17772">
    <dcterms:title><![CDATA[Oral history interview with William Somers]]></dcterms:title>
    <dcterms:subject><![CDATA[Somers, William]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[William Somers was born in 1964 in Lutchlade, England. He is married and has one child. He has a PhD in biophysics. Coming to the United States and dealing with our health care system was quite a shock. He has moderate factor VIII deficiency and hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of oral history interview with William Somers]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 September 28]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Somers, William]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (33 pages) and 1 .mp3 file (57.3 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17773">
    <dcterms:title><![CDATA[Oral history interview with Francis Story]]></dcterms:title>
    <dcterms:subject><![CDATA[Story, Francis]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Gray, Laura]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Francis Story was born in 1928 in Beverly, Massachusetts. <br />
Sonny, as he is known, is married and has six children. He has grandsons affected with hemophilia. Sonny grew up during the Depression and has vivid memories of that time. He played in a band and ran an insurance company and now is retired. He has mild Factor VIII deficiency]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of oral history interview with Francis Story]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 5]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Story, Francis]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (54 pages) and 1 .mp3 file (146 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description><rdf:Description rdf:about="https://collections.countway.harvard.edu/onview/index.php/items/show/17774">
    <dcterms:title><![CDATA[Oral history interview with Matthew Vieira]]></dcterms:title>
    <dcterms:subject><![CDATA[Vieira, Matthew]]></dcterms:subject>
    <dcterms:subject><![CDATA[Chronic illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Experience of illness]]></dcterms:subject>
    <dcterms:subject><![CDATA[Gray, Laura]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia]]></dcterms:subject>
    <dcterms:subject><![CDATA[Hemophilia -- Patients]]></dcterms:subject>
    <dcterms:subject><![CDATA[Oral history]]></dcterms:subject>
    <dcterms:description><![CDATA[Matthew Vieira was born in 1934 in East Boston, Massachusetts. His father, who was Portuguese, worked as a truck driver. Matty had two sisters and describes his home as “Just an average American family.” Mr. Vieira has one son. He and his wife Eleanor are very involved with the hemophilia community and feel support is critical in coping with the disease. Matty was diagnosed with severe Factor VIII deficiency at age six. He was successfully treated for his Hepatitis C]]></dcterms:description>
    <dcterms:abstract><![CDATA[Transcript and .mp3 file of oral history interview with Matthew Vieira]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Boston Hemophilia Center Oral History Project, A Gift of Experience]]></dcterms:creator>
    <dcterms:created><![CDATA[2004 August 12]]></dcterms:created>
    <dcterms:contributor><![CDATA[Gray, Laura<br />
Vieira, Matthew]]></dcterms:contributor>
    <dcterms:rights><![CDATA[The Harvard Medical Library does not hold copyright on all materials in this collection. For use information, consult Public Services at chm@hms.harvard.edu]]></dcterms:rights>
    <dcterms:accessRights><![CDATA[Access to the original work depicted requires advance notice. Contact Public Services at chm@hms.harvard.edu for additional information]]></dcterms:accessRights>
    <dcterms:isPartOf><![CDATA[Boston Hemophilia Center. Oral History Project. The gift of experience, 2004-2007, H MS c228]]></dcterms:isPartOf>
    <dcterms:format><![CDATA[text]]></dcterms:format>
    <dcterms:format><![CDATA[audio]]></dcterms:format>
    <dcterms:extent><![CDATA[1 transcript (35 pages) and 1 .mp3 file (70 MB)]]></dcterms:extent>
    <dcterms:medium><![CDATA[Digital text document, digital audio file]]></dcterms:medium>
    <dcterms:language><![CDATA[English]]></dcterms:language>
    <dcterms:type><![CDATA[text]]></dcterms:type>
    <dcterms:type><![CDATA[sound]]></dcterms:type>
    <dcterms:identifier><![CDATA[H MS c228]]></dcterms:identifier>
    <dcterms:provenance><![CDATA[These records were donated to the Harvard Medical Library by Laura Gray, the coordinator of the project, in July of 2006]]></dcterms:provenance>
</rdf:Description></rdf:RDF>
