Collaboration is the key! Sometimes we may be the pilot and other times the co-pilot on a project, but our mission always includes ~ Sickle Cell and saving lives!
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J R Perry
www.lovedropradio.com
Singer, Songwriter, Record Producer, DJ, Activist, Talk Show Host . J.R. Perry III is on a mission to help find a cure for sickle cell anemia. J.R. has a major motivation for his mission for a cure. J.R. has a 7 year old son who was born with this disease and he has educated himself with years of research, networking with the medical community and also he has personally witnessed the multiple symptoms that this disease produces in his son by the many hospital visits. |
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The K.I.S. Foundation, Inc.
thekisfoundation.org
Mission Statement: To inform and educate the public and raise awareness about Sickle Cell Disease through community outreach programs and educational scholarships. We will also financially help support the efforts of research institutions to find a universal cure. Donations toward this cause are most welcomed. The KIS Foundation is a 501(c) 3, as such; all contributions are tax deductible to the fullest extent of the relevant IRS laws and regulations. Contact Info: 13351-D Riverside Drive, Suite 178, Sherman Oaks, CA 91423. 818 981-7819 [email protected] |
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Sickle Cell Cure Foundation, Inc.
sicklecellcurefoundation.org/
The Sickle Cell Cure Foundation, Inc. (SCCF) is a non-profit 501(c)(3) research foundation incorporated in 2006. SCCF chose the PHF Research Park as its world headquarters to conduct translational research using patented treatments aimed at curing two of mankind’s most devastating diseases: malaria and its allied blood disorder, sickle cell disease (SCD). |
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Sickle Cell Disease Foundation of California
www.scdfc.org
The Sickle Cell Disease Foundation of California was the first non-profit, social service sickle cell disease organization established in the United States. Founded in 1957, the SCDFC has maintained a viable and reputable organization for over 45 years. With a growing population of individuals with sickle cell disease and sickle cell trait, the primary focus of the SCDFC is to educate, screen and counsel those persons at risk of having children with sickle cell disease and other hemoglobin disorders. Contact Info: Sickle Cell Disease Foundation of California -NEW ADDRESS 5777 W. Century Blvd, Suite 1230, Los Angeles, California 90045,Phone: (310) 693-0247, Fax: (310) 216-0307, Email: [email protected]; www.scdfc.org |
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The Sickle Cell Foundation of Orange County
SCDFOC.org
The Sickle Cell Foundation of Orange County is an organization that provides services to individuals and families with Sickle Cell Disease as well as at-risk individuals for Sickle Cell Disease. It is our mission to educate, empower & equip children, youth, young adults, and adults with the authority and power to overcome the challenges of Sickle Cell Disease. To provide education among those who are dealing with the physical, mental, emotional and psychological complications of Sickle Cell Disease. We believe that everyone have a choice to "Live by Design and Not by Diagnosis". Contact Info: Star Simmons - President P.O. Box 3780 Mission Viejo, CA 92690 Work: 949-331-8121 Fax: 949-215-9136 [email protected] |
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Southern California Adult Sickle Cell Support Group
www.cayennewellness.com/
Dr. Carolyn Rowley heads the Cayenne Wellness Center and Children's Foundation and is the Facilitator of the Southern California Adult Sickle Cell Support Group For activities contact Dr. Rowley: [email protected] |
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The White House Luncheon Project, Dominique Friend
www.sickle.us/
Watch Dominique on Youtube http://www.youtube.com/watch?v=wZldNXUkjgQ&feature=email. Contact her by emailing [email protected] |
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SCD Soldier Network., Phyllis Zachery-Thomas
scdsoldiernetwork.com/
RIP Phyllis ~ We will always be CP's (Collaborative Partners)!!!! SCD Soldier Anthem: www.youtube.com/watch?v=5Gl02eTMmx8 SCD Soldier Anthem Video Final http://www.youtube.com/watch?v=X4MyH-Ub9_8 SCD Soldier Network - VideoBlog Week Two: www.youtube.com/watch?v=o_EEWnZLVo4 Contact Phyllis at (404) 933-1838 Email: [email protected] |
