{"id":6424,"date":"2023-03-22T16:37:25","date_gmt":"2023-03-22T16:37:25","guid":{"rendered":"https:\/\/www.sicklecelldisease.org\/?p=6424"},"modified":"2023-03-22T18:06:21","modified_gmt":"2023-03-22T18:06:21","slug":"scdaa-names-new-board-members","status":"publish","type":"post","link":"https:\/\/www.sicklecelldisease.org\/2023\/03\/22\/scdaa-names-new-board-members\/","title":{"rendered":"SCDAA names new board members"},"content":{"rendered":"<p>The Sickle Cell Disease Association of America, a national nonprofit membership organization that advocates for people affected by sickle cell, named Melissa Creary and Monica Mitchell to the association\u2019s board of directors and Chris Ruffin Jr. to the Corporate Advisory Council.<\/p>\n<div class=\"large-4 columns\" style=\"\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-6273 size-thumbnail\" title=\"Thomas L. Johnson\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-250x250.jpg\" alt=\"\" width=\"250\" height=\"250\" style=\"font-size: 16px;\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-250x250.jpg 250w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-300x300.jpg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-1024x1024.jpg 1024w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-768x768.jpg 768w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-1536x1536.jpg 1536w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-200x200.jpg 200w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-400x400.jpg 400w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-600x600.jpg 600w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227-100x100.jpg 100w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/Melissa-Headshot-scaled-e1675435436227.jpg 1708w\" sizes=\"auto, (max-width: 250px) 100vw, 250px\" \/><\/p>\n<p style=\"text-align: left;\"><em>Melissa Creary<\/em><\/p>\n<\/div>\n<div class=\"large-4 columns\" style=\"\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-6274 size-thumbnail\" title=\"Gwendolyn Poles, PhD\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-250x250.jpg\" alt=\"\" width=\"250\" height=\"250\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-250x250.jpg 250w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-300x300.jpg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-1024x1024.jpg 1024w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-768x768.jpg 768w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-1536x1536.jpg 1536w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-200x200.jpg 200w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-400x400.jpg 400w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-600x600.jpg 600w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462-100x100.jpg 100w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/02\/monica-mitchell-7535-re-5-scaled-e1675435889462.jpg 1707w\" sizes=\"auto, (max-width: 250px) 100vw, 250px\" \/><\/p>\n<p style=\"text-align: left;\"><em>Monica Mitchell<\/em><\/p>\n<\/div>\n<div class=\"large-4 columns\" style=\"\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-6426 size-thumbnail\" title=\"Ed Flowers\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-250x250.jpg\" alt=\"\" width=\"250\" height=\"250\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-250x250.jpg 250w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-300x300.jpg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-1024x1024.jpg 1024w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-768x768.jpg 768w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-1536x1536.jpg 1536w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-200x200.jpg 200w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-400x400.jpg 400w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-600x600.jpg 600w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002-100x100.jpg 100w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2023\/03\/Chris-Ruffin-Jr-002.jpg 1799w\" sizes=\"auto, (max-width: 250px) 100vw, 250px\" \/><\/p>\n<p style=\"text-align: left;\"><em>Chris Ruffin Jr.<\/em><\/p>\n<\/div>\n<p><strong>Melissa Creary<\/strong> is senior director for the Office of Public Health Initiatives at the American Thrombosis and Hemostasis Network and an assistant professor in the department of health management and policy at the University of Michigan\u2019s School of Public Health. Over a nine-year career at the Centers for Disease Control and Prevention in the Division of Blood Disorders, she helped create and lead the first national program and data collection system for sickle cell disease at the agency. Creary received her doctorate in interdisciplinary studies focusing on health, history and culture, her Master of Public Health and her bachelor\u2019s degree in biology at Emory University in Atlanta, Georgia.<\/p>\n<p><strong>Monica Mitchell<\/strong> is founder and president of MERAssociates, an award-winning, woman- and minority-owned education, research and evaluation consultancy based in the Washington, D.C., area. She has been the principal investigator or co-principal investigator of National Science Foundation-funded grants totaling over $2,500,000. Prior to launching MERA, Mitchell was program officer at the National Science Foundation and managed portfolios in the Division of Research on Learning in Formal and Informal Settings and the Division of Undergraduate Education. She earned her Doctor of Education and master\u2019s degree in engineering at Columbia University and her bachelor\u2019s degree in economics at the University of California, Los Angeles.<\/p>\n<p>The Sickle Cell Disease Association of America\u2019s Corporate Advisory Council advises the association\u2019s board of directors with board recruitment, fundraising and general advisory information.<\/p>\n<p><strong>Chris Ruffin Jr.<\/strong> is a senior news producer for ABC24 TV in Memphis, Tennessee, and the author of \u201cSucceeding with Sickle Cell.\u201d Before moving to Memphis, he worked in TV news in Columbus, Georgia, and Winston-Salem and Charlotte, North Carolina, where he won an Emmy for Best Morning Newscast. Recently, he partnered with Aflac, Red Cross and Children\u2019s of Alabama to spread awareness about sickle cell disease and mentor other sickle cell patients. Ruffin earned his bachelor\u2019s degree in broadcast journalism from Stillman College in Tuscaloosa, Alabama.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Sickle Cell Disease Association of America, a national nonprofit membership organization that advocates for people affected by sickle cell, named Melissa Creary and Monica Mitchell to the association\u2019s board of directors and Chris Ruffin Jr. to the Corporate Advisory Council. Melissa Creary is senior director for the Office of Public Health Initiatives at the [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[],"class_list":["post-6424","post","type-post","status-publish","format-standard","hentry","category-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>SCDAA names new board members - Sickle Cell Disease Association of America Inc.<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.sicklecelldisease.org\/2023\/03\/22\/scdaa-names-new-board-members\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"SCDAA names new board members - Sickle Cell Disease Association of America Inc.\" \/>\n<meta property=\"og:description\" content=\"The Sickle Cell Disease Association of America, a national nonprofit membership organization that advocates for people affected by sickle cell, named Melissa Creary and Monica Mitchell to the association\u2019s board of directors and Chris Ruffin Jr. to the Corporate Advisory Council. 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