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Find A Cure Transit Sickle Cell Resources:
ASCAA     > website
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The American Sickle Cell Anemia Association (ASCAA) is an organization that provides quality and comprehensive services through diagnostic testing, evaluation, counseling and supportive services to individuals and families at-risk for Sickle Cell Disease.
Blood & Marrow Transplant Information Network (BMT InfoNet)     > website
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BMT InfoNet provide information and support to patients undergoing a bone marrow, stem cell or cord blood transplant. We support patient every step of the way 0- before, during and after transplant. Patients and their loved ones can visit us online, email us at help@bmtinfonet.org or phone 888-597-7674
book: Honest Medicine by Julia Schopick     > website
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HONEST MEDICINE introduces four lifesaving treatments that have been effectively treating--and in some cases curing--people for 25-90 years.
Book: Your Medical Mind     > website
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Book: Your Medical Mind by Dr. Jerome Groopman that focuses on patient decision making
Cells That Heal Us From Cradle To Grave: A Quantum Leap in Medical Science     > website
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book on stem cell research
Children's Sickle Cell Foundation     > website
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The mission of the Children’s Sickle Cell Foundation, Inc. (CSCF) is to provide social, educational and economic support for children with sickle cell disease (SCD) and their families. Our commitment to sickle cell disease and sickle trait outreach, and support for sickle cell disease research are natural extensions of this mission.
Disability Benefits Help     > website
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A resource for disabling conditions that can be considered severe enough by the Social Security Administration (SSA) to qualify a person for Social Security disability benefits. These conditions can interfere with an individual’s ability to achieve gainful employment, thereby making that person eligible for SSDI or SSI benefits.
IASCNAPA     > website
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International Association of Sickle Cell Nurses and Physician Assistants (IASCNAPA) is the only association of nurses, physician assistants, social workers, and other health care professionals caring for individuals with sickle cell disease.
Landis Vance     > website
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Resources to support spiritual well-being for those with chronic illness. Scholarly articles on the inter-relationship between spirituality and medicine. My personal struggles living with an incurable metastatic cancer.
Partnership for Prescription Assistance     > website
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Site that help people who are uninsured get treatment. Their services are free.
Rare Patient Voice     > website
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Helping patients and caregivers with rare diseases voice their opinions through surveys and interviews to improve medical products and services
Rock Scar Love     > website
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RockScar Love is inspiring passionate lives through clothing. We celebrate sexy scars, the lessons they teach us and the strength they create.
SCDAA     > website
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The vision for a national coordinated approach to addressing issues related to sickle cell disease was unveiled in 1971 when representatives of 15 community sickle cell organizations met at "Wingspread," a Racine, Wisconsin conference center, as guest of the Johnson Foundation. Out of that meeting, the National Association for Sickle Cell Disease was created.
Sickel Cell Foundation Support Group     > website
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The Sickle Cell Foundation Support Group, Inc. was established in 1997. Our mission is dedicated to engage with our global community in promoting Sickle Cell education to those afflicted with the disease and their care givers. Our vision is to be committed to total wellness through nutrition and supplementation for preventive health and management of Sickle Cell Disease and other hemoglobin disorders.
Sickle Cell Disease Association of Illinois (SCDAI)     > website
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ickle Cell Disease Association of Illinois’ (SCDAI) primary mission is to enhance the quality of life for people with sickle cell disease and their families. To effectively achieve this goal, SCDAI acts as an advocate for improved health care and services for sickle cell patients by educating and informing the community through outreach programs.
Sickle Cell Diva     > website
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Thank You for visiting my blog! Here you will find a glimpse of my life living with "Sickle Cell Anemia". This journey is in its 42nd year and it has been a long one. I hope along the way I can or have encouraged, educated, and engaged you in some form regarding this blood disorder.
Sickle Cell Information Center     > website
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The mission of this site is to provide sickle cell patient and professional education, news, research updates and world wide sickle cell resources.
State of California Sickle Cell Resources     > website
State of California sickle cell resources
The Sickle Cell Foundation of Georgia     > website
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Since 1971, the Sickle Cell Foundation of Georgia, Inc. has stood as a bastion of hope for victims of Sickle Cell and other abnormal hemoglobin. Dr. Delutha H. King, Jr. and the late Dr. Nelson McGhee, Jr. founded the organization to monitor Sickle Cell occurrences, share and advance knowledge and research with other organizations and, of course, to improve the quality of life of those battling the disease.
Very Bright Foundation     > website
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Very Bright Foundation is a non-profit organization formed to Break Sickle Silence® through education and inspiration.
Find A Cure Transit Sickle Cell Resources:
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