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Family Voices of California (FVCA)
www.familyvoicesofca.org/
MISSION Family Voices of California (FVCA) is a statewide collaborative of locally-based parent run centers working to ensure quality health care for children and youth with special health care needs. FVCA builds the capacity of parent centers throughout California to provide families with the information and support they need to make informed decisions about the health care of their children. FVCA provides information and a forum for parent centers and families to advocate for improved public and private policies, builds partnerships between professionals and families, and serves as a vital resource on health care. VISION The voice of families the vision of quality health care the future for children and youth with special health care needs Conrtact Info: Family Voices of California , 1663 Mission Street, 7th Floor, San Francisco, CA 94103, 415-282-7494; [email protected] |
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Sickle Cell Benefit Tour
sicklecellbenefittour.yolasite.com
A Future Activity - - - We're bring the real and updated facts about Sickle Cell through the arts, dialogue, and education. |
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WHAT'Z DA COUNT
www.whatzdacount.com
WDC on SCT has dedicated his Organization to educate the human race on Sickle Cell Trait (SCT is HbAS) also known as The Silent Killer, by distributing information and presentations, written and visual about SCT. Our Organization will travel the world to caution Children, Parents, Teachers, Coaches and all Branches of Service; the critical need of testing for the Sickle Cell Trait that can cause life-threatening complications of exercise, exertional heat illness (exertional rhabdomyolysis, heat stroke, or renal failure) or idiopathic sudden death. FOR MORE INFO CONTACT: SFC Farron Dozier, WHAT'Z DA COUNT, P O BOX 41416, Los Angeles, CA 90041. (323) 215-5384, [email protected] |
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Be The Match
www.marrow.org
Be The Match Registry/National Marrow Donor Program. Thousands of patients hope for a bone marrow donor who can make their life-saving transplant possible. They depend on people like you. You have the power to save a life. Take the first step today. |
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Cord Blood Forum
www.cordbloodforum.org
The primary mission of cordbloodforum.org is to serve patients for whom a hematopoietic cell transplant is indicated by disseminating information about the availability and effectiveness of cord blood transplants for children and adults. This will result in more appropriate utilization of this method of hematopoietic cell transplantation, which will serve many patients in need. Additionally, as the discipline of cord blood transplantation continues to evolve, communication among transplant physicians, transplant coordinators, cord blood bank personnel and patients will lead to clarification of numerous issues. |
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Parent's Guide to Cord Blood Foundation
parentsguidecordblood.org
Since 1998, the Parent's Guide to Cord Blood website has provided expectant parents with unbiased information about cord blood stem cells and cord blood banks. In 2007, the founder, Dr. Frances Verter, recruited a Board of Directors and we incorporated as a non-profit foundation. |
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StemCyte
www.stemcyteinc.com/home.html
StemCyte is dedicated to helping the world's physicians save more lives by providing high quality, safe and effective stem cell transplantation and therapy to all patients in need. Contact Info: StemCyte1589 W Industrial Park St. Covina, CA 91722 Toll Free: (866) 783-6298 (1-866-STEMCYTE) Local Ph: (626) 646-2500 [email protected] |
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National Cord Blood Program
www.nybloodcenter.org
Iraida Figueroa, Transplant Coordinator National Cord Blood Program, 45-01 Vernon Blvd., Long Island City, NY 11101 Ph: 718-752-4710 Fax: 718-752-4711 Email: [email protected] *Note: If you are not in the cord blood registry, please go to the PDF for Patient Registration, fill it out and send to Iraida! |
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Celebration Stem Cell Centre
www.csccaz.com
Rob Schemitsch Celebration Stem Cell Centre Director of Business Development 3495 S. Mercy Road Gilbert, AZ 85297 480-722-9963 Office 602-625-6910 Cell [email protected] |
