Searching for Sickle Cell Anemia Support Website information? Find all needed info by using official links provided below.
https://www.sicklecellsociety.org/
The Sickle Cell Society believes that individuals with sickle cell disorder have the right to quality care. This can only be achieved if funding is made available to educate health carers and other professionals about the condition. The Society aims to provide this.
https://www.sicklecelldisease.org/
SCDAA Partners with The Pain Community to Support the Sickle Cell Community by Providing Comprehensive Integrative Pain Management Educational Information. Sickle Cell Disease Association of America, Inc. (SCDAA) and The Pain Community are proud to announce a new partnership that will...
https://mythreesicklers.org/
MTS Sickle Cell Foundation, Inc. aims to increase the public’s awareness of sickle cell anemia. The organization will support awareness, education and research pertaining to sickle cell anemia as well as provide support to families affected by this life threatening disease …
The Sickle Cell Thalassemia Patients Network is committed to maintaining the privacy of our website visitors and donors and to maintain the confidentiality of all personal Information. The personal information you provide to us is solely utilized to receive and process your donation or to process any information requests you may have.
http://www.scdcoalition.org/
Sickle Cell Disease is an inherited blood disorder that causes red blood cells to form into a crescent shape, like a sickle. These cells break apart easily, clump together, and stick to the walls of blood vessels, blocking the flow of blood, which can lead to a range of serious health issues.
Please read this disclaimer carefully before using the American Sickle Cell Anemia Association’s website, or should you ask for advice or assistance on our website or through our social media direct messenger. All information is merely for educational and informational purposes for sickle cell anemia.
https://www.cdc.gov/ncbddd/sicklecell/links.html
Tips for preventing a sickle cell crisis. American Sickle Cell Anemia Association external icon Information and support groups. Clinical Trials external icon Up-to-date information on sickle cell disease clinical research trials. National Heart, Lung and Blood Institute external icon Sickle cell information, tips for healthy living, and resources.
https://www.sicklecelltx.org/
The Sickle Cell Association Marc Thomas Foundation has been a blessing to me. It has provided me with support during difficult times with my illness. I've met many other patients over the years through the agency that have became great friends.
Sickle cell disease affects about 100,000 people in the U.S., according to the U.S. Centers for Disease Control and Prevention (CDC). A 2009 study published in the journal Pediatric Blood and Cancer noted that in 2005, sickle disease cost an average of $11,702 for children under Medicaid and $14,772 for patients with employer-sponsored insurance.
https://sicklecellanemianews.com/2017/12/05/online-platform-created-support-sickle-cell-community/
Dec 05, 2017 · A new online platform, called oneSCDvoice.com, will help those affected by sickle cell disease (SCD) by offering free access to comprehensive support and a robust knowledge network .. rareLife solutions, the health tech, design and research team behind oneSCDvoice and other custom rare disease platforms, will launch the modular community system later this month.
How to find Sickle Cell Anemia Support Website information?
Follow the instuctions below:
- Choose an official link provided above.
- Click on it.
- Find company email address & contact them via email
- Find company phone & make a call.
- Find company address & visit their office.
