The Sickle Cell Disease Association of America will create a collection of occasions and support opportunities for member organizations at the National Sickle Cell Awareness Month in September. Nationwide Sickle Cell Awareness Month was nominated by Congress to focus on the need for analysis and remedy for sickle cell disease.

Beverley Francis-Gibson, president and CEO of Sickle Cell Disease Association mentioned that “People and organizations are redirecting public places, buildings, and sites by distributing instructional data to consider sickle cell disease and dispelling myths about sickle cell disease with the participation of elected officials about sickle cell diseases Huh,”

The 2020 Sickle Cell Disease Therapeutics Conference will be organized by World Blood Therapeutics Inc. on September 15 at 9 am. In partnership with the Sickle Cell Disease Association, the conference supplies a discussion board to discuss new developments and future developments for the treatment of victims. sickle cell disease.

Will present health care corporations, opinion leaders, victims, policymakers, and others at the conference. Additional teaching and on-line registration should be done.

A Sickle Cell Awareness Month Twitter Social Gathering, an Internet Twitter dialogue hosted by the Sickle Cell Disease Affiliation, a place where individuals work together, share, study, and post a tweet using the hashtag #SickleCMMatters Have a good time, will be on September 21, 23. And register on line 25 from 12:30 to 1:30 pm.

Fight sickle cell disease by donating blood to the American Red Cross. Donors can make an appointment by downloading the American Red Cross Blood Donor App, visiting RedCrossBlood.org, or calling 1-800-7-16-2767. Sickle cell groups across the country will maintain nationwide sickle cell consciousness month opportunities through September, with halls, webcasts, walks and races, summits and seminars, and foundation stones throughout the city. Be taught more on-line.

Invites sickle cell disease affiliation organizations, company and federal peers, and supporters to use the hashtags #SickleCellMatters, #SickleCellMatters, #SickleCellA Awareness Month, # SCDAA20LA Awareness Month, and #SCDSCTMatters in social media posts about sickle cell disease through September is. Additional data, with a press package, flyers, and truth sheets, is accessible on-line.

Sickle cell disease is an inherited blood disease, which causes red blood cells to take the form of a sickle, resulting in friable blood preventing blood from reaching the body’s components. Because of this, individuals with sickle cell problems may experience anemia, jaundice, gallstones, stroke, electrical pain, organ injury, and untimely death. No general remedy exists. (Sickle cell disease..net)

The Sickle Cell Disease Association of America advocates for people affected by sickle cell conditions and empowers community-based organizations to maximize the standard of living and elevate public consciousness while seeking a common remedy. Affiliations and more than 50 member organizations support sickle cell analysis, public {and professional} health education, and affected individuals and neighborhood providers.

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