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Save the Cord Foundation
www.savethecordfoundation.org
Contact info: Charis Ober, Co-Founder [email protected] 520-419-0269 120 S. Houghton Rd, Ste. 138, PMB 271, Tucson, AZ 85748 |
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Sereni Liquid Organix Green Tea Concentrate
www.liquidsereniteas.com
They are convenient concentrated liquid Green Teas tea packets in different flavored. Available at all Stater Bros. Markets in Southern California. You can also contact: Serenity Living LLC 8-D Village Loop RD PMB202 Pomona, CA 91766 (866) 780-2834 |
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Why Can't We Make A Difference
wcwmad.org
"Why Can't We Make A Difference" is here to help alleviate some of the stresses of individuals and families that can occur from life's trials and pressures. Our goal is to provide assistance and tangible aid to those individuals experiencing the difficulties that plague us all in our daily lives. We invite you to peruse our site, to find out how, together we can make a difference. If you are in need of assistance, we are here to serve. 5786 Rodeo Rd. Ste. 183 Los Angeles, CA. 90016 |
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Star's We Are and Associates
www.freewebs.com/starsweareandassociates
Nita L. Thompson Occupation: Business and Personal Empowerment Consultant / Success Coordinator; Health Advocate / Certified LAUSD Surrogate Parent Mission: To provide business and personal empowerment success techniques, that when applied, will redirect and change lives for the positive. Motto: "There are no problems, only solutions to your concerns!" |
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Sickle Cell Travel Arrangement website:
Myvortex365.com/surgesicklecell
I have a vision to set Sickle Cell Financially Free, globally!!! I ask each Sickle Cell Organization Globally to put the link with the Traveling info on every Sickle Cell and supporters website! Every Community Member tell everyone you know! Ask everyone you know to do what they normally do when finding their lowest fares, then check out our Surge Sickle Cell site! It will be lower, plus we have cost matching!!! With each purchase, 1/3 of our commission will go to any Sickle Cell non profit to grassroots organization of the client's choice or go into a nonrestrictive fund! I thought we don't have to beg for funds, we could ourselves and ask others to do what we do normally, just on our site! Everyone could help us help ourselves without coming out of our pockets any extra amounts!!! If you want to do this for your nonprofit, organization or for yourself, please see info below: Every Monday at 4 p.m. PST & Wednesday at 7 p.m. PST the travel membership has a webinar! Please log on 15mins early to join.Me/surge365ToFreedom2015 for audio dial 213-226-1066 pin number 714-545-836#. |
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Surge Sickle Cell Business Associates Membership Site:
Surge365.com/surgesicklecell
If you want to do this for your nonprofit, organization or for yourself, please see info below: Every Monday at 4 p.m. PST & Wednesday at 7 p.m. PST the travel membership has a webinar! Please log on 15mins early to join.Me/surge365ToFreedom2015 for audio dial 213-226-1066 pin number 714-545-836#. |
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American Pain Institute
www.AmericanPainInstitute.org/banner.htm
"Supporting physicians who treat chronic pain patients" |
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www.DoctorsofCourage
www.DoctorsofCourage.org
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Doctors of Courage
www.DoctorsofCourage.org
Pain Patient Physicians who are unfairly targeted by the USGovernment for properly treating Sickle Cell and other Pain Patients. |
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THE NATIONAL JUNETEENTH HOLIDAY CAMPAIGN! Wel
www.juneteenth.us
The official site for the: NATIONAL JUNETEENTH HOLIDAY CAMPAIGN! |
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Black Doctors Matter
www.BlackDoctorsMatter.com
Dedicated to black physician response to (1) the American Medical Association (AMA) Apology to African-American Physicians, (2) the ongoing attack on Black Physicians and (3) Advocating to stop the Mistreatment of Sickle Cell Patients! |
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National Pain Patients Coalition
www.PainPatientsCoalition.com
"Chronic pain patients helping chronic pain patients" |